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2 edition of Fluorescence derivatisation of some pharmacologically significant amines found in the catalog.

Fluorescence derivatisation of some pharmacologically significant amines

T. K. Hwang

Fluorescence derivatisation of some pharmacologically significant amines

by T. K. Hwang

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Published .
Written in English


Edition Notes

Thesis(Ph.D.) - Loughborough University of Technology 1976.

Statementby T.K. Hwang.
ID Numbers
Open LibraryOL19844135M


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Fluorescence derivatisation of some pharmacologically significant amines by T. K. Hwang Download PDF EPUB FB2

Fluorescence of several tertiary aliphatic amines has been excited in the gas phase by absorption of nm radiation, i.e. in the band corresponding to the à - X̃ transition of NH fluorescence was obtained from molecules having hydrogen Cited by: Fluorescence of Aromatic Amines and Their Fluorescamine Derivatives for Detection of Explosive Vapors Article (PDF Available) in Applied Spectroscopy 60(9).

Fluorescence derivatisation of amino acids in short and long-wavelengths. derivatisation is a needed to enhance both the selectivity and the sensitivity of amino acid analysis in biological samples.

or was not significant in its variation ( nm, 1a/ nm, 3c).Cited by: Primary aliphatic amines are reacted with 9‐isothiocyanatoacridine to yield the corresponding thiourea derivatives. These derivatives, after reaction in base, yield new.

The synthesis of two selective thiol derivatisation reagents (3, 4b) is described, starting from readily available 2-(4-aminophenyl)methyl-benzothiazole (1). The isocyanate6, being a known alcohol derivatisation reagent, is obtained from1 in a two step synthesis, in which the usual isocyanate synthesis using phosgen is by: 9.

Fluorescence Analysis for Amines on Plasma Functionalized Surfaces Simone Reichstein1, Jan-Eric Ehlers1, Karl-Heinz Gericke1, Stephen Kroll2, Kurosch Rezwan2 1TU Braunschweig, PCI, Braunschweig, Germany 2Advanced Ceramics, University of Bremen, Germany [email protected] Amino groups on polymer surfaces are exemplary used as anchor groups in.

Steric effects on the kinetics of quenching, namely a reduction by up to a factor of 50, became significant for amines with three secondary alkyl substituents, triisopropylamine, and N,N.

Acid- and aldehyde-induced fluorescence offers a highly sensitive and specific instrument for the histochemical demonstration of biogenic amines. This technique can be used to advantage for the selective identification of those neuronal structures that contain biogenic amines, namely the peripheral postganglionic sympathetic neurones and the central aminergic Cited by: 3.

Sigma-Aldrich Online Catalog Product List: Primary Amines. Chemistry C or H) is less than °; for instance, it is o in case of trimethylamine as shown in Fig. Amines are classified as primary (1o), secondary (2o) and tertiary (3o) depending upon the number of hydrogen atoms replaced by alkyl orFile Size: 1MB.

Publication list for members of E - Institute of Chemical Technologies and Analytics as authors or essentially involved persons. records ( - ) The complete list of publications of the Faculty of Chemistry is available from the publication database beginning with the publication year This banner text can have markup.

web; books; video; audio; software; images; Toggle navigation. Volume 40 issue 6 [doi _s] A. Lozhkin E. Sakanyan -- Natural coumarins- Methods of isolation and For some enzymes, a genetic polymorphism is not clearly demonstrated despite the fact that they display a wide interindividual variability in their activity.

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Biogenic amines (BAs), including tyramine, are heat stable: they are unaffected by cooking. Furthermore, decarboxylating enzymes are also heat-tolerant and may survive some cooking, allowing continued accumulation of BAs if cooked food is then poorly refrigerated.

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Amphetamine (AMP, “Speed”) was initially synthesized in Berlin in as 1-methylphenethylamine. It was the first of several chemicals, including methamphetamine (MET, “Ice”) and 3,4-methylenedioxymethamphetamine (MDMA. Transcript. 1 Plant-derived Natural Products.

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