N-Vinylacetamide

N-Vinylacetamide
structure
Names
Preferred IUPAC name
N-Ethenylacetamide
Other names
N-Vinylacetamide
NVA
N-Vinylcarboxylic acid amide
N-Carboxylic acid amide
Vinylamide
NVA monomer
Identifiers
  • 5202-78-8 checkY
  • polymer: 28408-65-3
3D model (JSmol)
  • Interactive image
ChemSpider
  • 71210
ECHA InfoCard 100.023.627
EC Number
  • 225-989-8
  • 78875
UNII
  • 227WR07D3L checkY
  • DTXSID201011002 DTXSID0063735, DTXSID201011002
  • InChI=1S/C4H7NO/c1-3-5-4(2)6/h3H,1H2,2H3,(H,5,6)
    Key: RQAKESSLMFZVMC-UHFFFAOYSA-N
  • CC(=O)NC=C
Properties
C4H7NO
Molar mass 85.106 g·mol−1
Appearance White solid
Melting point 54 °C (129 °F; 327 K)
Boiling point 96 °C (205 °F; 369 K)
soluble
Solubility in acetone soluble
Solubility in ether soluble
Solubility in ester soluble
Solubility in arene soluble
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H302, H315, H319
P264, P270, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, P501
Flash point 113 °C (235 °F; 386 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

N-Vinylacetamide (NVA) is a non-ionic monomer. Copolymers made of NVA and other monomers can exhibit practical characteristics in addition to those common with the existing hydrophilic polymers.

History

NVA is an amphipathic monomer. It was introduced and compounded in the U.S. in 1967. Today, it is recognized as a monomer that does polymerize; however, Showa Denko K.K. succeeded in its industrialization in 1997.[1]

Properties

NVA is soluble in water, various organic solvents and liquid vinyl monomers. It is polymerizable by various radical polymerization processes, depending on the objective. Since NVA itself is a solvent, it can act as a dissolution agent for poorly soluble substances.

References

  1. ^ http://www.sdk.co.jp/english/products/110/111/12508.html [dead link]
Retrieved from "https://en.wikipedia.org/w/index.php?title=N-Vinylacetamide&oldid=1073289766"