Quaternary ammonium cation

Quaternary ammonium compounds are prepared by the alkylation of tertiary amine. Industrial production of commodity quat salts usually involves hydrogenation of fatty nitriles, which can generate primary or secondary amines. These amines are then treated with methyl chloride.[4]

The quaternization of alkyl amines by alkyl halides is widely documented.[5] In older literature this is often called a Menshutkin reaction, however modern chemists usually refer to it simply as quaternization.[6] The reaction can be used to produce a compound with unequal alkyl chain lengths; for example when making cationic surfactants one of the alkyl groups on the amine is typically longer than the others.[7] A typical synthesis is for benzalkonium chloride from a long-chain alkyldimethylamine and benzyl chloride:

${\displaystyle {\ce {CH3(CH2)_{\mathit {n}}N(CH3)2{}+ClCH2C6H5->{}[CH3(CH2)_{\mathit {n}}N(CH3)2CH2C6H5]+Cl-}}}$

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. The halflife of Me₄NOH in 6M NaOH at 160 °C is >61 h.[8]

Because of their resilience, many unusual anions have been isolated as the quaternary ammonium salts. Examples include tetramethylammonium pentafluoroxenate, containing the highly reactive pentafluoroxenate (XeF⁻
₅) ion. Permanganate can be solubilized in organic solvents, when deployed as its NBu⁺
₄ salt.[9][10]

With exceptionally strong bases, quat cations degrade. They undergo Sommelet–Hauser rearrangement[11] and Stevens rearrangement,[12] as well as dealkylation under harsh conditions or in presence of strong nucleophiles, like thiolates. Quaternary ammonium cations containing N−C−C−H units can also undergo the Hofmann elimination and Emde degradation.

• Tetramethylammonium ion: (CH₃)₄N⁺, also denoted Me₄N⁺ (Me = methyl group)
• Tetraethylammonium ion: (C₂H₅)₄N⁺, also denoted Et₄N⁺ (Et = ethyl group)
• Tetrapropylammonium ion: (n-C₃H₇)₄N⁺, also denoted Pr₄N⁺ (Pr = propyl group)
• Tetrabutylammonium ion: (n-C₄H₉)₄N⁺, also denoted Bu₄N⁺ (Bu = butyl group)

Quaternary ammonium salts are used as disinfectants, surfactants, fabric softeners, and as antistatic agents (e.g. in shampoos). In liquid fabric softeners, the chloride salts are often used. In dryer anticling strips, the sulfate salts are often used. Older aluminium electrolytic capacitors and spermicidal jellies also contain quaternary ammonium salts. Quats are also used in contraception formulations, veterinary products, diagnostic testing, vaccine production, and nasal formulations. [14]

Concerns have been raised about the level of understanding of safety profile of quat disinfectants on people. As of August 2020, half of disinfectants the United States Environmental Protection Agency suggested as effective against COVID-19 contained one of the quats, and often a quat as the sole ingredient.[15] Salmonella and E. coli O157:H7 exposed to quats have developed cross resistance to antibiotics. A subject of concern is the potential effect of increased use of quats related to COVID-19 pandemic on antibiotic resistance in a larger microbial community in nature and engineered environment.[16]

Several quaternary ammonium derivatives exist in nature.[33] Prominent examples include glycine betaine, choline, carnitine. butyrobetaine, homarine, and trigonelline. Glycine betaine, an osmolyte, stabilizes osmotic pressure in cells.[34]

Choline is a precursor for the neurotransmitter acetylcholine. Choline is also a constituent of lecithin, which is present in many plants and animal organs.[35] It is found in phospholipids. For example, phosphatidylcholines, a major component of biological membranes, are a member of the lecithin group of fatty substances in animal and plant tissues.[36]

Carnitine participates in the beta-oxidation of fatty acids.

Quaternary ammonium compounds can display a range of health effects, amongst which are mild skin and respiratory irritation [37] up to severe caustic burns on skin and the gastrointestinal wall (depending on concentration), gastrointestinal symptoms (e.g., nausea and vomiting), coma, convulsions, hypotension and death.[38]

They are thought to be the chemical group responsible for anaphylactic reactions that occur with use of neuromuscular blocking drugs during general anaesthesia in surgery.[39] Quaternium-15 is the single most often found cause of allergic contact dermatitis of the hands (16.5% in 959 cases).[40]

The quantification of quaternary ammonium compounds can be challenging. Some methods include precipitation of solid salts with tetraphenylborate. Another method, an Epton titration, involves partitioning between water-chloroform in the presence of an anionic dye. Individual cations are detectable by ESI-MS and NMR spectroscopy.[4]

• Ammonium
• Benzyltrimethylammonium fluoride
• Iminium

• "Toxicities of quaternary ammonium". Internationally Peer Reviewed Chemical Safety Information (INCHEM). World Health Organization.