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{{Short description|Inorganic compound (KOH)}}
{{chembox {{chembox
|Verifiedfields = changed
| verifiedrevid = 449453670
|Watchedfields = changed
| Name = Potassium hydroxide
|verifiedrevid = 464361974
| ImageFile = Potassium hydroxide.jpg
|Name = Potassium hydroxide
| ImageSize = 200px
| ImageName = pellets of potassium hydroxide |ImageFile1 = Potassium hydroxide.jpg
| ImageFile1 = Potassium-hydroxide-xtal-3D-vdW.png |ImageName1 = Pellets of potassium hydroxide
|ImageFile = Potassium-hydroxide-xtal-3D-vdW.png
| ImageSize1 = 200px
| ImageName1 = crystal structure of KOH |ImageName = Crystal structure of KOH
| IUPACName = Potassium hydroxide |ImageSize = 150px
|IUPACName = Potassium hydroxide
| OtherNames = Caustic potash<br/>Potash lye<br/>Potassia<br/>Potassium hydrate |OtherNames = {{Unbulleted list|Caustic potash|]|Potash lye|Potassia|Potassium hydrate|KOH}}
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| UNII_Ref = {{fdacite|correct|FDA}} |UNII_Ref = {{fdacite|correct|FDA}}
| UNII = WZH3C48M4T |UNII = WZH3C48M4T
| InChI = 1/K.H2O/h;1H2/q+1;/p-1 |InChI = 1/K.H2O/h;1H2/q+1;/p-1
| InChIKey = KWYUFKZDYYNOTN-REWHXWOFAT |InChIKey = KWYUFKZDYYNOTN-REWHXWOFAT
| ChEBI_Ref = {{ebicite|correct|EBI}} |ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 32035 |ChEBI = 32035
| SMILES = . |SMILES = .
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/K.H2O/h;1H2/q+1;/p-1 |StdInChI = 1S/K.H2O/h;1H2/q+1;/p-1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = KWYUFKZDYYNOTN-UHFFFAOYSA-M |StdInChIKey = KWYUFKZDYYNOTN-UHFFFAOYSA-M
| CASNo = 1310-58-3 |CASNo = 1310-58-3
| CASNo_Ref = {{cascite|correct|CAS}} |CASNo_Ref = {{cascite|correct|CAS}}
| PubChem = 6093213 |PubChem = 14797
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 14113 |ChemSpiderID = 14113
| RTECS = TT2100000 |RTECS = TT2100000
| UNNumber = 1813 |UNNumber = 1813
| EINECS = 215-181-3 |EINECS = 215-181-3
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| Formula = KOH |Formula = KOH
|K=1|O=1|H=1
| MolarMass = 56.1056 g/mol
| Appearance = white solid, ] |Appearance = white solid, ]
|Odor = odorless
| Density = 2.044 g/cm<sup>3</sup><ref name=crc/>
| Solubility = 1210 g/L (25 °C) <br> 1780 g/L (100 °C)<ref name=crc>{{RubberBible86th|page=4-80}}</ref> |Density = 2.044 g/cm<sup>3</sup> (20 °C)<ref name=crc/><br/> 2.12 g/cm<sup>3</sup> (25 °C)<ref name=chemister />
|Solubility = 85 g/100 mL (-23.2 °C)<br/> 97 g/100 mL (0 °C)<br/> 121 g/100 mL (25 °C)<br/> 138.3 g/100 mL (50 °C)<br/> 162.9 g/100 mL (100 °C)<ref name=crc>{{RubberBible86th|page=4-80}}</ref><ref name=sioc>{{cite book|last1 = Seidell|first1 = Atherton|last2 = Linke|first2 = William F.|year = 1952|title = Solubilities of Inorganic and Organic Compounds|publisher = Van Nostrand|url = https://books.google.com/books?id=k2e5AAAAIAAJ|access-date = 2014-05-29}}</ref>
| SolubleOther = soluble in ], ] <br> insoluble in ], liquid ]
|SolubleOther = soluble in ], ] <br/> insoluble in ], liquid ]
| MeltingPt = 406 °C<ref name=crc/>
| BoilingPt = 1327 °C<ref name=crc/> |Solubility2 = 55 g/100 g (28 °C)<ref name=chemister />
|Solvent2 = methanol
| pKa = 13.5 (0.1 M)
|Solubility3 = ~14 g / 100 g (28 °C)
| RefractIndex = 1.409
|Solvent3 = isopropanol
|MeltingPtC = 410
<ref>{{cite journal | last1=Otto | first1=H.W | last2=Seward | first2=R.P. | title=Phase equilibria in the potassium hydroxide-sodium hydroxide system. | journal=J. Chem. Eng. Data | volume=9 | pages=507–508 | url=https://doi.org/10.1021/je60023a009 | doi=10.1021/je60023a009 | year=1964 | issue=4 }}</ref> <ref>{{cite journal | last1=Seward | first1=R.P | last2=Martin | first2=K.E. | title=The melting point of potassium hydroxide. | journal=J. Am. Chem. Soc. | volume=71 | pages=3564–3565 | url=https://doi.org/10.1021/ja01178a530 | doi=10.1021/ja01178a530 | year=1949 | issue=10 }}</ref>
|BoilingPtC = 1327
|pKa = 14.7<ref>{{cite journal | last1=Popov | first1=K. | last2=Lajunen | first2=L.H.J. | last3=Popov | first3=A. | last4=Rönkkömäki | first4=H. | last5=Hannu-Kuure | first5=M. | last6=Vendilo | first6=A. | title=<sup>7</sup>Li, <sup>23</sup>Na, <sup>39</sup>K and <sup>133</sup>Cs NMR comparative equilibrium study of alkali metal cation hydroxide complexes in aqueous solutions. First numerical value for CsOH formation | journal=Inorganic Chemistry Communications | volume=3 | issue=5 | issn=1387-7003 | pages=223–225 | url=https://www.infona.pl//resource/bwmeta1.element.elsevier-40fb73c1-ba37-32e0-914e-b264c7c0539b | access-date=October 20, 2018 |doi=10.1016/S1387-7003(02)00335-0 |display-authors=1| year=2002 }}</ref>
|RefractIndex = 1.409 (20 °C)
|MagSus = &minus;22.0·10<sup>−6</sup> cm<sup>3</sup>/mol
}} }}
| Section3 = {{Chembox Structure |Section3={{Chembox Thermochemistry
|DeltaHf = -425.8 kJ/mol<ref name=chemister>{{cite web|url=http://chemister.ru/Database/properties-en.php?dbid=1&id=325|title=potassium hydroxide|website=chemister.ru|access-date=8 May 2018|url-status=live|archive-url=https://web.archive.org/web/20140518070658/http://chemister.ru/Database/properties-en.php?dbid=1&id=325|archive-date=18 May 2014}}</ref><ref name=b1>{{cite book| author = Zumdahl, Steven S.|title =Chemical Principles 6th Ed.| publisher = Houghton Mifflin Company| year = 2009| isbn = 978-0-618-94690-7|page=A22}}</ref>
| Coordination =
|Entropy = 79.32 J/mol·K<ref name=chemister /><ref name=b1 />
| CrystalStruct =rhombohedral
|DeltaGf = -380.2 kJ/mol<ref name=chemister />
|HeatCapacity = 65.87 J/mol·K<ref name=chemister />
}} }}
| Section7 = {{Chembox Hazards |Section4={{Chembox Hazards
| ExternalMSDS = |ExternalSDS =
|GHSPictograms = {{GHS05}}{{GHS07}}<ref name="sigma">{{Sigma-Aldrich|id=757551|name=Potassium hydroxide|accessdate=2014-05-18}}</ref>
| EUIndex = 019-002-00-8
|GHSSignalWord = Danger
| EUClass = Corrosive ('''C''')<br/>Harmful ('''Xn''')
|HPhrases = {{H-phrases|290|302|314}}<ref name="sigma" />
| RPhrases = {{R22}}, {{R35}}
|PPhrases = {{P-phrases|280|305+351+338|310}}<ref name="sigma" />
| SPhrases = {{S1/2}}, {{S26}}, {{S36/37/39}}, {{S45}}
| NFPA-H = 3 |NFPA-H = 3
| NFPA-F = 0 |NFPA-F = 0
| NFPA-R = 1 |NFPA-R = 1
| NFPA-O = |NFPA-S = ALK
| FlashPt = Non-flammable |FlashPt = nonflammable
|LD50 = 273 mg/kg (oral, rat)<ref>{{cite web|url=https://chem.nlm.nih.gov/chemidplus/rn/1310-58-3|title=ChemIDplus - 1310-58-3 - KWYUFKZDYYNOTN-UHFFFAOYSA-M - Potassium hydroxide - Similar structures search, synonyms, formulas, resource links, and other chemical information.|first=Michael|last=Chambers|website=chem.sis.nlm.nih.gov|access-date=8 May 2018|url-status=live|archive-url=http://archive.wikiwix.com/cache/20140812085045/https://chem.nlm.nih.gov/chemidplus/rn/1310-58-3|archive-date=12 August 2014}}</ref>
| LD50 = 273 mg/kg
|PEL = none<ref name=PGCH>{{PGCH|0523}}</ref>
|IDLH = N.D.<ref name=PGCH/>
|REL = C 2 mg/m<sup>3</sup><ref name=PGCH/>
}} }}
| Section8 = {{Chembox Related |Section5={{Chembox Related
| OtherAnions = ]<br/>] |OtherAnions = ]<br/>]
| OtherCations = ]<br/>]<br/>]<br/>] |OtherCations = ]<br/>]<br/>]<br/>]
| OtherCpds = ] |OtherCompounds = ]
}} }}
}} }}
'''Potassium hydroxide''' is an ] with the formula ]], commonly called '''caustic potash'''. '''Potassium hydroxide''' is an ] with the formula ]], and is commonly called '''caustic potash'''.


