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Names | |
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IUPAC name
Tetrasodium [hexacyanoferrate(II)]
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Other names
Yellow prussiate of soda (YPS), Tetrasodium hexacyanoferrate, Gelbnatron, Ferrocyannatrium, sodium hexacyanoferrate(II), Yellow blood salt
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Identifiers | |
3D model (JSmol)
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EC Number |
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PubChem CID
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UNII | |
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Properties | |
Na4[Fe(CN)6] | |
Molar mass | 303.91 g/mol |
Appearance | pale yellow crystals |
Odor | odorless |
Density | 1.458 g/cm3 |
Melting point | 435 °C (815 °F; 708 K) (anhydrous) 81.5 °C (178.7 °F; 354.6 K) (decahydrate) (decomposes) |
10.2 g/100 mL (10 °C) 17.6 g/100 mL (20 °C) 39.7 g/100 mL (96.6 °C) | |
Refractive index (nD)
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1.530 |
Structure | |
monoclinic | |
Related compounds | |
Other anions
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Sodium ferricyanide (Red prussiate of soda) |
Other cations
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Potassium ferrocyanide |
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 ferrocyanide is the sodium salt of the coordination compound of formula [Fe(CN)6]4−. In its hydrous form, Na4Fe(CN)6 • 10H2O (sodium ferrocyanide decahydrate), it is sometimes known as yellow prussiate of soda. It is a yellow crystalline solid that is soluble in water and insoluble in alcohol. The yellow color is the color of ferrocyanide anion. Despite the presence of the cyanide ligands, sodium ferrocyanide has low toxicity (acceptable daily intake 0–0.025 mg/kg body weight[2]). The ferrocyanides are less toxic than many salts of cyanide, because they tend not to release free cyanide.[3] However, like all ferrocyanide salt solutions, addition of an acid can result in the production of hydrogen cyanide gas, which is extremely toxic.
When combined with an Fe(III) salt, it converts to a deep blue pigment called Prussian blue, FeIII4[FeII(CN)6]3.[4] It is used as a stabilizer for the coating on welding rods. In the petroleum industry, it is used for removal of mercaptans.
In the EU, ferrocyanides (E 535–538) were, as of 2018, solely authorized as additives in salt and salt substitutes, where they serve as anticaking agents. Kidneys are the organ for ferrocyanide toxicity, but according to the EFSA, ferrocyanides are of no safety concern at the levels at which they are used.[5]
Sodium ferrocyanide is produced industrially from hydrogen cyanide, ferrous chloride, and calcium hydroxide, the combination of which affords Ca2[Fe(CN)6] • 11H2O. A solution of this salt is then treated with sodium salts to precipitate the mixed calcium-sodium salt CaNa2[Fe(CN)6]2, which in turn is treated with sodium carbonate to give the tetrasodium salt.[6]
![]() | Original source: https://en.wikipedia.org/wiki/Sodium ferrocyanide.
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