NOAEL Studies Cosmetic Ingredient

Carvacrol NOAEL Studies

INCI: CARVACROL

CAS: 499-75-2

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

ECHA 15 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ECHA NOAEL 200 mg/kg bw/day rat oral: gavage - screening for reproductive / developmental toxicity dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=4d945f7c-5cbf-4305-8d6c-1f125daa241f_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=4d945f7c-5cbf-4305-8d6c-1f125daa241f/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=1996; basis=other:; key_result=false; entry_uuid=242f7ae8-e95f-4f81-8234-a99c31c65a4e
ECHA NOAEL 40 mg/kg bw/day rat oral: gavage - screening for reproductive / developmental toxicity dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=4d945f7c-5cbf-4305-8d6c-1f125daa241f_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=4d945f7c-5cbf-4305-8d6c-1f125daa241f/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=1996; basis=body weight and weight gain; key_result=false; entry_uuid=ccf911ed-556d-4cc3-97e9-af96aecaa875
ECHA NOAEL 300 mg/kg bw/day rat oral: gavage - screening for reproductive / developmental toxicity dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=3fdb9411-3842-456e-85a2-5a0cfcb4c05e_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=3fdb9411-3842-456e-85a2-5a0cfcb4c05e/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=2010; basis=clinical signs; key_result=false; entry_uuid=3062cb72-f970-468d-9e5f-c336d70550ea
ECHA NOAEL 400 mg/kg bw/day rat oral: gavage - chronic toxicity: oral dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=86e86ee8-b12b-440a-a9a7-4fbb557aece7_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=86e86ee8-b12b-440a-a9a7-4fbb557aece7/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=2006; basis=body weight and weight gain; key_result=false; entry_uuid=cfc1b194-575c-428b-b4d5-b37fba705ad1
ECHA NOAEL 200 mg/kg bw/day rat oral: gavage - screening for reproductive / developmental toxicity dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=4d945f7c-5cbf-4305-8d6c-1f125daa241f_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=4d945f7c-5cbf-4305-8d6c-1f125daa241f/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=1996; basis=other:; key_result=false; entry_uuid=242f7ae8-e95f-4f81-8234-a99c31c65a4e
ECHA NOAEL 40 mg/kg bw/day rat oral: gavage - screening for reproductive / developmental toxicity dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=4d945f7c-5cbf-4305-8d6c-1f125daa241f_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=4d945f7c-5cbf-4305-8d6c-1f125daa241f/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=1996; basis=body weight and weight gain; key_result=false; entry_uuid=ccf911ed-556d-4cc3-97e9-af96aecaa875
ECHA NOAEL 300 mg/kg bw/day rat oral: gavage - screening for reproductive / developmental toxicity dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=3fdb9411-3842-456e-85a2-5a0cfcb4c05e_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=3fdb9411-3842-456e-85a2-5a0cfcb4c05e/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=2010; basis=clinical signs; key_result=false; entry_uuid=3062cb72-f970-468d-9e5f-c336d70550ea
ECHA NOAEL 400 mg/kg bw/day rat oral: gavage - chronic toxicity: oral dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=86e86ee8-b12b-440a-a9a7-4fbb557aece7_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=86e86ee8-b12b-440a-a9a7-4fbb557aece7/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=2006; basis=body weight and weight gain; key_result=false; entry_uuid=cfc1b194-575c-428b-b4d5-b37fba705ad1
ECHA NOAEL 200 mg/kg bw/day rat oral: gavage - screening for reproductive / developmental toxicity dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=4d945f7c-5cbf-4305-8d6c-1f125daa241f_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=4d945f7c-5cbf-4305-8d6c-1f125daa241f/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=1996; basis=other:; key_result=false; entry_uuid=242f7ae8-e95f-4f81-8234-a99c31c65a4e
