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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Basic data given (no data on test substance purity, test material applied as 10% solution)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1983
Report date:
1983

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
Deviations:
yes
Remarks:
(6 animals used, test substance applied as 10% solution, no data on test substance purity)
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Esterification products of D-glucitol with C8 – C16 (even-numbered) and C18 unsaturated fatty acids
EC Number:
931-434-7
Cas Number:
1338-39-2
Molecular formula:
C18H34O6
IUPAC Name:
Esterification products of D-glucitol with C8 – C16 (even-numbered) and C18 unsaturated fatty acids
Constituent 2
Reference substance name:
931-434-7
EC Number:
931-434-7
IUPAC Name:
931-434-7

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: 4 kg (mean)
- Diet: rabbit Altromin 2023 diet, ad libitum
- Water: ad libitum

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20°C ± 3°C
- Humidity (%): 50%
- Photoperiod (hrs dark / hrs light): 12/12

Test system

Vehicle:
water
Controls:
other: the untreated eye served as control
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 mL
- Concentration (if solution): 10 % (g/g)
Duration of treatment / exposure:
single application
Observation period (in vivo):
72 h (all irritation reactions were reversible within 48 h after treatment)
reading time points: 1, 24, 48 and 72 h
Number of animals or in vitro replicates:
6
Details on study design:
SCORING SYSTEM: Draize Scoring System

TOOL USED TO ASSESS SCORE: macroscopic

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
cornea opacity score
Basis:
animal: #1, #2, #3, #4, #5 and #6
Remarks:
out of all 6 animals
Time point:
24/48/72 h
Score:
0
Max. score:
4
Reversibility:
other: reversibility not applicable
Irritation parameter:
iris score
Basis:
animal: #1, #2, #3, #4, #5 and #6
Time point:
24/48/72 h
Score:
0
Max. score:
2
Reversibility:
other: reversibility not applicable
Irritation parameter:
conjunctivae score
Basis:
animal: #1, #3 and #5
Time point:
24/48/72 h
Score:
0.33
Max. score:
3
Reversibility:
fully reversible within: 36 hours
Irritation parameter:
conjunctivae score
Basis:
animal: #2, #4 and #6
Time point:
24/48/72 h
Score:
0
Max. score:
3
Reversibility:
other: reversibility not applicable
Irritation parameter:
chemosis score
Basis:
animal: #1, #2, #3, #4, #5 and #6
Time point:
24/48/72 h
Score:
0
Max. score:
4
Reversibility:
other: reversibility: not applicable
Irritant / corrosive response data:
The test material did not induce any changes to iris and cornea of test animals. Conjunctivae of test animals showed a slight erythema 1 hour after application. All effects were fully reversible within 48 hours.
Other effects:
4 animals showed a slight exsudation 1 hour after application which was fully reversible within 24 hours.

Any other information on results incl. tables

Table 1. Results of eye irritation study.           
Rabbit # Time [h] conjunctivae   iris cornea   conjunctivae   iris cornea
redness swelling redness swelling    
1 1 2 0 0 0  
24 1 0 0 0
48 0 0 0 0
72 0 0 0 0
average 0.3 0 0 0 Time to reversion  48 0 0 0
2 1 2 0 0 0    
24 0 0 0 0
48 0 0 0 0
72 0 0 0 0
average 0 0 0 0 Time to reversion  24 0 0 0
3 1 2 1 0 0    
24 1 0 0 0
48 0 0 0 0
72 0 0 0 0
average 0.3 0 0 0 Time to reversion  48 24 0 0
4 1 1 0 0 0    
24 0 0 0 0
48 0 0 0 0
72 0 0 0 0
average 0 0 0 0 Time to reversion  24 0 0 0
5 1 2 0 0 0    
24 1 0 0 0
48 0 0 0 0
72 0 0 0 0
average 0.3 0 0 0 Time to reversion  48 0 0 0
6 1 1 0 0 0    
24 0 0 0 0
48 0 0 0 0
72 0 0 0 0
average 0 0 0 0 Time to reversion  24 0 0 0
       
Time [h] conjunctivae   iris cornea
  redness swelling     avg. time to reversion 36 4 0 0
average
score
1 1.67 0.17 0 0  
24 0.50 0 0 0
48 0 0 0 0
72 0 0 0 0
24+48+72 0.17 0 0 0

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
DSD: not classified
CLP: not classified