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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

In vitro

The test substance was tested for its mutagenic potential based on the ability to induce point mutations in selected loci of several strains of Salmonella typhimurium in a modified version of the traditional Ames test, i.e. the Ames II Assay (microtiter Version) both with and without the addition of a metabolizing system (S-9 mix) obtained from rat liver using the Salmonella strains TA 98 and mixed strains (TA 7001 - 7006). An increase in the number of positive wells (his+ revertants) was not observed either without S-9 mix or after the addition of a metabolizing system. The test substance was therefore not mutagenic under the experimental conditions chosen.


Short description of key information:
in vitro:
Ames-Test II: negative (BASF AG, 1999)

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

EU classification according to Annex VI of Directive 67/548/EEC: no classification required

GHS classification (1272/2008/EC): no classification required