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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
Not reported
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study conducted in accordance with generally accepted scientific principles but with incomplete reporting. It is considered adequate for classification and labelling purposes.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1994
Report date:
1994

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
The test material was applied topically to intact and abraded skin on the shaved abdomen of two male New Zealand White rabbits, one under dry conditions and the other under wet conditions in an occlusive fashion for 24 hours. Five consecutive daily doses were applied to the intact skin and three consecutive daily applications were made to the abraded abdominal site.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
5-ethoxy-2-({5-ethoxy-7-fluoro-[1,2,4]triazolo[1,5-c]pyrimidin-2-yl}disulfanyl)-7-fluoro-[1,2,4]triazolo[1,5-c]pyrimidine
EC Number:
695-187-4
Cas Number:
166524-75-0
Molecular formula:
C14H12F2N8O2S2
IUPAC Name:
5-ethoxy-2-({5-ethoxy-7-fluoro-[1,2,4]triazolo[1,5-c]pyrimidin-2-yl}disulfanyl)-7-fluoro-[1,2,4]triazolo[1,5-c]pyrimidine
Details on test material:
- Name of test material (as cited in study report): 2,2'-Dithiobis(5-ethoxy-7-fluoro[1,2,4]triazolo[1,5-c]pyrimidine)
- Synonym: DEDS
- Appearance: light beige solid

Test animals

Species:
rabbit
Strain:
New Zealand White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: Average weight of 3.5 kg on day 1 of the study

Test system

Type of coverage:
occlusive
Preparation of test site:
other: intact and abraded
Vehicle:
unchanged (no vehicle)
Controls:
no
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 g of the test material was applied to both the intact and abraded site under wet and dry conditions. To ensure sufficient contact of the test material with the skin, 0.6 mL of distilled water was used to moisten the test material for the wet patch application.
Duration of treatment / exposure:
24 hours per application.
Five consecutive daily doses of test material were applied to the intact skin, and three consecutive daily applications were made to the abraded abdominal sites.
Observation period:
Not reported
Number of animals:
2
Details on study design:
TEST SITE
- Area of exposure: Abdomen. The abdomen of each rabbit was shaved with a straight razor at least three days prior to test initiation.
- Type of wrap if used: The animals were bandaged for 24 hours after application of the test material to provide occlusion and prevent grooming of the application site.

SCORING SYSTEM: Not reported. Twenty four hours after application the bandages were removed and the application sites were graded.

Results and discussion

In vivo

Irritant / corrosive response data:
Very slight to slight erythema was observed at both abdominal application sites on the dry patch animal and very slight exfoliation was observed at the dry intact abdominal test site after five applications. No signs of irritation were observed on the wet patch animal.
Other effects:
No mortality was observed. No clinical signs indicative of systemic toxicity were observed. No substantial weight change was noted over the duration of the study (Table 1).

Any other information on results incl. tables

Table 1 Summary of Bodyweight Data (kg)

Animal Number

Test Day

1

8

93A0089 (Dry patch)

3.58

3.54

93A0097 (Wet patch)

3.47

3.44

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Very slight to slight erythema was observed at both abdominal application sites on the dry patch animal and very slight exfoliation was observed at the dry intact abdominal test site after five applications. No signs of irritation were observed on the wet patch animals.
Although the report does not include scoring of the effects observed there is sufficient information to conclude that classification of the substance as a skin irritant is not required.
Executive summary:

The skin irritation potential of the test material was investigated in the New Zealand White rabbit.

0.5 g of the test material was applied topically to intact and abraded skin on the shaved abdomen of two male rabbits, one under dry conditions and the other under wet conditions in an occlusive fashion for 24 hours. Five consecutive daily doses were applied to the intact skin and three consecutive daily applications were made to the abraded abdominal site.

No mortality was observed. No clinical signs indicative of systemic toxicity were observed. No substantial weight change was noted over the duration of the study.

Very slight to slight erythema was observed at both abdominal application sites on the dry patch animal and very slight exfoliation was observed at the dry intact abdominal test site after five applications. No signs of irritation were observed on the wet patch animal.

Although the report does not include scoring of the effects observed there is sufficient information to conclude that classification of the substance as a skin irritant is not required.