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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The registered substance has OECD 471, 473, and 476 studies to evluate genotoxicity.

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

Genetic toxicity in vivo

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

In vitro data

The potential of the registered substance to cause gene mutation was evaluated in an OECD 471 and OECD 476 study. Both studies were negative with and without metabolic activation.

The registered substance was also evaluated for chromosomal aberration in an OECD 473 study and was negative with and without metabolic activation.

The following information is taken into account for any hazard / risk assessment:

IN VITRO DATA

Gene mutation in mammalian cells: Negative, OECD 471, OECD 473, OECD 476

Value used for CSA:Genetic toxicity: No adverse effect observed (negative)

Justification for classification or non classification

In accordance with criteria for classification as defined in Annex I, Regulation 1272/2008, the test material does not require classification for genetic toxicity based on the overall negative response noted in the available genetic toxicity studies.

Justification for classification or non-classification

In accordance with criteria for classification as defined in Annex I, Regulation 1272/2008, the test material does not require classification for genetic toxicity based on the overall negative response noted in the available genetic toxicity studies.