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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: National Guideline study with acceptable restrictions.

Data source

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

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: The procedure described in Section 191.11 of the Federal Hazardous Substances Labeling Act was followed.
Deviations:
not specified
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Isooctyl 3-mercaptopropionate
EC Number:
250-157-6
EC Name:
Isooctyl 3-mercaptopropionate
Cas Number:
30374-01-7
Molecular formula:
C11H22O2S
IUPAC Name:
2-methylheptyl 3-sulfanylpropanoate
Details on test material:
- Name of test material (as cited in study report): Iso-octyl 3-mercaptopropionate
- Analytical purity: no data
- Other: sample number bl 1409

Test animals

Species:
rabbit
Strain:
New Zealand White
Details on test animals or test system and environmental conditions:
no data

Test system

Type of coverage:
occlusive
Preparation of test site:
shaved
Vehicle:
unchanged (no vehicle)
Controls:
not required
Amount / concentration applied:
TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 mL


Duration of treatment / exposure:
Removal of the test material from the skin after 24 hours .
Observation period:
The treated areas were scored according to the Federal Hazardous Substances Labeling Act, 24 and 72 hours after initiation of the test.
Number of animals:
6 rabbits
Details on study design:
REMOVAL OF TEST SUBSTANCE
- 24 hours after application of the test material, the gauze was removed and the skin gently cleaned


SCORING SYSTEM: The treated areas were scored according to the Federal Hazardous Substances Labeling Act.

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
4
Remarks on result:
other: no reading at 48 h
Irritation parameter:
edema score
Basis:
mean
Time point:
24/48/72 h
Score:
0
Max. score:
1
Remarks on result:
other: no reading at 48 h
Other effects:
A primary irritation index of 0 was calculated for the test material.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
Under the conditions of the study, the test material is not considered to be a dermal irritant.
GHS: not classifiable