Halogenated ether
Halogenated ethers are a subcategory of ethers—organic chemicals that containan oxygen atom connected to two alkyl groups or similar structures. An example of an ether is the solvent diethyl ether.[1] Halogenated ethers differ from other ethers because there are one or more halogen atoms—fluorine, chlorine, bromine, or iodine—as substituents on the carbon groups. .[2] Examples of commonly used halogenated ethers include isoflurane, sevofluorane and desflurane.[3]
History
[edit]
An ideal inhaled anesthetic wasn't found until 1950. Volatile substances like diethyl ether, which have severe risks of nausea, were used before.[4] Diethyl ether has the unfortunate disadvantage of being extremely flammable, especially in the presence of enriched oxygen mixtures.[5]
James Young Simpson, an obstetrics surgeon, used ethers to help women relieve their labor pains but ultimately deemed them unsuitable due to their drawbacks. Simpson and his friends tested the halogenated hydrocarbon, chloroform, as a substitute inhalation agent during a house party. They woke from unconsciousness pleasantly surprised with its effectiveness. This was the first recorded successful use of halogenated hydrocarbons as anesthetics.[4]
Applications
[edit]Anesthesia
[edit]Inhaled agents like diethyl ether are critical in anesthesia. Diethyl ether initially replaced non-flammable (but more toxic) halogenated hydrocarbons like chloroform and trichloroethylene. Halothane is a halogenated hydrocarbon anesthetic agent that was introduced into clinical practice in 1956. Due to its ease of use and improved safety profile with respect to organ toxicity, halothane quickly replaced chloroform and trichloroethylene.[6]
The anesthesia practice was significantly improved later in the 1950s with the introduction of halogenated ethers, like isoflurane, enflurane, and sevoflurane. Since its introduction in the 1980s, isoflurane has been widely used due to its decreased risk of hepatotoxicity and better hemodynamic stability when compared to halothane. The 1990s saw the development of sevoflurane, which was especially helpful in pediatric anesthesia because it provided even faster induction and recovery profiles.[7]
All inhalation anesthetics in current clinical use are halogenated ethers, except for halothane (which is a halogenated hydrocarbon or haloalkane), nitrous oxide, and xenon.[8]
Inhalation anesthetics are vaporized and mixed with other gases prior to their inhalation by the patient before or during surgery. These other gases always include oxygen or air, but may also include other gases such as nitrous oxide or helium. In most surgical situations, other drugs such as opiates are used for pain and skeletal muscle relaxants are used to cause temporary paralysis. Additional drugs such as midazolam may be used to produce amnesia during surgery. Although newer intravenous anesthetics (such as propofol) have increased the options of anesthesiologists, halogenated ethers remain a mainstay of general anesthesia. [9]
Polymers
[edit]Perfluorinated epoxides can be used as used as comonomers for the production of polytetrafluoroethylene (PTFE). [10]
Perfluorinated epoxides are a class of epoxides where all the hydrogen atoms on a carbon chain are replaced with fluorine atoms. The fluorine ensures compatibility with PTFE, while the epoxy group enables chemical bonding during polymerization. When used as comonomers, they can alter the microstructure of PTFE, reducing crystallinity and improving flexibility and toughness. This makes the polymer more suitable for applications like seals and gaskets, which require resilience under stress. Furthermore, perfluorinated epoxides enable the tailoring of specific functional properties, such as low surface energy, which is essential for applications requiring non-stick or low-friction surfaces. [10][11]
Flame Retardant
[edit]Halogenated ethers play a significant role in enhancing the thermal stability and fire resistance of polymers. When applied to materials, they are effective in preventing items from catching fire because of the chemical's resistance to decomposition and effective flame suppression properties. [12]
Most halogenated ethers contain bromine or chlorine. Brominated compounds are particularly effective because they release bromine radicals when exposed to heat. These radicals interrupt the combustion process by reacting with free radicals in the flame, thereby suppressing fire propagation. Chlorinated ethers can also function similarly by releasing chlorine radicals. Both types of halogens contribute to the flame-retardant properties, but brominated ethers are often favoured for their higher efficiency and lower required concentrations compared to their chlorinated counterparts. [12]
Decabromodiphenyl ether (deca-BDE), a type of Polybrominated diphenyl ether (PBDEs), is a brominated flame retardant. It was widely used in polystyrene, acrylonitrile butadiene styrene (ABS), flexible polyurethane foam, textile coatings, wire/cable insulation, electrical connectors, and other interior parts. Decabromodiphenyl ether is one of many halogenated flame retardants that are now are heavily regulated or banned in many regions because of bioaccumulation and potential toxicity hazards. Most industries are now transitioning to alternative, less hazardous flame retardants. However, because of the widespread use of these chemicals in many products, it is anticipated that they will continue to persist in the environment.
