Registration Dossier
Registration Dossier
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EC number: 306-797-4 | CAS number: 97404-33-6
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- 08 Apr - 14 Apr 1994
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Basic data given in summarized study report.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 994
- Report date:
- 1994
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- Deviations:
- yes
- Remarks:
- ; observation period post-treatment: 6 days; only female animals used
- GLP compliance:
- not specified
- Test type:
- standard acute method
- Limit test:
- yes
Test material
- Reference substance name:
- Decyl oleate
- EC Number:
- 222-981-6
- EC Name:
- Decyl oleate
- Cas Number:
- 3687-46-5
- Molecular formula:
- C28H54O2
- IUPAC Name:
- decyl octadec-9-enoate
- Details on test material:
- - Name of test material (as cited in study report): Oleate de Decyle S
- Analytical purity: no data given
- Code: 10117
- Lot/batch No.: 0609 G
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- other: NMRI EOPS
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Weight at study initiation: 19-21 g
Administration / exposure
- Route of administration:
- oral: unspecified
- Vehicle:
- not specified
- Doses:
- 2000 mg/kg bw
- No. of animals per sex per dose:
- 5 female animals
- Control animals:
- no
- Details on study design:
- Assessment of the acute oral toxicity of the test material after administration of a single dose.
Observation of the animals for 6 days post treatment.
Results and discussion
Effect levels
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: mouse
- Mortality:
- All animals survived.
- Clinical signs:
- other: No abnormalities were observed.
Any other information on results incl. tables
Under the experimental conditions of the test chosen, the LD50 was >2000 mg/kg bw in female mice. No mortality occurred.
Therefore the test material does not fulfill the requirements to be classified according to GHS- (1272/2008 EC) or EU-(67/548 EEC) criteria.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
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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