NOAEL Studies
Antioxidant
Tocopheryl Acetate NOAEL Studies
INCI: TOCOPHERYL ACETATE
CAS: 58-95-7
Raw No Observed Adverse Effect Level endpoint records grouped by source. This page does not render calculated Margin of Safety values.
COSMOS_DB 10 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| COSMOS_DB | NOAEL | 5.5 | mg/kg bw/day | rabbit | oral | 90 day | Subchronic | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
| COSMOS_DB | NOAEL | 6.6 | mg/kg bw/day | rabbit | oral | 63 day | Short Term Toxicity | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
| COSMOS_DB | NOAEL | 47 | mg/kg bw/day | rat | oral | 21 day | Short Term Toxicity | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
| COSMOS_DB | NOAEL | 83 | mg/kg bw/day | rat | oral | 480 day | Chronic | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
| COSMOS_DB | NOAEL | 125 | mg/kg bw/day | rat | oral | 90 day | Subchronic | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
| COSMOS_DB | NOAEL | 500 | mg/kg bw/day | rat | oral | 10 day | Short Term Toxicity | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
| COSMOS_DB | NOAEL | 833 | mg/kg bw/day | rat | oral | 480 day | Special Toxicology Study | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
| COSMOS_DB | NOAEL | 1000 | mg/kg bw/day | rat | oral | 20 day | Developmental | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
| COSMOS_DB | NOAEL | 1600 | mg/kg bw/day | mouse | oral | 10 day | Developmental | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
| COSMOS_DB | NOAEL | 4000 | mg/kg bw/day | rat | oral | 60 day | Short Term Toxicity | US FDA CFSAN PAFA; US FDA CFSAN PAFA Study |
EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx 2 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx | NOAEL | =540 | mg/day | Human | - | - | study with volunteers | EFSA FEEDAP - 2010 - OutputID 178 - haematology - hemopoietic - Scientific Opinion on the safety and efficacy of vitamin E as a feed additive for all animal species - doi:10.2903/j.efsa.2010.1635 |
| EFSA_OpenFoodTox_EFSA_ReferencePoints.xlsx | NOAEL | =540 | mg/day | Human | - | - | study with volunteers | EFSA FEEDAP - 2010 - OutputID 178 - haematology - hemopoietic - Scientific Opinion on the safety and efficacy of vitamin E as a feed additive for all animal species - doi:10.2903/j.efsa.2010.1635 |
ToxValDB_ECHA_IUCLID 1 endpoint
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| ToxValDB_ECHA_IUCLID | NOAEL | =2000 | mg/kg bw/day | Rat | oral | - | chronic | QUALITY=4 (not assignable); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669ea9e4e4b0a7c65d1b346e; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/en/registration-dossier/-/registered-dossier/25435?documentUUID=1b5482f2-44a9-41c3-a01c-c9ebf5a4b820; YEAR=2002; ORIGINAL_YEAR=2002; STUDY_GROUP=ECHA IUCLID:15820078: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_eb0d8dd698df47c52f8fd06571b02609 |
ToxValDB_ECOTOX 1 endpoint
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| ToxValDB_ECOTOX | NOEL | =35.7143 | mg/kg bw/day | Mouse | oral | subchronic; 42 days | subchronic | LONG_REF=Indian J. Exp. Biol.29(9): 823-825 Khan,S., M.A. Khan, D. Bhatnagar, P. Yadav, and S. Sarkar Zinc Protection Against Lipid Peroxidation from Cadmium 1991; TITLE=Zinc Protection Against Lipid Peroxidation from Cadmium; AUTHOR=Khan,S., M.A. Khan, D. Bhatnagar, P. Yadav, and S. Sarkar; QUALITY=Control type: Concurrent control; EXTERNAL_SOURCE_ID=82634; 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=1991; ORIGINAL_YEAR=1991; TOXICOLOGICAL_EFFECT=Enzyme(s): Catalase|Growth: Weight|Morphology: Organ weight in relationship to body weight|Physiology: Blood volume|Physiology: Lipid peroxidation; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|enzyme activity|hematology|organ weight|other; STUDY_GROUP=ECOTOX_dup_EPA ORD_15598178_15603493:M:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=79066f935e81f85a7d40f84821a44952 |
ToxValDB_EFSA 1 endpoint
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| ToxValDB_EFSA | NOAEL | =540 | mg/day | Human | oral | - | epidemiologic | LONG_REF=EFSA FEEDAP (2010). Scientific Opinion on the safety and efficacy of vitamin E as a feed additive for all animal species. doi:10.2903/j.efsa.2010.1635.; TITLE=Scientific Opinion on the safety and efficacy of vitamin E as a feed additive for all animal species; AUTHOR=EFSA FEEDAP; DOI=doi:10.2903/j.efsa.2010.1635; STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/65201d30e4b0f0a60ddd1165; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://zenodo.org/record/5076033#.Y9fEoXbMI2z; YEAR=2010; ORIGINAL_YEAR=2010; TOXICOLOGICAL_EFFECT=hematological; TOXICOLOGICAL_EFFECT_CATEGORY=hematology; STUDY_GROUP=EFSA:15614237:-:--; 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_a215a8d747e97a5fb6770b8a9a24aac2 |
openFDA substances 4 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| openFDA substances | FDA UNII substance identifier | A7E6112E4N | UNII | - | - | - | chemical | {"approval_status":null,"molecular_formula":"C31H52O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"A7E6112E4N"} |
| openFDA substances | FDA UNII substance identifier | A7E6112E4N | UNII | - | - | - | chemical | {"approval_status":null,"molecular_formula":"C31H52O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"A7E6112E4N"} |
| openFDA substances | FDA UNII substance identifier | A7E6112E4N | UNII | - | - | - | chemical | {"approval_status":null,"molecular_formula":"C31H52O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"A7E6112E4N"} |
| openFDA substances | FDA UNII substance identifier | A7E6112E4N | UNII | - | - | - | chemical | {"approval_status":null,"molecular_formula":"C31H52O3","source_table":"substance_identifiers_fda","substance_class":"chemical","unii_code":"A7E6112E4N"} |