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Key Documents

D0181

Sigma-Aldrich

Sodium 1-decanesulfonate

BioXtra, ~98%

Synonym(s):

1-Decanesulfonic acid sodium salt

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About This Item

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

product line

BioXtra

Assay

~98%

form

powder

mol wt

244.33 g/mol

technique(s)

HPLC: suitable

impurities

≤0.001% Phosphorus (P)
≤0.1% Insoluble matter

mp

>300 °C (lit.)

solubility

200 mg, clear, colorless (in 4 mL H2O)

anion traces

chloride (Cl-): ≤0.05%

cation traces

Al: ≤0.0005%
Ca: ≤0.0005%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Pb: ≤0.001%
Zn: ≤0.0005%

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

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Application

Sodium 1-decanesulfonate has been used in a study to assess transportation of atrazine and paraquat through nanochannels. It has also been used in a study to investigate the photocycle of bacteriorhodopsin upon chemical modification with surfactants.
Ion-associating reagent for HPLC, including analyses of peptides and proteins.

Storage Class Code

11 - Combustible Solids

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’.

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Influence of sodium 1-decanesulfonate on the enthalpy of activation of two-step Zn2+ ions electroreduction
Nieszporek
Journal of Electroanalytical Chemistry (Lausanne Switzerland), 662, 8-8 (2001)
Study of transportation of atrazine and paraquat through nanochannels
Yue, et al.
Journal of Membrane Science , 356, 6-6 (2010)
Li-Kang Chu et al.
Photochemistry and photobiology, 86(2), 316-323 (2009-12-17)
The spectroscopic and kinetic studies of the interaction between bacteriorhodopsin in the M-intermediate and several surfactants (cetyl trimethyl ammonium bromide, dodecyl trimethyl ammonium bromide, diethylene glycol mono-n-hexyl ether, ethylene glycol mono-n-hexyl ether, sodium 1-decanesulfonate and sodium 1-heptanesulfonate) have been investigated
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
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

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