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About This Item
Linear Formula:
Na2MoO4
CAS Number:
Molecular Weight:
205.92
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.55
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Quality Level
Assay
≥98%
form
granular
reaction suitability
reagent type: catalyst
core: molybdenum
mp
687 °C (lit.)
density
3.78 g/mL at 25 °C (lit.)
SMILES string
[Na+].[Na+].[O-][Mo]([O-])(=O)=O
InChI
1S/Mo.2Na.4O/q;2*+1;;;2*-1
InChI key
TVXXNOYZHKPKGW-UHFFFAOYSA-N
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General description
Sodium molybdate has corrosion resistant properties. On heating, it undergoes degradation and releases Na2O fumes.
Application
Sodium molybdate (Na2MO4) may be used as an electrolyte additive, for use in electrochemical capacitors. Addition of Na2MO4 as an electrolyte additive may result in enhanced capacitance, corrosion prevention and stabilized performance.
It may also be used as a catalyst during the manufacture of paints and dyes.
It may also be used as a catalyst during the manufacture of paints and dyes.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Q Abbas et al.
Faraday discussions, 172, 199-214 (2014-11-27)
Sodium molybdate (Na2MoO4) has been used as an additive to 1 mol L(-1) lithium sulfate electrolyte for electrochemical capacitors based on activated carbon (AC) electrodes, in order to reduce the corrosion of stainless steel current collectors. We demonstrate that the
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Two Anderson-type heteropolyanion-supported copper phenanthroline complexes, [Al(OH)6Mo6O18[Cu(phen)(H2O)2]2]1+ (1c) and [Al(OH)6Mo6O18[Cu(phen)(H2O)Cl]2]1- (1a) complement their charges in one of the title compounds [Al(OH)6Mo6O18[Cu(phen)(H2O)2]2][Al(OH)6Mo6O18[Cu(phen)(H2O)Cl]2].5H2O [1c][1a].5 H2O 1. Similar charge complementarity exists in the chromium analogue, [Cr(OH)6Mo6O18[Cu(phen)(H2O)2]2][Cr(OH)6Mo6O18[Cu(phen)(H2O)Cl]2].5 H2O [2c][2a].5 H2O 2. The chloride coordination
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Hsp90 functions to facilitate the folding of newly synthesized and denatured proteins. Hsp90 function is modulated through its interactions with cochaperones and the binding and hydrolysis of ATP. Recently, novobiocin has been shown to bind to a second nucleotide binding
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