Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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:
data from handbook or collection of data

Data source

Reference
Reference Type:
other company data
Title:
Unnamed
Year:
1992
Report date:
1992

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
Deviations:
yes
Remarks:
No single animal data provided; Relevant details on materials and methods (e.g. test substance concentration) not provided
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
1-[4-(2-methylpropyl)phenyl]ethan-1-ol
Cas Number:
40150-92-3
Molecular formula:
C12 H18 O
IUPAC Name:
1-[4-(2-methylpropyl)phenyl]ethan-1-ol
Details on test material:
No further data provided

Test animals / tissue source

Species:
rabbit
Strain:
New Zealand White

Test system

Vehicle:
not specified
Controls:
yes
Amount / concentration applied:
0.1 (unit not given) of liquid test material (not specified, if applied undiluted)
Duration of treatment / exposure:
7 days
Observation period (in vivo):
7 days
Number of animals or in vitro replicates:
3
Details on study design:
Ocular lesions were scored by Draize method approximately 1 hour, 1, 2, 3, 4 and 7 days after treatment.

Results and discussion

In vivo

Results
Irritation parameter:
overall irritation score
Remarks:
maximum mean Draize score
Basis:
mean
Time point:
24 h
Score:
44.7
Max. score:
110
Reversibility:
fully reversible within: 7 days
Irritant / corrosive response data:
- Conjunctivae: Slight to moderate irritation in 3/3 animals (1h and 24 hours),
cleared with time (minimal at day 4; no irritation at day 7).

- Cornea (dullling of the cornea) in 3/3 animals (1h); progress to scattered opacity over
most of the cornea for 4 days.

- Iris: Slight to moderate iritis for 3-4 days in 2/3 animals.

Treated eyes were free of effects 7 days after treatment.

Applicant's summary and conclusion

Interpretation of results:
Category 2 (irritating to eyes) based on GHS criteria