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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Tamip monoamide (ZK 39211) did not show any mutagenic potential in a bacterial reverse mutation assay with S. typhymurium (TA 1535, TA 100, TA 1537, TA 1538, TA 98) when tested up to 5.0 mg/plate in the absense and presense of intrinsic metabolic activation (liver mix from Aroclor 1254 -treated rats) (Schering AG, Report No. A483; 1993-06-28)

Tamip monoamide (ZK 39211) did not show any mutagenic potential in a bacterial reverse mutation assay with S. typhymurium (TA 1535, TA 100, TA 1537, TA 1538, TA 98) when tested with preincubation up to 5.0 mg/plate in the absense and presense of intrinsic metabolic activation (liver mix from Aroclor 1254 -treated rat) (Schering AG, Report No. A556; 1993-08-12)


Short description of key information:
Gene mutation (Bacterial reverse muation assay/AMES test, GLP): negative with and without metabolic activation
[Schering AG, Report No. A483; 1993-06-28]

Gene mutation (Bacterial reverse muation assay/AMES test, GLP): negative with and without metabolic activation
[Schering AG, Report No. A556; 1993-08-12]

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Tamip monoamide was tested in two standard genotoxicity tests and did not show any genotoxic potential. Thus, there is no sufficient evidence available to classify Tamip monoamide as genotoxic.

Tamip monoamide is not classified as genotoxic according to the German legislation (TRGS-905).

Classification according to Directive 67/548/EEC and Regulation (EC) 1272/2008 (CLP) is not required.