NOAEL Studies Cosmetic Ingredient

Triacetin NOAEL Studies

INCI: TRIACETIN

CAS: 102-76-1

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

COSMOS_DB 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
COSMOS_DB NOAEL 1650 mg/kg bw/day rat oral 708 day Chronic US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
COSMOS_DB NOAEL 9500 mg/kg bw/day rat oral 30 day Short Term Toxicity US FDA CFSAN PAFA; US FDA CFSAN PAFA Study
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip 12 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 12200 mg/kg bw/day rat oral: feed - sub-chronic toxicity: oral dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=58037e21-8443-45ae-829a-e9f238f1bb72_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=58037e21-8443-45ae-829a-e9f238f1bb72/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1975; basis=other:; key_result=false; entry_uuid=9218d597-32c1-4ed0-ba04-5ef25e10deb7
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 12200 mg/kg bw/day rat oral: feed - sub-chronic toxicity: oral dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=58037e21-8443-45ae-829a-e9f238f1bb72_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=58037e21-8443-45ae-829a-e9f238f1bb72/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1975; basis=other:; key_result=false; entry_uuid=9218d597-32c1-4ed0-ba04-5ef25e10deb7
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip LOAEL 12200 mg/kg bw/day rat oral: feed - sub-chronic toxicity: oral dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=58037e21-8443-45ae-829a-e9f238f1bb72_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=58037e21-8443-45ae-829a-e9f238f1bb72/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1975; basis=other:; key_result=false; entry_uuid=9218d597-32c1-4ed0-ba04-5ef25e10deb7
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL >=1000 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=375a1291-545e-4899-83e0-855af9f60797_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=375a1291-545e-4899-83e0-855af9f60797/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1998; basis=other:; key_result=false; entry_uuid=2f4f37bd-20d2-496d-b91b-ba7b084f7099
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 8000 mg/kg bw/day rat oral: feed - sub-chronic toxicity: oral dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=5db3ccdd-26e5-4c28-b971-98719b54160a_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=5db3ccdd-26e5-4c28-b971-98719b54160a/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1969; basis=other:; key_result=false; entry_uuid=523295da-ec3d-4839-8534-156d774dece2
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 10000 mg/kg bw/day rat oral: feed - sub-chronic toxicity: oral dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=656c2ed8-d7b4-40f4-9a89-b0b028fc6de3_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=656c2ed8-d7b4-40f4-9a89-b0b028fc6de3/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1969; basis=other:; key_result=false; entry_uuid=5a4b59d1-4aed-47b1-9f13-517eccd3d0c4
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL >=1000 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=375a1291-545e-4899-83e0-855af9f60797_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=375a1291-545e-4899-83e0-855af9f60797/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1998; basis=other:; key_result=false; entry_uuid=2f4f37bd-20d2-496d-b91b-ba7b084f7099
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 8000 mg/kg bw/day rat oral: feed - sub-chronic toxicity: oral dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=5db3ccdd-26e5-4c28-b971-98719b54160a_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=5db3ccdd-26e5-4c28-b971-98719b54160a/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1969; basis=other:; key_result=false; entry_uuid=523295da-ec3d-4839-8534-156d774dece2
