Registration Dossier
Registration Dossier
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EC number: 916-737-4 | CAS number: -
Endpoint summary
Administrative data
Description of key information
Brief summary reports in German. Only a very short description is reported. However, dose, number of animals and observation period are critical points which are mentioned in the studies.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Quality of whole database:
- The studies have a klimisch code 4.
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
Glycolierral was tested in two acute oral toxicity study with rats. No deaths occurred. Sedation and respiratory depression were observed among the animals.
Based on the results, an LD50 >8000 mg/kg bodyweight was determined.
Justification for selection of acute toxicity – oral endpoint
Glycolierral was tested in two acute oral toxicity studies with rats and mice.
Justification for classification or non-classification
Based on the results, Glycolierral does not have to be classified for acute oral toxicity according to Regulation (EC) No 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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