Examples of 'polar aprotic' in a sentence

Meaning of "polar aprotic"

polar aprotic - a term used in chemistry to describe a solvent that lacks acidic hydrogen atoms and has a specific polarity

How to use "polar aprotic" in a sentence

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polar aprotic
Any polar aprotic solvent can be used.
Suitable organic solvents are polar aprotic compounds.
The polar aprotic solvent is preferably biocompatible.
Said components being dissolved in a polar aprotic solvent.
Polar aprotic solvents lack an acidic hydrogen.
Suitable solvents are polar aprotic solvents such as tetrahydrofuran.
The reaction is generally conducted in a polar aprotic solvent.
An example of a polar aprotic solvent is dimethyl sulfoxide.
Dimethylformamide can suitable be used as polar aprotic solvent.
A mixture of polar aprotic solvents may also be used.
Certain adjuvants can also be polar aprotic solvents.
A suitable polar aprotic solvent is acetone.
The reaction is preferably conducted in a polar aprotic solvent.
Examples of polar aprotic solvents are tetrahydrofuran and dimethoxyethane.
Preferred solvents are polar aprotic solvents.

See also

Dissolving in a polar aprotic solvent a polyethersulfone of the general formula.
The adducts have an increased solubility in polar aprotic solvents.
The polar aprotic solvent.
The solvent employed can preferably be a polar aprotic solvent.
A known alkyl sulfoxide polar aprotic solvent is dimethyl sulfoxide.
The reaction is preferably carried out in a polar aprotic solvent.
Adjuvants as polar aprotic solvents.
Polar aprotic solvents are solvents that lack an acidic hydrogen.
The reaction can be carried out in a polar aprotic solvent.
Examples of suitable polar aprotic diluents are dimethylformamide and dichloromethane.
As solvent can a polar aprotic.
The use of polar aprotic solvent provides another benefit.
It can additionally comprise one or more liquid polar aprotic compounds.
Currently preferred polar aprotic organic solvents include acetonitrile.
The reactions described herein are preferably run in a polar aprotic solvent.
The abovementioned polar aprotic solvents can be used in this reaction.
The flowable composition also includes a biocompatible polar aprotic solvent.
The use of polar aprotic solvents is preferred among these solvents.
Suitable solvents for the reaction are polar aprotic organic solvents.
The preferred polar aprotic compounds are soluble in the elutriation liquid.
Preferred organic solvents include protic solvents or polar aprotic solvents.
If too much polar aprotic solvent is added gelation can occur.
A typical category of these solvents is the class of polar aprotic solvents.
Polar aprotic solvents which can be utilized include ether solvents.
This document does not mention the use of polar aprotic solvents.
Alkyl amine polar aprotic solvents include diethylenetriamine and hexamethylenetetramine.
The solvent may be a nonpolar organic solvent or a polar aprotic solvent.
Polar aprotic solvents are also a good choice for this chemistry.
Among the preferred organic solvents are the polar aprotic solvents.
A polar aprotic solvent may be added for inducing the crystallization.
The reaction is preferably carried out in a polar aprotic solvent such as dichloromethane.
The polar aprotic solvent according to the invention is an aprotic alkyl amine.
The solvent is a mixture of a polar aprotic solvent and a polar protic solvent.
Polar solvents include polar protic solvents and polar aprotic solvents.
The reaction is typically run in a polar aprotic solvent such as tetrahydrofuran or dimethylformamide.

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Examples of using Aprotic
In an aprotic solvent and in the presence of a base
Preferred solvents are aprotic solvents such a pyridine
An aprotic polar solvent is preferable as the solvent
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