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 10000 mg/kg bw/day rat oral: feed - sub-chronic toxicity: oral dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=656c2ed8-d7b4-40f4-9a89-b0b028fc6de3_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=656c2ed8-d7b4-40f4-9a89-b0b028fc6de3/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1969; basis=other:; key_result=false; entry_uuid=5a4b59d1-4aed-47b1-9f13-517eccd3d0c4
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL >=1000 mg/kg bw/day rat oral: gavage - developmental toxicity dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=375a1291-545e-4899-83e0-855af9f60797_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=375a1291-545e-4899-83e0-855af9f60797/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=DevelopmentalToxicityTeratogenicity; literature=Name=Unnamed; ReferenceYear=1998; basis=other:; key_result=false; entry_uuid=2f4f37bd-20d2-496d-b91b-ba7b084f7099
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 8000 mg/kg bw/day rat oral: feed - sub-chronic toxicity: oral dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=5db3ccdd-26e5-4c28-b971-98719b54160a_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=5db3ccdd-26e5-4c28-b971-98719b54160a/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1969; basis=other:; key_result=false; entry_uuid=523295da-ec3d-4839-8534-156d774dece2
ECHA_REACH_reach_study_results_dossiers_23-05-2023.zip NOAEL 10000 mg/kg bw/day rat oral: feed - sub-chronic toxicity: oral dossier=bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6z; document=656c2ed8-d7b4-40f4-9a89-b0b028fc6de3_bda14174-9ff7-4301-bd60-d9d6cc17ff01.i6d; document_key=656c2ed8-d7b4-40f4-9a89-b0b028fc6de3/bda14174-9ff7-4301-bd60-d9d6cc17ff01; document_subtype=RepeatedDoseToxicityOral; literature=Name=Unnamed; ReferenceYear=1969; basis=other:; key_result=false; entry_uuid=5a4b59d1-4aed-47b1-9f13-517eccd3d0c4
NTP_ICE_acute_inhalation 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_acute_inhalation LC50 >1.721 mg/L - Inhalation Duration=4 hr In Vivo; AcuteInhalNICEATM; Rat Acute Inhalation Toxicity sheet=Data; excel_row=2059; Record_ID=acute_inhalation_589; Data_Type=In Vivo; Internal_Data_Source=AcuteInhalNICEATM; Mixture=Chemical; DTXSID=DTXSID3026691; Assay=Rat Acute Inhalation Toxicity; Endpoint=LC50; Response_Modifier=>; Response=1.721; Response_Unit=mg/L; Reference=REACH; URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/15139/7/3/3/?documentUUID=fe31e1d9-8b6a-4508-9c7e-6577711c8742; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
NTP_ICE_adme_parameters 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_adme_parameters Clint 393 uL/min/10^6 cells Human - - Measured; httk, Human Hepatic Intrinsic Clearance sheet=Data; excel_row=1321; Record_ID=adme_parameters_1096; Data_Type=Measured; DTXSID=DTXSID3026691; Assay=httk, Human Hepatic Intrinsic Clearance; Endpoint=Clint; Response=393.0; 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/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
NTP_ICE_adme_parameters Fu 0.0000577 fraction Human - - Measured; httk, Human Plasma Fraction Unbound sheet=Data; excel_row=1322; Record_ID=adme_parameters_1096; Data_Type=Measured; DTXSID=DTXSID3026691; Assay=httk, Human Plasma Fraction Unbound; Endpoint=Fu; Response=5.77e-05; 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/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
NTP_ICE_endocrine 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_endocrine AC50 39.309013970844 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=15600; RecordID=ERPathway2016_349; DatasetName=ERPathway2016; DTXSID=DTXSID3026691; Assay=ER Pathway Model, Antagonist; Endpoint=AC50; Response=39.309013970844; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
NTP_ICE_endocrine ACC 33.120960836374 uM - - - ERPathway2016; ER Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=15601; RecordID=ERPathway2016_349; DatasetName=ERPathway2016; DTXSID=DTXSID3026691; Assay=ER Pathway Model, Antagonist; Endpoint=ACC; Response=33.120960836374; Response_Unit=uM; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
