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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Low concern regarding genotoxicity of 6-chlorohexyl methacrylate (6-CHMA) should be assumed based on in vitro and in vivo studies for similar substances belong to the category "short chain alkyl methacrylates".

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Genetic toxicity in vivo

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (negative)

Additional information

No data is available for genetic toxicity of 6-chlorohexyl methacrylate (6-CHMA). No concern regarding genetic toxicity of 6-CHMA is expected based on the similarity with short chain alkyl methacrylates and in particular with 2-ethylhexyl methacrylate CAS 688-84-6 (see document "Read -across hypothesis and justification" in section 13 of this IUCLID dossier).

 

In vitro studies

No in vitro genetic study is available for 6-chlorohexyl methacrylate (6-CHMA). No concern regarding  in vitro genetic toxicity of 6-CHMA is expected based on the experimental data reported in SIDS Dossier of " Short chain alkyl methacrylates" approved at SIAM 18 (20-23 April 2004) for these similar compounds: the methacrylate esters have been tested in vitro and in vivo for gene mutations, chromosome mutations and aneugenic effects over relevant dose ranges and there is no indication that the methacrylate esters in the category cause gene mutations. 

In particular, in SIDS Dossier of " Short chain alkyl methacrylates" approved at SIAM 18 (20-23 April 2004) inside the specific section of 2-ethylhexyl methacrylate CAS 688-84-6 (2 -EHMA) two in vitro genetic studies are reported:

1)Bacterial test: Negative result in a study conducted in 1998 according to OECD471 and OECD 472 on S. typh.(strains TA100, TA1535, TA98, TA1537) and E. coli WP2 uvr A at concentration of 0.6-5000μg/plate (Ref. Miyagawa et all, 1998, Reverse Mutation Test of Ethylhexyl Methacrylate on Bacteria. Study on behalf of Ministry of Health and Welfare, Japan).

2) Chromosome aberration test on chinese hamster lung: Negative result in a study conducted in 1998 according to OECD473 at concentration of 10-80 μg/ml(without S9) and 625-5000μg/ml (with S9)(Ref.Ohta et all, 1998,In Vitro Chromosome aberration Test of 2-Ethyl Hexyl Methacrylate on Cultured Chinese Hamster Cells, Mitsubishi Chemicals Safety Institute Ltd., unpublished report, study on behalf of Ministry of Health and Welfare, Japan).

 

In vivo studies

No in vivo study is available for 6-chlorohexyl methacrylate (6-CHMA) neither for most similar short chain alkyl methacrylates, 2-ethylhexyl methacrylate (2-EHMA) CAS 688-84-6. Some in vivo genetic studies are available for other short chain alkyl methacrylates with negative results.

In conclusion, low concern regarding genotoxicity of for 6-chlorohexyl methacrylate (6-CHMA) should be assumed based on in vitro and in vivo studies for similar substances.

Justification for classification or non-classification

Low concern regarding genotoxicity of 6-chlorohexyl methacrylate (6-CHMA) should be assumed based on its similarity with short chain alkyl methacrylates.

No classification for genetic toxicity of 6-chlorohexyl methacrylate (6-CHMA)is proposed according to the CLP Regulation (EC n.1272/2008).