NOAEL Studies Cosmetic Ingredient

Benzylparaben NOAEL Studies

INCI: BENZYLPARABEN

CAS: 94-18-8

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

NTP_ICE_adme_parameters 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_adme_parameters Clint 633 uL/min/10^6 cells Human - - Measured; httk, Human Hepatic Intrinsic Clearance sheet=Data; excel_row=3569; Record_ID=adme_parameters_791; Data_Type=Measured; DTXSID=DTXSID9022526; Assay=httk, Human Hepatic Intrinsic Clearance; Endpoint=Clint; Response=633.0; 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/DTXSID9022526
NTP_ICE_adme_parameters Clint 639.1 uL/min/10^6 cells Rat - - Measured; httk, Rat Hepatic Intrinsic Clearance sheet=Data; excel_row=3571; Record_ID=adme_parameters_791; Data_Type=Measured; DTXSID=DTXSID9022526; Assay=httk, Rat Hepatic Intrinsic Clearance; Endpoint=Clint; Response=639.1; Response_Unit=ul/min/10^6 cells; Species=Rat; Reference=httk2.3.1, Honda 2019; URL=https://cran.r-project.org/web/packages/httk/index.html; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID9022526
NTP_ICE_adme_parameters Fu 0.00674 fraction Human - - Measured; httk, Human Plasma Fraction Unbound sheet=Data; excel_row=3570; Record_ID=adme_parameters_791; Data_Type=Measured; DTXSID=DTXSID9022526; Assay=httk, Human Plasma Fraction Unbound; Endpoint=Fu; Response=0.00674; 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/DTXSID9022526
NTP_ICE_endocrine 6 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_endocrine AC50 5.84189349377303 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=5386; RecordID=ERPathway2016_195; DatasetName=ERPathway2016; DTXSID=DTXSID9022526; Assay=ER Pathway Model, Antagonist; Endpoint=AC50; Response=5.84189349377303; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID9022526
NTP_ICE_endocrine ACC 1.761544913204 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=5387; RecordID=ERPathway2016_195; DatasetName=ERPathway2016; DTXSID=DTXSID9022526; Assay=ER Pathway Model, Antagonist; Endpoint=ACC; Response=1.761544913204; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID9022526
NTP_ICE_endocrine LOEL 0.16 mg/kg bw/day Rat Oral Treatment_Duration=3 days; Age_at_First_Dose=PND 21; Time_Elapsed_Between_Last_Dose_and_Necropsy=24 hours; Number_of_Doses_Tested=2 to 5 In Vivo; Uterotrophic-Agonist sheet=Data_invivo; excel_row=1048; Record_ID=endocrine_invivo_411; Data_Type=In Vivo; Mixture=Chemical; DTXSID=DTXSID9022526; Assay=Uterotrophic-Agonist; Endpoint=LOEL; Response=0.16; Response_Unit=mg/kg/day; Species=Rat; Reported_Strain=SD; Strain=Sprague-Dawley; Sex=Female; Route=Oral; Maximum_Dose=100; Maximum_Dose_Units=mg/kg/day; Reference_Hormone=Estradiol; Reference=Hu et al. 2013; 23220609; 10.1016/j.fct.2012.11.043|Kleinstreuer et al. 2016; 26431337; 10.1289/ehp.1510183; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID9022526
NTP_ICE_endocrine Model Score 0 unitless - - - ARPathway2016; AR Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=5382; RecordID=ARPathway2016_1737; DatasetName=ARPathway2016; DTXSID=DTXSID9022526; Assay=AR Pathway Model, Antagonist; Endpoint=Model Score; Response=0; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID9022526
NTP_ICE_endocrine Model Score 0.234 unitless - - - ERPathway2016; ER Pathway Model, Agonist sheet=Integrated_approaches; excel_row=5388; RecordID=ERPathway2016_195; DatasetName=ERPathway2016; DTXSID=DTXSID9022526; Assay=ER Pathway Model, Agonist; Endpoint=Model Score; Response=0.234; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID9022526
NTP_ICE_endocrine Uterine weight increase vs control 120 % Rat Oral Treatment_Duration=3 days; Age_at_First_Dose=PND 21; Time_Elapsed_Between_Last_Dose_and_Necropsy=24 hours; Number_of_Doses_Tested=2 to 5 In Vivo; Uterotrophic-Agonist sheet=Data_invivo; excel_row=733; Record_ID=endocrine_invivo_411; Data_Type=In Vivo; Mixture=Chemical; DTXSID=DTXSID9022526; Assay=Uterotrophic-Agonist; Endpoint=Uterine weight increase vs control; Response=120; Response_Unit=%; Species=Rat; Reported_Strain=SD; Strain=Sprague-Dawley; Sex=Female; Route=Oral; Maximum_Dose=100; Maximum_Dose_Units=mg/kg/day; Reference_Hormone=Estradiol; Reference=Hu et al. 2013; 23220609; 10.1016/j.fct.2012.11.043|Kleinstreuer et al. 2016; 26431337; 10.1289/ehp.1510183; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID9022526