NTP_ICE_endocrine Model Score 0 unitless - - - ARPathway2016; AR Pathway Model, Antagonist sheet=Integrated_approaches; excel_row=15596; RecordID=ARPathway2016_428; DatasetName=ARPathway2016; DTXSID=DTXSID3026691; Assay=AR Pathway Model, Antagonist; Endpoint=Model Score; Response=0; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
NTP_ICE_endocrine Model Score 0.0182 unitless - - - ERPathway2016; ER Pathway Model, Agonist sheet=Integrated_approaches; excel_row=15602; RecordID=ERPathway2016_349; DatasetName=ERPathway2016; DTXSID=DTXSID3026691; Assay=ER Pathway Model, Agonist; Endpoint=Model Score; Response=0.0182; Response_Unit=Unitless; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
NTP_ICE_skin_sensitization 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
NTP_ICE_skin_sensitization Incidence of positive responses 0 % Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=1884; Record_ID=skin_sensitization_invivo_581; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=20.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID3026691; Assay=Human Maximization Test; Endpoint=Incidence of positive responses; Response=0; Response_Unit=%; Species=Human; Route=Dermal; Reference=Epstein 1976: report to RIFM|Anonymous 1978; Not available; 10.1016/S0015-6264(78)80155-2; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
NTP_ICE_skin_sensitization Induction dose per skin area 13500 ug/cm2 Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=1883; Record_ID=skin_sensitization_invivo_581; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=20.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID3026691; Assay=Human Maximization Test; Endpoint=Induction dose per skin area; Response=13500; Response_Unit=ug/cm2; Species=Human; Route=Dermal; Reference=Epstein 1976: report to RIFM|Anonymous 1978; Not available; 10.1016/S0015-6264(78)80155-2; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
NTP_ICE_skin_sensitization Relative reliability score 3 unitless Human Dermal - In Vivo; HPPT2020WIP; Human Maximization Test sheet=Data_invivo; excel_row=1886; Record_ID=skin_sensitization_invivo_581; Data_Type=In Vivo; Internal_Data_Source=HPPT2020WIP; Concentration=20.0; Concentration_Units=%; Mixture=Chemical; DTXSID=DTXSID3026691; Assay=Human Maximization Test; Endpoint=Relative reliability score; Response=3; Response_Unit=Unitless; Species=Human; Route=Dermal; Reference=Epstein 1976: report to RIFM|Anonymous 1978; Not available; 10.1016/S0015-6264(78)80155-2; URL_CompTox=https://comptox.epa.gov/dashboard/chemical/details/DTXSID3026691; URL_CEBS=https://doi.org/10.22427/NTP-DATA-DTXSID3026691
ToxValDB_DOE_Protective_Action_Criteria 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_DOE_Protective_Action_Criteria LEL =89245.8 mg/m3 Human inhalation - acute LONG_REF=U.S. Department of Energy (DOE) Protective Action Criteria (PAC). 2023. PAC Chemical Database. Updated 11 October 2023. Available: https://edms3.energy.gov/pac/ (Accessed November 16, 2023); TITLE=U.S. Department of Energy (DOE) Protective Action Criteria (PAC) Chemical Database; AUTHOR=U.S. Department of Energy; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65428efee4b045b9ff7cc432; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://edms3.energy.gov/pac/TeelDocs; YEAR=2012; ORIGINAL_YEAR=2012; STUDY_GROUP=DOE Protective Action Criteria:15520470:-:--; 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_ad22129d57288c5276345e13adbd0bb4
ToxValDB_ECHA_IUCLID 3 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_ECHA_IUCLID LOAEL =12200 mg/kg bw/day Rat oral subchronic; 13 weeks subchronic QUALITY=4 (not assignable); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eacb3e4b0a7c65d1c0616; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/15139/7/6/2?documentUUID=bda14174-9ff7-4301-bd60-d9d6cc17ff01; YEAR=2009; ORIGINAL_YEAR=2009; STUDY_GROUP=ECHA IUCLID:15835489: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_e48b78239587f970ab1da9bfbc80575d
