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Merck

P7425

Sigma-Aldrich

Tetraethylenglykol-monodecylether

~97% (GC)

Synonym(e):

C10E4, Decyl-tetraethylenglykolether, Decyl-tetraglykol

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About This Item

Lineare Formel:
CH3(CH2)9(OCH2CH2)4OH
CAS-Nummer:
Molekulargewicht:
334.49
Beilstein:
4247848
MDL-Nummer:
UNSPSC-Code:
12161900
PubChem Substanz-ID:

Beschreibung

non-ionic

Assay

~97% (GC)

Mol-Gew.

334.49 g/mol

bp

288-290 °C (lit.)

Dichte

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

InChIKey

ASMWIUUCZFNLHL-UHFFFAOYSA-N

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Allgemeine Beschreibung

Tetraethylene glycol monodecyl ether is a surfactant.

Anwendung

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.

Lagerklassenschlüssel

12 - Non Combustible Liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves


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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
Oliver Wrede et al.
Physical chemistry chemical physics : PCCP, 21(12), 6725-6731 (2019-03-13)
In our present work we present an approach which allows one to confine proteins in structurally nearly identical bicontinuous microemulsions with systematically decreasing water domain size. It is shown that sub-diffusive behaviour occurs already at water domain sizes below 13
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.

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