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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Repeated dose toxicity: inhalation

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Administrative data

Endpoint:
sub-chronic toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Study results summarized in inter-office correspondence. Insufficient experimental details provided to assess reliability.

Data source

Reference
Reference Type:
other: Inter-office correspondence
Title:
Unnamed
Year:
1953
Report date:
1953

Materials and methods

Test guideline
Qualifier:
no guideline followed
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Ethylene carbonate
EC Number:
202-510-0
EC Name:
Ethylene carbonate
Cas Number:
96-49-1
Molecular formula:
C3H4O3
IUPAC Name:
1,3-dioxolan-2-one
Test material form:
solid: crystalline
Details on test material:
- Name of test material (as cited in study report): Ethylene carbonate
- Purity: > 99%
- Physical state: fine crystals

Test animals

Species:
other: dogs, guinea pigs and rats
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
inhalation: aerosol
Type of inhalation exposure:
not specified
Vehicle:
other: no data
Details on inhalation exposure:
-Administered as an aerosol
Analytical verification of doses or concentrations:
yes
Details on analytical verification of doses or concentrations:
No data
Duration of treatment / exposure:
32 days
Frequency of treatment:
5 days/week over a period of 32 days
Doses / concentrationsopen allclose all
Dose / conc.:
8 ppm (analytical)
Remarks:
for the first 9 days of the experiment
Dose / conc.:
110 ppm (analytical)
Remarks:
for the remainder of the experiment
No. of animals per sex per dose:
2 dogs, 7 guinea pigs, 7 rats; sex not specified
Control animals:
not specified
Positive control:
No data

Examinations

Observations and examinations performed and frequency:
CAGE SIDE OBSERVATIONS: Yes
- Time schedule: No data

HAEMATOLOGY: Yes, dogs only
- Time schedule for collection of blood: Routine samples performed at intervals and at the end of the experiment for the dogs

URINALYSIS: Yes, dogs only
- Time schedule for collection of urine: End of experiment for dogs.



Sacrifice and pathology:
- At experiment termination, gross and microscopic pathology evaluated

Results and discussion

Results of examinations

Clinical signs:
no effects observed
Mortality:
no mortality observed
Body weight and weight changes:
not examined
Food consumption and compound intake (if feeding study):
not examined
Food efficiency:
not examined
Water consumption and compound intake (if drinking water study):
not examined
Ophthalmological findings:
not examined
Haematological findings:
no effects observed
Clinical biochemistry findings:
not examined
Urinalysis findings:
no effects observed
Behaviour (functional findings):
not examined
Organ weight findings including organ / body weight ratios:
not examined
Gross pathological findings:
no effects observed
Histopathological findings: non-neoplastic:
effects observed, treatment-related
Histopathological findings: neoplastic:
not examined
Details on results:
CLINICAL SIGNS AND MORTALITY: No signs of toxicity were noted in any of the animals during the course of the study.

HISTOPATHOLOGY: NON-NEOPLASTIC: Microscopically, mild interstitial irritation was observed in the lungs.






Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion

Conclusions:
Under the conditions of this study, there were no signs of toxicity and microscopically only mild interstitial irritation was observed in the lungs of dogs, guinea pigs, and rats exposed to aerosolized test substance.