15214-89-8

  • Product Name:2-Acrylamide-2-methylpropanesulfonic acid (AMPS)
  • Molecular Formula:C7H13NO4S
  • Purity:99%
  • Molecular Weight:207.251
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Product Details

pd_meltingpoint:195-200 °C (dec.)(lit.)

Appearance:white powder

Manufacturer Supply Best Quality 2-Acrylamide-2-methylpropanesulfonic acid (AMPS) 15214-89-8 with Efficient Transportation

  • Molecular Formula:C7H13NO4S
  • Molecular Weight:207.251
  • Appearance/Colour:white powder 
  • Vapor Pressure:<0.0000004 hPa (25 °C) 
  • Melting Point:195-200 °C (dec.)(lit.) 
  • Refractive Index:1.6370 (estimate) 
  • Boiling Point:412oC 
  • PKA:1.67±0.50(Predicted) 
  • Flash Point:160 °C 
  • PSA:91.85000 
  • Density:1.266 g/cm3 
  • LogP:1.42670 

2-Acrylamide-2-methylpropanesulfonic acid(Cas 15214-89-8) Usage

Uses and Mechanism of Action

In superabsorbent polymer (SAP) synthesis:
Enhances water absorption and saline-alkali resistance.[1]

In polymer gel formation:
Contributes to thermal stability and self-healing properties in oil and gas reservoirs.[2]

In fuel cell membranes:
Improves proton conductivity and flexibility, enabling use in fuel cells.[3]

Production Methods

Synthesized in labs using various methods including graft copolymerization and interpenetrating network formation.

Analysis Method

Characterized using FTIR, TGA, SEM, NMR, XRD, and conductivity measurements to understand structure and performance.

Preparation

2-Acrylamido-2-methylpropanesulfonic acid(AMPS) can be synthesized by one step and two steps. The one-step method is to react the raw materials acrylonitrile, isobutylene and oleum together. The two-step method is to sulfonate isobutylene in the presence of a reaction solvent to obtain a sulfonated intermediate, and then react with acrylonitrile in the presence of sulfuric acid. One-step method is more economical. Raw material consumption quota: isobutylene 300kg/t, acrylonitrile 290kg/t, oleum 560kg/t.

Application

2-Acrylamide-2-methylpropanesulfonic acid is an important monomer. Its copolymers or homopolymers with different molecular weight can be widely used in textile, oil drilling, water treatment, papermaking, dying, coating, cosmetics, electronics, etc. because of its unique formular structure—containing sulfonic acid group and unsaturated radical, thus showing excellent properties in many aspects.

InChI:InChI=1/C7H13NO4S/c1-4-6(9)8-7(2,3)5-13(10,11)12/h4H,1,5H2,2-3H3,(H,8,9)(H,10,11,12)/p-1

15214-89-8 Relevant articles

NEW METHOD FOR PRODUCING 2-ACRYLAMIDO-2-METHYLPROPANE SULPHONIC ACID

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Paragraph 0123-0144, (2020/02/10)

The present invention relates to a produ...

HYDRATED CRYSTALLINE FORM OF 2-ACRYLAMIDO-2-METHYLPROPANE SULFONIC ACID

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Paragraph 0194-0196, (2020/02/15)

The present invention relates to a hydra...

A 2 - acrylamide - 2 - methyl (alkanes) sulfonic acid

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Paragraph 0025; 0026; 0027; 0028; 0029-0045; 0052, (2018/04/03)

The invention relates to a preparation m...

METHOD FOR PRODUCING THE 2-ACRYLAMIDO-2-METHYLPROPANE SULFONIC ACID MONOMER AND POLYMER COMPRISING SAID MONOMER

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Paragraph 0057; 0060; 0058; 0059; 0060, (2018/09/16)

The invention relates to a method for pr...

15214-89-8 Process route

acrylonitrile
107-13-1,25014-41-9

acrylonitrile

isobutene
115-11-7,15220-85-6

isobutene

N-tert-Butylacrylamide
107-58-4,25267-41-8

N-tert-Butylacrylamide

2-acrylamido-2-methylpropanesulfonic acid
15214-89-8,27119-07-9

2-acrylamido-2-methylpropanesulfonic acid

2-propenamide
79-06-1,12624-24-7,25038-45-3,27754-57-0,33338-03-3,39387-77-4,68247-81-4,9082-06-8,79079-15-5

2-propenamide

Conditions
Conditions Yield
With sulfuric acid; at 20 ℃; for 2h;
87%
acrylonitrile
107-13-1,25014-41-9

acrylonitrile

isobutene
115-11-7,15220-85-6

isobutene

2-acrylamido-2-methylpropanesulfonic acid
15214-89-8,27119-07-9

2-acrylamido-2-methylpropanesulfonic acid

Conditions
Conditions Yield
With sulfur trioxide; at 8 - 35 ℃; Temperature;
92.2%
acrylonitrile; With sulfuric acid; In water; at -10 - -7 ℃; for 2h;
isobutene; With acetic acid; at 10 - 70 ℃; for 1.5h; Temperature;
92.09%
With methanesulfonic acid; sulfuric acid; at 0 - 45 ℃; for 1h; under 760.051 Torr; Reagent/catalyst; Temperature;
82.3%
With sulfur trioxide; at 23.4 ℃; Further Variations:; Temperatures; oleum concentration, reagent mixing order; Thermodynamic data;
With sulfuric acid; sulfur trioxide; at -15 - 50 ℃; for 1.66667h; Product distribution / selectivity;
acrylonitrile; With sulfur trioxide; at 5 - 10 ℃;
isobutene; With water; at 30 - 40 ℃;
acrylonitrile; With sulfuric acid; at -10 - 40 ℃; for 1h;
isobutene; With sulfuric acid; for 1h;
acrylonitrile; With sulfuric acid; at -5 - 0 ℃; for 0.366667h; Large scale;
isobutene; at 38 - 40 ℃; for 1h; Large scale;
243.1 kg
With sulfuric acid; sulfur trioxide; acetic anhydride; at 35 ℃; for 1.5h; Large scale;
With fuming sulphuric acid; at -20 - 50 ℃; for 2h;
acrylonitrile; With fuming sulphuric acid; In water; at -20 ℃; for 1h;
isobutene; In water; at 45 ℃; Temperature; Reagent/catalyst;
acrylonitrile; With sulfuric acid; In water; for 1h;
isobutene; In water; at -20 - 45 ℃;
acrylonitrile; With fuming sulphuric acid; at -15 - -5 ℃; for 0.166667h;
isobutene; at 40 - 60 ℃; for 0.666667h;

15214-89-8 Upstream products

  • 107-13-1
    107-13-1

    acrylonitrile

  • 115-11-7
    115-11-7

    isobutene

15214-89-8 Downstream products

  • 58374-69-9
    58374-69-9

    ammonium acryloyldimethyltaurate

  • 1161027-41-3
    1161027-41-3

    benzyltributylammonium 2-acrylamido-2-methyl-1-propanesulfonate

  • 5165-97-9
    5165-97-9

    sodium 2-acrylamido-2-methylpropane-1-sulfonate

  • 107-58-4
    107-58-4

    N-tert-Butylacrylamide