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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Guideline study, GLP

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1992
Report date:
1992

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
Deviations:
no
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)penta-1,4-dien-3-ol
EC Number:
226-006-5
EC Name:
3-methyl-1-(2,6,6-trimethylcyclohex-1-en-1-yl)penta-1,4-dien-3-ol
Cas Number:
5208-93-5
Molecular formula:
C15H24O
IUPAC Name:
(4E)-3-methyl-5-(2,6,6-trimethylcyclohex-1-en-1-yl)penta-1,4-dien-3-ol
Details on test material:
- Name of test material (as cited in study report): Vinyljonol

Test animals / tissue source

Species:
rabbit
Strain:
Vienna White
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Source: Gaukler
- Weight at study initiation: male: 3.28 kg; mean females: 3.40 kg
- Housing: single
- Diet: about 130 g per animal per day (Kliba 341)
- Water: about 250 ml tap water per animal per day
-Acclimation period: at least 8 days


ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-24
- Humidity (%): 30-70
- Photoperiod (hrs dark / hrs light): 12/12

Test system

Vehicle:
unchanged (no vehicle)
Controls:
other: untreated eye of the same animal
Amount / concentration applied:
TEST MATERIAL
- Amount applied: 0.1 ml

Duration of treatment / exposure:
see observation period (no washing out performed)
Observation period (in vivo):
72 hrs
Number of animals or in vitro replicates:
3 (one male, two females)
Details on study design:
REMOVAL OF TEST SUBSTANCE
- Washing: not performed

SCORING SYSTEM: according to OECD guideline 405/Draize

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
cornea opacity score
Basis:
mean
Remarks:
animal 1-3
Time point:
other: 24/48/72 hrs
Score:
0
Max. score:
4
Reversibility:
other: no effect
Irritation parameter:
iris score
Basis:
mean
Remarks:
animal 1-3
Time point:
other: 24/48/72 hrs
Score:
0
Max. score:
2
Reversibility:
other: no effect
Irritation parameter:
conjunctivae score
Basis:
animal #1
Time point:
other: 24/48/72 hrs
Score:
0.3
Max. score:
3
Reversibility:
fully reversible within: 48 hrs
Irritation parameter:
conjunctivae score
Basis:
animal #2
Time point:
other: 24/48/72 hrs
Score:
0.3
Max. score:
3
Reversibility:
fully reversible within: 48 hrs
Irritation parameter:
conjunctivae score
Basis:
animal #3
Time point:
other: 24/48/72 hrs
Score:
0.3
Max. score:
3
Reversibility:
fully reversible within: 48 hrs
Irritation parameter:
chemosis score
Basis:
mean
Remarks:
animal 1-3
Time point:
other: 24/48/72 hrs
Score:
0
Max. score:
4
Reversibility:
other: no effect
Other effects:
no other effects observed

Any other information on results incl. tables

Animal  Reading  Corneal Opacity Iris Conjunctiva Redness Chemosis
1 1 hr 0 0 2 0
2 1 hr 0 0 2 0
3 1 hr 0 0 2 0
1 24 hrs 0 0 1 0
2 24 hrs 0 0 1 0
3 24 hrs 0 0 1 0
1 48 hrs 0 0 0 0
2 48 hrs 0 0 0 0
3 48 hrs 0 0 0 0
1 72 hrs 0 0 0 0
2 72 hrs 0 0 0 0
3 72 hrs 0 0 0 0
mean animal 1-3 24/48/72 hrs 0.0 0.0 0.3 0.0

Applicant's summary and conclusion