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...]. Attempts to find anaesthetics with less metabolism led to [[halogenated ethers]] such as [[enflurane]] and [[isoflurane]]. The incidence of hepatic reacti

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...valent chromium, polybrominated biphenyls (PBB) or polybrominated diphenyl ethers (PBDE)."</ref> There are restrictions for mercury concentration in packagin

[[Category:Ethers]]

...special modifiers, organic compounds belonging to the classes of esters or ethers. The pre-catalysts are activated by combinations of organoaluminum compound

...ction products of one or more of the three hydroxyl groups, including: (1) ethers, e.g. methyl cellulose and hydroxyl-ethyl cellulose; (2) esters, e.g. cellu ...llulose ethers has been studied extensively and it is known that cellulose ethers with a DS of less than 1 will degrade due to attack of microorganisms at th

...lso contain organic modifiers, either aromatic acid esters and diesters or ethers. These catalysts are activated with special cocatalysts containing an orga

...kening agent]]s like [[carrageenan]] and [[Cellulose#Derivatives|cellulose ethers]]. Sugar-free syrup will not contribute to [[dental caries]].

Dimethyl ethers of PEG are the key ingredient of [[Selexol]], a solvent used by [[coal]]-bu

...ercial phenyl ether polymers belong to two chemical classes: '''polyphenyl ethers''' ('''PPE'''s) and '''[[Polyphenylene oxide]]s''' ('''PPO'''s). The pheno ...l polyether, but the name polyphenyl ether is widely accepted. Polyphenyl ethers (PPEs) are obtained by repeated application of the [[Ullmann condensation|U

...c hydrocarbons, esters, polyglycols, silicones. polyphenyl and fluorinated ethers are the "raw materials" for Nye lubricants. But the tradition that began mo

...[[ethylene glycol]], ethanolamines, simple and complex glycols, polyglycol ethers and other compounds. It is also a common gas-phase [[disinfectant]] which i Reactions with [[alcohol]]s proceed similarly yielding ethylene glycol ethers:

...ond number refers to the number of those atoms that are [[oxygen]]. Crown ethers are much broader than the oligomers of ethylene oxide; an important group a ...orm salts that are soluble in nonpolar solvents, and for this reason crown ethers are useful in [[phase transfer catalysis]]. The [[ligand|denticity]] of th

...their efforts in discovering and determining uses of cryptands and [[crown ethers]], thus launching the now flourishing field of [[supramolecular chemistry]] ...]], [[alkali]] metals, and [[alkaline earth metals]]. In contrast to crown ethers, cryptands bind the guest ions using both [[nitrogen]] and [[oxygen]] donor

...s a particular affinity for potassium cations. The synthesis of the crown ethers led to the Nobel Prize in Chemistry to [[Charles J. Pedersen]]. Crown ethers are useful as [[phase transfer catalyst]]s.<ref>Liotta, C. L.; Berknerin, J

...but the [[repeating unit]] (ethyleneimine) is always the same. Like crown ethers, cyclen compounds are capable of selectively binding [[cation]]s. They are

...lacrown nomenclature has been developed to mimic the nomenclature of crown ethers, which are named by the total number of atoms in the ring, followed by “C [[Category:Crown ethers]]

|Structures of common crown ethers: [[12-crown-4]], [[15-crown-5]], [[18-crown-6]], [[dibenzo-18-crown-6]], an ...tability constants and thermodynamic functions of metal complexes of crown ethers (IUPAC Technical Report)

...up>3+</sup> and [[Ferricyanide|[Fe(CN)₆]^3-]]. Crown-ethers bind to polyamine complexes through their second coordination sphere.<ref>L

...ground-state; that is, they have lone electron pairs (e.g. water, amines, ethers), so these substrates need an empty orbital to be able to react with a meta

...LM, Howell WC, Woolford RG. TOXIC FLUORINE COMPOUNDS: XIII. ω-FLUOROALKYL ETHERS. ''Canadian Journal of Chemistry''. 1957 Feb;35(2):141-148.]</ref> Fluoroac

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[[Category:Phenol ethers]]

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...omotive antifreeze as well as higher molecular weight glycols and [[glycol ethers]].

[[Category:Ethers]]

| title =Ethers, by Lawrence Karas and W. J. Piel Another reaction that can be used for the preparation of ethers is the [[Williamson ether synthesis]], in which an [[alkoxide]] (produced b

...4-B and GBL are all Class B illegal drugs, along with any possible esters, ethers and aldehydes. GABA itself is also listed as an illegal drug in these juris

*Exposure to [[polybrominated diphenyl ethers]] (PBDEs)