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71890

Sigma-Aldrich

Sodium persulfate

purum p.a., ≥98% (RT)

Synonym(s):

Sodium peroxodisulfate

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About This Item

Linear Formula:
Na2S2O8
CAS Number:
7775-27-1
Molecular Weight:
238.10
EC Number:
231-892-1
MDL number:
MFCD00003501
UNSPSC Code:
12352302
PubChem Substance ID:
329763615
NACRES:
NA.21

vapor pressure

<0.0001 hPa

grade

purum p.a.

Assay

≥98% (RT)

form

powder or crystals

reaction suitability

reagent type: oxidant

pH

2.5-4

anion traces

chloride (Cl-): ≤50 mg/kg

cation traces

Ca: ≤50 mg/kg
Cd: ≤50 mg/kg
Co: ≤50 mg/kg
Cu: ≤50 mg/kg
Fe: ≤50 mg/kg
Ni: ≤50 mg/kg
Pb: ≤50 mg/kg
Zn: ≤50 mg/kg

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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General description

Sodium persulfate (Sodium peroxodisulfate) is an inorganic sodium salt. It is a cheap, eco-friendly oxidizing reagent. It is widely employed in bleaches and hair-coloring formulations.

Application

Sodium persulfate (Sodium peroxodisulfate) may be employed as an oxidizing reagent for the palladium-catalyzed C-H bond functionalization reaction of O-phenylcarbamates with arenes. It may be used to compose the initiator solution required for the preparation of hydroxyethyl methacrylate (HEMA) gel disks.

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

Certificates of Analysis (COA)

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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
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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