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1-Octanol, also known as octan-1-ol, is the organic compound with the molecular formula CH 3 (CH 2) 7 OH. It is a fatty alcohol. Many other isomers are also known generically as octanols. 1-Octanol is manufactured for the synthesis of esters for use in perfumes and flavorings. It has a pungent odor.
Octanols are alcohols with the formula C 8 H 17 OH. A simple and important member is 1-octanol , with an unbranched chain of carbons. Other commercially important octanols are 2-octanol and 2-ethylhexanol .
It is classified as an ester that is formed from 1-octanol (octyl alcohol) and acetic acid. It is found in oranges, grapefruits, and other citrus products. [10] Octyl acetate can be synthesized by the Fischer esterification of 1-octanol and acetic acid: CH 3 (CH 2) 7 OH + CH 3 CO 2 H → CH 3 (CH 2) 7 O 2 CCH 3 + H 2 O
1-Octanol. Unsaturated compounds Ethylene. Acetylene. alpha-Linolenic acid, ... Unsaturation can be determined by NMR, mass spectrometry, and IR spectroscopy, ...
1-Octanol; 2-Octanol This page was last edited on 4 July 2024, at 00:41 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...
The higher-energy near-IR, approximately 14,000–4,000 cm −1 (0.7–2.5 μm wavelength) can excite overtone or combination modes of molecular vibrations. The mid-infrared, approximately 4,000–400 cm −1 (2.5–25 μm) is generally used to study the fundamental vibrations and associated rotational–vibrational structure.
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Cetyl alcohol (1-hexadecanol) 16 carbon atoms: C 16 H 34 O Palmitoleyl alcohol (cis-9-hexadecen-1-ol) 16 carbon atoms: unsaturated: C 16 H 32 O Heptadecyl alcohol (1-n-heptadecanol, heptadecanol) 17 carbon atoms: C 17 H 36 O Stearyl alcohol (1-octadecanol) 18 carbon atoms: C 18 H 38 O Oleyl alcohol (1-octadecenol) 18 carbon atoms: unsaturated ...