phenylamine


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Related to phenylamine: phenylalanine

phenylamine

(ˌfiːnaɪləˈmiːn; ˌfɛnɪl-)
n
(Elements & Compounds) another name for aniline
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014
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Noun1.phenylamine - oily poisonous liquid amine obtained from nitrobenzene and used to make dyes and plastics and medicinesphenylamine - oily poisonous liquid amine obtained from nitrobenzene and used to make dyes and plastics and medicines
amine, aminoalkane - a compound derived from ammonia by replacing hydrogen atoms by univalent hydrocarbon radicals
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References in periodicals archive ?
In this work, we performed graphene functionalization by the covalent bonding of the nitrophenyl group ([C.sub.6][H.sub.5][NO.sub.2]) followed by its reduction to the phenylamine group ([C.sub.6][H.sub.5][NH.sub.2]) by using a two-step cyclic voltammetry (CV) process.
GC-MS analysis of the ethyl acetate extract of Streptomycetes cavourensis SKCMM1 fermented broth Classification Compound % Aniline Compound 2,4-Dimethoxy-tri phenylamine 0.52 Fatty acid Pentanoic acid 1.76 2,4,6-Octatrienoic acid 2.74 Hydroxy Compound 1,4-Dioxane-2,6-dimethanol 13.06 Caryophyllenyl alcohol 0.67 3-Cyclohexen-1-ol 0.67 Geosmin 2.48 Hydrocarbons 1,5-Bis pentane 0.47 Docosane 0.50 Cycloheptanone 1.12 Benzene 2.12 Cycloalkane compound Cyclohexane 7.58 Cyclopropane 1.11 Aromatic compound 1,3-Bisbenzo thio phene 8.66 Carboxamide Cyclopropane carboxamide 0.8 Unknown compounds 55.74
After completely dried, the developed silica plate was visualized by dipping in a mixed solution containing 2% (w/v) N-phenylaniline, 2% (v/v) phenylamine and 85% (v/v) phosphoric acid in acetone, followed by heating at 85degC for 15 min.
In the brain and spinal cord, Paracetamol is conjugated with arachidonic acid to form N-arachidonoyl phenylamine (AM 404).
By this time, the method had evolved to be basically as it is used now: to a soil sample passing through a 0.5-mm screen (containing between 10 and 25 mg TOC), add 10mL of 0.167 M [K.sub.2][Cr.sub.2][0.sub.7] solution and 20 mL of [greater than or equal to] 96% sulfuric acid, shake and stand for 20-30 min; then, add 200-300 mL water, 10mL of 85% phosphoric acid and phenylamine indicator.
Sakar, "Structural and surface characterization of newly synthesized D-[pi]-D type Schiff base ligand: (1E,2E)-3-[4-(dimethylamino)phenyl]prop-2-en-1-ylidene) phenylamine," Journal of Chemistry, vol.

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