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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.
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For example, acetic acid and ethanol gives ethyl acetate and water. CH 3 COO−H + HO−CH 2 CH 3 → CH 3 COO−CH 2 CH 3 + H 2 O. Most acetate esters, however, are produced from acetaldehyde using the Tishchenko reaction. In addition, ether acetates are used as solvents for nitrocellulose, acrylic lacquers, varnish removers, and wood stains.
Ethyl Acetate: 77.1 [5] Acetic Anhydride: 139.0 [6] Ethylene Dichloride: 1.25 83.5 −35 [7] Acetonitrile: 0.78 81.6 −45 [8] Heptane: 98.4 [9] Isobutanol: 107.7 [10] n-Hexane: 0.66 68.7 [11] n-Butanol: 117.7 [12] Hydrochloric Acid: 84.8 [13] tert-Butanol: 82.5 [14] Chlorobenzene: 131.7 [15] p-chlorobenzotrifluoride: 1.34 136 –36.1 [16] MTBE ...
2-Ethoxyethanol, also known by the trademark Ethyl cellosolve, is a solvent used widely in commercial and industrial applications. It is a clear, colorless, nearly odorless liquid that is miscible with water, ethanol, diethyl ether, acetone, and ethyl acetate. [3] 2-Ethoxyethanol is manufactured by the reaction of ethylene oxide with ethanol.
1975 – Merger of Sigma Chemical and Aldrich Chemical to created Sigma-Aldrich. [13] Their first year earned $43 million in sales. [14] 1999 – Sigma-Aldrich reaches $1 billion in sales; 2005 – Announced membership in The RNAi Consortium [15] 2014 – Merck KGaA announced that it would purchase Sigma-Aldrich for approx. $17 billion (€13.1 ...
An ester of carboxylic acid.R stands for any group (organic or inorganic) and R′ stands for organyl group.. In chemistry, an ester is a compound derived from an acid (organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group (−OH) of that acid is replaced by an organyl group (−R).
The dianion of ethyl acetoacetate is also a useful building block, except that the electrophile adds to the terminal carbon. The strategy can be depicted in the following simplified form: [6] CH 3 C(O)CHNaCO 2 C 2 H 5 + BuLi → LiCH 2 C(O)CHNaCO 2 C 2 H 5 + BuH (Bu = butyl) Reduction of ethyl acetoacetate gives ethyl 3-hydroxybutyrate. [8]