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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Justification for selection of genetic toxicity endpoint
Both genetic toxicity sudies (in vitro and in vivo study) were negative.

Short description of key information:
The genetic toxicity potential was investigated with an Ames test following the OECD Guideline 471 (with exception for statistical analysis) and an in vivo micronucleus test following EU Method B.12 (Mutagenicity - In Vivo Mammalian Erythrocyte Micronucleus Test).
Both studies were performed more than 12 years ago, under GLP conditions.
Both studies did not observed a mutagenicity potential of the substance.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Both performed studies (in vitro and in vivo) did not observed a mutagenicity potential of the substance. A classification is not needed.