Registration Dossier
Registration Dossier
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EC number: 915-790-0 | CAS number: -
Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vitro
Description of key information
The substance gave a negative results, both with and without metabolic activation, in three reliable assays ie an in vitro bacterial mutation assay, an in vitro micronucleus assay and an in vitro gene mutation assay.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Genetic toxicity in vivo
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
The substance gave a negative results, both with and without metabolic activation, in three reliable assays ie an in vitro bacterial mutation assay, an in vitro micronucleus assay and an in vitro gene mutation assay. The bacterial mutation assay tested a formulation (69% active) however the dose levels were increased to correct for the content of active.
Justification for selection of genetic toxicity endpoint
All of the available in vitro studies were negative so no study has
been selected. All studies compliant with GLP and testing guidelines.
Short description of key information:
The substance gave negative, non-mutagenic results in three
different in vitro gentoxicity assays.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
The substance gave negative results in three in vitro gentoxicity assays. Therefore there is no requirement for classification.
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