Examples of 'tetraethylammonium' in a sentence
Meaning of "tetraethylammonium"
Tetraethylammonium (noun) - A quaternary ammonium compound with the chemical formula (C2H5)4N+, often used in chemistry and biochemistry research as an electrolyte or phase-transfer catalyst
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- A quaternary ammonium ion (C₂H₅)₄N⁺ containing four ethyl groups.
How to use "tetraethylammonium" in a sentence
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tetraethylammonium
The tetraethylammonium salt is also known.
The opposite effect is observed with tetraethylammonium chloride.
Tetraethylammonium perfluorooctane sulfonate.
A preferred organic cation is tetraethylammonium ion.
Tetraethylammonium perfluorooctane sulphonate.
The preferred organic cation is the tetraethylammonium ion.
By weight of tetraethylammonium hydroxide.
In this arrangement the first component is preferably tetraethylammonium chloride.
Cesium and tetraethylammonium ions block most types of potassium channels.
The preferred phase transfer catalyst used was tetraethylammonium chloride.
This is tetraethylammonium.
The exemplified catalysts are potassium iodide and tetraethylammonium bromide.
TEAC is tetraethylammonium chloride.
Particularly preferred catalysts include tetramethylammonium chloride and tetraethylammonium bromide.
The tetraalkylammonium cation may be tetraethylammonium or tetrabutylammonium but it is not so limited.
See also
Tetraethylammonium hydroxide, in the form of an aqueous solution containing.
The quaternary ammonium salts are exemplified by tetraethylammonium bromide and tetrabutylammonium bromide.
Tetraethylammonium hydroxide or tetra-n-butylammonium hydroxide are also well suited.
Preferably, the tetraalkylammonium iodide is tetraethylammonium iodide.
The solubility of tetraethylammonium iodide in benzene-ethylene dichloride mixtures.
In another embodiment, fluoride is provided as tetraethylammonium fluoride.
Tetramethylammonium hydroxide, tetraethylammonium hydroxide or tetrabutylammonium hydroxide is preferentially chosen.
As an example, such quaternary ammonium salt may be tetraethylammonium hydroxide.
The di-tetraethylammonium salt was prepared by treating this product with tetraethylammonium chloride in water.
Preferably, tetramethylammonium hydroxide, tetraethylammonium hydroxide or tetrabutylammonium hydroxide is used.
Salts of the complex are available with a variety of cations, but a common one is tetraethylammonium.
As the cationic electrolyte, a tetraethylammonium salt and the like are mentioned.
Silyl protecting groups are advantageously split off with fluorides, for example, tetraethylammonium fluoride.
Also in the solution was 90 ppm tetraethylammonium bromide to enhance solution conductivity.
Hofmann successfully converted ammonia into ethylamine and the compounds diethylamine, triethylamine, and tetraethylammonium.
Still more preferred are tetramethylammonium tetrafluoroborate, tetraethylammonium p-toluenesulfonate and tetrabutylammonium perchlorate.
Tetraethylammonium ( 1 mM ) on the cytoplasmic side caused a reversible decrease in the current amplitude.
Process as claimed in claim 2, wherein the electrolyte comprises tetraethylammonium tetrafluoroborate.
Tetramethylammonium chloride and / or tetraethylammonium chloride are even more preferred, and tetramethylammonium chloride is particularly preferred.
According to a preferred embodiment of the present invention, tetraethylammonium hydroxide is used.
Specific examples include without limitation tetraethylammonium hydroxide, tetraethylammonium bromide, diethyldimethylammonium hydroxide and the like.
Quaternary ammonium salts are generally tetraalkylammonium salts, preferably tetraethylammonium or tetrabutylammonium salts.
Preferable quaternary salts are tetraethylammonium chloride, tetraethylammonium bromide, triethylmethylammonium chloride, triethylmethylammonium bromide and the like.
The process of claim 5, wherein the organic template containing tetraethylammonium cations is tetraethylammonium chloride.
Tetraethylammonium hydroxide, tetramethylammonium hydroxide and Na2HPO4 have been found to be particularly effective.
In the present case, approximately one equivalent of tetraethylammonium fluoride was found to be sufficient.
Tetraethylammonium hydroxide solution ( 40 percent ) was added to the sodium hydroxide-sodium aluminate solution.
Typical phase transfer catalysts include benzyltrimethylammonium hydroxide, tetraethylammonium hydroxide and tetrabutylammonium hydroxide.
Tetraethylammonium tetrafluoroborate ( TEABF 4 ) was the supporting electrolyte that was used.
Materials which may be present may include methanol and tetraethylammonium hydroxide, or reaction products thereof.
See also = = * Tetraethylammonium bromide * Tetraethylammonium chloride * Tetraethylammonium iodide = = References.
Specific examples include without limitation tetramethylammonium hydroxide, tetraethylammonium hydroxide, hexamethonium bromide, tetramethylammonium chloride, methyltriethylammonium hydroxide.
The electrolyte is a solution of Y-butyrolactone or propylene carbonate and tetraethylammonium perchlorate.
The product was deprotected with tetraethylammonium fluoride hydrate as in Example 44.
More preferably NR4X is tetramethylammonium fluoride, tetramethylammonium chloride, tetraethylammonium chloride or NHaCl.
