16753-07-4

Basic information

• Product Name: N-acryloyl-beta-alanine
• CAS NO: 16753-07-4
• Molecular Formula: C₆H₉NO₃
• Molecular Weight: 143.1406
• Mol File: 16753-07-4.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 400.6°C at 760 mmHg
• Flash Point: 196.1°C
• Density: 1.161g/cm³
• Vapor Pressure: 1.55E-07mmHg at 25°C
• Refractive Index: 1.476
• CAS DataBase Reference: N-acryloyl-beta-alanine(CAS DataBase Reference)
• NIST Chemistry Reference: N-acryloyl-beta-alanine(16753-07-4)
• EPA Substance Registry System: N-acryloyl-beta-alanine(16753-07-4)

Safety Data

• Hazardous Substances Data: 16753-07-4(Hazardous Substances Data)

Upstream product

• 79-10-7 acrylic acid 
• 107-95-9 3-amino propanoic acid 
• 18664-78-3 3-aminopentanoic acid 
• 814-68-6 acryloyl chloride 

Downstream Products

• 219797-98-5 3-Acryloylamino-propionic acid pentafluorophenyl ester 
• 63406-12-2 acrylamido-3 N-benzyl propanamide 
• 65500-82-5 (acrylamido-3 propionamido)-3 N-benzyl propanamide 
• 65500-84-7 (acrylamido-3 propanamido)-3 N-phenyl propanamide 

Relevant articles and documents

Synthesis of amino acid-based polymers via atom transfer radical polymerization in aqueous media at ambient temperature

Well-defined acryloyl β-alanine (ABA) polymers were synthesized directly via atom transfer radical polymerization (ATRP) under near physiological conditions using various water soluble initiators with high yield and narrow molecular weight distributions. The Royal Society of Chemistry 2005.

Cooperativity of Catechols and Amines in High-Performance Dry/Wet Adhesives

The outstanding adhesive performance of mussel byssal threads has inspired materials scientists over the past few decades. Exploiting the amino-catechol synergy, polymeric pressure-sensitive adhesives (PSAs) have now been synthesized by copolymerizing tra

Novel 3-hydroxypyridin-4-one hexadentate ligand-based polymeric iron chelator: Synthesis, characterization and antimicrobial evaluation

A novel 3-hydroxypyridin-4-one (HPO) hexadentate monomeric chelator 14 has been synthesized and incorporated into polymers by copolymerization with 2-hydroxyethyl acrylate (HEA), using azobisisobutyronitrile (AIBN) as an initiator. The monomeric chelator was found to possess very high affinity for iron(III), with the log stability constant of the iron complex (log K1) = 33.61 and pFe3+ = 30.37. The iron binding capacity and monomer recovery of the copolymers were determined using spectrophotometry. The in vitro antimicrobial activity of monomeric chelator 14 and polymeric chelator 16-4 against both Gram-positive bacteria (Staphylococcus aureus and Bacillus subtilis) and Gram-negative bacteria (Escherichia coli, Salmonella spp., and Pseudomonas aeruginosa) was evaluated by inhibition zone and minimum inhibitory concentration (MIC) assays, which demonstrated that both monomeric and polymeric chelators possess inhibitory activity. The polymeric chelators possess potential application for the treatment of wound infection.