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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1990
Report date:
1990

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Pyrazole
EC Number:
206-017-1
EC Name:
Pyrazole
Cas Number:
288-13-1
Molecular formula:
C3H4N2
IUPAC Name:
1H-pyrazole
Details on test material:
Name of test substance: Pyrazol
Batch No.: Pyrazol 27/90
Purity: 100%
Date of manufacture: April 20, 1989
Physical state/appearance: solid (melt)/white-colourless
Storage conditions: was stored at room temperature
Stability: Stability was ensured for at least the study period.
Homogeneity: was guaranteed by purity

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
strain: SPF Wistar/Chbb : THOM ; breeding facility: Dr. K . Thomae GmbH, D-7950 Biberach, FRG)
Mean body weight at the beginning of the study: male animals 285 +- 4.0 g, female animals 188 +- 2 .1 g.
Age at the beginning of the study: approx . 8- 9 weeks
The animals were identified by color marking on the tail.
The animals were offered KLIBA rat/mouse laboratory diet 24-343-4 10 mm pellets, Klingentalmuhle AG, CH-4303 Kaiseraugst, Switzerland, and drinking water ad libitum during the post-exposure observation period.
The animals were kept in fully air-conditioned rooms in which a temperature in the range 20-24°C and relative humidity in the range 30-70% were regulated by means of a central air-conditioning system.

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
other: unchanged (no vehicle)
Analytical verification of test atmosphere concentrations:
yes
Duration of exposure:
4 h
Concentrations:
0.37 mg/l
No. of animals per sex per dose:
5

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 0.37 mg/L air

Any other information on results incl. tables

Cumulated lethality on day

male

female

0

0/5

0/5

1

0/5

0/5

2

0/5

0/5

7

0/5

0/5

14

0/5

0/5

Total at end of the study

0/5

0/5

Time after beginning of exposure

< ¼ h

¼ h

½ h

1 h

2 h

3 h

4 h

Animals without findings

10

10

10

Wiping of snouts

10

Restlessness

10

10

10

Attempts to escape

10

 

The body weight gain of male rats was not affected. The body weight gain of the female rats was retarded in the second week of the observation period.

Necropsy findings: Sacrificed animals: No pathologic findings noted.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Regarding the results of the study, the LC50 of the test substance Pyrazole exceeds the maximum concentration that could be technically achieved (0.37 mg/L air).