Skip to Content
Merck
All Photos(3)

Key Documents

661740

Sigma-Aldrich

Poly(vinylphosphonic acid)

greener alternative

Synonym(s):

PVPA, Polyethenylphosphonic acid

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(C2H5O3P)n
CAS Number:
MDL number:
UNSPSC Code:
26111700
NACRES:
NA.23

form

powder

Quality Level

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

greener alternative category

InChI

1S/C2H5O3P/c1-2-6(3,4)5/h2H,1H2,(H2,3,4,5)

InChI key

ZTWTYVWXUKTLCP-UHFFFAOYSA-N

General description

Poly(vinylphosphonic acid) (PVPA) is a polymeric diprotic acid, which can be synthesized by free-radical polymerization of VPA. It can also be synthesized by employing vinylphosphonic acid methyl ester as a monomer, followed by saponification.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Application

Poly(vinylphosphonic) acid is a versatile polyelectrolyte useful in several applications: proton conductor for fuel cells, chemical and biological sensors, biocomposite materials and surface modification and adhesion.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Minghan Ren et al.
Analytical chemistry, 77(9), 2700-2707 (2005-04-30)
We report here a chemical sensor based on detecting the mechanical response of a thin (approximately 10-microm) polymer wire stretched across the two prongs of a wristwatch quartz tuning fork (QTF). When the fork is set to oscillate, the wire
Y E Greish et al.
Biomaterials, 22(8), 807-816 (2001-03-15)
The formation of biocompatible organic-inorganic composites by reactions between tetracalcium phosphate (Ca4(PO4)2O, TetCP) and the biomedical polymer poly(vinyl phosphonic acid) (PVPA) is described. Composites were prepared by hot pressing mixtures of these powders at 80 kpsi and 300 degrees C
Van Den Brand, J.; Van Gils, S.; BeenTjes, P.C.J.; Terryn, H.; Sivel, V.; de Wit, J.H.W.
Progress in Organic Coatings, 51, 339-350 (2004)
Synthesis, microstructure, and acidity of poly (vinylphosphonic acid)
Bingol B, et al.
Macromolecular Rapid Communications, 27(20), 1719-1724 (2006)
Poly (vinylphosphonic acid) and its derivatives
Macarie L and Ilia G
Progress in Polymer Science, 35(8), 1078-1092 (2010)

Articles

Advances in electrochemical water conversion and understanding PEMFC degradation drive progress in hydrogen technologies.

Advances in electrochemical water conversion and understanding PEMFC degradation drive progress in hydrogen technologies.

Advances in electrochemical water conversion and understanding PEMFC degradation drive progress in hydrogen technologies.

Advances in electrochemical water conversion and understanding PEMFC degradation drive progress in hydrogen technologies.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service