O8380
1-Octanesulfonic acid sodium salt
≥98%
동의어(들):
Octane-1-sulfonic acid sodium salt, Sodium 1-octanesulfonate, Sodium octane-1-sulfonate, Sodium octanesulfonate
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
C8H17O3SNa
CAS 번호:
Molecular Weight:
216.27
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12161900
EC Number:
226-195-4
MDL number:
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
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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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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
저장 등급
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)
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
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
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
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
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