Registration Dossier
Registration Dossier
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EC number: 479-310-7 | CAS number: -
Endpoint summary
Administrative data
Description of key information
Acute skin irritation to the rabbit
Acute Eye irritation to the rabbit
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:
- no adverse effect observed (not irritating)
Additional information
Acute irritation studies were performed on the skin and eye of rabbits.
Skin irritation/corrosion: No skin irritation was caused after 4 hours exposure to E-AF098T (Fyrolflex SOL-DP) in any of the tested animals.
Eye irritation: Conjunctival redness and/or chemosis were seen in two rabbits at 1 -hour scoring interval and persisted in one rabbit at the 24 -hour interval. A small corneal opacity was seen in one of the rabbits at the 24 -hour scoring interval. All rabbits were completely recovered from all signs of ocular irritation by the 48 -hour scoring interval.
Justification for classification or non-classification
The above results triggered no classification under the EEC criteria for classification and labelling requirements for Dangerous Substances and Preparations (67/548/EEC) and the CLP Regulation (EC No 1272/2008). Therefore, Fyrolflex SOL-DP does not have to be classified and has no obligatory labelling requirement for skin irritation or eye irritation.
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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