Examples of 'trialkylamine' in a sentence
Meaning of "trialkylamine"
Trialkylamine: Refers to a type of organic compound that contains nitrogen, hydrogen, and carbon atoms. Trialkylamines are often used as solvents and chemical intermediates in various industrial processes
How to use "trialkylamine" in a sentence
Basic
Advanced
trialkylamine
Trialkylamine base includes tributylamine and tripropylamine.
In the presence of trialkylamine in an alcoholic solvent.
Examples of the suitable base are an alkali hydroxide or a trialkylamine.
Any known trialkylamine can be used in the above process.
Different concentrations of trialkylamine can be used.
Trialkylamine reagents are commercially available.
Alternatively the base may be a trialkylamine or a tetraalkylammonium hydroxide or alkoxide.
An organic base such as an trialkylamine.
The trialkylamine can contain same or different alkyl groups.
Alternatively the base may be selected from trialkylamine or tetraalkylammonium.
Examples of suitable trialkylamine reagents include trimethylamine and triethylamine.
A preferred base to effect acyl migration is a trialkylamine such as triethylamine.
Trialkylamine extraction has the highest efficiency when both acid moieties are carboxylated.
Preferred tertiary amines are trialkylamines and the most preferred trialkylamine is triethylamine.
Also disclosed is a process for the manufacture of materials of this type using trialkylamine catalysts.
See also
A preferred trialkylamine is triethylamine.
This example shows the efficient recovery of lactic acid from an aqueous solution using a trialkylamine.
Methyl gluconamides and trialkylamine oxides are also suitable nonionic surfactants.
In still another aspect, the amine is a trialkylamine.
Trialkylamine A group of organic chemical compounds derived from ammonia.
The acetyl halide may be converted in situ with a trialkylamine to the corresponding homochiral ketene.
The amines include monoalkylamine, dialkylamine and trialkylamine.
A suitable base is a trialkylamine or a picoline, or combinations thereof.
The amines include a monoalkylamine, a dialkylamine and a trialkylamine.
A suitable base is a trialkylamine or imidazole, or combinations thereof.
Process according to claim 3, characterized in that the trialkylamine is triisooctylamine.
In some embodiments, the trialkylamine base comprises diisopropylethylamine.
In various embodiments of the invention, different concentrations of trialkylamine are used.
Suitable bases include a trialkylamine base, preferably triethylamine.
A trialkylamine such as triethylamine etc, conveniently at about room temperature.
In another embodiment, the trialkylamine is triethylamine.
The trialkylamine functions as base and acid-binding agent.
In some embodiments, an excess of the trialkylamine base is used.
A trialkylamine salt where the alkyl groups are selected from methyl or ethyl ; and.
Preferably, a dialkylamine or trialkylamine is reacted with the unsaturated epoxide.
A process in accordance with claim 3 wherein the base is a trialkylamine.
The process as claimed in claim 7 wherein the trialkylamine is triethylamine or tributylamine.
Another process consists in carrying out an adsorption / desorption with a trialkylamine.
Tertiary amines are generally used ; of these, a trialkylamine such as triethylamine is especially desirable.
Process according to claim 2, characterized in that the organic amino compound is a trialkylamine.
Among these tertiary amines, a trialkylamine is preferred, and triethylamine is more preferred.
A weak basic catalyst may be utilized, such as a trialkylamine catalyst.
Specific examples of the trialkylamine include trimethylamine, triethylamine, tripropylamine and the like.
A tertiary amine such as pyridine, picoline, lutidine and trialkylamine may be added.
However, compositions prepared with trialkylamine catalysts, especially trimethylamine, are preferred for several reasons.
The amine is typically a cyclic amine or a tertiary amine, for example a trialkylamine.
A process according to claim 9, characterized in that a trialkylamine is reacted with the unsaturated epoxide.
However, in a preferred embodiment of the invention, the raw material is not a dialkylamine but a trialkylamine.
In some embodiments, the trialkylamine base is triethylamine, diisopropylethylamine, or a combination thereof.
As the suitable base, for example, an alkali hydroxide or a trialkylamine can be used.
