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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

Quality Level

200

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
Mushtaque Ahmad et al.
Journal of contaminant hydrology, 115(1-4), 34-45 (2010-05-05)
Persulfate dynamics in the presence of subsurface minerals was investigated as a basis for understanding persulfate activation for in situ chemical oxidation (ISCO). The mineral-mediated decomposition of persulfate and generation of oxidants and reductants was investigated with four iron and
Chenju Liang et al.
Water research, 42(15), 4091-4100 (2008-08-23)
The present study focused on evaluation of activated persulfate (PS) anion (S(2)O(8)(2-)) oxidative degradation of benzene, toluene, ethylbenzene, and xylene (constituents of gasoline and known collectively as BTEX) contamination. The results indicated that BTEX were effectively oxidized by PS in
Richard L Johnson et al.
Environmental science & technology, 42(24), 9350-9356 (2009-01-30)
Contaminant destruction with in situ chemical oxidation (ISCO) using persulfate (peroxydisulfate, S2O8(2-)) can be enhanced by activation, which increases the rate of persulfate decomposition to sulfate radicals (SO4*-). This step initiates a chain of radical reactions involving species (including SO4*-
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