Potassium permanganate

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Potassium permanganate
Potassium permanganate unit cellPotassium permanganate
General
Other names Potassium manganate(VII)
Molecular formula KMnO4
Molar mass 158.04 g/mol
Appearance black crystals;

bright purple in solution

CAS number [7722-64-7]
Properties
Density and phase 2.703 g/cm³, solid
Solubility in water 6.38 g/100 ml (20 °C)
Melting point 270 °C decomp.
Thermodynamic data
Standard enthalpy
of formation
ΔfH°solid
−813.4 kJ/mol
Standard molar entropy
S°solid
171.7 J.K−1.mol−1
Hazards
EU classification Oxidant (O)
Harmful (Xn)
Dangerous for
the environment (N)
NFPA 704

NFPA 704.svg

0
1
0
OX
Related compounds
Other anions Potassium hypomanganate
Other cations Sodium permanganate
Related compounds Potassium manganate
Manganese heptoxide
Except where noted otherwise, data are given for
materials in their standard state (at 25 °C, 100 kPa)
See Wikipedia:Disclaimer.

Potassium permanganate is an inorganic chemical compound. Its chemical formula is KMnO4. It contains potassium and permanganate ions. The manganese is in the +7 oxidation state. It is also known as permanganate of potash and Condy's crystals. Potassium permanganate is a strong oxidizing agent, which means it has a tendency to take electrons from other chemicals. It dissolves in water to give purple solutions. If it is evaporated, it makes purple-black shiny crystals.[2] It has a sweet taste and is odorless.[1]

History[change | edit source]

In 1659 a German chemist, J.R. Glauber, melted a mixture of the mineral pyrolusite and potassium carbonate to obtain a material that made a green solution (potassium manganate) when dissolved in water. It slowly changed colour to violet (potassium permanganate) and then finally red. This report is the first description of the production of potassium permanganate.

Just under 200 years later a Londoner named Henry Bollmann Condy was a chemist. He had an interest in disinfectants and made some things like ozonised water. He found that when he melted pyrolusite with sodium hydroxide and dissolved it in water, it made a solution that had good disinfectant properties. He patented this solution, and sold it as Condy's Fluid. The problem was that the solution was not very stable. This was fixed by using potassium hydroxide rather than sodium hydroxide. This gave a more stable material. It also was able to be dried to the just as good potassium permanganate powder. This powder was called Condy’s crystals or Condy’s powder. Potassium permanganate was easy to make so Condy tried to stop other people from making it and selling it themselves.

Early photographers used it in flash powder.

Uses[change | edit source]

Chemical applications[change | edit source]

Potassium permanganate is used as an oxidizing agent.[3] It also is used in disinfectants and in deodorizers. It can be used to make many different kinds of chemicals. In waste water treatment, it is used to get rid of hydrogen sulfide, a stinky toxic gas. In analytical chemistry, an accurate concentration of KMnO4 is sometimes used to see how much of a certain reducing agent is in the titration. In a related way, it is used as a reagent for wood pulp. Mixing potassium permanganate and formaldehyde makes a mild tear gas.

As an oxidant in organic synthesis[change | edit source]

Dilute solutions of KMnO4 convert alkenes into diols (glycols). This behaviour is also used as a qualitative test for the presence of double or triple bonds in a molecule, since the reaction makes the permanganate solution colorless. It is sometimes referred to as Baeyer's reagent.

Concentrated solutions oxidize a methyl group on an aromatic ring, e.g. toluene to benzoic acid.

KMnO4 oxidizes pseudoephedrine hydrochloride to produce methcathinone, a Schedule I drug in the United States. Consequently the DEA has restricted its use and sale by classifying it as a List I controlled precursor. Potassium permanganate is listed as a Table I precursor under the United Nations Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances.[2]

Acids and Potassium Permanganate[change | edit source]

Concentrated sulfuric acid reacts with potassium permanganate to give manganese(VII) oxide, which can be explosive. [4][5][6]. This reaction also makes ozone. The ozone can ignite paper soaked in alcohol. This reaction is very dangerous.

6 KMnO4 + 9 H2SO4 → 6 MnSO4 + 3 K2SO4 + 9 H2O + 5 O3

Concentrated HCl makes chlorine.

