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(Dyeing) a colourless insoluble solid obtained from coal tar and used in the production of some dyes. Formula: C12H9N. Also called: diphenylenimine
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014


(ˈkɑr bəˌzoʊl)

a white, crystalline compound, C12H9N, used chiefly in making dyes.
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 ?
The guluronic acid to manuronic acid ratio was estimated through colorimetric reaction with carbazole reagent at 546 nm [11].
The effect of P tenuiflorus extract on alginate production was evaluated as per the standard carbazole method.
On the basis of the research and analysis, Louzhen Fan and team, extend the study by fabricating an experimental LED from blue to red, with the NBE-T-CQDs blended with poly(N-vinyl carbazole) (PVK) as the active emission layer.
Carbazole oligomers [4] have been widely studied in recent years thanks to their optoelectronic [5] and photovoltaic properties [4] and their industrial applications [6].
Content of basic nitrogen compounds in the concentrated product 1 Nitrogen compound wt% Nitrogen compound wt% Pyridines 16.53 Naphthalenamine 0.16 Quinolines 25.33 Amides 3.14 Anilines 25.86 Acridine 0.10 Isoquinolinol 1.52 Carbazole 0.73 Indoles 1.33 -- -- Note: "--" represents no data.
[14] Lewandowski M.: "Hydrotreating activity of bulk NiB alloy in model reaction of hydrogenation of carbazole".
Per Guethlin, the markets for certain key feedstocks such as CLT acid, 2B acid (PR48.xx), carbazole (PV23) and DCB (PY12, 13,14, 83,174, etc.) have "become very tight, leading to extreme price volatility."
Huang et al., "A conjugated hyperbranched polymer constructed from carbazole and tetraphenylethylene moieties: convenient synthesis through one-pot "A2 + B4" suzuki polymerization, aggregation-induced enhanced emission, and application as explosive chemosensors and PLEDs," Journal of Materials Chemistry, vol.
A calibration curve was set up (y = 909.14x - 9891.9, [R.sup.2] = 0.9996), allowing for accurate [DELTA]-disaccharide quantitation in each sample, by loading known quantities (from 25 to 800 ng) of AMAC-derivatized [DELTA]-disaccharides obtained by depolymerisation of a highly purified UTI sample assayed for uronic acid (UA) content, according to the carbazole method by Bitter and Muir [44].
Carbazole (Supelco 442506) and cysteine hydrochloride (C7880) were purchased from Sigma-Aldrich Ltd.
Finally, the concentration of alginate in solution was determined using the carbazole method [26].