Along with ] (NaOH), this colorless solid is a prototypical ]. It has many industrial and niche applications. Most applications exploit its reactivity toward ] and its corrosive nature. In 2005, an estimated 700,000 to 800,000 ]s were produced. Approximately 100 times more NaOH than KOH is produced annually.<ref name=Ullmann>H. Schultz, G. Bauer, E. Schachl, F. Hagedorn, P. Schmittinger “Potassium Compounds” in Ullmann’s Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. {{DOI|10.1002/14356007.a22_039}}</ref><ref>"Caustic Potash." Retrieved on July 26, 2010.</ref><ref>"Potassium Hydroxide." Retrieved on January 24</ref> KOH is noteworthy as the precursor to most soft and liquid soaps as well as numerous potassium-containing chemicals. Along with ] (NaOH), KOH is a prototypical ]. It has many industrial and niche applications, most of which utilize its ] nature and its reactivity toward ]. An estimated 700,000 to 800,000 ]s were produced in 2005. KOH is noteworthy as the precursor to most soft and liquid ]s, as well as numerous potassium-containing chemicals. It is a white solid that is dangerously corrosive.<ref name=Ullmann>{{cite book| last1=Schultz | first1=Heinz | last2=Bauer | first2=Günter | last3=Schachl | first3=Erich | last4=Hagedorn | first4=Fritz | last5=Schmittinger | first5=Peter |title=Ullmann's Encyclopedia of Industrial Chemistry|publisher=Wiley-VCH|location=Weinheim, Germany| year=2005 | isbn=978-3-527-30673-2 | doi=10.1002/14356007.a22_039|chapter=Potassium Compounds}}</ref>


