Registration Dossier
Registration Dossier
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EC number: 939-401-9 | CAS number: 1469983-41-2
Acute Toxicity: other routes
Administrative data
- Endpoint:
- acute toxicity: other routes
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Study period:
- 1976
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- The study was performed before OECD test guidelines and GLP were established. The documentation is according to the best practice at the time the study was performed. However, some critical details of the test protocol and the results are not available.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 976
- Report date:
- 1976
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- BASF test
- GLP compliance:
- no
- Remarks:
- Pre-GLP
Test material
- Reference substance name:
- 2-Oxetanone, 3-C12-16-alkyl-4-C13-17-alkylidene derivs.
- EC Number:
- 284-932-5
- EC Name:
- 2-Oxetanone, 3-C12-16-alkyl-4-C13-17-alkylidene derivs.
- Cas Number:
- 84989-41-3
- Molecular formula:
- C28.H52.O2 - C36.H68.O2
- IUPAC Name:
- (4E)-4-(C13-C17)alkylidene-3-(C12-C16)alkyloxetan-2-one
- Details on test material:
- Test substance: other TS: Stearyldiketen TV 194/37
An AKD manufactured using a stearic acid rich blend of palmitic and stearic fatty acids.
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- not specified
- Sex:
- not specified
Administration / exposure
- Route of administration:
- intraperitoneal
- Vehicle:
- olive oil
- Doses:
- no data
- No. of animals per sex per dose:
- no data
Results and discussion
Effect levels
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- > 6 800 mg/kg bw
Any other information on results incl. tables
Clinical signs: Dyspnoe, Apathy, slow movement. Gross pathology: no signs of treatement.
Applicant's summary and conclusion
- Conclusions:
- Limited reporting interpretaion is not possible.
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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