Skip to Content
MilliporeSigma
All Photos(1)

Documents

P7425

Sigma-Aldrich

Tetraethylene glycol monodecyl ether

~97% (GC)

Synonym(s):

C10E4, Decyl tetraethylene glycol ether, Decyltetraglycol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3(CH2)9(OCH2CH2)4OH
CAS Number:
5703-94-6
Molecular Weight:
334.49
Beilstein/REAXYS Number:
4247848
MDL number:
MFCD00043359
UNSPSC Code:
12161900
PubChem Substance ID:
24898850

description

non-ionic

assay

~97% (GC)

mol wt

334.49 g/mol

bp

288-290 °C (lit.)

density

0.96 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCOCCOCCOCCOCCO

InChI

1S/C18H38O5/c1-2-3-4-5-6-7-8-9-11-20-13-15-22-17-18-23-16-14-21-12-10-19/h19H,2-18H2,1H3

InChI key

ASMWIUUCZFNLHL-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Tetraethylene glycol monodecyl ether is a surfactant.

Application

Tetraethylene glycol monodecyl ether has been used in a study to assess anomalous thickness variation of the foam films stabilized by weak non-ionic surfactants. It has also been used in a study to investigate removal of vaporous naphthalene using polyoxyethylenated nonionic surfactants.

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Hsiao-Lin Huang et al.
Journal of the Air & Waste Management Association (1995), 53(8), 983-991 (2003-08-29)
Previous research has demonstrated that an anionic surfactant can increase the solubility of the vapor phases of both naphthalene and sulfur dioxide in water. This study examines the feasibility of removing polycyclic aromatic hydrocarbons (PAHs) during gas absorption by adding
Cosima Stubenrauch et al.
Langmuir : the ACS journal of surfaces and colloids, 28(25), 9206-9210 (2012-06-08)
We showed in a previous study that a water-nonionic surfactant system, where the surfactant is a 9:1 mixture of tetraethylene glycol monodecyl ether (C(10)E(4)) and pentaethylene glycol monodecyl ether (C(10)E(5)), forms a disconnected lamellar (L(α)) phase. Thus, the isotropic phase
Christopher Hill et al.
Langmuir : the ACS journal of surfaces and colloids, 36(48), 14829-14840 (2020-11-25)
The interfacial properties and water-in-CO2 (W/CO2) microemulsion (μE) formation with double- and novel triple-tail surfactants bearing trimethylsilyl (TMS) groups in the tails are investigated. Comparisons of these properties are made with those for analogous hydrocarbon (HC) and fluorocarbon (FC) tail
Vishnu Sresht et al.
Langmuir : the ACS journal of surfaces and colloids, 33(33), 8319-8329 (2017-07-28)
A molecular modeling approach is presented with a focus on quantitative predictions of the surface tension of aqueous surfactant solutions. The approach combines classical Molecular Dynamics (MD) simulations with a molecular-thermodynamic theory (MTT) [ Y. J. Nikas, S. Puvvada, D.
Anne-Gaëlle Fournial et al.
Langmuir : the ACS journal of surfaces and colloids, 23(23), 11443-11450 (2007-10-13)
The binary phase diagram of tetraethylene glycol decanoyl ester (C9COE4) was investigated in the micellar region by PGSE-NMR (pulse field gradient spin echo nuclear magnetic resonance) and in the lamellar liquid crystalline state by 2H NMR. Its behavior was compared
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service