
15214-89-8
- Product Name:2-Acrylamide-2-methylpropanesulfonic acid (AMPS)
- Molecular Formula:C7H13NO4S
- Purity:99%
- Molecular Weight:207.251
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: |
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
-
Paragraph 0123-0144, (2020/02/10)
The present invention relates to a produ...
HYDRATED CRYSTALLINE FORM OF 2-ACRYLAMIDO-2-METHYLPROPANE SULFONIC ACID
-
Paragraph 0194-0196, (2020/02/15)
The present invention relates to a hydra...
A 2 - acrylamide - 2 - methyl (alkanes) sulfonic acid
-
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
-
Paragraph 0057; 0060; 0058; 0059; 0060, (2018/09/16)
The invention relates to a method for pr...
15214-89-8 Process route
-
-
107-13-1,25014-41-9
acrylonitrile

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

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

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

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

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

-
-
15214-89-8,27119-07-9
2-acrylamido-2-methylpropanesulfonic acid
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
-
acrylonitrile
-
isobutene
15214-89-8 Downstream products
-
ammonium acryloyldimethyltaurate
-
benzyltributylammonium 2-acrylamido-2-methyl-1-propanesulfonate
-
sodium 2-acrylamido-2-methylpropane-1-sulfonate
-
N-tert-Butylacrylamide
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-
(S)-2-HYDROXYMETHYL-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
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-
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