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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Data is from publication

Data source

Reference
Reference Type:
publication
Title:
Acute Oral Toxicity and Repellency of 933 Chemicals to House and Deer Mice
Author:
E. W. Schafer, Jr. and W. A. Bowles, Jr
Year:
1985
Bibliographic source:
Arch. Environ. Contain. Toxicol. 14, 111-129, 1985

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: as below
Principles of method if other than guideline:
An acute oral toxicity study was conducted to evaluate toxicity of Thiosemicarbazide in deer mice
GLP compliance:
not specified
Test type:
other: No data available
Limit test:
yes

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
- Analytical purity: No data available

Test animals

Species:
mouse
Strain:
other: Peromyscus maniculatus
Sex:
not specified
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Wild-trapped house and deer mice
or domestically bred house mice were used
- Age at study initiation: No data available
- Weight at study initiation: 20 g
- Fasting period before study: No data available
- Housing: No data available
- Diet (e.g. ad libitum): Wheat seeds
- Water (e.g. ad libitum): No data available
- Acclimation period: No data available

ENVIRONMENTAL CONDITIONS
- Temperature (°C): No data available
- Humidity (%): No data available
- Air changes (per hr): No data available
- Photoperiod (hrs dark / hrs light): No data available

IN-LIFE DATES: From: To: No data available

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: Water, corn oil, or 1.0% carbopol
Details on oral exposure:
No detailed data about vehicle available
Doses:
Dosing details not available
No. of animals per sex per dose:
6 animals
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 3 days
- Frequency of observations and weighing: No data available
- Necropsy of survivors performed: No data available
- Other examinations performed: Mortality was observed
Statistics:
Method of Thompson (1948) and Thompson and Weil (1952)

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
94 mg/kg bw
Based on:
test mat.

Applicant's summary and conclusion

Interpretation of results:
Toxicity Category III
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The acute oral median lethal dose (LD50) for the test compound thiosemicarbazide is found to be 94.0 mg/kg in deer mice.
Executive summary:

An acute oral toxicity study was conducted to evaluate toxicity ofThiosemicarbazidein deer mice.

 

The chemical was administered by gavage using water, corn oil, or 1.0% carbopol as carriers, followed by 3-days of observations for mortality.

 

The acute oral median lethal dose (LD50) for the test compound thiosemicarbazide is found to be 94.0 mg/kg.

 

According to the publication, the test materialThiosemicarbazide classifies as an acute oral toxicant Category 3 chemical.