46917-07-1

Basic information

• Product Name: METHACRYLOYL OXYETHYL DIMETHYLBENZYL AMMONIUM CHLORIDE
• Synonyms: METHACRYLOYL OXYETHYL DIMETHYLBENZYL AMMONIUM CHLORIDE;benzyldimethyl[2-[(2-methyl-1-oxoallyl)oxy]ethyl]ammonium chloride;Dimethylaminoethyl methacrylate benzylchloride salt;(Methacryloyloxyethyl)benzyldimethylammonium chloride;Benzenemethanaminium, N,N-dimethyl-N-2-(2-methyl-1-oxo-2-propenyl)oxyethyl-, chloride;N-Benzyl-N,N-dimethyl-N-[2-(methacryloyloxy)-ethyl]-ammonium chloride;[2-(Methacryloyloxy)ethyl]benzyldimethylaminium·chloride;[2-(Methacryloyloxy)ethyl]dimethylbenzylaminium·chloride
• CAS NO: 46917-07-1
• Molecular Formula: C15H20ClNO2
• Molecular Weight: 281.7778
• EINECS: 256-288-5
• Mol File: 46917-07-1.mol
• Article Data: 5

Chemical Properties

• Melting Point: 108-110 °C
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: METHACRYLOYL OXYETHYL DIMETHYLBENZYL AMMONIUM CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: METHACRYLOYL OXYETHYL DIMETHYLBENZYL AMMONIUM CHLORIDE(46917-07-1)
• EPA Substance Registry System: METHACRYLOYL OXYETHYL DIMETHYLBENZYL AMMONIUM CHLORIDE(46917-07-1)

Safety Data

• Hazardous Substances Data: 46917-07-1(Hazardous Substances Data)

Usage

General Description

Methacryloyl oxyethyl dimethylbenzyl ammonium chloride is a chemical compound that is commonly used in the production of polymers and as a disinfectant in various industrial and commercial applications. It is an ammonium salt with a quaternary ammonium group and a methacryloyl group, making it an effective antistatic agent and a powerful bactericide. METHACRYLOYL OXYETHYL DIMETHYLBENZYL AMMONIUM CHLORIDE is also used in the formulation of hair care products, where it acts as a conditioning agent and a preservative. Additionally, it is utilized in medical devices, water treatment systems, and as an antibacterial agent in various consumer products.

InChI:InChI=1/C15H22NO2.ClH/c1-13(2)15(17)18-11-10-16(3,4)12-14-8-6-5-7-9-14;/h5-9H,1,10-12H2,2-4H3;1H/q+1;/p-1

Upstream product

• 2867-47-2 2-(dimethylamino)ethyl methacrylate 
• 100-44-7 benzyl chloride 

Relevant articles and documents

Properties of polyelectrolytes prepared by polymerization of ionogenic monomers in micellar solutions of sodium dodecyl sulfate

The properties of polyelectrolytes obtained by the free radical and template polymerization of N-ethyl-N,N-dimethyl-N-methacryloyloxyethylammonium bromide, trimethylmethacryloyloxyethylammonium methyl sulfate, and [N-benzyl-N,N-dimethyl-N-(methacryloyloxyethyl)]ammonium chloride in micellar solutions of sodium dodecyl sulfate were studied by static and dynamic light scattering, viscosimetry, and differential refractometer. It was shown that the solubility of the polymerization products, being polyelectrolyte - surfactant complexes, is determined by the composition of the reaction mixture and chemical nature of the monomer. The introduction of a surfactant into the polymerization medium noticeably decreases the molecular weight of the formed polymers.

Titanium electrode modified by nano-PMDAH as a highly efficient polymer for removal of Reactive Red 13 using solar cells for energy-harvesting applications

Reactive and Azo dyes are among the major pollutants of surface water. As these dyes can be toxic, carcinogenic, and mutagenic, their contamination can bring about detrimental effects on public health. This study is an attempt to decolorization of a dye solution Reactive Red 13 (RR13), using a titanium electrode modified by a nano-polymer of methacryloxyethyl dimethylbenzyl ammoniumchloride homopolymer (PMDAH). The energy for conducting the experiment was supplied by solar cells. The optimum value of adsorbent (PMDAH) dose was shown to be 30?mg L? 1. Maximum dye removal occurred at pH 7, dye concentration 100?mg L? 1, and 25?°C. Stirring the solution during the treatment significantly improved the removal of dye. Langmuir equation was used to quantify the amount of RR13 adsorbed on PMDAH surface. Furthermore, UV irradiation had a positive effect on dye removal. FT-IR spectrometry results for PMDAH and PMDAH + RR13 verified the treatment efficiency. Finally, the adsorbent was surveyed by SEM, TGA, and H-NMR characterization. GS–MS analysis and cost analysis were used to identify the compounds of post-treatment products.

Hydrolysis of N,N-dimethylaminoethyl methacrylate and its salts in concentrated aqueous solutions

The influence exerted by the structure of the ammonium group and anion, pH, and surfactant and polymeric additives on hydrolysis of N,N-dimethylaminoethyl methacrylate and its salts in concentrated aqueous solutions was studied.