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228036

Sigma-Aldrich

OXONE®, monopersulfate compound

Synonym(s):

Potassium peroxymonosulfate

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About This Item

Linear Formula:
KHSO5 · 0.5KHSO4 · 0.5K2SO4
CAS Number:
70693-62-8
Molecular Weight:
307.38
MDL number:
MFCD00040551
UNSPSC Code:
12352300
PubChem Substance ID:
57648006
NACRES:
NA.21

vapor pressure

<0.0000017 hPa

Quality Level

200

form

powder

reaction suitability

reagent type: oxidant

concentration

>4.0% (active oxygen basis (by Na2S2O3, titration))

pH

2.1 (77 °C, 30 g/L)

SMILES string

[K+].[K+].[K+].[K+].[K+].OS([O-])(=O)=O.[O-]S([O-])(=O)=O.O[S+]([O-])([O-])(=O)=O.O[S+]([O-])([O-])(=O)=O

InChI

1S/5K.2H2O5S.2H2O4S/c;;;;;2*1-5-6(2,3)4;2*1-5(2,3)4/h;;;;;2*1H,(H,2,3,4);2*(H2,1,2,3,4)/q5*+1;;;;/p-5

InChI key

HJKYXKSLRZKNSI-UHFFFAOYSA-I

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General description

OXONE®, monopersulfate compound is a potassium triple salt mainly used as a stable, easy to handle and nontoxic oxidant.

Application

A rapid, efficient synthesis of oxaziridines from imines using buffered OXONE has been reported. Also used to study fading of an artist′s colorants.
OXONE®, monopersulfate compound may be used as an alternative to transition-metal oxidants for the conversion of aldehydes to carboxylic acids or esters.
Oxidant used for halogenation of α,β-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.
Oxidant used for halogenation of a,b-unsaturated carbonyl compounds and catalytic generation of hypervalent iodine reagents for alcohol oxidation.

2-Iodoxybenzenesulfonic Acid as an Extremely Active Catalyst for the Selective Oxidation of Alcohols to Aldehydes, Ketones, Carboxylic Acids, and Enones with Oxone

A Convenient Halogenation of α,β-Unsaturated Carbonyl Compounds with OXONE® and Hydrohalic Acid (HBr, HCl)

Legal Information

OXONE is a registered trademark of E. I. du Pont de Nemours and Company

Signal Word

Danger

Hazard Statements

H302,H314,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000375143
0000367257
0000358085
0000355727
0000355727

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Yifu Li et al.
Bioresource technology, 262, 294-301 (2018-05-08)
In this study, zero valent iron (ZVI) activated peroxymonosulfate (PMS) as novel technique (i.e. ZVI-PMS technology) was employed to enhance sludge dewatering. In optimal sludge dewatering conditions of ZVI and KHSO5 dosages, the specific resistance to filtration (SRF) was reduced
Yao-Hui Huang et al.
Journal of hazardous materials, 170(2-3), 1110-1118 (2009-06-23)
In order to generate powerful radicals as oxidizing species for the complete decolorization and degradation of azo dye Reactive Black B (RBB) at near neutral pH (pH 6), homogeneous activation of peroxymonosulfate (Oxone: PMS) by the trace Co2+-catalysts was explored.
Benjamin R Travis et al.
Organic letters, 5(7), 1031-1034 (2003-03-28)
[reaction: see text] A highly efficient, mild, and simple protocol is presented for the oxidation of aldehydes to carboxylic acids utilizing Oxone as the sole oxidant. Direct conversion of aldehydes in alcoholic solvents to their corresponding ester products is also
Yi-Fong Huang et al.
Journal of hazardous materials, 167(1-3), 418-426 (2009-02-14)
This study investigated the degradation and mineralization of Bisphenol A (BPA) at pH 7, taken as a model compound in the presence of the trace metal-ions, Co(2+), and peroxymonosulfate (Oxone: PMS). We took advantage of the high oxidation-reduction potential of
Sie King Ling et al.
Journal of hazardous materials, 178(1-3), 385-389 (2010-02-11)
Dye degradation using advanced oxidation processes with Co(2+)/H(2)O(2) and Co(2+)/peroxymonosulfate (PMS) systems has been investigated. Two types of dyes, basic blue 9 and acid red 183, were employed. Several parameters affecting dye degradation such as Co(2+), PMS, H(2)O(2), and dye
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