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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. Tris - Wikipedia

    en.wikipedia.org/wiki/Tris

    Tris is also used as a primary standard to standardize acid solutions for chemical analysis. Tris is used to increase permeability of cell membranes. [ 13 ] It is a component of the Moderna COVID-19 vaccine [ 14 ] and the Pfizer-BioNTech COVID-19 vaccine for use in children 5 through 11 years of age.

  4. Triethylenetetramine - Wikipedia

    en.wikipedia.org/wiki/Triethylenetetramine

    Triethylenetetramine (TETA and trien), also known as trientine when used medically, is an organic compound with the formula [CH 2 NHCH 2 CH 2 NH 2] 2.The pure free base is a colorless oily liquid, but, like many amines, older samples assume a yellowish color due to impurities resulting from air oxidation.

  5. 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 water.

  6. TEA chloride - Wikipedia

    en.wikipedia.org/wiki/TEA_chloride

    Triethylammonium chloride, the hydrochloride salt of triethylamine This page was last edited on 14 May 2022, at 17 ...

  7. Tris(2-aminoethyl)amine - Wikipedia

    en.wikipedia.org/wiki/Tris(2-aminoethyl)amine

    Tris(2-aminoethyl)amine is the organic compound with the formula N(CH 2 CH 2 NH 2) 3.This colourless liquid is soluble in water and is highly basic, consisting of a tertiary amine center and three pendant primary amine groups.

  8. Alkyl ketene dimer - Wikipedia

    en.wikipedia.org/wiki/Alkyl_ketene_dimer

    In 1901, Edgar Wedekind published the synthesis of alkyl ketene dimers by the reaction of carboxylic acid chlorides with tertiary amines: [5] [6] RCH 2 COCl + R 3 N → RCH=C=O + R 3 NHCl The molecular weight determined by the early researchers indicated (CH 3) 2 CH=C=O) n where n > 1 for the dehydrohalogenation of isobutyryl chloride with triethylamine.

  9. Diethylenetriamine - Wikipedia

    en.wikipedia.org/wiki/Diethylenetriamine

    Diethylenetriamine (abbreviated Dien or DETA) and also known as 2,2’-Iminodi(ethylamine) [2]) is an organic compound with the formula HN(CH 2 CH 2 NH 2) 2.This colourless hygroscopic liquid is soluble in water and polar organic solvents, but not simple hydrocarbons.