Registration Dossier
Registration Dossier
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EC number: 473-780-7 | 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:
In a sensitisation study according to OECD guideline 429 (local lymph node assay) female mice were exposed to 1, 2.5 or 5% NX 8000J. Stimulation index for 1%, 2.5% and 5% was 0.94, 0.69 and 1.10, respectively. There were no deaths and no signs of systemic toxicity.
Migrated from Short description of key information:
NX 8000J did not show skin sensitising properties.
Justification for classification or non-classification
Based on the results of a skin sensitisation study, NX 8000J does not need to be classified for skin sensitisation according to EU Directive 67/548/EEC and EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 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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