Registration Dossier
Registration Dossier
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EC number: 810-258-3 | CAS number: -
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
The negative results using in vitro and in vivo genotoxicity assays do not warrant the classification of the registered substance as genotoxic under the new Regulation (EC) 1272/2008 on classification, labeling and packaging of substances and mixtures (CLP) or under the Directive 67/518/EEC for dangerous substances and Directive 1999/45/EC for preparations.
Short description of key information:
The registered substance gave negative results in the genetic toxicity tests listed below
Genetic Toxicity in vitro – Bacterial reverse mutation assay (OECD TG 471)
Genetic Toxicity in vivo – Micronucleus Assay in Mouse Bone Marrow (OECD TG 474)
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
The negative results using in vitro and in vivo genotoxicity assays do not warrant the classification of the registered substance as genotoxic under the new Regulation (EC) 1272/2008 on classification, labeling and packaging of substances and mixtures (CLP) or under the Directive 67/518/EEC for dangerous substances and Directive 1999/45/EC for preparations.
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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