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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The aroma of ethyl acetate is most vivid in younger wines and contributes towards the general perception of “fruitiness” in the wine. Given that the chemical is naturally present in many organisms, there is little risk of toxicity. Ethyl acetate is used primarily as a solvent and diluentbeing favored because of its low cost, low toxicity, and agreeable odor. Retrieved from ” https: LC Lo lowest published.

Because it is not hygroscopicethyl acetate also keeps the insect soft enough to allow proper mounting suitable for a collection. For example, it is commonly used to clean circuit boards and in acehato nail varnish removers acetone and acetonitrile are also used.


Acidity p K a. Methyl acetate erilo, Propyl acetateButyl acetate. It is also prepared in industry using the Tishchenko reactionby combining two equivalents of acetaldehyde in the presence of an alkoxide catalyst:.

Ethyl acetate

In rare cases exposure may cause sensitization of the mucous membrane and eruptions of the skin. Overexposure to ethyl acetate may cause irritation of the eyes, nose, and throat.

This reaction gives ethanol and sodium acetatewhich is unreactive toward ethanol:. Ether -like, fruity [1]. International Labour Office,p. Catalytic technology for the sustainable society”. Propyl acetate Propyl propanoate Isopropyl acetate Isopropyl palmitate. Ethyl acetate is the ester of ethanol and acetic acid ; it is manufactured on a large scale for use as a solvent.

Ethyl acetate is the most common ester in winebeing the product of the most common volatile organic acid — acetic acid ettilo, and the ethyl alcohol generated during the fermentation. In perfumes, it evaporates quickly, leaving only the scent of the perfume on the skin.

Ethyl acetate | CH3COOC2H5 – PubChem

Excessive amounts of ethyl acetate are considered a wine fault. The use of an acid catalyst accelerates the hydrolysis, which is subject to the Fischer equilibrium dde above. In the field of entomologyethyl acetate is an effective asphyxiant for use in insect collecting and study. Surface area can be again increased by deposition onto a zeolitetypically ZSM The rate constant is 0. Lethal dose aetato concentration LDLC:.


LC 50 median concentration. Acetic ester Acetic ether Ethyl ester of acetic acid. Coffee beans and tea leaves are decaffeinated with this solvent. Refractive index n D. The Oxford Companion to Wine 3rd ed. Patty’s Industrial Hygiene and Toxicology. From Wikipedia, the free encyclopedia. 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.

Solubility in ethanolacetonediethyl etherbenzene.

This page was last edited on 29 Novemberat The irritant effect of ethyl etklo is weaker than that of propyl acetate or butyl acetate.