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Merck

672068

Sigma-Aldrich

Vinylphosphonsäure

≥90% (T)

Synonym(e):

Ethenephosphonic acid, Ethylenephosphonic acid, P-Ethenylphosphonic acid

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About This Item

Lineare Formel:
CH2=CHP(O)(OH)2
CAS-Nummer:
Molekulargewicht:
108.03
Beilstein:
1741622
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Assay

≥90% (T)

Verunreinigungen

≤7.0% water

mp (Schmelzpunkt)

36 °C (Lit. dry VPA) (lit.)

Dichte

1.37 g/mL at 20 °C (lit.)

SMILES String

OP(O)(=O)C=C

InChI

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

InChIKey

ZTWTYVWXUKTLCP-UHFFFAOYSA-N

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Anwendung

Vinylphosphonic acid (VPA) can be used as a monomer unit for the synthesis of poly(vinylphosphonic acid) via free radical polymerization. It is also used to develop copolymers of VPA with acrylonitrile, N-isopropylacrylamide, styrene, vinylpyrrolidone, and acrylic and methacrylic acid. These copolymers find potential application in hydrogels, drug delivery, biomimetic mineralization, and polymer electrolyte membranes in fuel cells.
It can also be used as an organic building block to prepare (E)-styryl phosphonic acid derivatives by reacting with various aryl halides via Pd-catalyzed Heck coupling reaction.

Piktogramme

Corrosion

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Met. Corr. 1 - Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flammpunkt (°F)

467.6 °F

Flammpunkt (°C)

242 °C

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Kunden haben sich ebenfalls angesehen

Noh-Seok Kwak et al.
Journal of hazardous materials, 203-204, 213-220 (2012-01-03)
Poly(vinylphosphonic acid-co-methacrylic acid) microbeads were synthesized by suspension polymerization, and their indium adsorption properties were investigated. The obtained microbeads were characterized by Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM). The microbeads were wrinkled spheres, irrespective of the
Synthesis, microstructure, and acidity of poly (vinylphosphonic acid)
Bingol B, et al.
Macromolecular Rapid Communications, 27(20), 1719-1724 (2006)
Richard D Bertram et al.
Biochemistry, 41(24), 7725-7731 (2002-06-12)
During the past 5 years a great deal of structural and biochemical information has given us a detailed insight into the molecular mechanism of action of the PcrA DNA helicase and challenged previous notions about the molecular mechanism of action
Young Kyung Kim et al.
Biomaterials, 31(25), 6618-6627 (2010-07-14)
The complex morphologies of mineralised collagen fibrils are regulated through interactions between the collagen matrix and non-collagenous extracellular proteins. In the present study, polyvinylphosphonic acid, a biomimetic analogue of matrix phosphoproteins, was synthesised and confirmed with FTIR and NMR. Biomimetic
Single-step synthesis of styryl phosphonic acids via palladium-catalyzed Heck coupling of vinyl phosphonic acid with aryl halides
McNichols BW, et al.
Chemical Communications (Cambridge, England), 53(92), 12454-12456 (2017)

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