Registration Dossier
Registration Dossier
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EC number: 700-502-6 | CAS number: -
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
F 213 Red was tested in an Ames test (EU Method B.13/14) an in vitro mammalian cell gene mutation test (EU Method B.17) and an in vitro mammalian chromosome aberration test (EU Method B.10). All tests were carried out up to cytotoxic concentrations/limit concentrations, without and with metabolic activation. All three tests were negative.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Based on the genetic toxicity results obtained for F 213 Red, no classification is warranted.
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