Registration Dossier
Registration Dossier
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EC number: - | CAS number: -
Endpoint summary
Administrative data
Description of key information
An in vivo skin irritation and an in vivo eye irration study in rabbits are available for the test substance, performed according to OECD and EU guidelines as well as GLP principles .
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Additional information
In an in vivo skin irritation study in rabbits with the test substance, no skin irritation was observed.
In an in vivo eye irritation study in rabbits with the test substance, slight eye irritation was observed. Irritation included redness of conjunctivae (mean scores 1 -2) and chemosis (mean scores 0.3 -1).
Based on these results the test substance does not have to be classified and has no obligatory labelling requirement for eye and skin irritation.
Effects on eye irritation: slightly irritating
Justification for classification or non-classification
Based on the results of in vivo skin and eye irritation studies in rabbits, classification for skin and eye irritation according to the CLP Regulation 1272/2008 and the Dangerous Substance Directive 67/548/EC is not necessary.
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.
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