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106437

Sigma-Aldrich

Sodium 1-dodecanesulfonate

ReagentPlus®, ≥99%

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Synonym(s):
1-Dodecanesulfonic acid sodium salt
Linear Formula:
CH3(CH2)11SO3Na
CAS Number:
2386-53-0
Molecular Weight:
272.38
Beilstein:
3919536
EC Number:
219-200-6
MDL number:
MFCD00007527
PubChem Substance ID:
24846734
NACRES:
NA.22

Quality Level

200

product line

ReagentPlus®

Assay

≥99%

mp

>300 °C (lit.)

solubility

H2O: 25 mg/mL

SMILES string

[Na+]

InChI

1S/C12H26O3S.Na/c1-2-3-4-5-6-7-8-9-10-11-12-16(13,14)15;/h2-12H2,1H3,(H,13,14,15);/q;+1/p-1

InChI key

DAJSVUQLFFJUSX-UHFFFAOYSA-M

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1 of 4

This Item
D34123063374885
Sodium 1-dodecanesulfonate ReagentPlus®, ≥99%

Sigma-Aldrich

106437

Sodium 1-dodecanesulfonate

Sodium 1-decanesulfonate ~98%

Sigma-Aldrich

D3412

Sodium 1-decanesulfonate

Sodium 1-decanesulfonate ≥99.0% (T)

Sigma-Aldrich

30633

Sodium 1-decanesulfonate

Sodium 1-octanesulfonate monohydrate ≥97.0% (T)

Sigma-Aldrich

74885

Sodium 1-octanesulfonate monohydrate

mp

>300 °C (lit.)

mp

>300 °C (lit.)

mp

>300 °C (lit.)

mp

≥300 °C (lit.)

solubility

H2O: 25 mg/mL

solubility

-

solubility

H2O: 0.05 g/mL, clear

solubility

H2O: 0.1 g/mL, clear, colorless

product line

ReagentPlus®

product line

-

product line

-

product line

-

General description

Sodium 1-dodecanesulfonate is an ion-pairing reagent and increases the retention of thiabendazole on the HPLC column during determination of thiabendazole in citrus fruit and banana. It is a surfactant standard.

Application

Sodium 1-dodecanesulfonate may be used in synthesis of metal oxide-graphene nanocomposites.

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Storage Class Code

11 - Combustible Solids

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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Y Ito et al.
Journal of chromatography. A, 810(1-2), 81-87 (1998-08-06)
A simple, rapid and reproducible analytical method for thiabendazole (TBZ) and imazalil (IMA) in citrus fruit and banana has been developed. The method involves the use of an ion-exchange cartridge for sample clean-up followed by ion-pair high-performance liquid chromatography with
Donghai Wang et al.
ACS nano, 4(3), 1587-1595 (2010-02-27)
Surfactant or polymer directed self-assembly has been widely investigated to prepare nanostructured metal oxides, semiconductors, and polymers, but this approach is mostly limited to two-phase materials, organic/inorganic hybrids, and nanoparticle or polymer-based nanocomposites. Self-assembled nanostructures from more complex, multiscale, and
Chengcheng Yu et al.
Polymers, 11(5) (2019-05-11)
In this work, the effect of doubly functionalized montmorillonite (MMT) on the structure, morphology, thermal, and tribological characteristics of the resulting polystyrene (PS) nanocomposites was investigated. The modification of the MMT was performed using a cationic surfactant and an anionic
Toshinori Fujie et al.
ACS applied materials & interfaces, 1(7), 1404-1413 (2010-04-02)
Freestanding quasi-two-dimensional ultrathin films (e.g., 41 nm thick polymer nanosheets) were produced, on which stimuli-responsive 47 nm thick polymer brushes were constructed by atom transfer radical polymerization (ATRP) of poly(N-isopropylacrylamide). The resulting surfaces of the multilayered polysaccharide ultrathin films were
Manuel Mora et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(3), 989-995 (2011-01-14)
An Mg/Al layered double hydroxide (LDH) containing carbonate ion in its interlayer region was examined by medium infrared (MIR) and near infrared reflectance spectroscopy (NIRS). The MIR and NIR spectroscopy techniques was also used to study two organo-hybrid LDHs containing
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