NOAEL Studies Cosmetic Ingredient

Propyl Gallate NOAEL Studies

INCI: PROPYL GALLATE

CAS: 121-79-9

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

COSMOS DB 14 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
COSMOS DB NOAEL 2.925 mg/kg bw/day dog oral 420 day Chronic US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 4.68 mg/kg bw/day guinea pig oral 450 day Carcinogenicity US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 75 mg/kg bw/day mouse oral 56 day Special Toxicology Study US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 250 mg/kg bw/day hamster oral 5 day Developmental US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 300 mg/kg bw/day rat oral 721 day Carcinogenicity US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 500 mg/kg bw/day rat oral 42 day Short Term Toxicity US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 585 mg/kg bw/day rat oral 728 day Carcinogenicity US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 900 mg/kg bw/day mouse oral 721 day Carcinogenicity US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 1250 mg/kg bw/day rat oral 91 day Subchronic US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 1500 mg/kg bw/day mouse oral 630 day Chronic US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 1875 mg/kg bw/day mouse oral 91 day Subchronic US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 2000 mg/kg bw/day rat oral 9 day Short Term Toxicity US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 3750 mg/kg bw/day mouse oral 14 day Short Term Toxicity US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS DB NOAEL 5000 mg/kg bw/day rat oral 14 day Short Term Toxicity US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
EFSA 5 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EFSA NOAEL =135 mg/kg bw/day Rat oral: feed 90 days subchronic EFSA ANS - 2014 - OutputID 2487 - haematology - hemopoietic - Scientific Opinion on the re-evaluation of propyl gallate (E 310) as a food additive - doi:10.2903/j.efsa.2014.3642
EFSA NOAEL =1910 mg/kg bw/day Rat oral: feed 91 days subchronic EFSA FEEDAP - 2020 - OutputID 3567 - clinical chemistry - systemic - Safety and efficacy of propyl gallate for all animal species - doi:10.2903/j.efsa.2020.6069
EFSA ADI =0.5 mg/kg bw/day Consumers - - ADI EFSA ANS - 2014 - OutputID 2487 - Consumers - Scientific Opinion on the re-evaluation of propyl gallate (E 310) as a food additive - doi:10.2903/j.efsa.2014.3642
EFSA ADI =0.5 mg/kg bw/day Consumers - - ADI EFSA ANS - 2014 - OutputID 2487 - Consumers - Scientific Opinion on the re-evaluation of propyl gallate (E 310) as a food additive - doi:10.2903/j.efsa.2014.3642
EFSA NOAEL =1910 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic LONG_REF=EFSA FEEDAP (2020). Safety and efficacy of propyl gallate for all animal species. doi:10.2903/j.efsa.2020.6069.; TITLE=Safety and efficacy of propyl gallate for all animal species; AUTHOR=EFSA FEEDAP; DOI=doi:10.2903/j.efsa.2020.6069; 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=clinical chemistry; TOXICOLOGICAL_EFFECT_CATEGORY=clinical chemistry; STUDY_GROUP=EFSA:15622614: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_17ab13348b84907aaa29c7bf55e1b7aa
NTP ICE adme parameters 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE adme parameters Clint 49.7 uL/min/10^6 cells Human - - Measured; httk, Human Hepatic Intrinsic Clearance sheet=Data; excel_row=1960; Record_ID=adme_parameters_1058; Data_Type=Measured; DTXSID=DTXSID5021201; Assay=httk, Human Hepatic Intrinsic Clearance; Endpoint=Clint; Response=49.7; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE adme parameters Fu 0.0258 fraction Human - - Measured; httk, Human Plasma Fraction Unbound sheet=Data; excel_row=1961; Record_ID=adme_parameters_1058; Data_Type=Measured; DTXSID=DTXSID5021201; Assay=httk, Human Plasma Fraction Unbound; Endpoint=Fu; Response=0.0258; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE cancer 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE cancer Top dose 12000 ppm Mouse Dosed feed - In Vivo; NTP Carcinogenicity sheet=Data; excel_row=5643; Record_ID=cancer_6178; Data_Type=In Vivo; Formulation_Name=Propyl gallate; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=NTP Carcinogenicity; Endpoint=Top dose; Response=12000; Response_Unit=ppm; Species=Mouse; Strain=B6C3F1; Sex=Female; Route=Dosed feed; Reference=TR-240; URL=https://ntp.niehs.nih.gov/publications/reports/tr/200s/tr240/index.html; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE endocrine 