==Properties and structure== ==Properties and structure==
Potassium hydroxide can be found in pure form by reacting ] with impure ]. Potassium hydroxide is usually sold as translucent pellets, which will become tacky in air because KOH is ]. Consequently, KOH typically contains varying amounts of water (as well as carbonates, see below). Its ] in water is strongly ], meaning the process gives off significant heat. Concentrated aqueous solutions are sometimes called potassium ]s. Even at high temperatures, solid KOH does not dehydrate readily.<ref>Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5.</ref> KOH exhibits high ]. Because of this high stability and relatively low ], 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 ]. Most commercial samples are ca. 90% pure, the remainder being water and carbonates.<ref name=Ullmann/> Its ] in water is strongly ]. Concentrated aqueous solutions are sometimes called potassium ]s. Even at high temperatures, solid KOH does not dehydrate readily.<ref>{{cite book|last1=Holleman|first1=A. F|last2=Wiberg|first2=E. |title=Inorganic Chemistry |publisher=Academic Press|location=San Diego|year=2001|isbn=978-0-12-352651-9}}</ref>


===Structure=== ===Structure===
At higher temperatures, solid KOH ] in the ] ]. The OH group is either rapidly or randomly disordered so that the {{chem|OH|-}} group is effectively a spherical ] of radius 1.53 Å (between {{chem|Cl|-}} and {{chem|F|-}} in size). At room temperature, the {{chem|OH|-}} groups are ordered and the environment about the {{chem|K|+}} centers is distorted, with {{chem|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 ]s, namely the monohydrate {{chem|KOH·H|2|O}}, the dihydrate {{chem|KOH·2H|2|O}}, and the tetrahydrate {{chem|KOH·4H|2|O}}.<ref>Wells, A.F. (1984) Structural Inorganic Chemistry, Oxford: Clarendon Press. ISBN 0-19-855370-6.</ref> At higher temperatures, solid KOH ] in the ] ]. The {{OH-}} group is either rapidly or randomly disordered so that it is effectively a spherical ] of radius 1.53 Å (between {{chem2|Cl-}} and {{chem2|F-}} in size). At room temperature, the {{chem2|OH-}} groups are ordered and the environment about the {{chem2|K+}} centers is distorted, with {{chem2|K+\sOH-}} distances ranging from 2.69 to 3.15 Å, depending on the orientation of the OH group. KOH forms a series of crystalline ]s, namely the monohydrate {{chem2|KOH * ]}}, the dihydrate {{chem2|KOH * 2]}} and the tetrahydrate {{chem2|KOH * 4]}}.<ref>{{cite book |last=Wells |first=A.F. |year=1984 |title=Structural Inorganic Chemistry |location=Oxford |publisher=Clarendon Press |isbn=978-0-19-855370-0}}</ref>


==Reactions==
===Solubility and desiccating properties=== ===Solubility and desiccating properties===
About 112 g of KOH ] in 100 mL water at room temperature, which contrasts with 100 g/100 mL for NaOH.<ref>{{cite book|last1 = Seidell|first1 = Atherton|last2 = Linke|first2 = William F.|year = 1952|title = Solubilities of Inorganic and Organic Compounds|publisher = Van Nostrand|url = https://books.google.com/books?id=k2e5AAAAIAAJ|access-date = 2014-05-29}}</ref> Thus on a molar basis, KOH is slightly more soluble than NaOH. Lower molecular-weight ]s such as ], ], and ]s are also excellent ]. They participate in an acid-base equilibrium. In the case of methanol the potassium ] (methylate) forms:<ref>{{Cite journal|last1=Platonov|first1=Andrew Y.|last2=Kurzin|first2=Alexander V.|last3=Evdokimov|first3=Andrey N.|date=2009|title=Composition of Vapor and Liquid Phases in the Potassium Hydroxide + Methanol Reaction System at 25 °С|journal=J. Solution Chem.|volume=39|issue=3|pages=335–342|doi=10.1007/s10953-010-9505-1|s2cid=97177429}}</ref>
Approximately 121 g of KOH will ] in 100 mL of water at room temperature (compared with 100 g of NaOH in the same volume). Lower ]s such as ], ], and ]s are also excellent ]. The solubility in ethanol is about 40 g KOH/100 mL.
: {{chem2|KOH + CH3OH -> CH3OK + H2O}}


Because of its high affinity for water, KOH serves as a ] in the laboratory. It is often used to dry basic solvents, especially ] and ]: distillation of these basic liquids from a ] of KOH yields the ] ]. Because of its high affinity for water, KOH serves as a ] in the laboratory. It is often used to dry basic solvents, especially ] and ].

