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Merck

S6172

Sigma-Aldrich

Sodium persulfate

BioXtra, ≥99%

Sinónimos:

Sodium peroxodisulfate

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About This Item

Fórmula lineal:
Na2S2O8
Número de CAS:
Peso molecular:
238.10
EC Number:
MDL number:
UNSPSC Code:
12161700
PubChem Substance ID:
NACRES:
NA.25

product line

BioXtra

Quality Level

assay

≥99%

reaction suitability

reagent type: oxidant

impurities

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

solubility

H2O: 1 M at 20 °C, clear, colorless

anion traces

chloride (Cl-): <0.05%

cation traces

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

SMILES string

[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

InChI key

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>

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

5.1B - Oxidizing hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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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
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.

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