NOAEL Studies Cosmetic Ingredient

Hexyl Salicylate NOAEL Studies

INCI: HEXYL SALICYLATE

CAS: 6259-76-3

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

EFSA 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EFSA NOAEL =5 mg/kg bw/day Rat oral: unspecified 91 days subchronic EFSA FEEDAP - 2012 - OutputID 607 - body weight - systemic - Scientific Opinion on the safety and efficacy of benzyl alcohols, aldehydes, acids, esters and acetals (chemical group 23) when used as flavourings for all animal species - doi:10.2903/j.efsa.2012.2785
EFSA NOAEL =5 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic LONG_REF=EFSA FEEDAP (2012). Scientific Opinion on the safety and efficacy of benzyl alcohols, aldehydes, acids, esters and acetals (chemical group 23) when used as flavourings for all animal species. doi:10.2903/j.efsa.2012.2785.; TITLE=Scientific Opinion on the safety and efficacy of benzyl alcohols, aldehydes, acids, esters and acetals (chemical group 23) when used as flavourings for all animal species; AUTHOR=EFSA FEEDAP; DOI=doi:10.2903/j.efsa.2012.2785; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2012; ORIGINAL_YEAR=2012; TOXICOLOGICAL_EFFECT=body weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=EFSA:15614581:-:--; 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_6ab5147820e47f46d6f593e5a882078d
NTP ICE adme parameters 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE adme parameters Clint 191.4 uL/min/10^6 cells Human - - Measured; httk, Human Hepatic Intrinsic Clearance sheet=Data; excel_row=1797; Record_ID=adme_parameters_1181; Data_Type=Measured; DTXSID=DTXSID4038924; Assay=httk, Human Hepatic Intrinsic Clearance; Endpoint=Clint; Response=191.4; Response_Unit=ul/min/10^6 cells; Species=Human; Reference=httk2.3.1, Paini 2020; URL=https://cran.r-project.org/web/packages/httk/index.html; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE adme parameters Fu 0 fraction Human - - Measured; httk, Human Plasma Fraction Unbound sheet=Data; excel_row=1796; Record_ID=adme_parameters_1181; Data_Type=Measured; DTXSID=DTXSID4038924; Assay=httk, Human Plasma Fraction Unbound; Endpoint=Fu; Response=0.0; Response_Unit=Unitless Fraction; Species=Human; Reference=httk2.3.1, Paini 2020; URL=https://cran.r-project.org/web/packages/httk/index.html; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE endocrine 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE endocrine AC50 57.7292004099647 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=10390; RecordID=ERPathway2016_356; DatasetName=ERPathway2016; DTXSID=DTXSID4038924; Assay=ER Pathway Model, Antagonist; Endpoint=AC50; Response=57.7292004099647; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE endocrine ACC 47.5953167173507 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=10391; RecordID=ERPathway2016_356; DatasetName=ERPathway2016; DTXSID=DTXSID4038924; Assay=ER Pathway Model, Antagonist; Endpoint=ACC; Response=47.5953167173507; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE endocrine Model Score 0 unitless - - - ARPathway2016; AR Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=10386; RecordID=ARPathway2016_1414; DatasetName=ARPathway2016; DTXSID=DTXSID4038924; Assay=AR Pathway Model, Antagonist; Endpoint=Model Score; Response=0; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE endocrine Model Score 0.0173 unitless - - - ERPathway2016; ER Pathway Model, Agonist sheet=Integrated_approaches; excel_row=10392; RecordID=ERPathway2016_356; DatasetName=ERPathway2016; DTXSID=DTXSID4038924; Assay=ER Pathway Model, Agonist; Endpoint=Model Score; Response=0.0173; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation 17 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin irritation Positive reaction 0 % Human Dermal - In Vivo; Four-hour Human Patch Test sheet=Data_invivo; excel_row=984; Record_ID=skin_irritation_invivo_22; Data_Type=In Vivo; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=Four-hour Human Patch Test; Endpoint=Positive reaction; Response=0; Response_Unit=%; Species=Human; Reference=Basketter et al. 2004; 15291823; 10.1111/j.0105-1873.2004.00385.x; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 80.7 % - Dermal - In Vitro; EpiDerm Irritation sheet=Data_invitro; excel_row=3339; Record_ID=skin_irritation_invitro_1053; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=EpiDerm Irritation; Endpoint=Viability; Response=80.7; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 88.4 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3342; Record_ID=skin_irritation_invitro_1077; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=88.4; Response_Unit=%; Reference=Katoh and Hata 2011; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 94.56 % - Dermal - In Vitro; EpiSkin Irritation sheet=Data_invitro; excel_row=3338; Record_ID=skin_irritation_invitro_1054; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=EpiSkin