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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
documentation insufficient for assessment

Data source

Reference
Reference Type:
publication
Title:
Effects of acute combined inhalation exposure to n-butyl alcohol and n-butyl acetate in experimental animals
Author:
Korsak et al.
Year:
1994
Bibliographic source:
Int J Occup Med Environ Health. 1994;7(3):273-80

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
Deviations:
yes
Remarks:
purpose of the investigations was to asses behavioural effects
GLP compliance:
not specified
Test type:
traditional method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Butan-1-ol
EC Number:
200-751-6
EC Name:
Butan-1-ol
Cas Number:
71-36-3
Molecular formula:
C4H10O
IUPAC Name:
butan-1-ol

Test animals

Species:
rat
Strain:
Wistar
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Strain: Imp: DAK
- Weight at study initiation: 250-300 g

ENVIRONMENTAL CONDITIONS: no data

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
air
Details on inhalation exposure:
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: dynamic inhalation chamber (1.3 m3)
- Generation: by heating of liquid substance in washer

TEST ATMOSPHERE
- Brief description of analytical method used: GC with FID
- Samples taken: every 30 min
Analytical verification of test atmosphere concentrations:
yes
Duration of exposure:
4 h
Concentrations:
ca 3500, 5750 and 7900 ppm (10.8, 17.7 and 24.3 mg/L)
No. of animals per sex per dose:
10 males
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: behavioural tests were performed immediately after the 4 hours exposure period
- Examinations performed:rotarod performance, hot plate performance

Rotarod performance was trained before exposure and only rats that were succesful in at least 10 trials were included in the study. Rotarod performance was measured before exposure and immediately therafter in 10 rats.
Hot plate perfomance was measured as latency to react immediately after exposure in 10 rats.
Statistics:
Probit (EC50), ANOVA and Kruskall-Wallis

Results and discussion

Effect levelsopen allclose all
Sex:
male
Dose descriptor:
other: EC50 rotarod
Effect level:
23.2 mg/L air
Based on:
test mat.
95% CL:
>= 19.5 - <= 29.2
Exp. duration:
4 h
Remarks on result:
other: 7559 ppm
Sex:
male
Dose descriptor:
other: EC50 hot plate test
Effect level:
18.2 mg/L air
Based on:
test mat.
95% CL:
>= 14.9 - <= 22.3
Exp. duration:
4 h
Remarks on result:
other: 5901 ppm
Sex:
male
Dose descriptor:
LC50
Effect level:
> 24.3 mg/L air
Based on:
test mat.
Exp. duration:
4 h
Mortality:
no maortality at any of the concentrations tested

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The LC 50 of the substance is > 24.3 mg/L. Below this concentration behavioural effects on rotarod performance and hot plate test are observed.