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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The test substance was found to be non-mutagenic and non-clastogenic.


In the Ames test, the test substance was not considered to be mutagenic to bacteria under the conditions of the test. The test substance was not found to be clastogenic in an in vitro mammalian chromosome aberration test in human peripheral lymphocytes. The test substance was found not to be mutagenic in an in vitro cell gene mutation test performed using mouse lymphoma cells. 


Overall, the test substance is considered non-mutagenic and non-clastogenic.

Justification for selection of genetic toxicity endpoint
No study was selected, since all three in vitro studies were negative

Short description of key information:
Clearly negative in the in vitro studies - both with and without metabolic activation

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

The test data does not support classification of the registered substance as mutagenic according to the criteria laid down in Regulation (EC) No 1272/2008 (i.e. CLP).