Registration Dossier
Registration Dossier
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EC number: 203-820-9 | CAS number: 110-97-4
Endpoint summary
Administrative data
Description of key information
No sensitisation potential was reported for DIPA in a Buehler test with guinea pigs, performed according to OECD guideline 406.
Key value for chemical safety assessment
Skin sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
Sensitisation potential was evaluated in a Buehler test (according to OECD guideline 406, under GLP) using Hartley guinea pigs (10 males). During a 3-week induction period, DIPA was given as 3 applications to the skin under occlusion at 50% and after two weeks, the animals were challenged with 50% DIPA again. No erythema was observed (1997, RL1).
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
- Additional information:
No data are available.
Justification for classification or non-classification
Based on the results of the Buehler test, DIPA does not need to be classified according to the 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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