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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:
key study
Study period:
From Aug. 18, 1992 to Sep. 24, 1992
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Guideline study (OECD 401/423). No GLP study.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1992
Report date:
1992

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Version / remarks:
year of guideline not reported
Deviations:
no
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
Version / remarks:
reliability scoring based on 2001
Deviations:
no
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
1H-1,2,4-triazole, sodium salt
EC Number:
255-280-9
EC Name:
1H-1,2,4-triazole, sodium salt
Cas Number:
41253-21-8
Molecular formula:
C2H3N3.Na
IUPAC Name:
sodium 1,2,4-triazol-1-ide
Details on test material:
- Name of test material (as cited in study report): 1, 2 , 4 - TRIAZOLE SODIUM SALT
- Physical state: white - yellow powder
- Analytical purity: = 99%
- Lot/batch No.: 92/492
- Expiration date of the lot/batch: after 1995 (received by laboratory on June 25, 1992)
- Storage condition of test material: in dark and at room temperature

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female
Details on test animals or test system and environmental conditions:
no

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: 0.5% (w/v) methylcellulose in water
Details on oral exposure:
no
Doses:
2000 mg/kg bw
No. of animals per sex per dose:
5/sex/dose
Control animals:
no
Details on study design:
no
Statistics:
no data

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
< 2 000 mg/kg bw
Mortality:
9 rats in 10 died in less than 24 hours. 3 animals (2 males, 1 female) died between 6 and 7 hours after the start of the test. The following day, 6 rats (3 males, 3 females) were found dead. The only one surviving animal (female) was in a coma. No amelioration of its state was observed during the following 48 hours. The last one, moribund was sacrificed 3 days after the treatment.
Clinical signs:
other: One hour after the treatment, the spontaneous motor activity of all animals decreased. Some showed symptoms of respiratory difficulties (gasping). A few rats showed symptoms like piloerection and hollow side. The first severe signs of toxicity were observ
Gross pathology:
The necropsy carried out on all animals revealed stomach (meteorism, glandular mucosa diffusely red) and intestinal (small intestine distended and inflamed) changes.
Other findings:
no

Applicant's summary and conclusion

Conclusions:
Under the experimental conditions adopted, the oral LD50 of the substance 1,2,4-TRIAZOLE SODIUM SALT in male and female rats is smaller than 2000 mg/kg.
Executive summary:

Groups of 5 rats/sexe were exposed to 1,2,4 -triazole sodium salt by gavage at 2000 mg/kg bw, according to the OECD guideline. 1,2,4 -triazole sodium salt was dilued in 0.5%(w/v) methylcellulose in water. 9 rats in 10 died in less than 24 hours. Under the experimental conditions adopted, the oral LD50 of 1,2,4 -triazole sodium salt in male and female rats is smaller than 2000 mg/kg.