Registration Dossier
Registration Dossier
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EC number: 212-789-0 | CAS number: 869-29-4
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1961
- Reliability:
- 4 (not assignable)
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- reference to same study
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 961
Materials and methods
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Allylidene di(acetate)
- EC Number:
- 212-789-0
- EC Name:
- Allylidene di(acetate)
- Cas Number:
- 869-29-4
- Molecular formula:
- C7H10O4
- IUPAC Name:
- 1-(acetyloxy)prop-2-en-1-yl acetate
- Reference substance name:
- 1-propene-1,3-diol,1,3-diacetate
- Cas Number:
- 1945-91-1
- Molecular formula:
- C7H10O4
- IUPAC Name:
- 1-propene-1,3-diol,1,3-diacetate
- Reference substance name:
- Acetic acid
- EC Number:
- 200-580-7
- EC Name:
- Acetic acid
- Cas Number:
- 64-19-7
- Molecular formula:
- C2H4O2
- IUPAC Name:
- acetic acid
- Reference substance name:
- Acetic anhydride
- EC Number:
- 203-564-8
- EC Name:
- Acetic anhydride
- Cas Number:
- 108-24-7
- Molecular formula:
- C4H6O3
- IUPAC Name:
- acetic anhydride
- Reference substance name:
- Non identified impurities
- Molecular formula:
- Not applicable
- IUPAC Name:
- Non identified impurities
- Test material form:
- liquid
Constituent 1
impurity 1
impurity 2
impurity 3
impurity 4
Test animals
- Species:
- rat
Administration / exposure
- Route of administration:
- oral: unspecified
Results and discussion
Effect levels
- Key result
- Dose descriptor:
- LD50
- Effect level:
- 35 mg/kg bw
Applicant's summary and conclusion
- Interpretation of results:
- Category 2 based on GHS criteria
- Conclusions:
- The oral LD50 of the test substance is 35 mg/kg bw in rats. Therefore it is classified H300 category 2 according to Regulation (EC) No. 1272/2008 and according to the GHS.
- Executive summary:
An acute oral toxicity study was performed on PROP-1-ENE-3,3-DIYL ACETATE.
The oral LD50 of the test substance is 35 mg/kg bw in rats.
Therefore it is classified H300 category 2 according to Regulation (EC) No. 1272/2008 and according to the GHS.
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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