===Thermal stability===
Like NaOH, KOH exhibits high ]. The ] species is ]ic. Because of its high stability and relatively low ], it is often melt-cast as pellets or rods, forms that have low surface area and convenient handling properties.

==Reactions==
===As a base===
KOH is highly ], forming strongly alkaline solutions in water and other ]. These solutions are capable of ] many acids, even weak ones. In ], ] using solutions of KOH are used to assay acids.


===As a nucleophile in organic chemistry=== ===As a nucleophile in organic chemistry===
KOH, like NaOH, serves as a source of {{chem|OH|-}}, a highly ] anion that attacks ] in both inorganic and organic materials. In perhaps its most well-known reaction, aqueous KOH ] ]s: KOH, like NaOH, serves as a source of {{chem2|OH-}}, a highly ] anion that attacks ] in both inorganic and organic materials. Aqueous KOH ] ]s:
: {{chem2|KOH + RCOOR' -> RCOOK + R'OH}}


When R is a long chain, the product is called a ]. This reaction is manifested by the "greasy" feel that KOH gives when touched; ]s on the skin are rapidly converted to soap and ].
: KOH + RCO<sub>2</sub>R' → RCO<sub>2</sub>K + R'OH


Molten KOH is used to displace ] and other ]s. The reaction is especially useful for ] ]s to give the corresponding ]s.<ref>{{OrgSynth|author = W. W. Hartman|title = ''p''-Cresol| collvol = 1|collvolpages = 175|prep = CV1P0175|year = 1923|volume = 3|pages = 37|doi = 10.15227/orgsyn.003.0037}}</ref>
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 — ] on the skin are rapidly converted to soap and ].

Molten KOH is used to displace ] and other leaving groups. The reaction is especially useful for ] ]s to give the corresponding ]s.<ref>{{OrgSynth|author = W. W. Hartman|title = p-Cresol| collvol = 1|collvolpages = 175|prep = CV1P0175}}</ref>


===Reactions with inorganic compounds=== ===Reactions with inorganic compounds===
Complementary to its reactivity toward acids, KOH attacks ]. Thus, SiO<sub>2</sub> is attacked by KOH to give soluble potassium silicates. KOH reacts with ] to give ]: Complementary to its reactivity toward acids, KOH attacks ]s. Thus, SiO<sub>2</sub> is attacked by KOH to give soluble potassium silicates. KOH reacts with ] to give ]:
:{{chem2|KOH + CO2 -> KHCO3}}
:KOH + CO<sub>2</sub> → KHCO<sub>3</sub>


==Manufacture== ==Manufacture==
Historically KOH was made by boiling a solution of ] (potash) with ] (]), leading to a ] which caused ] to precipitate, leaving potassium hydroxide in solution: Historically, KOH was made by adding ] to a strong solution of ] (slaked lime). The ] results in precipitation of solid ], leaving potassium hydroxide in solution:
:Ca(OH)<sub>2</sub> + K<sub>2</sub>CO<sub>3</sub> → CaCO<sub>3</sub> + 2 KOH :{{chem2|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 used potash extracted from wood ashes using slaked lime. It was the most important method of producing potassium hydroxide until the late 19th century, when it was largely replaced by the current method of electrolysis of ] solutions, analogous to the method of manufacturing ] (see ]): 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 ] solutions.<ref name=Ullmann/> The method is analogous to the manufacture of ] (see ]):
:2 KCl + 2 H<sub>2</sub>O → 2 KOH + Cl<sub>2</sub> + H<sub>2</sub> :{{chem2|2 KCl + 2 H2O -> 2 KOH + Cl2 + H2}}
] gas forms as a by-product on the ]; concurrently, an anodic oxidation of the ] ion takes place, forming ] gas as a byproduct. Separation of the anodic and cathodic spaces in the electrolysis cell is essential for this process.<ref>Römpp Chemie-Lexikon, 9th Ed. (in german)</ref>


] gas forms as a byproduct on the ]; concurrently, an anodic oxidation of the ] ion takes place, forming ] gas as a byproduct. Separation of the anodic and cathodic spaces in the electrolysis cell is essential for this process.<ref name="auto">Römpp Chemie-Lexikon, 9th Ed. (in German)</ref>
]


==Uses== ==Uses==
{{see also|Sodium hydroxide}}
KOH and NaOH can be used interchangeably for a number of applications, although in industry, NaOH is preferred because of its lower cost. KOH and NaOH can be used interchangeably for a number of applications, although in industry, NaOH is preferred because of its lower cost.