ToxValDB_ECHA_IUCLID NOAEL =1000 mg/kg bw/day Rat oral subchronic; 48 days subchronic QUALITY=1 (reliable without restriction); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eacb3e4b0a7c65d1c0614; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/15139/7/6/2?documentUUID=bda14174-9ff7-4301-bd60-d9d6cc17ff01; YEAR=2009; ORIGINAL_YEAR=2009; STUDY_GROUP=ECHA IUCLID:15830538: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_977aa5d776b17a590b8abe8ec5f0f56f
ToxValDB_ECHA_IUCLID NOAEL =8000 mg/kg bw/day Rat oral subchronic; 90 days subchronic QUALITY=4 (not assignable); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669eacb3e4b0a7c65d1c0618; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/registration-dossier/-/registered-dossier/15139/7/6/2?documentUUID=bda14174-9ff7-4301-bd60-d9d6cc17ff01; YEAR=2009; ORIGINAL_YEAR=2009; STUDY_GROUP=ECHA IUCLID:15835858: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_4f6fb2d7f49a8ac63629ddc2584e4186
ToxValDB_GESTIS_DNEL 1 endpoint
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_GESTIS_DNEL DNEL systemic =35.275 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:15632412:-:--; 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_fdf32e0d8ca161ee5b49d353c58931a4
ToxValDB_PPRTV_(CPHEA) 2 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
ToxValDB_PPRTV_(CPHEA) NOAEL (HED) =240 mg/kg bw/day Rat oral chronic (developmental) reproduction developmental LONG_REF=MHW (Ministry of Health and Welfare, Japan). (1998) Toxicity testing reports of environmental chemical. Tokyo: Ministry of Health & Welfare. 674892; TITLE=Toxicity testing reports of environmental chemical; AUTHOR=MHW; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/640754fce4b08a6b3934bdee; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.epa.gov/pprtv/basic-information-about-provisional-peer-reviewed-toxicity-values-pprtvs; SUBSOURCE_URL=https://cfpub.epa.gov/ncea/pprtv/chemicalLanding.cfm?pprtv_sub_id=1921; TOXICOLOGICAL_EFFECT=no effects; STUDY_GROUP=PPRTV (CPHEA):15654076:M/F:--; QC_CATEGORY=Manually extracted from unstructured data source; Source overall passed QC, and this record was manually checked; QC_STATUS=pass; SOURCE_HASH=ToxValhc_ab57ace19ef8a35b26f57ee93eee3ab0
ToxValDB_PPRTV_(CPHEA) RfD (provisional) =80 mg/kg bw/day Human oral - Toxicity Value LONG_REF=MHW (Ministry of Health and Welfare, Japan). (1998) Toxicity testing reports of environmental chemical. Tokyo: Ministry of Health & Welfare. 674892; TITLE=Toxicity testing reports of environmental chemical; AUTHOR=MHW; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/640754fce4b08a6b3934bdee; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://www.epa.gov/pprtv/basic-information-about-provisional-peer-reviewed-toxicity-values-pprtvs; SUBSOURCE_URL=https://cfpub.epa.gov/ncea/pprtv/chemicalLanding.cfm?pprtv_sub_id=1921; TOXICOLOGICAL_EFFECT=none in male/female rats; STUDY_GROUP=PPRTV (CPHEA):15654020:-:--; QC_CATEGORY=Manually extracted from unstructured data source; Source overall passed QC, and this record was manually checked; QC_STATUS=pass; SOURCE_HASH=ToxValhc_bd922d2cf150ed393d2a2a6b522f63db
openFDA substances 4 endpoints
Source Endpoint Type Value Unit Species Route Duration Study Type Reference
openFDA substances FDA UNII substance identifier XHX3C3X673 UNII - - - chemical {"approval_status":null,"molecular_formula":"C9H14O6","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"XHX3C3X673"}
openFDA substances FDA UNII substance identifier XHX3C3X673 UNII - - - chemical {"approval_status":null,"molecular_formula":"C9H14O6","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"XHX3C3X673"}
openFDA substances FDA UNII substance identifier XHX3C3X673 UNII - - - chemical {"approval_status":null,"molecular_formula":"C9H14O6","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"XHX3C3X673"}
openFDA substances FDA UNII substance identifier XHX3C3X673 UNII - - - chemical {"approval_status":null,"molecular_formula":"C9H14O6","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"XHX3C3X673"}