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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Adopted according to OECD SIDS (public available peer reviewed source). The original source is available and has been reviewed.
Cross-reference
Reason / purpose for cross-reference:
reference to same study

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Range-finding toxicity data: List IV
Author:
Smyth Jr. HF, Carpenter CP, Weil CS
Year:
1951
Bibliographic source:
Arch. Ind. Hyg. Occup. Med. 4, 119-122.
Reference Type:
secondary source
Title:
1,4-Dichlorobut-2-ene- CAS No: 764-41-0
Author:
OECD SIDS
Year:
2006
Bibliographic source:
SIDS Initial Assessment Report for 22th SIAM, UNEP Publications

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Dermal LD50 has been determined with rabbits, after 24-hour dermal exposure under occlusive conditions. Method described in: Smyth et al., J. Ind. Hyg. Toxicol. 30, 63-68 (1948).
GLP compliance:
no
Remarks:
GLP was not mandatory at the time of the study.
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1,4-dichlorobut-2-ene
EC Number:
212-121-8
EC Name:
1,4-dichlorobut-2-ene
Cas Number:
764-41-0
Molecular formula:
C4H6Cl2
IUPAC Name:
1,4-dichlorobut-2-ene
Details on test material:
- Name of test material (as cited in study report): 1,4-dichlorobut-2-ene.
- Analytical purity: no data.

Test animals

Species:
rabbit
Strain:
not specified
Sex:
not specified

Administration / exposure

Type of coverage:
occlusive
Vehicle:
not specified
Duration of exposure:
24 hours
Doses:
no data
No. of animals per sex per dose:
6 per dose group (sex of the animals not reported)
Details on study design:
- Duration of observation period following administration: 14 days.
Statistics:
Standard deviations calculated by the method of Thompson (1947)

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
735 mg/kg bw
Based on:
test mat.
95% CL:
557 - 960

Applicant's summary and conclusion