Registration Dossier
Registration Dossier
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EC number: 464-390-8 | CAS number: -
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- other company data
- Title:
- Unnamed
- Year:
- 2 006
- Report date:
- 2006
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Principles of method if other than guideline:
- OECD No.423 (2001) "Acute Toxicity-Oral, Acute Toxic Class
Method"
EC, Council Directive 67/548/EEC, Annex V, B.1 tris (2004)
"Acute Oral Toxicity"
EPA, OPPTS 870.1100 (2002), "Acute Oral Toxicity - Acute
Toxic Class Method"
JMAFF guidelines (2000) including the most recent partial
revisions. - GLP compliance:
- yes
- Test type:
- standard acute method
- Limit test:
- yes
Test material
Constituent 1
Test animals
- Species:
- other: Rat , Wistar strain Crl:(WI) BR
Administration / exposure
- Vehicle:
- other: Milli-U water
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Mortality:
- Female: 2000 mg/kg bw; Number of animals: 3; Number of deaths: 0
- Clinical signs:
- other: Signs of toxicity related to dose levels: No clinical signs of systemic toxicity were noted. Red faeces and urine was noted among all animals on day 2, which was considered to be related to staining properties of the formulation (red colour).
- Gross pathology:
- Effects on organs:
No abnormalities were found at macroscopic post mortem
examination of the animals.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
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