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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Key value for chemical safety assessment

Skin sensitisation

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (sensitising)
Additional information:

The skin sensitising potential of Ethyl acrylate was investigated in a Local Lymphnode Assay conducted according to OECD guideline 429 and GLP regulations (BAMM 2006). The application of the test substance at concentrations of 2.5, 5, 10, 25 or 50 % w/v in acetone : olive oil (4:1) resulted in an increase in isotope incorporation which was greater than 3-fold at the 50 % w/v concentration. Consequently, the test substance was shown to be a potential skin sensitiser. The concentration giving rise to a 3 fold increase in lymphocyte proliferation (EC3) was calculated to be 36.8 % w/v (9200 μg/cm2), indicative of a sensitiser of weak potency.

Several older studies in guinea pigs and mice gave ambigious or contradictory responses. Hence, the classification was based on the LLNA by BAMM (2006).

In the Freund’s complete adjuvant test, ethyl acrylate showed a sensitizing reaction in 7 of 8 animals, whereas in the guinea pig maximization test no positive reaction was found (Van der Walle et al., 1982). Guinea pigs sensitized to ethyl acrylate exhibited cross-sensitization to challenges with several other acrylates (Van der Walle and Bensink, 1982). A Mouse Ear Swelling Test (MEST) and a Local Lymph Node Assay (LLNA) were conducted in B6C3F1 mice (NTP, 1994). In the MEST, mice were treated with a maximal non-irritating concentration (MNC) of ethyl acrylate as well as 0.1 and 0.3 times the MNC for 3 consecutive days. Following a four-day resting period, a challenge was made with a minimal irritating concentration (MIC) of ethyl acrylate. Ethyl acrylate did not exhibit contact hypersensitivity in this assay. For the LLNA, mice were treated with the MIC, the MNC, or 0.5 times the MNC for 3 consecutive days. After 1 day of rest, tritiated thymidine was injected into the animals and 5 hours later lymph nodes were dissected and tritium uptake determined. No increase in response from controls was noted in the LLNA assay.

Migrated from Short description of key information:
After repeated skin contact with Ethyl acrylate sensitization is possible.

Respiratory sensitisation

Endpoint conclusion
Additional information:

There is no information available on the potential for EA to produce respiratory sensitisation in animals.

Justification for classification or non-classification

EU classification according to Annex I of Directive 67/548/EEC: Xi, R43

GHS/CLP classification:

GHS UN rev.4, 2011 - Category 1B

Regulation (EC) No 1272/2008 - Category 1