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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Study Results on Genotoxicity Tests

Mutagenicity Assay –(AMES)

In vitro bacteria gene mutation assay (AMES) has been conducted on this substances. The frequencies of reverse mutations in bacteria were not significantly changed after exposure to various concentrations of the test materials, with/without S9 mixture. The test substance is estimated to be non-mutagenic in bacteria

 

Cytogenicity Assay- in Mammalian Cells

In vitro mammalian chromosome abberation study was performed using Chinese Hamster V9 cell line after treated with various concentrations of the test materials. The test material did not cause cytogenic activity in the absence/presence of metabolic activation at any dose groups. 

CONCLUSION

It is concluded that the test substance is not expected to present a significant risk for genotoxicity.


Short description of key information:
The test substance is non-genotoxic.

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Classification is not required in accordance with Directive 67/548/EEC and EU CLP (Regulation (EC) No. 1272/2008).