Registration Dossier
Registration Dossier
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EC number: 202-592-8 | CAS number: 97-59-6
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:
- Migrated from Short description of key information:
No sensitization was observed in a reliable local lymph node assay (LLNA) on Allantoin.
Justification for selection of skin sensitisation endpoint:
Study was conducted under GLP according to OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay).
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
- Additional information:
- Migrated from Short description of key information:
No data are available on the respiratory sensitization endpoint for Allantoin.
Justification for classification or non-classification
Based on reliable LLNA results, Allantoin does not meet the criteria for classification as a skin sensitiser according to EU Directive 67/548/EEC and Regulation 1272/2008.
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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