NOAEL Studies Cosmetic Ingredient

Thiram NOAEL Studies

INCI: THIRAM (TETRAMETHYLTHIURAM DISULFIDE) — NO COSMETIC INCI ASSIGNMENT

CAS: 137-26-8

Raw No Observed Adverse Effect Level endpoint records grouped by source. This page does not render calculated Margin of Safety values.

ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip 36 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 1000 mg/kg bw/day rabbit - - short-term repeated dose toxicity: dermal dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=02e0c25b-686e-4b72-85ea-6b330c61cfe1_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=02e0c25b-686e-4b72-85ea-6b330c61cfe1/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityDermal; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-11-12; basis=body weight and weight gain; key_result=true; entry_uuid=ae19c21b-3d44-452d-8c3a-ef06d8070e24
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 15 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=83357a3a-e769-4c75-9f6b-910beffc2e5d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=83357a3a-e769-4c75-9f6b-910beffc2e5d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1988; ReportDate=1988-01-28; basis=fetal/pup body weight changes; key_result=true; entry_uuid=30b8e14a-ffe2-462f-b1a8-b0d3b9abf9c8
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 150 mg/kg bw/day rat oral: gavage - neurotoxicity: acute oral dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=0b9d24b8-0126-459d-89f7-eee317e75c76_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=0b9d24b8-0126-459d-89f7-eee317e75c76/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=Neurotoxicity; literature=Name=Unnamed; ReferenceYear=1993; ReportDate=1993-07-26; basis=other:; key_result=false; entry_uuid=1fd88ec5-3799-40da-87c0-22ed1046bd4b
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 20 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=3550e3a2-60e4-496f-9dd2-ae0a394500dd_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=3550e3a2-60e4-496f-9dd2-ae0a394500dd/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1986; ReportDate=1986-11-27; basis=body weight and weight gain; key_result=false; entry_uuid=f1df5349-dd7d-456a-93ae-bbc762caf009
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 300 mg/kg bw/day rat oral: gavage - short-term repeated dose toxicity: oral dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=72ea5e5e-e767-46bf-98aa-4b855be624fb_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=72ea5e5e-e767-46bf-98aa-4b855be624fb/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=2015; ReportDate=2015-04-01; basis=body weight and weight gain; key_result=true; entry_uuid=c7853f29-7237-43ae-b4b1-12fd28e11c02
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 1000 mg/kg bw/day rabbit - - short-term repeated dose toxicity: dermal dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=02e0c25b-686e-4b72-85ea-6b330c61cfe1_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=02e0c25b-686e-4b72-85ea-6b330c61cfe1/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityDermal; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-11-12; basis=body weight and weight gain; key_result=true; entry_uuid=ae19c21b-3d44-452d-8c3a-ef06d8070e24
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 15 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=83357a3a-e769-4c75-9f6b-910beffc2e5d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=83357a3a-e769-4c75-9f6b-910beffc2e5d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1988; ReportDate=1988-01-28; basis=fetal/pup body weight changes; key_result=true; entry_uuid=30b8e14a-ffe2-462f-b1a8-b0d3b9abf9c8
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 150 mg/kg bw/day rat oral: gavage - neurotoxicity: acute oral dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=0b9d24b8-0126-459d-89f7-eee317e75c76_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=0b9d24b8-0126-459d-89f7-eee317e75c76/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=Neurotoxicity; literature=Name=Unnamed; ReferenceYear=1993; ReportDate=1993-07-26; basis=other:; key_result=false; entry_uuid=1fd88ec5-3799-40da-87c0-22ed1046bd4b
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 20 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=3550e3a2-60e4-496f-9dd2-ae0a394500dd_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=3550e3a2-60e4-496f-9dd2-ae0a394500dd/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1986; ReportDate=1986-11-27; basis=body weight and weight gain; key_result=false; entry_uuid=f1df5349-dd7d-456a-93ae-bbc762caf009
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 300 mg/kg bw/day rat oral: gavage - short-term repeated dose toxicity: oral dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=72ea5e5e-e767-46bf-98aa-4b855be624fb_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=72ea5e5e-e767-46bf-98aa-4b855be624fb/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=2015; ReportDate=2015-04-01; basis=body weight and weight gain; key_result=true; entry_uuid=c7853f29-7237-43ae-b4b1-12fd28e11c02
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 1000 mg/kg bw/day rabbit - - short-term repeated dose toxicity: dermal dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=02e0c25b-686e-4b72-85ea-6b330c61cfe1_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=02e0c25b-686e-4b72-85ea-6b330c61cfe1/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityDermal; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-11-12; basis=body weight and weight gain; key_result=true; entry_uuid=ae19c21b-3d44-452d-8c3a-ef06d8070e24
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 15 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=83357a3a-e769-4c75-9f6b-910beffc2e5d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=83357a3a-e769-4c75-9f6b-910beffc2e5d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1988; ReportDate=1988-01-28; basis=fetal/pup body weight changes; key_result=true; entry_uuid=30b8e14a-ffe2-462f-b1a8-b0d3b9abf9c8
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 150 mg/kg bw/day rat oral: gavage - neurotoxicity: acute oral dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=0b9d24b8-0126-459d-89f7-eee317e75c76_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=0b9d24b8-0126-459d-89f7-eee317e75c76/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=Neurotoxicity; literature=Name=Unnamed; ReferenceYear=1993; ReportDate=1993-07-26; basis=other:; key_result=false; entry_uuid=1fd88ec5-3799-40da-87c0-22ed1046bd4b
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 20 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=3550e3a2-60e4-496f-9dd2-ae0a394500dd_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=3550e3a2-60e4-496f-9dd2-ae0a394500dd/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1986; ReportDate=1986-11-27; basis=body weight and weight gain; key_result=false; entry_uuid=f1df5349-dd7d-456a-93ae-bbc762caf009
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 300 mg/kg bw/day rat oral: gavage - short-term repeated dose toxicity: oral dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=72ea5e5e-e767-46bf-98aa-4b855be624fb_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=72ea5e5e-e767-46bf-98aa-4b855be624fb/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=2015; ReportDate=2015-04-01; basis=body weight and weight gain; key_result=true; entry_uuid=c7853f29-7237-43ae-b4b1-12fd28e11c02
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 300 mg/kg bw/day rabbit - - short-term repeated dose toxicity: dermal dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=02e0c25b-686e-4b72-85ea-6b330c61cfe1_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=02e0c25b-686e-4b72-85ea-6b330c61cfe1/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityDermal; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-11-12; basis=other:; key_result=true; entry_uuid=fa48b909-f577-42e9-bdb1-ec61768f007e
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL <=100 mg/kg bw/day rabbit - - short-term repeated dose toxicity: dermal dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=02e0c25b-686e-4b72-85ea-6b330c61cfe1_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=02e0c25b-686e-4b72-85ea-6b330c61cfe1/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityDermal; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-11-12; basis=other:; key_result=true; upper_value=100; entry_uuid=31828de1-b0ca-44be-b918-c3b5b62ce4a3
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL >=10 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=d4236cd5-b438-4af6-a776-9a9bf95a562d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=d4236cd5-b438-4af6-a776-9a9bf95a562d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-02-18; basis=other:; key_result=true; entry_uuid=749e69a4-2227-466a-8167-1fd6cf293cb2
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 5 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=d4236cd5-b438-4af6-a776-9a9bf95a562d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=d4236cd5-b438-4af6-a776-9a9bf95a562d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-02-18; basis=other:; key_result=true; entry_uuid=993cdc3d-78f6-47a7-96b1-0306745a2d50
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 2.5 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=9ceb7105-1ce3-4ddd-bb9d-d800552184bc_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=9ceb7105-1ce3-4ddd-bb9d-d800552184bc/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1988; ReportDate=1988-03-15; basis=other:; key_result=true; entry_uuid=0d755818-564f-4f44-88f4-08655e5d1798
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL <=7.5 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=83357a3a-e769-4c75-9f6b-910beffc2e5d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=83357a3a-e769-4c75-9f6b-910beffc2e5d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1988; ReportDate=1988-01-28; basis=body weight and weight gain; key_result=true; upper_value=7.5; entry_uuid=dbbc9da9-dc73-4c95-ad6e-b67f797e4fe2
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 1000 mg/kg bw/day rat oral: gavage - short-term repeated dose toxicity: oral dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=72ea5e5e-e767-46bf-98aa-4b855be624fb_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=72ea5e5e-e767-46bf-98aa-4b855be624fb/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=2015; ReportDate=2015-04-01; basis=other:; key_result=false; entry_uuid=ce3db584-176f-428c-8445-9d0cc3605978
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 300 mg/kg bw/day rabbit - - short-term repeated dose toxicity: dermal dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=02e0c25b-686e-4b72-85ea-6b330c61cfe1_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=02e0c25b-686e-4b72-85ea-6b330c61cfe1/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityDermal; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-11-12; basis=other:; key_result=true; entry_uuid=fa48b909-f577-42e9-bdb1-ec61768f007e
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL <=100 mg/kg bw/day rabbit - - short-term repeated dose toxicity: dermal dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=02e0c25b-686e-4b72-85ea-6b330c61cfe1_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=02e0c25b-686e-4b72-85ea-6b330c61cfe1/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityDermal; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-11-12; basis=other:; key_result=true; upper_value=100; entry_uuid=31828de1-b0ca-44be-b918-c3b5b62ce4a3
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL >=10 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=d4236cd5-b438-4af6-a776-9a9bf95a562d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=d4236cd5-b438-4af6-a776-9a9bf95a562d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-02-18; basis=other:; key_result=true; entry_uuid=749e69a4-2227-466a-8167-1fd6cf293cb2
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 5 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=d4236cd5-b438-4af6-a776-9a9bf95a562d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=d4236cd5-b438-4af6-a776-9a9bf95a562d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-02-18; basis=other:; key_result=true; entry_uuid=993cdc3d-78f6-47a7-96b1-0306745a2d50
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 2.5 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=9ceb7105-1ce3-4ddd-bb9d-d800552184bc_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=9ceb7105-1ce3-4ddd-bb9d-d800552184bc/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1988; ReportDate=1988-03-15; basis=other:; key_result=true; entry_uuid=0d755818-564f-4f44-88f4-08655e5d1798
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL <=7.5 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=83357a3a-e769-4c75-9f6b-910beffc2e5d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=83357a3a-e769-4c75-9f6b-910beffc2e5d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1988; ReportDate=1988-01-28; basis=body weight and weight gain; key_result=true; upper_value=7.5; entry_uuid=dbbc9da9-dc73-4c95-ad6e-b67f797e4fe2
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 1000 mg/kg bw/day rat oral: gavage - short-term repeated dose toxicity: oral dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=72ea5e5e-e767-46bf-98aa-4b855be624fb_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=72ea5e5e-e767-46bf-98aa-4b855be624fb/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=2015; ReportDate=2015-04-01; basis=other:; key_result=false; entry_uuid=ce3db584-176f-428c-8445-9d0cc3605978
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 300 mg/kg bw/day rabbit - - short-term repeated dose toxicity: dermal dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=02e0c25b-686e-4b72-85ea-6b330c61cfe1_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=02e0c25b-686e-4b72-85ea-6b330c61cfe1/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityDermal; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-11-12; basis=other:; key_result=true; entry_uuid=fa48b909-f577-42e9-bdb1-ec61768f007e
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL <=100 mg/kg bw/day rabbit - - short-term repeated dose toxicity: dermal dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=02e0c25b-686e-4b72-85ea-6b330c61cfe1_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=02e0c25b-686e-4b72-85ea-6b330c61cfe1/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityDermal; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-11-12; basis=other:; key_result=true; upper_value=100; entry_uuid=31828de1-b0ca-44be-b918-c3b5b62ce4a3
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL >=10 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=d4236cd5-b438-4af6-a776-9a9bf95a562d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=d4236cd5-b438-4af6-a776-9a9bf95a562d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-02-18; basis=other:; key_result=true; entry_uuid=749e69a4-2227-466a-8167-1fd6cf293cb2
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 5 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=d4236cd5-b438-4af6-a776-9a9bf95a562d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=d4236cd5-b438-4af6-a776-9a9bf95a562d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1992; ReportDate=1992-02-18; basis=other:; key_result=true; entry_uuid=993cdc3d-78f6-47a7-96b1-0306745a2d50
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 2.5 mg/kg bw/day rabbit oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=9ceb7105-1ce3-4ddd-bb9d-d800552184bc_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=9ceb7105-1ce3-4ddd-bb9d-d800552184bc/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1988; ReportDate=1988-03-15; basis=other:; key_result=true; entry_uuid=0d755818-564f-4f44-88f4-08655e5d1798
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL <=7.5 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=83357a3a-e769-4c75-9f6b-910beffc2e5d_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=83357a3a-e769-4c75-9f6b-910beffc2e5d/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1988; ReportDate=1988-01-28; basis=body weight and weight gain; key_result=true; upper_value=7.5; entry_uuid=dbbc9da9-dc73-4c95-ad6e-b67f797e4fe2
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 1000 mg/kg bw/day rat oral: gavage - short-term repeated dose toxicity: oral dossier=502ddbbe-8660-42be-8155-be5a2f6657e5.i6z; document=72ea5e5e-e767-46bf-98aa-4b855be624fb_502ddbbe-8660-42be-8155-be5a2f6657e5.i6d; document_key=72ea5e5e-e767-46bf-98aa-4b855be624fb/502ddbbe-8660-42be-8155-be5a2f6657e5; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=2015; ReportDate=2015-04-01; basis=other:; key_result=false; entry_uuid=ce3db584-176f-428c-8445-9d0cc3605978
EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx 6 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx NOAEL =1.6 mg/kg bw/day Rat - - chronic/long term toxicity EFSA - 2017 - OutputID 3606 - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx NOAEL =0.84 mg/kg bw/day Dog - 365 days chronic/long term toxicity EFSA - 2017 - OutputID 3606 - haematology - hepatotoxicity - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx NOAEL =1.5 mg/kg bw/day Rat - 730 days chronic/long term toxicity EFSA - 2017 - OutputID 3606 - body weight - systemic - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx NOAEL <7.5 mg/kg bw/day Rat - - reproduction toxicity EFSA - 2017 - OutputID 3606 - body weight - systemic - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx NOAEL =3 mg/kg bw/day Rat - - reproduction toxicity EFSA - 2017 - OutputID 3606 - body weight - systemic - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx NOAEL =2 mg/kg bw/day Dog - 90 days subchronic EFSA - 2017 - OutputID 3606 - haematology - hepatotoxicity - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EFSA_OpenFoodTox_EFSA_ReferenceValues.xlsx 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EFSA_OpenFoodTox_EFSA_ReferenceValues.xlsx ADI =0.01 mg/kg bw/day Consumers - - ADI EFSA - 2017 - OutputID 3606 - Consumers - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EFSA_OpenFoodTox_EFSA_ReferenceValues.xlsx ADI =0.01 mg/kg bw/day Consumers - - ADI EFSA - 2017 - OutputID 3606 - Consumers - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EFSA_OpenFoodTox_EFSA_ReferenceValues.xlsx ARfD =0.025 mg/kg bw/day Consumers - - ARfD EFSA - 2017 - OutputID 3606 - Consumers - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EFSA_OpenFoodTox_EFSA_ReferenceValues.xlsx ARfD =0.025 mg/kg bw/day Consumers - - ARfD EFSA - 2017 - OutputID 3606 - Consumers - Peer review of the pesticide risk assessment of the active substance thiram - doi:10.2903/j.efsa.2017.4700
EPA_IRIS_iris_rfd_systems.csv 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EPA_IRIS_iris_rfd_systems.csv NOEL =5 mg/kg/day - oral chronic IRIS chronic oral RfD system PoD row_hash=840487bde155d1b7; file=iris_rfd_systems.csv; kind=point_of_departure; raw_column=point_of_departure; raw_value=NOEL : 5 mg/kg-day; system=Nervous; basis=Neurotoxicity; point_of_departure=NOEL : 5 mg/kg-day; composite_uf=1000; confidence=Low; dtxsid=DTXSID5021332; detail_url=https://iris.epa.gov/ChemicalLanding/&substance_nmbr=267; rfd_pdf_url=https://iris.epa.gov/static/pdfs/0267_summary.pdf
EPA_IRIS_iris_rfd_systems.csv RfD =0.005 mg/kg/day - oral chronic IRIS chronic oral RfD system row_hash=f665b7bdf24592c5; file=iris_rfd_systems.csv; kind=reference_value; raw_column=rfd_mg_per_kg_day; raw_value=5e-3; system=Nervous; basis=Neurotoxicity; point_of_departure=NOEL : 5 mg/kg-day; composite_uf=1000; confidence=Low; dtxsid=DTXSID5021332; detail_url=https://iris.epa.gov/ChemicalLanding/&substance_nmbr=267; rfd_pdf_url=https://iris.epa.gov/static/pdfs/0267_summary.pdf
IARC Monographs 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
IARC Monographs IARC carcinogenicity classification 3 IARC group - - 1990 IARC Monographs {"additional_info":"volume_publication_year=1991","evaluation_year":1990,"source_table":"iarc_classifications","volume":"Sup 7, 53"}
IARC Monographs IARC carcinogenicity classification 3 IARC group - - 1990 IARC Monographs {"additional_info":"volume_publication_year=1991","evaluation_year":1990,"source_table":"iarc_classifications","volume":"Sup 7, 53"}
IARC Monographs IARC carcinogenicity classification 3 IARC group - - 1990 IARC Monographs {"additional_info":"volume_publication_year=1991","evaluation_year":1990,"source_table":"iarc_classifications","volume":"Sup 7, 53"}
INCHEM_WHO_jmpr_jmpmono_v065pr41 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
INCHEM_WHO_jmpr_jmpmono_v065pr41 ADI range:0-0.0250.025 mg/kg bw/day - - - Health guidance value document_id=jmpr_jmpmono_v065pr41; title=041. Thiram (FAO Meeting Report PL/1965/10/1); path=mirror/documents/jmpr/jmpmono/v065pr41.htm; row_hash=a626e3fa292ff37b; raw_unit=mg/kg; context=An effect was found in the chick at 6.8 mg/kg body-weight.) Estimate of acceptable daily intake for man 0-0.025 mg/kg body-weight.