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE endocrine AC50 30.4262745677929 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=9884; RecordID=ERPathway2016_268; DatasetName=ERPathway2016; DTXSID=DTXSID5021201; Assay=ER Pathway Model, Antagonist; Endpoint=AC50; Response=30.4262745677929; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE endocrine ACC 18.456602161568 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=9885; RecordID=ERPathway2016_268; DatasetName=ERPathway2016; DTXSID=DTXSID5021201; Assay=ER Pathway Model, Antagonist; Endpoint=ACC; Response=18.456602161568; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE endocrine Model Score 0 unitless - - - ARPathway2016; AR Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=9880; RecordID=ARPathway2016_692; DatasetName=ARPathway2016; DTXSID=DTXSID5021201; Assay=AR Pathway Model, Antagonist; Endpoint=Model Score; Response=0; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE endocrine Model Score 0.0601 unitless - - - ERPathway2016; ER Pathway Model, Agonist sheet=Integrated_approaches; excel_row=9886; RecordID=ERPathway2016_268; DatasetName=ERPathway2016; DTXSID=DTXSID5021201; Assay=ER Pathway Model, Agonist; Endpoint=Model Score; Response=0.0601; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization 35 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP ICE skin sensitization CD54, EC200 0.69 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3177; Record_ID=skin_sensitization_invitro_737; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=0.69; Reported_Response_Unit=ug/mL; Response=0.69; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD54, EC200 10 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3134; Record_ID=skin_sensitization_invitro_729; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=10; Reported_Response_Unit=ug/mL; Response=10; Response_Unit=ug/mL; Reference=Bauch et al. 2012; 22659254; 10.1016/j.yrtph.2012.05.013; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD54, EC200 20.19 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3144; Record_ID=skin_sensitization_invitro_731; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=20.187999999999899; Reported_Response_Unit=ug/mL; Response=20.19; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD54, EC200 23.77 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3168; Record_ID=skin_sensitization_invitro_736; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=23.77; Reported_Response_Unit=ug/mL; Response=23.77; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD54, EC200 26.369 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3154; Record_ID=skin_sensitization_invitro_733; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=26.369; Reported_Response_Unit=ug/mL; Response=26.369; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD54, EC200 29.29 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3162; Record_ID=skin_sensitization_invitro_735; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=29.29; Reported_Response_Unit=ug/mL; Response=29.29; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD54, EC200 32.4 ug/mL - Dermal - In Vitro; CE_hCLAT2018; h-CLAT sheet=Data_invitro; excel_row=1945; Record_ID=skin_sensitization_invitro_493; Data_Type=In Vitro; Internal_Data_Source=CE_hCLAT2018; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=32.4; Reported_Response_Unit=ug/mL; Response=32.4; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD54, EC200 32.5 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3124; Record_ID=skin_sensitization_invitro_727; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CD54, EC200; Reported_Response=32.5; Reported_Response_Unit=ug/mL; Response=32.5; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD86, EC120 1.74 ug/mL - Dermal - In Vitro; Urbisch_SkinSensitization2020; mMUSST sheet=Data_invitro; excel_row=7795; Record_ID=skin_sensitization_invitro_1893; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=mMUSST; Endpoint=CD86, EC120; Reported_Response=8.2; Reported_Response_Unit=uM; Conversion_Factor_Value=212.201; Conversion_Factor_Source=EPA Dashboard; Converted_Response=1.74; Converted_Response_Unit=ug/mL; Response=1.74; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD86, EC150 1.889 ug/mL - Dermal - In Vitro; Urbisch_SkinSensitization2020; U-SENS sheet=Data_invitro; excel_row=8320; Record_ID=skin_sensitization_invitro_2307; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=U-SENS; Endpoint=CD86, EC150; Reported_Response=8.9; Reported_Response_Unit=uM; Conversion_Factor_Value=212.201; Conversion_Factor_Source=EPA