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76954

Supelco

Sodium 1-pentanesulfonate solution

suitable for ion pair chromatography, LiChropur™, concentrate, ampule

Synonym(s):

1-Pentanesulfonic acid sodium salt

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About This Item

Linear Formula:
CH3(CH2)4SO3Na
CAS Number:
22767-49-3
Molecular Weight:
174.19
Beilstein:
3725147
MDL number:
MFCD00007541
UNSPSC Code:
12000000
PubChem Substance ID:
329767451
NACRES:
NB.21

description

anionic

Quality Level

100

form

solution

quality

LiChropur™
ampule

packaging

ampule of 25 mL

technique(s)

HPLC: suitable
ion pair chromatography: suitable

λ

in concentrate

UV absorption

λ: 210 nm Amax: 0.06
λ: 220 nm Amax: 0.04
λ: 230 nm Amax: 0.03
λ: 260 nm Amax: 0.01
λ: 500 nm Amax: 0.01

suitability

corresponds to standard for RP gradient test
corresponds to standard for filter test

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

Concentrate for 6x1 L ready-to-use solution. Dilute contents of one ampule (~0.3 M) to 1 L with HPLC grade water to obtain a 0.005 M eluent solution.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

76954-6AMP-F:
76954-1EA-F:
76954-BULK-F:
76954-VAR-F:
76954-0.1ML-F:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBX0120
BCBJ2992V
1386337
094143/1
94143/1

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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
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
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
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