ECHA NOAEL 40 mg/kg bw/day rat oral: gavage - screening for reproductive / developmental toxicity dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=4d945f7c-5cbf-4305-8d6c-1f125daa241f_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=4d945f7c-5cbf-4305-8d6c-1f125daa241f/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=1996; basis=body weight and weight gain; key_result=false; entry_uuid=ccf911ed-556d-4cc3-97e9-af96aecaa875
ECHA NOAEL 300 mg/kg bw/day rat oral: gavage - screening for reproductive / developmental toxicity dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=3fdb9411-3842-456e-85a2-5a0cfcb4c05e_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=3fdb9411-3842-456e-85a2-5a0cfcb4c05e/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=ToxicityReproduction; literature=Name=Unnamed; ReferenceYear=2010; basis=clinical signs; key_result=false; entry_uuid=3062cb72-f970-468d-9e5f-c336d70550ea
ECHA NOAEL 400 mg/kg bw/day rat oral: gavage - chronic toxicity: oral dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=86e86ee8-b12b-440a-a9a7-4fbb557aece7_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=86e86ee8-b12b-440a-a9a7-4fbb557aece7/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=2006; basis=body weight and weight gain; key_result=false; entry_uuid=cfc1b194-575c-428b-b4d5-b37fba705ad1
ECHA NOEL 8 mg/kg bw/day rat oral: gavage - repeated dose toxicity: oral, other dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=7b5ef2c0-6b9b-4fcd-911b-17799f3df51d_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=7b5ef2c0-6b9b-4fcd-911b-17799f3df51d/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1996; basis=histopathology: non-neoplastic; key_result=false; entry_uuid=0fdb6baa-85d7-4247-99f0-899364764287
ECHA NOEL 8 mg/kg bw/day rat oral: gavage - repeated dose toxicity: oral, other dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=7b5ef2c0-6b9b-4fcd-911b-17799f3df51d_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=7b5ef2c0-6b9b-4fcd-911b-17799f3df51d/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1996; basis=histopathology: non-neoplastic; key_result=false; entry_uuid=0fdb6baa-85d7-4247-99f0-899364764287
ECHA NOEL 8 mg/kg bw/day rat oral: gavage - repeated dose toxicity: oral, other dossier=b1058dde-3c09-433c-884f-6aa33c36bfde.i6z; document=7b5ef2c0-6b9b-4fcd-911b-17799f3df51d_b1058dde-3c09-433c-884f-6aa33c36bfde.i6d; document_key=7b5ef2c0-6b9b-4fcd-911b-17799f3df51d/b1058dde-3c09-433c-884f-6aa33c36bfde; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1996; basis=histopathology: non-neoplastic; key_result=false; entry_uuid=0fdb6baa-85d7-4247-99f0-899364764287
NTP ICE acute oral 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE acute oral LD50 =810 mg/kg bw Rat oral acute Rat Acute Oral Toxicity NLM ChemIDplus TEST (undated); record_id=acute_oral_6703; row=10857; data_type=In Vivo; mixture=Chemical; chemical_name=Isopropyl-o-cresol; preferred_name=Isopropyl-o-cresol; dtxsid=DTXSID6042074; url=https://chem.nlm.nih.gov/chemidplus/; url_comptox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074; source_file=acute_oral.xlsx
NTP ICE endocrine 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE endocrine Model Score 0 unitless - - - ARPathway2016; AR Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=10840; RecordID=ARPathway2016_1240; DatasetName=ARPathway2016; DTXSID=DTXSID6042074; Assay=AR Pathway Model, Antagonist; Endpoint=Model Score; Response=0; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin irritation 9 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin irritation Viability (240 minutes) 12.1 % - Dermal - In Vitro; EpiSkin Corrosion sheet=Data_invitro; excel_row=4372; Record_ID=skin_irritation_invitro_1891; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=EpiSkin Corrosion; Endpoint=Viability (240 minutes); Response=12.1; Response_Unit=%; Reference=Alepee et al. 2014; 24211528; 10.1016/j.tiv.2013.10.