Saltar al contenido
Merck

228036

Sigma-Aldrich

OXONE®, monopersulfate compound

Sinónimos:

Potassium peroxymonosulfate

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula lineal:
KHSO5 · 0.5KHSO4 · 0.5K2SO4
Número de CAS:
Peso molecular:
307.38
Número MDL:
Código UNSPSC:
12352300
ID de la sustancia en PubChem:
NACRES:
NA.21

grado

for analytical purposes

Nivel de calidad

presión de vapor

<0.0000017 hPa

Formulario

powder

idoneidad de la reacción

reagent type: oxidant

concentración

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

pH

2.1 (77 °C, 30 g/L)

cadena SMILES

[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

Clave InChI

HJKYXKSLRZKNSI-UHFFFAOYSA-I

¿Está buscando productos similares? Visita Guía de comparación de productos

Descripción general

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

Aplicación

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.

Información legal

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

Palabra de señalización

Danger

Frases de peligro

Clasificaciones de peligro

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

Clase de riesgo para el agua (WGK)

WGK 3

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number

¿No ve la versión correcta?

Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Los clientes también vieron

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
Jiamin Hu et al.
Water science and technology : a journal of the International Association on Water Pollution Research, 79(5), 911-920 (2019-04-27)
In this study, the difference in oxidative capacity for removing antibiotics and the mechanism between the Cu(II)/peroxymonosulfate (PMS)/UV and Cu(II)/persulfate (PDS)/UV systems were compared under various conditions. The optimal Cu(II) concentration in the Cu(II)/PMS/UV system was 30 μM, and in
Journal of chemical research. Synopses, 388-388 (1992)
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
George P Anipsitakis et al.
Water research, 42(12), 2899-2910 (2008-04-04)
Potassium peroxymonosulfate activation leads to the formation of highly reactive species, mainly the sulfate radicals. Activated potassium peroxymonosulfate (from now on peroxymonosulfate) was tested against specific pollutants such as ammonium ion, creatinine, chlorinated creatinine products, arginine and Escherichia coli (E.

Artículos

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.

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico