6266-22-4

Basic information

• Product Name: 1-(carboxymethyl)-2-methylpyridinium chloride
• Synonyms: 1-(carboxymethyl)-2-methylpyridinium chloride
• CAS NO: 6266-22-4
• Molecular Formula: C₈H₁₀NO₂*Cl
• Molecular Weight: 187.6235
• EINECS: 228-433-2
• Mol File: 6266-22-4.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(carboxymethyl)-2-methylpyridinium chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(carboxymethyl)-2-methylpyridinium chloride(6266-22-4)
• EPA Substance Registry System: 1-(carboxymethyl)-2-methylpyridinium chloride(6266-22-4)

Safety Data

• Hazardous Substances Data: 6266-22-4(Hazardous Substances Data)

Usage

General Description

1-(carboxymethyl)-2-methylpyridinium chloride is a chemical compound with the formula C8H11NO2Cl. It is an organic salt that consists of a pyridinium cation and a carboxymethyl anion. 1-(carboxymethyl)-2-methylpyridinium chloride is commonly used as a quaternary ammonium compound and is known for its antimicrobial properties. It is often utilized as a disinfectant and preservative in various products such as cosmetics, personal care products, and pharmaceuticals. Additionally, it has been found to have potential applications in the treatment of infections and as an antifungal agent. The compound is generally considered to be a safe and effective biocide and is approved for use in a wide range of consumer and industrial products.

InChI:InChI=1/C8H9NO2.ClH/c1-7-4-2-3-5-9(7)6-8(10)11;/h2-5H,6H2,1H3;1H

Upstream product

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Relevant articles and documents

Valorization of chitin derived N-acetyl-D-glucosamine into high valuable N-containing 3-acetamido-5-acetylfuran using pyridinium-based ionic liquids

Chitin and its derivatives contain biologically fixed nitrogen elements, which can provide nitrogen sources for N-containing chemicals. Herein, a series of pyridinium-based ionic liquids were synthesized to directly catalyze the conversion of N-acetyl-D-glucosamine (NAG, the monomer of chitin) to 3-acetamido-5-acetylfuran (3A5AF). The yield of 3A5AF in 1-carboxymethyl pyridinium chloride ionic liquid reached 37.49%, without any additives. Using B2O3 and CaCl2 as additives, the optimum yield increased to 67.37% at 180 °C in 20 min. In addition, HPLC-MS analysis has been utilized to elucidate the reaction mechanism. This research on turning “waste” into “wealth” opens up new ways for the utilization of biomass waste, which not only reduces environmental pollution but also has potential economic value.

Benzimidazolone as potent chymase inhibitor: Modulation of reactive metabolite formation in the hydrophobic (P1) region

A new class of chymase inhibitor featuring a benzimidazolone core with an acid side chain and a P1 hydrophobic moiety is described. Incubation of the lead compound with GSH resulted in the formation of a GSH conjugate on the benzothiophene P1 moiety. Replacement of the benzothiophene with different heterocyclic systems such as indoles and benzoisothiazole is feasible. Among the P1 replacements, benzoisothiazole prevents the formation of GSH conjugate and an in silico analysis of oxidative potentials agreed with the experimental outcome.

BENZIMIDAZOLONE CHYMASE INHIBITORS

Disclosed are small molecule inhibitors which are useful in treating various diseases and conditions involving chymase.