10196-75-5 Usage
Description
N-[(diethylamino)methyl]methacrylamide, commonly referred to as DMAEMA, is a versatile chemical compound with the molecular formula C9H18N2O. It serves as a key monomer in the synthesis of polymers, playing a crucial role in organic synthesis and polymer chemistry. Characterized by its capacity for free radical polymerization, DMAEMA is instrumental in creating a diverse array of polymeric structures, such as copolymers, homopolymers, and graft polymers. Its applications extend across various industries, including adhesives, coatings, and biomedical materials, while also functioning as a stabilizer in emulsion polymerization processes. However, due to its hazardous nature, it is imperative to handle DMAEMA with care and adhere to stringent safety measures.
Uses
Used in Polymer Synthesis:
DMAEMA is utilized as a monomer in the production of polymers for its ability to undergo free radical polymerization, which is essential in creating various types of polymers, including copolymers, homopolymers, and graft polymers. This property makes it valuable in the development of materials with specific properties tailored for different applications.
Used in Adhesives Industry:
In the adhesives industry, DMAEMA is used as a component in the formulation of adhesives, contributing to the development of strong, durable, and versatile bonding agents that can be applied across a wide range of substrates.
Used in Coatings Industry:
DMAEMA plays a role in the coatings industry, where it is employed in the creation of coatings with enhanced properties, such as improved adhesion, durability, and resistance to environmental factors.
Used in Biomedical Materials:
Within the biomedical field, DMAEMA is used in the development of materials for various medical applications, including drug delivery systems, tissue engineering scaffolds, and biocompatible coatings for medical devices.
Used as a Stabilizer in Emulsion Polymerization:
DMAEMA is also used as a stabilizer in emulsion polymerization processes, where it helps to control the size and distribution of polymer particles, leading to improved product quality and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 10196-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,9 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10196-75:
(7*1)+(6*0)+(5*1)+(4*9)+(3*6)+(2*7)+(1*5)=85
85 % 10 = 5
So 10196-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H18N2O/c1-5-11(6-2)7-10-9(12)8(3)4/h3,5-7H2,1-2,4H3,(H,10,12)
10196-75-5Relevant articles and documents
Synthesis of: N -[(dialkylamino)methyl]acrylamides and N -[(dialkylamino)methyl]methacrylamides from Schiff base salts: Useful building blocks for smart polymers
Alzahrani, Abdullah,Mirallai, Styliana I.,Chalmers, Benjamin A.,McArdle, Patrick,Aldabbagh, Fawaz
, p. 4108 - 4116 (2018)
The traditional thermal Mannich reaction is unsuitable for preparing polymerizable N-methylene amino substituted acrylamides and methacrylamides. Herein we provide a facile multi-gram high yield synthesis of these monomeric precursors to stimuli-responsive polymers by the addition of acrylamides and methacrylamides onto in situ generated or freshly isolated methylene Schiff base (iminium) salts. The X-ray crystal structure of the hydrated iminium salt, 1-(hydroxymethyl)azocan-1-ium chloride and monomer·HCl salt (N-[(azocan-1-yl)methyl]prop-2-enamide hydrochloride) is described.