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin irritation Viability (240 minutes) 12.5 % - Dermal - In Vitro; EpiSkin Corrosion sheet=Data_invitro; excel_row=4371; Record_ID=skin_irritation_invitro_1892; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=EpiSkin Corrosion; Endpoint=Viability (240 minutes); Response=12.5; Response_Unit=%; Reference=Alepee et al. 2014; 24211528; 10.1016/j.tiv.2013.10.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin irritation Viability (240 minutes) 14.7 % - Dermal - In Vitro; EpiSkin Corrosion sheet=Data_invitro; excel_row=4370; Record_ID=skin_irritation_invitro_1893; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=EpiSkin Corrosion; Endpoint=Viability (240 minutes); Response=14.7; Response_Unit=%; Reference=Alepee et al. 2014; 24211528; 10.1016/j.tiv.2013.10.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin irritation Viability (3 minutes) 48.9 % - Dermal - In Vitro; EpiSkin Corrosion sheet=Data_invitro; excel_row=4367; Record_ID=skin_irritation_invitro_1891; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=EpiSkin Corrosion; Endpoint=Viability (3 minutes); Response=48.9; Response_Unit=%; Reference=Alepee et al. 2014; 24211528; 10.1016/j.tiv.2013.10.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin irritation Viability (3 minutes) 57.3 % - Dermal - In Vitro; EpiSkin Corrosion sheet=Data_invitro; excel_row=4366; Record_ID=skin_irritation_invitro_1892; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=EpiSkin Corrosion; Endpoint=Viability (3 minutes); Response=57.3; Response_Unit=%; Reference=Alepee et al. 2014; 24211528; 10.1016/j.tiv.2013.10.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin irritation Viability (3 minutes) 73.4 % - Dermal - In Vitro; EpiSkin Corrosion sheet=Data_invitro; excel_row=4364; Record_ID=skin_irritation_invitro_1893; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=EpiSkin Corrosion; Endpoint=Viability (3 minutes); Response=73.40; Response_Unit=%; Reference=Alepee et al. 2014; 24211528; 10.1016/j.tiv.2013.10.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin irritation Viability (60 minutes) 23.4 % - Dermal - In Vitro; EpiSkin Corrosion sheet=Data_invitro; excel_row=4363; Record_ID=skin_irritation_invitro_1891; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=EpiSkin Corrosion; Endpoint=Viability (60 minutes); Response=23.4; Response_Unit=%; Reference=Alepee et al. 2014; 24211528; 10.1016/j.tiv.2013.10.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin irritation Viability (60 minutes) 26.5 % - Dermal - In Vitro; EpiSkin Corrosion sheet=Data_invitro; excel_row=4362; Record_ID=skin_irritation_invitro_1892; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=EpiSkin Corrosion; Endpoint=Viability (60 minutes); Response=26.5; Response_Unit=%; Reference=Alepee et al. 2014; 24211528; 10.1016/j.tiv.2013.10.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin irritation Viability (60 minutes) 31.1 % - Dermal - In Vitro; EpiSkin Corrosion sheet=Data_invitro; excel_row=4361; Record_ID=skin_irritation_invitro_1893; Data_Type=In Vitro; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=EpiSkin Corrosion; Endpoint=Viability (60 minutes); Response=31.1; Response_Unit=%; Reference=Alepee et al. 2014; 24211528; 10.1016/j.tiv.2013.10.016; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin sensitization 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin sensitization Incidence of positive responses 0 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=7513; Record_ID=skin_sensitization_invivo_1713; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=4.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=0; Response_Unit=%; Species=Human; Route=Dermal; Reference=Epstein 1977: report to RIFM|Anonymous 1979; Not available; 10.1016/S0015-6264(79)80018-8; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin sensitization Induction dose per skin area 2700 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=7511; Record_ID=skin_sensitization_invivo_1713; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=4.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=Human Maximization Test; Endpoint=Induction dose per skin area; Response=2700; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Epstein 1977: report to RIFM|Anonymous 1979; Not available; 10.1016/S0015-6264(79)80018-8; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
