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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 has been assessed in Ames and in the in vitro micronucleus test and in an in vivo micronucleus test. The substance is negative, positive and negative in these tests, respectively, resulting in absence of genotoxicity.

Key value for chemical safety assessment

Carcinogenicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Mode of Action Analysis / Human Relevance Framework

Mode of Action is not relevant in absence of adverse effects.

Justification for classification or non-classification

The genotoxicity of the substance has been assessed with three genotoxicity tests. The substance is negative in Ames. The substance is positive in the in vitro micronucleus test but negative in an in vivo micronucleus test. Therefore the substance does not have a genotoxic potential and therefore the substance does not need to be classified for genotoxic carcinogenicity according to EU CLP (EC 1272/2008 and its amendments).

Additional information