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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Skin irritation / corrosion

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Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
read-across based on grouping of substances (category approach)
Adequacy of study:
supporting study
Study period:
Prior to May 1976
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: early study report; short study description
Justification for type of information:
Read across is based on the category approach. Please refer to attached category document.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976

Materials and methods

Principles of method if other than guideline:
according to BASF-internal standards
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3,6,9-trioxaundecane-1,11-diol
EC Number:
203-989-9
EC Name:
3,6,9-trioxaundecane-1,11-diol
Cas Number:
112-60-7
Molecular formula:
C8H18O5
IUPAC Name:
2,2'-[oxybis(ethane-2,1-diyloxy)]diethanol
Test material form:
not specified
Details on test material:
purity about 90%

Test animals

Species:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
Body weight male rabbit: 3.48 kg
Body weight female rabbit: 3.49

Test system

Type of coverage:
occlusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Controls:
other: untreated skin of the same animal
Amount / concentration applied:
0.5 g
Duration of treatment / exposure:
20 h
Observation period:
Readings after 24 hours and 8 days
Number of animals:
2
Details on study design:
The test substance was applied to a 2.5 x 2.5 cm application site of white Vienna rabbits for 20 h under occlusive conditions. The skin was either intact or abraded. After the application time, the skin was washed with water which may have contained a mild detergent. Animals were observed for 8 days and skin changes were observed on working days. Findings were recorded after 1 min, 5 min, 15 min and 20 hours and at the end of the observation period. Findings were graded as described in OECD test guideline 404.

Results and discussion

In vivo

Results
Irritation parameter:
overall irritation score
Basis:
mean
Time point:
other: 24 h
Score:
0
Irritant / corrosive response data:
No irritation was observed.
Other effects:
After 20-hour exposure a slight reddening (ear) was observed, which was reversible within 8 days.

Any other information on results incl. tables

No additional information available.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
No dermal irritation was noted at the application site following 20 hour exposure to the test material.
Executive summary:

The dermal irritation potential was examined in a pre-guideline study. No dermal irritation was noted at the application site following 20 hour exposure to the test material.