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S6172

Sigma-Aldrich

Sodium persulfate

BioXtra, ≥99%

Synonyme(s) :

Sodium peroxodisulfate

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About This Item

Formule linéaire :
Na2S2O8
Numéro CAS:
Poids moléculaire :
238.10
Numéro CE :
Numéro MDL:
Code UNSPSC :
12161700
ID de substance PubChem :
Nomenclature NACRES :
NA.25

Gamme de produits

BioXtra

Niveau de qualité

Pureté

≥99%

Pertinence de la réaction

reagent type: oxidant

Impuretés

<0.0005% Phosphorus (P)
<0.1% Insoluble matter

Solubilité

H2O: 1 M at 20 °C, clear, colorless

Traces d'anions

chloride (Cl-): <0.05%

Traces de cations

Al: <0.0005%
Ca: <0.005%
Cu: <0.0005%
Fe: <0.0005%
K: <0.02%
Mg: <0.001%
Pb: <0.001%
Zn: <0.0005%

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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Application

<ul>
<li><strong>Electrochemical treatment of organic pollutants in landfill leachate using a three-dimensional electrode system.</strong>: This study explores the electrochemical treatment of landfill leachate using a three-dimensional electrode system. Sodium persulfate is used as an oxidizing agent to degrade organic pollutants effectively, providing a potential method for waste management and environmental protection (Yu et al., 2020).</li>
<li><strong>The Box-Benkhen experimental design for the optimization of the electrocatalytic treatment of wastewaters with high concentrations of phenol and organic matter.</strong>: This paper discusses the optimization of electrocatalytic treatment processes for wastewater containing high levels of phenol and organic matter using sodium persulfate. The study provides valuable insights for improving wastewater treatment efficiency (GilPavas et al., 2009).</li>
<li><strong>Reaction of pectin and glycidyl methacrylate and ulterior formation of free films by reticulation.</strong>: This research involves the chemical modification of pectin with glycidyl methacrylate followed by cross-linking using sodium persulfate, leading to the formation of free-standing films. These films have potential applications in pharmaceuticals and food packaging (Maior et al., 2008).</li>
</ul>

Pictogrammes

Flame over circleHealth hazardExclamation mark

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

Équipement de protection individuelle

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


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Consulter la Bibliothèque de documents

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
Ya-Ting Lin et al.
Chemosphere, 82(8), 1168-1172 (2011-01-12)
Using ultraviolet photolytic persulfate activation to produce two sulfate radicals (SO(4)(-)) exhibits a potential for destroying organic contaminants in wastewater treatment applications. This study investigated both the feasibility of using a UV/SPS (sodium persulfate) process to treat phenol in aqueous
Zhiguo Zhang et al.
The Journal of organic chemistry, 77(17), 7665-7670 (2012-08-02)
Mediated by sodium persulfate (Na(2)S(2)O(8)), a series of polysubstituted 4-pyridones were synthesized via self-condensation of N-aryl acetoacetamides, during which a novel N to C 1,3-acyl migration should be involved. The structure of 4-pyridone was unequivocally confirmed by X-ray diffraction analysis.
Olha S Furman et al.
Environmental science & technology, 44(16), 6423-6428 (2010-08-14)
Base is the most commonly used activator of persulfate for the treatment of contaminated groundwater by in situ chemical oxidation (ISCO). A mechanism for the base activation of persulfate is proposed involving the base-catalyzed hydrolysis of persulfate to hydroperoxide anion

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