28384-61-4

Basic information

• Product Name: N-N-BUTYL METHACRYLAMIDE
• Synonyms: N-N-BUTYL METHACRYLAMIDE;N-butylmethacrylamide;N-BUTYLMETHACRYLAMIDE(WXC07250)
• CAS NO: 28384-61-4
• Molecular Formula: C₈H₁₅NO
• Molecular Weight: 141.21
• Product Categories: monomer
• Mol File: 28384-61-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 265.376 °C at 760 mmHg
• Flash Point: 150.548 °C
• Appearance: /
• Density: 0.875 g/cm³
• Vapor Pressure: 0.009mmHg at 25°C
• Refractive Index: 1.437
• Storage Temp.: 2-8°C
• CAS DataBase Reference: N-N-BUTYL METHACRYLAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N-N-BUTYL METHACRYLAMIDE(28384-61-4)
• EPA Substance Registry System: N-N-BUTYL METHACRYLAMIDE(28384-61-4)

Safety Data

• Hazardous Substances Data: 28384-61-4(Hazardous Substances Data)

Usage

General Description

N-N-butyl methacrylamide is a chemical compound with the molecular formula C10H19NO2. It is a colorless, transparent liquid with a mild odor. This chemical is mainly used as a raw material for the synthesis of various polymers and copolymers. It is often employed in the production of water-based paints, adhesives, and coatings, as well as in the manufacturing of specialty polymers and resins. N-N-butyl methacrylamide can also be used as a crosslinking agent in the textile and paper industries. Additionally, it has applications in the medical field for the development of biocompatible polymers and hydrogels. Due to its versatile nature and unique chemical properties, N-N-butyl methacrylamide is an important ingredient in the production of a wide range of industrial and commercial products.

InChI:InChI=1/C8H15NO/c1-4-5-6-9-8(10)7(2)3/h2,4-6H2,1,3H3,(H,9,10)

Upstream product

• 109-73-9 N-butylamine 
• 920-46-7 Methacryloyl chloride 
• 80-62-6 methacrylic acid methyl ester 

Downstream Products

• 1309763-10-7 1-n-butyl-3-methyl-5,6-diphenylpyridin-2(1H)-one 
• 173007-38-0 C₃₁H₅₂N₂O₄ 
• 172900-95-7 N-tert-butoxycarbonyl-2-methylene-4(S)-hydroxy-5(S)-amino-7(S)-isopropyl-8-(p-tert-butyl-phenyl)-octanoic acid (N-butyl) amide 
• 180183-00-0 (2R,3S,5S)-2-[3-(tert-butoxycarbonyl)amino-5-(benzyloxymethyl)-2-hydroxy-6-methylheptyl]-N-(butyl)acrylamide 
• 180182-99-4 (2S,3S,5S)-2-[3-(tert-butoxycarbonyl)amino-5-(benzyloxymethyl)-2-hydroxy-6-methylheptyl]-N-(butyl)acrylamide 
• 198641-73-5 N-tert-butoxycarbonyl-2-methylene-4(S)-hydroxy-5(S)-amino-7(S)-isopropyl-8-(3-benzyloxy-4-tert-butyl-phenyl)-octanoic acid (N-butyl) amide 

Relevant articles and documents

Effect of Transition Metals on Chemodivergent Cross-Coupling of Acrylamides with Vinyl Acetate via C-H Activation

A novel chemodivergent cross-coupling of acrylamides and vinyl acetates has been realized via metal-catalyzed vinylic C-H activation. The selective olefinic C-H vinylation and alkenylation reaction was examined with a variety of differently functionalized acrylamides. The reaction efficiently generates a range of highly synthetically valuable butadienes with good functional group tolerance in good to moderate yields. A possible catalytic reaction mechanism involving the chelation-assisted olefinic C-H activation via an acetate-assisted deprotonation pathway is proposed.

Lipase catalyzed aminolysis of ethyl propiolate and acrylic esters. Synthesis of chiral acrylamides

Candida cylindracea lipase is a useful catalyst for the preparation of propiolamides. Candida antarctica lipase efficiently catalyzes the aminolysis of different acrylic esters and aliphatic amines; if racemic amines are used, the corresponding optically active acrylic amide is obtained in moderate-high enantiomeric excess.