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CS-W001157 4
Total: USD 88.00

N,N-Dimethylacrylamide,98% (stabilized with MEHQ)

  • CAS No. 2680-03-7

  • Cat. No. CS-0016062
  • Purity97% (stabilized with MEHQ)
  • MDL No.MFCD00008626

*For research and further manufacturing use only, not for direct human use.

N,N-Dimethylacrylamide,98% (stabilized with MEHQ)|CS-0016062

Structure of 2680-03-7

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General Information

  • CAS No. 2680-03-7
  • Cat. No. CS-0016062
  • Purity 97% (stabilized with MEHQ)
  • MDL No. MFCD00008626
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₉NO
  • Molecular Weight 99.13
  • Synonym(s) N,N-Dimethyl-2-propenamide
  • SMILES C=CC(N(C)C)=O

Description

N,N-Dimethylacrylamide (DMAA) is a non-ionic monomer with high reactivity and low initiation temperature. It is commonly used as a monomer in the production of polymers and copolymers for various applications such as hydrogels, polymeric flocculants, biomedical and drug delivery applications, polymer coatings, smart coatings, adhesives, sensors, self-healing materials, and water treatment agents. The unique structure of DMMA can form a three-dimensional network with other hydrogels and enhance their water retention capacity. It is also used as a crosslinking agent in polymerization reactions.N, N-Dimethylacrylamide(DMAA) can be used in the following applications:Synthesis of poly(N,N-dimethylacrylamide) (PDMAA) nanoparticles which are used in biomedical and drug delivery applications.Use as a co-monomer in the synthesis of thermoresponsive polymers used in smart coatings, adhesives, and sensors.As a reactive diluent in the manufacture of UV-cured coatings and inks.Use as a co-monomer with polyethylene glycol dimethacrylate (PEGDMA) and a chitosan derivative to develop an injectable hydrogel that can be used as a bone tissue engineering matrix.A series of DMMA-based hydrogels for the removal of heavy metals and organic dyes from polluted water. These hydrogels are highly efficient in removing cationic dyes due to electrostatic interaction and hydrogen bonding in the DMMA backbone.Non-toxic luminescent carbon dot/poly(DMMA) nanocomposite via surface-initiated reversible addition-fragmentation chain transfer polymerization. Polymer coating for quartz crystal microbalance(QCM) sensor. The poly(DMMA) gel acts as a sensing material to adsorb Au(III) ions from HCl aqueous solution and it is inactive to most other metal ions and organic compounds.

Synthesis

  • Route1
    • 3-(Dimethylamino)-N,N-dimethyl-propanamide|CS-0771628
      17268-47-2
    • ~98%
    • In-stock
      N,N-Dimethylacrylamide,98% (stabilized with MEHQ)|CS-0016062
      2680-03-7

    References

    • Idemitsu Kosan Co., Ltd. Patent: EP2426103 A1, 2012 ; Location in patent: Page/Page column 20-21; 23 ;
  • Route2
    • null|null
      110-88-3
    • In-stock
      N,N-Dimethylacetamide|CS-W023195
      127-19-5
    • ~46%
    • In-stock
      N,N-Dimethylacrylamide,98% (stabilized with MEHQ)|CS-0016062
      2680-03-7

    References

    • Foo, Siong Wan; Oishi, Shun; Saito, Susumu Tetrahedron Letters, 2012 , vol. 53, # 40 p. 5445 - 5448
  • Route3
    • null|null
      124-40-3
    • null|null
      79-10-7
    • ~%
    • In-stock
      N,N-Dimethylacrylamide,98% (stabilized with MEHQ)|CS-0016062
      2680-03-7

    References

    • Tetrahedron, , vol. 68, # 4 p. 1177 - 1184

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05,GHS06
Signal Word : Danger
UN#: 2810
Class : 6.1
Packing Group : Ⅲ
Hazard Statements : H227-H301+H311-H318
Precautionary Statements : P210-P264-P270-P280-P302+P352-P330-P361+P364-P370+P378-P403-P405-P501

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Computational Chemistry Data

  • TPSA   20.31
  • LogP   0.2606
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   1

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