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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Data is from authoritative database

Data source

Reference
Reference Type:
other: Authoritative database
Title:
Skin irritation study on rats
Author:
US National Library of Medicine (NLM)
Year:
2015
Bibliographic source:
Canadian Centre for Occupational Health and Chemistry

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Draize method
Principles of method if other than guideline:
Range finding study was conducted to evaluate the skin irritation potential of the test compound Thiosemicarbazide
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Thiosemicarbazide
EC Number:
201-184-7
EC Name:
Thiosemicarbazide
Cas Number:
79-19-6
Molecular formula:
CH5N3S
IUPAC Name:
hydrazinecarbothioamide
Details on test material:
- Name of test material (as cited in study report): Thiosemicarbazide
- Molecular formula (if other than submission substance): CH5N3S
- Molecular weight (if other than submission substance): 91.1375 g/mol
- Substance type: Organic
- Physical state: Solid

Test animals

Species:
rat
Strain:
other: CD
Details on test animals or test system and environmental conditions:
Sex: Male

Test system

Type of coverage:
occlusive
Preparation of test site:
not specified
Vehicle:
physiological saline
Remarks:
0.85% saline, 1:1
Controls:
not specified
Amount / concentration applied:
0, 20, and 200 mg/kg
Duration of treatment / exposure:
24 hrs
Observation period:
14 days
Number of animals:
6
Details on study design:
TEST SITE
- Area of exposure: No data available
- % coverage: No data available
- Type of wrap if used: No data available

REMOVAL OF TEST SUBSTANCE
- Washing (if done): yes
- Time after start of exposure: No data available

SCORING SYSTEM: No data available

Results and discussion

In vivo

Results
Irritation parameter:
overall irritation score
Basis:
mean
Time point:
other: 14 days
Reversibility:
no data
Remarks on result:
other: Dermal irritation not observed
Other effects:
Mortality was observed on day 1 of 14 day post treatment and 1 on the day of treatment
Convulsions, tremors, salivation, aggressiveness, and red stained muzzle were observed in the decedent rats. Terminal necropsy disclosed wet and/or tan or red-stained muzzles and darkened livers.

Applicant's summary and conclusion

Interpretation of results:
not irritating
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Thiosemicarbazide is not irritating to the skin of male CD rats.
Executive summary:

Thiosemicarbazide was evaluated in range-finding study for acute dermal toxicity in male CD rats administered single occluded dermal applications (0.85% saline, 1:1) of 0, 20, and 200 mg/kg for 24 hours.

 

Dermal exposure was associated with mortality in 5/6 high dose rats only, 4 on Day 1 of 14-day post-treatment observation and 1 on the day of treatment. Prior to death, the decedent rats unanimously exhibited convulsions, tremors, salivation, aggressiveness, and red stained muzzle. Terminal necropsy disclosed wet and/or tan or red-stained muzzles and darkened livers. No apparent toxicity was reported among the solitary surviving rat of a 200 mg/kg application or rats of a 20 mg/kg dose, and no dermal irritation (Draize) was noted in any treated animal.

 

Thiosemicarbazide is not irritating to the skin of male CD rats.

 

In accordance with the CLP classification, the test material Thiosemicarbazide does not classify as a skin irritant.