90450
Triethylene glycol monomethyl ether
Triethylene glycol monomethyl ether
purum, ≥97.0% (GC)
Synonym(s):
Methyltriglycol
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About This Item
Linear Formula:
CH3(OCH2CH2)3OH
CAS Number:
Molecular Weight:
164.20
Beilstein:
1700198
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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vapor density
5.66 (vs air)
Quality Level
vapor pressure
<0.01 mmHg ( 20 °C)
description
non-ionic
grade
purum
Assay
≥97.0% (GC)
form
liquid
mol wt
164.20 g/mol
refractive index
n20/D 1.439 (lit.)
n20/D 1.439
bp
122 °C/10 mmHg (lit.)
density
1.026 g/mL at 25 °C (lit.)
SMILES string
COCCOCCOCCO
InChI
1S/C7H16O4/c1-9-4-5-11-7-6-10-3-2-8/h8H,2-7H2,1H3
InChI key
JLGLQAWTXXGVEM-UHFFFAOYSA-N
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Application
Triethylene glycol monomethyl ether (TEGME) was used in the following studies:
- To study the structural and thermosensitive properties of phosphazene derivatives having glycol and amino acids groups.[1]
- Synthesis of amphiphilic o-phenylene ethylene oligomers.[2]
- Preparation of pegylated zinc(II) phthalocyanines.[1]
- Modification of 2-OH positions in cyclodextrin thioethers, which are used for transport of hydrophobic drugs.[3]
- Functionalizing polymethacrylic acid (PMMA), hence increasing inhibition in crack generation in TEGMA-PMMA compared to unmodified PMMA electrodes.[4]
- Preparation of difunctionalized ionic liquids (ILs). [5]
- As terminal groups for cationic dendrons, which was further used to encapsulate an inorganic polyanionic cluster. [6]
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
230.0 °F - closed cup
Flash Point(C)
110 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Sandra D Hojniak et al.
The journal of physical chemistry. B, 118(26), 7440-7449 (2014-06-05)
Novel difunctionalized ionic liquids (ILs) containing a triethylene glycol monomethyl ether chain and a nitrile group on a pyrrolidinium or imidazolium cation have been synthesized and incorporated into supported ionic liquid membranes (SILMs). These ILs exhibit ca. 2.3 times higher
Synthesis and Characterization of amphiphilic -co-Phenylene ethynylene oligomers
<B>Slutsky MM, et al.</B>
New. J. Chem., 32, 670-675 (2008)
Lisa F Becker et al.
Beilstein journal of organic chemistry, 10, 2920-2927 (2015-01-01)
Methyl and ethyl thioether groups were introduced at all primary positions of α-, β-, and γ-cyclodextrin by nucleophilic displacement reactions starting from the corresponding per-(6-deoxy-6-bromo)cyclodextrins. Further modification of all 2-OH positions by etherification with iodo terminated triethylene glycol monomethyl ether
A Systematic Investigation of Polymer Binder Flexibility on the Electrode Performance of Lithium-Ion Batteries
Yuca N, et al.
ACS Applied Materials & Interfaces, 6(19), 17111-17118 (2014)
Hailong Chen et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(33), 11051-11061 (2013-07-03)
A series of cationic dendrons bearing triethylene glycol monomethyl ether terminal groups of different generations have been synthesized and used to encapsulate an inorganic polyanionic cluster [K(12.5)Na(1.5)(NaP5W30O110)] through electrostatic interactions. The resulting dendritic cation-encapsulated polyoxometalate (POM) complexes, cluster-dendrimers, are soluble
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