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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Genetic toxicity in vitro

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Additional information

Following test substance treatments no mutagenic potential was obtained in reverse bacteria mutation assays performed with and without photoactivation. A mouse lymphoma assay did not show any relevant increases in mutant frequency following treatment with the test substance in two experimental series in the absence and presence of S9 mix.


Short description of key information:
The test substance was not mutagenic in Ames and Photo Ames tests and did not increase the mutant frequency in a mouse lymphome assay.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Based on the results obtained, the test substance must not be classified for mutagenicity according to CLP directive.