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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Eye irritation

Currently viewing:

Administrative data

Endpoint:
eye irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1966
Report date:
1966

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
Principles of method if other than guideline:
BASF test. 50 µl of the test substance were applied to the conjunctival sac of one eye in 2 animals. The animals were observed after 10 min, 1 and 3 h on the day of treatment and up to 8 days afterwards. Findings were recorded daily. The eyes were not washed out after 24 hours as specified in OECD Guideline 405. The report describes findings after 1 and 24 hours and at the end of the observation period.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2-methylimidazole
EC Number:
211-765-7
EC Name:
2-methylimidazole
Cas Number:
693-98-1
Molecular formula:
C4H6N2
IUPAC Name:
2-methyl-1H-imidazole
Details on test material:
- Name of test material (as cited in study report): 2-Methylimidazol

Test animals / tissue source

Species:
rabbit
Strain:
Vienna White

Test system

Vehicle:
unchanged (no vehicle)
Controls:
other: The adjacent eye served as control with talc powder.
Amount / concentration applied:
TEST MATERIAL
- Amount applied: 50 µl
Duration of treatment / exposure:
single application, no washing was performed
Observation period (in vivo):
8 days
Number of animals or in vitro replicates:
2
Details on study design:
REMOVAL OF TEST SUBSTANCE
- Washing (if done): no

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
chemosis score
Basis:
mean
Time point:
other: 1 h
Score:
4
Max. score:
4
Reversibility:
fully reversible within: 24 h
Remarks on result:
other: Cauterization of mucous membrane was observed from observation time period 1 hour and this was not reversible.
Irritation parameter:
cornea opacity score
Basis:
mean
Time point:
other: 1 h - 24 h - 8d
Score:
3
Max. score:
4
Reversibility:
not reversible
Remarks on result:
other: Cauterization of mucous membrane was observed from observation time period 1 hour and this was not reversible.
Irritation parameter:
conjunctivae score
Basis:
mean
Time point:
other: 1 h - 24 h
Score:
3
Max. score:
3
Reversibility:
fully reversible within: 8 d
Remarks on result:
other: Cauterization of mucous membrane was observed from observation time period 1 hour and this was not reversible.
Irritant / corrosive response data:
Cauterization of mucous membrane was observed from observation time period 1 hour and this was not reversible.

Applicant's summary and conclusion