KMnO4 And Glycerol

Potassium permanganate is an inorganic compound with the chemical formula KMnO₄. It is a purplish-black crystalline salt, that dissolves in water as K⁺ and , an intensely pink to purple solution.

Potassium permanganate is widely used in the chemical industry and laboratories as a strong oxidizing agent, and also as a medication for dermatitis, for cleaning wounds, and general disinfection. It is on the World Health Organization's List of Essential Medicines. In 2000, worldwide production was estimated at 30,000 tonnes.

Properties

Potassium permanganate is the potassium salt of the tetrahedral transition metal oxo complex permanganate, in which four O^2- ligands are bound to a manganese(VII) center.

Structure

KMnO₄ forms orthorhombic crystals with constants: ''a'' = 910.5  pm, ''b'' = 572.0 pm, ''c'' = 742.5 pm. The overall motif is similar to that for barium sulfate, with which it forms solid solutions. In the solid (as in solution), each MnO₄⁻ centre is tetrahedral. The Mn–O distances are 1.62 Å.

Color

The purplish-black color of solid potassium permanganate, and the intensely pink to purple color of its solutions, is caused by its permanganate anion, which gets its color from a strong charge-transfer absorption band caused by excitation of electrons from oxo ligand orbitals to empty orbitals of the manganese(VII) center.

Uses

Almost all applications of potassium permanganate exploit its oxidizing properties. As a strong oxidant that does not generate toxic byproducts, KMnO₄ has many niche uses.

Medical uses

Potassium permanganate is used for a number of skin conditions. This includes fungal infections of the foot, impetigo, pemphigus, superficial wounds, dermatitis, and tropical ulcers. It is on the World Health Organization's List of Essential Medicines.

Water treatment

Potassium permanganate is used extensively in the water treatment industry. It is used as a regeneration chemical to remove iron and hydrogen sulfide (rotten egg smell) from well water via a "manganese greensand" filter. "Pot-Perm" is also obtainable at pool supply stores and is used additionally to treat wastewater. Historically it was used to disinfect drinking water and can turn the water pink. It currently finds application in the control of nuisance organisms such as zebra mussels in fresh water collection and treatment systems.

Synthesis of organic compounds

A major application of KMnO₄ is as a reagent for the synthesis of organic compounds. Significant amounts are required for the synthesis of ascorbic acid, chloramphenicol, saccharin, isonicotinic acid, and pyrazinoic acid.

KMnO₄ is used in qualitative organic analysis to test for the presence of unsaturation. It is sometimes referred to as Baeyer's reagent after the German organic chemist Adolf von Baeyer . The reagent is an alkaline solution of potassium permanganate. Reaction with double or triple bonds (-C=C- or -C≡C-) causes the color to fade from purplish-pink to brown. Aldehydes and formic acid (and formates) also give a positive test. The test is antiquated.

KMnO₄ solution is a common thin layer chromatography stain for the detection of oxidizable functional groups, such as alcohols, aldehydes, alkenes, and ketones. Such compounds result in a white to orange spot on TLC plates.

Analytical use

Potassium permanganate can be used to quantitatively determine the total oxidizable organic material in an aqueous sample. The value determined is known as the ''permanganate value.'' In analytical chemistry, a standardized aqueous solution of KMnO₄ is sometimes used as an oxidizing titrant for redox titrations ( permanganometry). As potassium permanganate is titrated, the solution becomes a light shade of purple, which darkens as excess of the titrant is added to the solution. In a related way, it is used as a reagent to determine the Kappa number of wood pulp. For the standardization of KMnO₄ solutions, reduction by oxalic acid is often used. In agricultural chemistry, it is used for estimation of active carbon in soil.

Aqueous, acidic solutions of KMnO₄ are used to collect gaseous mercury in flue gas during stationary source emissions testing.

In histology, potassium permanganate was used as a bleaching agent.

Fruit preservation

Ethylene absorbents extend storage time of bananas even at high temperatures. This effect can be exploited by packing bananas in polyethylene together with potassium permanganate. By removing ethylene by oxidation, the permanganate delays the ripening, increasing the fruit's shelf life up to 4 weeks without the need for refrigeration.

Survival kits

Potassium permanganate is sometimes included in survival kits: as a hypergolic fire starter (when mixed with glycerol antifreeze from a car radiator; as a water sterilizer; and for creating distress signals on snow).

Fire service

Potassium permanganate is added to "plastic sphere dispensers" to create backfires, burnouts, and controlled burns. Polymer spheres resembling ping-pong balls containing small amounts of permanganate are injected with ethylene glycol and projected towards the area where ignition is desired, where they spontaneously ignite seconds later. Both handheld and helicopter- or boat-mounted plastic sphere dispensers are used.

Other uses

Potassium permanganate is one of the principal chemicals used in the film and television industries to "age" props and set dressings. Its ready conversion to brown MnO₂ creates "hundred-year-old" or "ancient" looks on hessian cloth (burlap), ropes, timber, and glass.