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Tetrabromobisphenol A bis(2,3-dibromopropyl) ether (TBBPA-DBPE) is another type of brominated flame retardant. It is widely used in electronic casings and circuit boards due to its high efficiency in reducing flammability. TBBPA-DBPE is also a flame retardant in plastics, paper, and textiles, and as plasticizer in adhesives and coatings. [13]
Common halogenated ethers
[edit]| Halogenated Ether | Chemical Formula | Chemical Structure | Use |
|---|---|---|---|
| Sevoflurane | C4H3F7O |  |
Induction and maintenance of general anesthesia for adults and children. [14] |
| Isoflurane | C3H2ClF5O |  |
Induction and maintenance of general anesthesia for adults and children. [15] |
| Desflurane | C3H2F6O | 
|
Induction and maintenance of general anesthesia for adults. Maintenance in children following induction by other agents. [16] |
| Methoxyflurane | C3H4Cl2F2O | 
|
Short term pain relief; rarely used for chronic pain or as an anesthetic because of nephrotoxicity risks. [17] |
| Enflurane | C3H2ClF5O | 
|
Induction and maintenance of general anesthesia. Used to reduce pain during vaginal delivery. [18] |
Toxicology
[edit]Respiratory Depression
[edit]Halogenated ethers can cause respiratory depression by reducing the body's response to carbon dioxide and hypoxia, which affects breathing rates and depth. Some, like desflurane and isoflurane, are also known for causing airway irritation. This can cause coughing, breath-holding, or laryngospasm, particularly during inhalational induction of anesthesia. Sevoflurane has minimal airway irritation and is generally preferred for induction, particularly in children or those with sensitive airways. [19]
Environmental Impact
[edit]Greenhouse Gas Emissions
[edit]Halogenated ethers are greenhouse gases and contribute to global warming. Compounds like desflurane and isoflurane have high global warming potentials (GWP), which measure their heat-trapping abilities relative to carbon dioxide (CO₂). The GWP of a halogenated anesthetic is up to 2,000 times greater than CO₂. The use of these anesthetics in healthcare is a significant contributor to hospital-related greenhouse gas emissions. There is a growing focus on identifying lower-GWP alternatives or enhancing recovery and recycling technologies for anesthetic gases. [20]
Persistence and Bioaccumulation
[edit]Halogenated ethers can persist in the atmosphere for years due to their stability. These compounds do not readily degrade and thus remain in circulation long after their release, adding to the atmospheric burden of greenhouse gases. They are generally not bioaccumulative due to its high volatility and low tendency to dissolve in water or adhere to biological tissues, but the persistent nature of these compounds raises concerns for long-term environmental effects. This is especially concerning in areas surrounding healthcare facilities where they may be routinely released. [21]
See also
[edit]References
[edit]- ^ "Ether | Chemical Structure & Properties | Britannica". www.britannica.com. 2024-11-29. Retrieved 2024-12-02.
- ^ Tang, Shaokun; Baker, Gary A.; Zhao, Hua (2012). "Ether- and alcohol-functionalized task-specific ionic liquids: attractive properties and applications". Chemical Society Reviews. 41 (10): 4030–4066. doi:10.1039/c2cs15362a. ISSN 0306-0012. PMC 3341508. PMID 22456483.
- ^ Bertram-Ralph, Elliott; Amare, Muataz (2022-01-01). "Inhalational anaesthesia". Anaesthesia & Intensive Care Medicine. 23 (1): 60–68. doi:10.1016/j.mpaic.2021.10.003. ISSN 1472-0299.
- ^ a b Whalen, Francis X.; Bacon, Douglas R.; Smith, Hugh M. (2005-09-01). "Inhaled anesthetics: an historical overview". Best Practice & Research Clinical Anaesthesiology. Renaissance of Inhalational Anaesthesia. 19 (3): 323–330. doi:10.1016/j.bpa.2005.02.001. ISSN 1521-6896.
- ^ insideout (2015-04-27). "Understanding the Safety Risks of Diethyl Ether". VelocityEHS. Retrieved 2024-11-04.
- ^ "Halothane". go.drugbank.com. Retrieved 2024-11-04.
