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:
Molecular Weight:
216.27
EC Number:
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
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
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comparable product
Signal Word
Danger
Hazard Statements
Precautionary 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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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
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
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
Rachel C Evans et al.
Langmuir : the ACS journal of surfaces and colloids, 28(33), 12348-12356 (2012-07-31)
The absorption and photoluminescence spectra of the cationic conjugated polyelectrolyte poly[3-(6-trimethylammoniumhexyl)thiophene] (P3TMAHT) were observed to be dramatically altered in the presence of anionic surfactants due to self-assembly through ionic complex formation. Small-angle neutron scattering (SANS), UV/vis, and photoluminescence spectroscopy were
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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