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  Vol. 73 No. 5, November 1956 TABLE OF CONTENTS
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Anesthetic Properties of Trifluoroethyl Vinyl Ether and Common Ethers

ERNST TRIER MORCH, M.D., Ph.D.; GEORGE EDWARD COADE, B.A., B.S.

AMA Arch Surg. 1956;73(5):768-774.

Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings.

The purpose of this investigation is to compare the anesthetic effectiveness of one of the less explosive ethers, trifluoroethyl vinyl ether, with well known ethers.

It is known that halogenation of organic compounds decreases their flammability. The substitution of chlorine atoms in the methane molecule shows progressively decreasing flammability to where the triple and tertiary substituted compounds, chloroform and carbon tetrachloride, can be used as fire extinguishers. Halogenation also increases toxicity, e. g., carbon tetrachloride is an anesthetic but lethal at surgical levels. Fluorine has the same property of diminishing flammability in compounds but is less toxic and more stable. Trifluorethyl vinyl ether (Fluoromar) is a colorless liquid having a pleasant, sweetish odor. The physical properties of the ethers used in these studies are given in Table 1.

In studies of trifluorethyl vinyl ether by Krantz and co-workers, in 1953,1 four dogs and one monkey were anesthetized by means . . . [Full Text PDF of this Article]


Author Affiliations

Chicago

Department of Surgery, Division of Anesthesia, The University of Chicago. Professor of Surgery and Director of Anesthesia (Dr. Mörch).


Footnotes

Submitted for publication April 7, 1956.

The trifluoroethyl vinyl ether (Fluoromar) used in these experiments was supplied by the Ohio Chemical & Surgical Equipment Company.



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