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30633

Sodium 1-decanesulfonate

≥99.0% (T)

Synonym(s):

1-Decanesulfonic acid sodium salt

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About This Item

Linear Formula:
CH3(CH2)8CH2SO3Na
CAS Number:
13419-61-9
Molecular Weight:
244.33
UNSPSC Code:
12161900
NACRES:
NA.25
PubChem Substance ID:
57648452
EC Number:
236-525-9
Beilstein/REAXYS Number:
3918920
MDL number:
MFCD00007526

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description

anionic

Quality Level

100

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

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1 of 4

This Item
30631D3412106437
Sodium 1-decanesulfonate ≥99.0% (T)

Sigma-Aldrich

30633

Sodium 1-decanesulfonate

Sodium 1-decanesulfonate suitable for ion pair chromatography, LiChropur™, ≥99.0%

Supelco

30631

Sodium 1-decanesulfonate

Sodium 1-decanesulfonate ~98%

Sigma-Aldrich

D3412

Sodium 1-decanesulfonate

Sodium 1-dodecanesulfonate ReagentPlus®, ≥99%

Sigma-Aldrich

106437

Sodium 1-dodecanesulfonate

technique(s)

electrophoresis: suitable

technique(s)

ion pair chromatography: suitable

technique(s)

LC/MS: suitable

technique(s)

-

assay

≥99.0% (T)

assay

≥99.0% (T)

assay

~98%

assay

≥99%

mp

>300 °C (lit.)

mp

>300 °C (lit.)

mp

>300 °C (lit.)

mp

>300 °C (lit.)

solubility

H2O: 0.05 g/mL, clear

solubility

-

solubility

-

solubility

H2O: 25 mg/mL

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

200

description

anionic

description

anionic

description

anionic

description

-

General description

Sodium 1-decanesulfonate is an ion-associating reagent.

Application

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM4357
BCCK9601
BCCH4125
BCCG5959
BCCG5574

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Journal of medicinal chemistry, 52(14), 4338-4344 (2009-06-19)
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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
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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
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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
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
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Global Trade Item Number

SKUGTIN
30633-5G04061835541232
30633-10G04061826672914

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