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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

The genotoxicity of the substance has been assessed in vitro and in vivo. Based on the results of the negative Ames test, the negative mouse lymphoma assay and the negative in vivo micronucleus study no genotoxic carcinogenicity is expected, via the oral, inhalation and dermal route.

Key value for chemical safety assessment

Carcinogenicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Justification for classification or non-classification

The genotoxicity of the substance has been assessed in vitro and in vivo. Based on the results of the negative Ames test, the negative mouse lymphoma assay and the negative in vivo micronucleus study no genotoxic carcinogenicity is expected, via the oral, inhalation and dermal route. Therefore the substance does not have to be classified for genotoxic carcinogenicity via the oral, inhalation and dermal route in accordance with the criteria of EU CLP (EC 1272/2008 and its updates).

Additional information