Registration Dossier
Registration Dossier
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EC number: 227-527-0 | CAS number: 5872-08-2
Endpoint summary
Administrative data
Description of key information
No data were found in the scientific literature.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
No data were found in the scientific literature. For the substance LD50 oral >316 mg/kg is reported in USP SDS. This information is not reliable due to the fact that it is not supported by any scientific data. This property is judged as inconclusive.
Specific target organ toxicity - single: No data were found in the scientific literature. USP SDS reports that the substance causes possible gastrointestinal, and/or respiratory tract irritation. This information is not reliable due to the fact that it is not supported by any
scientific data.
Justification for classification or non-classification
According to Regulation (EC) n. 1272/2008, the substance is classified for acute oral toxicity as inconclusive.
According to Regulation (EC) n. 1272/2008, the substance is not classified for acute dermal and inhalation toxicity for data lacking.
According to Regulation (EC) n. 1272/2008, the substance is classified for Specific target organ toxicity - single as inconclusive.
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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