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P0299

Sigma-Aldrich

Sodium pentanesulfonate

≥95% (elemental analysis)

Synonym(s):

1-Pentanesulfonic acid sodium salt

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About This Item

Linear Formula:
C5H11O3SNa
CAS Number:
22767-49-3
Molecular Weight:
174.19
EC Number:
245-208-4
MDL number:
MFCD00007541
UNSPSC Code:
12161900
PubChem Substance ID:
24898092
NACRES:
NA.21

description

anionic

Quality Level

100

Assay

≥95% (elemental analysis)

form

powder

mol wt

174.19 g/mol

SMILES string

[Na+].CCCCCS([O-])(=O)=O

InChI

1S/C5H12O3S.Na/c1-2-3-4-5-9(6,7)8;/h2-5H2,1H3,(H,6,7,8);/q;+1/p-1

InChI key

ROBLTDOHDSGGDT-UHFFFAOYSA-M

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General description

Sodium pentanesulfonate is an anionic surfactant, which is used in the analysis of small organic molecular compounds, pharmaceutical products, and metabolites using reversed-phase high-performance liquid (RP-HPLC) and micellar electrokinetic chromatography. Sonochemical and sonoluminescent studies by electron paramagnetic resonance spectroscopy (EPR) and spin-trapping techniques have been reported on various ion-pairing reagents, like sodium pentanesulfonate.

Application

Ion-associating reagent for HPLC, including analyses of peptides and proteins.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000404936
0000404935
0000387422
0000396914
0000387409

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B R Thomas et al.
Journal of pharmaceutical and biomedical analysis, 12(1), 85-90 (1994-01-01)
The five active drug substances and two of the excipients present in Frenadol, a cold medication, were separated. The active drug components dextromethorphan HBr monohydrate, ascorbic acid, caffeine, paracetamol and chlorpheniramine maleate were quantitatively assayed by a mixed ion pair
Hsin-Hua Yeh et al.
Electrophoresis, 26(4-5), 947-953 (2005-01-26)
A simple and selective micellar electrokinetic chromatography (MEKC) with UV detection is described for simultaneous determination of amikacin, tobramycin, and kanamycin A, performed in Tris buffer (180 mM; pH 9.1) with 300 mM sodium pentanesulfonate (SPS) as an anionic surfactant.
Joe Z Sostaric
Ultrasonics sonochemistry, 15(6), 1043-1048 (2008-05-13)
Sonolysis of aqueous solutions of n-alkyl anionic surfactants results in the formation of secondary carbon-centered radicals (-*CH-). The yield of -*CH- depends on the bulk surfactant concentration up to a maximum attainable radical yield (the 'plateau yield') where an increasing
Limei Yang et al.
The journal of physical chemistry. B, 111(6), 1361-1367 (2007-01-26)
Sonolysis of argon-saturated aqueous solutions of the nonvolatile surfactants sodium dodecyl sulfate (SDS) and sodium 1-pentanesulfonate (SPSo) was investigated at three ultrasonic frequencies under both continuous wave (CW) and pulsed ultrasound. Secondary carbon-centered radicals were detected by spin trapping using
Rahmat Sadeghi et al.
Journal of colloid and interface science, 346(1), 107-117 (2010-03-24)
Thermodynamic properties for aqueous solutions containing sodium pentane-1-sulfonate (C(5)SO(3)Na) in the absence and presence of poly(ethyleneglycol) (PEG) or poly(vinylpyrrolidone) (PVP) determined as a function of surfactant concentration from the density, sound velocity, viscosity, conductivity and vapor-liquid equilibria data, are reported
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