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Merck
CN

86140

Docusate sodium salt

purum, ≥96.0% (TLC)

Synonym(s):

AOT, Bis(2-ethylhexyl) sulfosuccinate sodium salt, Sodium bis(2-ethylhexyl) sulfosuccinate, Sulfobutanedioic acid bis(2-ethylhexyl ester) sodium salt, Sulfosuccinic acid bis(2-ethylhexyl) ester sodium salt, ‘Dioctyl’ sulfosuccinate sodium salt

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About This Item

Empirical Formula (Hill Notation):
C20H37NaO7S
CAS Number:
Molecular Weight:
444.56
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-406-4
Beilstein/REAXYS Number:
4117588
MDL number:
Assay:
≥96.0% (TLC)
Form:
solid
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Product Name

Docusate sodium salt, purum, ≥96.0% (TLC)

InChI key

APSBXTVYXVQYAB-UHFFFAOYSA-M

InChI

1S/C20H38O7S.Na/c1-5-9-11-16(7-3)14-26-19(21)13-18(28(23,24)25)20(22)27-15-17(8-4)12-10-6-2;/h16-18H,5-15H2,1-4H3,(H,23,24,25);/q;+1/p-1

SMILES string

[Na+].CCCCC(CC)COC(=O)CC(C(=O)OCC(CC)CCCC)S([O-])(=O)=O

grade

purum

assay

≥96.0% (TLC)

form

solid

impurities

≤2% water

functional group

ester
sulfonic acid

Quality Level

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Application

Docusate sodium salt can be used as a surfactant in the synthesis of magnetic nanoparticles by co-precipitation method.
Forms reverse micelles in hydrocarbon solvents; Suitable for the solubilization of the major myelin transmembrane proteolipid

General description

Docusate sodium salt is an emollient which can combine with the active pharmaceutical ingredients (APIs) such as ranitidine hydrochloride and lidocaine hydrochloride to form hydrophobic ionic liquids (IL-APIs)).

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Nanomedicine: Nanotechnology, Biology, and Medicine, 6(2), 355-361 (2010)
The third evolution of ionic liquids: active pharmaceutical ingredients
Hough WL, et al.
New. J. Chem., 31(8), 1429-1436 (2007)
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U Thapa et al.
Journal of colloid and interface science, 406, 172-177 (2013-07-06)
Understanding the mechanism that controls the folding/unfolding of proteins in the presence of urea continues to be a subject of research, and since micelles mimic biological aggregates, equal importance has been given to the study of surfactants in the presence

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