Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Available studies for mutagenicity, EU Method B13/14, EU Method B10 and Ames test show negative results both with and without metabolic activation.

Justification for selection of genetic toxicity endpoint
Three in-vitro studies available, GLP compliant, same results.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

A non-classification for mutagenicity germ cells is based on the available results according to different in-vitro tests results.