cyanohydrin


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Related to cyanohydrin: acetal, lactic acid, Acetone cyanohydrin

cy·a·no·hy·drin

 (sī′ə-nō-hī′drĭn, sī-ăn′ō-)
n.
An organic compound or functional group containing both a CN group and a hydroxyl group, usually on adjacent carbon atoms.

American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

cyanohydrin

(ˌsaɪənəʊˈhaɪdrɪn)
n
(Biochemistry) any of a class of organic compounds containing a cyanide group and a hydroxyl group bound to the same carbon atom
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

cy•a•no•hy•drin

(ˌsaɪ ə noʊˈhaɪ drɪn, saɪˌæn oʊ-)

n.
an organic compound containing both the cyanogen and hydroxyl groups.
[1920–25]
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.cyanohydrin - any organic compound in which the cyano radical -CN and the hydroxyl radical -OH are attached to the same carbon atom
organic compound - any compound of carbon and another element or a radical
Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.
References in periodicals archive ?
When the possible risks of the filter and its cleaning on human health are examined, the polymer film filter in the tobacco unit is observed to easily melt during use (90[degrees]C), and even though in low amounts formaldehyde cyanohydrin, which is a very toxic substance, is formed.
Analysis of the polymer-film filter showed release of formaldehyde cyanohydrin at 90 degrees Celsius, which is well below the maximum temperature reached during normal usage.
The interaction of cyanohydrin of 1-(2-ethoxyethyl)-4oxopiperidine 2, obtained with 67.5% yield from 1, with ammonium carbonate gives the compound 3HCl with 24% yield (Scheme 1).
Gelman et al., "Efficient synthesis of cyanohydrin trimethylsilyl ethers via 1,2-chemoselective cyanosilylation of carbonyls," Green Chemistry, vol.
In order to provide the cyanohydrins, first sulfonic is produced which is a sediment and then by adding potassium cyanide to the sulfonic compound, the nitrile group is replaced and the compound of 4-t-butyl-2-(Npiperidinomethyl)cyanocyclohexane is obtained which had active optical chiral centers and is a new analog of active optical cyanohydrin family.