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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:
Molecular Weight:
307.38
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.21

vapor pressure

<0.0000017 hPa

Quality Level

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.

Legal Information

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

Signal Word

Danger

Hazard Statements

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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Atmos. Environ., Part A, 27A, 765-765 (1993)
Raf Dewil et al.
Journal of hazardous materials, 146(3), 577-581 (2007-05-29)
During the anaerobic digestion of wastewater treatment sludge, commonly called biosolids, an energy rich biogas is formed which is now considered as renewable energy source and widely used for the production of heat and/or electricity. Pre-treatment methods, which achieve a
Masami Fukushima et al.
Chemosphere, 80(8), 860-865 (2010-06-19)
Tetrabromobisphenol A (TBBPA), a commercially used brominated flame retardant, also functions as an endocrine disruptor and is of serious concern in terms of environmental pollution. TBBPA has been detected in leachates from landfills, because hydrophobic interactions with humic acids (HAs)
J Rodríguez-Chueca et al.
Journal of hazardous materials, 372, 94-102 (2018-05-08)
This study explores the enhancement of UV-C tertiary treatment by sulfate radical based Advanced Oxidation Processes (SR-AOPs), including photolytic activation of peroxymonosulfate (PMS) and persulfate (PS) and their photocatalytic activation using Fe(II). Their efficiency was assessed both for the inactivation
Journal of chemical research. Synopses, 388-388 (1992)

Articles

Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis, and are some of the organic chemist’s most powerful tools for creating novel products. Below is a list of the most commonly used oxidizing and reducing agents currently available in our catalog.

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