Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 203-466-5
CAS number: 107-13-1
A positive result is reported in a Maximisation assay performed with
No signs of systemic toxicity were noted during the primary irritation
experiments and during the main study. No mortality occurred/ Average
body weight gain was similar in treated guinea pigs and controls.
Four animals showed skin irritation after the 48 hours occluded
epicutaneous induction exposure. No positive skin reactions were
observed in the controls following the challenge exposure.
Nineteen animals showed a positive sensitisation reaction in response to
the 1% and 0.5% test concentrations, and 16 animals in response to the
0.2% concentration. Two animals showed a skin reaction to the vehicle
alone. It was therefore concluded that leakage of the test material
across the Square chambers had cocurred. Another minor reaction to the
test material was scaliness.
The resulting sensitisation rate was 95%, indicating that acrylonitrile
is an extreme sensitiser according to the Kligman (1966) rating.
Positive skin reactions scored after challenge exposure
Experimental group – no. animals with positive reaction
Control group – no. animals with positive reaction
* it was considered possible that some test material
leaked from the other chambers
The sensitising properties of acrylonitrile were evaluated in the Guinea
Pig Maximisation Test. Under the conditions of the study, acrylonitrile
resulted in a 95% sensitisation rate after intracutaneous and
epicutaneous application. Acrylonitrile should therefore be classified
as a skin sensitiser in Category 1B according to Regulation (EC)
Acrylonitrile is listed on Annex VI of the CLP Regulation with
classification for skin sensitisation (H317: may cause an allergic skin
reaction'. In addition, there are also reports of sensitisation in
A guideline-compliant Maximisation assay is also reported (Koopmans &
Daamen. 1989). In this study, sensitisation was induced by intradermal
injection of 2.5% acrylonitrile and an epidermal application of 2%
acrylonitrile. Animals challenged with acrylonitrile concentrations of
0.5% and 1.0% acrylonitrile showed a 95% positive sensitisation rate.
Exposure to 0.2% on challenge caused an 80% sensitisation rate.
No animal data are available; there is no recognised validated test
guideline for the investigation of this endpoint. There are no reports,
from exposed workers of occupational asthma, which indicates that
acrylonitrile does not have the potential to cause respiratory
Acrylonitrile is listed on Annex VI of Regulation 1272/2008/EC with H317
'May cause an allergic skin reaction' . Based on the results of the key
maximisation assay, classification in Category 1B is appropriate;
however it is notable that there are very few reports of skin
sensitisation in exposed workers. No classification for respiratory
sensitisation is proposed in the absence of any evidence that
acrylonitrile can cause respiratory sensitisation.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
Welcome to the ECHA website. This site is not fully supported in Internet Explorer 7 (and earlier versions). Please upgrade your Internet Explorer to a newer version.
Do not show this message again