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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: acceptable well-documented publication which meets basic scientific principles

Data source

Reference
Reference Type:
publication
Title:
Toxicity of chloroprene in an acute test during oral administration
Author:
Asmamgulian, T., A.; et al.
Year:
1971
Bibliographic source:
Proceedings of the Yerevan Medical Institute, vol. XV, 461-465

Materials and methods

Principles of method if other than guideline:
other: acute oral toxicity study
GLP compliance:
no
Test type:
other: acute oral toxicity study

Test material

Constituent 1
Chemical structure
Reference substance name:
2-chlorobuta-1,3-diene
EC Number:
204-818-0
EC Name:
2-chlorobuta-1,3-diene
Cas Number:
126-99-8
Molecular formula:
C4H5Cl
IUPAC Name:
2-chlorobuta-1,3-diene
Details on test material:
chloroprene

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: sunflower seed oil
Doses:
150 to 400 mg/kg bw
No. of animals per sex per dose:
total number of rats used: 54
Control animals:
yes

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
251 mg/kg bw
Based on:
test mat.
Remarks on result:
other: clinical signs, death, pathological changes in the inner organs and brain membrane

Any other information on results incl. tables

Clinical signs: symptoms of a depressed nervous system, animals were apathetic, death occured usually within the first day, survivors were comparable to the control at study termination

Autopsy of decedent: irregular blood content of the inner organs, hemorrhages foci in the brain membrane

Microscopic evaluations of decedents: blood vessels of the liver plethoric showed a turbid swelling, some lung alveoles were collapsed, lung tissue with formolic pigment, diapedesis of erythrocytes, epicardium was loosened up in spots, muscle fibers showed a turbid swelling, the fatty tissue of myocardium under epicardium and endocardium with foci of hemorrhages, the pulp of the spleen was plethoric with aggregated of eosinophiles, epithelium of the convoluted channels in the kidneys with distinct granular dystrophy, vessel of the brain cortex showed plethoric, the brain vessels were severely plethoric and had foci of hemorrhages, the brain tissue was swollen, stomach with a moderate leuco- and lymphocytic infiltration and a pronounced accumulation of eosinophiles

Applicant's summary and conclusion

Executive summary:

Oral LD50 value in rats: 251 mg/kg bw; the clinical picture of acute poisoning is characterized by depression of the central nervous system. Patho-morphological changes in decedents after single oral application were mainly plethora, hemorrhages and dystropic changes in the central nervous system and in the inner organs.