NTP_ICE_acute_dermal 5 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_acute_dermal EPA classification 3 unitless Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=1283; Record_ID=acute_dermal_234; Data_Type=In Vivo; Formulation_ID=MIX227; Formulation_Name=Foundation Lite; Percent_Active_Ingredient=6.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Dermal Toxicity; Endpoint=EPA classification; Response=3.0; Response_Unit=Unitless; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_dermal EPA classification 4 unitless Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=1287; Record_ID=acute_dermal_436; Data_Type=In Vivo; Formulation_ID=MIX430; Formulation_Name=Sativa IMX Max; Percent_Active_Ingredient=10.78; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Dermal Toxicity; Endpoint=EPA classification; Response=4.0; Response_Unit=Unitless; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_dermal GHS classification 5 unitless Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=1284; Record_ID=acute_dermal_148; Data_Type=In Vivo; Formulation_ID=MIX144; Formulation_Name=DeerPro Winter Animal Repellant; Percent_Active_Ingredient=25.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Dermal Toxicity; Endpoint=GHS classification; Response=5; Response_Unit=Unitless; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_dermal LD50 >5000 mg/kg Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=1281; Record_ID=acute_dermal_148; Data_Type=In Vivo; Formulation_ID=MIX144; Formulation_Name=DeerPro Winter Animal Repellant; Percent_Active_Ingredient=25.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Dermal Toxicity; Endpoint=LD50; Response_Modifier=>; Response=5000; Response_Unit=mg/kg; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_dermal LD50 >2000 mg/kg Rat Dermal - In Vivo; Rat Acute Dermal Toxicity sheet=Data; excel_row=1282; Record_ID=acute_dermal_234; Data_Type=In Vivo; Formulation_ID=MIX227; Formulation_Name=Foundation Lite; Percent_Active_Ingredient=6.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Dermal Toxicity; Endpoint=LD50; Response_Modifier=>; Response=2000.0; Response_Unit=mg/kg; Species=Rat; Route=Dermal; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_inhalation 9 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_acute_inhalation EPA Classification 3 unitless - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2814; Record_ID=acute_inhalation_160; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX227; Formulation_Name=Foundation Lite; Percent_Active_Ingredient=6.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Inhalation Toxicity; Endpoint=EPA Classification; Response=3; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_inhalation GHS Classification 4 unitless - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2804; Record_ID=acute_inhalation_160; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX227; Formulation_Name=Foundation Lite; Percent_Active_Ingredient=6.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Inhalation Toxicity; Endpoint=GHS Classification; Response=4; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_inhalation GHS Classification 5 unitless - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2808; Record_ID=acute_inhalation_343; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX430; Formulation_Name=Sativa IMX Max; Percent_Active_Ingredient=10.78; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Inhalation Toxicity; Endpoint=GHS Classification; Response=5; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_inhalation LC50 4.42 mg/L - Inhalation Duration=4 hr In Vivo; AcuteInhalNICEATM; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2802; Record_ID=acute_inhalation_1665; Data_Type=In Vivo; Internal_Data_Source=AcuteInhalNICEATM; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response=4.42; Response_Unit=mg/L; Reference=NIOSH; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_inhalation LC50 >5.13 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2803; Record_ID=acute_inhalation_343; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX430; Formulation_Name=Sativa IMX Max; Percent_Active_Ingredient=10.78; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response_Modifier=>; Response=5.13; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_inhalation LC50 0.5 mg/L - Inhalation Duration=4 hr In Vivo; AcuteInhalNICEATM; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2805; Record_ID=acute_inhalation_1185; Data_Type=In Vivo; Internal_Data_Source=AcuteInhalNICEATM; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response=0.5; Response_Unit=mg/L; Reference=ChemIDplus; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_inhalation LC50 >2.54 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2806; Record_ID=acute_inhalation_400; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX494; Formulation_Name=Tital FL; Percent_Active_Ingredient=9.49; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response_Modifier=>; Response=2.54; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_inhalation LC50 1.4 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2810; Record_ID=acute_inhalation_160; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX227; Formulation_Name=Foundation Lite; Percent_Active_Ingredient=6.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response=1.4; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_inhalation LC50 2.06 mg/L - Inhalation - In Vivo; AcuteInhal6pack; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2811; Record_ID=acute_inhalation_90; Data_Type=In Vivo; Internal_Data_Source=AcuteInhal6pack; Formulation_ID=MIX144; Formulation_Name=DeerPro Winter Animal Repellant; Percent_Active_Ingredient=25.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response=2.06; Response_Unit=mg/L; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_acute_oral 15 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_acute_oral EPA classification =4 Unitless Rat (Male/Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12601; row=8587; data_type=In Vivo; mixture=Mixture; formulation_id=MIX227; formulation_name=Foundation Lite; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=6.8; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral EPA classification =3 Unitless Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12960; row=8591; data_type=In Vivo; mixture=Mixture; formulation_id=MIX430; formulation_name=Sativa IMX Max; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=10.78; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral EPA classification =4 Unitless Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12457; row=8596; data_type=In Vivo; mixture=Mixture; formulation_id=MIX144; formulation_name=DeerPro Winter Animal Repellant; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=25.8; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral EPA classification =4 Unitless Rat (Male/Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_13028; row=8601; data_type=In Vivo; mixture=Mixture; formulation_id=MIX494; formulation_name=Tital FL; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=9.49; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral GHS classification =5 Unitless Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12457; row=8604; data_type=In Vivo; mixture=Mixture; formulation_id=MIX144; formulation_name=DeerPro Winter Animal Repellant; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=25.8; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral GHS classification =5 Unitless Rat (Male) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_13030; row=8605; data_type=In Vivo; mixture=Mixture; formulation_id=MIX494; formulation_name=Tital FL; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=9.49; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral GHS classification =5 Unitless Rat (Male/Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12601; row=8606; data_type=In Vivo; mixture=Mixture; formulation_id=MIX227; formulation_name=Foundation Lite; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=6.8; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral GHS classification =5 Unitless Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12960; row=8609; data_type=In Vivo; mixture=Mixture; formulation_id=MIX430; formulation_name=Sativa IMX Max; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=10.78; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral LD50 =3129 mg/kg bw Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12960; row=8585; data_type=In Vivo; mixture=Mixture; formulation_id=MIX430; formulation_name=Sativa IMX Max; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=10.78; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral LD50 >5000 mg/kg bw Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12457; row=8586; data_type=In Vivo; mixture=Mixture; formulation_id=MIX144; formulation_name=DeerPro Winter Animal Repellant; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=25.8; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral LD50 >5000 mg/kg bw Rat (Male) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_12605; row=8590; data_type=In Vivo; mixture=Mixture; formulation_id=MIX227; formulation_name=Foundation Lite; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=6.8; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral LD50 >5000 mg/kg bw Rat (Female) oral acute Rat Acute Oral Toxicity Studies submitted to EPA in support of pesticide registration applications (undated); record_id=acute_oral_13029; row=8593; data_type=In Vivo; mixture=Mixture; formulation_id=MIX494; formulation_name=Tital FL; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; percent_active_ingredient=9.49; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral LD50 =560 mg/kg bw Rat oral acute Rat Acute Oral Toxicity NLM Hazardous Substances Data Bank (undated); record_id=acute_oral_2410; row=8597; data_type=In Vivo; mixture=Chemical; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; dtxsid=DTXSID5021332; url=https://pubchem.ncbi.nlm.nih.gov/; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral LD50 >1800 mg/kg bw Rat oral acute Rat Acute Oral Toxicity record_id=acute_oral_2412; row=8598; data_type=In Vivo; mixture=Chemical; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_acute_oral LD50 <2700 mg/kg bw Rat oral acute Rat Acute Oral Toxicity record_id=acute_oral_2414; row=8599; data_type=In Vivo; mixture=Chemical; chemical_name=Thiram; preferred_name=Bis(dimethylaminothiocarbonyl) disulfide; dtxsid=DTXSID5021332; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; url_cebs=https://doi.org/10.22427/NTP-DATA-DTXSID5021332; source_file=acute_oral.xlsx
NTP_ICE_adme_parameters 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_adme_parameters Clint 816 uL/min/10^6 cells Human - - Measured; httk, Human Hepatic Intrinsic Clearance sheet=Data; excel_row=1969; Record_ID=adme_parameters_1093; Data_Type=Measured; DTXSID=DTXSID5021332; Assay=httk, Human Hepatic Intrinsic Clearance; Endpoint=Clint; Response=816.0; Response_Unit=ul/min/10^6 cells; Species=Human; Reference=httk2.3.1, Wambaugh 2019; URL=https://cran.r-project.org/web/packages/httk/index.html; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_adme_parameters Fu 3.86e-8 fraction Human - - Measured; httk, Human Plasma Fraction Unbound sheet=Data; excel_row=1968; Record_ID=adme_parameters_1093; Data_Type=Measured; DTXSID=DTXSID5021332; Assay=httk, Human Plasma Fraction Unbound; Endpoint=Fu; Response=3.86e-08; Response_Unit=Unitless Fraction; Species=Human; Reference=httk2.3.1, Wambaugh 2019; URL=https://cran.r-project.org/web/packages/httk/index.html; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_cancer 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_cancer IARC group 3 unitless - - - WOE; IARC Carcinogenicity sheet=Data; excel_row=5698; Record_ID=cancer_6778; Data_Type=WOE; Formulation_Name=Thiram; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=IARC Carcinogenicity; Endpoint=IARC group; Response=3; Response_Unit=Unitless; URL=http://publications.iarc.fr/139; http://publications.iarc.fr/71; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_dart 7 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_dart LOEL 7.5 mg/kg bw/day Rat Oral - In Vivo; DART, In life observation sheet=Data; excel_row=78621; Record_ID=dart_17126; Data_Type=In Vivo; DTXSID=DTXSID5021332; Assay=DART, In life observation; Endpoint=LOEL; Response=7.5; Response_Unit=mg/kg/day; Species=Rat; Strain=Sprague Dawley (CD); Sex=Female; Life_Stage=Adult; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C0005910;CUI;Body Weight|UMLS;C3540840;CUI;Sign or Symptom|UMLS;C0043094;CUI;Weight Gain; Reference=ToxRefDB v2 , ID = 3546; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_dart LOEL 7.5 mg/kg bw/day Rat Oral - In Vivo; DART, In life observation sheet=Data; excel_row=78622; Record_ID=dart_17127; Data_Type=In Vivo; DTXSID=DTXSID5021332; Assay=DART, In life observation; Endpoint=LOEL; Response=7.5; Response_Unit=mg/kg/day; Species=Rat; Strain=Sprague Dawley (CD); Sex=Female; Life_Stage=Adult; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C3540840;CUI;Sign or Symptom; Reference=ToxRefDB v2 , ID = 3546; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_dart LOEL 7.5 mg/kg bw/day Rat Oral - In Vivo; DART, In life observation sheet=Data; excel_row=78623; Record_ID=dart_17188; Data_Type=In Vivo; DTXSID=DTXSID5021332; Assay=DART, In life observation; Endpoint=LOEL; Response=7.5; Response_Unit=mg/kg/day; Species=Rat; Strain=Sprague Dawley (CD); Sex=Female; Life_Stage=Adult; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C3540840;CUI;Sign or Symptom|UMLS;C0205204;CUI;Scab; Reference=ToxRefDB v2 , ID = 3546; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_dart LOEL 7.5 mg/kg bw/day Rat Oral - In Vivo; DART, In life observation sheet=Data; excel_row=78624; Record_ID=dart_17189; Data_Type=In Vivo; DTXSID=DTXSID5021332; Assay=DART, In life observation; Endpoint=LOEL; Response=7.5; Response_Unit=mg/kg/day; Species=Rat; Strain=Sprague Dawley (CD); Sex=Female; Life_Stage=Adult; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C3540840;CUI;Sign or Symptom|UMLS;C0151907;CUI;Discoloration of skin; Reference=ToxRefDB v2 , ID = 3546; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_dart LOEL 15 mg/kg bw/day Rat Oral - In Vivo; DART, Developmental malformation sheet=Data; excel_row=78625; Record_ID=dart_17207; Data_Type=In Vivo; DTXSID=DTXSID5021332; Assay=DART, Developmental malformation; Endpoint=LOEL; Response=15; Response_Unit=mg/kg/day; Species=Rat; Strain=Sprague Dawley (CD); Sex=Male/Female; Life_Stage=Fetal; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C0000768;CUI;Congenital Abnormality|UMLS;C0265509;CUI;Congenital anomaly of skeletal bone|UMLS;C1282719;CUI;Incomplete ossification; Reference=ToxRefDB v2 , ID = 3546; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_dart LOEL 15 mg/kg bw/day Rat Oral - In Vivo; DART, Developmental malformation sheet=Data; excel_row=78626; Record_ID=dart_17208; Data_Type=In Vivo; DTXSID=DTXSID5021332; Assay=DART, Developmental malformation; Endpoint=LOEL; Response=15; Response_Unit=mg/kg/day; Species=Rat; Strain=Sprague Dawley (CD); Sex=Male/Female; Life_Stage=Fetal; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C0000768;CUI;Congenital Abnormality|UMLS;C0265509;CUI;Congenital anomaly of skeletal bone|UMLS;C1806781;CUI;Short|UMLS;C1883702;CUI;Supernumerary; Reference=ToxRefDB v2 , ID = 3546; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_dart LOEL 7.5 mg/kg bw/day Rat Oral - In Vivo; DART, In life observation sheet=Data; excel_row=78627; Record_ID=dart_17128; Data_Type=In Vivo; DTXSID=DTXSID5021332; Assay=DART, In life observation; Endpoint=LOEL; Response=7.5; Response_Unit=mg/kg/day; Species=Rat; Strain=Sprague Dawley (CD); Sex=Female; Life_Stage=Adult; Route=Oral; Critical_Effect=Yes; Unified_Medical_Language_System=UMLS;C3540840;CUI;Sign or Symptom|UMLS;C0002170;CUI;Alopecia; Reference=ToxRefDB v2 , ID = 3546; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_endocrine 7 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_endocrine AC50 25.92490805 uM - - - ARPathway2016; AR Pathway Model, Agonist sheet=Integrated_approaches; excel_row=5628; RecordID=ARPathway2016_70; DatasetName=ARPathway2016; DTXSID=DTXSID5021332; Assay=AR Pathway Model, Agonist; Endpoint=AC50; Response=25.92490805; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_endocrine AC50 15.8495315173844 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=5634; RecordID=ERPathway2016_442; DatasetName=ERPathway2016; DTXSID=DTXSID5021332; Assay=ER Pathway Model, Antagonist; Endpoint=AC50; Response=15.8495315173844; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_endocrine ACC 1.69650633256529 uM - - - ARPathway2016; AR Pathway Model, Agonist sheet=Integrated_approaches; excel_row=5629; RecordID=ARPathway2016_70; DatasetName=ARPathway2016; DTXSID=DTXSID5021332; Assay=AR Pathway Model, Agonist; Endpoint=ACC; Response=1.69650633256529; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_endocrine ACC 13.9488404367794 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=5635; RecordID=ERPathway2016_442; DatasetName=ERPathway2016; DTXSID=DTXSID5021332; Assay=ER Pathway Model, Antagonist; Endpoint=ACC; Response=13.9488404367794; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_endocrine Model Score 0.0731 unitless - - - ARPathway2016; AR Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=5630; RecordID=ARPathway2016_70; DatasetName=ARPathway2016; DTXSID=DTXSID5021332; Assay=AR Pathway Model, Antagonist; Endpoint=Model Score; Response=0.0731; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_endocrine Model Score 0 unitless - - - ARPathway2016; AR Pathway Model, Agonist sheet=Integrated_approaches; excel_row=5631; RecordID=ARPathway2016_70; DatasetName=ARPathway2016; DTXSID=DTXSID5021332; Assay=AR Pathway Model, Agonist; Endpoint=Model Score; Response=0; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_endocrine Model Score 0.00506 unitless - - - ERPathway2016; ER Pathway Model, Agonist sheet=Integrated_approaches; excel_row=5636; RecordID=ERPathway2016_442; DatasetName=ERPathway2016; DTXSID=DTXSID5021332; Assay=ER Pathway Model, Agonist; Endpoint=Model Score; Response=0.00506; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_eye_irritation 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_eye_irritation EPA Classification 4 unitless Rabbit Ocular - In Vivo; Draize Eye Irritation/Corrosion Test sheet=Data; excel_row=1490; Record_ID=eye_irritation_481; Data_Type=In Vivo; Formulation_ID=EyeIrritation6pack_PID303; Formulation_Name=DeerPro Winter Animal Repellant; Percent_Active_Ingredient=25.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Draize Eye Irritation/Corrosion Test; Endpoint=EPA Classification; Response=4; Response_Unit=Unitless; Species=Rabbit; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_eye_irritation EPA Classification 3 unitless Rabbit Ocular - In Vivo; Draize Eye Irritation/Corrosion Test sheet=Data; excel_row=1493; Record_ID=eye_irritation_626; Data_Type=In Vivo; Formulation_ID=EyeIrritation6pack_PID475; Formulation_Name=Foundation Lite; Percent_Active_Ingredient=6.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Draize Eye Irritation/Corrosion Test; Endpoint=EPA Classification; Response=3; Response_Unit=Unitless; Species=Rabbit; Reference=FIFRA data; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_irritation 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_skin_irritation EPA classification 4 unitless Rabbit Dermal - In Vivo; Draize Skin Irritation/Corrosion Test sheet=Data_invivo; excel_row=1011; Record_ID=skin_irritation_invivo_1316; Data_Type=In Vivo; Formulation_ID=MIX227; Formulation_Name=Foundation Lite; Percent_Active_Ingredient=6.