Irritation; Endpoint=Viability; Response=94.56; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 96.6 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3337; Record_ID=skin_irritation_invitro_1056; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=96.6; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 96.66 % - Dermal - In Vitro; EpiDerm Irritation sheet=Data_invitro; excel_row=3336; Record_ID=skin_irritation_invitro_1058; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=EpiDerm Irritation; Endpoint=Viability; Response=96.66; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 98.6 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3326; Record_ID=skin_irritation_invitro_1059; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=98.6; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 99.85 % - Dermal - In Vitro; EpiSkin Irritation sheet=Data_invitro; excel_row=3325; Record_ID=skin_irritation_invitro_1061; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=EpiSkin Irritation; Endpoint=Viability; Response=99.85; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 100.49 % - Dermal - In Vitro; EpiSkin Irritation sheet=Data_invitro; excel_row=3318; Record_ID=skin_irritation_invitro_1063; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=EpiSkin Irritation; Endpoint=Viability; Response=100.49; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 102.17 % - Dermal - In Vitro; EpiDerm Irritation sheet=Data_invitro; excel_row=3317; Record_ID=skin_irritation_invitro_1065; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=EpiDerm Irritation; Endpoint=Viability; Response=102.17; Response_Unit=%; Reference=Spielmann et al. 2007; 18186667; 10.1177/026119290703500614; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 103.6 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3316; Record_ID=skin_irritation_invitro_1067; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=103.6; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 104.1 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3315; Record_ID=skin_irritation_invitro_1069; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=104.1; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 105.1 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3314; Record_ID=skin_irritation_invitro_1071; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=105.1; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 108.1 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3313; Record_ID=skin_irritation_invitro_1073; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=108.1; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 112.2 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3341; Record_ID=skin_irritation_invitro_1079; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=112.2; Response_Unit=%; Reference=Katoh and Hata 2011; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 113 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3343; Record_ID=skin_irritation_invitro_1075; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=113; Response_Unit=%; Reference=Kojima et al. 2012; 22558976; 10.1177/026119291204000108; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin irritation Viability 119.5 % - Dermal - In Vitro; LabCyte EPI-MODEL24 Irritation sheet=Data_invitro; excel_row=3340; Record_ID=skin_irritation_invitro_1081; Data_Type=In Vitro; Formulation_Name=hexyl salicylate; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LabCyte EPI-MODEL24 Irritation; Endpoint=Viability; Response=119.5; Response_Unit=%; Reference=Katoh and Hata 2011; Not available; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization 16 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin sensitization CD54, EC200 52.73 ug/mL - Dermal - In Vitro; Urbisch_SkinSensitization2020; h-CLAT sheet=Data_invitro; excel_row=1733; Record_ID=skin_sensitization_invitro_446; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=52.73; Reported_Response_Unit=ug/mL; Response=52.73; 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/DTXSID4038924
NTP ICE skin sensitization CD86, EC150 27.29 ug/mL - Dermal - In Vitro; CE_USENSE2018; U-SENS sheet=Data_invitro; excel_row=8629; Record_ID=skin_sensitization_invitro_2385; Data_Type=In Vitro; Internal_Data_Source=CE_USENSE2018; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=U-SENS; Endpoint=CD86, EC150; Reported_Response=27.29; Reported_Response_Unit=ug/mL; Response=27.29; 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/DTXSID4038924
NTP ICE skin sensitization CV75 147.7 ug/mL - Dermal - In Vitro; Urbisch_SkinSensitization2020; h-CLAT sheet=Data_invitro; excel_row=1718; Record_ID=skin_sensitization_invitro_446; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=h-CLAT; Endpoint=CV75; Reported_Response=147.7; Reported_Response_Unit=ug/mL; Response=147.7; 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/DTXSID4038924
