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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

3 -Mercapto-1,2,4 -triazole was administered one-time orally to rats to determine its acute toxicity. The test product was present as a crystalline substance and was applied in an aqueous tragacanth suspension (0.5%).Using application volumes of 4.64 and 10.0 ml / kg with test substance contents of 215 to 464 mg / ml, the dosis in the male and female animals ranged from 1000 to 4640 mg / kg. The intoxication was characterized by tremor, clonic convulsions, loss of muscle tone, generalized reflex failure, diarrhea and poor general condition. Occasionally, stilt walk, ruffled fur, sunken flanks and red-colored tears flow and strenuous breathing were observed. Initial symptoms of poisoning occurred 1 hour after substance administration and lasted up to 5 days. Deaths occurred between 2 hours and 5 days p.appl. A dose of 1000 mg / kg caused no signs of intoxication in female rats.

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records
Reference
Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Qualifier:
according to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
not specified
GLP compliance:
not specified
Test type:
standard acute method
Limit test:
no
Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
water and food ad libitum;
Route of administration:
oral: gavage
Vehicle:
water
Remarks:
binder suspension (0.5%)
Details on oral exposure:
food withdrawal 16 h before application
Doses:
1000 / 1470/ 2150/ 4640 mg/kg
No. of animals per sex per dose:
5
Details on study design:
daily obervasion of animals, observation period 14 days
Statistics:
95% probit analysis
Sex:
male/female
Dose descriptor:
LD50
Effect level:
1 353 mg/kg bw
Based on:
test mat.
Sex:
female
Dose descriptor:
LD50
Effect level:
1 457 mg/kg bw
Based on:
test mat.
Key result
Sex:
male
Dose descriptor:
LD50
Effect level:
1 297 mg/kg bw
Based on:
test mat.
Mortality:
Dosis (mg/kg) death rate
male 1000 1/5
1470 3/5
2150 5/5
4640 5/5

female 1000 0/5
1470 3/5
2150 5/5
4640 5/5
Clinical signs:
other: The poisoning pattern in the two low dose groups was characterized by diarrhea and poor general health. Occasionally, moderate tremors, ruffled fur, stilts and sunken flanks were observed. After application of a dose of 1000 mg / kg, there were no symptom
Gross pathology:
In the autopsy of the deceased animals and intestinal mucosa and in 2 animals additionally the cecum reddened. The intestine contained aqueous, occasionally red-colored fluid. In one animal, the stomach or intestine was bloated. The spleen of one female animal in the lowest dose group was littered with 1 mm white bumps.
Interpretation of results:
Category 4 based on GHS criteria
Conclusions:
LD 50 male: 1279 mg/kg
Executive summary:
3 -Mercapto-1,2,4 -triazole was administered one-time orally to rats to determine its acute toxicity.The test product was present as a crystalline substance and was applied in an aqueous tragacanth suspension (0.5%).Using application volumes of 4.64 and 10.0 ml / kg with test substance contents of 215 to 464 mg / ml, the dosis in the male and female animals ranged from 1000 to 4640 mg / kg.
The intoxication was characterized by tremor, clonic convulsions, loss of muscle tone, generalized reflex failure, diarrhea and poor general condition.Occasionally, stilt walk, ruffled fur, sunken flanks and red-colored tears flow and strenuous breathing were observed.
Initial symptoms of poisoning occurred 1 hour after substance administration and lasted up to 5 days.Deaths occurred between 2 hours and 5 days p.appl.
A dose of 1000 mg / kg caused no signs of intoxication in female rats.
Endpoint conclusion
Endpoint conclusion:
adverse effect observed
Dose descriptor:
LD50
Value:
1 297 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for classification or non-classification

CLP ((EG) Nr. 1272/2008) criteria for acute toxicity are met. Based on the LD 50 (male: 1297 mg/kg) the substance is classified in Category 4.