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Draize Skin Irritation/Corrosion Test; Endpoint=EPA classification; Response=4; Response_Unit=Unitless; Species=Rabbit; Reported_Strain=New Zealand white; Strain=New Zealand White; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_irritation EPA classification 3 unitless Rabbit Dermal - In Vivo; Draize Skin Irritation/Corrosion Test sheet=Data_invivo; excel_row=1013; Record_ID=skin_irritation_invivo_435; Data_Type=In Vivo; Formulation_ID=MIX430; Formulation_Name=Sativa IMX Max; Percent_Active_Ingredient=10.78; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Draize Skin Irritation/Corrosion Test; Endpoint=EPA classification; Response=3; Response_Unit=Unitless; Species=Rabbit; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_irritation EPA classification 4 unitless Rabbit Dermal - In Vivo; Draize Skin Irritation/Corrosion Test sheet=Data_invivo; excel_row=1014; Record_ID=skin_irritation_invivo_690; Data_Type=In Vivo; Formulation_ID=MIX227; Formulation_Name=Foundation Lite; Percent_Active_Ingredient=6.8; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=Draize Skin Irritation/Corrosion Test; Endpoint=EPA classification; Response=4; Response_Unit=Unitless; Species=Rabbit; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization 123 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_skin_sensitization CD54, EC200 2.7 ug/mL - Dermal - In Vitro; CE_hCLAT2018; h-CLAT sheet=Data_invitro; excel_row=2174; Record_ID=skin_sensitization_invitro_537; Data_Type=In Vitro; Internal_Data_Source=CE_hCLAT2018; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=2.7; Reported_Response_Unit=ug/mL; Response=2.7; Response_Unit=ug/mL; Reference=Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD54, EC200 2.46 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3313; Record_ID=skin_sensitization_invitro_769; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=2.46; Reported_Response_Unit=ug/mL; Response=2.46; Response_Unit=ug/mL; Reference=Ashikaga et al. 2010; 20822320; 10.1177/026119291003800403|Nukada et al. 2011; 21767275; 10.1111/j.1600-0536.2011.01952.x|Nukada et al. 2012; 22796097; 10.1016/j.tiv.2012.07.001|Nukada personal communication (undated)|Nukada et al. 2013; 23149339; 10.1016/j.tiv.2012.11.006; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD54, EC200 3.9 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3324; Record_ID=skin_sensitization_invitro_771; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=3.9; Reported_Response_Unit=ug/mL; Response=3.9; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD54, EC200 5.2 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3334; Record_ID=skin_sensitization_invitro_773; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=5.2; Reported_Response_Unit=ug/mL; Response=5.2; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD54, EC200 0.1 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3344; Record_ID=skin_sensitization_invitro_775; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=0.1; Reported_Response_Unit=ug/mL; Response=0.1; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD54, EC200 3 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3354; Record_ID=skin_sensitization_invitro_777; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=3; Reported_Response_Unit=ug/mL; Response=3; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD86, EC150 9.11 ug/mL - Dermal - In Vitro; CE_hCLAT2018; h-CLAT sheet=Data_invitro; excel_row=2176; Record_ID=skin_sensitization_invitro_537; Data_Type=In Vitro; Internal_Data_Source=CE_hCLAT2018; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD86, EC150; Reported_Response=9.11; Reported_Response_Unit=ug/mL; Response=9.11; Response_Unit=ug/mL; Reference=Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD86, EC150 8.1 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3326; Record_ID=skin_sensitization_invitro_771; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD86, EC150; Reported_Response=8.1; Reported_Response_Unit=ug/mL; Response=8.1; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD86, EC150 14.6 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3335; Record_ID=skin_sensitization_invitro_773; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD86, EC150; Reported_Response=14.6; Reported_Response_Unit=ug/mL; Response=14.6; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD86, EC150 <8.9 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3346; Record_ID=skin_sensitization_invitro_775; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD86, EC150; Response_Modifier=<; Reported_Response_Modifier=<; Reported_Response=8.9; Reported_Response_Unit=ug/mL; Response=8.9; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD86, EC150 3.8 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3355; Record_ID=skin_sensitization_invitro_777; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CD86, EC150; Reported_Response=3.8; Reported_Response_Unit=ug/mL; Response=3.8; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD86, EC150 0.06 ug/mL - Dermal - In Vitro; Urbisch_SkinSensitization2020; U-SENS sheet=Data_invitro; excel_row=8245; Record_ID=skin_sensitization_invitro_2268; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=U-SENS; Endpoint=CD86, EC150; Reported_Response=0.249543543; Reported_Response_Unit=uM; Conversion_Factor_Value=240.42; Conversion_Factor_Source=EPA Dashboard; Converted_Response=0.06; Converted_Response_Unit=ug/mL; Response=0.06; Response_Unit=ug/mL; Reference=Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CD86, EC150 <0.1 ug/mL - Dermal - In Vitro; CE_USENSE2018; U-SENS sheet=Data_invitro; excel_row=8480; Record_ID=skin_sensitization_invitro_2336; Data_Type=In Vitro; Internal_Data_Source=CE_USENSE2018; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=U-SENS; Endpoint=CD86, EC150; Response_Modifier=<; Reported_Response_Modifier=<; Reported_Response=0.1; Reported_Response_Unit=ug/mL; Response=0.1; Response_Unit=ug/mL; Reference=Piroird et al. 2015; 25820135; 10.1016/j.tiv.2015.03.009; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CV70 3.06 ug/mL - Dermal - In Vitro; CE_USENSE2018; U-SENS sheet=Data_invitro; excel_row=8481; Record_ID=skin_sensitization_invitro_2336; Data_Type=In Vitro; Internal_Data_Source=CE_USENSE2018; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=U-SENS; Endpoint=CV70; Reported_Response=3.06; Reported_Response_Unit=ug/mL; Response=3.06; Response_Unit=ug/mL; Reference=Piroird et al. 2015; 25820135; 10.1016/j.tiv.2015.03.009; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CV75 10 ug/mL - Dermal - In Vitro; CE_hCLAT2018; h-CLAT sheet=Data_invitro; excel_row=2178; Record_ID=skin_sensitization_invitro_537; Data_Type=In Vitro; Internal_Data_Source=CE_hCLAT2018; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CV75; Reported_Response=10; Reported_Response_Unit=ug/mL; Response=10; Response_Unit=ug/mL; Reference=Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CV75 8.2 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3328; Record_ID=skin_sensitization_invitro_771; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CV75; Reported_Response=8.1999999999999904; Reported_Response_Unit=ug/mL; Response=8.2; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CV75 14.7 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3337; Record_ID=skin_sensitization_invitro_773; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CV75; Reported_Response=14.7; Reported_Response_Unit=ug/mL; Response=14.7; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CV75 26.7 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3345; Record_ID=skin_sensitization_invitro_775; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CV75; Reported_Response=26.7; Reported_Response_Unit=ug/mL; Response=26.7; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization CV75 11.5 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3356; Record_ID=skin_sensitization_invitro_777; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=h-CLAT; Endpoint=CV75; Reported_Response=11.5; Reported_Response_Unit=ug/mL; Response=11.5; Response_Unit=ug/mL; Reference=Sakaguchi et al. 2010; 20510347; 10.1016/j.tiv.2010.05.012|h-CLAT RingTrial EC values for NICEATM (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, 5% incidence of positive responses 5.5 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4895; Record_ID=skin_sensitization_invivo_1171; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, 5% incidence of positive responses; Response=5.5; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159|Akkan et al. 2003; Not available; Not available|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, 5% incidence of positive responses 1.5 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4908; Record_ID=skin_sensitization_invivo_1172; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, 5% incidence of positive responses; Response=1.5; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, 5% incidence of positive responses 7.8125 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4923; Record_ID=skin_sensitization_invivo_1175; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, 5% incidence of positive responses; Response=7.8125; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160|Marzulli and Maibach 1976; 801606; 10.1111/j.1600-0536.1976.tb02972.x|Basketter et al. 1996; 9012774; 10.1016/s0278-6915(96)00059-2|Gerberick et al. 2000; 10684384; 10.1053/ajcd.2000.0003|Akkan et al. 2003; Not available; Not available|Griem et al. 2003; 14623479; 10.1016/j.yrtph.2003.07.001|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, 5% incidence of positive responses 6.875 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4937; Record_ID=skin_sensitization_invivo_1177; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, 5% incidence of positive responses; Response=6.875; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, 5% incidence of positive responses 31.25 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4940; Record_ID=skin_sensitization_invivo_1178; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, 5% incidence of positive responses; Response=31.25; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, 5% incidence of positive responses 28.75 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4954; Record_ID=skin_sensitization_invivo_1176; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, 5% incidence of positive responses; Response=28.75; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, one positive response 5 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4893; Record_ID=skin_sensitization_invivo_1171; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, one positive response; Response=5; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159|Akkan et al. 2003; Not available; Not available|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, one positive response 1.667 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4904; Record_ID=skin_sensitization_invivo_1172; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, one positive response; Response=1.667; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, one positive response 6.25 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4920; Record_ID=skin_sensitization_invivo_1175; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, one positive response; Response=6.25; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160|Marzulli and Maibach 1976; 801606; 10.1111/j.1600-0536.1976.tb02972.x|Basketter et al. 1996; 9012774; 10.1016/s0278-6915(96)00059-2|Gerberick et al. 2000; 10684384; 10.1053/ajcd.2000.0003|Akkan et al. 2003; Not available; Not available|Griem et al. 2003; 14623479; 10.1016/j.yrtph.2003.07.001|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Concentration, one positive response 25 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4936; Record_ID=skin_sensitization_invivo_1178; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Concentration, one positive response; Response=25; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Depletion Cys 99.5 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1164; Record_ID=skin_sensitization_invitro_315; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=DPRA; Endpoint=Depletion Cys; Reported_Response=99.5; Reported_Response_Unit=%; Response=99.5; Response_Unit=%; Reference=Jaworska 2011; 23670904; 10.1002/jat.2869|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Depletion Cys 100 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1174; Record_ID=skin_sensitization_invitro_317; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=DPRA; Endpoint=Depletion Cys; Reported_Response=100; Reported_Response_Unit=%; Response=100; Response_Unit=%; Reference=Nukada et al. 2013; 23149339; 10.1016/j.tiv.2012.11.006|Nukada personal communication (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Depletion Lys 6.9 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1163; Record_ID=skin_sensitization_invitro_315; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=DPRA; Endpoint=Depletion Lys; Reported_Response=6.9; Reported_Response_Unit=%; Response=6.9; Response_Unit=%; Reference=Jaworska 2011; 23670904; 10.1002/jat.2869|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Depletion Lys 1.6 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1172; Record_ID=skin_sensitization_invitro_317; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=DPRA; Endpoint=Depletion Lys; Reported_Response=1.6; Reported_Response_Unit=%; Response=1.6; Response_Unit=%; Reference=Nukada et al. 2013; 23149339; 10.1016/j.tiv.2012.11.006|Nukada personal communication (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Depletion Lys + Cys 53.2 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1168; Record_ID=skin_sensitization_invitro_315; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=DPRA; Endpoint=Depletion Lys + Cys; Reported_Response=53.2; Reported_Response_Unit=%; Response=53.2; Response_Unit=%; Reference=Jaworska 2011; 23670904; 10.1002/jat.2869|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Depletion Lys + Cys 51 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1176; Record_ID=skin_sensitization_invitro_317; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=DPRA; Endpoint=Depletion Lys + Cys; Reported_Response=51; Reported_Response_Unit=%; Response=51; Response_Unit=%; Reference=Nukada et al. 2013; 23149339; 10.1016/j.tiv.2012.11.006|Nukada personal communication (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 0.827 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=5030; Record_ID=skin_sensitization_invitro_1163; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=0.82699999999999996; Reported_Response_Unit=uM; Response=0.827; Response_Unit=uM; Reference=Emter et al. 2010; 20307559; 10.1016/j.taap.2010.03.009|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 0.89 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5031; Record_ID=skin_sensitization_invitro_1164; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=0.89; Reported_Response_Unit=uM; Response=0.89; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 0.9 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5032; Record_ID=skin_sensitization_invitro_1165; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=0.9; Reported_Response_Unit=uM; Response=0.9; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 <0.97 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5033; Record_ID=skin_sensitization_invitro_1166; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Response_Modifier=<; Reported_Response_Modifier=<; Reported_Response=0.97; Reported_Response_Unit=uM; Response=0.97; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 <0.98 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5036; Record_ID=skin_sensitization_invitro_1169; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Response_Modifier=<; Reported_Response_Modifier=<; Reported_Response=0.98; Reported_Response_Unit=uM; Response=0.98; Response_Unit=uM; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 1.6 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5043; Record_ID=skin_sensitization_invitro_1176; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=1.6; Reported_Response_Unit=uM; Response=1.6; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 1.9 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5044; Record_ID=skin_sensitization_invitro_1177; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=1.9; Reported_Response_Unit=uM; Response=1.9; Response_Unit=uM; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 2.33 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5045; Record_ID=skin_sensitization_invitro_1178; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=2.33; Reported_Response_Unit=uM; Response=2.33; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 3.11 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5046; Record_ID=skin_sensitization_invitro_1179; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=3.11; Reported_Response_Unit=uM; Response=3.11; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 3.32 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5047; Record_ID=skin_sensitization_invitro_1180; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=3.32; Reported_Response_Unit=uM; Response=3.32; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 4.1 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5049; Record_ID=skin_sensitization_invitro_1181; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=4.0999999999999996; Reported_Response_Unit=uM; Response=4.1; Response_Unit=uM; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 4.39 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5050; Record_ID=skin_sensitization_invitro_1182; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=4.3899999999999997; Reported_Response_Unit=uM; Response=4.39; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 5.12 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5052; Record_ID=skin_sensitization_invitro_1183; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=5.12; Reported_Response_Unit=uM; Response=5.12; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 9.8 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5054; Record_ID=skin_sensitization_invitro_1184; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=9.8000000000000007; Reported_Response_Unit=uM; Response=9.8; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 0.8 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5117; Record_ID=skin_sensitization_invitro_1187; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=0.8; Reported_Response_Unit=uM; Response=0.8; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC1.5 <20.82 uM - Dermal - In Vitro; Urbisch_SkinSensitization2020; LuSens sheet=Data_invitro; excel_row=7598; Record_ID=skin_sensitization_invitro_1837; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=LuSens; Endpoint=EC1.5; Response_Modifier=<; Reported_Response_Modifier=<; Reported_Response=20.82; Reported_Response_Unit=uM; Response=20.82; Response_Unit=uM; Reference=Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC3 10.676 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=5056; Record_ID=skin_sensitization_invitro_1163; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=EC3; Reported_Response=10.676; Reported_Response_Unit=uM; Response=10.676; Response_Unit=uM; Reference=Emter et al. 2010; 20307559; 10.1016/j.taap.2010.03.009|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC3 5.2 % Mouse Dermal - In Vivo; LLNAdb2013; LLNA sheet=Data_invivo; excel_row=12905; Record_ID=skin_sensitization_invivo_2840; Data_Type=In Vivo; Internal_Data_Source=LLNAdb2013; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=LLNA; Endpoint=EC3; Response=5.2; Response_Unit=%; Species=Mouse; Route=Dermal; Reference=Gerberick et al. 2005; 16536334; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization EC3 0.13 % Mouse Dermal - In Vivo; LLNAdb2013; LLNA sheet=Data_invivo; excel_row=12908; Record_ID=skin_sensitization_invivo_2841; Data_Type=In Vivo; Internal_Data_Source=LLNAdb2013; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=LLNA; Endpoint=EC3; Response=0.13; Response_Unit=%; Species=Mouse; Route=Dermal; Reference=De Jong et al. 2002; 12062936; 10.1016/s0300-483x(02)00131-2; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization GHS Classification 1 unitless Mouse Dermal - In Vivo; SkinSensitization6pack; LLNA sheet=Data_invivo; excel_row=13884; Record_ID=skin_sensitization_invivo_3949; Data_Type=In Vivo; Internal_Data_Source=SkinSensitization6pack; Formulation_ID=MIX430; Formulation_Name=Sativa IMX Max; Percent_Active_Ingredient=10.78; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=LLNA; Endpoint=GHS Classification; Response=1; Response_Unit=Unitless; Species=Mouse; Route=Dermal; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization GHS Classification 1 unitless Mouse Dermal - In Vivo; SkinSensitization6pack; LLNA sheet=Data_invivo; excel_row=13884; Record_ID=skin_sensitization_invivo_3949; Data_Type=In Vivo; Internal_Data_Source=SkinSensitization6pack; Formulation_ID=MIX430; Formulation_Name=Sativa IMX Max; Percent_Active_Ingredient=10.78; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=LLNA; Endpoint=GHS Classification; Response=1; Response_Unit=Unitless; Species=Mouse; Route=Dermal; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization GHS Classification 1 unitless Mouse Dermal - In Vivo; SkinSensitization6pack; LLNA sheet=Data_invivo; excel_row=13884; Record_ID=skin_sensitization_invivo_3949; Data_Type=In Vivo; Internal_Data_Source=SkinSensitization6pack; Formulation_ID=MIX430; Formulation_Name=Sativa IMX Max; Percent_Active_Ingredient=10.78; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=LLNA; Endpoint=GHS Classification; Response=1; Response_Unit=Unitless; Species=Mouse; Route=Dermal; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization GHS Classification 1 unitless Mouse Dermal - In Vivo; SkinSensitization6pack; LLNA sheet=Data_invivo; excel_row=13884; Record_ID=skin_sensitization_invivo_3949; Data_Type=In Vivo; Internal_Data_Source=SkinSensitization6pack; Formulation_ID=MIX430; Formulation_Name=Sativa IMX Max; Percent_Active_Ingredient=10.78; Mixture=Mixture; DTXSID=DTXSID5021332; Assay=LLNA; Endpoint=GHS Classification; Response=1; Response_Unit=Unitless; Species=Mouse; Route=Dermal; Reference=FIFRA (undated); URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 11.8 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5058; Record_ID=skin_sensitization_invitro_1171; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=11.8; Reported_Response_Unit=uM; Response=11.8; Response_Unit=uM; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 12.35 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5060; Record_ID=skin_sensitization_invitro_1176; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=12.35; Reported_Response_Unit=uM; Response=12.35; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 13.74 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5062; Record_ID=skin_sensitization_invitro_1175; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=13.74; Reported_Response_Unit=uM; Response=13.74; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 