Potassium permanganate can be used to oxidize cocaine paste to purify it and increase its stability. This led to the Drug Enforcement Administration launching Operation Purple in 2000, with the goal of monitoring the world supply of potassium permanganate; however, potassium permanganate derivatives and substitutes were soon used thereafter to avoid the operation.

Potassium permangate used as an oxidizing agent in the synthesis of cocaine and methcathinone.

History

In 1659, Johann Rudolf Glauber fused a mixture of the mineral pyrolusite (manganese dioxide, MnO₂) and potassium carbonate to obtain a material that, when dissolved in water, gave a green solution ( potassium manganate) which slowly shifted to violet and then finally red. The reaction that produced the color changes that Glauber observed in his solution of potassium permanganate and potassium manganate (K₂MnO₄) is now known as the "chemical chameleon had an interest in disinfectants; he found that fusing pyrolusite with sodium hydroxide (NaOH) and dissolving it in water produced a solution with disinfectant properties. He patented this solution, and marketed it as 'Condy's Fluid'. Although effective, the solution was not very stable. This was overcome by using potassium hydroxide (KOH) rather than NaOH. This was more stable, and had the advantage of easy conversion to the equally effective potassium permanganate crystals. This crystalline material was known as 'Condy's crystals' or 'Condy's powder'. Potassium permanganate was comparatively easy to manufacture, so Condy was subsequently forced to spend considerable time in litigation to stop competitors from marketing similar products.

Early photographers used it as a component of flash powder. It is now replaced with other oxidizers, due to the instability of permanganate mixtures.

Preparation

Potassium permanganate is produced industrially from manganese dioxide, which also occurs as the mineral pyrolusite. In 2000, worldwide production was estimated at 30,000 tonnes. The MnO₂ is fused with potassium hydroxide and heated in air or with another source of oxygen, like potassium nitrate or potassium chlorate. This process gives potassium manganate:
:2 MnO₂ + 4 KOH + O₂ → 2 K₂MnO₄ + 2 H₂O
(With sodium hydroxide, the end product is not sodium manganate but an Mn(V) compound, which is one reason why the potassium permanganate is more commonly used than sodium permanganate. Furthermore, the potassium salt crystallizes better.)

The potassium manganate is then converted into permanganate by electrolytic oxidation in alkaline media:
:2 K₂MnO₄ + 2 H₂O → 2 KMnO₄ + 2 KOH + H₂

Other methods

Although of no commercial importance, potassium manganate can be oxidized by chlorine or by disproportionation under acidic conditions. The chlorine oxidation reaction is
:2 K₂MnO₄ + Cl₂ → 2 KMnO₄ + 2 KCl

and the acid-induced disproportionation reaction may be written as
:3 K₂MnO₄ + 4 HCl → 2 KMnO₄ + MnO₂ + 2 H₂O + 4 KCl

A weak acid such as carbonic acid is sufficient for this reaction:
:3 K₂MnO₄ + 2 CO₂ → 2 KMnO₄ + 2 K₂CO₃ + MnO₂

Permanganate salts may also be generated by treating a solution of Mn²⁺ ions with strong oxidants such as lead dioxide (PbO₂), sodium bismuthate (NaBiO₃), or peroxydisulfate. Tests for the presence of manganese exploit the vivid violet color of permanganate produced by these reagents.

Reactions

Organic chemistry

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 decolorizes the initially purple permanganate solution and generates a brown precipitate (MnO₂). In this context, it is sometimes called ''Baeyer's reagent''. However, bromine serves better in measuring unsaturation (double or triple bonds) quantitatively, since KMnO₄, being a very strong oxidizing agent, can react with a variety of groups.

Under acidic conditions, the alkene double bond is cleaved to give the appropriate carboxylic acid:
: CH₃(CH₂)₁₇CH=CH₂ + 2 KMnO₄ + 3 H₂SO₄ → CH₃(CH₂)₁₇COOH + CO₂ + 4 H₂O + K₂SO₄ + 2 MnSO₄

Potassium permanganate oxidizes aldehydes to carboxylic acids, illustrated by the conversion of ''n''-heptanal to heptanoic acid:
:5 C₆H₁₃CHO + 2 KMnO₄ + 3 H₂SO₄ → 5 C₆H₁₃COOH + 3 H₂O + K₂SO₄ + 2 MnSO₄

Even an alkyl group (with a benzylic hydrogen) on an aromatic ring is oxidized, e.g. toluene to benzoic acid.

:5 C₆H₅CH₃ + 6 KMnO₄ + 9 H₂SO₄ → 5 C₆H₅COOH + 14 H₂O + 3 K₂SO₄ + 6 MnSO₄

Glycols and polyols are highly reactive toward KMnO₄. For example, addition of potassium permanganate to an aqueous solution of sugar and sodium hydroxide produces the chemical chameleon

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