Dashboard; Converted_Response=1.889; Converted_Response_Unit=ug/mL; Response=1.889; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CD86, EC150 1.97 ug/mL - Dermal - In Vitro; CE_USENSE2018; U-SENS sheet=Data_invitro; excel_row=8500; Record_ID=skin_sensitization_invitro_2342; Data_Type=In Vitro; Internal_Data_Source=CE_USENSE2018; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=U-SENS; Endpoint=CD86, EC150; Reported_Response=1.97; Reported_Response_Unit=ug/mL; Response=1.97; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CV70 32.75 ug/mL - Dermal - In Vitro; CE_USENSE2018; U-SENS sheet=Data_invitro; excel_row=8501; Record_ID=skin_sensitization_invitro_2342; Data_Type=In Vitro; Internal_Data_Source=CE_USENSE2018; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=U-SENS; Endpoint=CV70; Reported_Response=32.75; Reported_Response_Unit=ug/mL; Response=32.75; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CV75 14.8 ug/mL - Dermal - In Vitro; hCLAT2015; h-CLAT sheet=Data_invitro; excel_row=3135; Record_ID=skin_sensitization_invitro_729; Data_Type=In Vitro; Internal_Data_Source=hCLAT2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CV75; Reported_Response=14.8; Reported_Response_Unit=ug/mL; Response=14.8; Response_Unit=ug/mL; Reference=Bauch et al. 2012; 22659254; 10.1016/j.yrtph.2012.05.013; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization CV75 125 ug/mL - Dermal - In Vitro; CE_hCLAT2018; h-CLAT sheet=Data_invitro; excel_row=1947; Record_ID=skin_sensitization_invitro_493; Data_Type=In Vitro; Internal_Data_Source=CE_hCLAT2018; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=h-CLAT; Endpoint=CV75; Reported_Response=125; Reported_Response_Unit=ug/mL; Response=125; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Depletion Cys 24.8 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1018; Record_ID=skin_sensitization_invitro_278; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=DPRA; Endpoint=Depletion Cys; Reported_Response=24.8; Reported_Response_Unit=%; Response=24.8; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Depletion Cys 59.2 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1010; Record_ID=skin_sensitization_invitro_276; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=DPRA; Endpoint=Depletion Cys; Reported_Response=59.2; Reported_Response_Unit=%; Response=59.2; Response_Unit=%; Reference=Bauch et al. 2012; 22659254; 10.1016/j.yrtph.2012.05.013; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Depletion Cys 59.9 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1014; Record_ID=skin_sensitization_invitro_277; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=DPRA; Endpoint=Depletion Cys; Reported_Response=59.9; Reported_Response_Unit=%; Response=59.9; Response_Unit=%; Reference=Gerberick et al. 2007; 17400584; 10.1093/toxsci/kfm064|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Depletion Lys -303 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1017; Record_ID=skin_sensitization_invitro_278; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=DPRA; Endpoint=Depletion Lys; Reported_Response=-303; Reported_Response_Unit=%; Response=-303; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Depletion Lys 26.6 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1013; Record_ID=skin_sensitization_invitro_277; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=DPRA; Endpoint=Depletion Lys; Reported_Response=26.6; Reported_Response_Unit=%; Response=26.6; Response_Unit=%; Reference=Gerberick et al. 2007; 17400584; 10.1093/toxsci/kfm064|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Depletion Lys 63.6 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1009; Record_ID=skin_sensitization_invitro_276; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=DPRA; Endpoint=Depletion Lys; Reported_Response=63.6; Reported_Response_Unit=%; Response=63.6; Response_Unit=%; Reference=Bauch et al. 2012; 22659254; 10.1016/j.yrtph.2012.05.013; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Depletion Lys + Cys 12 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1019; Record_ID=skin_sensitization_invitro_278; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=DPRA; Endpoint=Depletion Lys + Cys; Reported_Response=12; Reported_Response_Unit=%; Response=12; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Depletion Lys + Cys 43.25 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1015; Record_ID=skin_sensitization_invitro_277; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=DPRA; Endpoint=Depletion