=== Catalyst for hydrothermal gasification process ===
===Precursor to other potassium compounds===
In industry, KOH is a good catalyst for ] process. In this process, it is used to improve the yield of gas and amount of hydrogen in process. For example, production of ] from coal often produces much coking wastewater. In order to degrade it, ] water is used to convert it to the syngas containing ], ], ] and ]. Using ], we could separate various gases and then use ] technology to convert them to fuel.<ref>{{Cite journal |date=2020-01-13 |title=Gasification of coking wastewater in supercritical water adding alkali catalyst |journal=International Journal of Hydrogen Energy |language=en |volume=45 |issue=3 |pages=1608–1614 |doi=10.1016/j.ijhydene.2019.11.033 |issn=0360-3199|last1=Chen |first1=Fu |last2=Li |first2=Xiaoxiao |last3=Qu |first3=Junfeng |last4=Ma |first4=Jing |last5=Zhu |first5=Qianlin |last6=Zhang |first6=Shaoliang |s2cid=213336330 |doi-access=free |bibcode=2020IJHE...45.1608C }}</ref> On the other hand, the hydrothermal gasification process could degrade other waste such as sewage sludge and waste from food factories.
Many potassium salts are prepared by neutralization reactions involving KOH. The potassium salts of ], ], ], ], and various silicates are prepared by treating either the oxides or the acids with KOH.<ref name=Ullmann/> The high solubility of potassium phosphate is desirable in ]s.


===Precursor to other potassium compounds===
===Manufacture of biodiesel===
Many potassium salts are prepared by neutralization reactions involving KOH. The potassium salts of ], ], ], ], and various silicates are prepared by treating either the oxides or the acids with KOH.<ref name=Ullmann/> The high solubility of ] is desirable in ]s.
Although more expensive than using sodium hydroxide, KOH works well in the manufacture of ] by ] of the triglycerides in ]. ] from potassium hydroxide-processed biodiesel is useful as an inexpensive food supplement for livestock, once the toxic methanol is removed.<ref>James K. Drackley </ref>


===Manufacture of soft soaps=== ===Manufacture of soft soaps===
The ] of ]s with KOH is used to prepare the corresponding "potassium ]", which are softer than the more common ]-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.<ref>K. Schumann, K. Siekmann “Soaps” in Ullmann’s Encyclopedia of Industrial Chemistry 2005, Wiley-VCH, Weinheim. {{DOI|10.1002/14356007.a24_247}}</ref> The ] of ]s with KOH is used to prepare the corresponding "potassium ]", which are softer than the more common ]-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.<ref>{{cite book |author=K. Schumann |author2=K. Siekmann |chapter=Soaps|title=Ullmann's Encyclopedia of Industrial Chemistry |year=2005|publisher=Wiley-VCH |location=Weinheim|doi=10.1002/14356007.a24_247|isbn=978-3527306732 }}</ref>


===As an electrolyte=== ===As an electrolyte===
]
Aqueous potassium hydroxide is employed as the ] in ] based on ]-] and ]-]. Potassium hydroxide is preferred over sodium hydroxide because its solutions are more conductive.<ref>D. Berndt, D. Spahrbier, "Batteries" in Ullmann’s Encyclopedia of Industrial Chemistry 2005, Wiley-VCH, Weinheim. {{DOI|10.1002/14356007.a03_343}}</ref> The ] in the ] use a mixture of potassium hydroxide and sodium hydroxide.<ref>{{Cite web|title= Toyota Prius Hybrid 2010 Model Emergency Response Guide |publisher=Toyota Motor Corporation |year=2009 |url=http://www.toyota-tech.eu/HYBRID/ERG/EN/Prius%20ZVW30%20ERG.pdf |archiveurl=http://www.webcitation.org/62ngVS3FD |archivedate=2011-10-29 }}</ref>
] potassium hydroxide is employed as the ] in ] based on ]-], ]-], and ]-]. Potassium hydroxide is preferred over ] because its solutions are more conductive.<ref>{{cite book |author=D. Berndt |author2=D. Spahrbier |chapter=Batteries |title=Ullmann's Encyclopedia of Industrial Chemistry |year=2005 |publisher=Wiley-VCH |location=Weinheim |doi=10.1002/14356007.a03_343|isbn=978-3527306732 }}</ref> The ] in the ] use a mixture of potassium hydroxide and sodium hydroxide.<ref>{{Cite web |title=Toyota Prius Hybrid 2010 Model Emergency Response Guide |publisher=Toyota Motor Corporation |year=2009 |url=http://www.toyota-tech.eu/HYBRID/ERG/EN/Prius%20ZVW30%20ERG.pdf |archive-url=https://web.archive.org/web/20120320175142/http://www.toyota-tech.eu/HYBRID/ERG/EN/Prius%20ZVW30%20ERG.pdf |archive-date=2012-03-20 |url-status=dead }}</ref> ] also use potassium hydroxide electrolyte.

===Food industry===
In food products, potassium hydroxide acts as a food thickener, pH control agent and food stabilizer. The ] considers it generally safe as a direct food ingredient when used in accordance with ].<ref>{{cite web |title=Compound Summary for CID 14797 - Potassium Hydroxide |url=https://pubchem.ncbi.nlm.nih.gov/compound/potassium_hydroxide |publisher=PubChem}}</ref> It is known in the ] system as '''E525'''.


