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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Key value for chemical safety assessment

Additional information

Negative results were observed in an in vitro gene mutation study in bacterial cells (Salmonella typhimurium and E. coli), an in vitro gene mutation study in mammalian cells (Chinese hamster ovary cells), an in vitro cytogenicity study in mammalian cells (Chinese hamster ovary cells), and an in vivo micronucleus (mouse bone marrow) study. Overall, the test substance is considered negative for genotoxicity.


Short description of key information:
In Vitro (Mutagenic effects - bacterial): OECD 471; Bacterial reverse mutation assay. Negative. Reliability = 1.
In Vitro (Clastogenic effects - mammalian): OECD 473; Chinese hamster ovary cells. Negative. Reliability = 2
In Vitro (Mutagenic effects - mammalian): OECD 476; Mammalian Cell Forward Gene Mutation (CHO/HPRT) Assay . Negative. Reliability = 1
In Vivo (Clastogenic effects - mammalian): OECD 474; in vivo mouse micronucleus study; Negative. Reliability = 1.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Overall, the test substance is negative for genotoxicity when evaluated in bacterial or mammalian cell cultures or in laboratory animals. Based on an assessment of the robust genetic toxicity data for this substance, the substance does not need to be classified for mutagenicity according the EU Directive 67/548/EEC and EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008.