Sodium dichromate is the inorganic compound with the formula Na2Cr2O7. Usually, however, the salt is handled as its dihydrate Na2Cr2O7·2H2O. Virtually all chromium ore is processed via conversion to sodium dichromate and virtually all compounds and materials based on chromium are prepared from this salt. In terms of reactivity and appearance, sodium dichromate and potassium dichromate are very similar. The sodium salt is, however, around twenty times more soluble in water than the potassium salt (49 g/L at 0 °C) and its equivalent weight is also lower, which is often desirable.
Chromic acid disodium salt
3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||261.97 g/mol (anhydrous)|
298.00 g/mol (dihydrate)
|Melting point||356.7 °C (674.1 °F; 629.8 K)|
|Boiling point||400 °C (752 °F; 673 K) decomposes|
|73 g/100 mL at 25 °C|
|Solubility in other solvents||soluble in methanol, ethanol|
Refractive index (nD)
|Safety data sheet||ICSC 1369|
Carc. Cat. 2
Muta. Cat. 2
Repr. Cat. 2
Very toxic (T+)
Dangerous for the environment (N)
|R-phrases (outdated)||R45, R46, R60, R61, R8, R21, R25, R26, R34, R42/43, R48/23, R50/53,|
|S-phrases (outdated)||S53, S45, S60, S61|
|NFPA 704 (fire diamond)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Sodium dichromate is generated on a large scale from ores containing chromium(III) oxides. The ore is fused with a base, typically sodium carbonate, at around 1000 °C in the presence of air (source of oxygen):
This step solubilizes the chromium and allows it to be extracted into hot water. At this stage, other components of the ore such as aluminium and iron compounds, are poorly soluble. Acidification of the resulting aqueous extract with sulfuric acid or carbon dioxide affords the dichromate:
The dichromate is isolated as the dihydrate by crystallization. In this way, many millions of kilograms of sodium dichromate are produced annually.
Since chromium(VI) is toxic, especially as the dust, such factories are subject to stringent regulations. For example, effluent from such refineries is treated with reducing agents to return any chromium(VI) to chromium(III), which is less threatening to the environment. A variety of hydrates of this salt are known, ranging from the decahydrate below 19.5 °C (CAS# 13517-17-4 ) as well as hexa-, tetra-, and dihydrates. Above 62 °C, these salts lose water spontaneously to give the anhydrous material. It is crystallised around 30 to 35 degrees C
In the area of organic synthesis, this compound oxidizes benzylic and allylic C-H bonds to carbonyl derivatives. For example, 2,4,6-trinitrotoluene is oxidized to the corresponding carboxylic acid. Similarly, 2,3-dimethylnaphthalene is oxidized by Na2Cr2O7 to 2,3-naphthalenedicarboxylic acid.
- 3 R2CHOH + Cr2O72− + 2 H+ → 3 R2C=O + Cr2O3 + 4 H2O
Relative to the potassium salt, the main advantage of sodium dichromate is its greater solubility in water and polar solvents like acetic acid.
- Gerd Anger, Jost Halstenberg, Klaus Hochgeschwender, Christoph Scherhag, Ulrich Korallus, Herbert Knopf, Peter Schmidt, Manfred Ohlinger, "Chromium Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. doi:10.1002/14356007.a07_067
- Freeman, F. "Sodium Dichromate" in Encyclopedia of Reagents for Organic Synthesis (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. doi:10.1002/047084289.
- Clarke, H. T.; Hartman, W. W. (1941). "2,4,6-Trinitrobenzoic Acid". Organic Syntheses.CS1 maint: multiple names: authors list (link); Collective Volume, 1, p. 543
- Friedman, L. (1973). "2,3-Naphthalenedicarboxylic Acid". Organic Syntheses.; Collective Volume, 5, p. 810
- L. T. Sandborn (1929). "l-Menthone". Organic Syntheses. 9: 59.; Collective Volume, 1, p. 340
- W. F. Bruce (1941). "Cholestanone". Organic Syntheses.; Collective Volume, 2, p. 139
- ILO 1369 - Sodium Dichromate