===Niche applications=== ===Niche applications===
Like ], 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 "]", potassium hydroxide hastens the decomposition of soft tissues, both animal and human, to leave behind only the bones and other hard tissues.{{citation needed|date=April 2010}} ] wishing to study the fine structure of ] ] may use a 10% aqueous solution of KOH to apply this process.<ref>Thomas Eisner, For the Love of Insects, Harvard University Press 2003, p. 71</ref> An example of chemical cremation outside of a laboratory environment is the use of a potassium hydroxide solution as the principal agent in the ] process, an alternative to the well-known, thermal ] process for the disposal of human remains after death. 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 "]", potassium hydroxide hastens the decomposition of soft tissues, both animal and human, to leave behind only the bones and other hard tissues.<ref>{{cite journal|last=Green|first=Margaret|title=A RAPID METHOD FOR CLEARING AND STAINING SPECIMENS FOR THE DEMONSTRATION OF BONE|journal=The Ohio Journal of Science|date=January 1952|volume=52|issue=1|pages=31–33|hdl=1811/3896}}</ref> ] wishing to study the fine structure of ] ] may use a 10% aqueous solution of KOH to apply this process.<ref>{{cite book |author=Thomas Eisner |title=For the Love of Insects |publisher=Harvard University Press |year=2003 |page=71}}</ref>


In chemical synthesis, the choice between the use of KOH and the use of ], NaOH, is guided by the solubility of the resulting ]. 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 ].


The corrosive properties of potassium hydroxide make it a useful ingredient in agents and preparations that clean and ] surfaces and materials that can themselves resist corrosion by KOH.<ref>Römpp Chemie-Lexikon, 9th Ed. (in German)</ref> The corrosive properties of potassium hydroxide make it a useful ingredient in agents and preparations that clean and ] surfaces and materials that can themselves resist ] by KOH.<ref name="auto"/>

KOH is also used for semiconductor chip fabrication (for example ]).


Potassium hydroxide is often the main active ingredient in chemical "cuticle removers" used in ] treatments. Potassium hydroxide is often the main active ingredient in chemical "cuticle removers" used in ] treatments.


Because aggressive bases like KOH damage the ] of the ] 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 ] stage of the ] process. This same effect is also used to weaken human hair in preparation for shaving. Pre-shave 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. Because aggressive bases like KOH damage the ] of the ] 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 ] 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 ]. 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 ], ], ], and ]<ref>{{cite book|last1=Elix|first1=J.A.|title=Lichen Biology|last2=Stocker-Wörgötter|first2=Elfie|date=2008|publisher=]|isbn=978-0-521-69216-8|editor-last=Nash III|editor-first=Thomas H.|edition=2nd|location=New York|pages=118–119|chapter=Chapter 7: Biochemistry and secondary metabolites|author-link=John Alan Elix}}</ref> are identifiable based on this color-change reaction.<ref> {{webarchive|url=https://web.archive.org/web/20091015000955/http://www.mushroomexpert.com/macrochemicals.html |date=2009-10-15 }} at MushroomExpert.com</ref>

==Safety==
Potassium hydroxide is a ] alkali and its solutions range from irritating to skin and other tissue in low concentrations, to highly corrosive in high concentrations. Eyes are particularly vulnerable, and dust or mist is severely irritating to lungs and can cause ].<ref>{{Cite web |title=Hazardous Substance Fact Sheet: Potassium Hydroxide |url=https://nj.gov/health/eoh/rtkweb/documents/fs/1571.pdf |access-date=7 October 2024 |website=New Jersey Department of Health}}</ref> Safety considerations are similar to ].


The caustic effects arise from being highly alkaline, but if potassium hydroxide is ] with a non-toxic acid then it becomes a non-toxic potassium salt. It is approved as a food additive under the code E525.
Potassium hydroxide is used to identify certain kinds of ]. 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 ], ], and many ] are identified based on this color-change reaction.<ref> at MushroomExpert.com</ref>
]]]


==See also== ==See also==
*] * ]
* ]
* ] – sailors' soap


==References== ==References==
{{reflist}} {{reflist|30em}}


==External links== ==External links==
{{Commons category}}
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*
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{{Potassium compounds}} {{Potassium compounds}}
{{Hydroxides}}

{{Authority control}}


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Latest revision as of 06:28, 7 October 2024

