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S6172

Sigma-Aldrich

Sodium persulfate

BioXtra, ≥99%

Synonym(s):

Sodium peroxodisulfate

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About This Item

Linear Formula:
Na2S2O8
CAS Number:
Molecular Weight:
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>

Signal Word

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 Code

5.1B - Oxidizing hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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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