Skip to Content
Merck
CN
All Photos(1)

Documents

30633

Sigma-Aldrich

Sodium 1-decanesulfonate

≥99.0% (T)

Sign Into View Organizational & Contract Pricing

Synonym(s):
1-Decanesulfonic acid sodium salt
Linear Formula:
CH3(CH2)8CH2SO3Na
CAS Number:
Molecular Weight:
244.33
Beilstein:
3918920
EC Number:
MDL number:
UNSPSC Code:
12161900
PubChem Substance ID:
NACRES:
NA.25

description

anionic

Quality Level

Assay

≥99.0% (T)

mol wt

244.33 g/mol

technique(s)

electrophoresis: suitable

mp

>300 °C (lit.)

solubility

H2O: 0.05 g/mL, clear

SMILES string

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

InChI

1S/C10H22O3S.Na/c1-2-3-4-5-6-7-8-9-10-14(11,12)13;/h2-10H2,1H3,(H,11,12,13);/q;+1/p-1

InChI key

AIMUHNZKNFEZSN-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

General description

Sodium 1-decanesulfonate is an ion-associating reagent.

Application

Ion-associating reagent for HPLC, including analyses of peptides and proteins.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Luigi Battaglia et al.
Journal of pharmaceutical sciences, 103(7), 2157-2165 (2014-05-16)
The major obstacle to glioblastoma pharmacological therapy is the overcoming of the blood-brain barrier (BBB). In literature, several strategies have been proposed to overcome the BBB: in this experimental work, solid lipid nanoparticles (SLN), prepared according to fatty acid coacervation
N M Kovalchuk et al.
Journal of colloid and interface science, 459, 250-256 (2015-08-25)
Mixed solutions of cationic and anionic surfactants show considerable synergism in their wetting behaviour, but their spreading is affected considerably by the phase separation processes. The valuable information about wetting properties of synergetic mixtures can be obtained by using mixtures
Miriam Gochin et al.
Journal of medicinal chemistry, 52(14), 4338-4344 (2009-06-19)
The hydrophobic pocket within the coiled coil domain of HIV-1 gp41 is considered to be a hot-spot suitable for small molecule intervention of fusion, although so far it has yielded only microM inhibitors. Previous peptide studies have identified specific hydrophobic
Hongyan Yang et al.
ACS chemical neuroscience, 6(8), 1487-1501 (2015-07-15)
In vivo microdialysis is widely used to investigate how neurotransmitter levels in the brain respond to biologically relevant challenges. Here, we combined recent improvements in the temporal resolution of online sampling and analysis for serotonin with a brief high-K(+) stimulus
Franziska Mohr et al.
PloS one, 10(10), e0141136-e0141136 (2015-10-28)
The muscarinic M2 receptor (M2R) acts as a negative feedback regulator in central cholinergic systems. Activation of the M2 receptor limits acetylcholine (ACh) release, especially when ACh levels are increased because acetylcholinesterase (AChE) activity is acutely inhibited. Chronically high ACh

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service