Registration Dossier
Registration Dossier
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EC number: - | CAS number: -
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vitro
- Data waiving:
- study technically not feasible
- Justification for data waiving:
- other:
- Justification for type of information:
- JUSTIFICATION FOR DATA WAIVING
The study cannot be completed because the test substance is completely insoluble in all solvents indicated by the respective OECD guidelines at the required concentrations. Under these circumstances, in vitro skin sensitization testing in accordance with OECD 442C, OECD 442D, and OECD 442E of the test substance, Cesium Tungsten Oxide, is not possible. Testing with precipitates is technically not feasible in case of DPRA and h-CLAT, and it is not recommended in case of the LuSens test, since a significant result cannot be obtained.
Data source
Materials and methods
Results and discussion
Applicant's summary and conclusion
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
