112-50-5 Usage
Description
Triethylene glycol monoethyl ether is an odorless, colorless liquid that is soluble in water and has combustible properties. It is a chemical intermediate with a variety of applications across different industries.
Uses
Used in Chemical Industry:
Triethylene glycol monoethyl ether is used as a chemical intermediate for the synthesis of various compounds and materials due to its versatile chemical properties.
Used in Solvent Applications:
It is used as a solvent in the manufacturing process of different products, such as resins, dyes, and pharmaceuticals, because of its ability to dissolve a wide range of substances.
Used in Paint and Coating Industry:
Triethylene glycol monoethyl ether is used as a component in the formulation of paints and coatings, enhancing their properties and performance.
Used in Automotive Industry:
In the automotive industry, it is utilized as a component in the production of certain types of lubricants and coolants, taking advantage of its chemical stability and solubility.
Used in Textile Industry:
Triethylene glycol monoethyl ether is employed in the textile industry as a component in the production of various types of fibers and fabrics, contributing to their quality and performance.
Used in Personal Care Industry:
It is also used in the personal care industry, particularly in the formulation of cosmetics and toiletries, due to its ability to act as a solvent and improve the texture of the products.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 112-50-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112-50:
(5*1)+(4*1)+(3*2)+(2*5)+(1*0)=25
25 % 10 = 5
So 112-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O4/c1-2-10-5-6-12-8-7-11-4-3-9/h9H,2-8H2,1H3
112-50-5Relevant articles and documents
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 effective reagent for the radical reduction of organic halides. Treatment of 1-bromododecane with tri-2-furylgermane in THF at 25 °C in the presence of a catalytic amount of triethylborane afforded dodecane almost quantitatively. Radical cyclization of 2-iodoethanal allyl acetal afforded five-membered products under the same reaction conditions. These reactions proceeded with NaBH4 in the presence of a catalytic amount of germanium hydride. The reaction took place in water as well as in THF to give the corresponding reduced compounds in good yields.
Process for preventing consolidation of p-dichlorobenzene
-
, (2008/06/13)
A triethylene glycol derivative is added to p-dichlorobenzene so as to prevent consolidation and improve flowability of p-dichlorobenzene.