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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Key value for chemical safety assessment

Genetic toxicity in vitro

Description of key information
The genetic toxicity was screened with a QSAR prediction using Software DEREK Nexus, version 2.0.3 LHASA Ltd, Leeds, UK
Link to relevant study records
Reference
Endpoint:
genetic toxicity in vitro
Remarks:
Type of genotoxicity: other: chromosome damage, genotoxicity, mutagenicity
Type of information:
(Q)SAR
Adequacy of study:
supporting study
Study period:
2010
Reliability:
2 (reliable with restrictions)
Justification for type of information:
QSAR prediction: migrated from IUCLID 5.6
Principles of method if other than guideline:
Software used: DEREK Nexus, version 2.0.3 LHASA Ltd, Leeds, UK
GLP compliance:
no
Type of assay:
other: QSAR using Derek Nexus, version 2.0.3
Species / strain:
not specified
Metabolic activation:
not specified
Genotoxicity:
other: PLAUSIBLE alert for chromosome damage and mutagenicity
Cytotoxicity / choice of top concentrations:
not specified
Conclusions:
Interpretation of results (migrated information):
other: no alert for genotoxicity
other: PLAUSIBLE alert for chromosome damage and mutagenicity

No alert for genotoxicity was detected.
A plausible alert for chromosome damage and mutagenicity of the Acetic acid, 2-chloro-, 1-methylpropyl ester was detected by DEREK Nexus version 2.0.3.
Plausible - The weight of evidence supports the proposition
Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Additional information from genetic toxicity in vitro:

No alert for genotoxicity was detected.

A plausible alert for chromosome damage and mutagenicity of the Acetic acid, 2-chloro-, 1-methylpropyl ester was detected by DEREK Nexus version 2.0.3.


Justification for selection of genetic toxicity endpoint
Only available data

Justification for classification or non-classification

Following REGULATION (EC) No 1272/2008, to arrive at a classification test results are considered from experiments determining mutagenic and/or genotoxic effects in germ and/or somatic cells of exposed animals. Mutagenic and/or genotoxic effects determined in in vitro tests shall also be considered.

The only available study is a QSAR prediction.

The test result is not judged sufficient to arrive at a classification.