95984-11-5

Usage

Uses

Used in Polymer and Resin Production:
N-(2,2-dimethoxyethyl)methacrylamide is used as a monomer for the synthesis of high-performance polymers and resins. Its ability to undergo polymerization reactions allows it to form strong and durable materials.
Used in Protective Coatings, Adhesives, and Sealants:
N-(2,2-dimethoxyethyl)methacrylamide is used as a component in protective coatings, adhesives, and sealants due to its excellent adhesion properties and resistance to abrasion and chemicals. This makes it suitable for use in various industrial and commercial applications where durability and protection are required.

InChI:InChI=1/C8H15NO3/c1-6(2)8(10)9-5-7(11-3)12-4/h7H,1,5H2,2-4H3,(H,9,10)

Upstream product

• 38862-25-8 methacrylic acid N-hydroxysuccinimide ester 
• 22483-09-6 2,2-dimethoxyethylamine 
• 920-46-7 Methacryloyl chloride 

Relevant academic research and scientific papers

Injectable and tunable poly(ethylene glycol) analogue hydrogels based on poly(oligoethylene glycol methacrylate)

Injectable PEG-analogue hydrogels based on poly(oligoethylene glycol methacrylate) have been developed based on complementary hydrazide and aldehyde reactive linear polymer precursors. These hydrogels display the desired biological properties of PEG, form

PARAMAGNETIC SUPPORTS FOR USE AS ASSAY REAGENTS

A composition for use as an assay reagent includes a paramagnetic solid support comprising a coating of a synthetic copolymer. The synthetic copolymer comprises two or three of a first copolymerized monomer, a second copolymerized monomer and a third copolymerized monomer and further comprises a polyethylenic backbone.

POLY(OLIGOETHYLENE GLYCOL METHACRYLATE) HYDROGEL COMPOSITIONS, AND METHODS OF USE THEREOF

The present application relates to hydrogel compositions comprising first and second precursor polymers, wherein the precursor polymers are modified poly(oligoethylene glycol methacrylate) copolymers that are crosslinked through electrophile-nucleophile reactions.

Tuning gelation time and morphology of injectable hydrogels using Ketone-Hydrazide cross-linking

Injectable, covalently in situ forming hydrogels based on poly(N-isopropylacrylamide) have been designed on the basis of mixing hydrazide-functionalized nucleophilic precursor polymers with electrophilic precursor polymers functionalized with a combination of ketone (slow reacting) and aldehyde (fast reacting) functional groups. By tuning the ratio of aldehyde:ketone functional groups as well as the total number of ketone groups in the electrophilic precursor polymer, largely independent control over hydrogel properties including gelation time (from seconds to hours), degradation kinetics (from hours to months), optical transmission (from 1 to 85%), and mechanics (over nearly 1 order of magnitude) can be achieved. In addition, ketone-functionalized precursor polymers exhibit improved cytocompatibility at even extremely high concentrations relative to polymers functionalized with aldehyde groups, even at 4-fold higher functional group densities. Overall, increasing the ketone content of the precursor copolymers can result in in situ-gellable hydrogels with improved transparency and biocompatibility and equivalent mechanics and stimuli-responsiveness while only modestly sacrificing the speed of gel formation.