14401-93-5

Usage

Uses

Used in Pharmaceutical Synthesis:
4-methylpyridinium chloride is used as a precursor in the synthesis of various pharmaceuticals, due to its ability to form stable complexes with metal ions, enhancing the development of new drugs.
Used in Agrochemical Production:
In the agrochemical industry, 4-methylpyridinium chloride is utilized as a precursor for the synthesis of various agrochemicals, contributing to the development of effective pesticides and fertilizers.
Used in Dye Manufacturing:
4-methylpyridinium chloride is employed as a starting material in the production of dyes, owing to its chemical properties that facilitate the creation of diverse colorants for various applications.
Used in Materials Science:
4-methylpyridinium chloride is used as a component in the development of ionic liquids and nanoparticle synthesis, capitalizing on its capacity to form stable complexes with a range of metal ions, which is crucial for advancing material technologies.
Used in Disinfectants and Preservatives:
Due to its antimicrobial and antifungal properties, 4-methylpyridinium chloride is considered for use in disinfectants and preservatives, offering potential applications in healthcare and food industries to ensure sterility and prevent spoilage.

InChI:InChI=1/C6H7N.ClH/c1-6-2-4-7-5-3-6;/h2-5H,1H3;1H

Upstream product

• 108-89-4 picoline 
• 6608-47-5 vinylsulfonyl chloride 
• 1358544-05-4 N-(p-fluorophenyldiphenylmethyl)-4-picolinium chloride 

Downstream Products

• 22796-40-3 4-trichloromethyl-pyridine 
• 151477-57-5 α,α,2-trichloro-4-picoline 
• 80636-01-7 2-(4-methoxyphenyl)-4-methylpyridine 

Relevant academic research and scientific papers

Controlling hydrolysis reaction rates with binary ionic liquid mixtures by tuning hydrogen-bonding interactions

The ability of a binary ionic liquid (IL) system consisting of a phosphonium transition state analogue (TSA) and 1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([BMIM][NTf2]) to accelerate the rate of the well-studied hydrolysis of a tert-alkyl picolinium salt by influencing the solvent structure was investigated. A significant rate enhancement was observed in the presence of the TSA; however, comparison with other cations illustrated that this enhancement was not unique to the chosen TSA. Instead, the rate enhancements were correlated with the dilution of hydrogen bonding by the added cations. This phenomenon was further examined by the use of 1-butyl-2,3-dimethylimidazolium bis(trifluoromethanesulfonyl)imide ([BMMIM][NTf2]) as a cosolvent and the use of Reichardt's dye to measure the extent of hydrogen bonding on solutes in these systems. The rate increases are rationalized in terms of weaker hydrogen bonding from the solvent system to water. ? 2012 American Chemical Society.