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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
weight of evidence
Study period:
This study was conducted in 1970.
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Abstract only

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1970
Report date:
1970

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
The test substance was administered to the eyes of rabbits for 24 hours at a range of concentrations (3 - 50 %) and observations were made for seven days.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
1,2,3,4,4a,7,8,8a-octahydro-2,4a,5,8a-tetramethyl-1-naphthyl formate
EC Number:
265-742-1
EC Name:
1,2,3,4,4a,7,8,8a-octahydro-2,4a,5,8a-tetramethyl-1-naphthyl formate
Cas Number:
65405-72-3
Molecular formula:
C15H24O2
IUPAC Name:
1,2,3,4,4a,7,8,8a-octahydro-2,4a,5,8a-tetramethyl-1-naphthyl formate
Test material form:
liquid

Test animals / tissue source

Species:
rabbit
Strain:
not specified
Details on test animals or tissues and environmental conditions:
No data

Test system

Vehicle:
not specified
Controls:
not specified
Amount / concentration applied:
3 %, 10 %, 30 % and 50 %.
Duration of treatment / exposure:
24 hours
Observation period (in vivo):
Seven days
Number of animals or in vitro replicates:
No data
Details on study design:
No data

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
chemosis score
Basis:
mean
Time point:
24 h
Score:
1
Max. score:
4
Reversibility:
fully reversible within: 4 days
Irritation parameter:
chemosis score
Basis:
mean
Time point:
48 h
Score:
1
Max. score:
4
Reversibility:
fully reversible within: 4 days
Irritation parameter:
chemosis score
Basis:
mean
Time point:
72 h
Score:
1
Max. score:
4
Reversibility:
fully reversible within: 4 days

Any other information on results incl. tables

Irritation score

Concentration

Reactions, days following application

1

2

3

4

5

6

7

3 %

-

-

-

-

-

-

-

10 %

(+)

-

-

-

-

-

-

30 %

(+)

-

-

-

-

-

-

50 %

+

(+)

(+)

-

-

-

-

- = No redness

(+) = weak redness

+ = moderate redness and secretion

++ strong redness and strong secretion

+++ strong redness and strong secretion with oedema

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The test substance was administered to the eyes of rabbits for 24 hours at a range of concentrations (3 - 50 %). Observations indicated weak to moderate redness of the conjunctiva, which was reversed within a maximum of four days.
Executive summary:

The test substance was administered to the eyes of rabbits for 24 hours at a range of concentrations (3 - 50 %). Observations indicated weak to moderate redness of the conjunctiva, which was reversed within a maximum of four days.