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Potassium peroxymonosulfate

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"Oxone" redirects here. Not to be confused with the gas ozone.
Potassium peroxymonosulfate
Names
IUPAC name
Potassium peroxysulfate
Other names
Caroat
Oxone
potassium monopersulfate
MPS
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.158 Edit this at Wikidata
UNII
  • InChI=1S/K.H2O5S/c;1-5-6(2,3)4/h;1H,(H,2,3,4)/q+1;/p-1 ☒N
    Key: OKBMCNHOEMXPTM-UHFFFAOYSA-M ☒N
  • InChI=1S/K.H2O4S/c;1-4-5(2)3/h;1H,(H,2,3)/q+1;/p-1
  • Key: GZHFEBOLZPYNER-UHFFFAOYSA-M
  • InChI=1/K.H2O5S/c;1-5-6(2,3)4/h;1H,(H,2,3,4)/q+1;/p-1
    Key: OKBMCNHOEMXPTM-REWHXWOFAJ
  • [K+].[O-]S(=O)(=O)OO
Properties
KHSO5
Molar mass 152.2 g/mol (614.76 as triple salt)
Appearance off-white powder
decomposes
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
 Oxidant, Corrosive
NFPA 704 (fire diamond)
[1]
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 hazards (white): no code
3
0
1
Safety data sheet (SDS) Degussa Caroat MSDS
Related compounds
Related compounds
 Potassium persulfate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Potassium peroxymonosulfate (also known as MPS, potassium monopersulfate, potassium caroate, and the trade names Caroat and Oxone) is widely used as an oxidizing agent. It is the potassium salt of peroxymonosulfuric acid.

The triple salt 2KHSO5·KHSO4·K2SO4 (known by the tradename Oxone) is a form with higher stability.[2] The standard electrode potential for this compound is +1.81 V with a half reaction generating the hydrogen sulfate (pH=0).[3]

HSO5− + 2 H+ + 2 e− → HSO4− + H2O

Reactions

MPS is a versatile oxidant. It oxidizes aldehydes to carboxylic acids; in the presence of alcoholic solvents, the esters may be obtained.[4] Internal alkenes may be cleaved to two carboxylic acids (see below), while terminal alkenes may be epoxidized. Thioethers give sulfones, tertiary amines give amine oxides, and phosphines give phosphine oxides.

Illustrative of the oxidation power of this salt is the conversion of an acridine derivative to the corresponding acridine-N-oxide.[5]

MPS will also oxidize a thioether to a sulfone with 2 equivalents.[6] With one equivalent the reaction converting sulfide to sulfoxide is much faster than that of sulfoxide to sulfone, so the reaction can conveniently be stopped at that stage if so desired.

MPS can also react with ketones to form dioxiranes, with the synthesis of dimethyldioxirane (DMDO) being representative. These are versatile oxidising agents and may be used for the epoxidation of olefins. In particular, if the starting ketone is chiral then the epoxide may be generated enantioselectively, this forms the basis of the Shi epoxidation.[7]

The Shi epoxidation
The Shi epoxidation

Uses

Potassium peroxymonosulfate can be used in swimming pools to keep the water clear, thus allowing chlorine in pools to work to sanitize the water rather than clarify the water, resulting in less chlorine needed to keep pools clean.[8] One of the drawbacks of using potassium peroxymonosulfate in pools is it can cause the common DPD #3 water test for combined chlorine to read incorrectly high.[9]

References

  1. ^ "DuPont MSDS" (PDF).
  2. ^ Crandall, Jack K.; Shi, Yian; Burke, Christopher P.; Buckley, Benjamin R. (2001). Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons, Ltd. doi:10.1002/047084289x.rp246.pub3. ISBN 978-0-470-84289-8.
  3. ^ Spiro, M. "The standard potential of the peroxosulphate/sulphate couple". Electrochimica Acta. 24 (3): 313–314. doi:10.1016/0013-4686(79)85051-3. ISSN 0013-4686.
  4. ^ Benjamin R. Travis; Meenakshi Sivakumar; G. Olatunji Hollist; Babak Borhan (2003). "Facile Oxidation of Aldehydes to Acids and Esters with Oxone". Organic Letters. 5 (7): 1031–4. doi:10.1021/ol0340078. PMID 12659566. {{cite journal}}: Unknown parameter |last-author-amp= ignored (|name-list-style= suggested) (help)
  5. ^ Thomas W. Bell, Young-Moon Cho, Albert Firestone, Karin Healy, Jia Liu, Richard Ludwig, and Scott D. Rothenberger (1993). "9-n-Butyl-1,2,3,4,5,6,7,8-Octahydroacridin-4-ol". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 8, p. 87.
  6. ^ James R. McCarthy, Donald P. Matthews, and John P. Paolini (1998). "Reaction of Sulfoxides with Diethylaminosulfur Trifluoride". Organic Syntheses{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 9, p. 446.
  7. ^ Frohn, Michael; Shi, Yian (2000). "Chiral Ketone-Catalyzed Asymmetric Epoxidation of Olefins". Synthesis. 2000 (14): 1979–2000. doi:10.1055/s-2000-8715.
  8. ^ "Benefits of Using a Non-Chlorine Shock Oxidizer Powered by DuPont Oxone" Dupont.com Archived 2011-07-15 at the Wayback Machine. Accessed July 2011.
  9. ^ "How to accurately measure chlorine levels in water shocked with potassium monopersulfate". Tech note from water test maker Taylor Technologies, originally appeared in Aquatics International. Accessed November 2011
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