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216232

Sigma-Aldrich

Sodium persulfate

reagent grade, ≥98%

Synonyme(s) :

Sodium peroxodisulfate

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About This Item

Formule linéaire :
Na2S2O8
Numéro CAS:
7775-27-1
Poids moléculaire :
238.10
Numéro CE :
231-892-1
Numéro MDL:
MFCD00003501
Code UNSPSC :
12352302
ID de substance PubChem :
329752185
Nomenclature NACRES :
NA.21

Qualité

reagent grade

Niveau de qualité

200

Pureté

≥98%

Forme

powder, crystals or granules

Pertinence de la réaction

reagent type: oxidant

Chaîne SMILES 

[Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O

InChI

1S/2Na.H2O8S2/c;;1-9(2,3)7-8-10(4,5)6/h;;(H,1,2,3)(H,4,5,6)/q2*+1;/p-2

Clé InChI

CHQMHPLRPQMAMX-UHFFFAOYSA-L

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Description générale

Sodium persulfate, also known as Sodium peroxodisulfate is an inorganic compound and is a water-soluble strong oxidizing agent, that is stable and easy to handle. It is commonly used as an oxidant in organic synthesis reactions such as transition-metal-catalyzed or metal-free reactions. Additionally, it is used as a polymerization initiator and in the synthesis of sulfate radical anions through heat-activated decomposition.

Application

Sodium persulfate can be used as an oxidant:
  • For the radical cyclization cascade reaction of 2-alkynylbenzonitriles and sodium arylsulfinates to synthesize sulfonated indenones.
  • In the silica-supported aluminum chloride-catalyzed Baeyer-Villiger oxidation of cyclic and acyclic ketones to lactones or esters.
It can also be used as an initiator for the polymerization of styrene to synthesize polystyrene.

Pictogrammes

Flame over circleHealth hazardExclamation mark
GHS03,GHS08,GHS07

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 4 Oral - Ox. Sol. 3 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

5.1B - Oxidizing hazardous materials

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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PCE oxidation by sodium persulfate in the presence of solids
Jed C, et al.
Environmental Science & Technology, 44, 9445-9450 (2010)
Esther Eljarrat-Binstock et al.
Investigative ophthalmology & visual science, 45(8), 2543-2548 (2004-07-28)
To assess the corneal iontophoretic delivery of gentamicin by drug-loaded hydrogel probe, and to determine the resultant ocular disposition and elimination of the drug from the cornea and anterior chamber. Corneal iontophoresis of gentamicin sulfate was studied in healthy white
Xiaodan Zhao et al.
Journal of the American Chemical Society, 132(16), 5837-5844 (2010-04-03)
By palladium catalysis, the C-H bond functionalization of O-phenylcarbamates with simple arenes has been achieved using sodium persulfate (Na(2)S(2)O(8)), an inexpensive, easy-to-handle, and environmentally friendly oxidant. This oxidative cross-coupling involves two aromatic C-H bonds undergoing concomitant oxidation to furnish a
Chenju Liang et al.
Chemosphere, 70(3), 426-435 (2007-08-19)
In situ chemical oxidation with persulfate anion (S2O82*) is a viable technique for remediation of groundwater contaminants such as trichloroethylene (TCE). An accelerated reaction using S2O82* to destroy TCE can be achieved via chemical activation with ferrous ion to generate
Chia-Hsien Yen et al.
Journal of hazardous materials, 186(2-3), 2097-2102 (2011-01-25)
In this study, batch experiments were conducted to evaluate the feasibility of petroleum-hydrocarbon contaminated soil remediation using persulfate oxidation. Various controlling factors including different persulfate and ferrous ion concentrations, different oxidants (persulfate, hydrogen peroxide, and permanganate), and different contaminants (diesel
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