Registration Dossier
Registration Dossier
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EC number: 467-290-2 | CAS number: -
Specific investigations: other studies
Administrative data
- Endpoint:
- specific investigations: other studies
- Adequacy of study:
- other information
Data source
Reference
- Reference Type:
- other: Body responsible for the test
- Title:
- Unnamed
Materials and methods
- Principles of method if other than guideline:
- Test procedure:
EEC Directive 2004/73, B.42.
Test material
Constituent 1
Results and discussion
- Details on results:
- A dose response relationship was observed:
Concentration(% w/v) S.I.
Group 2 5 2.9
Group 3 10 3.9
Group 4 25 8.7
Viability/Mortality:
No deaths occurred during the study period.
Clinical Signs:
Slight ear erythema was observed in all mice of Group 3 and
4, about 2 hours after application and persisting for the
remainded of the in-life phase. Slight swelling was observed
in one animal of Group 5 and all of Group 3 and 4.
Body weights were in the range commonly recorded for the
strain and age.
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.
