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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).
Ethyl acrylate is an organic compound with the formula CH 2 CHCO 2 CH 2 CH 3. It is the ethyl ester of acrylic acid. It is a colourless liquid with a characteristic acrid odor. It is mainly produced for paints, textiles, and non-woven fibers. [5] It is also a reagent in the synthesis of various pharmaceutical intermediates.
Ethyl propionate is an organic compound with formula C 2 H 5 O 2 CCH 2 CH 3. It is the ethyl ester of propionic acid. It is a colorless volatile liquid with a pineapple-like odor. [3] Some fruits such as kiwis [4] and strawberries [5] contain ethyl propionate in small amounts.
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 cyanoacrylate (ECA), a cyanoacrylate ester, is an ethyl ester of 2-cyano-acrylic acid. It is a colorless liquid with low viscosity and a faint sweet smell in pure form. It is the main component of cyanoacrylate glues and can be encountered under many trade names . [ 2 ]
E. EA-2098; Edifenphos; Efloxate; Enalapril; EPN (insecticide) Etazolate; Ethion; Ethoheptazine; Ethonam; 2-Ethoxycarbonyl-1-methylvinyl cyclohexyl methylphosphonate
Ethyl benzoate, C 9 H 10 O 2, is an ester formed by the condensation of benzoic acid and ethanol. It is a colorless liquid that is almost insoluble in water, but miscible with most organic solvents. As with many volatile esters, ethyl benzoate has a pleasant odor described as sweet, wintergreen, fruity, medicinal, cherry and grape. [1]
2-Ethylhexyl acrylate polymerizes easily. The polymerization can be initiated by light, peroxides, heat, or contaminants.It can react violently when combined with strong oxidants and can form explosive mixtures with air at temperatures above 82 °C (180 °F). [2]