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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.
6.02 ε 0 at 25 °C Bond strength? ... for Ethyl Acetate/Water [3] P = 760 mmHg BP Temp. ... 78.3 75.6: 90.8: 82.3 76.1: 93.2: 86.8 76.4: 94.2: 88.0 77.7:
141-43-5: 0152: Ethanolamine: 75 mg/m 3: 30 ppm: 141435: 110-80-5: 0060: 2-Ethoxyethanol: 1845 mg/m 3: 500 ppm: 110805: 111-15-9: 0364: 2-Ethoxyethyl acetate: 2705 mg/m 3: 500 ppm: 111159: 141-78-6: 0367: Ethyl acetate: 7200 mg/m 3: 2000 ppm: 141786 (10% Lower explosive limit LEL) 140-88-5: 0267: Ethyl acrylate: 1227 mg/m 3: 500 ppm: 140885 ...
At large scale, ethyl acetoacetate is industrially produced by treatment of diketene with ethanol. [2] The small scale preparation of ethyl acetoacetate is a classic laboratory procedure. [3] It involves Claisen condensation of ethyl acetate. Two moles of ethyl acetate condense to form one mole each of ethyl acetoacetate and ethanol. [4]
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
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.
Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers. [1] Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds.
118-78-5 C 4 H 6: cyclobutene: 822-35-5 C 4 H 6: methylenecyclopropane: 6142-73-0 C 4 H 6 Br 2 O 2: ethyl dibromoacetate: 617-33-4 C 4 H 6 MgO 4: magnesium acetate: 142-72-3 C 4 H 6 N 2 O 2: dihydrouracil: 504-07-4 C 4 H 6 N 2 O 2: dimethylfurazan monoxide: 2518-42-5 C 4 H 6 N 2 O 2: ethyl diazoacetate: 623-73-4 C 4 H 6 N 2 S: methimazole: 60 ...