NTP ICE skin sensitization Depletion Cys 3.9 % - Dermal - In Vitro; Urbisch_SkinSensitization2020; DPRA sheet=Data_invitro; excel_row=145; Record_ID=skin_sensitization_invitro_54; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=DPRA; Endpoint=Depletion Cys; Reported_Response=3.9; Reported_Response_Unit=%; Response=3.9; Response_Unit=%; Reference=Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization Depletion Lys 1.1 % - Dermal - In Vitro; Urbisch_SkinSensitization2020; DPRA sheet=Data_invitro; excel_row=164; Record_ID=skin_sensitization_invitro_54; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=DPRA; Endpoint=Depletion Lys; Reported_Response=1.1; Reported_Response_Unit=%; Response=1.1; Response_Unit=%; Reference=Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization EC1.5 >2000 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=6267; Record_ID=skin_sensitization_invitro_1481; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=KeratinoSens; Endpoint=EC1.5; Response_Modifier=>; Reported_Response_Modifier=>; Reported_Response=2000; Reported_Response_Unit=uM; Response=2000; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization EC1.5 4000 uM - Dermal - In Vitro; Urbisch_SkinSensitization2020; KeratinoSens sheet=Data_invitro; excel_row=6269; Record_ID=skin_sensitization_invitro_1482; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=4000; Reported_Response_Unit=uM; Response=4000; 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/DTXSID4038924
NTP ICE skin sensitization EC3 0.2 % Mouse Dermal - In Vivo; LLNAdb2013; LLNA sheet=Data_invivo; excel_row=13324; Record_ID=skin_sensitization_invivo_3433; Data_Type=In Vivo; Internal_Data_Source=LLNAdb2013; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=LLNA; Endpoint=EC3; Response=0.2; Response_Unit=%; Species=Mouse; Route=Dermal; Reference=Kern et al. 2010; 20137736; Not available; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization IC50 53.7 uM - Dermal - In Vitro; Urbisch_SkinSensitization2020; KeratinoSens sheet=Data_invitro; excel_row=6273; Record_ID=skin_sensitization_invitro_1482; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=53.69715902; Reported_Response_Unit=uM; Response=53.7; 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/DTXSID4038924
NTP ICE skin sensitization IC50 67.4 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=6275; Record_ID=skin_sensitization_invitro_1481; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=67.400000000000006; Reported_Response_Unit=uM; Response=67.4; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization Imax 1.37 ratio - Dermal - In Vitro; Urbisch_SkinSensitization2020; KeratinoSens sheet=Data_invitro; excel_row=6277; Record_ID=skin_sensitization_invitro_1482; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=1.369557416; Reported_Response_Unit=Unitless; Response=1.37; 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/DTXSID4038924
NTP ICE skin sensitization Imax 1.5 ratio - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=6279; Record_ID=skin_sensitization_invitro_1481; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=1.5; Reported_Response_Unit=Unitless; Response=1.5; Response_Unit=Ratio; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization Incidence of positive responses 0 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=9164; Record_ID=skin_sensitization_invivo_2027; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=3.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=0; Response_Unit=%; Species=Human; Route=Dermal; Reference=Epstein 1975: report to RIFM|RIFM 1975; https://www.rifm.org/rifm-science-database.php#gsc.tab=0|Opdyke 1975; Not available; 10.1016/0015-6264(75)90230-8|Api et al. 2015; 25430073; 10.3109/15569527.2014.979425; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization Induction dose per skin area 2025 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=9161; Record_ID=skin_sensitization_invivo_2027; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=3.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=Human Maximization Test; Endpoint=Induction dose per skin area; Response=2025; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Epstein 1975: report to RIFM|RIFM 1975; https://www.rifm.org/rifm-science-database.php#gsc.tab=0|Opdyke 1975; Not available; 10.1016/0015-6264(75)90230-8|Api et al. 2015; 25430073; 10.3109/15569527.2014.979425; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization Induction dose per skin area 35430 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Repeat Insult Patch Test sheet=Data_invivo; excel_row=9171; Record_ID=skin_sensitization_invivo_2028; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=30.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=Human Repeat Insult Patch Test; Endpoint=Induction dose per skin area; Response=35430; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=RIFM 2004; https://www.rifm.org/rifm-science-database.php#gsc.tab=0|Belsito et al. 2007; 18022746; 10.1016/j.fct.2007.09.066|Lapczynski et al. 2007; 18022307; 10.1016/j.fct.2007.09.045|Basketter et al. 2014; 24407057; 10.1097/der.0000000000000003|Api et al. 2015; 25430073; 10.3109/15569527.2014.979425; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
