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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1998
Report date:
1998

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
Thioacetic acid
EC Number:
208-063-8
EC Name:
Thioacetic acid
Cas Number:
507-09-5
Molecular formula:
C2H4OS
IUPAC Name:
ethanethioic S-acid
Test material form:
other: liquid
Details on test material:
- Name of test material (as cited in study report): Thioacetic acid
- batch 47956,
- purity 99.20%.

Test animals

Species:
rabbit
Strain:
New Zealand White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Elevage Cunicole de Val de Selle, 80160 Prouzel, France.
- Age at study initiation: no data
- Weight at study initiation: 3.1 ± 0.1. kg
- Housing: housed individually in polystyrene cages
- Diet: 112 C pelleted diet, ad libitum
- Water: filtered by a F.G. Miilipore membrane (0.22 micron) ad libitum
- Acclimation period: at least 5 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18 ± 3
- Humidity (%): 30 to 70
- Air changes (per hr): 12
- Photoperiod (hrs dark / hrs light): 12 h/12 h

Test system

Type of coverage:
semiocclusive
Preparation of test site:
clipped
Vehicle:
unchanged (no vehicle)
Controls:
not required
Amount / concentration applied:
0.5 ml
Duration of treatment / exposure:
3 min and 4 hours
Observation period:
up to 15 days
Number of animals:
3
Details on study design:
TEST SITE
- Area of exposure: 6 cm²
- Type of wrap if used: semi occlusive

REMOVAL OF TEST SUBSTANCE
- Washing (if done): not done

SCORING SYSTEM: Draize scale

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
animal #1
Time point:
other: 24+48+72 h
Score:
2
Max. score:
4
Reversibility:
fully reversible within: 12 days
Irritation parameter:
erythema score
Basis:
animal #2
Time point:
other: 24+48+72 h
Score:
1.7
Max. score:
4
Reversibility:
fully reversible within: 9 days
Irritation parameter:
erythema score
Basis:
animal #3
Time point:
other: 24+48+72 h
Score:
1.7
Max. score:
4
Reversibility:
fully reversible within: 9 days
Irritation parameter:
edema score
Basis:
animal #1
Time point:
other: 24+48+72 h
Score:
2
Max. score:
4
Reversibility:
fully reversible within: 6 days
Irritation parameter:
edema score
Basis:
animal: # 2 & 3
Time point:
other: 24+48+72 h
Score:
0
Max. score:
4
Irritant / corrosive response data:
After a 3-minute exposure (one animal): No cutaneous reactions were observed during the study.
After a 4-hour exposure (three animals): A well-defined erythema was observed in all animals on day 1; it persisted up to day 11 at the latest. A slight oedema was noted in all animals from day 1 or 2; it persisted  for 24, 48 or 72 hours. Dryness of the skin was recorded in all animals  from day 5 or 6 up to day 12, 13 or 15. 
Other effects:
A slight yellow colouration of  the skin was also observed in all animals between day 1 and day 4.

Applicant's summary and conclusion

Interpretation of results:
slightly irritating
Remarks:
Migrated information not classified Criteria used for interpretation of results: EU
Conclusions:
Mean scores over 24, 48 and 72 hours for each animal were 2.0, 1.7 and 1.7 for erythema and 2.0, 0 and 0 for oedema.
Executive summary:

The potential of THIOACETIC ACID to induce skin irritation was evaluated in rabbits according to O.E.C.D. (No. 404, 17th July 1992) and E.C. (92/69/E.E.C., B4, 31 st July 1992) guidelines. The study was conducted in compliance with the Principles of Good Laboratory Practice Regulations. The test substance was applied in a first assay for periods of 3 minutes and 4 hours to one male New Zealand White rabbit. Since the test substance was not strongly irritant in this first assay, it was applied for 4 hours to two other males in a second assay. A single dose of 0.5 ml of the test substance in its original form was applied to the closely clipped skin of one flank. The test substance was held in contact with the skin by means of a semi-occlusive dressing. Cutaneous reactions were observed approximately 1 hour, 24, 48 and 72 hours after removal of the dressing and the end of the observation period.The mean values of the scores for erythema and oedema were calculated for each animal.After a 3-minute exposure (one animal), no cutaneous reactions were observed during the study. After a 4-hour exposure (three animals), a well-defined erythema was observed in ail animals on day 1; it persisted up to day 11 at the latest.A slight oedema was noted in ail animals from day 1 or 2; it persisted for 24, 48 or 72 hours.Dryness of the skin was recorded in ail animals from day 5 or 6 up to day 12, 13 or 15. A slight yellow colouration of the skin was also observed in ail animals between day 1 and day 4. Mean scores over 24, 48 and 72 hours for each animal were 2.0, 1.7 and 1.7 for erythema and 2.0, 0 and 0 for oedema.