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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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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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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