Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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.