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Merck

O8380

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:
5324-84-5
Molecular Weight:
216.27
NACRES:
NA.21
PubChem Substance ID:
24898057
UNSPSC Code:
12161900
EC Number:
226-195-4
MDL number:
MFCD00007544

Product Name

1-Octanesulfonic acid sodium salt, ≥98%

InChI key

HRQDCDQDOPSGBR-UHFFFAOYSA-M

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

SMILES string

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

biological source

synthetic (oragnic)

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)

Quality Level

100

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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

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.

Other Notes

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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SHBT0603
SHBS2843
SHBR6765
SHBQ9124
SHBP1420

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H T Jung et al.
Proceedings of the National Academy of Sciences of the United States of America, 98(4), 1353-1357 (2001-02-15)
Equilibrium unilamellar vesicles are stabilized by one of two distinct mechanisms depending on the value of the bending constant. Helfrich undulations ensure that the interbilayer potential is always repulsive when the bending constant, K, is of order k(B)T. When K
M T Veciana-Nogues et al.
Journal of AOAC International, 78(4), 1045-1050 (1995-07-01)
A liquid chromatographic method with postcolumn derivatization is described for determination of biogenic amines in fish and fish products. Histamine, tyramine, serotonin, beta-phenylethylamine, tryptamine, putrescine, cadaverine, agmatine, spermine, and spermidine can be determined in less than 60 min. Routine sample
W Xie et al.
Biochimica et biophysica acta, 1768(5), 1299-1308 (2007-03-14)
Perfluorooctanesulfonic acid (PFOS) is a persistent environmental pollutant that may cause adverse effects by inhibiting pulmonary surfactant. To gain further insights in this potential mechanism of toxicity, we investigated the interaction of PFOS potassium salt with dipalmitoylphosphatidylcholine (DPPC) - the
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
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
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