Registration Dossier
Registration Dossier
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EC number: - | CAS number: -
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
No study was selected, since all in vitro genotoxicity studies showed no genotoxic effects.
Short description of key information:
Under the present test conditions the test item tested up to cytotoxic concentrations in the in vitro bacterial mutagenicity assay (Salmonella reverse mutation Assay), the in vitro mammalian mutagenicity assay (Mouse lymphoma Assay) and the in vitro mammalian cytogenetic assay (Micronucleus Test) each assay carried out without and with metabolic activation, revealed no genotoxic activity.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Because all in vitro genotoxicity studies revealed clearly negative results, it can be conluded that the test item is not genotoxic in vitro and therefore must not be classifed according to the criteria of EC Directive 67/548/EEC and EC Regulation 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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