Examples of 'ml of methylene' in a sentence
Meaning of "ml of methylene"
In chemistry and laboratory settings, 'ml' stands for milliliters, which is a unit of measurement for volume. 'Methylene' refers to a compound called methylene chloride, commonly used as a solvent or paint stripper. So 'ml of methylene' signifies a specific quantity of methylene chloride being measured
How to use "ml of methylene" in a sentence
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ml of methylene
This is extracted with a few ml of methylene chloride.
Ml of methylene blue solution was added to each test tube.
The acid chloride was dissolved in 1 mL of methylene chloride.
Ml of methylene chloride is stirred in.
The solution was extracted with 2 mL of methylene chloride.
Ml of methylene chloride.
The crude product was dissolved in 2 mL of methylene chloride.
Ml of methylene chloride, and mg of undecane as an internal standard.
The product obtained was taken up in 6 ml of methylene chloride.
Another 20 ml of methylene chloride and excess saturated aqueous sodium bicarbonate were added.
The obtained residue was dissolved into 5 ml of methylene chloride.
The residue is redissolved in 20 ml of methylene chloride and filtrate through a glass sinter funnel.
The entirety of this crude product was dissolved in 5 mL of methylene chloride.
The residue is dissolved in 60 ml of methylene chloride and used further reactions.
The filtrate was concentrated in vacuo and redissolved in 50 mL of methylene chloride.
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Add 50 ml of methylene chloride to extraction beaker.
The resin was washed once more with 1 mL of methylene chloride.
A further 30 mL of methylene chloride is added and the layers are separated.
The solvent was evaporated and the residue was taken up in 50 ml of methylene chloride.
To the flask was added 3.5 mL of methylene chloride for dissolution.
The solvent is evaporated off and the residue is dissolved in 10 ml of methylene chloride.
The dried product was dissolved in 2 mL of methylene chloride / 2 ml trifluoroacetic acid.
The mixture was transferred to a separatory funnel with the addition of 50 ml of methylene chloride.
This was dissolved in 40 mL of methylene chloride and 3 mL of trifluoroacetic acid was added.
The combined aqueous layers were extracted with 50 mL of methylene chloride chloride.
Approximately 30 mL of methylene chloride was added to the mixture in the funnel.
The residue of the toluene extract was then extracted with 40 ml of methylene chloride.
Then 15 ml of methylene chloride were added and the aqueous phase was decanted.
The water layer was further extracted two times with 5 ml of methylene chloride.
After 3 hours, 1 mL of methylene chloride was added to help dissolve the solid.
The suspension is extracted three times with 50 ml of methylene chloride each time.
After adding 1.5 mL of methylene chloride, the reaction was stirred at room temperature overnight.
The filtrate is decanted and the aqueous phase is washed with 50 ml of methylene chloride.
This crude material was dissolved in 4 ml of methylene chloride and 2.4 ml of trifluoroacetic acid.
The reaction mixture is then filtered and the residue washed with 50 ml of methylene chloride.
Ten ml of boron tribromide in 10 ml of methylene chloride is added dropwise over 25 minutes.
Of the product of preparation 6 is dissolved in 25 ml of methylene chloride.
The resin was swelled with 8 mL of methylene chloride for 15 minutes then drained.
Of pyridinium chlorochromate is dissolved in 250 ml of methylene chloride.
After cooling, 25 ml of methylene chloride are added and the suspension is filtered and washed.
The distillation residue is taken up in 10 ml of methylene chloride.
The residue was treated with 100 ml of methylene chloride whereupon residual phthalimide precipitated.
The precipitate was dissolved by heating in 50 ml of methylene chloride.
The solid was suspended in 500 ml of methylene chloride and agitated for 1 hour under nitrogen.
Mg of the protected product was dissolved in 15 ml of methylene chloride.
The residue is taken up in 100 ml of methylene chloride and extracted with 1N hydrochloric acid.
Millimols of dicobalt octacarbonyl were dissolved in 250 ml of methylene chloride.
The residue was dissolved in 200 mL of methylene chloride and 1 L of ethyl ether then filtered.
G of the product silica were suspended in 150 ml of methylene chloride.
Separately, 10 ml of methylene chloride was added to the filtrate.
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