Inorganic compound (KOH)
Potassium hydroxide
Crystal structure of KOH
Pellets of potassium hydroxide
Names
IUPAC name Potassium hydroxide
Other names
  • Caustic potash
  • Lye
  • Potash lye
  • Potassia
  • Potassium hydrate
  • KOH
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.013.802 Edit this at Wikidata
EC Number
  • 215-181-3
E number E525 (acidity regulators, ...)
PubChem CID
RTECS number
  • TT2100000
UNII
UN number 1813
CompTox Dashboard (EPA)
InChI
  • InChI=1S/K.H2O/h;1H2/q+1;/p-1Key: KWYUFKZDYYNOTN-UHFFFAOYSA-M
  • InChI=1/K.H2O/h;1H2/q+1;/p-1Key: KWYUFKZDYYNOTN-REWHXWOFAT
SMILES
  • .
Properties
Chemical formula KOH
Molar mass 56.105 g·mol
Appearance white solid, deliquescent
Odor odorless
Density 2.044 g/cm (20 °C)
2.12 g/cm (25 °C)
Melting point 410 °C (770 °F; 683 K)
Boiling point 1,327 °C (2,421 °F; 1,600 K)
Solubility in water 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)
Acidity (pKa) 14.7
Magnetic susceptibility (χ) −22.0·10 cm/mol
Refractive index (nD) 1.409 (20 °C)
Thermochemistry
Heat capacity (C) 65.87 J/mol·K
Std molar
entropy
(S298)
79.32 J/mol·K
Std enthalpy of
formation
fH298)
-425.8 kJ/mol
Gibbs free energyfG) -380.2 kJ/mol
Hazards
GHS labelling:
Pictograms GHS05: CorrosiveGHS07: Exclamation mark
Signal word Danger
Hazard statements H290, H302, H314
Precautionary statements P280, P305+P351+P338, P310
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 0: Will not burn. E.g. waterInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazard ALK: Alkaline
3 0 1ALK
Flash point nonflammable
Lethal dose or concentration (LD, LC):
LD50 (median dose) 273 mg/kg (oral, rat)
NIOSH (US health exposure limits):
PEL (Permissible) none
REL (Recommended) C 2 mg/m
IDLH (Immediate danger) N.D.
Safety data sheet (SDS) ICSC 0357
Related compounds
Other anions Potassium hydrosulfide
Potassium amide
Other cations Lithium hydroxide
Sodium hydroxide
Rubidium hydroxide
Caesium hydroxide
Related compounds Potassium oxide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

Potassium hydroxide is an inorganic compound with the formula KOH, and is commonly called caustic potash.

Along with sodium hydroxide (NaOH), KOH is a prototypical strong base. It has many industrial and niche applications, most of which utilize 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 structure

KOH exhibits high thermal stability. Because of this 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.

Structure

At higher temperatures, solid KOH crystallizes in the NaCl crystal structure. The  OH group is either rapidly or randomly disordered so that it 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.

Reactions

Solubility and desiccating properties

About 112 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:

KOH + CH3OH → CH3OK + H2O

Because of its high affinity for water, KOH serves as a desiccant in the laboratory. It is often used to dry basic solvents, especially amines and pyridines.

As a nucleophile in organic chemistry

KOH, like NaOH, serves as a source of OH, a highly nucleophilic anion that attacks polar bonds in both inorganic and organic materials. Aqueous KOH saponifies esters:

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.

Molten KOH is used to displace halides and other leaving groups. The reaction is especially useful for aromatic reagents to give the corresponding phenols.

Reactions with inorganic compounds

Complementary to its reactivity toward acids, KOH attacks oxides. Thus, SiO2 is attacked by KOH to give soluble potassium silicates. KOH reacts with carbon dioxide to give potassium bicarbonate:

KOH + CO2 → KHCO3

Manufacture

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.

Uses

KOH and NaOH can be used interchangeably for a number of applications, although in industry, NaOH is preferred because of its lower cost.

Catalyst for hydrothermal gasification process

In industry, KOH is a good catalyst for hydrothermal gasification process. In this process, it is used to improve the yield of gas and amount of hydrogen in process. For example, production of coke (fuel) from coal often produces much coking wastewater. In order to degrade it, supercritical water is used to convert it to the syngas containing carbon monoxide, carbon dioxide, hydrogen and methane. Using pressure swing adsorption, we could separate various gases and then use power-to-gas technology to convert them to fuel. On the other hand, the hydrothermal gasification process could degrade other waste such as sewage sludge and waste from food factories.

Precursor to other potassium compounds

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 soaps

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 electrolyte

Potassium carbonate, formed from the hydroxide solution leaking from an alkaline battery
Potassium carbonate, formed from the hydroxide solution leaking from an alkaline battery

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.

Food industry

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.

Niche applications

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.

The corrosive properties of potassium hydroxide make it a useful ingredient in agents and preparations that clean and disinfect surfaces and materials that can themselves resist corrosion by KOH.

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.

Safety

Potassium hydroxide is a caustic alkali and its solutions range from irritating to skin and other tissue in low concentrations, to highly corrosive in high concentrations. Eyes are particularly vulnerable, and dust or mist is severely irritating to lungs and can cause pulmonary edema. Safety considerations are similar to those of sodium hydroxide.

The caustic effects arise from being highly alkaline, but if potassium hydroxide is neutralised with a non-toxic acid then it becomes a non-toxic potassium salt. It is approved as a food additive under the code E525.