Lys + Cys; Reported_Response=43.25; Reported_Response_Unit=%; Response=43.25; Response_Unit=%; Reference=Gerberick et al. 2007; 17400584; 10.1093/toxsci/kfm064|Natsch et al. 2013; 23576290; 10.1002/jat.2868; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Depletion Lys + Cys 61.4 % - Dermal - In Vitro; DPRA2015; DPRA sheet=Data_invitro; excel_row=1011; Record_ID=skin_sensitization_invitro_276; Data_Type=In Vitro; Internal_Data_Source=DPRA2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=DPRA; Endpoint=Depletion Lys + Cys; Reported_Response=61.4; Reported_Response_Unit=%; Response=61.4; Response_Unit=%; Reference=Bauch et al. 2012; 22659254; 10.1016/j.yrtph.2012.05.013; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization EC1.5 132.8 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=4944; Record_ID=skin_sensitization_invitro_1143; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=132.83699999999999; Reported_Response_Unit=uM; Response=132.8; Response_Unit=uM; Reference=Natsch et al. 2013; 23576290; 10.1002/jat.2868|Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization EC1.5 >140 uM - Dermal - In Vitro; Urbisch_SkinSensitization2020; LuSens sheet=Data_invitro; excel_row=7611; Record_ID=skin_sensitization_invitro_1853; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=LuSens; Endpoint=EC1.5; Response_Modifier=>; Reported_Response_Modifier=>; Reported_Response=140; Reported_Response_Unit=uM; Response=140; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization EC1.5 191 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=4946; Record_ID=skin_sensitization_invitro_1145; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=191; Reported_Response_Unit=uM; Response=191; Response_Unit=uM; Reference=Bauch et al. 2012; 22659254; 10.1016/j.yrtph.2012.05.013; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization EC1.5 199.8 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=4948; Record_ID=skin_sensitization_invitro_1144; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=EC1.5; Reported_Response=199.8; Reported_Response_Unit=uM; Response=199.8; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization EC3 202.727 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=4950; Record_ID=skin_sensitization_invitro_1143; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=EC3; Reported_Response=202.727; Reported_Response_Unit=uM; Response=202.727; Response_Unit=uM; Reference=Natsch et al. 2013; 23576290; 10.1002/jat.2868|Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization IC50 605 uM - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=4951; Record_ID=skin_sensitization_invitro_1143; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=605; Reported_Response_Unit=uM; Response=605; Response_Unit=uM; Reference=Natsch et al. 2013; 23576290; 10.1002/jat.2868|Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization IC50 650.3 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=4952; Record_ID=skin_sensitization_invitro_1144; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=650.29999999999995; Reported_Response_Unit=uM; Response=650.3; Response_Unit=uM; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization IC50 731.5 uM - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=4954; Record_ID=skin_sensitization_invitro_1145; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=IC50; Reported_Response=731.5; Reported_Response_Unit=uM; Response=731.5; Response_Unit=uM; Reference=Bauch et al. 2012; 22659254; 10.1016/j.yrtph.2012.05.013; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Imax 0.8886 ratio - Dermal - In Vitro; Urbisch_SkinSensitization2020; LuSens sheet=Data_invitro; excel_row=7730; Record_ID=skin_sensitization_invitro_1853; Data_Type=In Vitro; Internal_Data_Source=Urbisch_SkinSensitization2020; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=LuSens; Endpoint=Imax; Reported_Response=0.888575576; Reported_Response_Unit=Unitless; Response=0.8886; 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/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Imax 8.2 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=4956; Record_ID=skin_sensitization_invitro_1144; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=8.1999999999999993; Reported_Response_Unit=Unitless; Response=8.2; Response_Unit=Ratio; Reference=Joint Research Centre of the European Union 2014; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Imax 8.68 ratio - Dermal - In Vitro; KeratinoSens2015; KeratinoSens sheet=Data_invitro; excel_row=4958; Record_ID=skin_sensitization_invitro_1145; Data_Type=In Vitro; Internal_Data_Source=KeratinoSens2015; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=8.68; Reported_Response_Unit=Unitless; Response=8.68; Response_Unit=Ratio; Reference=Bauch et al. 2012; 22659254; 10.1016/j.yrtph.2012.05.013; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