17.39 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5064; Record_ID=skin_sensitization_invitro_1184; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=17.39; Reported_Response_Unit=uM; Response=17.39; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 22.94 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5066; Record_ID=skin_sensitization_invitro_1166; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=22.94; Reported_Response_Unit=uM; Response=22.94; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 22.98 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5068; Record_ID=skin_sensitization_invitro_1167; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=22.98; Reported_Response_Unit=uM; Response=22.98; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 23.59 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5070; Record_ID=skin_sensitization_invitro_1173; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=23.59; Reported_Response_Unit=uM; Response=23.59; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 23.8 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5072; Record_ID=skin_sensitization_invitro_1169; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=23.8; Reported_Response_Unit=uM; Response=23.8; Response_Unit=uM; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 25.68 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5076; Record_ID=skin_sensitization_invitro_1168; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=25.68; Reported_Response_Unit=uM; Response=25.68; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 26.8 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5078; Record_ID=skin_sensitization_invitro_1170; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=26.8; Reported_Response_Unit=uM; Response=26.8; Response_Unit=uM; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 27.03 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5080; Record_ID=skin_sensitization_invitro_1164; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=27.03; Reported_Response_Unit=uM; Response=27.03; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 36.6 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5082; Record_ID=skin_sensitization_invitro_1177; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=36.6; Reported_Response_Unit=uM; Response=36.6; Response_Unit=uM; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 38.65 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5084; Record_ID=skin_sensitization_invitro_1178; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=38.65; Reported_Response_Unit=uM; Response=38.65; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 39.1 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=5086; Record_ID=skin_sensitization_invitro_1163; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=39.1; Reported_Response_Unit=uM; Response=39.1; Response_Unit=uM; Reference=Emter et al. 2010; 20307559; 10.1016/j.taap.2010.03.009|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 46.8 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5088; Record_ID=skin_sensitization_invitro_1172; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=46.8; Reported_Response_Unit=uM; Response=46.8; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 47.01 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5090; Record_ID=skin_sensitization_invitro_1180; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=47.01; Reported_Response_Unit=uM; Response=47.01; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 52.85 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5092; Record_ID=skin_sensitization_invitro_1179; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=52.85; Reported_Response_Unit=uM; Response=52.85; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 53.65 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5094; Record_ID=skin_sensitization_invitro_1182; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=53.65; Reported_Response_Unit=uM; Response=53.65; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 53.7 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5096; Record_ID=skin_sensitization_invitro_1181; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=53.7; Reported_Response_Unit=uM; Response=53.7; Response_Unit=uM; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 54.57 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5098; Record_ID=skin_sensitization_invitro_1183; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=54.57; Reported_Response_Unit=uM; Response=54.57; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 9.78 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5100; Record_ID=skin_sensitization_invitro_1174; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=9.7799999999999994; Reported_Response_Unit=uM; Response=9.78; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization IC50 49.5 uM - Dermal - In Vitro; Urbisch_SkinSensitization2020; LuSens sheet=Data_invitro; excel_row=7668; Record_ID=skin_sensitization_invitro_1837; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=LuSens; Endpoint=IC50; Reported_Response=49.49606853; Reported_Response_Unit=uM; Response=49.5; Response_Unit=uM; Reference=Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 1.978 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5102; Record_ID=skin_sensitization_invitro_1184; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=1.978; Reported_Response_Unit=Unitless; Response=1.978; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 13.119 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5104; Record_ID=skin_sensitization_invitro_1167; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=13.119; Reported_Response_Unit=Unitless; Response=13.119; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 13.24 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5106; Record_ID=skin_sensitization_invitro_1172; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=13.244999999999999; Reported_Response_Unit=Unitless; Response=13.24; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 15.413 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5108; Record_ID=skin_sensitization_invitro_1179; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=15.413; Reported_Response_Unit=Unitless; Response=15.413; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 16.36 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5110; Record_ID=skin_sensitization_invitro_1168; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=16.364000000000001; Reported_Response_Unit=Unitless; Response=16.36; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 17.7 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5111; Record_ID=skin_sensitization_invitro_1181; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=17.7; Reported_Response_Unit=Unitless; Response=17.7; Response_Unit=Ratio; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 18.52 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5114; Record_ID=skin_sensitization_invitro_1182; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=18.515999999999998; Reported_Response_Unit=Unitless; Response=18.52; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 19.16 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5116; Record_ID=skin_sensitization_invitro_1183; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=19.155999999999999; Reported_Response_Unit=Unitless; Response=19.16; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 22.3 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5118; Record_ID=skin_sensitization_invitro_1169; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=22.3; Reported_Response_Unit=Unitless; Response=22.3; Response_Unit=Ratio; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 3.021 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5119; Record_ID=skin_sensitization_invitro_1173; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=3.0209999999999999; Reported_Response_Unit=Unitless; Response=3.021; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 37.32 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5120; Record_ID=skin_sensitization_invitro_1166; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=37.316000000000003; Reported_Response_Unit=Unitless; Response=37.32; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 48.11 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5121; Record_ID=skin_sensitization_invitro_1164; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=48.110999999999997; Reported_Response_Unit=Unitless; Response=48.11; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 58.427 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5122; Record_ID=skin_sensitization_invitro_1178; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=58.427; Reported_Response_Unit=Unitless; Response=58.427; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 6.18 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5124; Record_ID=skin_sensitization_invitro_1187; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=6.18; Reported_Response_Unit=Unitless; Response=6.18; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 6.75 ratio - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=5126; Record_ID=skin_sensitization_invitro_1163; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=6.75; Reported_Response_Unit=Unitless; Response=6.75; Response_Unit=Ratio; Reference=Emter et al. 2010; 20307559; 10.1016/j.taap.2010.03.009|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 67.9 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5128; Record_ID=skin_sensitization_invitro_1177; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=67.900000000000006; Reported_Response_Unit=Unitless; Response=67.9; Response_Unit=Ratio; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 7.321 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5130; Record_ID=skin_sensitization_invitro_1165; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=7.3209999999999997; Reported_Response_Unit=Unitless; Response=7.321; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 8.1 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5132; Record_ID=skin_sensitization_invitro_1170; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=8.1; Reported_Response_Unit=Unitless; Response=8.1; Response_Unit=Ratio; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 8.739 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5134; Record_ID=skin_sensitization_invitro_1176; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=8.7390000000000008; Reported_Response_Unit=Unitless; Response=8.739; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 9.3 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5135; Record_ID=skin_sensitization_invitro_1171; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=9.3000000000000007; Reported_Response_Unit=Unitless; Response=9.3; Response_Unit=Ratio; Reference=Natsch et al. 2011; 22023385; 10.1021/tx2003678; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 9.513 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5137; Record_ID=skin_sensitization_invitro_1175; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=9.5129999999999999; Reported_Response_Unit=Unitless; Response=9.513; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 9.6 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5139; Record_ID=skin_sensitization_invitro_1174; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=9.6; Reported_Response_Unit=Unitless; Response=9.6; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 97.17 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=5141; Record_ID=skin_sensitization_invitro_1180; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=97.17; Reported_Response_Unit=Unitless; Response=97.17; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Imax 5.287 ratio - Dermal - In Vitro; Urbisch_SkinSensitization2020; LuSens sheet=Data_invitro; excel_row=7571; Record_ID=skin_sensitization_invitro_1837; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=LuSens; Endpoint=Imax; Reported_Response=5.287027612; Reported_Response_Unit=Unitless; Response=5.287; Response_Unit=Ratio; Reference=Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Incidence of positive responses 33.33 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4900; Record_ID=skin_sensitization_invivo_1172; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=33.33; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Incidence of positive responses 0 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4905; Record_ID=skin_sensitization_invivo_1173; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=0; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159|Akkan et al. 2003; Not available; Not available|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Incidence of positive responses 16 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4916; Record_ID=skin_sensitization_invivo_1175; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=16; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160|Marzulli and Maibach 1976; 801606; 10.1111/j.1600-0536.1976.tb02972.x|Basketter et al. 1996; 9012774; 10.1016/s0278-6915(96)00059-2|Gerberick et al. 2000; 10684384; 10.1053/ajcd.2000.0003|Akkan et al. 2003; Not available; Not available|Griem et al. 2003; 14623479; 10.1016/j.yrtph.2003.07.001|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Incidence of positive responses 9.091 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4921; Record_ID=skin_sensitization_invivo_1171; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=9.091; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159|Akkan et al. 2003; Not available; Not available|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Incidence of positive responses 18.18 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4929; Record_ID=skin_sensitization_invivo_1177; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=18.18; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Incidence of positive responses 4 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4932; Record_ID=skin_sensitization_invivo_1178; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=4; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Incidence of positive responses 4.348 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4946; Record_ID=skin_sensitization_invivo_1176; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=4.348; Response_Unit=%; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area 6207 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4898; Record_ID=skin_sensitization_invivo_1172; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area; Response=6207; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area 15520 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4913; Record_ID=skin_sensitization_invivo_1175; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area; Response=15520; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160|Marzulli and Maibach 1976; 801606; 10.1111/j.1600-0536.1976.tb02972.x|Basketter et al. 1996; 9012774; 10.1016/s0278-6915(96)00059-2|Gerberick et al. 2000; 10684384; 10.1053/ajcd.2000.0003|Akkan et al. 2003; Not available; Not available|Griem et al. 2003; 14623479; 10.1016/j.yrtph.2003.07.001|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area, 5% incidence of positive responses 3414 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4896; Record_ID=skin_sensitization_invivo_1171; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area, 5% incidence of positive responses; Response=3414; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159|Akkan et al. 2003; Not available; Not available|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area, 5% incidence of positive responses 931 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4910; Record_ID=skin_sensitization_invivo_1172; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area, 5% incidence of positive responses; Response=931; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area, 5% incidence of positive responses 4849 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4924; Record_ID=skin_sensitization_invivo_1175; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area, 5% incidence of positive responses; Response=4849; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160|Marzulli and Maibach 1976; 801606; 10.1111/j.1600-0536.1976.tb02972.x|Basketter et al. 1996; 9012774; 10.1016/s0278-6915(96)00059-2|Gerberick et al. 2000; 10684384; 10.1053/ajcd.2000.0003|Akkan et al. 2003; Not available; Not available|Griem et al. 2003; 14623479; 10.1016/j.yrtph.2003.07.001|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area, 5% incidence of positive responses 17840 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4925; Record_ID=skin_sensitization_invivo_1176; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area, 5% incidence of positive responses; Response=17840; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area, 5% incidence of positive responses 4267 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4939; Record_ID=skin_sensitization_invivo_1177; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area, 5% incidence of positive responses; Response=4267; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area, 5% incidence of positive responses 19400 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4942; Record_ID=skin_sensitization_invivo_1178; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area, 5% incidence of positive responses; Response=19400; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area, one positive response 3103 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4894; Record_ID=skin_sensitization_invivo_1171; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area, one positive response; Response=3103; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159|Akkan et al. 2003; Not available; Not available|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area, one positive response 1034 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4906; Record_ID=skin_sensitization_invivo_1172; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area, one positive response; Response=1034; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Induction dose per skin area, one positive response 3879 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4922; Record_ID=skin_sensitization_invivo_1175; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=25.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Induction dose per skin area, one positive response; Response=3879; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924294; 10.1038/jid.1966.160|Marzulli and Maibach 1976; 801606; 10.1111/j.1600-0536.1976.tb02972.x|Basketter et al. 1996; 9012774; 10.1016/s0278-6915(96)00059-2|Gerberick et al. 2000; 10684384; 10.1053/ajcd.2000.0003|Akkan et al. 2003; Not available; Not available|Griem et al. 2003; 14623479; 10.1016/j.yrtph.2003.07.001|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
NTP_ICE_skin_sensitization Relative reliability score 1 unitless Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=4897; Record_ID=skin_sensitization_invivo_1171; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=10.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID5021332; Assay=Human Maximization Test; Endpoint=Relative reliability score; Response=1; Response_Unit=Unitless; Species=Human; Route=Dermal; Reference=Kligman 1966; 5924293; 10.1038/jid.1966.159|Akkan et al. 2003; Not available; Not available|Schneider and Akkan 2004; 15135206; 10.1016/j.yrtph.2004.02.002; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021332; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021332
