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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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.
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 237-853-5 | CAS number: 14024-18-1
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- Jusqu'à 2016
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- documentation insufficient for assessment
Data source
Reference
- Reference Type:
- other company data
- Title:
- Unnamed
- Year:
- 2 016
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- GLP compliance:
- not specified
- Remarks:
- Précision non disponible
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Tris(pentane-2,4-dionato)iron(II)
- EC Number:
- 237-853-5
- EC Name:
- Tris(pentane-2,4-dionato)iron(II)
- Cas Number:
- 14024-18-1
- Molecular formula:
- C15H21FeO6
- IUPAC Name:
- iron(3+) tris(4-oxopent-2-en-2-olate)
- Test material form:
- solid: crystalline
Constituent 1
- Specific details on test material used for the study:
- Aucun
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- Non disponible
Administration / exposure
- Route of administration:
- oral: unspecified
- Vehicle:
- unchanged (no vehicle)
- Details on oral exposure:
- Non disponible
- Doses:
- Non disponible
- No. of animals per sex per dose:
- Non disponible
- Control animals:
- no
- Details on study design:
- Non disponible
- Statistics:
- Non disponible
Results and discussion
- Preliminary study:
- Pas applicable
Effect levels
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 1 872 mg/kg bw
- Based on:
- test mat.
- Mortality:
- Non disponible
- Clinical signs:
- other: Non disponible
- Gross pathology:
- Non disponible
- Other findings:
- Non disponible
Applicant's summary and conclusion
- Interpretation of results:
- Category 4 based on GHS criteria
- Conclusions:
- La substance à enregistrer (Acétylacétonate de fer) apparait comme nocive (DL50 comprise entre 300 et 2000 mg/kg de poids corporel) pour les rats dans les conditions de test utilisées.
- Executive summary:
L'acétylacétonate de fer a été administré à des groupes de rats par voie orale. Une DL50 de 1872 mg/kg de poids corporel a été établie pour l'acétylacétonate de fer.
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.
