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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Comparable to guideline study with acceptable restrictions. Restriction: purity of TS not reported; non-fasted animals; no data about vehicle; no data about clinical signs, necropsy or body weight.

Data source

Reference
Reference Type:
publication
Title:
Range-finding toxicity data: List VII.
Author:
Smyth HF, Carpenter CP, Weil CS, Pozzani U, Striegel JA, Nygum JS
Year:
1969
Bibliographic source:
Am Ind Hyg Assoc J 30: 470-476

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
no
Principles of method if other than guideline:
Methods according to Smyth et al., Am Ind Hyg Assoc J 23: 95ff (1962).
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Ethyl vinyl ether
EC Number:
203-718-4
EC Name:
Ethyl vinyl ether
Cas Number:
109-92-2
Molecular formula:
C4H8O
IUPAC Name:
ethoxyethene
Details on test material:
Ethyl vinyl ether, no further data

Test animals

Species:
rat
Strain:
Wistar
Sex:
male
Details on test animals or test system and environmental conditions:
Male Carworth-Wistar rats were used, four to five weeks of age and 90 to 120 g in weight. Animals were kept on complete diet.

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
not specified
Details on oral exposure:
no further details
Doses:
Dose levels were arranged in a logarithmic series differing by a factor of 2.
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
Post exposure observation period 14 days
Statistics:
LD50-values were estimated by the method of Thompson using the tables of Weil, based on mortalities.

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
6 150 mg/kg bw
95% CL:
5 300 - 7 150
Remarks on result:
other: original value: 8.16 mL/kg bw

Any other information on results incl. tables

No further details given. 
Density: 0.754 g/mL at 20°C.

Applicant's summary and conclusion

Conclusions:
The LD50 in male Wistar rats was 8.16 mL/kg bw corresponding to 6150 mg/kg bw; the post exposure observation period was 14 days.