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Reputable factory supply Triethylene glycol monoethyl ether 112-50-5 in bulk at low price
- Molecular Formula: C8H18O4
- Molecular Weight: 178.229
- Appearance/Colour: Odorless colorless liquid
- Vapor Pressure: 0.00238mmHg at 25°C
- Melting Point: -19°C(lit.)
- Refractive Index: n20/D 1.438(lit.)
- Boiling Point: 255.999 °C at 760 mmHg
- PKA: 14.36±0.10(Predicted)
- Flash Point: 106.443 °C
- PSA： 47.92000
- Density: 1.006 g/cm3
- LogP: 0.04840
Triethylene glycol monoethyl ether(Cas 112-50-5) Usage
|
Air & Water Reactions |
Water soluble. |
|
Reactivity Profile |
Triethylene glycol monoethyl ether is a ethoxy-alcohol derivative. The ether being relatively unreactive. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert alcohols to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides. |
|
Safety Profile |
Mildly toxic by ingestion and slm contact. An eye irritant. Combustible when exposed to heat or flame; can react with oxidizing materials. Tofight fire, use foam, alcohol foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also GLYCOL ETHERS. |
|
General Description |
Odorless colorless liquid. Sinks and mixes with water. |
InChI:InChI=1/C8H18O4/c1-2-10-5-6-12-8-7-11-4-3-9/h9H,2-8H2,1H3
112-50-5 Relevant articles
Reduction of organic halides with tri-2-furylgermane: Stoichiometric and catalytic reduction
Nakamura,Yorimitsu,Shinokubo,Oshima
, p. 747 - 752 (2007/10/03)
Tri-2-furylgermane proved to be an effec...
Formation of macrocyclic ethers by free radical cyclization: Effects of chain length, substituents, and solvents
Philippen, Annie,Degueil-Castaing, Marie,Beckwith, Athelstan L. J.,Maillard, Bernard
, p. 6814 - 6819 (2007/10/03)
Free radical reduction by tributylstanna...
Process for preventing consolidation of p-dichlorobenzene
-
, (2008/06/13)
A triethylene glycol derivative is added...
112-50-5 Process route
-
-
75-21-8,99932-75-9
oxirane
-
-
111-90-0
ethoxyethoxyethanol
-
-
112-50-5
monoethyl ether of triethylene glycol
-
-
5650-20-4
3,6,9,12-tetraoxatetradecan-1-ol
Conditions
| Conditions | Yield |
|---|---|
|
With
ethanolamine;
at 50 - 60 ℃;
|
-
-
75-21-8,99932-75-9
oxirane
-
-
111-90-0
ethoxyethoxyethanol
-
-
141-43-5
ethanolamine
-
-
112-50-5
monoethyl ether of triethylene glycol
-
-
5650-20-4
3,6,9,12-tetraoxatetradecan-1-ol
Conditions
| Conditions | Yield |
|---|---|
|
at 50 - 63 ℃;
|
112-50-5 Upstream products
-
75-21-8
oxirane
-
64-17-5
ethanol
-
111-90-0
ethoxyethoxyethanol
-
141-43-5
ethanolamine
112-50-5 Downstream products
-
136814-66-9
1-ethoxy-8-(2-nitro-phenoxy)-3,6-dioxa-octane
-
62921-75-9
2-(2-(2-ethoxyethoxy)ethoxy)ethyl 4-methylbenzenesulfonate
-
23601-39-0
1,14-diethoxy-3,6,9,12-tetraoxa-tetradecane
-
45180-95-8
3,6,9-trioxaundecyl acrylate
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