Registration Dossier
Registration Dossier
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EC number: 300-339-7 | CAS number: 93925-37-2
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
None of the in-vitro tests revealed a mutagenic potential of the test substance. It can therefore be concluded that the substance is non mutagenic in-vitro, and possible in vivo.
Short description of key information:
In-vitro: negative in Ames Test with Salmonella typhimurium strains TA1535, TA1537, TA98 and TA100 and Escherichia coli strain WP2uvrA (with and without metabolic activation)
in-vitro: negative in Chromosome-Aberration in Chinese Hamster Lung (CHL) cell line (CHL/IU)
in-vitro: negative in Mouse Lymphoma Assay
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
There are conclusive but not sufficient data to classify the substance with regard to mutagenicity. The test substance is not classified for this endpoint in accordance to Directive 67/548/EEC or the CLP Regulation (EC) No 1272/2008.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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