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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

According to the key study, the procedures described in this report were based on the Guideline OECD 471 and B.13/14. The substance was tested in the Salmonella typhimurium reverse mutation assay with four histidine-requiring strains of Salmonella typhimurium (TA1535, TA1537, TA98 and TA100) and in the Escherichia coli reverse mutation assay with a tryptophan-requiring strain of Escherichia coli. The test was performed in two independent experiments in the presence and absence of S9 -mix. To obtain more information about the possible mutagenicity of the susbtance, an additional experiment was performed with the tester strains TA1535 and TA1537 in the absence and presence of 10% (v/v) S9 -mix.

Based on the results of this study it is concluded that the substance is not mutagenic in the Salmonella typhimurium reverse mutation assay and in the Escherichia coli reverse mutation assay.

Short description of key information:
Full details of these endpoints are provided in the IUCLID dossier and they are considered reliable.
Results for the substance decyldimethylamine are presented below:
The test material did not exhibit any mutagenic activity under the conditions of test.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification