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  2. Triethylamine - Wikipedia

    en.wikipedia.org/wiki/Triethylamine

    Triethylamine is the chemical compound with the formula N(CH 2 CH 3) 3, commonly abbreviated Et 3 N. Like triethanolamine and tetraethylammonium, it is often abbreviated TEA. [8] [9] It is a colourless volatile liquid with a strong fishy odor reminiscent of ammonia.

  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. Triethylammonium acetate - Wikipedia

    en.wikipedia.org/wiki/Triethylammonium_acetate

    Print/export Download as PDF; ... Chemical formula (CH 3 CH 2) 3 NHOCOCH 3 Molar mass: ... Toggle the table of contents. Triethylammonium acetate.

  5. Triethanolamine - Wikipedia

    en.wikipedia.org/wiki/Triethanolamine

    Triethanolamine, or TEOA, is an organic compound with the chemical formula N(CH 2 CH 2 OH) 3. It is a colourless, viscous liquid. It is both a tertiary amine and a triol. A triol is a molecule with three alcohol groups. Approximately 150,000 tonnes were produced in 1999. [3] It is a colourless compound although samples may appear yellow because ...

  6. Ethylammonium nitrate - Wikipedia

    en.wikipedia.org/wiki/Ethylammonium_nitrate

    Ethylammonium nitrate can be produced by heating ethyl nitrate with an alcoholic solution of ammonia [8] or by reacting ethylamine with concentrated nitric acid. [6] It has a relatively low viscosity of 0.28 poise or 0.028 Pa·s at 25 °C and therefore a high electrical conductivity of about 20 mS·cm −1 at 25 °C.

  7. Kornblum oxidation - Wikipedia

    en.wikipedia.org/wiki/Kornblum_oxidation

    The first step is an S N 2 reaction, so it is subject to the usual leaving group limitations of that reaction. While iodides work well, even bromides are often not reactive enough to be displaced by the DMSO.

  8. Triphenylamine - Wikipedia

    en.wikipedia.org/wiki/Triphenylamine

    Triphenylamine is an organic compound with formula (C 6 H 5) 3 N. In contrast to most amines, triphenylamine is nonbasic.At room temperature it appears as a colorless crystalline solid, with monoclinic structure.

  9. Nitroethylene - Wikipedia

    en.wikipedia.org/wiki/Nitroethylene

    The main use of nitroethylene is as an intermediate reagent in chemical synthesis. One example is the production of N-(2-nitroethyl)-aniline with aniline at room temperature. The reaction utilizes benzene as a solvent and proceeds to about 90% yield in 12 hours. [9] Reaction of nitroethylene and aniline