Registration Dossier
Registration Dossier
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
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EC number: 204-118-5 | CAS number: 115-96-8
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- other: No experimental details, but published in peer-reviewed publication.
Data source
Reference
- Reference Type:
- grey literature
- Title:
- Further Toxicologic Studies with Commercial and Candidate Flame Retardant Chemicals. Part II.
- Author:
- A.T. Eldefrawi et al
- Year:
- 1 977
- Bibliographic source:
- Bulletin of Environmental Comtamination and Toxicology, Vol.17, No.6.
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- No information available other than report of LD50 (rat) as part of a wider investigation.
- GLP compliance:
- no
- Test type:
- other: LD50
Test material
- Reference substance name:
- Fyrol CEF
- IUPAC Name:
- Fyrol CEF
- Details on test material:
- Not available
Constituent 1
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- Not available
Administration / exposure
- Route of administration:
- oral: unspecified
- Vehicle:
- not specified
- Details on oral exposure:
- Not available
- Doses:
- Not available
- No. of animals per sex per dose:
- Not available
- Control animals:
- not specified
- Details on study design:
- Not available
- Statistics:
- Not available
Results and discussion
Effect levels
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 1 230 mg/kg bw
- Based on:
- test mat.
- Mortality:
- No data
- Clinical signs:
- No data
- Body weight:
- No data
- Gross pathology:
- No data
Any other information on results incl. tables
No further data available.
Applicant's summary and conclusion
- Interpretation of results:
- Toxicity Category IV
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Rat oral LD50, 1230 mg/kg bw
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
