V900633
Sodium 1-dodecanesulfonate
Vetec™, reagent grade
Synonym(s):
1-Dodecanesulfonic acid sodium salt
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About This Item
Linear Formula:
CH3(CH2)11SO3Na
CAS Number:
Molecular Weight:
272.38
EC Number:
219-200-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
3919536
MDL number:
Product Name
Sodium 1-dodecanesulfonate, Vetec™, reagent grade
InChI key
DAJSVUQLFFJUSX-UHFFFAOYSA-M
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
SMILES string
[Na+]
grade
reagent grade
product line
Vetec™
mp
>300 °C (lit.)
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Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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Jamil Rima et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 74(1), 10-15 (2009-07-14)
The solubilization of pyrene in aqueous solution of beta-cyclodextrin (beta-CD) or its derivatives such as beta-CD-hexanoyl, beta-CD-benzoyl and beta-CD-dodecylsulfonate was investigated by spectrophotometry. Linear and non-linear regression methods were used to estimate the association constants (K(1)). A 1:1 stoichiometric ratio
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
D Zielinska et al.
Chemosphere, 40(3), 327-330 (2000-02-09)
The objective of this study was to determine the interaction of modified bilayer lipid membranes (BLMs) with lead and tin organoderivatives. The relative depolarization, of the lipid membrane, caused by organo metals, was used to estimate their activity. Dodecyltrimethylammonium bromide
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
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