Registration Dossier
Registration Dossier
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EC number: 423-340-5 | CAS number: 162881-26-7 CGI 819
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
The 3 available in vitro studies showed negative results.
Short description of key information:
The test substance is negative in the Ames test, in the in vitro HPRT assay and in the in vivo micronucleus assay.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
The test substance is negative in the Ames test, in the in vitro mouse lymphoma assay and in the in vitro chromosome aberration assay. Therefore, the substance does not need to be classified and labelled as a mutagen, according to the Regulation 1271/2008 and the Directive 67/548/EEC.
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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