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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The genetic toxicity of TSP/DSP was tested in a bacterial reverse gene mutation assay on S. typhimurium strains (RBM study No. 970075, 1997), using both plate incorporation and pre-incubation methods. This Ames test was a key study of validity 1 according to Klimisch cotation criteria.

 

The test substance showed no mutagenic activity up to the limit concentration of 5000 µg/plate in the presence or absence of mammalian metabolic activation.

 

Therefore, the test item was considered non mutagenic in the Ames test.


Short description of key information:
No in vitro mutagenic activity

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Due to the absence of induced mutant colonies over background in an Ames test up to the limit concentration of 5000 µg/plate in the presence or absence of mammalian metabolic activation, no classification is warranted for mutagenicity.