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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Three in vitro tests were performed according to OECD guidelines n° 471, 473 and 476 and are GLP studies. No mutagenic or genotoxic effect was detected according to these tests

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

Genetic toxicity in vivo

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

Additional information

Additional information from genetic toxicity in vitro:


Justification for selection of genetic toxicity endpoint
Three in vitro tests were performed according to OECD guidelines n° 471, 473 and 476 and are GLP studies

Justification for classification or non-classification

The registered substance is not classified as mutagenic according to GHS