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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 403 (Acute Inhalation Toxicity)
GLP compliance:
no
Test type:
acute toxic class method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
sec-butylamine
EC Number:
237-732-7
EC Name:
sec-butylamine
Cas Number:
13952-84-6
Molecular formula:
C4H11N
IUPAC Name:
butan-2-amine

Test animals

Species:
mouse
Strain:
other: WBS/S
Details on test animals or test system and environmental conditions:
5 MALES OF wbs/s MICE 527+/- g BW) were placed in each of a series of 20-liter exposure chambers and the latter sealed airtight. A measured volume of the sample was then injected upon a disc of filter paper suspended in each chamber. (The sample was seen to evaporate completely within 20 seconds). The mice were observed continuously during an exposure period of one hour and suviving animals were observed for 11 days.

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
not specified
Details on inhalation exposure:
5 MALES OF wbs/s MICE 527+/- g BW) were placed in each of a series of 20-litter exposure chambers and the latter sealed airtight. A measured volume of the sample was then injected upon a disc of filter paper suspended in each chamber. (The sample was seen to evaporate completely within 20 seconds). The mice were observed continuously during an exposure period of one hour and suviving animals were observed for 11 days.
Analytical verification of test atmosphere concentrations:
not specified
Duration of exposure:
1 h
Concentrations:
8, 10, 12.5, 16, 20 and 25 mg/l
No. of animals per sex per dose:
5 males
Control animals:
no
Details on study design:
5 MALES OF wbs/s MICE 527+/- g BW) were placed in each of a series of 20-litter exposure chambers and the latter sealed airtight. A measured volume of the sample was then injected upon a disc of filter paper suspended in each chamber. (The sample was seen to evaporate completely within 20 seconds). The mice were observed continuously during an exposure period of one hour and suviving animals were observed for 11 days.
Statistics:
none

Results and discussion

Effect levels
Key result
Sex:
male
Dose descriptor:
LC50
Effect level:
11.2 mg/L air
Based on:
test mat.
Exp. duration:
1 h
Mortality:
0 % mortality at 8 mg/L
20% mortality at 10 mg/l
80% mortality at 12.5 mg/L
100% mortality at 16 mg/L
100% mortality at 20 mg/l
100% mortality at 25 mg/l
Clinical signs:
other: severe sensory irritation, dffrantic escape activity, salivation and bronchospastic gasping.
Body weight:
not recorded
Gross pathology:
not examined

Applicant's summary and conclusion

Interpretation of results:
Category 3 based on GHS criteria
Executive summary:

5 males of wbs/s MICE 527+/- g BW were placed in each of a series of 20-litter exposure chambers and the latter sealed airtight. A measured volume of the sample was then injected upon a disc of filter paper suspended in each chamber. (The sample was seen to evaporate completely within 20 seconds). The mice were observed continuously during an exposure period of one hour and suviving animals were observed for 11 days. The LC 50 was set at 11.2 mg/l (3680 ppm).