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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Additional information

The genetic toxicity data collected on the test substance have in both studies found negative genetic toxicity.


Short description of key information:
A bacterial reverse mutation assay was performed (2011) in accordance with OECD 471. The study was GLP compliant and the results indicate the test substance was negative, without and with metabolic activation, under the test conditions and according to the criteria of the test protocol.

An in vitro micronucleus assay in human lymphocytes was performed (2011) in accordance with OECD 487. The study was GLP compliant and the results indicate the test article was considered negative for inducing micronuclei in binucleated cells in cultured human lymphocytes, without and with metabolic activation.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

The substance does not meet classification criteria under EU Directive 67/548/EEC for genotoxicity.

The substance does not meet classification criteria under Regulation (EC) No 1272/2008 for genotoxicity.