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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1982
Report date:
1982

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
Deviations:
yes
Remarks:
: scoring system
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Bis(isopropyl)naphthalene
EC Number:
254-052-6
EC Name:
Bis(isopropyl)naphthalene
Cas Number:
38640-62-9
Molecular formula:
C16H20
IUPAC Name:
1,2-bis(propan-2-yl)naphthalene

Test animals / tissue source

Species:
rabbit
Strain:
New Zealand White
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Source: H. Fortkamp, Lengerich, Germany
- Age at study initiation: 11 - 17 weeks
- Weight at study initiation: 2.36 - 2.46 kg
- Housing: singly in steel cages with perforated plate floors above litter-filled dung troughs
- Diet: Ssniff K complete rabbit diet (Ssniff Versuchstier-Diäten GmbH, Soest, Germany), ad libitum
- Water: drinking water, ad libitum
- Acclimation period: 6 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 - 23
- Humidity (%): 40 - 70
- Air changes (per hr): 10
- Photoperiod (hrs dark / hrs light): 12 / 12

Test system

Vehicle:
unchanged (no vehicle)
Controls:
other: The untreated eye of the animals served as control
Amount / concentration applied:
TEST MATERIAL
- Amount applied: 0.1 mL
Duration of treatment / exposure:
single exposure
Observation period (in vivo):
72 h
Number of animals or in vitro replicates:
3
Details on study design:
APPLICATION DETAILS: The test substance was instilled into the conjunctival sac of the left eye. Then, the eye was held closed by gently pressing both eye lids together for about 1 - 2 seconds.

REMOVAL OF TEST SUBSTANCE
- Washing: Following application no further treatment of the eye.

SCORING SYSTEM: According to Draize; grading scale (additional parameters included: discharge of conjunctiva and area of cornea involved) and scoring differently from OECD TG 405.

TOOL USED TO ASSESS SCORE: The eyes of test animals were examined after application of 2% fluorescein solution.

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
cornea opacity score
Basis:
mean
Remarks:
all 3 animals
Time point:
24/48/72 h
Score:
0
Max. score:
4
Reversibility:
other: reversibility not applicable
Irritation parameter:
iris score
Basis:
mean
Remarks:
all 3 animals
Time point:
24/48/72 h
Score:
0
Max. score:
2
Reversibility:
other: reversibility not applicable
Irritation parameter:
conjunctivae score
Basis:
mean
Remarks:
all 3 animals
Time point:
24/48/72 h
Score:
0
Max. score:
3
Reversibility:
other: reversibility not applicable
Irritation parameter:
chemosis score
Basis:
mean
Remarks:
all 3 animals
Time point:
24/48/72 h
Score:
0
Max. score:
4
Reversibility:
other: reversibility not applicable
Irritant / corrosive response data:
Only a slight irritating effect (conjunctivae redness score 1) was observed in all test animals at 1 h after test substance administration. At 24 h, this finding had subsided and was not seen any more. Scores for all eye irritation parameters were 0 starting from 24 h onwards. Observation ended at 72 h due to the lack of any visible effects.

Applicant's summary and conclusion

Interpretation of results:
other: CLP/EU GHS criteria not met, no classification required according to Regulation (EC) No. 1272/2008
Conclusions:
No occular reactions were observed following application of the unchanged test substance to the eyes of rabbits. The mean scores of all effects at 24/48/72 h for each animal was 0.