106437
Sodium 1-dodecanesulfonate
ReagentPlus®, ≥99%
동의어(들):
1-Dodecanesulfonic acid sodium salt
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제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
CH3(CH2)11SO3Na
CAS 번호:
Molecular Weight:
272.38
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-200-6
Beilstein/REAXYS Number:
3919536
MDL number:
Assay:
≥99%
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
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
저장 등급
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
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