- ^ Goa, Karen L.; Noble, Stuart; Spencer, Caroline M. (1999-04-01). "Sevoflurane in Paediatric Anaesthesia". Pediatric Drugs. 1 (2): 127–153. doi:10.2165/00128072-199901020-00005. ISSN 1179-2019. PMID 10937447.
- ^ Miller, Amanda L.; Theodore, Danny; Widrich, Jason (2024), "Inhalational Anesthetic", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 32119427, retrieved 2024-11-04
- ^ Clar, Derek T.; Patel, Samir; Richards, John R. (2024), "Anesthetic Gases", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30725698, retrieved 2024-11-04
- ^ a b Siegemund, Günter; Schwertfeger, Werner; Feiring, Andrew; Smart, Bruce; Behr, Fred; Vogel, Herward; McKusick, Blaine; Kirsch, Peer (2016-01-28). "Fluorine Compounds, Organic". Ullmann's Encyclopedia of Chemical Technology. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA. pp. 1–56. doi:10.1002/14356007.a11_349.pub2. ISBN 978-3-527-30673-2.
- ^ Cı́rkva, Vladimı́r; Gaboyard, Manuel; Paleta, Oldřich (2000-03-01). "Fluorinated epoxides: 5. Highly selective synthesis of diepoxides from α,ω-diiodoperfluoroalkanes. Regioselectivity of nucleophilic epoxide-ring opening and new amphiphilic compounds and monomers". Journal of Fluorine Chemistry. 102 (1): 349–361. Bibcode:2000JFluC.102..349C. doi:10.1016/S0022-1139(99)00301-2. ISSN 0022-1139.
- ^ a b Martinez, Guillaume; Niu, Jianjun; Takser, Larissa; Bellenger, Jean-Phillipe; Zhu, Jiping (2021-09-15). "A review on the analytical procedures of halogenated flame retardants by gas chromatography coupled with single quadrupole mass spectrometry and their levels in human samples". Environmental Pollution. 285: 117476. Bibcode:2021EPoll.28517476M. doi:10.1016/j.envpol.2021.117476. ISSN 0269-7491. PMC 8355089. PMID 34082369.
- ^ Knudsen, Gabriel A.; Hughes, Michael F.; Birnbaum, Linda S. (2019-02-01). "Dermal disposition of Tetrabromobisphenol A Bis(2,3-dibromopropyl) ether (TBBPA-BDBPE) using rat and human skin". Toxicology Letters. 301: 108–113. doi:10.1016/j.toxlet.2018.11.011. ISSN 0378-4274. PMC 6309208. PMID 30481582.
- ^ "Sevoflurane (inhalation route)". Mayo Clinic. Retrieved 2024-12-01.
- ^ "Isoflurane (inhalation route)". Mayo Clinic. Retrieved 2024-12-01.
- ^ Khan, Joohi; Patel, Preeti; Liu, Mark (2024), "Desflurane", StatPearls, Treasure Island (FL): StatPearls Publishing, PMID 30725791, retrieved 2024-12-01
- ^ Methoxyflurane Inhalation as an Analgesic for Minor Gynecological, Ambulatory, or Emergency Procedures: Rapid Review. CADTH Health Technology Review. Ottawa (ON): Canadian Agency for Drugs and Technologies in Health. 2024. PMID 39466939.
- ^ PubChem. "Enflurane". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-12-01.
- ^ TerRiet, M. F.; DeSouza, G. J. A.; Jacobs, J. S.; Young, D.; Lewis, M. C.; Herrington, C.; Gold, M. I. (2000-08-01). "Which is most pungent: isoflurane, sevoflurane or desflurane?". British Journal of Anaesthesia. 85 (2): 305–307. doi:10.1093/bja/85.2.305. ISSN 0007-0912.
- ^ Gadani, Hina; Vyas, Arun (2011-06-01). "Anesthetic gases and global warming: Potentials, prevention and future of anesthesia". Anesthesia Essays and Researches. 5 (1): 5–10. doi:10.4103/0259-1162.84171. ISSN 0259-1162. PMC 4173371. PMID 25885293.
- ^ Wu, Qiong; Munschy, Catherine; Bodin, Nathalie; Vetter, Walter (2024-07-17). "Persistent and Bioaccumulative Halogenated Natural Products in Various Tropical Reef Fish Species from the Seychelles, Western Indian Ocean". Journal of Agricultural and Food Chemistry. 72 (28): 15643–15652. Bibcode:2024JAFC...7215643W. doi:10.1021/acs.jafc.4c03503. ISSN 1520-5118. PMID 38967173.