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|Systematic (IUPAC) name|
|ATC code||N01AB04 (WHO)|
|Molar mass||184.492 g/mol[[Script error: No such module "String".]]|
Enflurane (2-chloro-1,1,2,-trifluoroethyl-difluoromethyl ether) is a halogenated ether that was commonly used for inhalational anesthesia during the 1970s and 1980s. Developed by Ross Terrell in 1963, it was first used clinically in 1966.
Enflurane is a structural isomer of isoflurane. It vaporizes readily, but is a liquid at room temperature.
|Boiling point at 1 atm||56.5 °C|
|Vapor pressure at 20 °C||22.9 kPa (172 mm Hg)|
|Blood: Gas Partition Coefficient||1.9|
|Oil: Gas Partition Coefficient||98|
Clinically, enflurane produces a dose-related depression of myocardial contractility with an associated decrease in myocardial oxygen consumption. Between 2% and 5% of the inhaled dose is oxidised in the liver, producing fluoride ions and difluoromethoxy-difluoroacetic acid. This is significantly higher than the metabolism of its structural isomer isoflurane.
Enflurane also lowers the threshold for seizures and should especially not be used on people with epilepsy. It is also known to cause malignant hyperthermia.
Relaxes the uterus in pregnant women.
Enflurane and Methoxyflurane have a nephrotoxic effect and cause acute renal failure usually by its nephrotoxic metabolite. By G. Edward Morgan, Maged S. Mikhail, Michael J. Murray, C. Philip Larson; clinical anaesthesiology third edition,142.
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de:Enfluran fa:انفلوران fr:Enflurane it:Enflurano nl:Enfluraan ja:エンフルラン pt:Enflurano
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