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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

In-vitro experiments comprised bacterial and mammalian cell genotoxicity as well as the chromosome aberration test. All tests revealed the absence of genotoxicity. Furthermore, an in-vivo micronucleus test that was performed in NMRI mice by gavage administration, gave no evidence of a genotoxic potential of the test substance.


Short description of key information:
In-vitro and in-vivo experiments with the test substance were devoid of a genotoxic result.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

There are conclusive data that classification of the test item with regard to genotoxicity is not necessary.

The test item is not classified for this endpoint in accordance with Directive 67/548/EEC or with the CLP Regulation (EC) No 1272/2008 reflecting GHS regulations.