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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Adopted according to OECD SIDS (public available peer reviewed source). The original source is not available and has not been reviewed.

Data source

Referenceopen allclose all

Reference Type:
secondary source
Title:
SIDS Initial Assessment Report for 11th SIAM, UNEP Publications
Author:
OECD SIDS
Year:
2003
Reference Type:
study report
Title:
Unnamed
Year:
1967

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
An acute single dose inhalation toxicity test was performed on 6 male rats in order to determine the LC50.
GLP compliance:
no
Remarks:
GLP was not mandatory at the time of the study
Test type:
other: Single Dose Inhalation Toxicity Test

Test material

Constituent 1
Chemical structure
Reference substance name:
3,4-dichlorobut-1-ene
EC Number:
212-079-0
EC Name:
3,4-dichlorobut-1-ene
Cas Number:
760-23-6
Molecular formula:
C4H6Cl2
IUPAC Name:
3,4-dichlorobut-1-ene
Details on test material:
- Name of test material (as cited in study report): 3,4-Dichlorobut-1-ene
- Analytical purity: 98%

Test animals

Species:
rat
Strain:
other: ChR;CD (SD)
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 246-295 g bw

Administration / exposure

Route of administration:
inhalation: vapour
Vehicle:
not specified
Details on inhalation exposure:
The test material was metered by a syringe drive into a stainless steel T tube where it was vaporized at 120-150°C. The resulting vapours were carried by a stream of air into a 16 liter exposure chamber.
Analytical verification of test atmosphere concentrations:
yes
Remarks:
The chamber atmosphere was analyzed at least once every hour by a gas chromatographic method.
Duration of exposure:
4 h
Concentrations:
1000, 2250, 3000 ppm
No. of animals per sex per dose:
6 (only male animals were tested)
Control animals:
other: not necessary
Details on study design:
- Necropsy of survivors performed: yes
- Organs examined at necropsy: kidney, liver, trachea, lung, brain, testes, bone marrow, spleen, thymus, gastro intestinal tract were examined.
- Other examinations performed: clinical signs, histopathology.
Statistics:
Statistical analysis by metod of Litchfield, J. T., Jr., and F. Wilcoxon, J. Pharmacol. And Exper. Ther., 96, 99 (1949).

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LC50
Effect level:
10.89 mg/L air
Based on:
test mat.
Exp. duration:
4 h
Mortality:
Deaths occurred 2-6 days post-exposure.
Clinical signs:
other: Clinical signs of irregular breathing, incoordination, unresponsiveness and lacrimation (only at the beginning of the exposure) were observed.
Body weight:
No data
Gross pathology:
No data
Other findings:
Inhalation at both high and low dosage levels was followed by degenerative lesions of the livers and/or kidneys of rats which died or killed within two days of exposure. Observable lesions were not present in the tissues examined from rats killed at seven days following low level exposure or fourteen days following medium level exposure.

Any other information on results incl. tables

On the basis of the results, 3,4 -dichlorobut-1 -ene is to be classified as Xn, R20 (Harmful by inhalation), according to the DSD classification criteria and Acute Tox. 4 (Harmful by inhalation) according to CLP classification criteria.

Applicant's summary and conclusion