Ad
related to: quaternary ammonium salt
Search results
Results From The WOW.Com Content Network
Quaternary ammonium cations are unreactive toward even strong electrophiles, oxidants, and acids.They also are stable toward most nucleophiles.The latter is indicated by the stability of the hydroxide salts such as tetramethylammonium hydroxide and tetrabutylammonium hydroxide even at elevated temperatures.
Berberine is a quaternary ammonium salt from the protoberberine group of benzylisoquinoline alkaloids, occurring naturally as a secondary metabolite in some plants including species of Berberis, from which its name is derived. Due to their yellow pigmentation, raw Berberis materials were once commonly used to dye wool, leather, and wood. [4]
Dimethyldioctadecylammonium chloride (also commonly distearyl dimethyl ammonium chloride or distearyldimonium chloride) is an organic compound classified as quaternary ammonium salt. The nitrogen center substituted with two methyl groups and two stearyl groups.
It is a quaternary ammonium salt, consisting of choline cations ([(CH 3) 3 NCH 2 CH 2 OH] +) and chloride anions (Cl −). It is a bifunctional compound, meaning, it contains both a quaternary ammonium functional group and a hydroxyl functional group. The cation of this salt, choline, occurs in nature in living beings. [2]
Tetramethylammonium (TMA) is the simplest quaternary ammonium cation. It has the chemical formula [Me 4 N] + and consists of four methyl groups (−CH 3, denoted Me) attached to a central nitrogen atom. The cation is isoelectronic with neopentane (Me 4 C). It is positively-charged and can only be isolated in association with a counter-ion.
In another use of the term in organic chemistry, a quaternary compound is or has a cation consisting of a central positively charged atom with four substituents, especially organic (alkyl and aryl) groups, discounting hydrogen atoms. [1] The best-known quaternary compounds are quaternary ammonium salts, having a nitrogen atom at the center. [2]
In organic chemistry, the Menshutkin reaction converts a tertiary amine into a quaternary ammonium salt by reaction with an alkyl halide. Similar reactions occur when tertiary phosphines are treated with alkyl halides. Menshutkin-reaction. The reaction is the method of choice for the preparation of quaternary ammonium salts. [1]
Benzyltrimethylammonium hydroxide, also known as Triton B or trimethylbenzylammonium hydroxide, is a quaternary ammonium salt that functions as an organic base. It is usually handled as a solution in water or methanol. The compound is colourless, although the solutions often appear yellowish. [1]