Registration Dossier
Registration Dossier
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EC number: 200-021-7 | CAS number: 50-24-8
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 biological assay (OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay) and the criteria given in Annex I of Regulation (EC) 1272/2008), shows that the test item Prednisolone, as described in this report is expected to have no sensitising properties and therefore should not be regarded as a dermal sensitiser. (BSL Bioservice 104857)
The QSAR study carried out with QSAR Toolbox v.2.0 (2010), based on the general model for Skin sensitisation (Danish EPA DB), showed that prednisolone is skin sensitising. Due to the reliability of the source of this software, OECD, it was considered reliable for the first evaluation of this assessment.
Migrated from Short description of key information:
Prednisolone is not a skin sensitising.
Justification for classification or non-classification
In accordance to Directive 67/548/EEC, classification is not necessary for sensitisation based on the available data.
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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