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Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.
Ethyl acetoacetate is subject to keto-enol tautomerism.In the neat liquid at 33 °C, the enol consists of 15% of the total. [5]The enol is moderately acidic. Thus ethyl acetoacetate behaves similarly to acetylacetone: [6]
Isopropyl acetate is a solvent with a wide variety of manufacturing uses that is miscible with most other organic solvents, and slightly soluble in water (although less so than ethyl acetate). It is used as a solvent for cellulose, plastics, oil and fats. It is a component of some printing inks [4] and perfumes.
The acetate anion, [CH 3 COO] −,(or [C 2 H 3 O 2] −) is one of the carboxylate family. It is the conjugate base of acetic acid. Above a pH of 5.5, acetic acid converts to acetate: [1] CH 3 COOH ⇌ CH 3 COO − + H + Many acetate salts are ionic, indicated by their tendency to dissolve well in water.
Propyl acetate, also known as propyl ethanoate, is an organic compound. Nearly 20,000 tons are produced annually for use as a solvent . This colorless liquid is known by its characteristic odor of pears.
This page provides supplementary chemical data on ethyl acetate. Material Safety Data Sheet. The handling of this chemical may incur notable safety precautions. It is ...
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Aluminium acetate or aluminium ethanoate [1] (also "aluminum ~"), sometimes abbreviated AlAc in geochemistry, [2] can refer to a number of different salts of aluminium with acetic acid. In the solid state, three salts exist under this name: basic aluminium monoacetate , (HO) 2 AlCH 3 CO 2 , basic aluminium diacetate , HOAl(CH 3 CO 2 ) 2 , [ 3 ...
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