Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
7 Nov 1991 to 21 Nov 1991
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1991
Report date:
1991

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
Version / remarks:
May 12, 1981
Deviations:
no
Qualifier:
equivalent or similar to guideline
Guideline:
EU Method B.2 (Acute Toxicity (Inhalation))
GLP compliance:
yes
Test type:
traditional method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
6-methyl-4-[(E)-[(pyridin-3-yl)methylidene]amino]-2,3,4,5-tetrahydro-1,2,4-triazin-3-one
EC Number:
602-927-1
Cas Number:
123312-89-0
Molecular formula:
C10H11N5O
IUPAC Name:
6-methyl-4-[(E)-[(pyridin-3-yl)methylidene]amino]-2,3,4,5-tetrahydro-1,2,4-triazin-3-one
Test material form:
solid: particulate/powder

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 1 800 mg/m³ air
Based on:
test mat.
Exp. duration:
4 h

Any other information on results incl. tables

No mortality was recorded during the study. Clinical signs in both sexes included piloerection, hunched posture, and dyspnea, which cleared by day 4. Body weight gain was in the expected range. Gross necropsy revealed no observable abnormalities. At autopsy, no compound-related deviations from normal morphology were seen. The acute inhalation LC50 in albino rats was determined to be greater than 1800 mg/m³.

Applicant's summary and conclusion

Interpretation of results:
study cannot be used for classification
Conclusions:
Under the conditions of the study, the acute inhalation LC50 in male and female rats was determined to be greater than 1800 mg/m³.
Executive summary:

In a GLP compliant acute inhalation toxicity study performed according to OECD guideline 403, groups of 5 male and 5 female Tif: RAI f (SPF) rats were exposed to the test material. Because of the high variability of particle size of technical material as such, it was not possible to generate an aerosol of sufficient concentration and respirable particle size. For the inhalation study the test material had to be milled twice using a jet mill adding 1 % Sipernat 50S, a highly disperse amorphic siliciumoxide. 5 male and 5 female rats (Tif:RAIf (SPF)) were exposed to milled test material for 4 hours (nose only exposure) at the maximum attainable concentration of 1800 mg/m3 air. The main exposure parameters are given in the following Table:

Nominal concentration

2767 mg/m3

Mean exposure concentration determined gravimetrically + standard deviation

1806 ± 103 mg/m3

Mass median aerodynamic diameter

1.5 - 2.9 µm

Particles < 7 μm (% w/w)

79 - 89

Air flow through generator

32 L/min

Mean chamber temperature

22.8 °C

Mean relative humidity

47 %

No mortality was recorded during the study. Clinical signs in both sexes included piloerection, hunched posture, and dyspnea, which cleared by day 4. Body weight gain was in the expected range. Gross necropsy revealed no observable abnormalities. At autopsy, no compound-related deviations from normal morphology were seen.The acute inhalation LC50 in albino rats was determined to be greater than 1800 mg/m³.