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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
other: Comparable to guideline study, acceptable for assessment.

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1980
Report date:
1980
Reference Type:
other company data
Title:
Unnamed
Year:
2002
Report date:
2002

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
Version / remarks:
(adopted 1981)
Deviations:
yes
Remarks:
Only 0.05 mL applied (instead of 0.1 mL), observation period: only 8 days (instead of 21 days)
Principles of method if other than guideline:
The study was conducted following a protocol based on BASF-internal standards.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Hexahydro-4,7-methano-1H-indenyl acrylate
EC Number:
235-697-2
EC Name:
Hexahydro-4,7-methano-1H-indenyl acrylate
Cas Number:
12542-30-2
Molecular formula:
C13 H16 O2
IUPAC Name:
2-Propenoic acid hexahydro-4,7-methano-1H-indenyl ester
Details on test material:
- Name of the test substance used in the study report: Dihydrodicyclopentadienylacrylat
- Analytical purity: 99%

Test animals / tissue source

Species:
rabbit
Strain:
New Zealand White
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 2.99 kg (male) and 2.82 kg (female)


ENVIRONMENTAL CONDITIONS
no details given

Test system

Vehicle:
unchanged (no vehicle)
Controls:
other: untreated eye of the same animal
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.05 mL
Duration of treatment / exposure:
once
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): not rinsed


SCORING SYSTEM: Draize Scoring System


TOOL USED TO ASSESS SCORE: none

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
conjunctivae score
Basis:
mean
Time point:
other: 24 - 48 hours
Score:
1
Max. score:
3
Reversibility:
fully reversible within: 5 days
Remarks on result:
other: (animals 1 and 2 had identical scores)
Irritation parameter:
cornea opacity score
Basis:
mean
Time point:
other: 24 - 48 hours
Score:
0
Max. score:
4
Reversibility:
other: no effects
Irritation parameter:
iris score
Basis:
mean
Time point:
other: 24 - 48 hours
Score:
0
Max. score:
2
Reversibility:
other: no effects
Irritation parameter:
chemosis score
Basis:
mean
Time point:
other: 24 - 48 hours
Score:
0
Max. score:
4
Reversibility:
other: no effects

Any other information on results incl. tables

Mean scores after 24 and 48 h*:

 

Scores

24 h

48 h

mean

 

Animal 1

Animal 2

Animal 1

Animal 2

Animal 1

Animal 2

Conjunctivae

1

1

1

1

1

1

Cornea

0

0

0

0

0

0

Chemosis

0

0

0

0

0

0

Iritis

0

0

0

0

0

0

Discharge

0

0

0

0

0

0

*72 hrs-scores were missing in the raw data.

 

 

 

Findings at test termination:

 

Scores

8 d

 

Animal 1

Animal 2

Conjunctivae

0

0

Cornea

0

0

Chemosis

0

0

Iritis

0

0

Discharge

0

0

 

 

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information