Examples of 'polar aprotic solvents' in a sentence
Meaning of "polar aprotic solvents"
polar aprotic solvents - In chemistry, polar aprotic solvents are a specific type of solvent that lacks acidic hydrogen atoms and have a high polarity, commonly used in reactions that involve ionic compounds or reactive intermediates
How to use "polar aprotic solvents" in a sentence
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polar aprotic solvents
Polar aprotic solvents lack an acidic hydrogen.
Suitable solvents are polar aprotic solvents such as tetrahydrofuran.
The adducts have an increased solubility in polar aprotic solvents.
A mixture of polar aprotic solvents may also be used.
Certain adjuvants can also be polar aprotic solvents.
Examples of polar aprotic solvents are tetrahydrofuran and dimethoxyethane.
Preferred solvents are polar aprotic solvents.
Polar aprotic solvents are solvents that lack an acidic hydrogen.
Adjuvants as polar aprotic solvents.
Polar aprotic solvents which can be utilized include ether solvents.
Preferred organic solvents include protic solvents or polar aprotic solvents.
The abovementioned polar aprotic solvents can be used in this reaction.
A typical category of these solvents is the class of polar aprotic solvents.
The use of polar aprotic solvents is preferred among these solvents.
This document does not mention the use of polar aprotic solvents.
See also
Alkyl amine polar aprotic solvents include diethylenetriamine and hexamethylenetetramine.
Among the preferred organic solvents are the polar aprotic solvents.
Polar aprotic solvents are also a good choice for this chemistry.
Polar solvents include polar protic solvents and polar aprotic solvents.
Different polar aprotic solvents may impart different properties on the compositions.
Polar protic solvents such as alcohols or polar aprotic solvents such as esters.
The polar aprotic solvents mentioned above can advantageously be used in this reaction.
Crop oils in combination with surfactants can also act as polar aprotic solvents.
Polar aprotic solvents such as dichloromethane or acetonitrile are preferred solvents for this transformation.
These dioxetanes also yield bright chemiluminescence in polar aprotic solvents such as acetonitrile.
Alcohols and polar aprotic solvents are preferred for use with inorganic bases.
DMSO and DMF are considered polar aprotic solvents.
Any conventional polar aprotic solvents can be utilized in preparing compounds of the invention.
Tetrahydrofurane or dioxane or polar aprotic solvents e . g.
Some polar aprotic solvents may produce stronger signals in one phase or another.
Typical solvents for this reaction include polar aprotic solvents such as dioxane or dimethylformamide.
Polar aprotic solvents include those defined according to the Hansen Solubility Parameters discussed below.
Suitable organic solvents can be selected from polar aprotic solvents and aliphatic or aromatic hydrocarbons.
Examples of polar aprotic solvents are chloroform, tetrahydrofuran, dimethylsulfoxide and dimethylformamide.
It is preferred to use non-polar or polar aprotic solvents or mixtures thereof.
Examples of polar aprotic solvents are tetrahydrofuran, dimethylsulfoxide and toluene.
Suitable organic solvents are, in general, polar or slightly polar aprotic solvents.
Preferred polar aprotic solvents include DMSO and DMF.
Exemplary solvents include non-polar solvents and polar aprotic solvents.
All concentrations of polar aprotic solvents are provided as v / v percentages.
Preferably, the hydrogenation may be conducted in anhydrous polar protic or polar aprotic solvents.
Polar protic and / or polar aprotic solvents are preferred in principle.
Generally, formation of the imidazolidinone may be conducted in polar protic or polar aprotic solvents.
Preferred solvents are polar aprotic solvents such as dichloromethane, tetrahydrofuran, or dimethylformamide.
The study is conducted in the presence of nonpolar, polar protic and polar aprotic solvents.
Examples of polar aprotic solvents are acetone, tetrahydrofuran and ethyl acetate.
Suitable polar solvents include alcohols, polar aprotic solvents or hydroxyalkylamine itself.
Suitable polar aprotic solvents include dimethylformamide or tetrahydrofuran, preferably dimethylformamide.
The reactions can be run in a wide range of solvent systems, including polar aprotic solvents.
In one aspect, the polar aprotic solvents are acetonitrile and chloroform.
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Examples of using Aprotic
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In an aprotic solvent and in the presence of a base
Preferred solvents are aprotic solvents such a pyridine
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Examples of using Solvents
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Do not use solvents or other aggressive or abrasive
Do not use harsh or abrasive cleaners or solvents
Do not use solvents or immerse the product
