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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: although limited documented sufficient information for assessment

Data source

Reference
Reference Type:
publication
Title:
Range-Finding Toxicity Data: List VI
Author:
Smyth, H.F. et al.,
Year:
1962
Bibliographic source:
Am. Ind. Hyg. Ass. J. 23, 95-107

Materials and methods

Principles of method if other than guideline:
Penetration o f rabbits skin is estimated by a technique closely akinto the one-day cuff method of Draize and associates, using groups of 4 male albino New Zealand rabbits weighing 2.5 to 3.5 kg . the fur was removed from the entire trunk by clipping and the dose is retainded beneath an imperious plastic film. The animals were immobilized during tge 24-hour contact period, after which the film was removed and the rabbits are caged for subsequent 14 day observation period
GLP compliance:
no
Test type:
other: acute dermal toxicity study

Test material

Constituent 1
Chemical structure
Reference substance name:
Cyclohex-3-ene-1-carbaldehyde
EC Number:
202-858-3
EC Name:
Cyclohex-3-ene-1-carbaldehyde
Cas Number:
100-50-5
Molecular formula:
C7H10O
IUPAC Name:
cyclohex-3-ene-1-carbaldehyde
Details on test material:
4-Cyclohexene-1-carboxaldehyde

Test animals

Species:
rabbit
Strain:
New Zealand White
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 2.5-3.5 kg
- Fasting period before study:
- Housing: no data
- Diet ad libitum
- Water ad libitum
- Acclimation period: no data

ENVIRONMENTAL CONDITIONS
details not given

Administration / exposure

Type of coverage:
semiocclusive
Vehicle:
unchanged (no vehicle)
Details on dermal exposure:
Penetration o f rabbits skin is estimated by a technique closely akinto the one-day cuff method of Draize and associates (1944, J Pharmacol Exp Therap 82, 377), using groups of 4 male albino New Zealand rabbits weighing 2.5 to 3.5 kg . The fur was removed from the entire trunk by clipping and the dose is retained beneath an imperious plastic film. The animals were immobilized during the 24-hour contact period, after which the film was removed and the rabbits are caged for subsequent 14 day observation period
Duration of exposure:
24 h
Doses:
no data
No. of animals per sex per dose:
4
Control animals:
no
Details on study design:
Penetration o f rabbits skin is estimated by a technique closely akinto the one-day cuff method of Draize and associates (1944, J Pharmacol Exp Therap 82, 377), using groups of 4 male albino New Zealand rabbits weighing 2.5 to 3.5 kg . The fur was removed from the entire trunk by clipping and the dose is retained beneath an imperious plastic film. The animals were immobilized during the 24-hour contact period, after which the film was removed and the rabbits are caged for subsequent 14 day observation period
Statistics:
LD50 was estimated by the method of Thompson (1947) Bacteriol Rev 11, 115 using the tables of Weil (1952) Biometrics 8, 249

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
1 770 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

original value: 1.77 ml/kg; density: 0.967 g/cm3

Applicant's summary and conclusion

Executive summary:

LD50 rabbit: 1712 mg/kg