ToxRefDB_ToxRefDB_v3_pod.csv 32 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxRefDB_ToxRefDB_v3_pod.csv LEL =2.35 mg/kg bw/day dog (beagle; beagle) oral 0 day to 90 day SUB study_id=3542; toxval_study_source_id=studyid3542_Adult_F0_F_systemic; toxval_effect_list=hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|clinical chemistry-cholesterol-cholesterol|hematology-hemoglobin (hgb)-hemoglobin (hgb)|hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|clinical chemistry-albumin-albumin|hematology-hematocrit (hct)-hematocrit (hct)|hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|clinical chemistry-protein-protein|in life observation-clinical signs-emesis|clinical chemistry-calcium-calcium|in life observation-food consumption-food consumption|in life observation-body weight-body weight|hematology-platelet-platelet|hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc); dose_level=1; study_year=1990; study_citation=Kehoe, D. (1990) 13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017. Unpublished study prepar- ed Hazleton Laboratories America, Inc. 237 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =2.26 mg/kg bw/day dog (beagle; beagle) oral 0 day to 90 day SUB study_id=3542; toxval_study_source_id=studyid3542_Adult_F0_M_systemic; toxval_effect_list=hematology-hematocrit (hct)-hematocrit (hct)|hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|clinical chemistry-cholesterol-cholesterol|in life observation-body weight-body weight|clinical chemistry-calcium-calcium|hematology-platelet-platelet|in life observation-clinical signs-emesis|in life observation-food consumption-food consumption|hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|clinical chemistry-protein-protein|clinical chemistry-albumin-albumin|hematology-hemoglobin (hgb)-hemoglobin (hgb)|hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc); dose_level=1; study_year=1990; study_citation=Kehoe, D. (1990) 13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017. Unpublished study prepar- ed Hazleton Laboratories America, Inc. 237 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =7.5 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 6 GD to 15 GD DEV study_id=3546; toxval_study_source_id=studyid3546_Adult_F0_F_systemic; toxval_effect_list=in life observation-clinical signs-skin discoloration|in life observation-clinical signs-scabbing|in life observation-clinical signs-alopecia|in life observation-body weight-body weight gain|in life observation-clinical signs-[other]|in life observation-clinical signs-salivation|organ weight-placenta-nos; dose_level=1; study_year=1988; study_citation=Tesh, J.; McAnulty, P.; Willoughby, C.; et al. (1988) Thiram: Teratology Study in the Rat: 87/TRK002/179. Unpublished study prepared by Life Science Research. 91 p.; dsstox_substance_id=DTXSID5021332; admin_method=Gavage/Intubation; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =4.7 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 90 days (premating) to 2 generation MGR study_id=3549; toxval_study_source_id=studyid3549_Adult_F0_F_systemic; toxval_effect_list=in life observation-body weight-body weight gain|in life observation-food consumption-food consumption|in life observation-body weight-body weight|pathology microscopic-pituitary gland-angiectasis; dose_level=2; study_year=1997; study_citation=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =12.2 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 90 days (premating) to 2 generation MGR study_id=3549; toxval_study_source_id=studyid3549_Adult_F0_M_systemic; toxval_effect_list=pathology microscopic-prostate-inflammation|in life observation-food consumption-food consumption; dose_level=3; study_year=1997; study_citation=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =5.4 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 90 days (premating) to 2 generation MGR study_id=3549; toxval_study_source_id=studyid3549_Adult_F1_F_systemic; toxval_effect_list=in life observation-body weight-body weight gain; dose_level=2; study_year=1997; study_citation=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =4.9 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 90 days (premating) to 2 generation MGR study_id=3549; toxval_study_source_id=studyid3549_Juvenile_F1_M_systemic; toxval_effect_list=in life observation-body weight-offspring (pup) weight gain|in life observation-body weight-offspring (pup) weight; dose_level=2; study_year=1997; study_citation=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =0.9 mg/kg bw/day dog (beagle; beagle) oral 0 week to 52 week CHR study_id=3550; toxval_study_source_id=studyid3550_Adult_F0_F_systemic; toxval_effect_list=hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|clinical chemistry-cholesterol-cholesterol|clinical chemistry-albumin-albumin|organ weight-liver-relative to body weight|clinical chemistry-protein-protein; dose_level=1; study_year=1991; study_citation=Kehoe, D. (1991) 52-Week Dietary Chronic Toxicity Study with Thiram in Dogs: Final Report: Lab Project Number: HLA 6111-112. Unpublished study prepared by Hazleton Laboratories America, Inc. 545 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =0.84 mg/kg bw/day dog (beagle; beagle) oral 0 week to 52 week CHR study_id=3550; toxval_study_source_id=studyid3550_Adult_F0_M_systemic; toxval_effect_list=clinical chemistry-cholesterol-cholesterol|clinical chemistry-protein-protein|hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|organ weight-liver-relative to body weight|hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|clinical chemistry-albumin-albumin|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|in life observation-body weight-body weight; dose_level=1; study_year=1991; study_citation=Kehoe, D. (1991) 52-Week Dietary Chronic Toxicity Study with Thiram in Dogs: Final Report: Lab Project Number: HLA 6111-112. Unpublished study prepared by Hazleton Laboratories America, Inc. 545 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =57 mg/kg bw/day mouse (cd1; Crl:CD-1(ICR)BR) oral 0 day to 97 week CHR study_id=3551; toxval_study_source_id=studyid3551_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-spleen-pigmentation|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|pathology microscopic-urinary bladder-[other]|in life observation-body weight-body weight gain|hematology-platelet-platelet|pathology microscopic-eye-atrophy|pathology microscopic-stomach-hyperkeratosis|pathology microscopic-skin-inflammation|in life observation-body weight-body weight|hematology-hemoglobin (hgb)-hemoglobin (hgb)|hematology-hematocrit (hct)-hematocrit (hct)|pathology microscopic-skin-necrosis; dose_level=2; study_year=1992; study_citation=Trutter, J. (1992) Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223. Unpublished study prepared by Hazleton Washington, Inc. 2965 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =24 mg/kg bw/day mouse (cd1; Crl:CD-1(ICR)BR) oral 0 day to 97 week CHR study_id=3551; toxval_study_source_id=studyid3551_Adult_F0_M_systemic; toxval_effect_list=pathology microscopic-skin-necrosis|in life observation-body weight-body weight|pathology microscopic-eye-atrophy|in life observation-body weight-body weight gain|pathology microscopic-skin-inflammation|hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc)|pathology microscopic-urinary bladder-[other]|pathology microscopic-stomach-hyperkeratosis; dose_level=2; study_year=1992; study_citation=Trutter, J. (1992) Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223. Unpublished study prepared by Hazleton Washington, Inc. 2965 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =1.8 mg/kg bw/day rat (sprague dawley; CD(SD)BR) oral 0 day to 104 week CHR study_id=3552; toxval_study_source_id=studyid3552_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-spleen-hematopoietic cell proliferation|hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc)|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|hematology-hemoglobin (hgb)-hemoglobin (hgb)|hematology-hematocrit (hct)-hematocrit (hct)|pathology gross-adrenal gland-cyst|pathology microscopic-liver-hyperplasia|pathology microscopic-pancreas-steatosis|pathology microscopic-thyroid gland-hyperplasia|in life observation-body weight-body weight gain|clinical chemistry-urea nitrogen-urea nitrogen|pathology microscopic-pancreas-infiltration cellular|clinical chemistry-glucose-glucose|pathology microscopic-liver-hematopoietic cell proliferation|organ weight-ovary-relative to brain weight|organ weight-ovary-absolute; dose_level=1; study_year=1991; study_citation=Kehoe, D. (1991) 104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113. Unpublished study prepared by Hazleton Labs America, Inc. 2513 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =7.3 mg/kg bw/day rat (sprague dawley; CD(SD)BR) oral 0 day to 104 week CHR study_id=3552; toxval_study_source_id=studyid3552_Adult_F0_M_systemic; toxval_effect_list=pathology microscopic-pancreas-infiltration cellular|pathology microscopic-pancreas-steatosis|in life observation-body weight-body weight gain|pathology microscopic-pancreas-atrophy|pathology gross-kidney-discolored|hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|clinical chemistry-glucose-glucose|organ weight-kidney-absolute|pathology gross-lymph node-discolored|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|pathology gross-liver-foci|organ weight-kidney-relative to brain weight; dose_level=2; study_year=1991; study_citation=Kehoe, D. (1991) 104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113. Unpublished study prepared by Hazleton Labs America, Inc. 2513 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =1.6 mg/kg bw/day rat (Sprague Dawley (SD) rat; Crl: CD(SD)IGS BR) oral 3 GD (gestation day) to 1 Generation DNT study_id=776296; toxval_study_source_id=studyid776296_Adult_F0_F_systemic; toxval_effect_list=in life observation-food consumption-food consumption|in life observation-body weight-body weight|in life observation-body weight-body weight gain; dose_level=1; study_year=2005; study_citation=Fulcher, S.M. (2005) Thiram: developmental neurotoxicity study in the CD rat by dietary administration. Huntingdon Life Sciences, Ltd., Wooley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Laboratory study no. PFX/004; January 18, 2005. MRID 46455201. Piccirillo, V. (2008) Response to Data Evaluation Record for Developmental Neurotoxicity Study in Rats With Thiram (MRID 46455201). Huntingdon Life Sciences, Ltd., Wo'oley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Project Number: 2008/1, PFX/004, PFX004/042634; January 1, 2008. MRID 47429501. Stannard, D. (2010) Thiram: Morphometric Examination of Brains Derived from a Developmental Neurotoxicity Study in the CD Rat. Huntingdon Life Sciences, Eye Research Center, Eye, Suffolk, IP23 7PX, UK. Project Number: SMJ000l, PFX/004/042634. MRID 48291001.; dsstox_substance_id=DTXSID5021332; admin_method=Diet; vehicle=diet; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LEL =1.6 mg/kg bw/day rat (Sprague Dawley (SD) rat; Crl: CD(SD)IGS BR) oral 3 GD (gestation day) to 1 Generation DNT study_id=776296; toxval_study_source_id=studyid776296_Adult_F0_F_systemic; toxval_effect_list=in life observation-food consumption-food consumption|in life observation-body weight-body weight|in life observation-body weight-body weight gain; dose_level=1; study_year=2005; study_citation=Fulcher, S.M. (2005) Thiram: developmental neurotoxicity study in the CD rat by dietary administration. Huntingdon Life Sciences, Ltd., Wooley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Laboratory study no. PFX/004; January 18, 2005. MRID 46455201. Piccirillo, V. (2008) Response to Data Evaluation Record for Developmental Neurotoxicity Study in Rats With Thiram (MRID 46455201). Huntingdon Life Sciences, Ltd., Wo'oley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Project Number: 2008/1, PFX/004, PFX004/042634; January 1, 2008. MRID 47429501. Stannard, D. (2010) Thiram: Morphometric Examination of Brains Derived from a Developmental Neurotoxicity Study in the CD Rat. Huntingdon Life Sciences, Eye Research Center, Eye, Suffolk, IP23 7PX, UK. Project Number: SMJ000l, PFX/004/042634. MRID 48291001.; dsstox_substance_id=DTXSID5021332; admin_method=Diet; vehicle=diet; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LOAEL =7.34 mg/kg bw/day dog (beagle; beagle) oral 0 day to 90 day SUB study_id=3542; toxval_study_source_id=studyid3542_Adult_F0_F_systemic; toxval_effect_list=hematology-hemoglobin (hgb)-hemoglobin (hgb)|clinical chemistry-cholesterol-cholesterol|hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|in life observation-food consumption-food consumption|clinical chemistry-albumin-albumin|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|clinical chemistry-protein-protein|clinical chemistry-calcium-calcium|hematology-hematocrit (hct)-hematocrit (hct)|hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch); dose_level=2; study_year=1990; study_citation=Kehoe, D. (1990) 13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017. Unpublished study prepar- ed Hazleton Laboratories America, Inc. 237 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LOAEL =7.01 mg/kg bw/day dog (beagle; beagle) oral 0 day to 90 day SUB study_id=3542; toxval_study_source_id=studyid3542_Adult_F0_M_systemic; toxval_effect_list=in life observation-food consumption-food consumption|hematology-platelet-platelet|clinical chemistry-cholesterol-cholesterol|in life observation-body weight-body weight|clinical chemistry-calcium-calcium|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|hematology-hematocrit (hct)-hematocrit (hct)|hematology-hemoglobin (hgb)-hemoglobin (hgb)|clinical chemistry-albumin-albumin|hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|clinical chemistry-protein-protein; dose_level=2; study_year=1990; study_citation=Kehoe, D. (1990) 13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017. Unpublished study prepar- ed Hazleton Laboratories America, Inc. 237 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LOAEL =15 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 6 GD to 15 GD DEV study_id=3546; toxval_study_source_id=studyid3546_Fetal_Fetal_MF_developmental; toxval_effect_list=developmental malformation-bone-short supernumerary|developmental malformation-bone-incomplete ossification; dose_level=2; study_year=1988; study_citation=Tesh, J.; McAnulty, P.; Willoughby, C.; et al. (1988) Thiram: Teratology Study in the Rat: 87/TRK002/179. Unpublished study prepared by Life Science Research. 91 p.; dsstox_substance_id=DTXSID5021332; admin_method=Gavage/Intubation; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LOAEL =2.54 mg/kg bw/day dog (beagle; beagle) oral 0 week to 52 week CHR study_id=3550; toxval_study_source_id=studyid3550_Adult_F0_F_systemic; toxval_effect_list=clinical chemistry-cholesterol-cholesterol|clinical chemistry-albumin-albumin|organ weight-liver-relative to body weight|clinical chemistry-protein-protein; dose_level=2; study_year=1991; study_citation=Kehoe, D. (1991) 52-Week Dietary Chronic Toxicity Study with Thiram in Dogs: Final Report: Lab Project Number: HLA 6111-112. Unpublished study prepared by Hazleton Laboratories America, Inc. 545 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LOAEL =8.9 mg/kg bw/day rat (sprague dawley; CD(SD)BR) oral 0 day to 104 week CHR study_id=3552; toxval_study_source_id=studyid3552_Adult_F0_F_systemic; toxval_effect_list=hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|hematology-hemoglobin (hgb)-hemoglobin (hgb)|hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc)|pathology microscopic-liver-hyperplasia|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|in life observation-body weight-body weight gain|clinical chemistry-urea nitrogen-urea nitrogen|hematology-hematocrit (hct)-hematocrit (hct); dose_level=2; study_year=1991; study_citation=Kehoe, D. (1991) 104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113. Unpublished study prepared by Hazleton Labs America, Inc. 2513 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LOAEL =6.6 mg/kg bw/day rat (Sprague Dawley (SD) rat; Crl: CD(SD)IGS BR) oral 3 GD (gestation day) to 1 Generation DNT study_id=776296; toxval_study_source_id=studyid776296_Adult_F0_F_neurological; toxval_effect_list=detailed clin obs: dam lactation #2-convulsive behavior-tremors|detailed clin obs: dam lactation #2-unusual behavior or appearance-rearing activity|detailed clin obs: dam lactation #2-autonomic function-palpebral closure (ptosis)|detailed clin obs: dam lactation #2-unusual behavior or appearance-activity; dose_level=3; study_year=2005; study_citation=Fulcher, S.M. (2005) Thiram: developmental neurotoxicity study in the CD rat by dietary administration. Huntingdon Life Sciences, Ltd., Wooley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Laboratory study no. PFX/004; January 18, 2005. MRID 46455201. Piccirillo, V. (2008) Response to Data Evaluation Record for Developmental Neurotoxicity Study in Rats With Thiram (MRID 46455201). Huntingdon Life Sciences, Ltd., Wo'oley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Project Number: 2008/1, PFX/004, PFX004/042634; January 1, 2008. MRID 47429501. Stannard, D. (2010) Thiram: Morphometric Examination of Brains Derived from a Developmental Neurotoxicity Study in the CD Rat. Huntingdon Life Sciences, Eye Research Center, Eye, Suffolk, IP23 7PX, UK. Project Number: SMJ000l, PFX/004/042634. MRID 48291001.; dsstox_substance_id=DTXSID5021332; admin_method=Diet; vehicle=diet; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv LOAEL =6.6 mg/kg bw/day rat (Sprague Dawley (SD) rat; Crl: CD(SD)IGS BR) oral 3 GD (gestation day) to 1 Generation DNT study_id=776296; toxval_study_source_id=studyid776296_Adult_F0_F_neurological; toxval_effect_list=detailed clin obs: dam lactation #2-convulsive behavior-tremors|detailed clin obs: dam lactation #2-unusual behavior or appearance-rearing activity|detailed clin obs: dam lactation #2-autonomic function-palpebral closure (ptosis)|detailed clin obs: dam lactation #2-unusual behavior or appearance-activity; dose_level=3; study_year=2005; study_citation=Fulcher, S.M. (2005) Thiram: developmental neurotoxicity study in the CD rat by dietary administration. Huntingdon Life Sciences, Ltd., Wooley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Laboratory study no. PFX/004; January 18, 2005. MRID 46455201. Piccirillo, V. (2008) Response to Data Evaluation Record for Developmental Neurotoxicity Study in Rats With Thiram (MRID 46455201). Huntingdon Life Sciences, Ltd., Wo'oley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Project Number: 2008/1, PFX/004, PFX004/042634; January 1, 2008. MRID 47429501. Stannard, D. (2010) Thiram: Morphometric Examination of Brains Derived from a Developmental Neurotoxicity Study in the CD Rat. Huntingdon Life Sciences, Eye Research Center, Eye, Suffolk, IP23 7PX, UK. Project Number: SMJ000l, PFX/004/042634. MRID 48291001.; dsstox_substance_id=DTXSID5021332; admin_method=Diet; vehicle=diet; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NEL >0 mg/kg bw/day dog (beagle; beagle) oral 0 day to 90 day SUB study_id=3542; toxval_study_source_id=studyid3542_Adult_F0_F_systemic; toxval_effect_list=in life observation-clinical signs-emesis|clinical chemistry-calcium-calcium|clinical chemistry-protein-protein|hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc)|hematology-hematocrit (hct)-hematocrit (hct)|hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|clinical chemistry-cholesterol-cholesterol|hematology-hemoglobin (hgb)-hemoglobin (hgb)|in life observation-food consumption-food consumption|clinical chemistry-albumin-albumin|hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|hematology-platelet-platelet|in life observation-body weight-body weight; dose_level=0; study_year=1990; study_citation=Kehoe, D. (1990) 13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017. Unpublished study prepar- ed Hazleton Laboratories America, Inc. 237 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NEL =1.6 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 90 days (premating) to 2 generation MGR study_id=3549; toxval_study_source_id=studyid3549_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-pituitary gland-angiectasis|in life observation-body weight-body weight|in life observation-body weight-body weight gain|in life observation-food consumption-food consumption; dose_level=1; study_year=1997; study_citation=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NEL =4.2 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 90 days (premating) to 2 generation MGR study_id=3549; toxval_study_source_id=studyid3549_Adult_F0_M_systemic; toxval_effect_list=pathology microscopic-prostate-inflammation|in life observation-food consumption-food consumption; dose_level=2; study_year=1997; study_citation=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NEL =1.8 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 90 days (premating) to 2 generation MGR study_id=3549; toxval_study_source_id=studyid3549_Adult_F1_F_systemic; toxval_effect_list=in life observation-body weight-body weight gain; dose_level=1; study_year=1997; study_citation=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NEL =1.7 mg/kg bw/day rat (sprague dawley; Sprague Dawley (CD)) oral 90 days (premating) to 2 generation MGR study_id=3549; toxval_study_source_id=studyid3549_Juvenile_F1_M_systemic; toxval_effect_list=in life observation-body weight-offspring (pup) weight|in life observation-body weight-offspring (pup) weight gain; dose_level=1; study_year=1997; study_citation=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NEL =3.1 mg/kg bw/day mouse (cd1; Crl:CD-1(ICR)BR) oral 0 day to 97 week CHR study_id=3551; toxval_study_source_id=studyid3551_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-skin-inflammation|in life observation-body weight-body weight|pathology microscopic-stomach-hyperkeratosis|hematology-hematocrit (hct)-hematocrit (hct)|hematology-hemoglobin (hgb)-hemoglobin (hgb)|pathology microscopic-spleen-pigmentation|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|pathology microscopic-urinary bladder-[other]|in life observation-body weight-body weight gain|hematology-platelet-platelet|pathology microscopic-skin-necrosis|pathology microscopic-eye-atrophy; dose_level=1; study_year=1992; study_citation=Trutter, J. (1992) Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223. Unpublished study prepared by Hazleton Washington, Inc. 2965 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NEL =2.5 mg/kg bw/day mouse (cd1; Crl:CD-1(ICR)BR) oral 0 day to 97 week CHR study_id=3551; toxval_study_source_id=studyid3551_Adult_F0_M_systemic; toxval_effect_list=pathology microscopic-urinary bladder-[other]|pathology microscopic-skin-inflammation|hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc)|in life observation-body weight-body weight gain|pathology microscopic-eye-atrophy|pathology microscopic-stomach-hyperkeratosis|pathology microscopic-skin-necrosis|in life observation-body weight-body weight; dose_level=1; study_year=1992; study_citation=Trutter, J. (1992) Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223. Unpublished study prepared by Hazleton Washington, Inc. 2965 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NEL =1.5 mg/kg bw/day rat (sprague dawley; CD(SD)BR) oral 