Potassium hydroxide spillage, stained red by phenolphthalein

See also

References

  1. ^ Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton, Florida: CRC Press. p. 4-80. ISBN 0-8493-0486-5.
  2. ^ "potassium hydroxide". chemister.ru. Archived from the original on 18 May 2014. Retrieved 8 May 2018.
  3. Otto, H.W; Seward, R.P. (1964). "Phase equilibria in the potassium hydroxide-sodium hydroxide system". J. Chem. Eng. Data. 9 (4): 507–508. doi:10.1021/je60023a009.
  4. Seward, R.P; Martin, K.E. (1949). "The melting point of potassium hydroxide". J. Am. Chem. Soc. 71 (10): 3564–3565. doi:10.1021/ja01178a530.
  5. Seidell, Atherton; Linke, William F. (1952). Solubilities of Inorganic and Organic Compounds. Van Nostrand. Retrieved 2014-05-29.
  6. Popov, K.; et al. (2002). "Li, Na, K and Cs 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.
  7. ^ Zumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. p. A22. ISBN 978-0-618-94690-7.
  8. ^ Sigma-Aldrich Co., Potassium hydroxide. Retrieved on 2014-05-18.
  9. ^ NIOSH Pocket Guide to Chemical Hazards. "#0523". National Institute for Occupational Safety and Health (NIOSH).
  10. 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.
  11. ^ 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.
  12. Holleman, A. F; Wiberg, E. (2001). Inorganic Chemistry. San Diego: Academic Press. ISBN 978-0-12-352651-9.
  13. Wells, A.F. (1984). Structural Inorganic Chemistry. Oxford: Clarendon Press. ISBN 978-0-19-855370-0.
  14. Seidell, Atherton; Linke, William F. (1952). Solubilities of Inorganic and Organic Compounds. Van Nostrand. Retrieved 2014-05-29.
  15. 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.
  16. W. W. Hartman (1923). "p-Cresol". Organic Syntheses. 3: 37. doi:10.15227/orgsyn.003.0037; Collected Volumes, vol. 1, p. 175.
  17. ^ Römpp Chemie-Lexikon, 9th Ed. (in German)
  18. Chen, Fu; Li, Xiaoxiao; Qu, Junfeng; Ma, Jing; Zhu, Qianlin; Zhang, Shaoliang (2020-01-13). "Gasification of coking wastewater in supercritical water adding alkali catalyst". International Journal of Hydrogen Energy. 45 (3): 1608–1614. Bibcode:2020IJHE...45.1608C. doi:10.1016/j.ijhydene.2019.11.033. ISSN 0360-3199. S2CID 213336330.
  19. K. Schumann; K. Siekmann (2005). "Soaps". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a24_247. ISBN 978-3527306732.
  20. D. Berndt; D. Spahrbier (2005). "Batteries". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_343. ISBN 978-3527306732.
  21. "Toyota Prius Hybrid 2010 Model Emergency Response Guide" (PDF). Toyota Motor Corporation. 2009. Archived from the original (PDF) on 2012-03-20.
  22. "Compound Summary for CID 14797 - Potassium Hydroxide". PubChem.
  23. 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.
  24. Thomas Eisner (2003). For the Love of Insects. Harvard University Press. p. 71.
  25. 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.
  26. Testing Chemical Reactions Archived 2009-10-15 at the Wayback Machine at MushroomExpert.com
  27. "Hazardous Substance Fact Sheet: Potassium Hydroxide" (PDF). New Jersey Department of Health. Retrieved 7 October 2024.

External links

Potassium compounds
H, (pseudo)halogens
chalcogens
pnictogens
B, C group
transition metals
organic
Hydroxides
HOH He
LiOH Be(OH)2 B(OH)3 C(OH)4 N(OH)3
[NH4]OH
O(OH)2 FOH Ne
NaOH Mg(OH)2 Al(OH)3 Si(OH)4 P(OH)3 S(OH)2 ClOH Ar
KOH Ca(OH)2 Sc(OH)3 Ti(OH)2
Ti(OH)3
Ti(OH)4
V(OH)2
V(OH)3
Cr(OH)2
Cr(OH)3
Mn(OH)2 Fe(OH)2
Fe(OH)3
Co(OH)2 Ni(OH)2 CuOH
Cu(OH)2
Zn(OH)2 Ga(OH)3 Ge(OH)2 As(OH)3 Se BrOH Kr
RbOH Sr(OH)2 Y(OH)3 Zr(OH)4 Nb Mo Tc(OH)4 Ru Rh(OH)3 Pd AgOH Cd(OH)2 In(OH)3 Sn(OH)2
Sn(OH)4
Sb(OH)3 Te(OH)6 IOH Xe
CsOH Ba(OH)2 * Lu(OH)3 Hf Ta W Re Os Ir Pt Au(OH)3 Hg(OH)2 TlOH
Tl(OH)3
Pb(OH)2
Pb(OH)4
Bi(OH)3 Po At Rn
FrOH Ra(OH)2 ** Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
 
* La(OH)3 Ce(OH)3
Ce(OH)4
Pr(OH)3 Nd(OH)3 Pm(OH)3 Sm(OH)3 Eu(OH)2
Eu(OH)3
Gd(OH)3 Tb(OH)3 Dy(OH)3 Ho(OH)3 Er(OH)3 Tm(OH)3 Yb(OH)3
** Ac(OH)3 Th(OH)4 Pa U(OH)2
U(OH)3
UO2(OH)2
Np(OH)3
Np(OH)4
NpO2(OH)3
Pu Am(OH)3 Cm(OH)3 Bk Cf Es Fm Md No
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