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)|
Refractive index (nD)
|1.409 (20 °C)|
Heat capacity (C)
Std enthalpy of
Gibbs free energy (ΔfG˚)
|P280, P305+P351+P338, P310|
|NFPA 704 (fire diamond)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
|273 mg/kg (oral, rat)|
|NIOSH (US health exposure limits):|
|C 2 mg/m3|
IDLH (Immediate danger)
|Safety data sheet (SDS)||ICSC 0357|
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), KOH 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. 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.
Properties and structureEdit
KOH exhibits high thermal stability. 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. These pellets become tacky in air because KOH is hygroscopic. Most commercial samples are ca. 90% pure, the remainder being water and carbonates. 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 Cl− and F− in size). At room temperature, the OH− groups are ordered and the environment about the K+ centers is distorted, with K+−OH− 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 · H2O, the dihydrate KOH · 2H2O and the tetrahydrate KOH · 4H2O.
Solubility and desiccating propertiesEdit
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, NaOH is slightly more soluble than KOH. 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: 
- KOH + CH3OH → CH3OK + H2O
As a nucleophile in organic chemistryEdit
- KOH + RCOOR' → RCOOK + R'OH
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.
Reactions with inorganic compoundsEdit
- KOH + CO2 → KHCO3
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:
- Ca(OH)2 + K2CO3 → CaCO3 + 2 KOH
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):
- 2 KCl + 2 H2O → 2 KOH + Cl2 + H2
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.
Precursor to other potassium compoundsEdit
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.
Manufacture of soft soapsEdit
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.
As an electrolyteEdit
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 generally safe as a direct food ingredient when used in accordance with Good Manufacturing Practices. 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 (for example 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.
- Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. p. 4-80. ISBN 0-8493-0486-5.
- "potassium hydroxide". chemister.ru. Archived from the original on 18 May 2014. Retrieved 8 May 2018.
- "A18854 Potassium hydroxide". Alfa Aesar. Thermo Fisher Scientific. Archived from the original on 19 October 2015. Retrieved 26 October 2015.
- Seidell, Atherton; Linke, William F. (1952). Solubilities of Inorganic and Organic Compounds. Van Nostrand. Retrieved 2014-05-29.
- Popov, K.; et al. (2002). "7Li, 23Na, 39K and 133Cs NMR comparative equilibrium study of alkali metal cation hydroxide complexes in aqueous solutions. First numerical value for CsOH formation". Inorganic Chemistry Communications. 3 (5): 223–225. doi:10.1016/S1387-7003(02)00335-0. ISSN 1387-7003. Retrieved October 20, 2018.
- Zumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. p. A22. ISBN 978-0-618-94690-7.
- Sigma-Aldrich Co., Potassium hydroxide. Retrieved on 2014-05-18.
- NIOSH Pocket Guide to Chemical Hazards. "#0523". National Institute for Occupational Safety and Health (NIOSH).
- Chambers, Michael. "ChemIDplus - 1310-58-3 - KWYUFKZDYYNOTN-UHFFFAOYSA-M - Potassium hydroxide [JAN:NF] - Similar structures search, synonyms, formulas, resource links, and other chemical information". chem.sis.nlm.nih.gov. Archived from the original on 12 August 2014. Retrieved 8 May 2018.
- Schultz, Heinz; Bauer, Günter; Schachl, Erich; Hagedorn, Fritz; Schmittinger, Peter (2005). "Potassium Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim, Germany: Wiley-VCH. doi:10.1002/14356007.a22_039. ISBN 978-3-527-30673-2.
- Holleman, A. F; Wiberg, E. (2001). Inorganic Chemistry. San Diego: Academic Press. ISBN 978-0-12-352651-9.
- Wells, A.F. (1984). Structural Inorganic Chemistry. Oxford: Clarendon Press. ISBN 978-0-19-855370-0.
- Platonov, Andrew Y.; Kurzin, Alexander V.; Evdokimov, Andrey N. (2009). "Composition of Vapor and Liquid Phases in the Potassium Hydroxide + Methanol Reaction System at 25 °С". J. Solution Chem. 39 (3): 335–342. doi:10.1007/s10953-010-9505-1. S2CID 97177429.
- W. W. Hartman (1923). "p-Cresol". Organic Syntheses. 3: 37. doi:10.15227/orgsyn.003.0037.; Collective Volume, vol. 1, p. 175
- Römpp Chemie-Lexikon, 9th Ed. (in German)
- K. Schumann; K. Siekmann (2005). "Soaps". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a24_247. ISBN 978-3527306732.
- D. Berndt; D. Spahrbier (2005). "Batteries". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_343. ISBN 978-3527306732.
- "Toyota Prius Hybrid 2010 Model Emergency Response Guide" (PDF). Toyota Motor Corporation. 2009. Archived from the original (PDF) on 2012-03-20.
- "Compound Summary for CID 14797 - Potassium Hydroxide". PubChem.
- Green, Margaret (January 1952). "A RAPID METHOD FOR CLEARING AND STAINING SPECIMENS FOR THE DEMONSTRATION OF BONE". The Ohio Journal of Science. 52 (1): 31–33. hdl:1811/3896.
- Thomas Eisner (2003). For the Love of Insects. Harvard University Press. p. 71.
- Elix, J.A.; Stocker-Wörgötter, Elfie (2008). "Chapter 7: Biochemistry and secondary metabolites". In Nash III, Thomas H. (ed.). Lichen Biology (2nd ed.). New York: Cambridge University Press. pp. 118–119. ISBN 978-0-521-69216-8.
- Testing Chemical Reactions Archived 2009-10-15 at the Wayback Machine at MushroomExpert.com
- Potassium hydroxide, SIDS Initial Assessment Report For SIAM 13. Bern, Switzerland, 6-9 November 2001. Archived 3 January 2018 at the Wayback Machine By Dr. Thaly LAKHANISKY. Date of last Update: February 2002
|Wikimedia Commons has media related to Potassium hydroxide.|