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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Animal experimental study, published in peer reviewed literature, limitations in design and/or reporting but otherwise adequate for assessment

Data source

Reference
Reference Type:
publication
Title:
Toxicity of pyrazole and 4-methylpyrazole in mice and rats.
Author:
Magnusson G. et al
Year:
1972
Bibliographic source:
Experientia. 1972 Oct 15;28(10):1198-200.

Materials and methods

Principles of method if other than guideline:
Six male Sprague-Dawley rats per dose were exposed orally to the test substance diluted in physiological saline. Animals were observed for 7 days and mortalities were recorded.
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
4-methylpyrazole
EC Number:
231-445-0
EC Name:
4-methylpyrazole
Cas Number:
7554-65-6
Molecular formula:
C4H6N2
IUPAC Name:
4-methyl-1H-pyrazole
Details on test material:
Name of test material (as cited in study article): 4-methylpyrazole

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 170 g (mean)

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
physiological saline
Details on oral exposure:
Administered as solution in 6 dose levels.
No. of animals per sex per dose:
6 male animals
Control animals:
no
Details on study design:
Duration of observation period following administration: 7 days
Statistics:
Values for LD50 were calculated from the recorded mortalities by the method of Litchfield and Wilcoxon (1949).

Results and discussion

Effect levelsopen allclose all
Sex:
male
Dose descriptor:
LD50
Effect level:
6.5 other: mmol/kg bw
Based on:
test mat.
95% CL:
5.9 - 7.1
Sex:
male
Dose descriptor:
LD50
Effect level:
534 mg/kg bw
Based on:
test mat.

Applicant's summary and conclusion

Interpretation of results:
harmful
Remarks:
Migrated information