Synonyms: Ethyl acetic ester, Ethyl ester, Ethyl ethanoate, Acetoxyethane. Other Languages: De: Ethylacetat. Es: Acetato de etilo. Ethyl acetate for liquid chromatography LiChrosolv®. CAS , EC Number , chemical formula CH₃COOC₂H₅. – Find MSDS or SDS, a COA. Details of the supplier of the safety data sheet Wordt ervan verdacht de vruchtbaarheid te schaden. STOT RE acetato de etilo.

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Ethyl acetate is synthesized in industry mainly via the classic Fischer esterification reaction of ethanol and acetic acid. Separations of the byproducts are complicated by the fact that ethanol forms an azeotrope with water, as does ethyl acetate with ethanol and water, and methyl ethyl ketone MEK, which forms from 2-butanol with both ethanol and ethyl acetate.

S16S26S International Labour Office,p. In rare cases exposure may cause sensitization of the mucous membrane and eruptions of the skin. Acidity p K a. Ethyl acetate is the most common ester in winebeing the product of the most common volatile organic acid — acetic acidand the ethyl alcohol generated during the fermentation.

Coffee beans and tea leaves are decaffeinated with this solvent. Ethyl acetate can be hydrolyzed in acidic or basic conditions to regain acetic acid and ethanol. This reaction gives ethanol and sodium acetatewhich is unreactive toward ethanol:.

The Oxford Companion to Wine 3rd ed. The reaction can be accelerated by acid catalysis and the etiloo can be shifted to the right by removal of water. In a killing jar charged with ethyl acetate, the vapors will kill the collected insect quickly without destroying it. R11R36R66R Acetate esters Ethyl esters Flavors Ester solvents Commodity chemicals.


Traces of rare-earth and alkali metals are beneficial to the process. Refractive index n D.

Ethyl acetate – Wikipedia

From Wikipedia, the free encyclopedia. Due to these properties, it can be removed from a sample by heating in a hot water bath and providing ventilation with compressed air. In the field of entomologyethyl acetate is an effective asphyxiant for use in insect collecting and study. Ether -like, fruity [1]. The irritant effect of ethyl acetate is weaker than that of propyl acetate or butyl acetate. The rate constant is 0. Overexposure to ethyl acetate may cause irritation of the eyes, nose, and throat.

Byproducts of the dehydrogenation include diethyl etherwhich is thought to arise primarily due to aluminum sites in the catalyst, acetaldehyde and its aldol products, higher esters, and ketones. By using this site, you agree to the Terms of Use and Privacy Policy.

Retrieved from ” https: Propyl acetate Propyl propanoate Isopropyl acetate Isopropyl palmitate. Acetic ester Acetic ether Ethyl ester of acetic acid. It is also prepared in industry using the Tishchenko reactionby combining two equivalents of acetaldehyde in the presence of an alkoxide catalyst:.

Views Read Edit View history. Surface area can be again increased by deposition onto a zeolitetypically ZSM Catalytic technology for the sustainable society”. This page was last edited on 29 Novemberat A specialized industrial route entails the catalytic dehydrogenation of ethanol.

The copper may have its surface area increased by depositing it on zincpromoting the growth of snowflake -like fractal structures dendrites.

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For example, it is commonly used to clean circuit boards and in some nail varnish removers acetone and acetonitrile are also used.

Ethyl acetate

Other names Acetic ester Acetic ether Ethyl ester of acetic acid. The aroma of ethyl acetate is most vivid in younger wines and contributes towards the general perception of “fruitiness” in the wine. The use of an acid catalyst accelerates the hydrolysis, which is subject to the Fischer equilibrium mentioned above.

Ethyl acetate is rarely selected as a reaction solvent because it is prone to hydrolysis and transesterification.

LC 50 median concentration. Ethyl acetate is zcetato ester of ethanol and acetic acid ; it is manufactured on a large scale for use as a solvent. This method is more cost effective than the esterification xcetato is applied with surplus ethanol in a chemical ehilo.

In perfumes, it evaporates quickly, leaving only the scent of the perfume on the skin. Lethal dose or concentration LDLC:. In the laboratory, and usually for illustrative purposes only, ethyl esters are typically hydrolyzed in a two-step process starting with a stoichiometric amount of a strong base, such as sodium hydroxide. Exposure to oxygen can exacerbate the fault due to the oxidation of ethanol to acetaldehydewhich leaves the wine with a sharp vinegar -like taste.

In other projects Wikimedia Commons. Severe overexposure may cause weakness, drowsiness, and unconsciousness.