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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

The results of three performed in vitro tests for genetic toxicity were negative.

Short description of key information:
Three tests in vitro for the determination of genetic toxicity were performed:
The tests were performed according to the following methods:
1/ EU Method B.13/14 (Mutagenicity - Reverse Mutation Test Using Bacteria)
2/ EU Method B.10 (Mutagenicity - In Vitro Mammalian Chromosome Aberration Test)
3/ EU Method B.17 (Mutagenicity - In vitro Mammalian Cell Gene Mutation Test)

The obtaining of information concerning of mutagenicity in the tests in vitro are in accordance with reccomendations stated in Annexes VII - X of the Regulation (EC) No 1907/2006.

All testst were carried out in accordance with internationally valid GLP principles.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Because the results of all performed genotoxicity tests are negative, the test item could not be clasiffied as mutagenic.