Registration Dossier
Registration Dossier
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EC number: 221-201-1 | CAS number: 3030-47-5
Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vitro
Description of key information
3 in vitro tests for mutagenicity were performed:
1/ Genetic toxicity in vitro: Bacterial reverse mutation test (Ames) -
negative
2/ Genetic toxicity in vitro: Chromosome aberration test - negative
3/ Genetic toxicity in vitro: Mouse Lymphoma Assay - negative
All tests were carried out in accordance with internationally valid GLP principles.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Additional information
All three in vitro tests in genetic toxicity showed negative results. Therefore, there is no need to carry out in vivo studies in genetic toxicity.
Justification for selection of genetic toxicity endpoint
No endpoint selection was performed because the results of three various in vitro mutagenicity tests are available - all negative.
See section 7.6.1 - Genetic toxicity in vitro.
Justification for classification or non-classification
Based on the available data, the substance is not classified.
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