N-Vinyl-2-pyrrolidone(NVP)


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  • N-Vinyl-2-pyrrolidone(NVP)
  • 88-12-0
  • C6H9NO
  • 111.144
  • liquid
Inquiry

Factory Sells Best Quality N-Vinyl-2-pyrrolidone(NVP) 88-12-0 with GMP standards

  • Molecular Formula:C6H9NO
  • Molecular Weight:111.144
  • Appearance/Colour:liquid 
  • Vapor Pressure:0.1 mm Hg ( 24 °C) 
  • Melting Point:13-14 °C 
  • Refractive Index:n20/D 1.512(lit.)  
  • Boiling Point:217.6 °C at 760 mmHg 
  • PKA:-0.34±0.20(Predicted) 
  • Flash Point:93.9 °C 
  • PSA:20.31000 
  • Density:1.144 g/cm3 
  • LogP:0.69020 

N-Vinyl-2-pyrrolidone(Cas 88-12-0) Usage

General Description

1-Vinyl-2-pyrrolidinone is a colorless to yellow liquid, with a characteristic odor. Its melting point is around 13.5oC and boils at about 90-92oC. VP is completely miscible in water and in most organic solvents but partially miscible in aliphatic hydrocarbons. Industrial production of VP by reacting 2-pyrrolidone with acetylene at high pressure and temperature has been reported. The vinylation process proceeds in liquid phase and is catalyzed by 3-pyrrolidone -potassium hydroxide.

Safety Profile

Confirmed carcinogen. Moderately toxic by ingestion, inhalation, and skin contact. A severe eye irritant. Probably irritating and narcotic in high concentrations. Combustible when exposed to heat or flame; can react vigorously with oxibzing materials. To fight fire, use alcohol foam, CO2, dry chemical. When heated to decomposition it emits highly toxic fumes of NOx.

InChI:InChI=1/C6H9NO/c1-2-7-5-3-4-6(7)8/h2H,1,3-5H2

88-12-0 Relevant articles

SYNTHESIS OF N-VINYL COMPOUNDS BY REACTING CYLIC NH-COMPOUNDS WITH ACETYLENE IN PRESENCE OF HOMOGENOUS CATALYST

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Page/Page column 17; 20, (2021/06/26)

Process to produce N-vinyl compounds by ...

Phosphine-Catalyzed Vinylation at Low Acetylene Pressure

Bienewald, Frank,Comba, Peter,Hashmi, A. Stephen K.,Menche, Maximilian,Rominger, Frank,Schafer, Ansgar,Schaub, Thomas,Sitte, Nikolai A.,Tuzina, Pavel

, p. 13041 - 13055 (2021/09/18)

The vinylation of various nucleophiles w...

Ruthenium-catalyzed synthesis of vinylamides at low acetylene pressure

Semina, Elena,Tuzina, Pavel,Bienewald, Frank,Hashmi,Schaub, Thomas

supporting information, p. 5977 - 5980 (2020/06/04)

The reaction of cyclic amides with acety...

Efficient palladium catalysis for the upgrading of itaconic and levulinic acid to 2-pyrrolidones followed by their vinylation into value-added monomers

Haus, Moritz O.,Hofmann, Jan P.,Konrad, Marc,Louven, Yannik,Palkovits, Regina

, p. 4532 - 4540 (2020/11/02)

The production of monomers from bio-base...

88-12-0 Process route

1-(2-hydroxyethyl)-2-pyrrolidinone
3445-11-2

1-(2-hydroxyethyl)-2-pyrrolidinone

1-ethenyl-2-pyrrolidinone
88-12-0

1-ethenyl-2-pyrrolidinone

Conditions
Conditions Yield
With Na/SiO2; ammonia; at 350 ℃; for 10h; under 750.075 Torr; Reagent/catalyst; Temperature; Catalytic behavior;
90%
Ca/Zn oxide; at 348 ℃; for 1h;
82%
Ca/Zn oxide; at 331 - 359 ℃; for 1h;
67.5%
zinc-magnesium mixed oxide; at 356 - 360 ℃; for 2 - 4h;
66.7%
Ca/Zn oxide calcined in air to 500 C; at 366 ℃; for 1h;
44%
magnesium oxide; at 368 ℃; for 1h;
26.6%
Ca/Zn oxide calcined in air to 700 C; at 359 ℃; for 1h;
11.5%
calcium carbonate; at 377 ℃; for 1h;
2.7%
With aluminum oxide; at 300 - 340 ℃; under 56 Torr; Beim Leiten des Dampfes von Edukt ueber Reagens;
Multi-step reaction with 2 steps
1: benzene; thionyl chloride
2: benzene; sodium amide
With thionyl chloride; sodium amide; benzene;
Product distribution / selectivity;
With Cs2O#SiO2; at 500 ℃; for 2h;
Gas phase;
With Cs1Si10 catalyst; for 1h; under 760.051 Torr; Inert atmosphere; Sealed tube;
87 %Chromat.
With sodium oxide-silicon dioxide; at 350 ℃; Temperature; Catalytic behavior; Flow reactor; Green chemistry;
2-pyrrolidinon
616-45-5

2-pyrrolidinon

[1,3]-dioxolan-2-one
96-49-1

[1,3]-dioxolan-2-one

1-ethenyl-2-pyrrolidinone
88-12-0

1-ethenyl-2-pyrrolidinone

Conditions
Conditions Yield
With TEMPOL; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 5,5-dimethyl-1,3-cyclohexadiene; at 100 - 120 ℃; for 3.5h; Dean-Stark;
82.13%

88-12-0 Upstream products

  • 616-45-5
    616-45-5

    2-pyrrolidinon

  • 51333-90-5
    51333-90-5

    1-(2-chloro-ethyl)-pyrrolidin-2-one

  • 3445-11-2
    3445-11-2

    1-(2-hydroxyethyl)-2-pyrrolidinone

  • 14468-90-7
    14468-90-7

    N-trimethylsilyl-pyrrolidin-2-one

88-12-0 Downstream products

  • 123055-49-2
    123055-49-2

    {2-(2-oxo-N-pyrrolidinyl)ethyl}triphenyltin

  • 125330-80-5
    125330-80-5

    3-benzoyl-N-vinylpyrrolidin-2-one

  • 19853-24-8
    19853-24-8

    1-(1-Methoxyethyl)-2-pyrrolidinon

  • 135604-63-6
    135604-63-6

    1-(pyrrolidinyl-2-on-1-yl)-1-triethylsilylethane

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