Potassium ferrocyanide

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(pə′tas·ē·əm ′fer·ō′sī·ə′nīd)

(inorganic chemistry) K4Fe(CN)6·3H2O Yellow crystals with saline taste; soluble in water, insoluble in alcohol; loses water at 60°C; used in medicine, dry colors, explosives, and as an analytical reagent. Also known as yellow prussiate of potash.


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Potassium ferrocyanide

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Potassium ferrocyanide
Identifiers
CAS number 13943-58-3 YesY, (anhydrous)
14459-95-1 (trihydrate)
PubChem 161067
Properties
Molecular formula C6N6FeK4
Molar mass 368.35 g/mol (anhydrous)
422.388 g/mol (trihydrate)
Appearance Light yellow, crystalline granules.
Density 1.85 g/cm3 (trihydrate)
Melting point

69−71 °C

Boiling point

400 °C (decomp)

Solubility in water trihydrate
28.9 g/100 mL (20 °C)
Solubility insoluble in ethanol, ether
Hazards
EU Index Not listed
R-phrases R32, R52, R53
S-phrases S50(B), S61
NFPA 704
NFPA 704.svg
0
1
0
Flash point Non-flammable
Related compounds
Other anions Potassium ferricyanide
Other cations Sodium ferrocyanide
Prussian blue
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Potassium ferrocyanide is the inorganic compound with formula K4[Fe(CN)6] · 3H2O. It is the potassium salt of the coordination complex [Fe(CN)6]4-. This salt forms lemon-yellow monoclinic crystals.

Contents

Synthesis

Potassium ferrocyanide is produced industrially from hydrogen cyanide, ferrous chloride, calcium hydroxide, the combination of which affords Ca2[Fe(CN)6] · 11H2O. This solution is then treated with potassium salts to precipitate the mixed calcium-potassium salt CaK2[Fe(CN)6], which in turn is treated with potassium carbonate to give the tetrapotassium salt.[2]

Chemical reactions

Treatment of potassium ferrocyanide with nitric acid givesH2[Fe(NO)(CN)5]. After neutralization of this intermediate with sodium carbonate, red crystals of sodium nitroprusside can be selectively crystallized.[3]

Upon treatment with chlorine gas, potassium ferrocyanide converts to potassium ferricyanide:

2 K4[Fe(CN)6] + Cl2 → 2 K3[Fe(CN)6] + 2 KCl

This reaction can be used to remove potassium ferrocyanide from a solution.[citation needed]

A famous reaction involves treatment with ferric salts to give Prussian blue. With the approximate composition KFe2(CN)6, this insoluble but deeply coloured material is the blue of blueprinting.

Potassium ferrocyanide, potassium ferricyanide, and Prussian blue account for over 97% of cyanides in the environment.[4]

Applications

Potassium ferrocyanide finds many niche applications in industry. It and the related sodium salt are widely used as anti-caking agents for both road salt and table salt. The potassium and sodium ferrocyanides are also used in the purification of tin and the separation of copper from molybdenum ores. Potassium ferrocyanide is used in the production of wine and citric acid.[2]

In the laboratory, potassium ferrocyanide is used to determine the concentration of potassium permanganate, a compound often used in titrations based on redoxreactions. Potassium ferrocyanide is used in a mixture with potassium ferricyanide and phosphate buffered solution (PBS) to provide a buffer for X-Gal, which is used to cleave Beta-galactosidase, giving a bright blue visualization where an antibody (or other molecule), conjugated to Beta-gal, has bonded to its target.

Potassium ferrocyanide can be used as a fertilizer for plants.[citation needed]

Toxicity

Potassium ferrocyanide is nontoxic, although upon contact with strong acid it can release toxic hydrogen cyanide gas. It is not decomposed to cyanide in the body. The toxicity in rats is low, with lethal dose (LD50) at 6400 mg/kg.[1]

See also

References

  1. ^ a b "POTASSIUM FERROCYANIDE MSDS Number: P5763 - Effective Date: 12/08/96". J. T. Baker Inc.. http://hazard.com/msds/mf/baker/baker/files/p5763.htm. Retrieved 2012-04-08. 
  2. ^ a b Gail, E.; Gos, S.; Kulzer, R.; Lorösch, J.; Rubo, A.; Sauer, M.; Kellens, R.; Reddy, J.; Steier, N.; Hasenpusch, W. (October 2011). "Cyano Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a08_159.pub3. 
  3. ^ Seel, F. (1965). "Sodium Nitrosyl Cyanoferrate". In Brauer, G.. Handbook of Preparative Inorganic Chemistry. 2 (2nd ed.). New York: Academic Press. p. 1768. LCCN 63-14307. http://www.scribd.com/doc/27443280/Handbook-of-Preparative-Inorganic-Chemistry-Vol-2-2d-Ed-George-Brauer. 
  4. ^ Yu, X. Z.; Gu, J. D.; Li, T. P. (August 2008). "Availability of ferrocyanide and ferricyanide complexes as a nitrogen source to cyanogenic plants". Archives of Environmental Contamination and Toxicology 55 (2): 229–237. doi:10.1007/s00244-007-9101-6. PMID 18180862. 

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