NTP ICE skin sensitization Relative reliability score 3 unitless Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=7516; Record_ID=skin_sensitization_invivo_1713; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=4.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID6042074; Assay=Human Maximization Test; Endpoint=Relative reliability score; Response=3; Response_Unit=Unitless; Species=Human; Route=Dermal; Reference=Epstein 1977: report to RIFM|Anonymous 1979; Not available; 10.1016/S0015-6264(79)80018-8; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID6042074
ToxValDB ECOTOX 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB ECOTOX LOEL =4 mg Mouse oral acute; 1 days acute LONG_REF=J. Chem. Ecol.21(3): 263-271 Ahn,Y.J., S.B. Lee, T. Okubo, and M. Kim Antignawing Factor of Crude Oil Derived from Thujopsis dolabrata S. et Z. var. hondai Sawdust Against Mice 1995; TITLE=Antignawing Factor of Crude Oil Derived from Thujopsis dolabrata S. et Z. var. hondai Sawdust Against Mice; AUTHOR=Ahn,Y.J., S.B. Lee, T. Okubo, and M. Kim; DOI=10.1007/BF02036716; QUALITY=Control type: Carrier or solvent control; EXTERNAL_SOURCE_ID=102568; 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=1995; ORIGINAL_YEAR=1995; TOXICOLOGICAL_EFFECT=Behavior: Bite or biting; TOXICOLOGICAL_EFFECT_CATEGORY=neurobehavior; STUDY_GROUP=ECOTOX:15605461:F:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=9a7833a30cbbb3f44b51d30ac3f62794
EFSA 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EFSA LEL =2000 mg/kg bw/day Pig oral subchronic; 6 weeks subchronic LONG_REF=EFSA FEEDAP (2020). Safety and efficacy of Nimicoat (carvacrol) as a zootechnical additive for weaned piglets. doi:10.2903/j.efsa.2020.6070.; TITLE=Safety and efficacy of Nimicoat (carvacrol) as a zootechnical additive for weaned piglets; AUTHOR=EFSA FEEDAP; DOI=doi:10.2903/j.efsa.2020.6070; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2020; ORIGINAL_YEAR=2020; TOXICOLOGICAL_EFFECT=no effects; STUDY_GROUP=EFSA:15621592: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_8f9d55eedc595eb1a2d00a30a5fdfdb9
ToxValDB GESTIS DNEL 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB GESTIS DNEL DNEL systemic =0.439 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_dup_-_15630593_15630594_15630595:-:--; 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_25e7efcba46d858d3b0e8240e623a947
ToxValDB GESTIS DNEL DNEL systemic =9.87 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_dup_-_15630593_15630594_15630595:-:--; 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_162190e65b8d0cc6305f28f5a8fa56fa
ToxValDB GESTIS DNEL DNEL systemic =14.8 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_dup_-_15630593_15630594_15630595:-:--; 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_211acdba878f97f3898630bd6e54b933
openFDA substances 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier 9B1J4V995Q UNII - - - chemical {"approval_status":null,"molecular_formula":"C10H14O","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"9B1J4V995Q"}
openFDA substances FDA UNII substance identifier 9B1J4V995Q UNII - - - chemical {"approval_status":null,"molecular_formula":"C10H14O","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"9B1J4V995Q"}
openFDA substances FDA UNII substance identifier 9B1J4V995Q UNII - - - chemical {"approval_status":null,"molecular_formula":"C10H14O","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"9B1J4V995Q"}
openFDA substances FDA UNII substance identifier 9B1J4V995Q UNII - - - chemical {"approval_status":null,"molecular_formula":"C10H14O","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"9B1J4V995Q"}