Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: see 'Remark'
Remarks:
Acceptable (pre-GLP; pre-guidelines), study containing basic data which suggests that basic scientific principles have been met. This is sufficient to judge the results reliable as a contribution to the understanding of the toxicity of this substance.

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1950

Materials and methods

Principles of method if other than guideline:
other
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Crotonaldehyde
EC Number:
224-030-0
EC Name:
Crotonaldehyde
Cas Number:
4170-30-3
Molecular formula:
C4H6O
IUPAC Name:
but-2-enal

Test animals

Species:
other: rat and mouse
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
Subcutaneous injections of aqueous solutions of crotonaldehyde at 10% concentration were applied to the rats and 1% to the mice. Animals were observed for 21 days.

Administration / exposure

Route of administration:
subcutaneous
Vehicle:
water
Details on exposure:
A single exposure was applied.
Doses:
0.1 - 0.18 g/kg for the rats
0.12 - 0.26 g/kg for the mice
No. of animals per sex per dose:
96 animals total
Control animals:
no
Details on study design:
no additional data
Statistics:
no data

Results and discussion

Effect levels
Dose descriptor:
LD50
Effect level:
140 mg/kg bw
Mortality:
There was a total mortality of 43 animals, 6 between 0-1hr, 26 1and 6 hr and 11 between 6-24 hr.
Clinical signs:
intense excitation, nose, ears and feet became strongly red.
Gross pathology:
Lungs: hyperemia, haemorrhages, perivascular edema, slight peribronchrial pneumonic changes.
Heart, liver, kidneys: hyperemia
Other organs: no changes
Other findings:
Survivors appeared recovered after 24 to 48 hr.

Any other information on results incl. tables

"A few minutes after injection a stage of intense excitation activity set in, lasting 10 -15 minutes, during which the animals ran about squeaking in the cage. At the same time peripheral parts of the body (nose, ears and feet) became strongly reddened. With the larger doses there were also general tremors or convulsions. The peripheral reddening subsided and disappeared in about an hour. With the larger doses death occured during or close to the stage of excitation. With the smaller doses the animals died most oftern during the night after the injections and no death occured later than 24 hours afterwards. The survivors seemed to have recovered after one to two days."

Applicant's summary and conclusion

Conclusions:
Crotonaldehyde resulted toxic via subcutaneous and more toxic in rats than in mice.
Executive summary:

A subcutaneous toxicity study with crotonaldehyde indicated that the substance is toxic to rats and mice and suggested that the lungs and respiratory tract were the target organs. The LD50 was 0.16 g/kg in the mouse and 0.14 g/kg in the rat.