0 day to 104 week CHR study_id=3552; toxval_study_source_id=studyid3552_Adult_F0_M_systemic; toxval_effect_list=organ weight-kidney-relative to brain weight|pathology gross-liver-foci|hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|clinical chemistry-glucose-glucose|organ weight-kidney-absolute|pathology gross-lymph node-discolored|hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|pathology gross-kidney-discolored|pathology microscopic-pancreas-atrophy|in life observation-body weight-body weight gain|pathology microscopic-pancreas-steatosis|pathology microscopic-pancreas-infiltration cellular; dose_level=1; study_year=1991; study_citation=Kehoe, D. (1991) 104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113. Unpublished study prepared by Hazleton Labs America, Inc. 2513 p.; dsstox_substance_id=DTXSID5021332; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NOAEL =3.8 mg/kg bw/day rat (Sprague Dawley (SD) rat; Crl: CD(SD)IGS BR) oral 3 GD (gestation day) to 1 Generation DNT study_id=776296; toxval_study_source_id=studyid776296_Adult_F0_F_neurological; toxval_effect_list=detailed clin obs: dam lactation #2-autonomic function-palpebral closure (ptosis)|detailed clin obs: dam lactation #2-convulsive behavior-tremors|detailed clin obs: dam lactation #2-unusual behavior or appearance-rearing activity|detailed clin obs: dam lactation #2-unusual behavior or appearance-activity; dose_level=2; study_year=2005; study_citation=Fulcher, S.M. (2005) Thiram: developmental neurotoxicity study in the CD rat by dietary administration. Huntingdon Life Sciences, Ltd., Wooley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Laboratory study no. PFX/004; January 18, 2005. MRID 46455201. Piccirillo, V. (2008) Response to Data Evaluation Record for Developmental Neurotoxicity Study in Rats With Thiram (MRID 46455201). Huntingdon Life Sciences, Ltd., Wo'oley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Project Number: 2008/1, PFX/004, PFX004/042634; January 1, 2008. MRID 47429501. Stannard, D. (2010) Thiram: Morphometric Examination of Brains Derived from a Developmental Neurotoxicity Study in the CD Rat. Huntingdon Life Sciences, Eye Research Center, Eye, Suffolk, IP23 7PX, UK. Project Number: SMJ000l, PFX/004/042634. MRID 48291001.; dsstox_substance_id=DTXSID5021332; admin_method=Diet; vehicle=diet; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxRefDB_ToxRefDB_v3_pod.csv NOAEL =3.8 mg/kg bw/day rat (Sprague Dawley (SD) rat; Crl: CD(SD)IGS BR) oral 3 GD (gestation day) to 1 Generation DNT study_id=776296; toxval_study_source_id=studyid776296_Adult_F0_F_neurological; toxval_effect_list=detailed clin obs: dam lactation #2-autonomic function-palpebral closure (ptosis)|detailed clin obs: dam lactation #2-convulsive behavior-tremors|detailed clin obs: dam lactation #2-unusual behavior or appearance-rearing activity|detailed clin obs: dam lactation #2-unusual behavior or appearance-activity; dose_level=2; study_year=2005; study_citation=Fulcher, S.M. (2005) Thiram: developmental neurotoxicity study in the CD rat by dietary administration. Huntingdon Life Sciences, Ltd., Wooley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Laboratory study no. PFX/004; January 18, 2005. MRID 46455201. Piccirillo, V. (2008) Response to Data Evaluation Record for Developmental Neurotoxicity Study in Rats With Thiram (MRID 46455201). Huntingdon Life Sciences, Ltd., Wo'oley Road, Alconbury, Huntingdon, Cambridgeshire, PE28 4HS, England. Project Number: 2008/1, PFX/004, PFX004/042634; January 1, 2008. MRID 47429501. Stannard, D. (2010) Thiram: Morphometric Examination of Brains Derived from a Developmental Neurotoxicity Study in the CD Rat. Huntingdon Life Sciences, Eye Research Center, Eye, Suffolk, IP23 7PX, UK. Project Number: SMJ000l, PFX/004/042634. MRID 48291001.; dsstox_substance_id=DTXSID5021332; admin_method=Diet; vehicle=diet; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ToxValDB_AU_DWG 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_AU_DWG NOEL =0.4 mg/kg bw/day Dog oral chronic; 2 years chronic STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/68c82db5e4b02565fc7d237c; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.nhmrc.gov.au; SUBSOURCE_URL=https://www.nhmrc.gov.au/sites/default/files/documents/attachments/publications/Australian_Drinking_Water_Guidelines_ADWG_V3-8_Sep2022.pdf; TOXICOLOGICAL_EFFECT=neurological disturbances, anaemia and changes in the liver; STUDY_GROUP=AU DWG:15951776:-:--; QC_CATEGORY=Manually extracted from unstructured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_3418a97c60dd5a7e534fc96f6523b768
ToxValDB_ECHA_IUCLID 34 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_ECHA_IUCLID LOAEL =11.7 mg/kg bw/day Rat oral - chronic GUIDELINE=OECD Guideline 453 (Combined Chronic Toxicity / Carcinogenicity Studies); QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c80fe4b0a7c65d2166c6; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/8?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=liver: body weight and weight gain|food consumption and compound intake|gross pathology|haematology|histopathology: non-neoplastic|liver: histopathology: neoplastic; TOXICOLOGICAL_EFFECT_CATEGORY=cancer|food and/or water consumption|gross pathology|hematology|nonneoplastic histopathology|organ weight; STUDY_GROUP=ECHA IUCLID_dup_Carcinogenicity_15817560_15817561:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_62c17fe71608959eddc92ed98dad4abb
ToxValDB_ECHA_IUCLID LOAEL =27.75 mg/kg bw/day Mouse oral - chronic GUIDELINE=OECD Guideline 451 (Carcinogenicity Studies); QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c80fe4b0a7c65d2166c8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/8?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=body weight and weight gain|food consumption and compound intake|haematology|histopathology: non-neoplastic; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption|hematology|nonneoplastic histopathology; STUDY_GROUP=ECHA IUCLID_dup_Carcinogenicity_15817939_15817942:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_fb812a7a377a9544e238f592f9a269b8
ToxValDB_ECHA_IUCLID LOAEL =88.65 mg/kg bw/day Mouse oral - subchronic QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c851e4b0a7c65d217e7e; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=hepatobiliary: spleen: immunology; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECHA IUCLID_dup_Immunotoxicity_15825513_15825514:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_2fd8ea3a51ac07daeaf9ca5a3128ca28
ToxValDB_ECHA_IUCLID LOAEL =150 mg/kg bw/day Rat oral - repeat dose other GUIDELINE=OECD Guideline 418 (Delayed Neurotoxicity of Organophosphorus Substances Following Acute Exposure); QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c85ae4b0a7c65d218169; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/1?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Neurotoxicity_15825580_15825581:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_71506f0b6d992279f283dfe7e4840716
ToxValDB_ECHA_IUCLID LOAEL =90 ppm Rat oral - repeat dose other QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c85ae4b0a7c65d21816b; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/1?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=body weight and weight gain|clinical signs|food consumption and compound intake; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|food and/or water consumption; STUDY_GROUP=ECHA IUCLID_dup_Neurotoxicity_15825586_15825587:F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_c2e6aee59ec40f534a00e14c565cf1cd
ToxValDB_ECHA_IUCLID LOAEL =125 ppm Rat oral - repeat dose other GUIDELINE=OECD Guideline 424 (Neurotoxicity Study in Rodents); QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c85ae4b0a7c65d21816f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/1?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=body weight and weight gain|food consumption and compound intake; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption; STUDY_GROUP=ECHA IUCLID_dup_Neurotoxicity_15825588_15825589_15825590_15825763_15825764_15825765_15825766:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_3cdb2af307e8a89287f4ddb47260273e
ToxValDB_ECHA_IUCLID LOAEL =500 ppm Rat oral - repeat dose other GUIDELINE=OECD Guideline 424 (Neurotoxicity Study in Rodents); QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c85ae4b0a7c65d21816f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/1?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=behavior: functional findings; TOXICOLOGICAL_EFFECT_CATEGORY=neurobehavior; STUDY_GROUP=ECHA IUCLID_dup_Neurotoxicity_15825588_15825589_15825590_15825763_15825764_15825765_15825766:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_99144b3df616a6c10f6df6edb26d9643
ToxValDB_ECHA_IUCLID LOAEL =60 mg/kg bw/day Rat oral - repeat dose other QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c85ae4b0a7c65d218171; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/1?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=body weight and weight gain|food consumption and compound intake; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption; STUDY_GROUP=ECHA IUCLID_dup_Neurotoxicity_15825800_15825801:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_5c98116772e335e72435b5b44a870f0e
ToxValDB_ECHA_IUCLID LOAEL =1000 mg/kg bw/day Rabbit dermal short-term; 21 days short-term GUIDELINE=OECD Guideline 410 (Repeated Dose Dermal Toxicity: 21/28-Day Study); QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/67c61d3ae4b096bca8774fa1; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/4?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Dermal_15826099_15826100_15826101:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_65b8c9c571b5b8af8e2efefa13bfa934
ToxValDB_ECHA_IUCLID LOAEL =48 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca77e4b0a7c65d222053; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=body weight and weight gain|clinical biochemistry|gross pathology|haematology|histopathology: non-neoplastic; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical chemistry|gross pathology|hematology|nonneoplastic histopathology; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15833271_15833272_15836628_15836629:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_71820374655bcfefffbe15e76eefa9a1
ToxValDB_ECHA_IUCLID LOAEL =300 mg/kg bw/day Rat oral - short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca77e4b0a7c65d222074; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=body weight and weight gain|food consumption and compound intake|gross pathology; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption|gross pathology; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15837261_15837262:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_3ae84defe7c6bc6697c36519a3d66540
ToxValDB_ECHA_IUCLID LOAEL =9.25 mg/kg bw/day Dog oral subchronic; 90 days subchronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca78e4b0a7c65d2220c8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=body weight and weight gain|clinical biochemistry|food consumption and compound intake|haematology; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical chemistry|food and/or water consumption|hematology; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15837590_15837591_15840866_15840867:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_855b7bae3079447eaae58885373e3495
ToxValDB_ECHA_IUCLID LOAEL =300 ppm Mouse oral short-term; 4 weeks short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca78e4b0a7c65d2220d0; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=body weight and weight gain|food consumption and compound intake|haematology|organ weights and organ / body weight ratios; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption|hematology|organ weight; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15838325_15838327_15839196:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_0cb7211e2c4b0e9b180010c612947276
ToxValDB_ECHA_IUCLID LOAEL =600 ppm Mouse oral short-term; 4 weeks short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca78e4b0a7c65d2220d0; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=body weight and weight gain|food consumption and compound intake|haematology|organ weights and organ / body weight ratios; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption|hematology|organ weight; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15838325_15838327_15839196:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_c05d35a88ab9d3a9b4d77fc448a37735
ToxValDB_ECHA_IUCLID LOAEL =5 mg/kg bw/day Dog oral chronic; 52 weeks chronic QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca78e4b0a7c65d2220d8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=liver: clinical biochemistry|haematology|organ weights and organ / body weight ratios; TOXICOLOGICAL_EFFECT_CATEGORY=clinical chemistry|hematology|organ weight; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15841286_15841288:F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_6f078eff30aed043b4024b90ee13bc34
ToxValDB_ECHA_IUCLID LOAEL =60 ppm Rat oral - reproduction developmental QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c8bde4b0a7c65d219fbc; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/9/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Toxicity Reproduction_15855336_15856171_15856717:M/F:P0-; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_a150a952b16e525e9ba3b5ce36b0ac55
ToxValDB_ECHA_IUCLID NOAEL =2.34 mg/kg bw/day Rat oral - chronic GUIDELINE=OECD Guideline 453 (Combined Chronic Toxicity / Carcinogenicity Studies); QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c80fe4b0a7c65d2166c6; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/8?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=liver; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECHA IUCLID_dup_Carcinogenicity_15817560_15817561:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_7426a733f94e671aa9196191282587f4
ToxValDB_ECHA_IUCLID NOAEL =55.5 mg/kg bw/day Mouse oral - chronic GUIDELINE=OECD Guideline 451 (Carcinogenicity Studies); QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c80fe4b0a7c65d2166c8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/8?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Carcinogenicity_15817939_15817942:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_2ce959a42caa75611a7d0e0387b960d1
ToxValDB_ECHA_IUCLID NOAEL =111 mg/kg bw/day Mouse oral - chronic GUIDELINE=OECD Guideline 451 (Carcinogenicity Studies); QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c80fe4b0a7c65d2166c8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/8?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Carcinogenicity_15817940_15817943:F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_f705b0fb57d0ca1c745029e66c4e2848
ToxValDB_ECHA_IUCLID NOAEL =2.775 mg/kg bw/day Mouse oral - chronic GUIDELINE=OECD Guideline 451 (Carcinogenicity Studies); QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c80fe4b0a7c65d2166c8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/8?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID:15817941:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_791ecdb9f2c3342c33a9b053b36a09e8
ToxValDB_ECHA_IUCLID NOAEL >5 mg/kg bw/day Rabbit oral - developmental GUIDELINE=OECD Guideline 414 (Prenatal Developmental Toxicity Study); QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eac93e4b0a7c65d1bfdf4; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11549/7/9/3?documentUUID=bffc9e90-e74d-4644-9f2b-e987470690fd; YEAR=1977; ORIGINAL_YEAR=1977; STUDY_GROUP=ECHA IUCLID_dup_Developmental Toxicity Teratogenicity_15820672_15821426:M/F:-fetal; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_5b5d3065cc32ca5fa0e4b693fd14189c
ToxValDB_ECHA_IUCLID NOAEL =29.55 mg/kg bw/day Mouse oral - subchronic QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c851e4b0a7c65d217e7e; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=hepatobiliary: spleen; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECHA IUCLID_dup_Immunotoxicity_15825513_15825514:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_116c9323993ab82e309bc7c385a9e3e8
ToxValDB_ECHA_IUCLID NOAEL =45 ppm Rat oral - repeat dose other QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c85ae4b0a7c65d21816b; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/1?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Neurotoxicity_15825586_15825587:F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_6b01a256d02f7c6847f267cf34606955
ToxValDB_ECHA_IUCLID NOAEL =20 ppm Rat oral - repeat dose other QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c85ae4b0a7c65d21816b; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/1?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Neurotoxicity_15825588_15825589_15825590_15825763_15825764_15825765_15825766:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_64cd00f94483e75b4f464f68c44d0827
ToxValDB_ECHA_IUCLID NOAEL =30 ppm Rat oral - repeat dose other GUIDELINE=OECD Guideline 424 (Neurotoxicity Study in Rodents); QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c85ae4b0a7c65d21816f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/1?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Neurotoxicity_15825588_15825589_15825590_15825763_15825764_15825765_15825766:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_e5b1961a511623b564ffcdd97302df16
ToxValDB_ECHA_IUCLID NOAEL =25 mg/kg bw/day Rat oral - repeat dose other QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c85ae4b0a7c65d218171; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/10/1?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Neurotoxicity_15825800_15825801:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_01c17850d2d8ce1533d2175de6d9251d
ToxValDB_ECHA_IUCLID NOAEL =300 mg/kg bw/day Rabbit dermal short-term; 21 days short-term GUIDELINE=OECD Guideline 410 (Repeated Dose Dermal Toxicity: 21/28-Day Study); QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/67c61d3ae4b096bca8774fa1; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/4?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Dermal_15826099_15826100_15826101:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_0d88efcd686eaf467f2137440d12cd9e
ToxValDB_ECHA_IUCLID NOAEL <100 mg/kg bw/day Rabbit dermal short-term; 21 days short-term GUIDELINE=OECD Guideline 410 (Repeated Dose Dermal Toxicity: 21/28-Day Study); QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/67c61d3ae4b096bca8774fa1; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/4?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Dermal_15826099_15826100_15826101:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_4885b3ba2167b8208c4b52fb9d02629e
ToxValDB_ECHA_IUCLID NOAEL =4.8 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca77e4b0a7c65d222053; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15833271_15833272_15836628_15836629:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_a7cc4d0aba969ea2fb9939248a4154ff
ToxValDB_ECHA_IUCLID NOAEL =125 ppm Dog oral short-term; 4 weeks short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca77e4b0a7c65d222060; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15834088_15834089_15836232_15836233:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_2c4885936a628f20dfdcf0b9bd534f13
ToxValDB_ECHA_IUCLID NOAEL =1000 mg/kg bw/day Rat oral - short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca77e4b0a7c65d222074; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15837261_15837262:M/F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_9efa4253c6fd1508336a2d82c2e4819b
ToxValDB_ECHA_IUCLID NOAEL =0.6 mg/kg bw/day Dog oral chronic; 52 weeks chronic QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca78e4b0a7c65d2220d8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=liver; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15841285_15841287:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_b9e35fc3510947ee0217551f9f299fe5
ToxValDB_ECHA_IUCLID NOAEL =1.8 mg/kg bw/day Dog oral chronic; 52 weeks chronic QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca78e4b0a7c65d2220d8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/6/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=liver; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Oral_15841286_15841288:F:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_77cb92ccb35364e4e94345fc0b12d9ae
ToxValDB_ECHA_IUCLID NOAEL =180 ppm Rat oral - reproduction developmental QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c8bde4b0a7c65d219fbc; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/11311/7/9/2?documentUUID=502ddbbe-8660-42be-8155-be5a2f6657e5; YEAR=1985; ORIGINAL_YEAR=1985; STUDY_GROUP=ECHA IUCLID_dup_Toxicity Reproduction_15855336_15856171_15856717:M/F:P0-; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_7f23de17ff1dcb95bfe35f0fad8a5580
