Caustic potash, Lye, Potash lye, Potassia, Potassium hydrate, KOH
3D model (JSmol)
|E number||E525 (acidity regulators, ...)|
CompTox Dashboard (EPA)
|Molar mass||56.11 g mol-1|
|Appearance||white solid, deliquescent|
|Density||2.044 g/cm3 (20 °C)|
2.12 g/cm3 (25 °C)
|Melting point||360 °C (680 °F; 633 K)|
|Boiling point||1,327 °C (2,421 °F; 1,600 K)|
|85 g/100 mL (-23.2 °C)|
97 g/100 mL (0 °C)
121 g/100 mL (25 °C)
138.3 g/100 mL (50 °C)
162.9 g/100 mL (100 °C)
|Solubility||soluble in alcohol, glycerol |
insoluble in ether, liquid ammonia
|Solubility in methanol||55 g/100 g (28 °C)|
|Solubility in isopropanol||~14 g / 100 g (28 °C)|
|Basicity (pKb)||−0.7(KOH(aq) = K+ + OH-)|
Refractive index (nD)
|1.409 (20 °C)|
Heat capacity (C)
Std enthalpy of
Gibbs free energy (ΔfG?)
|Safety data sheet||ICSC 0357|
|GHS signal word||Danger|
|P280, P305+351+338, P310|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
|273 mg/kg (oral, rat)|
|US health exposure limits (NIOSH):|
|C 2 mg/m3|
IDLH (Immediate danger)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Along with sodium hydroxide (NaOH), this colorless solid is a prototypical strong base. It has many industrial and niche applications, most of which exploit its caustic nature and its reactivity toward acids. An estimated 700,000 to 800,000 tonnes were produced in 2005. About 100 times more NaOH than KOH is produced annually. KOH is noteworthy as the precursor to most soft and liquid soaps, as well as numerous potassium-containing chemicals. It is a white solid that is dangerously corrosive. Most commercial samples are ca. 90% pure, the remainder being water and carbonates.
Potassium hydroxide is usually sold as translucent pellets, which become tacky in air because KOH is hygroscopic. Consequently, KOH typically contains varying amounts of water (as well as carbonates - see below). Its dissolution in water is strongly exothermic. Concentrated aqueous solutions are sometimes called potassium lyes. Even at high temperatures, solid KOH does not dehydrate readily.
At higher temperatures, solid KOH crystallizes in the NaCl crystal structure. The OH group is either rapidly or randomly disordered so that the OH− group is effectively a spherical anion of radius 1.53 Å (between and in size). At room temperature, the OH− groups are ordered and the environment about the centers is distorted, with distances ranging from 2.69 to 3.15 Å, depending on the orientation of the OH group. KOH forms a series of crystalline hydrates, namely the monohydrate KOH o H2O, the dihydrate KOH o 2H2O and the tetrahydrate KOH o 4H2O.
Like NaOH, KOH exhibits high thermal stability. The gaseous species is dimeric. Because of its high stability and relatively low melting point, it is often melt-cast as pellets or rods, forms that have low surface area and convenient handling properties.
About 121 g of KOH dissolve in 100 mL water at room temperature, which contrasts with 100 g/100 mL for NaOH. Thus on a molar basis, KOH is slightly more soluble than NaOH. Lower molecular-weight alcohols such as methanol, ethanol, and propanols are also excellent solvents. They participate in an acid-base equilibrium. In the case of methanol the potassium methoxide (methylate) forms: 
When R is a long chain, the product is called a potassium soap. This reaction is manifested by the "greasy" feel that KOH gives when touched -- fats on the skin are rapidly converted to soap and glycerol.
Historically, KOH was made by adding potassium carbonate to a strong solution of calcium hydroxide (slaked lime) The salt metathesis reaction results in precipitation of solid calcium carbonate, leaving potassium hydroxide in solution:
Filtering off the precipitated calcium carbonate and boiling down the solution gives potassium hydroxide ("calcinated or caustic potash"). This method of producing potassium hydroxide remained dominant until the late 19th century, when it was largely replaced by the current method of electrolysis of potassium chloride solutions. The method is analogous to the manufacture of sodium hydroxide (see chloralkali process):
Hydrogen gas forms as a byproduct on the cathode; concurrently, an anodic oxidation of the chloride ion takes place, forming chlorine gas as a byproduct. Separation of the anodic and cathodic spaces in the electrolysis cell is essential for this process.
KOH and NaOH can be used interchangeably for a number of applications, although in industry, NaOH is preferred because of its lower cost.
Many potassium salts are prepared by neutralization reactions involving KOH. The potassium salts of carbonate, cyanide, permanganate, phosphate, and various silicates are prepared by treating either the oxides or the acids with KOH. The high solubility of potassium phosphate is desirable in fertilizers.
The saponification of fats with KOH is used to prepare the corresponding "potassium soaps", which are softer than the more common sodium hydroxide-derived soaps. Because of their softness and greater solubility, potassium soaps require less water to liquefy, and can thus contain more cleaning agent than liquefied sodium soaps.
Aqueous potassium hydroxide is employed as the electrolyte in alkaline batteries based on nickel-cadmium, nickel-hydrogen, and manganese dioxide-zinc. Potassium hydroxide is preferred over sodium hydroxide because its solutions are more conductive. The nickel-metal hydride batteries in the Toyota Prius use a mixture of potassium hydroxide and sodium hydroxide.Nickel-iron batteries also use potassium hydroxide electrolyte.
In food products, potassium hydroxide acts as a food thickener, pH control agent and food stabilizer. The FDA considers it (as a direct human food ingredient) as generally safe when combined with "good" manufacturing practice conditions of use. It is known in the E number system as E525.
Like sodium hydroxide, potassium hydroxide attracts numerous specialized applications, virtually all of which rely on its properties as a strong chemical base with its consequent ability to degrade many materials. For example, in a process commonly referred to as "chemical cremation" or "resomation", potassium hydroxide hastens the decomposition of soft tissues, both animal and human, to leave behind only the bones and other hard tissues.Entomologists wishing to study the fine structure of insect anatomy may use a 10% aqueous solution of KOH to apply this process.
In chemical synthesis, the choice between the use of KOH and the use of NaOH is guided by the solubility or keeping quality of the resulting salt.
KOH is also used for semiconductor chip fabrication. See also: anisotropic wet etching.
Potassium hydroxide is often the main active ingredient in chemical "cuticle removers" used in manicure treatments.
Because aggressive bases like KOH damage the cuticle of the hair shaft, potassium hydroxide is used to chemically assist the removal of hair from animal hides. The hides are soaked for several hours in a solution of KOH and water to prepare them for the unhairing stage of the tanning process. This same effect is also used to weaken human hair in preparation for shaving. Preshave products and some shave creams contain potassium hydroxide to force open the hair cuticle and to act as a hygroscopic agent to attract and force water into the hair shaft, causing further damage to the hair. In this weakened state, the hair is more easily cut by a razor blade.
Potassium hydroxide is used to identify some species of fungi. A 3-5% aqueous solution of KOH is applied to the flesh of a mushroom and the researcher notes whether or not the color of the flesh changes. Certain species of gilled mushrooms, boletes, polypores, and lichens are identifiable based on this color-change reaction.
Potassium hydroxide and its solutions are severe irritants to skin and other tissue.