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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non-GLP non-guideline, available as unpublished report, limitations in design and/or reporting but otherwise adequate for assessment.

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1970
Report date:
1970
Reference Type:
other: English translation (summary)
Title:
Unnamed
Year:
2005
Report date:
2005

Materials and methods

Principles of method if other than guideline:
Ten rats were exposed to the test substance for 1 hour via inhalation. After an exposure period of 14 days animals were necropsied.
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Butyl chloroformate
EC Number:
209-750-5
EC Name:
Butyl chloroformate
Cas Number:
592-34-7
Molecular formula:
C5H9ClO2
IUPAC Name:
butyl carbonochloridate
Details on test material:
- Name of the test substance used in the study report: n-Butylchlorkohlensäureester; Chloroformic acid butyl ester
- Physical state: liquid

Test animals

Species:
rat
Strain:
not specified
Sex:
male/female
Details on test animals or test system and environmental conditions:
- Weight at study initiation (mean): Males: 158 g; Females 136 g

Administration / exposure

Route of administration:
inhalation
Type of inhalation exposure:
not specified
Vehicle:
not specified
Details on inhalation exposure:
4185 L/h
Analytical verification of test atmosphere concentrations:
not specified
Duration of exposure:
1 h
Concentrations:
about 200 ppm
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
> 200 ppm
Based on:
test mat.
Exp. duration:
1 h
Mortality:
4 out of 10 animals exposed to 200 ppm died.
Clinical signs:
other: Eyelid closure, after a few minutes forced breathing, and partially thoracic breathing was observed. In the first days after exposure no abnormal signs were observed. However, on the sixth day of the observation period 3 animals died. One animal showed ga
Body weight:
- Weight at start study: Males: 158 g; Females 136 g
- Weight at end study: Males: 201.7 g; Females 178.3 g
Gross pathology:
- Animals that died: Pulmonary emphysema
- Sacrificed animals: no effects observed

Applicant's summary and conclusion