Registration Dossier
Registration Dossier
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EC number: 249-200-1 | CAS number: 28754-28-1
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Sep 1975
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 975
- Report date:
- 1975
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- yes
Test material
- Reference substance name:
- 3-(5-chlorobenzoxazol-2-yl)-7-(diethylamino)-2-benzopyrone
- EC Number:
- 252-722-2
- EC Name:
- 3-(5-chlorobenzoxazol-2-yl)-7-(diethylamino)-2-benzopyrone
- Cas Number:
- 35773-43-4
- Molecular formula:
- C20H17ClN2O3
- IUPAC Name:
- 3-(5-chloro-1,3-benzoxazol-2-yl)-7-(diethylamino)-2H-chromen-2-one
- Test material form:
- solid: particulate/powder
- Details on test material:
- Disperse Yellow 184:1
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Winkelmann, Borchen, Germany
- Age at study initiation: 10 wks (male)
- Weight at study initiation: 150 - 200 g
- Fasting period before study: 16 h
- Housing: Makrolon Type III cages (group of 5 animals)
- Diet (e.g. ad libitum): ad lib.
- Water (e.g. ad libitum): ad lib.
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20.5 - 23.5
- Humidity (%): 55 - 65
- Light/darkness (h): 12/12
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- poloxamer
- Remarks:
- Lutrol
- Details on oral exposure:
- 25% in medium
- Doses:
- 5000 mg/kg bw
- No. of animals per sex per dose:
- 5
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: daily
- Necropsy of survivors performed: not reported
- Other examinations performed: clinical signs
Results and discussion
- Preliminary study:
- Probit analysis
Effect levels
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- > 5 000 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- not determinable due to absence of adverse toxic effects
- Mortality:
- No mortality
- Clinical signs:
- other: No clinical signs observed
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The LD50 (oral, gavage) in male rats was determined to be >5000 mg/kg bw. The substance is not classifiable according to CLP criteria.
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