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Key Documents

O8380

Sigma-Aldrich

1-Octanesulfonic acid sodium salt

≥98%

Synonym(s):

Octane-1-sulfonic acid sodium salt, Sodium 1-octanesulfonate, Sodium octane-1-sulfonate, Sodium octanesulfonate

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About This Item

Linear Formula:
C8H17O3SNa
CAS Number:
Molecular Weight:
216.27
EC Number:
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.21

biological source

synthetic (oragnic)

Quality Level

description

anionic

Assay

≥98%

form

powder

mol wt

216.27 g/mol

technique(s)

HPLC: suitable

impurities

<2.0% water (Karl Fischer)

mp

300  °C (572 °F)

solubility

9.8 g/L at 20 °C

cation traces

Na: 10.1-11.1 % (w/v) (Anhydrous)

SMILES string

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

InChI

1S/C8H18O3S.Na/c1-2-3-4-5-6-7-8-12(9,10)11;/h2-8H2,1H3,(H,9,10,11);/q;+1/p-1

InChI key

HRQDCDQDOPSGBR-UHFFFAOYSA-M

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General description

1-Octanesulfonic acid sodium is an anionic detergent and a surfactant with excellent coupling properties. This versatile molecule finds application as a buffer component, in cell biology, analytical chemistry, and biochemical research.

Application

1-Octanesulfonic acid sodium salt has been used:
  • as a component of 9 parts buffer to determine the concentration of L-Dopa in extracts of seed flour
  • in mobile phase solution to measure dopamine in rats using high-performance liquid chromatography (HPLC) analysis
  • in neurochemistry for the preparation of mobile phase buffer for HPLC analysis.

Ion-pairing reagent for HPLC analysis of peptides and proteins.

Features and Benefits

  • Highly versatile surfactant for your cell biology and biochemical research
  • Suitable for HPLC applications

Other Notes

For additional information on our range of Biochemicals, please complete this form.

comparable product

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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I T James et al.
Journal of chromatography, 525(1), 43-57 (1990-01-26)
Following a detailed study, a rapid and sensitive assay for the naturally fluorescent collagen cross-links pyridinoline and deoxypyridinoline has been developed using ion-pair reversed-phase high-performance liquid chromatography in the presence of 1-octanesulphonic acid (OSA). Pyridinoline and deoxypyridinoline were separated on
Tejwant Singh et al.
Physical chemistry chemical physics : PCCP, 12(37), 11728-11735 (2010-08-10)
We have observed dual transitions in various physical properties while investigating the surfactant-like behavior of the ionic liquid (IL) 1-butyl-3-methylimidazolium octylsulfate [C(4)mim][C(8)SO(4)] in aqueous media. Interestingly, in conductivity measurements, it was found that the second transition, which is comparatively weak
P G Jaison et al.
Journal of chromatography. A, 1216(9), 1383-1389 (2009-01-27)
Studies were carried out for the separation of uranium (U) and thorium (Th) on reversed-phase (RP) C18 columns using mandelic acid as an eluent. Retention of thorium-mandelate on the unmodified stationary phase was found to be greater than that of
J L Razak et al.
Pharmaceutical research, 18(1), 104-111 (2001-05-05)
The aim of this study was to develop a method based upon electrokinetic chromatography (EKC) using oppositely charged surfactant vesicles as a buffer modifier to estimate hydrophobicity (log P) for a range of neutral and charged compounds. Vesicles were formed
Yingjie Ma et al.
Chemical communications (Cambridge, England), 47(45), 12340-12342 (2011-10-21)
By the introduction of trimethylammonium groups at both upper and lower rims, a cationic water-soluble pillar[5]arene was prepared, which forms a stable 1 : 1 host-guest complex with sodium 1-octanesulfonate in water.

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