Registration Dossier

Diss Factsheets

Administrative data

Description of key information

Key value for chemical safety assessment

Skin sensitisation

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed (not sensitising)
Additional information:

The potential of E-AF098T (SOL-DP) to induce and elicit delayed dermal sensitisation was assessed in the albino guinea pig (Maximization test). The results indicate sensitisation rate of 0% at challenge. Hence, this substance was found to be non sensitizer.

Migrated from Short description of key information:
Assessment of contact hypersensitivity in the albino guinea pig.

Respiratory sensitisation

Endpoint conclusion
Additional information:
Migrated from Short description of key information:
No data available.

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 sensitisation by skin contact .