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Ammonium heptamolybdate
IUPAC name
Other names Ammonium molybdate
Ammonium paramolybdate
(see text)
Identifiers
CAS number 12027-67-7 Yes check.svgY,
12054-85-2 (tetrahydrate)
PubChem 24867009
EC number 234-320-9
Properties
Molecular formula (NH4)6Mo7O24
Molar mass 1163.9 g/mol
1235.86 g/mol (tetrahydrate)
Appearance white crystalline solid
Density 2.498 g/cm3
Melting point

~90 ˚C

Solubility in water 43 g/100 ml (tetrahydrate)
Hazards
EU Index Not listed
Main hazards Irritant
NFPA 704
NFPA 704.svg
0
2
0
 
Flash point Non-flammable
Related compounds
Other anions Ammonium orthomolybdate
Ammonium dimolybdate
Other cations Potassium paramolybdate
Related compounds Molybdenum(VI) oxide
Molybdic acid
 Yes check.svgY (what is this?)  (verify)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Ammonium heptamolybdate is an odourless crystalline compound ranging in colour from white to yellow-green. It is usually encoutered as the tetrahydrate, whose chemical formula is (NH4)6Mo7O24·4H2O. It is often referred to as ammonium paramolybdate or simply as ammonium molybdate, although the latter name can also refer to ammonium orthomolybdate, (NH4)2MoO4, and several other species.

Contents

[edit] Synthesis

Ammonium paramolybdate is easily prepared by dissolving molybdenumtrioxide in an excess of ammonia (a solution of NH3 in water), and evaporating the solution at room temperature. While the solution evaporates, the excess of ammonia escapes. This method results in the formation of six-sides prisms of the tetrahydrate of ammonium paramolybdate, which are transparent as water [1].
Solutions of ammoniumparamolybdate react acid. The pH value of a concentrated solution will lie between 5 and 6.

[edit] Uses

  • as an analytical reagent to find the presence of phosphates, silicates, arsenates and lead in pigments
  • in the production of molybdenum metal and ceramics
  • in the preparation of dehydrogenation and desulphurisation catalysts
  • in the fixing of metals
  • in electroplating
  • in fertilizers for crops.
  • as a negative stain in biological electron microscopy, typically in the 3-5% (vol/vol) concentration range and in the presence of trehalose [2]; or at saturated concentration to perform cryo-negative staining [3,4].

[edit] References

  1. L. Svanberg & H. Struve, J. pr. Ch. 44 [1848], 282; cited in Gmelin's Handbuch für Anorganische Chemie, 53 255
  2. Harris, J.R. and Horne, R.W. 1991. Negative staining, in Harris J. R. (Ed.), Electron Microscopy in Biology, Oxford University Press, Oxford.
  3. Adrian, M., Dubochet, J., Fuller, S.D. and Harris, J.R. 1998. Cryo-negative Staining. Micron 29, 145-160.
  4. De Carlo, S., El-Bez, C., Alvarez-Rúa, C., Borge, J. and Dubochet, J. 2002. Cryo-negative staining reduces electron-beam sensitivity of vitrified biological particles. J. Struct. Biol. 138, 216-226.

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