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Safety Information

106437

Sigma-Aldrich

Sodium 1-dodecanesulfonate

ReagentPlus®, ≥99%

Synonym(s):

1-Dodecanesulfonic acid sodium salt

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About This Item

Linear Formula:
CH3(CH2)11SO3Na
CAS Number:
2386-53-0
Molecular Weight:
272.38
Beilstein:
3919536
EC Number:
219-200-6
MDL number:
MFCD00007527
UNSPSC Code:
12352100
PubChem Substance ID:
24846734
NACRES:
NA.22

Quality Level

200

product line

ReagentPlus®

Assay

≥99%

mp

>300 °C (lit.)

solubility

H2O: 25 mg/mL

functional group

sulfonic acid

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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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 Merck KGaA, Darmstadt, Germany

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

106437-VAR:
106437-250MG:
106437-BULK:
106437-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBK4343V
1451815V
1451815
06820HJ
1253931

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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
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
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
Toshihide Tsukatani et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 22(2), 199-200 (2006-03-04)
The tetraoctylammonium cation forms water-immiscible room temperature ionic liquids with dodecylsulfate and dodecylbenzenesulfonate anions. The ionic liquids are halogen-free and can be considered environmentally friendly solvents. At 25 degrees C, the solubilities of water in tetraoctylammonium dodecylsulfate and tetraoctylammonium dodecylbenzenesulfonate
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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