Registration Dossier
Registration Dossier
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EC number: 203-005-8 | CAS number: 102-09-0
Repeated dose toxicity: inhalation
Administrative data
- Endpoint:
- short-term repeated dose toxicity: inhalation
- Data waiving:
- study scientifically not necessary / other information available
- Justification for data waiving:
- a short-term toxicity study does not need to be conducted because a reliable sub-chronic (90 days) or chronic toxicity study is available, conducted with an appropriate species, dosage, solvent and route of administration
- Justification for type of information:
- JUSTIFICATION FOR DATA WAIVING
In accordance with sections 8.6.1 of Column 1 of REACH Annex VIII, repeated dose toxicity testing should be carried out using the most appropriate route of administration, having regard to the likely route of human exposure. For this substance, the oral route was deemed to be the most appropriate and a robust and reliable oral sub-chronic study is available to address the information requirement of section 8.6.1.
Data source
Materials and methods
Results and discussion
Target system / organ toxicity
- Critical effects observed:
- not specified
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.
