Examples of 'carbonate esters' in a sentence
Meaning of "carbonate esters"
Carbonate esters: Carbonate esters are organic compounds that contain a carbonate functional group. They are commonly used in various industrial applications, such as solvents, plasticizers, and chemical intermediates
How to use "carbonate esters" in a sentence
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carbonate esters
Cyclic ethers made by pyrolysis of carbonate esters.
Other carbonate esters may subsequently be prepared by transesterification.
Process for preparing carbonate esters.
Carbonate esters can be converted to other carbonates by transesterification.
These compounds are thus quaternary ammonium carbonate esters.
Carbonate esters can be divided into three categories by their structures.
This process enables efficient preparation of carbonate esters.
These carbonate esters may be used singly or in combinations of two or more.
Propylene carbonate product may be converted to other carbonate esters by transesterification as well.
Cyclic carbonate esters of diols decompose to oxetanes and carbon dioxide.
These hydrofluorocarbons are prepared from corresponding alcohols or carbonate esters of said alcohols.
Such carbonate esters generate carbon dioxide on contact with the acid.
Preferred solvents for the process of this invention include dinitriles and cyclic carbonate esters.
Diaryl carbonate esters are known as materials for polycarbonates produced by melt process.
Useful solvents for the process of this invention include certain dinitriles and cyclic carbonate esters.
See also
Specific examples of carbonate esters which can be used include those listed previously.
In short, with this conventional process, it is impossible to efficiently prepare carbonate esters.
The carbonate esters react with hydrogen peroxide and peroxide sources to increase bleaching activity.
Illustrative examples of such precursors include carbonyl halides, diaryl carbonate esters and haloformates.
Small carbonate esters like dimethyl carbonate, ethylene carbonate, propylene carbonate are used as solvents.
A process for preparation of sulphophenyl quaternary ammonium and phosphonium carbonate esters of the formula, wherein,.
Examples of cyclic carbonate esters include ethylene carbonate, propylene carbonate, and butylene carbonate.
Illustrative esters include dibasic acid esters, polyol esters, complex esters and polyol carbonate esters.
The position 42 carbonate esters are the major reaction product.
Preferred co-solvents are selected from glycols, sugar alcohols, carbonate esters and chlorinated hydrocarbons.
Carbonate esters of PEG can be used to form the PEG-EphB4 conjugates.
Useful solvents include, for example, water, aqueous alcohols, glycols, and phosphonate or carbonate esters.
Category, Carbonate esters.
Raw carbonate esters represented by formula ( 4 ) are hereinafter referred to as carbonate esters ( 4 ).
Useful solvents include, for example, water, aqueous alcohols, glycols, and phosphate or carbonate esters.
These carbonate esters ( 4 ) may be suitably mixed for use.
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