NTP ICE skin sensitization Relative reliability score 3 unitless Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=9170; Record_ID=skin_sensitization_invivo_2027; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=3.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID4038924; Assay=Human Maximization Test; Endpoint=Relative reliability score; Response=3; Response_Unit=Unitless; Species=Human; Route=Dermal; Reference=Epstein 1975: report to RIFM|RIFM 1975; https://www.rifm.org/rifm-science-database.php#gsc.tab=0|Opdyke 1975; Not available; 10.1016/0015-6264(75)90230-8|Api et al. 2015; 25430073; 10.3109/15569527.2014.979425; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID4038924
SCCS Opinion 21 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
SCCS Opinion NOAEL =0.1 % human oral developmental reproductive toxicity p.37
SCCS Opinion NOAEL =3 - - - - NOAEL study p.17
SCCS Opinion NOAEL =13 - - - 3 years NOAEL study p.46
SCCS Opinion NOAEL =13.4 % - dermal 3 years NOAEL study p.17
SCCS Opinion NOAEL =15 - - oral - NOAEL study p.45
SCCS Opinion NOAEL =29 mg/kg/day rat - developmental reproductive toxicity p.45
SCCS Opinion NOAEL =75 mg/kg bw/day human oral developmental developmental toxicity p.37
SCCS Opinion NOAEL =75 mg/kg/day rat - developmental reproductive toxicity p.49
SCCS Opinion NOAEL =75 - - - - NOAEL study p.17
SCCS Opinion NOAEL =180 mg/kg bw/day rat - - NOAEL study p.36
SCCS Opinion NOAEL =370 mg/kg bw/day rat oral 13-week NOAEL study p.35
SCCS Opinion NOAEL =540 mg/kg bw/day rat - - NOAEL study p.36
SCCS Opinion NOAEL =736 - - - 3 years NOAEL study p.46
SCCS Opinion NOAEL =801 - - - 3 years NOAEL study p.46
SCCS Opinion NOAEL =822 - - - 3 years NOAEL study p.46
SCCS Opinion NOAEL =1000 mg/kg bw/day rat oral 13-week NOAEL study p.35
SCCS Opinion NOAEL =1000 mg/kg bw/day rat oral sub-chronic repeated dose toxicity p.38
SCCS Opinion NOAEL =1127 mg/kg rat oral sub-acute repeated dose toxicity p.35
SCCS Opinion NOAEL =1668 - - - 3 years NOAEL study p.46
SCCS Opinion NOAEL =35433 μg/cm2 human - 2 weeks sensitisation p.32
SCCS Opinion NOAEL =75000 - - - 3 years NOAEL study p.46
ECHA 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ECHA NOAEL =360 mg/kg bw/day Rat oral - developmental QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eac4ae4b0a7c65d1be527; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/14766/7/9/3?documentUUID=4af4dd5e-02c7-473f-bf7e-03a480be8b21; YEAR=2000; ORIGINAL_YEAR=2000; STUDY_GROUP=ECHA IUCLID:15821877:M/F:-fetal; 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_6675801f54a514a3e3eab72a4c83652b
ToxValDB GESTIS DNEL 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB GESTIS DNEL DNEL systemic =1.7 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:15632551:-:--; 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_ca10a1c526a3243384907a5b212f70db
Regulatory source 23 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
Regulatory source - 3 - - - - - p.17
Regulatory source - 13 - - - 3 years - p.46
Regulatory source - 13.4 % - dermal 3 years - p.17
Regulatory source - 15 - - oral - - p.45
Regulatory source - 75 - - - - - p.17
Regulatory source - 180 mg/kg bw/day rat - - - p.36
Regulatory source - 370 mg/kg bw/day rat oral 13-week - p.35
Regulatory source - 540 mg/kg bw/day rat - - - p.36
Regulatory source - 736 - - - 3 years - p.46
Regulatory source - 801 - - - 3 years - p.46
Regulatory source - 822 - - - 3 years - p.46
Regulatory source - 1000 mg/kg bw/day rat oral 13-week - p.35
Regulatory source - 1668 - - - 3 years - p.46
Regulatory source - =75000 - - - 3 years - p.46
Regulatory source developmental toxicity 0.1 % human oral developmental developmental toxicity p.48
Regulatory source developmental toxicity 75 mg/kg bw/day human oral developmental developmental toxicity p.37
Regulatory source developmental toxicity 180 mg/kg bw/day rat - - developmental toxicity p.36
Regulatory source repeated dose toxicity 1000 mg/kg bw/day rat oral sub-chronic repeated dose toxicity p.38
Regulatory source repeated dose toxicity 1127 mg/kg rat oral sub-acute repeated dose toxicity p.35
Regulatory source reproductive toxicity 0.1 % human oral developmental reproductive toxicity p.37
Regulatory source reproductive toxicity 29 mg/kg/day rat - developmental reproductive toxicity p.45
Regulatory source reproductive toxicity 75 mg/kg/day rat - developmental reproductive toxicity p.49
Regulatory source sensitisation 35433 μg/cm2 human - 2 weeks sensitisation p.32
openFDA substances 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier 8F78EY72YL UNII - - - chemical -