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  2. Triethylamine - Wikipedia

    en.wikipedia.org/wiki/Triethylamine

    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. Triethylamine is soluble in water to the extent of 112.4 g/L at ...

  3. Triethanolamine - Wikipedia

    en.wikipedia.org/wiki/Triethanolamine

    Triethanolamine is used primarily in making surfactants, such as for emulsifier.It is a common ingredient in formulations used for both industrial and consumer products. The triethanolamine neutralizes fatty acids, adjusts and buffers the pH, and solubilizes oils and other ingredients that are not completely soluble in wate

  4. Triethylammonium acetate - Wikipedia

    en.wikipedia.org/wiki/Triethylammonium_acetate

    This page was last edited on 8 September 2024, at 15:40 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  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.

  6. 1-Ethyl-3- (3-dimethylaminopropyl)carbodiimide - Wikipedia

    en.wikipedia.org/wiki/1-Ethyl-3-(3-dimethylamino...

    1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC, EDAC or EDCI) is a water-soluble carbodiimide usually handled as the hydrochloride. [1]It is typically employed in the 4.0-6.0 pH range.

  7. Tetraethylammonium iodide - Wikipedia

    en.wikipedia.org/wiki/Tetraethylammonium_iodide

    Examples include: Stereoselective formation of (Z)-diiodoalkenes by treatment of alkynes with ICl in the presence of tetraethylammonium iodide. [4]2-Hydroxyethylation (attachment of −CH 2 −CH 2 −OH) by ethylene carbonate of carboxylic acids and certain heterocycles bearing an acidic N-H.

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  9. Triethylaluminium - Wikipedia

    en.wikipedia.org/wiki/Triethylaluminium

    Triethylaluminium can be formed via several routes. The discovery of an efficient route was a significant technological achievement. The multistep process uses aluminium, hydrogen gas, and ethylene, summarized as follows: [4]