Chemistry:Sodium orthovanadate

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Sodium orthovanadate
File:Na3VO4dihydrate.tif
Names
IUPAC name
Sodium vanadate(V)
Other names
Sodium vanadium oxide
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
RTECS number
  • YW1120000
UNII
Properties
Na
3
VO
4
Molar mass 183.908 g/mol
Appearance white powder
Density 2.16 g/cm3, solid
Melting point 858 °C (1,576 °F; 1,131 K)
22.17 g/100 mL
Solubility insoluble in ethanol
Structure
cubic
Thermochemistry
164.8 J/mol K
190 J/mol K
−1757 kJ/mol
Hazards
Main hazards Harmful.
NFPA 704 (fire diamond)
Flammability code 0: Will not burn. E.g. waterHealth code 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
0
3
0
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
330 mg/kg (oral, rat)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Sodium orthovanadate is the inorganic compound with the chemical formula Na
3
V O
4
. It forms a dihydrate Na
3
VO
4
 · 2H2O
. Sodium orthovanadate is a salt of the VO3−
4
oxyanion. It is a colorless, water-soluble solid.[2]

Synthesis and structure

Sodium orthovanadate is produced by dissolving vanadium(V) oxide in a solution of sodium hydroxide:

V
2
O
5
+ 6 NaOH → 2 Na
3
VO
4
+ 3 H
2
O

The salt features tetrahedral VO3−
4
anion centers linked to octahedral Na+
cation sites.[3]

Condensation equilibria

Like many oxometalates, orthovanadate is subject to a number of reactions, which have been analyzed by 51V NMR studies. At high pH, VO3−
4
ions exist in equilibrium with HVO2−
4
.[4] At lower pH's, condensation ensues to give various polyoxovanadates. Ultimately, decavanadate is formed.[5]

Biochemistry

Vanadates exhibit a variety of biological activities, in part because they serve as structural mimics of phosphates.[6][7] It acts as a competitive inhibitor of ATPases, alkaline and acid phosphatases, and protein-phosphotyrosine phosphatases,[8] and its inhibitory effects can be reversed by dilution or the addition of ethylenediaminetetraacetic acid (EDTA).[9]

Orthovanadate is activated by boiling and adjusting pH to ~10; this depolymerizes decavanadate into the active inhibitor, monovanadate.[8]

References

  1. "Archived copy". http://www.sciencelab.com/msds.php?msdsId=9925008. 
  2. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8. 
  3. Kato, K.; Takayama-Muromachi, E. (1987). "Die Struktur des Trinatriumvanadattrihydrats". Acta Crystallogr. C43 (6): 1030–1032. doi:10.1107/S0108270187093120. Bibcode1987AcCrC..43.1030K. http://journals.iucr.org/c/issues/1987/06/00/a27117/a27117.pdf. 
  4. Rehder, D.; Polenova, T.; Bühl, M. (2007). Vanadium-51 NMR. Annual Reports on NMR Spectroscopy. 62. pp. 49–114. doi:10.1016/S0066-4103(07)62002-X. ISBN 9780123739193. 
  5. Klemperer, W. G.; Yaghi, O. (1983). "Tetrabutylammonium Trihydrogen Decavanadate(V)". Inorg. Synth. 27: 83. doi:10.1002/9780470132586.ch15. 
  6. Korbecki, Jan; Baranowska-Bosiacka, Irena; Gutowska, Izabela; Chlubek, Dariusz (2012). "Biochemical and medical importance of vanadium compounds". Acta Biochim. Pol. 59 (2): 195–200. doi:10.18388/abp.2012_2138. PMID 22693688. http://www.actabp.pl/pdf/2_2012/195.pdf. 
  7. Crans, D. C.; Chatterjee, P. B. (2013). "Comprehensive Inorganic Chemistry II: From Elements to Applications". in Reedijk, Jan; Poeppelmeier, Kenneth. Comprehensive Inorganic Chemistry II. 3. pp. 323–342. doi:10.1016/B978-0-08-097774-4.00324-7. ISBN 978-0-08-097774-4. 
  8. 8.0 8.1 "Sodium orthovanadate". https://www.sigmaaldrich.com/content/dam/sigma-aldrich/docs/Sigma/Product_Information_Sheet/1/s6508pis.pdf. 
  9. Biolabs, New England. "Sodium Orthovanadate (Vanadate) | NEB" (in en). https://www.neb.com/products/p0758-sodium-orthovanadate-activated-vanadate#Product%20Information. 

See also