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Ethyl acetate has many advantages and is very widely used.
Today, scientists use the less toxic, but fragrant, ethyl acetate.
However, ethyl acetate is a handy and less toxic substitute.
Excessive amounts of ethyl acetate are considered a wine fault.
Ethyl acetate is generally the solvent in nail polish itself.
Studies show that this insect is attracted by ethyl acetate, 2-mehoxy.4.
The most common killing agents are ether, chloroform and ethyl acetate.
The key active ingredient in non-acetone removers is usually ethyl acetate.
The sensory threshold for ethyl acetate is 150-200 mg/L.
Ethyl acetate is present in confectionery, perfumes, and fruits.
It is prepared via the Claisen condensation of ethyl acetate.
Plates were developed in ethyl acetate: acetic acid, 90:1, together with unlabeled standards.
It has a similar polarity to ethyl acetate, but greater stability towards aqueous acid and base.
The compound is soluble in ethyl acetate and chloroform but not in petrol.
It reacts with acetone, ethyl acetate, tetrahydrofuran, ethanol, and water.
SDK is the leader of the Asian ethyl acetate market.
Organic solvents such as acetone and ethyl acetate are very effective at removing Sharpie ink.
For example, the reaction of acetic anhydride with ethanol yields ethyl acetate:
Ethyl acetate distills off as pressure is slowly reduced to leave small spheres of nitrocellulose and additives.
Then the beans are removed and either dichloromethane or ethyl acetate is used to extract the caffeine from the water.
The sharp taste resulting from small amounts of ethyl acetate in wine is known to drinkers as "volatile acidity."
I would suggest ethanol, ethyl acetate and acetone due to their low toxicity and ease of getting them.
Made from ethanol and acetic acid, ethyl acetate is colorless and also flammable.
Among the esters most generally employed are ethyl acetate and ethyl butyrate.
Carbonyl-containing solvents, such as acetone and ethyl acetate, are also incompatible with the reagent.