Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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.

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1967-07-04 to 1967-07-05
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non-GLP but equivalent to guideline study.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1967
Report date:
1967

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
no
Principles of method if other than guideline:
according to BASF-internal standard
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2-ethylimidazole
EC Number:
214-011-5
EC Name:
2-ethylimidazole
Cas Number:
1072-62-4
Molecular formula:
C5H8N2
IUPAC Name:
2-ethylimidazole

Test animals

Species:
rat
Strain:
other: "US" rats
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Details on oral exposure:
VEHICLE
- Concentration in vehicle: 2, 8, 10 and 16% (w/v)
Doses:
200, 800, 1250 and 1600 mg/kg
No. of animals per sex per dose:
10 per dose level
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
ca. 1 400 mg/kg bw
Based on:
test mat.
Mortality:
200 and 800 mg/kg: no deaths; 1250 mg/kg: 3/10 after 7 days; 1600 mg/kg: 8/10 after 7 days
Clinical signs:
Dyspnea, apathy, abdominal and lateral position
Gross pathology:
Animals that died: all animals with bloody-serous snouts and blurred anus; 1 x diarrhea, 1 x severe distended ectatic stomach, 1 x suspicion of necrosis and hemorrhages of the liver (with putrescence)
Sacrificed animals: nothing abnormal detected

Applicant's summary and conclusion

Interpretation of results:
Category 4 based on GHS criteria