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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Range-finding toxicity data
Author:
Smyth H.F.
Year:
1954
Bibliographic source:
AMA Arch Ind Hyg Occup Med. 1954 Jul;10(1):61-8.
Reference Type:
publication
Title:
Unnamed
Year:
1991
Report date:
1991
Reference Type:
publication
Title:
Industrial hygiene and toxicology, Second Revised Edition, Volume II
Author:
Fassett D.W.
Year:
1962
Bibliographic source:
p. 1966-1978

Materials and methods

Principles of method if other than guideline:
Penetration of rabbit skin is estimated by a technique closely to the one-day cuff method of Draize and associates (Draize, J.H. et al.: J. Pharmacol. Exp. Therap. 82, 377, 1944), using groups of four male rabbits. The fur is removed from the entire trunk by clipping, and the dose is retained beneath an impervious plastic film. Animals were observed for 14 days.
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Isobutyraldehyde
EC Number:
201-149-6
EC Name:
Isobutyraldehyde
Cas Number:
78-84-2
Molecular formula:
C4H8O
IUPAC Name:
2-methylpropanal
Details on test material:
- Name of test material: isobutyraldehyde

Test animals

Species:
rabbit
Strain:
New Zealand White
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Age at study initiation: 3-5 months
- Weight at study initiation: average 2.5 – 3.5 kg
- Diet: Rockland rabbit ration

Administration / exposure

Type of coverage:
occlusive
Vehicle:
not specified
Details on dermal exposure:
Penetration of rabbit skin is estimated by a technique closely to the one-day cuff method of Draize and associates, using groups of four male rabbits weighing. The fur is removed from the entire trunk by clipping, and the dose is retained beneath an impervious plastic film. The animals are immobilized during the 24-hour contact period, after which the film is removed and the rabbits are caged for the subsequent 14-day observation period.
Duration of exposure:
24 h
Doses:
5, 10 mL/kg
No. of animals per sex per dose:
2 (low dose), 4 (high dose)
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 14 days
Statistics:
Thompson's method was used for calculating the LD50.

Results and discussion

Effect levelsopen allclose all
Sex:
male
Dose descriptor:
LD50
Effect level:
ca. 7.13 mL/kg bw
Based on:
test mat.
Remarks on result:
other: original value
Sex:
male
Dose descriptor:
LD50
Effect level:
5 583 mg/kg bw
Based on:
test mat.
Remarks on result:
other: density used for conversion: 0.783 g/cm3
Mortality:
Four animals dosed at 10 mL/kg died
The 2 animals dosed at 5 mL/kg survived.
Clinical signs:
other: erythema, edema and necrosis of the skin at the site of contact, with congestion and hemorrhage of the lungs in rabbits dying on study.

Applicant's summary and conclusion