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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1966
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study well documented, acceptable for assessment

Data source

Reference
Reference Type:
publication
Title:
Untersuchungen zur Toxikologie von Diaethylcarbonat
Author:
Bornmann G & Loeser A
Year:
1966
Bibliographic source:
Arch Toxicol 22, 98-114

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
see below
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Diethyl carbonate
EC Number:
203-311-1
EC Name:
Diethyl carbonate
Cas Number:
105-58-8
Molecular formula:
C5H10O3
IUPAC Name:
diethyl carbonate
Test material form:
other: liquid
Details on test material:
Purity: > 99.5%

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
Weight at study initiation: 200-340 g
Housing: individually
Diet: ad libitum
Water: ad libitum

ENVIRONMENTAL CONDITIONS
Temperature (°C): 26-28

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
olive oil
Details on oral exposure:
Concentration in vehicle: 60 % (w/v)
Doses:
22-37 mL/kg
No. of animals per sex per dose:
5 m / 5 f
Control animals:
not specified
Details on study design:
Duration of observation period following administration: up to 10 days
Necropsy of survivors performed: no data
Other examinations performed: clinical signs
Statistics:
no data

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 15 000 mg/kg bw
Mortality:
yes, but not further specified
Clinical signs:
other: predominant sign of toxicity was narcosis
Gross pathology:
no data

Applicant's summary and conclusion

Interpretation of results:
practically nontoxic
Remarks:
Migrated information Criteria used for interpretation of results: OECD GHS
Conclusions:
In male and female Wistar rats a LD50 value of > 15000 mg/kg bw was reported. The predominant sign of toxicity was narcosis.
Executive summary:

In male and female Wistar rats a LD50 value of > 15000 mg/kg bw was reported. The predominant sign of toxicity was narcosis.