2397-75-3

Basic information

• Product Name: 2-(dibutylamino)ethyl methacrylate
• Synonyms: 2-(dibutylamino)ethyl methacrylate;2-Methylpropenoic acid 2-(dibutylamino)ethyl ester;Einecs 219-262-4
• CAS NO: 2397-75-3
• Molecular Formula: C₁₄H₂₇NO₂
• Molecular Weight: 241.36968
• EINECS: 219-262-4
• Mol File: 2397-75-3.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 311.5°Cat760mmHg
• Flash Point: 95.2°C
• Appearance: /
• Density: 0.909g/cm³
• Vapor Pressure: 0.00056mmHg at 25°C
• Refractive Index: 1.455
• CAS DataBase Reference: 2-(dibutylamino)ethyl methacrylate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(dibutylamino)ethyl methacrylate(2397-75-3)
• EPA Substance Registry System: 2-(dibutylamino)ethyl methacrylate(2397-75-3)

Safety Data

• Hazardous Substances Data: 2397-75-3(Hazardous Substances Data)

Usage

General Description

2-(dibutylamino)ethyl methacrylate is a chemical compound with the formula C14H27NO2. It is commonly used as a monomer in the production of polymers, particularly in the manufacturing of adhesives, coatings, and medical devices. 2-(dibutylamino)ethyl methacrylate is a clear, colorless liquid with a slight odor, and is highly soluble in organic solvents. Due to its ability to undergo polymerization, 2-(dibutylamino)ethyl methacrylate is used to create durable and flexible materials with good adhesion properties. It is important to handle this compound with caution, as it may cause irritation to the skin, eyes, and respiratory system, and should only be used in well-ventilated areas with the appropriate protective equipment.

InChI:InChI=1/C14H27NO2/c1-5-7-9-15(10-8-6-2)11-12-17-14(16)13(3)4/h3,5-12H2,1-2,4H3

Upstream product

• 102-81-8 N,N-dibutyl amino-2 ethanol 
• 80-62-6 methacrylic acid methyl ester 
• 920-46-7 Methacryloyl chloride 

Relevant articles and documents

Ultrasensitive (Co)polymers based on poly(methacrylamide) structure with fining-tunable pH responsive value

Novel pH responsive copolymers with tertiary amine groups were prepared by free radical polymerization with 2-(dialkylamino)ethyl methacrylate monomers. These polymers were pH sensitive with the ability to be responsively fine-tuned in aqueous solution, which was proven through titration, transmittance measurements, and proton nuclear magnetic resonance spectroscopy. The polymers were soluble in water at low pH values, induced by electrostatic repulsion between amine groups, and aggregated above their pKa value due to the hydrophobic effect of the alkyls. The pH responsive values were precisely tuned from 7.4 to 4.8 by increasing the hydrophobic monomer ratio. Our work provides a novel approach for the development of ultrasensitive pH-responsive polymers for application in biomedical materials.

PH RESPONSIVE BLOCK COPOLYMER COMPOSITIONS AND MICELLES THAT INHIBIT MCT 1 AND RELATED PROTEINS

Described herein are therapeutic pH responsive compositions comprising a block copolymer and a therapeutic agent useful for the treatment of cancer.

(Meth) acrylic acid ester manufacturing method of N, N-substituted amino alcohol

The present invention relates to a process for preparing (meth)acrylic esters (F) of N,N-substituted amino alcohols, by transesterifying N,N-substituted amino alcohols (I) in which Y and Z are each independently C1-C20-alkyl, C3-C15-cycloalkyl, aryl, or Y and Z together with the nitrogen atom connecting them form a 5- to 9-membered saturated heterocyclic radical which optionally has oxygen, sulfur, nitrogen or C1-C4-alkyl-substituted nitrogen as a further heteroatom, and X is C2-C20-alkylene which may be interrupted by 1 to 10 nonadjacent oxy groups and/or unsubstituted or methoxy-substituted C1-C4-alkylimino groups, or C3-C15-cycloalkylene, with at least one (meth)acrylic ester (D) in the presence of at least one heterogeneous catalyst (K), wherein the heterogeneous catalyst (K) is used without any further solvent and the content of polymerization inhibitors in the reaction mixture is 450 ppm, and to the use of the (meth)acrylic esters (F) of N,N-substituted amino alcohols.