Registration Dossier
Registration Dossier
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EC number: 241-304-5 | CAS number: 17268-47-2
Endpoint summary
Administrative data
Description of key information
In the key study the test substance was found to be moderately toxic to mice following intraperitoneal injection. There were no adverse effects noted in any animal receiving intraperitoneal control doses with distilled water. There was no evidence that the test substance either suppressed or stimulated proliferation of polychromatophilic erythrocytes.
LD50 (males) 354 mg/kg
LD50 (females) 374 mg/kg
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- LD50
- Value:
- 354 mg/kg bw
Additional information
Justification for classification or non-classification
According to the criteria in CLP Annex I, 3.1.2 to 3.1.3.4, a substance is a Category 4 for acrute toxicioty if it has an Oral LD50 >300 but = 2000 mg/kg bodyweight.
DDPA has an LD50 (males) of 354 mg/kg, and LD50 (females) of 374 mg/kg, therefore is considered a Category 4 for acute toxicity.
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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