Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
C5H11O3SNa
CAS Number:
Molecular Weight:
174.19
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12161900
EC Number:
245-208-4
MDL number:
description
anionic
Quality Segment
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
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.
Still not finding the right product?
Explore all of our products under Sodium pentanesulfonate
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
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
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| P0299-5G | 04061834290971 |
| P0299-25G | 04061835547210 |
| P0299-100G | 04061835547203 |