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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

For the Ames study and the two of the three in vitro mammalian cell gene mutation tests the results are: negative with metabolic activation; negative without metabolic activation. One in vitro study indicated a positive result with and without activation; chromosome aberration study indicates a positive result with activation at the highest concentration tested due to polyploid cells, although there was no increase in frequency of chromosome aberrations.


Short description of key information:
For the Ames study and the two of the three in vitro mammalian cell gene mutation tests the results are: negative with metabolic activation; negative without metabolic activation. One in vitro study indicated a positive result with and without activation; chromosome aberration study indicates a positive result with activation at the highest concentration tested due to polyploid cells, although there was no increase in frequency of chromosome aberrations.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

The substance does not meet classification criteria under EU Directive 67/548/EEC for genetic toxicity.

The substance does not meet classification criteria under Regulation (EC) No 1272/2008 for genetic toxicity.