Fluroxene

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Fluroxene
Fluroxene.svg
Clinical data
ATC code
  • None
Identifiers
CAS Number
PubChem CID
ChemSpider
ECHA InfoCard 100.006.344 Edit this at Wikidata
Chemical and physical data
Formula C4H5F3O
Molar mass 126.077 g/mol
3D model (JSmol)

Fluroxene (INN, USAN; brand name Fluoromar), or 2,2,2-trifluoroethyl vinyl ether, is a volatile, inhalational anesthetic, and was the first halogenated hydrocarbon anesthetic to be introduced.[1][2] It was synthesized in 1951, and was introduced for clinical use in 1954, but was voluntarily withdrawn from the market in 1974 due to its potential flammability and accumulating evidence that it could cause organ toxicity.[2][1][3] In any case, prior to being discontinued, it had largely been superseded by halothane.[4] Fluroxene is metabolized to 2,2,2-trifluoroethanol, a compound responsible for some of the toxicity seen with fluroxene use.[5][6]

See also[edit]

References[edit]

  1. ^ a b Robert K. Stoelting; Simon C. Hillier (11 January 2012). Pharmacology and Physiology in Anesthetic Practice. Lippincott Williams & Wilkins. pp. 142–. ISBN 978-1-4511-6583-8. 
  2. ^ a b Paul G Barash; Bruce F Cullen; Robert K Stoelting; Michael Cahalan; M Christine Stock (1 January 2011). Clinical Anesthesia. Lippincott Williams & Wilkins. pp. 113–. ISBN 978-1-4511-2297-8. 
  3. ^ Monte Lichtiger; Frank Moya (1 January 1978). Introduction to the practice of anesthesia. Medical Dept., Harper & Row. ISBN 978-0-06-141534-0. 
  4. ^ Acta anaesthesiologica Belgica. Acta Medica Belgica. 1974. 
  5. ^ V. Fiserova-Bergerova (1977). "Metabolism and toxicity of 2,2,2-trifluoroethyl vinyl ether". Environmental Health Perspectives. 21: 225–230. PMC 1475355Freely accessible. PMID 25763. 
  6. ^ L. S. Kaminsky & J. M. Fraser (1988). "Multiple aspects of the toxicity of fluroxene and its metabolite 2,2,2-trifluoroethanol". Critical reviews in toxicology. 19 (2): 87–112. doi:10.3109/10408448809014901. PMID 2906849.