P8199
Sodium pentanesulfonate
BioXtra
Synonym(s):
1-Pentanesulfonic acid sodium salt
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 Level
product line
BioXtra
form
powder
mol wt
174.19 g/mol
impurities
≤0.001% Phosphorus (P), ≤0.1% Insoluble matter
solubility
H2O: 0.5 M at 20 °C, clear, colorless
anion traces
chloride (Cl-): ≤0.05%
cation traces
Al: ≤0.0005%, Ca: ≤0.001%, Cu: ≤0.0005%, Fe: ≤0.0005%, K: ≤0.005%, Mg: ≤0.0005%, NH4+: ≤0.05%, Pb: ≤0.001%, Zn: ≤0.0005%
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
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.
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