Enflurane
File:Enflurane2.png | |
File:Enflurane-3D-balls.png | |
Clinical data | |
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ATC code | |
Pharmacokinetic data | |
Protein binding | 97% |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C3H2ClF5O |
Molar mass | 184.492 g/mol |
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.
Physical properties
Property | Value |
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Boiling point at 1 atm | 56.5 °C |
MAC | 1.68 |
Vapor pressure at 20 °C | 22.9 kPa (172 mm Hg) |
Blood: Gas Partition Coefficient | 1.9 |
Oil: Gas Partition Coefficient | 98 |
Side Effects
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.
External links
de:Enfluran it:Enflurano nl:Enfluraan Template:WikiDoc Sources
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- Anesthetics
- Ethers
- Organohalides