Registration Dossier
Registration Dossier
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EC number: 612-831-1 | CAS number: 61967-98-4
Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vitro
Description of key information
Ames: in progress
CHO mammalian cell gene mutation assay: NEGATIVE
IHMA intrasanguineous host-mediated assay: NEGATIVE
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Genetic toxicity in vivo
Description of key information
Micronucleus: NEGATIVE
UDS: NEGATIVE
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Additional information
An ames test is in progress and it is expected to be negative.
Other genetic toxicity studies of the analogue substance were available, namely: mammalian cells in vitro (CHO, hamster; HGPRT assay), mammalian cells in a combined in vitro/in vivo study (UDS test) and whole animals (in vivo micronucleus test). In all the present experiments, the substance did not show any genetic activity.
Justification for classification or non-classification
Based on the information currently available, the substance does not meet the criteria for mutagenic effects classification under the Regulation EC 1272/2008 (CLP).
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