ToxValDB_ECOTOX 12 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_ECOTOX LOEL =50 ul/org Mouse dermal short-term; 18 days short-term LONG_REF=Toxicology176(1-2): 123-134 De Jong,W.H., M. Tentij, S.W. Spiekstra, R.J. Vandebriel, and H. Van Loveren Determination of the Sensitising Activity of the Rubber Contact Sensitisers TMTD, ZDMC, MBT and DEA in a Modified Local Lymph Node Assay and the Effect of Sodium Dodecyl Sulfate Pretreatment on Local Lymph Node Response 2002; TITLE=Determination of the Sensitising Activity of the Rubber Contact Sensitisers TMTD, ZDMC, MBT and DEA in a Modified Local Lymph Node Assay and the Effect of Sodium Dodecyl Sulfate Pretreatment on Local Lymph Node Response; AUTHOR=De Jong,W.H., M. Tentij, S.W. Spiekstra, R.J. Vandebriel, and H. Van Loveren; DOI=10.1016/s0300-483x(02)00131-2; QUALITY=Control type: Carrier or solvent control; EXTERNAL_SOURCE_ID=99302; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=2002; ORIGINAL_YEAR=2002; TOXICOLOGICAL_EFFECT=Cell(s): Number of cells|Histology: Proliferation|Morphology: Weight; TOXICOLOGICAL_EFFECT_CATEGORY=nonneoplastic histopathology|other; STUDY_GROUP=ECOTOX:15594832:M/F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=4e4c92acdbe6b0dd46089db4031e8f9e
ToxValDB_ECOTOX LOEL =25 mg/kg bw/day Mouse injection short-term; 2 days short-term LONG_REF=Teratog. Carcinog. Mutagen.12(3): 97-112 Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test 1992; TITLE=Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test; AUTHOR=Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere; DOI=10.1002/tcm.1770120302; QUALITY=Control type: Multiple control types; EXTERNAL_SOURCE_ID=99049; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1992; ORIGINAL_YEAR=1992; TOXICOLOGICAL_EFFECT=Cell(s): Polychromatic cells; STUDY_GROUP=ECOTOX_dup_EPA ORD_15594976_15594977_15596212_15607992:F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=fb34e74e94c486d49fb7f1bf6e4ecf54
ToxValDB_ECOTOX LOEL =76 mL/454 g diet Mouse oral short-term; 4 days short-term LONG_REF=Int. Biodeterior. Biodegrad.45:169-174 Nolte,D.L., and J.P. Barnett A Repellent to Reduce Mouse Damage to Longleaf Pine Seed 2000; TITLE=A Repellent to Reduce Mouse Damage to Longleaf Pine Seed; AUTHOR=Nolte,D.L., and J.P. Barnett; DOI=10.1016/S0964-8305(00)00060-3; QUALITY=Control type: Baseline control |::| Control type: Concurrent control; EXTERNAL_SOURCE_ID=74471; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=2000; ORIGINAL_YEAR=2000; TOXICOLOGICAL_EFFECT=Avoidance: Food avoidance; TOXICOLOGICAL_EFFECT_CATEGORY=food and/or water consumption; STUDY_GROUP=ECOTOX:15605086:unknown:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=2eb5f8208a8bca04f0e00551af4ad9c8
ToxValDB_ECOTOX LOEL =1 mmol/kg Mouse oral acute; 1 days acute LONG_REF=Toxicol. Lett.42(1): 87-98 Borg,K., and H. Tjalve Effect of Thiram and Dithiocarbamate Pesticides on the Gastrointestinal Absorption and Distribution of Nickel in Mice 1988; TITLE=Effect of Thiram and Dithiocarbamate Pesticides on the Gastrointestinal Absorption and Distribution of Nickel in Mice; AUTHOR=Borg,K., and H. Tjalve; DOI=10.1016/0378-4274(88)90106-3; QUALITY=Control type: Carrier or solvent control; EXTERNAL_SOURCE_ID=90179; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1988; ORIGINAL_YEAR=1988; TOXICOLOGICAL_EFFECT=Biochemistry: Nickel content; STUDY_GROUP=ECOTOX:15605694:F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=ccaef8edfd8ec15b83da2e2c8768c857
ToxValDB_ECOTOX NOEL =12.5 mg/kg bw/day Mouse injection short-term; 2 days short-term LONG_REF=Teratog. Carcinog. Mutagen.12(3): 97-112 Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test 1992; TITLE=Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test; AUTHOR=Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere; DOI=10.1002/tcm.1770120302; QUALITY=Control type: Multiple control types; EXTERNAL_SOURCE_ID=99049; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1992; ORIGINAL_YEAR=1992; TOXICOLOGICAL_EFFECT=Cell(s): Polychromatic cells; STUDY_GROUP=ECOTOX_dup_EPA ORD_15594976_15594977_15596212_15607992:F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=f24b2917b921e7f5b8bfbd9ff52aaed1
ToxValDB_ECOTOX NOEL =37.5 mg/kg bw/day Mouse injection short-term; 2 days short-term LONG_REF=Teratog. Carcinog. Mutagen.12(3): 97-112 Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test 1992; TITLE=Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test; AUTHOR=Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere; DOI=10.1002/tcm.1770120302; QUALITY=Control type: Carrier or solvent control; EXTERNAL_SOURCE_ID=99049; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1992; ORIGINAL_YEAR=1992; TOXICOLOGICAL_EFFECT=Cell(s): Polychromatic cells|Cell(s): Polychromatic cells, micronucleated; TOXICOLOGICAL_EFFECT_CATEGORY=nonneoplastic histopathology; STUDY_GROUP=ECOTOX_dup_EPA ORD_15594976_15594977_15596212_15607992:F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=3a9c98231fec70f81126969008162427
ToxValDB_ECOTOX NOEL =50 mg/kg bw/day Mouse injection acute; 1 days acute LONG_REF=Teratog. Carcinog. Mutagen.12(3): 97-112 Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test 1992; TITLE=Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test; AUTHOR=Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere; DOI=10.1002/tcm.1770120302; QUALITY=Control type: Multiple control types; EXTERNAL_SOURCE_ID=99049; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1992; ORIGINAL_YEAR=1992; TOXICOLOGICAL_EFFECT=Cell(s): Polychromatic cells, micronucleated; TOXICOLOGICAL_EFFECT_CATEGORY=nonneoplastic histopathology; STUDY_GROUP=ECOTOX_dup_EPA ORD_15596604_15599023_15609795_15609796:F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=4874ab26437ec2a74945282c3aaa7197
ToxValDB_ECOTOX NOEL =80 mg/kg bw/day Rat injection short-term; 5 days short-term LONG_REF=Arch. Toxicol.8:77-79 Komulainen,H., and K. Savolainen Effect of Dithiocarbamate Fungicides and Thiurams on 3H-Haloperidol Binding in Rat Brain 1985; TITLE=Effect of Dithiocarbamate Fungicides and Thiurams on 3H-Haloperidol Binding in Rat Brain; AUTHOR=Komulainen,H., and K. Savolainen; DOI=10.1007/978-3-642-69928-3_8; QUALITY=Control type: Carrier or solvent control; EXTERNAL_SOURCE_ID=90501; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1985; ORIGINAL_YEAR=1985; TOXICOLOGICAL_EFFECT=Biochemistry: Protein binding; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECOTOX:15599546:M:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=a76d61c06246f5004256399de43d537b
ToxValDB_ECOTOX NOEL =366.7 mg/kg bw/day Mouse injection short-term; 2 days short-term LONG_REF=Mutat. Res.518(2): 145-150 Grisolia,C.K. A Comparison Between Mouse and Fish Micronucleus Test Using Cyclophosphamide, Mitomycin C and Various Pesticides 2002; TITLE=A Comparison Between Mouse and Fish Micronucleus Test Using Cyclophosphamide, Mitomycin C and Various Pesticides; AUTHOR=Grisolia,C.K.; DOI=10.1016/s1383-5718(02)00086-4; QUALITY=Control type: Multiple control types; EXTERNAL_SOURCE_ID=74478; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=2002; ORIGINAL_YEAR=2002; TOXICOLOGICAL_EFFECT=Cell(s): Polychromatic cells; STUDY_GROUP=ECOTOX:15606416:M/F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=8344a78ba71d20d4dcaa6f19b2ca3a72
ToxValDB_ECOTOX NOEL =250 mg/kg bw/day Mouse oral short-term; 1.25 days short-term LONG_REF=Mutat. Res.48(2): 225-236 Seiler,J.P. Nitrosation In Vitro and In Vivo by Sodium Nitrite, and Mutagenicity of Nitrogenous Pesticides 1977; TITLE=Nitrosation In Vitro and In Vivo by Sodium Nitrite, and Mutagenicity of Nitrogenous Pesticides; AUTHOR=Seiler,J.P.; DOI=10.1016/0027-5107(77)90164-6; QUALITY=Control type: Concurrent control; EXTERNAL_SOURCE_ID=88676; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1977; ORIGINAL_YEAR=1977; TOXICOLOGICAL_EFFECT=Cell(s): Polychromatic cells, micronucleated; TOXICOLOGICAL_EFFECT_CATEGORY=nonneoplastic histopathology; STUDY_GROUP=ECOTOX:15609136:M/F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=03144c9447194fdcee7e5302dfd13404
ToxValDB_ECOTOX NOEL =25 mg/kg bw/day Mouse injection acute; 1 days acute LONG_REF=Teratog. Carcinog. Mutagen.12(3): 97-112 Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test 1992; TITLE=Further In Vitro and In Vivo Mutagenicity Assays with Thiram and Ziram Fungicides: Bacterial Reversion Assays and Mouse Micronucleus Test; AUTHOR=Crebelli,R., A. Zijno, L. Conti, B. Crochi, P. Leopardi, F. Marcon, L. Renzi, and A. Carere; DOI=10.1002/tcm.1770120302; QUALITY=Control type: Multiple control types; EXTERNAL_SOURCE_ID=99049; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1992; ORIGINAL_YEAR=1992; TOXICOLOGICAL_EFFECT=Cell(s): Polychromatic cells; STUDY_GROUP=ECOTOX_dup_EPA ORD_15596604_15599023_15609795_15609796:F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=0de1ccecb035bdda920efdf305bb566e
ToxValDB_ECOTOX NOEL =10 mg/kg bw/day Mouse oral chronic; 547.92 days chronic LONG_REF=J. Natl. Cancer Inst.42:1101-1114 Innes,J.R.M., B.M. Ulland, M.G. Valerio, L. Petrucelli, L. Fishbein, E.R. Hart, A.J. Pallotta, R.R. Bates, H.L. Falk, J Bioassay of Pesticides and Industrial Chemicals for Tumorigenicity in Mice: A Preliminary Note 1969; TITLE=Bioassay of Pesticides and Industrial Chemicals for Tumorigenicity in Mice: A Preliminary Note; AUTHOR=Innes,J.R.M., B.M. Ulland, M.G. Valerio, L. Petrucelli, L. Fishbein, E.R. Hart, A.J. Pallotta, R.R. Bates, H.L. Falk, J; QUALITY=Control type: Multiple entries; EXTERNAL_SOURCE_ID=71346; EXTERNAL_SOURCE_ID_DESC=ECOTOX Reference Number; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759bce8e4b0a7c65d37bc5f; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://cfpub.epa.gov/ecotox/; YEAR=1969; ORIGINAL_YEAR=1969; TOXICOLOGICAL_EFFECT=Injury: Tumor induction; TOXICOLOGICAL_EFFECT_CATEGORY=cancer; STUDY_GROUP=ECOTOX:15611931:unknown:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=9bc8d73f3fcbc419ee2ee58aa7d545c0
ToxValDB_EFSA 7 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_EFSA NOAEL =1.5 mg/kg bw/day Rat oral chronic; 2 years chronic LONG_REF=EFSA (2017). Peer review of the pesticide risk assessment of the active substance thiram. doi:10.2903/j.efsa.2017.4700.; TITLE=Peer review of the pesticide risk assessment of the active substance thiram; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2017.4700; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2017; ORIGINAL_YEAR=2017; TOXICOLOGICAL_EFFECT=body weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=EFSA:15623339:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_bf3c3dfee4c734740417e9fa939557f9
ToxValDB_EFSA NOAEL =0.84 mg/kg bw/day Dog oral chronic; 1 years chronic LONG_REF=EFSA (2017). Peer review of the pesticide risk assessment of the active substance thiram. doi:10.2903/j.efsa.2017.4700.; TITLE=Peer review of the pesticide risk assessment of the active substance thiram; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2017.4700; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2017; ORIGINAL_YEAR=2017; TOXICOLOGICAL_EFFECT=hematological; TOXICOLOGICAL_EFFECT_CATEGORY=hematology; STUDY_GROUP=EFSA:15623340:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_f32149ef25c5b2291cebd1b92accbf77
ToxValDB_EFSA NOAEL <7.5 mg/kg bw/day Rat oral - reproduction developmental LONG_REF=EFSA (2017). Peer review of the pesticide risk assessment of the active substance thiram. doi:10.2903/j.efsa.2017.4700.; TITLE=Peer review of the pesticide risk assessment of the active substance thiram; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2017.4700; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2017; ORIGINAL_YEAR=2017; TOXICOLOGICAL_EFFECT=body weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=EFSA_dup_-_15623341_15623344:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_be3468867fe35cb65c7b0402ca8ddbd4
ToxValDB_EFSA NOAEL =2 mg/kg bw/day Dog oral subchronic; 90 days subchronic LONG_REF=EFSA (2017). Peer review of the pesticide risk assessment of the active substance thiram. doi:10.2903/j.efsa.2017.4700.; TITLE=Peer review of the pesticide risk assessment of the active substance thiram; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2017.4700; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2017; ORIGINAL_YEAR=2017; TOXICOLOGICAL_EFFECT=hematological; TOXICOLOGICAL_EFFECT_CATEGORY=hematology; STUDY_GROUP=EFSA:15623343:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_1351304bc95f0785803e296ecc5df7e5
ToxValDB_EFSA NOAEL =3 mg/kg bw/day Rat oral - reproduction developmental LONG_REF=EFSA (2017). Peer review of the pesticide risk assessment of the active substance thiram. doi:10.2903/j.efsa.2017.4700.; TITLE=Peer review of the pesticide risk assessment of the active substance thiram; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2017.4700; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2017; ORIGINAL_YEAR=2017; TOXICOLOGICAL_EFFECT=body weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=EFSA_dup_-_15623341_15623344:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_64d314bfe070c03d4252a652a2742be7
ToxValDB_EFSA NOAEL =1.6 mg/kg bw/day Rat oral - chronic LONG_REF=EFSA (2017). Peer review of the pesticide risk assessment of the active substance thiram. doi:10.2903/j.efsa.2017.4700.; TITLE=Peer review of the pesticide risk assessment of the active substance thiram; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2017.4700; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2017; ORIGINAL_YEAR=2017; STUDY_GROUP=EFSA:15623345:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_c4948426c199a3861759771567c38a30
ToxValDB_EFSA NOEC =37.5 mg/kg bw/day Northern Bobwhite Quail inhalation - reproduction developmental LONG_REF=EFSA (2017). Peer review of the pesticide risk assessment of the active substance thiram. doi:10.2903/j.efsa.2017.4700.; TITLE=Peer review of the pesticide risk assessment of the active substance thiram; AUTHOR=EFSA; DOI=doi:10.2903/j.efsa.2017.4700; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2017; ORIGINAL_YEAR=2017; STUDY_GROUP=EFSA:15623350:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_8f3a2acd27e59c676c74e3777facd629
ToxValDB_EPA_OPP 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_EPA_OPP PAD (RfD) =0.014 mg/kg bw/day Human oral - Toxicity Value STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/63d99625e4b02a0c3a37c5d8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.epa.gov/sdwa/2021-human-health-benchmarks-pesticides; YEAR=2021; ORIGINAL_YEAR=2021; STUDY_GROUP=EPA OPP_dup_HHBP_15790228_15790230:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_693e7e84b82389d2671019141b726f52
ToxValDB_EPA_OPP PAD (RfD) =0.015 mg/kg bw/day Human oral - Toxicity Value STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/63d99625e4b02a0c3a37c5d8; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.epa.gov/sdwa/2021-human-health-benchmarks-pesticides; YEAR=2021; ORIGINAL_YEAR=2021; STUDY_GROUP=EPA OPP_dup_HHBP_15790228_15790230:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_b997a0afacd7db6a1e70308df4ffe0af
ToxValDB_GESTIS_DNEL 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_GESTIS_DNEL DNEL systemic =0.118 mg/m3 Human inhalation - Toxicity Value STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6543dd69e4b045b9ff7cd87e; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.dguv.de/ifa/gestis/gestis-dnel-liste/index-2.jsp; STUDY_GROUP=GESTIS DNEL:15635243:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_cb8f47db92215504b43a784a65c4819d
ToxValDB_HPVIS 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_HPVIS NOAEL ~2.5 mg/kg bw/day Rat oral subchronic; 90 days subchronic LONG_REF=HLA 6111-110 (1988)Posting date of document from which data were extracted for entry into HPVIS: July 25, 2003.; QUALITY=1; EXTERNAL_SOURCE_ID=61975; EXTERNAL_SOURCE_ID_DESC=HPVIS ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/63861d6de4b04f6bb1480596; RECORD_SOURCE_LEVEL=Extraction document; YEAR=1982; ORIGINAL_YEAR=1982; STUDY_GROUP=HPVIS:15639828:M:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_e29623f43b7ca213d3e0bcc90f1dc6bf
ToxValDB_HPVIS NOAEL =7.5 mg/kg bw/day Rat oral short-term; 10 days developmental LONG_REF=Thiram Task Force, 1987Posting date of document from which data were extracted for entry into HPVIS: July 25, 2003.; QUALITY=2; EXTERNAL_SOURCE_ID=58346; EXTERNAL_SOURCE_ID_DESC=HPVIS ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/63861d6de4b04f6bb1480590; RECORD_SOURCE_LEVEL=Extraction document; YEAR=1987; ORIGINAL_YEAR=1987; STUDY_GROUP=HPVIS:15642417:F:F1offspring; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_dcf77757deefbf1b0e82e28df33347cd
ToxValDB_HPVIS NOAEL =5 mg/kg bw/day Rabbit oral short-term; 14 days reproduction developmental LONG_REF=LSR 87/TRK 004/541 (1988)Posting date of document from which data were extracted for entry into HPVIS: July 25, 2003.; QUALITY=1; EXTERNAL_SOURCE_ID=59944; EXTERNAL_SOURCE_ID_DESC=HPVIS ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/63861d6de4b04f6bb1480590; RECORD_SOURCE_LEVEL=Extraction document; YEAR=1988; ORIGINAL_YEAR=1988; STUDY_GROUP=HPVIS:15642914:F:-maternal; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_7c8655204d490c478c27cc38b37fdb9e
ToxValDB_IRIS 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_IRIS LEL =15 mg/kg bw/day Rat oral chronic; 2 years chronic LONG_REF=E.I. duPont de Nemours & Co., Inc. 1954. MRID. No. 0045162. HED Doc. No. 004550. Available from EPA. Write to FOI, EPA, Washington, DC 20460.; AUTHOR=E.I. duPont de Nemours & Co., Inc; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/652e8a35e4b045b9ff7a542d; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.epa.gov/iris; SUBSOURCE_URL=https://iris.epa.gov/ChemicalLanding/&substance_nmbr=267; TOXICOLOGICAL_EFFECT=neurotoxicity; TOXICOLOGICAL_EFFECT_CATEGORY=nonneoplastic histopathology; STUDY_GROUP=IRIS_dup_IRIS Summary_15644769_15644771:M/F:--; QC_CATEGORY=Manually extracted from unstructured data source; Source overall passed QC, and this record was manually checked; QC_STATUS=pass; SOURCE_HASH=ToxValhc_f70f1eb808c5d7349799b1f207cb879d
ToxValDB_IRIS NOEL =5 mg/kg bw/day Rat oral chronic; 2 years chronic LONG_REF=E.I. duPont de Nemours & Co., Inc. 1954. MRID. No. 0045162. HED Doc. No. 004550. Available from EPA. Write to FOI, EPA, Washington, DC 20460.; AUTHOR=E.I. duPont de Nemours & Co., Inc; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/652e8a35e4b045b9ff7a542d; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.epa.gov/iris; SUBSOURCE_URL=https://iris.epa.gov/ChemicalLanding/&substance_nmbr=267; TOXICOLOGICAL_EFFECT=neurotoxicity; TOXICOLOGICAL_EFFECT_CATEGORY=nonneoplastic histopathology; STUDY_GROUP=IRIS_dup_IRIS Summary_15644769_15644771:M/F:--; QC_CATEGORY=Manually extracted from unstructured data source; Source overall passed QC, and this record was manually checked; QC_STATUS=pass; SOURCE_HASH=ToxValhc_aa6138f13f03ff074b2dfe3675d3ddc3
ToxValDB_IRIS RfD =0.005 mg/kg bw/day Human oral - Toxicity Value LONG_REF=E.I. duPont de Nemours & Co., Inc. 1954. MRID. No. 0045162. HED Doc. No. 004550. Available from EPA. Write to FOI, EPA, Washington, DC 20460.; AUTHOR=E.I. duPont de Nemours & Co., Inc; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/652e8a35e4b045b9ff7a542d; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.epa.gov/iris; SUBSOURCE_URL=https://iris.epa.gov/ChemicalLanding/&substance_nmbr=267; TOXICOLOGICAL_EFFECT=Neurotoxicity in male/female rats; STUDY_GROUP=IRIS:15645482:-:--; QC_CATEGORY=Manually extracted from unstructured data source; Source overall passed QC, and this record was manually checked; QC_STATUS=pass; SOURCE_HASH=ToxValhc_6a36ced23cca8bf6a386b20a402f136d
ToxValDB_RSL 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_RSL RfD =0.006 mg/kg bw/day Human oral - Toxicity Value STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759b87ce4b0a7c65d37b4e2; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.epa.gov/risk/regional-screening-levels-rsls-generic-tables; STUDY_GROUP=RSL:15663807:-:--; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, but this record was not manually checked; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_3911e6e1405e290bea642788b8b361a4
ToxValDB_ToxRefDB 22 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_ToxRefDB LEL =2.35 mg/kg bw/day Dog oral subchronic; 90 days subchronic LONG_REF=Kehoe, D. (1990) 13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017. Unpublished study prepar- ed Hazleton Laboratories America, Inc. 237 p.; TITLE=13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017; AUTHOR=Kehoe, D; EXTERNAL_SOURCE_ID=3542; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1990; ORIGINAL_YEAR=1990; TOXICOLOGICAL_EFFECT=systemic: clinical chemistry-cholesterol-cholesterol|systemic: hematology-hemoglobin (hgb)-hemoglobin (hgb)|systemic: clinical chemistry-protein-protein|systemic: hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|systemic: in life observation-clinical signs-emesis|systemic: hematology-hematocrit (hct)-hematocrit (hct)|systemic: clinical chemistry-calcium-calcium|systemic: hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|systemic: clinical chemistry-albumin-albumin|systemic: hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|systemic: in life observation-food consumption-food consumption|systemic: hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc)|systemic: in life observation-body weight-body weight|systemic: hematology-platelet-platelet; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical chemistry|clinical signs|food and/or water consumption|hematology; STUDY_GROUP=ToxRefDB_dup_-_15702529_15702530_15702531:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_e02033e71d6f8f0437d234d22def0f5f
