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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: inhalation

Currently viewing:

Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
1967
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: short summary, non GLP, no guideline followed

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1967
Report date:
1967

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
4 h whole body exposure to an unknown air concentration of the test substance.
GLP compliance:
no
Remarks:
Study performed prior to implementation of GLP
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
trans-crotonic acid
EC Number:
203-533-9
EC Name:
trans-crotonic acid
Cas Number:
107-93-7
Molecular formula:
C4H6O2
IUPAC Name:
but-2-enoic acid

Test animals

Species:
other: rats (wistar) and guinea pig
Sex:
female
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Route of administration:
inhalation
Type of inhalation exposure:
whole body
Vehicle:
air
Details on inhalation exposure:
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION

- Exposure chamber volume: 28 L
- Method of conditioning air: 24.5 g of the product was vapoured at 125-130°C, Airflow: 500 liter/hour
- Temperature in air chamber: 29°C
Duration of exposure:
4 h
Concentrations:
less than 1.2 mg/L, exact concentration unknown (the evaporated test item recrystallised partly before the vapour reached the inhalation chamber)
No. of animals per sex per dose:
5 rats and 5 guinea pigs
Details on study design:
- Duration of observation period following administration: 7 days

Results and discussion

Effect levels
Key result
Sex:
female
Dose descriptor:
LC0
Effect level:
> 0.9 - < 1.2 mg/L air
Based on:
test mat.
Exp. duration:
4 h
Remarks on result:
other: rats and guinea pigs were tested; actual exposure concentration unknown as the evaporated test item recrystallised partly before the vapour reached the inhalation chamber
Mortality:
no
Clinical signs:
other: no
Body weight:
no data
Gross pathology:
no data
Other findings:
no data

Any other information on results incl. tables

Based on the equation for saturated vapour concentrations it can be estimated that the concentration of the substance is approx. 0.88 mg/L saturated air at 20 °C. Therefore, it is assumed that at a temperature of 29 °C the test item concentration was between 0.88 and 1.2 mg/L.

Applicant's summary and conclusion

Interpretation of results:
study cannot be used for classification
Conclusions:
Under the conditions of the present acute toxicity study the inhalation of the test item crotonic acid showed no abnormal behaviour in rats and guinea pigs.