2-Sulfoethyl methacrylate

Product Information

Molecular Formula:
C6H10O5S
Molecular Weight:
194.21
Description
Water-soluble monomer. Used to introduce polar sites into polymer chains, confer shear stability to aqueous polymer dispersions.
Synonyms
2-SULFOETHYL METHACRYLATE; 2-methyl-2-propenoicaci2-sulfoethylester; 2-Propenoicacid,2-methyl-,2-sulfoethylester; sulphoethyl methacrylate; 2-SULPHOETHYLMETHACRYLATE; METHACRYLICACID,2-SULPHOETHYLESTER; 2-SULFOETHYL METHACRYLATE 95%; 2-(2-Methylacryloyloxy)etha
IUPAC Name
2-(2-methylprop-2-enoyloxy)ethanesulfonic acid
Canonical SMILES
CC(=C)C(=O)OCCS(=O)(=O)O
InChI
InChI=1S/C6H10O5S/c1-5(2)6(7)11-3-4-12(8,9)10/h1,3-4H2,2H3,(H,8,9,10)
InChI Key
PRAMZQXXPOLCIY-UHFFFAOYSA-N
Purity
>90%
Density
1,324 g/cm3
Storage
Store at 4 degrees celsius
Refractive Index
n20/D 1.477

Safety Information

Hazards
Corrosive

Computed Properties

XLogP3
0
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
5
Rotatable Bond Count
5
Exact Mass
194.02489459 g/mol
Monoisotopic Mass
194.02489459 g/mol
Topological Polar Surface Area
89Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
271
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114058450-A Stable granular detergent composition and preparation method thereof 2021-12-03
CN-114149868-A Tablet detergent composition with hardness and solubility and preparation method thereof 2021-12-03
CN-113930121-A Antifogging coating composition based on amphiphilic copolymer and preparation method and application thereof 2021-11-11
CN-113817883-A Sulfonate-containing polymer retanning fatliquor and preparation method thereof 2021-10-15
JP-6994600-B1 Primer composition 2021-08-31
JP-6994601-B1 Primer composition 2021-08-31
CN-113350047-A Anion sanitary towel 2021-06-03
JP-6948484-B1 Ink set 2021-04-27
JP-6918263-B1 Cleaning liquid, ink set, and cleaning method 2021-03-23
JP-6919082-B1 Ink set 2021-02-22

Literatures

PMID Publication Date Title Journal
21529818 2011-07-15 Controlling photochromism between fluoroalkyl end-capped oligomer/polyaniline and N,N'-diphenyl-1,4-phenylenediamine nanocomposites induced by UV-light-responsive titanium oxide nanoparticles Journal of colloid and interface science
18666170 2008-08-01 Mixed-mode reversed-phase and ion-exchange monolithic columns for micro-HPLC Journal of separation science
17952566 2008-05-01 Equilibrium and non-equilibrium charge-dependent quantification of endothelial cell hydrogel scaffolds Journal of materials science. Materials in medicine
18262200 2008-04-15 Preparation and applications of a variety of fluoroalkyl end-capped oligomer/hydroxyapatite composites Journal of colloid and interface science
18052165 2007-12-26 Scanning Kelvin probe imaging of the potential profiles in fixed and dynamic planar LECs Journal of the American Chemical Society
17583965 2007-08-01 Polymer monoliths with low hydrophobicity for strong cation-exchange capillary liquid chromatography of peptides and proteins Analytical chemistry
15351818 2004-09-21 Atrazine transformation using synthetic enzymes prepared by molecular imprinting Organic & biomolecular chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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