Registration Dossier
Registration Dossier
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EC number: 945-131-2 | CAS number: -
Endpoint summary
Administrative data
Description of key information
LD50(oral) > 15000 mg/kg bw
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 15 000 mg/kg bw
- Quality of whole database:
- Method equivalent or similar to guidelines internationally accepted.
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 information about the "Acute oral toxicity" of the Target Substance is available. Nevertheless a study on a Similar Substance (Similar Substance 01) was used in order to fulfill regulatory requirements. Details about the structural similarity between the two substances are reported in section 13.
The substance was tested in 1977 by oral administration. The results of the test show a very high value of LD50. No death occurred during the test.
Justification for classification or non-classification
According to the CLP Regulation (EC) n. 1272/2008, acute toxicity means those adverse effects occurring following oral or dermal administration of a single dose of a substance or a mixture, or multiple doses given within 24 hours, or an inhalation exposure of 4 hours.
The substance is not classified according to table 3.1.1 of the CLP Regulation (EC) n. 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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