Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

The genotoxicity of the substance has been assessed in vitro for three genotoxicity endpoints: genotoxicity in bacteria, cytogenicity in a chromosomal aberration assay and genemutation test in mammalian cells, resulting in the absence of genotoxicity.

Key value for chemical safety assessment

Mode of Action Analysis / Human Relevance Framework

In view of the absence of in vitro genotoxicity the substance does not have a genotoxic Mode of Action.

Justification for classification or non-classification

The genotoxicity of the substance has been assessed in vitro for three genotoxicity endpoints: genotoxicity in bacteria, cytogenicity in a chromosomal aberration assay and genemutation test in mammalian cells, resulting in the absence of genotoxicity. Therefore no genotoxic carcinogenicity is expected, via the oral, inhalation and dermal route. The substance does not need to be classified for genotoxic carcinogenicity via the oral, inhalation and dermal route in accordance with the criteria outlined in the EU CLP (EC no. 1272/2008/EC and its updates).

Additional information