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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.
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.
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.
IUPAC name IARC carcinogen group Toxic metabolite(s) Alcohol by volume (ABV) [1] LD50 in rat, oral [2]; Ethanol: Group 1: Acetaldehyde → acetic acid Up to 95.6% in rectified spirit
Arachidyl alcohol (1-eicosanol) 20 carbon atoms: C 20 H 42 O Heneicosyl alcohol (1-heneicosanol) 21 carbon atoms: C 21 H 44 O Behenyl alcohol (1-docosanol) 22 carbon atoms: C 22 H 46 O Erucyl alcohol (cis-13-docosen-1-ol) 22 carbon atoms: unsaturated: C 22 H 44 O Lignoceryl alcohol (1-tetracosanol) 24 carbon atoms: C 24 H 50 O Ceryl alcohol (1 ...
Download as PDF; Printable version; In other projects ... move to sidebar hide. Phenylethanol may refer to: 1-Phenylethanol; 2 -Phenylethanol (phenethyl ...
At room temperature, acetaldehyde (H 3 CC(O)H) is more stable than vinyl alcohol (H 2 C=CHOH) by 42.7 kJ/mol. [3] Vinyl alcohol gas isomerizes to the aldehyde with a half-life of 30 min at room temperature. [1] H 2 C=CHOH → H 3 CC(O)H The industrial synthesis of acetaldehyde (Wacker process) proceeds via the intermediacy of a vinyl alcohol ...
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