Registration Dossier
Registration Dossier
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EC number: 701-371-8 | CAS number: -
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
The substance was non mutagenic in a GLP-compliant Ames test performed according to OECD guideline 471 (Dainippon 1994).
It was non clastogenic in a GLP-compliant in-vitro chromosome abberration test performed according to OECD guideline 473 (SunChemical 1997).
The substance is assessed to be non genotoxic in mammalian cells in vitro based on read-across. The read-across justifcation is attached to the endpoint study record.
Justification for classification or non-classification
No signs of genotoxic effects in-vitro were observed, neither in bacterial systems nor in mammalian cells.
Additionally, no signs of genotoxic effects in-vivo were seen, neither in the Micronucleus Test, nor in the Nucleus Anomaly Test or the Mouse Spot test.
Thererefore, there is no indication given for classification for mutagenic effects.
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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