2 KMnO4 + 16 HCl → 2 MnCl2 + 2 KCl + 8 H2O + 5 Cl2

The Mn-containing products from redox reactions depend on the pH. Acidic solutions of permanganate are reduced to the faintly pink Mn2+ ion, as in manganese(II) chloride. In neutral solution, permanganate is reduced to brown manganese(IV) oxide, where Mn is in a +4 oxidation state. Manganese(IV) oxide is the stuff that stains skin when potassium permanganate is put on it. Potassium permanganate spontaneously reduces in an basic solution to green-coloured potassium manganate, where manganese is in the +6 oxidation state.

Biomedical uses[change | edit source]

  • Dilute solutions are used as a treatment for canker sores (ulcers) (0.25%), disinfectant for the hands (about 1%) and treatment for mild pompholyx dermatitis or fungal infections of the hands or feet.
  • A dilute solution of acidified potassium permanganate is used in histology to bleach melanin which obscures tissue detail.
  • Potassium permanganate can be used to differentiate amyloid AA from other types of amyloid pathologically deposited in body tissues. Incubation of fixed tissue with potassium permanganate will prevent amyloid AA from staining with congo red whereas other types of amyloid are unaffected.[7][8]

Miscellaneous uses[change | edit source]

Dissolved potassium permanganate
  • Solutions of KMnO4 have been used together with 80% hydrogen peroxide to propel a rocket. In this use, it was called Z-Stoff. This propellant is still used in torpedoes.
  • A dilute (10 mg/l) of potassium permanganate can be used to eliminate snails from plants prior to placing them in a fresh-water aquarium.
  • High-grade potassium permanganate can be found at pool supply stores and is used in rural areas to remove iron and hydrogen sulfide (rotten egg smell) from well water.
  • KMnO4 is often included in survival kits along with either glycerine or a glucose tablet for the purposes of making fire. The glucose tablet can be ground up, mixed with the potassium permanganate and caused to combust by applying friction. It can also be mixed with anti-freeze from a vehicle to produce flame, although this can be dangerous and should be done in a controlled manner i.e. dipping some paper into the anti-freeze and then adding a small amount of potassium permanganate. The ability to sterilize water and wounds is also advantageous and another reason for inclusion in a survival kit.
  • KMnO4 is employed to treat some parasitic diseases of fish, in treatment of drinking water, as well as an antidote in phosphorus poisoning. In Africa, it has been used as a disinfectant for vegetables such as lettuce.

Hazards[change | edit source]

Solid potassium permanganate is a strong oxidizer and in general it should be kept separated from reducing agents. Some reactions need a bit of water. For example, powdered potassium permanganate and powdered sugar will ignite (but not explode) a few seconds after a drop of water is added. Dilute solutions of KMnO4 are not dangerous. KMnO4 forms dangerous products when mixed with concentrated acids.

Potassium permanganate stains skin and clothing and should be handled with care. Clothing stains may be washed away using acetic acid. Skin stains disappear within 48 hours.

References[change | edit source]

  1. ^ F. Burriel, F. Lucena, S. Arribas and J. Hernández, (1985), Química Analítica Cualitativa, page 688, ISBN 84-9732-140-5.
  2. ^  Fatiadi, A. J. Synthesis 1987, 85-127. (Review) (doi:10.1055/s-1987-27859)
  3. ^  F. A. Cotton, G. Wilkinson, C. A. Murillo, and M. Bochmann (April 1999). Advanced Inorganic Chemistry, 6th Edition. Wiley-VCH. ISBN 0-471-19957-5
  4. ^  van Rijswijk MH, van Heusden CW.American Journal of Pathology.1979Oct;97(1):43-58. PMID 495695
  5. ^ Dzhabiev, T. S.; Denisov, N. N.; Moiseev, D. N. and Shilov, A. E., "Formation of Ozone During the Reduction of Potassium Permanganate in Sulfuric Acid Solutions", Russian Journal of Physical Chemistry, 2005, volume 79, pages 1755-1760.
  6. ^ Barthel, H. and Duvinage, B., "Clemens Winkler. His Experiments with Ozone in 1892", Praxis der Naturwissenschaften, Chemie, 2000, volume 49, page 18ff.
  7. ^ Wright JR, Calkins E, Humphrey RL.Laboratory Investigation. 1977 Mar;36(3):274-81. PMID 839739

Other websites[change | edit source]