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Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH. It is a colourless liquid with a pleasant floral odor. It occurs widely in nature, being found in a variety of essential oils. It is slightly soluble in water (2 ml per 100 ml of H 2 O), but miscible with most organic solvents.
1-Phenylethanol is the organic compound with the formula C 6 H 5 CH(OH)CH 3. It is one of the most commonly available chiral alcohols. It is a colorless liquid with a mild gardenia-hyacinth scent. [4] Phenylethanol is an aromatic alcohol, it has the role of mouse metabolite.
Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite.
1-propanol; Other higher alcohols that can be produced during fermentation include: isopropanol (isopropyl alcohol), oxidized to form acetone by alcohol dehydrogenase in the liver, leading to ketosis when ingested in large quantities. 1-butanol; 1-pentanol (n-amyl alcohol) 1-hexanol; 2-phenylethanol; tyrosol; tryptophol; methionol
Like many esters, it is found in a range of fruits and biological products. [1] It is a colorless liquid with a rose and honey scent and a raspberry-like taste. [ 2 ] [ 3 ]
Phenylethanol may refer to: 1-Phenylethanol; 2-Phenylethanol (phenethyl alcohol) This page was last edited on 22 October 2023, at 17:24 (UTC). Text is available ...
2,3-Dimethyl-1-butanol; 3,3-Dimethyl-1-butanol This page was last edited on 27 March 2024, at 19:55 (UTC). Text is available under the Creative Commons Attribution ...
Under the usual laboratory conditions, it is unstable, tending instead to undergo self-condensation. [1] Aminoacetaldehyde diethylacetal is a stable surrogate. [2] In nature, aminoacetaldehyde is produced by oxygenation of taurine catalyzed by taurine dioxygenase, which produces the sulfite H 2 NCH 2 CH(OH)SO 3 −.