10471-14-4

Usage

Uses

Used in Chemical Industry:
1-ethoxy-1-methoxyethane is used as a solvent for cellulose acetate, which is a common ingredient in various products such as photographic film and plastic materials, due to its ability to dissolve a wide range of substances.
Used in Coatings and Adhesives:
1-ethoxy-1-methoxyethane is used as a solvent for nitrocellulose, which is a key component in the production of lacquers and coatings, providing a fast-drying and durable finish.
Used in Paints and Varnishes:
1-ethoxy-1-methoxyethane is used as a solvent for various natural and synthetic resins, which are essential in the formulation of paints and varnishes, enhancing their performance and application properties.
Used in Pharmaceutical Industry:
1-ethoxy-1-methoxyethane is used as a solvent in the production of pharmaceuticals, aiding in the manufacturing process by facilitating the dissolution of active ingredients and excipients.
Used in Natural Product Extraction:
1-ethoxy-1-methoxyethane is used in the extraction of natural products, such as essential oils and botanical compounds, due to its ability to dissolve a variety of organic substances.
Used in Fuel Industry:
1-ethoxy-1-methoxyethane is used as a component in specialty fuel formulations, contributing to the performance and efficiency of certain types of fuels.
Used in Pesticide Formulations:
1-ethoxy-1-methoxyethane is used as an inert ingredient in pesticide formulations, serving as a carrier or solvent for the active ingredients, ensuring their proper application and distribution.
Safety Considerations:
It is crucial to handle 1-ethoxy-1-methoxyethane with care due to its high flammability. It should be stored and used in well-ventilated areas, away from sources of ignition, to prevent potential hazards.

InChI:InChI=1/C5H12O2/c1-4-7-5(2)6-3/h5H,4H2,1-3H3

Upstream product

• 67-56-1 methanol 
• 64-17-5 ethanol 
• 7081-78-9 1-chloroethyl ethyl ether 
• 124-41-4 sodium methylate 
• 109-92-2 ethyl vinyl ether 
• 105-57-7 diethyl acetal 
• 201230-82-2 carbon monoxide 
• 109-87-5 Dimethoxymethane 
• 534-15-6 1,1-dimethoxyethane 

Downstream Products

• 105-57-7 diethyl acetal 
• 534-15-6 1,1-dimethoxyethane 
• 7081-78-9 1-chloroethyl ethyl ether 
• 67-56-1 methanol 
• 20680-10-8 1-(1-ethoxyethoxy)-propane 
• 64-17-5 ethanol 

Relevant academic research and scientific papers

HCo(CO)4 AS AN ACID CATALYST IN VINYL ETHER REACTIONS

At room conditions in the presence of alcohols, HCo(CO)4 instead of being consumed by vinyl ethers, functions as an acid catalyst for acetal formation.

THE HOMOLOGATION OF METHANOL. THE MODIFICATION OF COBALT CATALYST BY DIPHOSPHINES

Cobalt iodide modified by α,ω-bis(diphenylphosphino)alkane (PCnP; n=1-6) efficiently catalyzes the homologation of methanol to ethanol.The ethanol selectivity as high as 89percent was achieved by using PC6P as the ligand.

Process and catalysts for the oxidation of methanol and/or ethanol

A process for oxidation of methanol, ethanol, or a mixture of methanol and ethanol comprising contacting the methanol and/or ethanol with an oxygen-containing gas and a supported catalyst comprising one or more platinum group oxides. The process conditions and/or catalyst may be selected to as to selectively produce methyl formate from methanol or diethoxyethane from ethanol. The invention also includes certain novel supported platinum group metal oxide catalysts. Preferred catalysts include one or more ruthenium oxides.

Kinetische Untersuchungen zur Methanolyse von Acetalen

It has been shown that the acid-catalyzed methanolysis of the diethylacetales RCH(OEt)2 of acetaldehyde (R=CH3), propionaldehyde (R = C2H5), butyraldehyde (R = C3H7) and caprylaldehyde (R = C7H15) at temperatures between 283 and 318 K proceeds as a consecutive reaction involving a reversible second step.The pseudo first order rate constants of the three reaction steps, their activation parameters and equilibrium constants were estimated by measuring the concentration-time-curves of starting product, intermediate and final product and using a large excess of methanol.There is a linear dependence be tween rate constants of methanolysis and concentration of the catalyst.

SYNTHESIS OF UNSYMMETRICAL 1,1-DIALKOXYALKANES AND THEIR SULFUR-CONTAINING ANALOGS

Acyclic acetals and 1,1-di(alkylthio)alkanes enter into exchange reactions in the presence of aprotic acids and of the KU-2 cation-exchange resin with the formation of the unsymmetric acetals and 1-alkoxy-1-alkylthioalkanes.In reaction with ethylal di(ethylthio)methane forms 3,5,7-trioxanonane in addition to ethylthioethoxymethane. 2-Methyl-4-thia-2-hexene was found in the products from the reaction of 1,1-di(ethylthio)-2-methylpropane with methylal.