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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Results of available in vitro studies:

- Ames test for the strain TA 98 in the presence of metabolic activation S9 at 5000 µg/plate: positive.

- Mammalian cell gene mutation test: negative.

- Ames test for the strain TA 98 in presence and absence of metabolic activation S9 at 5000 µg/plate: negative.

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

Genetic toxicity in vivo

Description of key information

Results of available in vitro study:

Single cell gel/Comet assay in rats: negative.

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

Additional information

Justification for classification or non-classification

The available experimental test data are reliable and suitable for classification purposes under Regulation 1272/2008. No hazard for genotoxicity was identified. As a result, according to the CLP Regulation (EC 1272/2008), the substance is not considered to be classified for genetic toxicity.