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Merck
CN

282731

2-Acrylamido-2-methyl-1-propanesulfonic acid

99%

Synonym(s):

(1 1-Dimethyl-2-sulfoethyl)acrylamide, 2-Acrylamido-2 2-dimethylethanesulfonic acid, AMPS

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About This Item

Linear Formula:
H2C=CHCONHC(CH3)2CH2SO3H
CAS Number:
Molecular Weight:
207.25
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
EC Number:
239-268-0
MDL number:
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Quality Level

assay

99%

mp

195 °C (dec.) (lit.)

SMILES string

CC(C)(CS(O)(=O)=O)NC(=O)C=C

InChI

1S/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)

InChI key

XHZPRMZZQOIPDS-UHFFFAOYSA-N

General description

2-Acrylamido-2-methyl-1-propanesulfonicacid (AMPS) is a reactive and hydrophilic monomer that belongs to the class of sulfonic acid acrylic monomers. It is used in the synthesis of various polymers such as poly(2-acrylamido-2-methylpropanesulfonic acid-CO-acrylic acid), poly(acrylamidomethylpropanesulfonic acid-co-acrylicacid), and poly(acrylic acid-co-2-acrylamido-2-methyl propane sulfonic acid). These polymers are used in a wide range of applications, such as textiles, flocculants, dispersants, scale control agents, personal care products, water treatment, oil fields, and emulsion coatings. AMPS has an ionic character due to the sulfonic acid group, which is valuable for applications such as ion exchange, flocculation, and water treatment.

Application

2-Acrylamido-2-methyl-1-propanesulfonic acid can be used as a monomer:
  • In the synthesis of polyampholyte hydrogels for Potential Biomedical Applications, including tissue engineering, drug delivery, antibacterial and antifouling materials.
  • To graft bacterial cellulose membranes for fuel cell applications. AMPS potentially improves the proton conductivity and fuel cell application of the bacterial cellulose membranes.
  • In the preparation of a superabsorbent hydrogel. The presence of AMPS enhances the superabsorbent properties, which are important for applications such as wastewater treatment, wound healing medical devices, and agriculture.
  • In the formation of a polyelectrolyte with enhanced electrochemical properties for supercapacitor applications.


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pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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Articles

Discover hydrogels, biocompatible materials for drug delivery, tissue engineering, wound care, and 3D bioprinting in innovative biomedical applications


Vanessa Martínez-Cornejo et al.
Polymers, 12(8) (2020-07-31)
The first example of quasiliving radical polymerization and copolymerization of 2-acrylamido-2-methylpropane sulfonic acid (AMPS) without previous protection of its strong acid groups catalyzed by [Ru(o-C6H4-2-py)(phen)(MeCN)2]PF6 complex is reported. Nuclear magnetic resonance (RMN) and gel permeation chromatography (GPC) confirmed the diblock
Xi Ke et al.
Polymers, 11(7) (2019-07-25)
Polymer electrolyte membranes (PEM) for potential applications in fuel cells or vanadium redox flow batteries were synthesized and characterized. ETFE (poly (ethylene-alt-tetrafluoroethylene)) and PVDF (poly (vinylidene fluoride)) serving as base materials were activated by electron beam treatment with doses ranging
Yongjun Sun et al.
Journal of environmental management, 248, 109241-109241 (2019-07-16)
Carboxylated chitosan (CPCTS) is used as substrates in the design and synthesis of CPCTS-based flocculants through UV-initiated polymerization techniques. The synthesized flocculants are applied to remove Cr and Ni ions from chromic acid lotion and electroplating wastewater through two-stage flocculation.



Global Trade Item Number

SKUGTIN
282731-250G04061826235768
282731-1KG04061835383016