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Vinylphosphonic acid

Base Information Edit
  • Chemical Name:Vinylphosphonic acid
  • CAS No.:27754-99-0
  • Molecular Formula:(C2H5O3P)n
  • Molecular Weight:108.033061
  • Hs Code.:
  • European Community (EC) Number:217-123-2,677-765-8
  • DSSTox Substance ID:DTXSID40862745
  • Nikkaji Number:J203.156F
  • Wikipedia:Vinylphosphonic_acid
  • Wikidata:Q15634162
  • Mol file:27754-99-0.mol
Vinylphosphonic acid

Synonyms:vinylphosphonic acid

Suppliers and Price of Vinylphosphonic acid
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • Poly(vinylphosphonic acid)
  • 1g
  • $ 360.00
Total 58 raw suppliers
Chemical Property of Vinylphosphonic acid Edit
Chemical Property:
  • Boiling Point:266.2 °C at 760 mmHg 
  • Flash Point:114.8 °C 
  • Density:1.425 g/cm3 
  • XLogP3:-1.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:107.99763101
  • Heavy Atom Count:6
  • Complexity:91
Purity/Quality:

98%,99%, *data from raw suppliers

Poly(vinylphosphonic acid) *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes: Xi:;
     
MSDS Files:

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C=CP(=O)(O)O
  • Uses Poly(vinylphosphonic) acid is a versatile polyelectrolyte useful in several applications: proton conductor for fuel cells1, chemical and biological sensors2, biocomposite materials3 and surface modification and adhesion. 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.
Technology Process of Vinylphosphonic acid

There total 19 articles about Vinylphosphonic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With trifluorormethanesulfonic acid; In benzene; at 120 ℃; for 24h; Inert atmosphere;
Guidance literature:
With water; at 140 ℃; for 38h;
Guidance literature:
With hydrogenchloride; In water; at 80 ℃; for 8h;
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