Examples of 'dissolved in acetonitrile' in a sentence
Meaning of "dissolved in acetonitrile"
dissolved in acetonitrile - This phrase describes a process where a substance has been mixed or combined with acetonitrile to form a solution. It is commonly used in chemistry or scientific contexts to indicate the dissolution of a compound in a specific solvent
How to use "dissolved in acetonitrile" in a sentence
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dissolved in acetonitrile
The dry residue was dissolved in acetonitrile.
Substrate is dissolved in acetonitrile and diluted to equal volume with water for injection.
The oily residue was dissolved in acetonitrile.
CDAP is dissolved in acetonitrile and added immediately to the polysaccharide solution.
The residue was concentrated to a syrup and dissolved in acetonitrile.
The solids were dissolved in acetonitrile and a nitrogen sparge was applied.
The organic soluble compound may be dissolved in acetonitrile.
This oil was dissolved in acetonitrile and washed with heptane.
The solid is collected by filtration and dissolved in acetonitrile.
The foam was dissolved in acetonitrile and cooled in an ice bath.
The residual free base was immediately dissolved in acetonitrile and used.
Were dissolved in acetonitrile.
It reacts with water, but can be dissolved in acetonitrile.
The solid was dissolved in acetonitrile and precipitated with ethyl ether.
Next, disuccinimidyl suberate is dissolved in acetonitrile.
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This white powder was dissolved in acetonitrile and concentrated under reduced pressure.
Volatiles were evaporated and the residue was dissolved in acetonitrile ( 3 mL ).
The evaporation rest was dissolved in acetonitrile and injected on the chromatograph.
The solvent was evaporated to produce a colourless oil which was dissolved in acetonitrile ( 30 ml ).
The resulting solid was dissolved in acetonitrile and evaporated in vacuo.
Volatiles were removed by evaporation in vacuo, and the residue was dissolved in acetonitrile ( 5 mL ).
The solids were dissolved in acetonitrile.
After 10 minutes, the reaction solution was concentrated and dissolved in acetonitrile.
The residue was dissolved in acetonitrile and water was added to induce precipitation of solids.
The solution is evaporated to dryness, the residue is dissolved in acetonitrile and evaporated again.
The residue was dissolved in acetonitrile water and lithium hydroxide was added until basic.
The oil contained a white precipitate, so this was dissolved in acetonitrile and filtered again.
The residue was dissolved in acetonitrile and treated with a solution of anhydrous HCl in ethanol.
The residues E-i were dissolved in acetonitrile.
The residue was dissolved in acetonitrile and treated with a 1.5 fold molar excess of hydrochloric acid.
The solution was stirred for 1 hour, concentrated and dissolved in acetonitrile.
PEO and the sulfonimide were dissolved in acetonitrile in a glovebox under argon.
The reaction mixture was concentrated to give a colourless oil which was dissolved in acetonitrile ( 30 mL ).
The obtained oily product was dissolved in acetonitrile and quantitatively analyzed by HPLC.
After the solvent was evaporated in vacuo, the residue was dissolved in acetonitrile ( 2 mL ).
The product is dissolved in acetonitrile which contains 2 equivalents of pyrrolidine.
After the solvent was evaporated in vacuo, the resulting methylthioamidate was dissolved in acetonitrile ( 2 mL ).
The oil / crystals were dissolved in acetonitrile and gravity filtered.
Following filtration, the solvents were removed by evaporation and the residue dissolved in acetonitrile ( 3 mL ).
The oil obtained was dissolved in acetonitrile and left at room temperature for 2 h.
After 4h, the mixture was filtered through celite, evaporated and the residue dissolved in acetonitrile.
These phenacyl bromide derivatives were dissolved in acetonitrile in preparation for HPLC.
This was dissolved in acetonitrile and the solution was allowed to stand at -15°C for 3 hours.
The crude product ( consisting of a mixture of regioisomers ) is dissolved in acetonitrile ( 1 L ) at room temperature.
The oil obtained was dissolved in acetonitrile and left at room temperature for 4 hrs.
The nucleotides are preferably applied in 0.1 M concentration dissolved in acetonitrile.
The product, which was dissolved in acetonitrile was stable in the freezer for months.
The resultant dark red solution was concentrated in vacuo and dissolved in acetonitrile ( 1.8 ml ).
The solid obtained was dissolved in acetonitrile and left at room temperature for 2 hrs.
The dimethylformamide was removed in vacuo, and the resulting residue was dissolved in acetonitrile ( 250 mL ).
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Dissolved one of the coins in hydrochloric acid
No association may be dissolved by order of the executive
Examples of using Acetonitrile
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The solvent acetonitrile is a byproduct of this process
The solids were washed with additional acetonitrile
Acetonitrile is a byproduct from the manufacture of acrylonitrile
