hydroxylamine

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hy·drox·yl·a·mine

 (hī-drŏk′sə-lə-mēn′, hī′drŏk-sĭl′ə-mēn′, -sə-lăm′ĭn)
n.
A colorless crystalline compound, H3NO, explosive when heated, that is used as a reducing agent and in organic synthesis.
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.

hydroxylamine

(haɪˌdrɒksɪləˈmiːn; -ˈæmɪn; -ˈsaɪləˌmiːn)
n
(Elements & Compounds) a colourless crystalline compound that explodes when heated: a reducing agent. Formula: NH2OH
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

hy•drox•yl•a•mine

(haɪˌdrɒk sə ləˈmin, -səlˈæm ɪn)

n.
an unstable, weakly basic, crystalline compound, NH3O, used as a reducing agent, analytical reagent, and chemical intermediate.
[1865–70]
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.
References in periodicals archive ?
Additive Function of additive Grinding aid (O1) Grinding aid/energy saving Grinding aid (O2) Grinding aid/energy saving Strength enhancer (E) Early-age strength enhancer Strength enhancer (N) Final-age strength enhancer Additive Raw material Density Grinding aid (O1) Polyethanolamine acetate 1.14 Grinding aid (O2) Polyethanolamine acetate 1.12 modified with glycol Strength enhancer (E) Modified hydroxylamines 1.15 Strength enhancer (N) Modified hydroxylamines 1.16 Additive PH Color Grinding aid (O1) 6-7 Light brown Grinding aid (O2) 6-7 Brown Strength enhancer (E) 10-12 Brown Strength enhancer (N) 11-12 Brown TABLE 3: Results of ANOVA test for Blaine fineness (significance level-[alpha] = 0.05).
Hydroxylamines and tocopherols are representative examples of "hyperactive" stabilizers that can supplement the performance of traditional stabilizers, such as phenolics and phosphites.
The ease detachment of the benzoyl group from the cycloadducts 9a,b was achieved through NaOH/MeOH treatment at room temperature for 24 h, affording the fairly stable hydroxylamines 10a,b.
It was shown [21, 22] that cyclic hydroxylamines as CMH can be used to assay formation of reactive oxidant species resulting from differently generated oxidative stress, detecting a 10-fold lower superoxide radical level than other spin-traps, thereby providing superior sensitivity for quantification of superoxide radical in vitro.
It provides guidance on selecting the appropriate aminating agent--whether haloamines, hydroxylamines, diazonium salts, azo compounds, or azides--for different types of carbon nucleophile.
(21,22) A one-pot synthesis of [beta]-lactams by a multi-component coupling (23) of N-alkyl hydroxylamines, aldehydes, and alkynes catalyzed by copper were reported under mild conditions (Scheme 2).
Hydroxylamines and hydroxylamine salts as combustion improvers for liquid biomass-derived and hydrocarbon-based fuels.
Biological formation and pharmacological, toxicological, and pathological properties of hydroxylamines and hydroxamic acids.