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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
disregarded due to major methodological deficiencies
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: see 'Remark'
Remarks:
The study contains no details on test substance source, purity, composition, batch number or storage conditions. Although test results are reported there are significant deficiencies in experimental details such as the method of atmosphere generation.

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1988
Report date:
1992

Materials and methods

Test guideline
Qualifier:
no guideline followed
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1,3-dimethylimidazolidin-2-one
EC Number:
201-304-8
EC Name:
1,3-dimethylimidazolidin-2-one
Cas Number:
80-73-9
Molecular formula:
C5H10N2O
IUPAC Name:
1,3-dimethylimidazolidin-2-one
Constituent 2
Reference substance name:
N,N'-dimethylethyleneurea
IUPAC Name:
N,N'-dimethylethyleneurea
Constituent 3
Reference substance name:
1,3-dimethyl-2-imidazolidinone
IUPAC Name:
1,3-dimethyl-2-imidazolidinone
Constituent 4
Reference substance name:
1,3-Dimethylethyleneurea
IUPAC Name:
1,3-Dimethylethyleneurea

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female
Details on test animals or test system and environmental conditions:
200-300g
placed into a sealed 120-L chamber containing sample vapour (near saturation)

Administration / exposure

Route of administration:
other: not specified
Type of inhalation exposure:
whole body
Vehicle:
not specified
Analytical verification of test atmosphere concentrations:
no
Duration of exposure:
6 h
Details on study design:
14 day observation period

Results and discussion

Mortality:
no deaths
Clinical signs:
other: no signs
Gross pathology:
no gross legions

Applicant's summary and conclusion