Registration Dossier
Registration Dossier
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EC number: 479-310-7 | CAS number: -
Endpoint summary
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 .
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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