NTP ICE skin sensitization Imax 9.24 ratio - Dermal - In Vitro; CE_KeratinoSense2018; KeratinoSens sheet=Data_invitro; excel_row=4959; Record_ID=skin_sensitization_invitro_1143; Data_Type=In Vitro; Internal_Data_Source=CE_KeratinoSense2018; Mixture=Chemical; DTXSID=DTXSID5021201; Assay=KeratinoSens; Endpoint=Imax; Reported_Response=9.24; Reported_Response_Unit=Unitless; Response=9.24; Response_Unit=Ratio; Reference=Natsch et al. 2013; 23576290; 10.1002/jat.2868|Urbisch et al. 2015; 25541156; 10.1016/j.yrtph.2014.12.008; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID5021201; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID5021201
EPA ToxRefDB v3 6 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
EPA ToxRefDB v3 LEL =300 mg/kg bw/day rat (fischer; Fischer 344) oral 0 week to 103 week CHR study_id=5627; toxval_study_source_id=studyid5627_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-eye-cataract|pathology microscopic-eye-retinopathy|pathology microscopic-kidney-nephropathy|in life observation-body weight-body weight; dose_level=1; study_year=1982; study_citation=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Chronic_Rats; dsstox_substance_id=DTXSID5021201; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =900 mg/kg bw/day mouse (b6c3f1; B6C3F1) oral 0 week to 103 week CHR study_id=5628; toxval_study_source_id=studyid5628_Adult_F0_F_systemic; toxval_effect_list=in life observation-body weight-body weight; dose_level=1; study_year=1982; study_citation=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Chronic_Mice; dsstox_substance_id=DTXSID5021201; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 LEL =1250 mg/kg bw/day rat (fischer; Fischer 344) oral 0 week to 13 week SUB study_id=5620; toxval_study_source_id=studyid5620_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-stomach-ulcer|in life observation-clinical signs-skin discoloration|pathology gross-intestine small-discolored|pathology microscopic-stomach-inflammation|pathology gross-stomach-thickened|pathology microscopic-stomach-necrosis|in life observation-body weight-body weight gain; dose_level=5; study_year=1982; study_citation=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Subchronic_Rats; dsstox_substance_id=DTXSID5021201; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 NEL >0 mg/kg bw/day rat (fischer; Fischer 344) oral 0 week to 103 week CHR study_id=5627; toxval_study_source_id=studyid5627_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-eye-cataract|pathology microscopic-eye-retinopathy|pathology microscopic-kidney-nephropathy|in life observation-body weight-body weight; dose_level=0; study_year=1982; study_citation=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Chronic_Rats; dsstox_substance_id=DTXSID5021201; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 NEL =300 mg/kg bw/day rat (fischer; Fischer 344) oral 0 week to 13 week SUB study_id=5620; toxval_study_source_id=studyid5620_Adult_F0_M_systemic; toxval_effect_list=in life observation-body weight-body weight gain|pathology microscopic-stomach-inflammation|pathology microscopic-stomach-ulcer|in life observation-clinical signs-skin discoloration|pathology microscopic-stomach-necrosis|pathology gross-intestine small-discolored|pathology gross-stomach-thickened; dose_level=3; study_year=1982; study_citation=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Subchronic_Rats; dsstox_substance_id=DTXSID5021201; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
EPA ToxRefDB v3 NEL =625 mg/kg bw/day rat (fischer; Fischer 344) oral 0 week to 13 week SUB study_id=5620; toxval_study_source_id=studyid5620_Adult_F0_F_systemic; toxval_effect_list=pathology microscopic-stomach-inflammation|pathology gross-intestine small-discolored|in life observation-clinical signs-skin discoloration|pathology microscopic-stomach-ulcer|in life observation-body weight-body weight gain|pathology microscopic-stomach-necrosis|pathology gross-stomach-thickened; dose_level=4; study_year=1982; study_citation=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Subchronic_Rats; dsstox_substance_id=DTXSID5021201; admin_method=Feed; cas_source=toxval_ToxRefDB.xlsx:DTXSID; blob_url=https://clowder.edap-cluster.com/files/688cbadae4b02565bc3f8c07/blob; blob_sha256=69dd2da06ffc6a98a1bed684c347d8b2f31e6d35d607d4f2f83ebb6845a708d5