ToxValDB_ECHA_IUCLID 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_ECHA_IUCLID LEL =0.16 mg/kg bw/day Rat oral short-term; 3 days short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7cc27e4b0a7c65d2292fc; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/17658/7/6/2?documentUUID=9b735672-9ba2-473a-af73-e79c9b9f63d1; YEAR=2018; ORIGINAL_YEAR=2018; STUDY_GROUP=ECHA IUCLID:15841986: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_84785213e86c1690ba60be8cb45dcc08
ToxValDB_ECHA_IUCLID LOAEL =33 mg/kg bw/day Mouse dermal short-term; 3 days short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/67c61f82e4b096bca877dccc; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/17658/7/6/4?documentUUID=9b735672-9ba2-473a-af73-e79c9b9f63d1; YEAR=2018; ORIGINAL_YEAR=2018; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Dermal_15826870_15826871: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_b93f0059274d962c50ce7a8424301f2b
ToxValDB_ECHA_IUCLID NOAEL =10 mg/kg bw/day Mouse dermal short-term; 3 days short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/67c61f82e4b096bca877dccc; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/17658/7/6/4?documentUUID=9b735672-9ba2-473a-af73-e79c9b9f63d1; YEAR=2018; ORIGINAL_YEAR=2018; STUDY_GROUP=ECHA IUCLID_dup_Repeated Dose Toxicity Dermal_15826870_15826871: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_149a5ba56347fb4bdfb21348b5944f39
ToxValDB_ECHA_IUCLID NOAEL =3000 mg/kg bw/day Mouse oral short-term; 5 days short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7cc27e4b0a7c65d2292f2; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/17658/7/6/2?documentUUID=9b735672-9ba2-473a-af73-e79c9b9f63d1; YEAR=2018; ORIGINAL_YEAR=2018; STUDY_GROUP=ECHA IUCLID:15840987: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_9c98bee243f6aea3056aecd18057d81c
ToxValDB_GESTIS_DNEL 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_GESTIS_DNEL DNEL systemic =0.33 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:15630069:-:--; 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_eb76f3d1cfd2bbce595f1305aae94171
ToxValDB_Uterotrophic_Hershberger_DB 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_Uterotrophic_Hershberger_DB LEL =0.16 mg/kg bw/day Rat oral short-term; 3 days uterotrophic LONG_REF=Kleinstreuer et al., A Curated Database of Rodent Uterotrophic Bioactivity, EHP Vol 124 2106, https://doi.org/10.1289/ehp.1510183; TITLE=A Curated Database of Rodent Uterotrophic Bioactivity; AUTHOR=Kleinstreuer et al., A Curated Database of Rodent Uterotrophic Bioactivity, EHP Vol 124; DOI=10.1289/ehp.1510183; GUIDELINE=1; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759abc7e4b0a7c65d37b40c; RECORD_SOURCE_LEVEL=Extraction document; TOXICOLOGICAL_EFFECT=Active; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=Uterotrophic Hershberger DB:15713443:-:--; 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_fcdf87201af9e79d87761cf7931d3095
ToxValDB_Uterotrophic_Hershberger_DB LEL =100 mg/day Mouse dermal short-term; 3 days uterotrophic LONG_REF=Kleinstreuer et al., A Curated Database of Rodent Uterotrophic Bioactivity, EHP Vol 124 2106, https://doi.org/10.1289/ehp.1510183; TITLE=A Curated Database of Rodent Uterotrophic Bioactivity; AUTHOR=Kleinstreuer et al., A Curated Database of Rodent Uterotrophic Bioactivity, EHP Vol 124; DOI=10.1289/ehp.1510183; GUIDELINE=0; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/6759abc7e4b0a7c65d37b40c; RECORD_SOURCE_LEVEL=Extraction document; TOXICOLOGICAL_EFFECT=Active; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=Uterotrophic Hershberger DB:15713377:-:--; 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_736e16752c6803fe679ea0f892a46a3d
openFDA substances 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier 8Y41DYV4VG UNII - - - chemical {"approval_status":null,"molecular_formula":"C14H12O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"8Y41DYV4VG"}
openFDA substances FDA UNII substance identifier 8Y41DYV4VG UNII - - - chemical {"approval_status":null,"molecular_formula":"C14H12O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"8Y41DYV4VG"}
openFDA substances FDA UNII substance identifier 8Y41DYV4VG UNII - - - chemical {"approval_status":null,"molecular_formula":"C14H12O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"8Y41DYV4VG"}
openFDA substances FDA UNII substance identifier 8Y41DYV4VG UNII - - - chemical {"approval_status":null,"molecular_formula":"C14H12O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"8Y41DYV4VG"}