ToxValDB_ToxRefDB LEL =2.26 mg/kg bw/day Dog oral subchronic; 90 days subchronic LONG_REF=Kehoe, D. (1990) 13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017. Unpublished study prepar- ed Hazleton Laboratories America, Inc. 237 p.; TITLE=13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017; AUTHOR=Kehoe, D; EXTERNAL_SOURCE_ID=3542; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1990; ORIGINAL_YEAR=1990; TOXICOLOGICAL_EFFECT=systemic: clinical chemistry-cholesterol-cholesterol|systemic: hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|systemic: clinical chemistry-protein-protein|systemic: clinical chemistry-albumin-albumin|systemic: hematology-hemoglobin (hgb)-hemoglobin (hgb)|systemic: in life observation-body weight-body weight|systemic: hematology-hematocrit (hct)-hematocrit (hct)|systemic: clinical chemistry-calcium-calcium|systemic: hematology-platelet-platelet|systemic: in life observation-clinical signs-emesis|systemic: hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|systemic: hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|systemic: in life observation-food consumption-food consumption|systemic: hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc); TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical chemistry|clinical signs|food and/or water consumption|hematology; STUDY_GROUP=ToxRefDB_dup_-_15702532_15702533_15702534:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_172a81f62317fefa461707d1c80f2441
ToxValDB_ToxRefDB LEL =4.7 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; TITLE=Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180; AUTHOR=Turck, P; EXTERNAL_SOURCE_ID=3549; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1997; ORIGINAL_YEAR=1997; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight gain|systemic: in life observation-food consumption-food consumption|systemic: in life observation-body weight-body weight|systemic: pathology microscopic-pituitary gland-angiectasis; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15702540_15702541_15702542_15702543:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_4d5db3998579058abb9cb7dbae00b316
ToxValDB_ToxRefDB LEL =12.2 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; TITLE=Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180; AUTHOR=Turck, P; EXTERNAL_SOURCE_ID=3549; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1997; ORIGINAL_YEAR=1997; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-prostate-inflammation|systemic: in life observation-food consumption-food consumption; TOXICOLOGICAL_EFFECT_CATEGORY=food and/or water consumption|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15702544_15702545:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_5f03fdfa6b0ee108faec68acd41e9d64
ToxValDB_ToxRefDB LEL =5.4 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; TITLE=Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180; AUTHOR=Turck, P; EXTERNAL_SOURCE_ID=3549; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1997; ORIGINAL_YEAR=1997; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight gain; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ToxRefDB_dup_-_15702546_15702547_15702548_15702549:F:F1adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_2f25cad235c439e7b0410ff4b162a591
ToxValDB_ToxRefDB LEL =4.9 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; TITLE=Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180; AUTHOR=Turck, P; EXTERNAL_SOURCE_ID=3549; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1997; ORIGINAL_YEAR=1997; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-offspring (pup) weight|systemic: in life observation-body weight-offspring (pup) weight gain; TOXICOLOGICAL_EFFECT_CATEGORY=development; STUDY_GROUP=ToxRefDB_dup_-_15702554_15702555_15702556_15702557:M:F1juvenile; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_1f0b98231c4a5977b48fe4757c3ac834
ToxValDB_ToxRefDB LEL =0.9 mg/kg bw/day Dog oral chronic; 52 weeks chronic LONG_REF=Kehoe, D. (1991) 52-Week Dietary Chronic Toxicity Study with Thiram in Dogs: Final Report: Lab Project Number: HLA 6111-112. Unpublished study prepared by Hazleton Laboratories America, Inc. 545 p.; TITLE=52-Week Dietary Chronic Toxicity Study with Thiram in Dogs: Final Report: Lab Project Number: HLA 6111-112; AUTHOR=Kehoe, D; EXTERNAL_SOURCE_ID=3550; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1991; ORIGINAL_YEAR=1991; TOXICOLOGICAL_EFFECT=systemic: hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|systemic: hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|systemic: clinical chemistry-albumin-albumin|systemic: clinical chemistry-cholesterol-cholesterol|systemic: organ weight-liver-relative to body weight|systemic: clinical chemistry-protein-protein; TOXICOLOGICAL_EFFECT_CATEGORY=clinical chemistry|hematology|organ weight; STUDY_GROUP=ToxRefDB_dup_-_15702566_15702567_15702568:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_1fda1665314c8292ade9e771bed0c31a
ToxValDB_ToxRefDB LEL =57 mg/kg bw/day Mouse oral chronic; 97 weeks chronic LONG_REF=Trutter, J. (1992) Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223. Unpublished study prepared by Hazleton Washington, Inc. 2965 p.; TITLE=Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223; AUTHOR=Trutter, J; EXTERNAL_SOURCE_ID=3551; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1992; ORIGINAL_YEAR=1992; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight gain|systemic: hematology-platelet-platelet|systemic: pathology microscopic-stomach-hyperkeratosis|systemic: pathology microscopic-eye-atrophy|systemic: pathology microscopic-skin-inflammation|systemic: pathology microscopic-spleen-pigmentation|systemic: hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|systemic: pathology microscopic-urinary bladder-[other]|systemic: in life observation-body weight-body weight|systemic: pathology microscopic-skin-necrosis|systemic: hematology-hemoglobin (hgb)-hemoglobin (hgb)|systemic: hematology-hematocrit (hct)-hematocrit (hct); TOXICOLOGICAL_EFFECT_CATEGORY=body weight|hematology|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15702571_15702572_15702573_15702574:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_0d04a8f6fdcad36c2255d0028b4d1b06
ToxValDB_ToxRefDB LEL =24 mg/kg bw/day Mouse oral chronic; 97 weeks chronic LONG_REF=Trutter, J. (1992) Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223. Unpublished study prepared by Hazleton Washington, Inc. 2965 p.; TITLE=Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223; AUTHOR=Trutter, J; EXTERNAL_SOURCE_ID=3551; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1992; ORIGINAL_YEAR=1992; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-skin-necrosis|systemic: pathology microscopic-skin-inflammation|systemic: pathology microscopic-eye-atrophy|systemic: in life observation-body weight-body weight gain|systemic: hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc)|systemic: in life observation-body weight-body weight|systemic: pathology microscopic-urinary bladder-[other]|systemic: pathology microscopic-stomach-hyperkeratosis; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|hematology|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15702575_15702576_15702577_15702578:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_a907fed8a11788c2b0319a2ab12b0f40
ToxValDB_ToxRefDB LEL =1.8 mg/kg bw/day Rat oral chronic; 104 weeks chronic LONG_REF=Kehoe, D. (1991) 104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113. Unpublished study prepared by Hazleton Labs America, Inc. 2513 p.; TITLE=104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113; AUTHOR=Kehoe, D; EXTERNAL_SOURCE_ID=3552; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1991; ORIGINAL_YEAR=1991; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-spleen-hematopoietic cell proliferation|systemic: hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc)|systemic: hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|systemic: hematology-hemoglobin (hgb)-hemoglobin (hgb)|systemic: hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|systemic: hematology-hematocrit (hct)-hematocrit (hct)|systemic: clinical chemistry-urea nitrogen-urea nitrogen|systemic: pathology microscopic-liver-hyperplasia|systemic: pathology microscopic-thyroid gland-hyperplasia|systemic: in life observation-body weight-body weight gain|systemic: pathology gross-adrenal gland-cyst|systemic: pathology microscopic-pancreas-steatosis|systemic: pathology microscopic-pancreas-infiltration cellular|systemic: organ weight-ovary-relative to brain weight|systemic: organ weight-ovary-absolute|systemic: clinical chemistry-glucose-glucose|systemic: pathology microscopic-liver-hematopoietic cell proliferation; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical chemistry|gross pathology|hematology|nonneoplastic histopathology|organ weight; STUDY_GROUP=ToxRefDB_dup_-_15702579_15702580_15702581:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_7e4c31addd126e86131a0866394ae65a
ToxValDB_ToxRefDB LEL =7.3 mg/kg bw/day Rat oral chronic; 104 weeks chronic LONG_REF=Kehoe, D. (1991) 104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113. Unpublished study prepared by Hazleton Labs America, Inc. 2513 p.; TITLE=104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113; AUTHOR=Kehoe, D; EXTERNAL_SOURCE_ID=3552; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1991; ORIGINAL_YEAR=1991; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-pancreas-infiltration cellular|systemic: pathology microscopic-pancreas-steatosis|systemic: in life observation-body weight-body weight gain|systemic: pathology microscopic-pancreas-atrophy|systemic: clinical chemistry-glucose-glucose|systemic: organ weight-kidney-absolute|systemic: pathology gross-lymph node-discolored|systemic: hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|systemic: pathology gross-liver-foci|systemic: pathology gross-kidney-discolored|systemic: organ weight-kidney-relative to brain weight|systemic: hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv); TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical chemistry|gross pathology|hematology|nonneoplastic histopathology|organ weight; STUDY_GROUP=ToxRefDB_dup_-_15702582_15702583_15702584_15702585:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_fcce5407c1b1177b71a93e26596414ec
ToxValDB_ToxRefDB LOAEL =7.34 mg/kg bw/day Dog oral subchronic; 90 days subchronic LONG_REF=Kehoe, D. (1990) 13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017. Unpublished study prepar- ed Hazleton Laboratories America, Inc. 237 p.; TITLE=13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017; AUTHOR=Kehoe, D; EXTERNAL_SOURCE_ID=3542; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1990; ORIGINAL_YEAR=1990; TOXICOLOGICAL_EFFECT=systemic: hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|systemic: hematology-hemoglobin (hgb)-hemoglobin (hgb)|systemic: clinical chemistry-cholesterol-cholesterol|systemic: clinical chemistry-protein-protein|systemic: hematology-hematocrit (hct)-hematocrit (hct)|systemic: clinical chemistry-calcium-calcium|systemic: hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|systemic: hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|systemic: in life observation-food consumption-food consumption|systemic: clinical chemistry-albumin-albumin; TOXICOLOGICAL_EFFECT_CATEGORY=clinical chemistry|food and/or water consumption|hematology; STUDY_GROUP=ToxRefDB_dup_-_15702529_15702530_15702531:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_09900eb5c06dea2ea9faceb8b1d75ff7
ToxValDB_ToxRefDB LOAEL =7.01 mg/kg bw/day Dog oral subchronic; 90 days subchronic LONG_REF=Kehoe, D. (1990) 13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017. Unpublished study prepar- ed Hazleton Laboratories America, Inc. 237 p.; TITLE=13-Week Toxicity Study with Thiram in Dogs: Lab Project Number: HLA 6111-121: 90-017; AUTHOR=Kehoe, D; EXTERNAL_SOURCE_ID=3542; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1990; ORIGINAL_YEAR=1990; TOXICOLOGICAL_EFFECT=systemic: hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|systemic: in life observation-food consumption-food consumption|systemic: hematology-platelet-platelet|systemic: hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|systemic: clinical chemistry-cholesterol-cholesterol|systemic: hematology-mean corpuscular hemoglobin (mch)-mean corpuscular hemoglobin (mch)|systemic: in life observation-body weight-body weight|systemic: hematology-hematocrit (hct)-hematocrit (hct)|systemic: hematology-hemoglobin (hgb)-hemoglobin (hgb)|systemic: clinical chemistry-calcium-calcium|systemic: clinical chemistry-protein-protein|systemic: clinical chemistry-albumin-albumin; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical chemistry|food and/or water consumption|hematology; STUDY_GROUP=ToxRefDB_dup_-_15702532_15702533_15702534:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_ee7305999a0e4a0032c921e443e5409e
ToxValDB_ToxRefDB LOAEL =15 mg/kg bw/day Rat oral short-term (developmental); 10 days developmental LONG_REF=Tesh, J.; McAnulty, P.; Willoughby, C.; et al. (1988) Thiram: Teratology Study in the Rat: 87/TRK002/179. Unpublished study prepared by Life Science Research. 91 p.; TITLE=Thiram: Teratology Study in the Rat: 87/TRK002/179; AUTHOR=Tesh, J.; McAnulty, P.; Willoughby, C.; et al; EXTERNAL_SOURCE_ID=3546; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1988; ORIGINAL_YEAR=1988; TOXICOLOGICAL_EFFECT=developmental: developmental malformation-bone-incomplete ossification|developmental: developmental malformation-bone-short supernumerary; TOXICOLOGICAL_EFFECT_CATEGORY=development; STUDY_GROUP=ToxRefDB_dup_-_15702537_15702538_15702539:M/F:fetusfetal; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_7dd1cd690f6a00e50612fff600e17ce7
ToxValDB_ToxRefDB LOAEL =2.54 mg/kg bw/day Dog oral chronic; 52 weeks chronic LONG_REF=Kehoe, D. (1991) 52-Week Dietary Chronic Toxicity Study with Thiram in Dogs: Final Report: Lab Project Number: HLA 6111-112. Unpublished study prepared by Hazleton Laboratories America, Inc. 545 p.; TITLE=52-Week Dietary Chronic Toxicity Study with Thiram in Dogs: Final Report: Lab Project Number: HLA 6111-112; AUTHOR=Kehoe, D; EXTERNAL_SOURCE_ID=3550; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1991; ORIGINAL_YEAR=1991; TOXICOLOGICAL_EFFECT=systemic: clinical chemistry-albumin-albumin|systemic: clinical chemistry-cholesterol-cholesterol|systemic: organ weight-liver-relative to body weight|systemic: clinical chemistry-protein-protein; TOXICOLOGICAL_EFFECT_CATEGORY=clinical chemistry|organ weight; STUDY_GROUP=ToxRefDB_dup_-_15702566_15702567_15702568:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_f954c0714817e7ad873592a768d99377
ToxValDB_ToxRefDB LOAEL =8.9 mg/kg bw/day Rat oral chronic; 104 weeks chronic LONG_REF=Kehoe, D. (1991) 104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113. Unpublished study prepared by Hazleton Labs America, Inc. 2513 p.; TITLE=104-Week Combined Chronic Toxicity and Carcino- genicity Study with Thiram in Rats: Lab Project Number: HLA 6111 113; AUTHOR=Kehoe, D; EXTERNAL_SOURCE_ID=3552; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1991; ORIGINAL_YEAR=1991; TOXICOLOGICAL_EFFECT=systemic: hematology-mean corpuscular (cell) volume (mcv)-mean corpuscular (cell) volume (mcv)|systemic: hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc)|systemic: clinical chemistry-urea nitrogen-urea nitrogen|systemic: pathology microscopic-liver-hyperplasia|systemic: in life observation-body weight-body weight gain|systemic: hematology-hematocrit (hct)-hematocrit (hct)|systemic: hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|systemic: hematology-hemoglobin (hgb)-hemoglobin (hgb); TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical chemistry|hematology|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15702579_15702580_15702581:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_c045a6e894047ac14ec87a19cb4f4cf5
ToxValDB_ToxRefDB NEL =1.6 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; TITLE=Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180; AUTHOR=Turck, P; EXTERNAL_SOURCE_ID=3549; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1997; ORIGINAL_YEAR=1997; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight gain|systemic: in life observation-food consumption-food consumption|systemic: pathology microscopic-pituitary gland-angiectasis|systemic: in life observation-body weight-body weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15702540_15702541_15702542_15702543:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_10f960d3ad1de1ab80d433995d8f7d98
ToxValDB_ToxRefDB NEL =4.2 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; TITLE=Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180; AUTHOR=Turck, P; EXTERNAL_SOURCE_ID=3549; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1997; ORIGINAL_YEAR=1997; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-prostate-inflammation|systemic: in life observation-food consumption-food consumption; TOXICOLOGICAL_EFFECT_CATEGORY=food and/or water consumption|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15702544_15702545:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_7d9d4691033ef70efa4d9bcee90d3ea5
ToxValDB_ToxRefDB NEL =1.8 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; TITLE=Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180; AUTHOR=Turck, P; EXTERNAL_SOURCE_ID=3549; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1997; ORIGINAL_YEAR=1997; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight gain; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ToxRefDB_dup_-_15702546_15702547_15702548_15702549:F:F1adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_e6f61234b6276c54cf698eed574b82a2
ToxValDB_ToxRefDB NEL =1.7 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=Turck, P. (1997) Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180. Unpublished study prepared by MPI Research. 1579 p.; TITLE=Two Generation Reproduction/Fertility Study in Rats with Thiram: Lab Project Number: 399-180; AUTHOR=Turck, P; EXTERNAL_SOURCE_ID=3549; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1997; ORIGINAL_YEAR=1997; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-offspring (pup) weight gain|systemic: in life observation-body weight-offspring (pup) weight; TOXICOLOGICAL_EFFECT_CATEGORY=development; STUDY_GROUP=ToxRefDB_dup_-_15702554_15702555_15702556_15702557:M:F1juvenile; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_2613d6d33b35aff5fda3f1063cd37680
ToxValDB_ToxRefDB NEL =3.1 mg/kg bw/day Mouse oral chronic; 97 weeks chronic LONG_REF=Trutter, J. (1992) Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223. Unpublished study prepared by Hazleton Washington, Inc. 2965 p.; TITLE=Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223; AUTHOR=Trutter, J; EXTERNAL_SOURCE_ID=3551; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1992; ORIGINAL_YEAR=1992; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-skin-inflammation|systemic: pathology microscopic-spleen-pigmentation|systemic: hematology-erythrocyte (rbc) count differential-erythrocyte (rbc)|systemic: pathology microscopic-urinary bladder-[other]|systemic: hematology-hematocrit (hct)-hematocrit (hct)|systemic: in life observation-body weight-body weight|systemic: hematology-hemoglobin (hgb)-hemoglobin (hgb)|systemic: in life observation-body weight-body weight gain|systemic: hematology-platelet-platelet|systemic: pathology microscopic-skin-necrosis|systemic: pathology microscopic-stomach-hyperkeratosis|systemic: pathology microscopic-eye-atrophy; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|hematology|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15702571_15702572_15702573_15702574:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_d8ab16dfc92fec546d0ceff7a2595f11
ToxValDB_ToxRefDB NEL =2.5 mg/kg bw/day Mouse oral chronic; 97 weeks chronic LONG_REF=Trutter, J. (1992) Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223. Unpublished study prepared by Hazleton Washington, Inc. 2965 p.; TITLE=Oncogenicity Study in Mice with Thiram: Lab Project Number: 798-223; AUTHOR=Trutter, J; EXTERNAL_SOURCE_ID=3551; EXTERNAL_SOURCE_ID_DESC=ToxRefDB Study ID; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66bca4a3e4b0a7c65d2a792a; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://github.com/USEPA/CompTox-ToxRefDB; YEAR=1992; ORIGINAL_YEAR=1992; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight gain|systemic: pathology microscopic-eye-atrophy|systemic: pathology microscopic-skin-inflammation|systemic: pathology microscopic-skin-necrosis|systemic: pathology microscopic-stomach-hyperkeratosis|systemic: pathology microscopic-urinary bladder-[other]|systemic: in life observation-body weight-body weight|systemic: hematology-mean corpuscular hemoglobin concentration (mchc)-mean corpuscular hemoglobin concentration (mchc); TOXICOLOGICAL_EFFECT_CATEGORY=body weight|hematology|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15702575_15702576_15702577_15702578:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_a4a71fbd810c3f6bfa895cc778feff4c
openFDA substances 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier 0D771IS0FH UNII - - - chemical {"approval_status":null,"molecular_formula":"C6H12N2S4","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"0D771IS0FH"}
openFDA substances FDA UNII substance identifier 0D771IS0FH UNII - - - chemical {"approval_status":null,"molecular_formula":"C6H12N2S4","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"0D771IS0FH"}
openFDA substances FDA UNII substance identifier 0D771IS0FH UNII - - - chemical {"approval_status":null,"molecular_formula":"C6H12N2S4","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"0D771IS0FH"}
openFDA substances FDA UNII substance identifier 0D771IS0FH UNII - - - chemical {"approval_status":null,"molecular_formula":"C6H12N2S4","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"0D771IS0FH"}