Registration Dossier
Registration Dossier
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EC number: 916-331-7 | CAS number: -
Carcinogenicity
Administrative data
Description of key information
In accordance with Annex VIII information on carcinogenicity is not required for a substance manufactured/imported in amounts 10-100 tons. The genotoxicity of the substance has been assessed for three genotoxicity endpoints: genotoxicity in bacteria, genotoxicity in mammalian cells and information on chromosomal aberrations all assessed in vitro, resulting in the absence of genotoxicity. Therefore no genotoxic carcinogenicity is expected.
Key value for chemical safety assessment
Carcinogenicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
Justification for classification or non-classification
The genotoxicity of the substance has been assessed (see IUCLID section 7.6 and CSR section 5.7) resulting in absence of genotoxicity in vitro. Therefore no genotoxic carcinogenicity is expected. Classification for carcinogenicity of the substance is therefore not warranted in accordance with EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008 and its updates.
Additional information
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
