6427-70-9

Usage

Uses

Used in Organic Synthesis:
BENZYLTRIMETHYLAMMONIUM HEXAFLUOROPHOSPHATE is used as a phase-transfer catalyst for enhancing the efficiency of chemical reactions. Its ability to transfer ions or molecules between immiscible phases allows for smoother reaction processes and improved yields.
Used in Ion Exchange Chromatography:
In the industry of ion exchange chromatography, BENZYLTRIMETHYLAMMONIUM HEXAFLUOROPHOSPHATE is used as a cation-exchange resin. This application capitalizes on its structural properties to effectively separate ions during the chromatographic process.
Used in Industrial Processes:
BENZYLTRIMETHYLAMMONIUM HEXAFLUOROPHOSPHATE is utilized as a key reagent in various industrial applications. Its high efficiency and wide-ranging applicability make it an indispensable tool for numerous chemical processes and reactions.

InChI:InChI=1/C10H16N.F6P/c1-11(2,3)9-10-7-5-4-6-8-10;1-7(2,3,4,5)6/h4-8H,9H2,1-3H3;/q+1;-1

Upstream product

• 16056-11-4 N,N,N-trimethylanilinium bromide 
• 5350-41-4 trimethylbenzylammonium bromide 

Downstream Products

• 62992-33-0 ethoxy-N,N-dimethylaminomethane 
• 28149-27-1 N,N-dimethylmethyleneammonium ion 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 108-88-3 toluene 
• 75-50-3 trimethylamine 
• 39580-58-0 bis-trideuteriomethoxy-methane 

Relevant academic research and scientific papers

Catechol[4]arene: The Missing Chiral Member of the Calix[4]arene Family

A missing, inherently chiral member of the calix[4]arene family denoted catechol[4]arene was synthesized. Its properties were studied and compared to the ones of its close relatives resorcin[4]arene and pyrogallol[4]arene. This novel supramolecular host exhibits binding capabilities that are superior to its sister molecules in polar media. The enantiomerically pure forms of the macrocycle display modest recognition of chiral ammonium salts.

Effects of Quaternary Ammonium Salts on Reactions of Aromatic radical Anions Formed in Tetrahydrofuran by Pulse Radiolysis

Pulse radiolysis of biphenyl (BP) and pyrene (Py) in tetrahydrofuran (THF) solution was carried out in the presence of various kinds of quaternary ammonium salts, such as Bu4NPF6, Bu4NBF4, Bu4NI, BzMe3NPF6 and PhMe3NPF6 (Bu, butyl; Me, mthyl; Bz, benzyl; and Ph, phenyl).The decay behaviors of the radical anions, BP-. and Py-., are significantly affected by the addition of the salts.The anions of the salts, PF6-, BF4-, and I-, are considered to form ion pairs with the solvent counterions, THF(H+), resulting in a retardation of the neutralization reactions.The rate constants for the neutralization reactions have been determined in the absence and presence of Bu4NPF6.The addition of BzMe3NPF6 (or PhMe3NPF6) accelerates the decay of BP-. and retards the decay of Py-., depending on the rates of reactions of the radical anions with BzMe3N+ (or PhMe3N+).The reactivity of BP-. in the electron transfer to Py seems to be reduced in the presence of Bu4NPF6.The effect of Bu4N+ on the reactions of the radical anions is discussed.