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Ethyl butyrate, also known as ethyl butanoate, or butyric ether, is an ester with the chemical formula CH 3 CH 2 CH 2 COOCH 2 CH 3. It is soluble in propylene glycol, paraffin oil, and kerosene. It has a fruity odor, similar to pineapple, and is a key ingredient used as a flavor enhancer in processed orange juices. [1]
Butyl butyrate, or butyl butanoate, is an organic compound that is an ester formed by the condensation of butyric acid and n-butanol. It is a clear, colorless liquid that is insoluble in water, but miscible with ethanol and diethyl ether. Its refractive index is 1.406 at 20 °C.
The butyrate or butanoate ion, C 3 H 7 COO −, is the conjugate base of butyric acid. It is the form found in biological systems at physiological pH . A butyric (or butanoic) compound is a carboxylate salt or ester of butyric acid.
Paramagnetic nuclear magnetic resonance spectroscopy refers to nuclear magnetic resonance (NMR) spectroscopy of paramagnetic compounds. [1] [2] Although most NMR measurements are conducted on diamagnetic compounds, paramagnetic samples are also amenable to analysis and give rise to special effects indicated by a wide chemical shift range and broadened signals.
Ethyl butyrate; Isobutyl acetate; Isoamyl formate; Methyl pentanoate; Methyl pivalate; Propyl propanoate; Other organic compounds with formula C 6 H 12 O 2: Cyclohexane-1,2-diol, a chemical compound found in castoreum; Diacetone alcohol
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Isobutyric acid is a colorless liquid with a somewhat unpleasant odor. It is soluble in water and organic solvents. It is found naturally in carobs (Ceratonia siliqua), in vanilla, and in the root of Arnica dulcis, and as an ethyl ester in croton oil. [6]
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