Poly(ethylene glycol) 4-nonylphenyl 3-sulfopropyl ether potassium salt

Product Information

Molecular Formula:
C6H14O4C6H14O4C6H14O4C6H14O4
Molecular Weight:
150.17
Description
Anionic surfactant.
Synonyms
Triglycol; 2,2'-(Ethane-1,2-diylbis(oxy))diethanol; 2-[2-(2-Hydroxyethoxy)ethoxy]ethanol; Triethyleneglycol; Trigen; Triethylenglykol; 2,2'-Ethylenedioxydiethanol; 1,2-Bis(2-hydroxyethoxy)ethane; 2,2'-(Ethylenedioxy)diethanol; 2,2'-Ethylenedioxybis(ethanol); 3,6-Dioxaoctane-1,8-diol; Di-beta-hydroxyethoxyethane; 2,2'-Ethylenedioxyethanol; Ethanol, 2,2'-[1,2-ethanediylbis(oxy)]bis-; Triethylene glcol; Glycol bis(hydroxyethyl) ether; 2,2'-[ethane-1,2-diylbis(oxy)]diethanol; Ethylene glycol dihydroxydiethyl ether; Trigol
IUPAC Name
2-[2-(2-hydroxyethoxy)ethoxy]ethanol
Canonical SMILES
C(COCCOCCO)O
InChI
InChI=1S/C6H14O4/c7-1-3-9-5-6-10-4-2-8/h7-8H,1-6H2
InChI Key
ZIBGPFATKBEMQZ-UHFFFAOYSA-N
Boiling Point
81 °C(lit.)
Melting Point
24.3 °F
Flash Point
>235.4 °F
Density
1 g/mL at 25 °C (lit.)
Solubility
greater than or equal to 100 mg/mL at 68 °F
Appearance
powder
Application
Used as a fragrance (cosmetics), solvent (resins, pesticides, textile dyeing), humectant (printing inks and tobacco), plasticizer, and disinfectant.
Refractive Index
1.473
LogP
log Kow = -1.98
Vapor Pressure
less than 0.001 mmHg at 68 °F
Henry's Law Constant
2.61X10-10 atm-cu m/mol at 25 °C (est)
Decomposition
When heated to decomposition it emits acrid smoke and irritating fumes.
Odor
Practically odorless

Computed Properties

XLogP3
-1.6
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
7
Exact Mass
150.08920892 g/mol
Monoisotopic Mass
150.08920892 g/mol
Topological Polar Surface Area
58.9Ų
Heavy Atom Count
10
Formal Charge
0
Complexity
49.7
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
US-11034664-B1 Synthesis of cyclic carbonate monomers 2020-05-11
US-2020377656-A1 Polyurethane polyol and preparation method and application thereof 2020-04-23
US-11007134-B1 Ceramide containing capsules, ceramide compositions, and cosmetic compositions thereof 2020-03-31
US-11028217-B1 Thermoplastic polyurethane compositions comprising nitro-substituted polyester diols 2020-03-13
US-10767119-B1 Amphiphilic asphaltene ionic liquids as demulsifiers for heavy petroleum crude oil-water emulsions 2020-01-23
US-10907107-B1 Amphiphilic asphaltene ionic liquids as demulsifiers for heavy petroleum crude oil-water emulsions 2020-01-23
US-10799444-B1 Wax for hair removal with thermally activated pigment 2020-01-07
US-10995258-B1 Removing filter cake with delayed enzymatic breakers 2020-01-02
US-10807063-B1 Device and method for continuously manufacturing acrylate compound 2019-12-31
EP-3842469-A1 Material for forming organic film, method for forming organic film, patterning process, and compound 2019-12-26

Literatures

PMID Publication Date Title Journal
23021892 2012-12-01 Investigation of crystal structure influence on spectroscopic and photoluminescent properties of terbium-picrate triethylene glycol complex Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
22465497 2012-11-01 Dendrimers reduce toxicity of Aβ 1-28 peptide during aggregation and accelerate fibril formation Nanomedicine : nanotechnology, biology, and medicine
21894502 2012-08-01 The impact of three strains of oral bacteria on the surface and mechanical properties of a dental resin material Clinical oral investigations
22488581 2012-05-14 Rational design and synthesis of optimized glycoclusters for multivalent lectin-carbohydrate interactions: influence of the linker arm Chemistry (Weinheim an der Bergstrasse, Germany)
21552619 2011-08-07 Supramolecular construction of vesicles based on core-substituted naphthalene diimide appended with triethyleneglycol motifs Chemical communications (Cambridge, England)
21536113 2011-07-15 Comprehensive comparison of two new biodegradable gene carriers International journal of pharmaceutics
21457991 2011-06-15 Confinement effects on water structure in membrane lyotropic phases Journal of colloid and interface science
21524091 2011-06-13 Bifunctional dendronized cellulose surfaces as biosensors Biomacromolecules
21538866 2011-05-23 Tuning stamp surface energy for soft lithography of polar molecules to fabricate bioactive small-molecule microarrays Small (Weinheim an der Bergstrasse, Germany)
21480622 2011-05-05 Aggregation behavior modulation of 1-dodecyl-3-methylimidazolium bromide by organic solvents in aqueous solution The journal of physical chemistry. B
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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