ECHA 14 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ECHA LEL =1152 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669ead10e4b0a7c65d1c2438; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/6/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=clinical signs|gross pathology; TOXICOLOGICAL_EFFECT_CATEGORY=clinical signs|gross pathology; STUDY_GROUP=ECHA IUCLID:15850548: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_3096575d0f2bd5baa1dbe02c893863b1
ECHA LEL =2462.5 mg/kg bw/day Mouse oral subchronic; 13 weeks subchronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669ead05e4b0a7c65d1c21d7; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/6/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; STUDY_GROUP=ECHA IUCLID:15850542: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_e9ad66edda36a5d7e047e2a9d7399e24
ECHA LEL =12500 ppm Mouse oral short-term; 14 days short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca41e4b0a7c65d220fdb; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/6/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=body weight and weight gain|clinical signs|mortality; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|mortality/survival; STUDY_GROUP=ECHA IUCLID:15846191: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_9aaa4ad783b2094f22db001c1131c869
ECHA LEL =25000 ppm Rat oral short-term; 14 days short-term QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7ca41e4b0a7c65d220fbe; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/6/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=body weight and weight gain|clinical signs|mortality; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|mortality/survival; STUDY_GROUP=ECHA IUCLID:15831253: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_492903acb4399ca3fe2e2666e00943ab
ECHA LOAEL =298 mg/kg bw/day Rat oral chronic; 721 days chronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669ead10e4b0a7c65d1c2435; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/6/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=body weight and weight gain|histopathology: non-neoplastic; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|nonneoplastic histopathology; STUDY_GROUP=ECHA IUCLID:15850546: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_6a9033b54f68fd390cbd6e9bba9f1d37
ECHA LOAEL =332 mg/kg bw/day Rat oral chronic; 721 days chronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669ead10e4b0a7c65d1c2435; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/6/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=body weight and weight gain|histopathology: non-neoplastic; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|nonneoplastic histopathology; STUDY_GROUP=ECHA IUCLID:15850547: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_ab6802bcad7bb20c33ae39484fc84c44
ECHA LOAEL =468 mg/kg bw/day Rat oral - chronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c805e4b0a7c65d2162f6; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/8?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=histopathology: neoplastic; TOXICOLOGICAL_EFFECT_CATEGORY=cancer; STUDY_GROUP=ECHA IUCLID:15816316: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_8921f15627a54d7247db42a30f47213e
ECHA LOAEL =1141 mg/kg bw/day Mouse oral chronic; 721 days chronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669ead10e4b0a7c65d1c2430; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/6/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=body weight and weight gain; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ECHA IUCLID:15850543: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_52e7b78d68c0fa24a903c5ca5abcbb69
ECHA LOAEL =1591 mg/kg bw/day Mouse oral chronic; 721 days chronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669ead10e4b0a7c65d1c2430; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/6/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=body weight and weight gain; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ECHA IUCLID:15850544: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_6cea96a80d15e827ec63bfa06c367153
