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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
key study
Study period:
1979-05-01
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Meets generally accepted standards with acceptable restrictions (limited documentation; raw data generally available on request)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1979
Report date:
1979

Materials and methods

Principles of method if other than guideline:
Method: other: no data
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Butyl(ethyl)amine
EC Number:
236-415-0
EC Name:
Butyl(ethyl)amine
Cas Number:
13360-63-9
Molecular formula:
C6H15N
IUPAC Name:
butyl(ethyl)amine
Details on test material:
- Name of test material (as cited in study report): N-Ethyl-N-n-butylamin; no further details

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Route of administration:
inhalation: aerosol
Type of inhalation exposure:
nose/head only
Vehicle:
air
Details on inhalation exposure:
no data
Analytical verification of test atmosphere concentrations:
yes
Duration of exposure:
1 h
Concentrations:
2.45, 9.66, 10.18, and 11.87 mg/m3 (analytical)
No. of animals per sex per dose:
10
Control animals:
other: not required
Details on study design:
- Duration of observation period following administration: no data
- Frequency of observations and weighing: no data
- Necropsy of survivors performed: no data
- Other examinations performed: clinical signs, body weight,organ weights, histopathology, other: no data

Results and discussion

Effect levelsopen allclose all
Sex:
male
Dose descriptor:
LC50
Effect level:
10.6 mg/L air (analytical)
Exp. duration:
1 h
Sex:
female
Dose descriptor:
LC50
Effect level:
> 11.9 mg/L air (analytical)
Exp. duration:
1 h

Any other information on results incl. tables

 

Concentration

(mg/L; analytical

Mortality

No. dead /No. exposed

Male

female

2.45

0/10

0/10

9.66

2/10

0/10

10.18

5/10

0/10

11.87

8/10

0/10

 

Applicant's summary and conclusion

Executive summary:

10 male and female Wistar rats were exposed (head-nose only) to Butylethylamine for 1 hour at analytical concentrations of 2.45 to 11.87 mg/L. All females survived whereas male mortality increased with dose up to 80% at the top dose. The LC50(1hr)was 10.6 mg/L for the male rat (BASF, 1979).

The study may be used for assessment using the LC50, 1 -hr -value for male rats. There is no explanation why no deaths occurred in females.