Registration Dossier
Registration Dossier
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EC number: 479-100-5 | CAS number: 577705-90-9
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
The evaluation of the potential mutagenicity of the substance is based on two in vitro experimental studies:
- A bacterial reverse mutation assay, according to OECD 471
- AnIn vitro mammalian chromosome aberration test, according to OECD 473
All studies were performed under GLP and all of them included a preliminary study on citoxicity of the test item under the specific experimental test condition.
Both the bacterial reverse mutation assay and thein vitro chromosome aberration tests sowed negative results and identify the substance as non mutagenic.
Short description of key information:
The evaluation of the potential mutagenicity of the test item is based on two different experimental studies.
Basing on the results of the studies, it was concluded that the test item does not show genotoxic hazard.
Therefore, according to the criteria reported in the REGULATION (EC) No 1272/2008 , it would indicate the following:
Classification: not required
Signal word: none indicated
Hazard statement: none indicated
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Basing on the results of the reported studies, according to the criteria reported in theREGULATION (EC) No 1272/2008, the test item would indicate the following:
Classification: not required
Signal word: none indicated
Hazard statement: none indicated
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