ECHA LOAEL =2220 mg/kg bw/day Mouse oral - chronic QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7c805e4b0a7c65d216300; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/8?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=histopathology: neoplastic; TOXICOLOGICAL_EFFECT_CATEGORY=cancer; STUDY_GROUP=ECHA IUCLID:15818427: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_3ffde3e2708ab63a1f969b40aff1e342
ECHA NOAEL =135 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669ead10e4b0a7c65d1c2432; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/6/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=blood: haematology; TOXICOLOGICAL_EFFECT_CATEGORY=hematology; STUDY_GROUP=ECHA IUCLID:15850545: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_bbdc7ebbf3721eeb1b82e1abdcc3250f
ECHA NOAEL =250 mg/kg bw/day Hamster oral - developmental QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/66a7d199e4b0a7c65d22f44c; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/9/3?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; STUDY_GROUP=ECHA IUCLID:15821916:-:-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_1545fba00b227b620558fa9c1f906f94
ECHA NOAEL =260 mg/kg bw/day Rat oral - reproduction developmental QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eaa71e4b0a7c65d1b5e46; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/9/2?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; STUDY_GROUP=ECHA IUCLID:15862587:M/F:F1-; QC_CATEGORY=Programmatically extracted from structured data source; Source overall passed QC, and this record was expert reviewed; QC_STATUS=pass; SOURCE_HASH=ToxValhc_658952a23ecb321a3b9c87b0538fff81
ECHA NOAEL =880 mg/kg bw/day Rat oral - reproduction developmental QUALITY=2 (reliable with restrictions); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eabc6e4b0a7c65d1bbbba; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/24203/7/9/3?documentUUID=8e00c401-75a8-4d55-8e9a-1e207d5fdfec; YEAR=2011; ORIGINAL_YEAR=2011; TOXICOLOGICAL_EFFECT=maternal: body weight and weight gain|maternal: food consumption and compound intake; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|food and/or water consumption; STUDY_GROUP=ECHA IUCLID:15824123: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_5099709e1e5f18ddb513ca5da056e78d
ToxValDB ECOTOX 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB ECOTOX NOEL =2000 mg/kg bw/day Mouse oral acute; 1 days acute LONG_REF=Mutat. Res.519(1/2): 103-119 Sasaki,Y.F., S. Kawaguchi, A. Kamaya, M. Ohshita, K. Kabasawa, K. Iwama, K. Taniguchi, and S. Tsuda The Comet Assay with 8 Mouse Organs: Results with 39 Currently Used Food Additives 2002; TITLE=The Comet Assay with 8 Mouse Organs: Results with 39 Currently Used Food Additives; AUTHOR=Sasaki,Y.F., S. Kawaguchi, A. Kamaya, M. Ohshita, K. Kabasawa, K. Iwama, K. Taniguchi, and S. Tsuda; DOI=10.1016/s1383-5718(02)00128-6; QUALITY=Control type: Concurrent control; EXTERNAL_SOURCE_ID=75840; 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=Genetics: Damage; TOXICOLOGICAL_EFFECT_CATEGORY=other; STUDY_GROUP=ECOTOX:15596960:M:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=d6407bbaf8f6e38cc92e4dc3f6949400
ToxValDB GESTIS DNEL 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB GESTIS DNEL DNEL systemic =6.66 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:15634408:-:--; 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_725a296a3ea1a8f93ba8b06ceaef3885
ToxValDB ToxRefDB 5 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB ToxRefDB LEL =300 mg/kg bw/day Rat oral chronic; 103 weeks chronic LONG_REF=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Chronic_Rats; TITLE=Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Chronic_Rats; AUTHOR=NTP; EXTERNAL_SOURCE_ID=5627; 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=1982; ORIGINAL_YEAR=1982; TOXICOLOGICAL_EFFECT=systemic: pathology microscopic-eye-cataract|systemic: pathology microscopic-eye-retinopathy|systemic: pathology microscopic-kidney-nephropathy|systemic: in life observation-body weight-body weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15709726_15709727:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_75176ea9ed831b3555bd2beb92e5e02b
ToxValDB ToxRefDB LEL =900 mg/kg bw/day Mouse oral chronic; 103 weeks chronic LONG_REF=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Chronic_Mice; TITLE=Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Chronic_Mice; AUTHOR=NTP; EXTERNAL_SOURCE_ID=5628; 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=1982; ORIGINAL_YEAR=1982; TOXICOLOGICAL_EFFECT=systemic: in life observation-body weight-body weight; TOXICOLOGICAL_EFFECT_CATEGORY=body weight; STUDY_GROUP=ToxRefDB_dup_-_15709730_15709731:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_0db26d611405948ad8b52368d260709c
