Registration Dossier

Administrative data

Key value for chemical safety assessment

Additional information

The substance showed no evidence of mutagenic potential in a battery of three different in vitro assays (as required by Annexes VII and VIII of REACH): a reverse mutation test in Salmonella typhimurium and E. coli; a chromosome aberration assay using human lymphocytes, and a mouse lymphoma gene mutation assay.


Short description of key information:
The substance showed no evidence of mutagenic potential in three different in vitro assays.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

The substance showed no evidence of mutagenic potential in the standard battery of three in vitro assays (bacterial mutation, mammalian gene mutation, and mammalian cytogenetic). Consequently, no classification for gene mutagenicity is required under CLP.