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  2. Triethylamine - Wikipedia

    en.wikipedia.org/wiki/Triethylamine

    nh 3 + 3 c 2 h 5 oh → n(c 2 h 5) 3 + 3 h 2 o The pK a of protonated triethylamine is 10.75, [ 4 ] and it can be used to prepare buffer solutions at that pH. The hydrochloride salt , triethylamine hydrochloride (triethylammonium chloride), is a colorless, odorless, and hygroscopic powder, which decomposes when heated to 261 °C.

  3. Tetraethylammonium - Wikipedia

    en.wikipedia.org/wiki/Tetraethylammonium

    Tetraethylammonium (TEA) is a quaternary ammonium cation with the chemical formula [Et 4 N] +, consisting of four ethyl groups (−C 2 H 5, denoted Et) attached to a central nitrogen atom. It is a counterion used in the research laboratory to prepare lipophilic salts of inorganic anions.

  4. Tetraethylammonium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Tetraethylammonium_hydroxide

    Tetraethylammonium hydroxide is the organic compound with the formula (C 2 H 5) 4 NOH, abbreviated Et 4 NOH. It is the tetraethylammonium salt of hydroxide. It is used and dispensed as solutions in water or alcohols, which are colorless and highly alkaline. The compound is a common reagent in organic synthesis.

  5. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    Ethylamine, also known as ethanamine, is an organic compound with the formula CH 3 CH 2 NH 2. This colourless gas has a strong ammonia-like odor. It condenses just below room temperature to a liquid miscible with virtually all solvents. It is a nucleophilic base, as is typical for amines.

  6. Triethylammonium acetate - Wikipedia

    en.wikipedia.org/wiki/Triethylammonium_acetate

    teaa, triethylamine/acetate buffer. ... [2] [3] [4] Since unadjusted triethylammonium acetate salt solutions contain neither a conjugate acid nor a conjugate base, ...

  7. Tetraethylammonium iodide - Wikipedia

    en.wikipedia.org/wiki/Tetraethylammonium_iodide

    For example, benzoic acid is converted to the ester, 2-hydroxyethyl benzoate, by treatment with ethylene carbonate in the presence of tetraethylammonium iodide. [ 5 ] Phase-transfer catalyst in geminal di- alkylation of fluorene , N,N-dialkylation of aniline and N-alkylation of carbazole using aqueous sodium hydroxide and alkyl halides .

  8. Burgess reagent - Wikipedia

    en.wikipedia.org/wiki/Burgess_reagent

    The Burgess reagent (methyl N-(triethylammoniumsulfonyl)carbamate) is a mild and selective dehydrating reagent often used in organic chemistry. [1] [2] It was developed in the laboratory of Edward M. Burgess at Georgia Tech.

  9. Anion exchanger family - Wikipedia

    en.wikipedia.org/wiki/Anion_Exchanger_Family

    The anion exchanger family (TC# 2.A.31, also named bicarbonate transporter family) is a member of the large APC superfamily of secondary carriers. [1] Members of the AE family are generally responsible for the transport of anions across cellular barriers, although their functions may vary. All of them exchange bicarbonate. Characterized protein ...