ToxValDB ToxRefDB LEL =1250 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic LONG_REF=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Subchronic_Rats; TITLE=Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Subchronic_Rats; AUTHOR=NTP; EXTERNAL_SOURCE_ID=5620; 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=1982; ORIGINAL_YEAR=1982; TOXICOLOGICAL_EFFECT=systemic: pathology gross-intestine small-discolored|systemic: pathology gross-stomach-thickened|systemic: pathology microscopic-stomach-ulcer|systemic: pathology microscopic-stomach-necrosis|systemic: in life observation-body weight-body weight gain|systemic: pathology microscopic-stomach-inflammation|systemic: in life observation-clinical signs-skin discoloration; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|gross pathology|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15709702_15709703:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_e3738fcd0e9c1fe46f32e2603849b286
ToxValDB ToxRefDB NEL =300 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic LONG_REF=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Subchronic_Rats; TITLE=Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Subchronic_Rats; AUTHOR=NTP; EXTERNAL_SOURCE_ID=5620; 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=1982; ORIGINAL_YEAR=1982; TOXICOLOGICAL_EFFECT=systemic: in life observation-clinical signs-skin discoloration|systemic: pathology gross-intestine small-discolored|systemic: in life observation-body weight-body weight gain|systemic: pathology gross-stomach-thickened|systemic: pathology microscopic-stomach-necrosis|systemic: pathology microscopic-stomach-inflammation|systemic: pathology microscopic-stomach-ulcer; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|gross pathology|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15709704_15709705_15709706_15709707:M:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_f0fd65f02f1fabf356d9ab9550814f4b
ToxValDB ToxRefDB NEL =625 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic LONG_REF=NTP_1982_Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Subchronic_Rats; TITLE=Carcinogenesis Bioassay of Propyl Gallate (CAS No. 121-79-9) in F344/N Rats and B6C3F1 Mice (Feed Study)_Subchronic_Rats; AUTHOR=NTP; EXTERNAL_SOURCE_ID=5620; 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=1982; ORIGINAL_YEAR=1982; TOXICOLOGICAL_EFFECT=systemic: in life observation-clinical signs-skin discoloration|systemic: pathology microscopic-stomach-inflammation|systemic: in life observation-body weight-body weight gain|systemic: pathology microscopic-stomach-necrosis|systemic: pathology microscopic-stomach-ulcer|systemic: pathology gross-stomach-thickened|systemic: pathology gross-intestine small-discolored; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical signs|gross pathology|nonneoplastic histopathology; STUDY_GROUP=ToxRefDB_dup_-_15709702_15709703:F:F0adult; QC_CATEGORY=Data source QC'd by data provider prior to ToxRefDB import; QC_STATUS=not determined; SOURCE_HASH=ToxValhc_8ae1d4806a42b94182bb36d17dc70203
WHO/JECFA 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
WHO/JECFA ADI <=1.4 mg/kg Human oral - Toxicity Value STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/650b0374e4b0d99f5a887e40; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://apps.who.int/food-additives-contaminants-jecfa-database/; SUBSOURCE_URL=https://apps.who.int/food-additives-contaminants-jecfa-database/Home/Chemical/1272; YEAR=1996; ORIGINAL_YEAR=1996; STUDY_GROUP=WHO JECFA ADI:15715691:-:--; 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_c406c455e9edb5586d390f7ae69b6d38
openFDA substances 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier 8D4SNN7V92 UNII - - - chemical {"approval_status":null,"molecular_formula":"C10H12O5","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"8D4SNN7V92"}
openFDA substances FDA UNII substance identifier 8D4SNN7V92 UNII - - - chemical {"approval_status":null,"molecular_formula":"C10H12O5","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"8D4SNN7V92"}
openFDA substances FDA UNII substance identifier 8D4SNN7V92 UNII - - - chemical {"approval_status":null,"molecular_formula":"C10H12O5","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"8D4SNN7V92"}
openFDA substances FDA UNII substance identifier 8D4SNN7V92 UNII - - - chemical {"approval_status":null,"molecular_formula":"C10H12O5","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"8D4SNN7V92"}