Examples of 'diethylamine' in a sentence
Meaning of "diethylamine"
diethylamine (noun): A chemical compound commonly used in the production of pharmaceuticals, pesticides, and other products
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- The secondary amine (CH₃CH₂)₂NH
How to use "diethylamine" in a sentence
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diethylamine
The insoluble diethylamine hydrobromide was separated by filtration.
Suitable bases include alkylamines such as diethylamine.
Diethylamine may be added to quench excess reagent.
Preferred bases include diethylamine and triethylamine.
The title compound was prepared using diethylamine.
Diethylamine may be used as the base.
You are just going to end up with a little bit of diethylamine.
Diethylamine and its salts.
Of these dimethylamine and diethylamine are preferred.
In the invention the pharmaceutically acceptable salt is diethylamine.
Hexane and diethylamine levels were monitored over several days.
A suitable chemical absorbent is methyl diethylamine.
Especially the use of diethylamine turned out to be very useful.
The preferred amine solvent is diethylamine.
The diethylamine is removed in vacuo.
See also
An acceptable organic base includes diethylamine and triethylamine.
Diethylamine is then added in a rapid continuous stream into the vessel.
The filtrate was neutralized with diethylamine.
It is commonly synthesized by reacting diethylamine with an activated form of lysergic acid.
A preferred alkylamine initiator is diethylamine.
Immediately upon addition of the diethylamine a dark red precipitate formed.
The title compound was prepared using dimethylamine instead of diethylamine.
Diethylamine is also preferred.
Examples of secondary amine compounds include diethylamine and diisopropylamine.
Diethylamine is especially preferred.
The title compound was prepared using pyrrolidine instead of diethylamine.
Drops of diethylamine.
Dicyclohexylamine dicyclohexylammonium diethylamine.
Diethylamine was used to assess the reactivity of surface epoxide groups towards amines.
Diethylethanolamine is prepared commercially by the reaction of diethylamine and ethylene oxide.
The solvent and the residual diethylamine were removed by rotary evaporation in vacua.
You could imagine that now you have this diethylamine.
At this point add excess diethylamine and stir overnight at room temperature.
The organic base employed may be primary amines such as diethylamine.
Then remove the solvent and residual diethylamine by rotary vacuum evaporation.
Appropriate organic bases of tertiary and secondary amines are triethylamine and diethylamine.
This would be diethylamine.
The precipitated diethylamine hydrochloride was removed by filtration and the solvent removed exvacuo.
An acceptable organic base includes among others diethylamine and triethylamine.
The precipitate of diethylamine hydrochloride is filtered off and washed with a small amount of tetrahydrofuran.
Dimethylamine and diethylamine.
The DCM and diethylamine was removed by rotary evaporation.
The reaction can be carried out with either diethylamine or triethylamine.
The DCM and diethylamine were removed by rotary evaporation.
The water was changed several times to remove all diethylamine from me pores.
Diethylamine is also sometimes used in the illicit production of LSD.
It would be diethylamine.
The lower quantisising limit is due to the chromatography of dibutylamine being better than diethylamine.
The DCM and diethylamine is then removed by rotary evaporation.
The fluorinating agent used in the present invention is a reaction product of hexafluoropropene and diethylamine.
