NOAEL Studies
Cosmetic Ingredient
Acid Red 52 NOAEL Studies
INCI: CI 45100
CAS: 3520-42-1
Raw No Observed Adverse Effect Level endpoint records grouped by source. This page does not render calculated Margin of Safety values.
COSMOS DB 1 endpoint
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| COSMOS DB | LOAEL | 100 | mg/kg bw/day | rat | oral | 90 day | Subchronic | SCCP; H.J. Hamann, D. Richard, K. Weber, C.Knuppe, Acid Red 52 (CI 45100): 13-week oral toxicity (gavage) study in rat, RCC Project No. 736334, Itingen /CH |
SCCNFP Opinion 2 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| SCCNFP Opinion | NOAEL | =1000 | mg/kg bw/day | rabbit | oral | 13 weeks | repeated dose toxicity | p.7 |
| SCCNFP Opinion | NOAEL | =1000 | mg/kg | human | - | - | NOAEL study | p.15 |
SCCS Opinion 3 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| SCCS Opinion | NOAEL | =0.013 | mg/kg bw | rat | oral | 13-week | dermal absorption | p.20 |
| SCCS Opinion | NOAEL | =1000 | mg/kg bw/day | - | oral | 13 weeks | genotoxicity | p.16 |
| SCCS Opinion | NOAEL | =1000 | mg/kg bw | rat | oral | 13-week | dermal absorption | p.20 |
ECHA 1 endpoint
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| ECHA | NOAEL | =1000 | mg/kg bw/day | Rat | oral | subchronic; 13 weeks | subchronic | QUALITY=4 (not assignable); STORED_SOURCE_RECORD=https://clowder.edap-cluster.com/files/669ead10e4b0a7c65d1c2568; RECORD_SOURCE_LEVEL=Extraction document; SOURCE_URL=https://echa.europa.eu/; SUBSOURCE_URL=https://echa.europa.eu/en/registration-dossier/-/registered-dossier/12094?documentUUID=b300c255-029d-42ea-8cad-836bc333cae7; YEAR=1975; ORIGINAL_YEAR=1975; TOXICOLOGICAL_EFFECT=behaviour (functional findings)|organ weights and organ / body weight ratios|urinalysis|body weight and weight gain|clinical biochemistry|clinical signs|food consumption and compound intake|gross pathology|haematology|histopathology: non-neoplastic|mortality|ophthalmological examination; TOXICOLOGICAL_EFFECT_CATEGORY=body weight|clinical chemistry|clinical signs|food and/or water consumption|gross pathology|hematology|mortality/survival|neurobehavior|nonneoplastic histopathology|organ weight|urinalysis; STUDY_GROUP=ECHA IUCLID:15836696: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_36816715f00a44eb3b5268beedbb6dac |
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:15598651:M:--; QC_CATEGORY=Data source QC'd by data provider prior to ECOTOX import; QC_STATUS=not determined; SOURCE_HASH=4e67c3961a62320bf75f3c5765493d2b |
Regulatory source 10 endpoints
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| Regulatory source | - | =1000 | mg/kg | human | - | - | - | p.15 |
| Regulatory source | - | 1000 | mg/kg | - | - | - | - | p.15 |
| Regulatory source | dermal absorption | 1000 | mg/kg bw/day | pig | - | - | dermal absorption | p.11 |
| Regulatory source | dermal absorption | 1000 | mg/kg bw/day | pig | - | 3 months | dermal absorption | p.11 |
| Regulatory source | irritation | 1000 | mg/kg bw/day | - | oral | 13 weeks | irritation | p.16 |
| Regulatory source | repeated dose toxicity | 1000 | mg/kg bw/day | rabbit | oral | 13 weeks | repeated dose toxicity | p.7 |
| Regulatory source | - | 1000 | mg/kg bw/day | human | - | - | - | p.20 |
| Regulatory source | dermal absorption | =0.013 | mg/kg bw | rat | oral | 13-week | dermal absorption | p.20 |
| Regulatory source | dermal absorption | =1000 | mg/kg bw | rat | oral | 13-week | dermal absorption | p.20 |
| Regulatory source | genotoxicity | 1000 | mg/kg bw/day | - | oral | 13 weeks | genotoxicity | p.16 |
openFDA substances 1 endpoint
| Source | Endpoint Type | Value | Unit | Species | Route | Duration | Study Type | Reference |
|---|---|---|---|---|---|---|---|---|
| openFDA substances | FDA UNII substance identifier | 821LWZ3R6R | UNII | - | - | - | chemical | - |