Use of 11C as a tracer for studying the synthesis of [ 11C]urea from [ 11C]cyanide

The use of reversed-phase liquid chromotography and radiochemical detection with carbon-11 (t 1 2 = 20.4 min) as a tracer allowed the study of the preparation of [ 11C]urea from [ 11C]cyanide at no carrier-added concentrations. [ 11C]cyanate was readily prepared by permanganate oxidation of [ 11C]cy...

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Veröffentlicht in:The International journal of applied radiation and isotopes 1985-02, Vol.36 (2), p.141-144
Hauptverfasser: Boothe, Thomas E., Emran, Ali M., Finn, Ronald D., Vora, Manhar M., Kothari, Paresh J.
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container_end_page 144
container_issue 2
container_start_page 141
container_title The International journal of applied radiation and isotopes
container_volume 36
creator Boothe, Thomas E.
Emran, Ali M.
Finn, Ronald D.
Vora, Manhar M.
Kothari, Paresh J.
description The use of reversed-phase liquid chromotography and radiochemical detection with carbon-11 (t 1 2 = 20.4 min) as a tracer allowed the study of the preparation of [ 11C]urea from [ 11C]cyanide at no carrier-added concentrations. [ 11C]cyanate was readily prepared by permanganate oxidation of [ 11C]cyanide at 75°C. The conversion of NH 4O 11CN (≈0.03 mM) to [ 11C]urea in the presence of excess ammonium ions (0.28 M) was found to best fit pseudo first order reaction kinetics with a rate constant of 0.065 ± 0.008 min −1 at 75°C. Heating at higher temperatures (180–200°C) revealed that the conversion of NH 4O 11CN to [ 11C]urea occured in high yield in less than 3 min. The hydrolysis of [ 11C]cyanate to [ 11C]carbonate, a possible side reaction, was found to proceed at a rate of 0.010 ± 0.001 min −1 at 113°C.
doi_str_mv 10.1016/0020-708X(85)90229-7
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[ 11C]cyanate was readily prepared by permanganate oxidation of [ 11C]cyanide at 75°C. The conversion of NH 4O 11CN (≈0.03 mM) to [ 11C]urea in the presence of excess ammonium ions (0.28 M) was found to best fit pseudo first order reaction kinetics with a rate constant of 0.065 ± 0.008 min −1 at 75°C. Heating at higher temperatures (180–200°C) revealed that the conversion of NH 4O 11CN to [ 11C]urea occured in high yield in less than 3 min. 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[ 11C]cyanate was readily prepared by permanganate oxidation of [ 11C]cyanide at 75°C. The conversion of NH 4O 11CN (≈0.03 mM) to [ 11C]urea in the presence of excess ammonium ions (0.28 M) was found to best fit pseudo first order reaction kinetics with a rate constant of 0.065 ± 0.008 min −1 at 75°C. Heating at higher temperatures (180–200°C) revealed that the conversion of NH 4O 11CN to [ 11C]urea occured in high yield in less than 3 min. The hydrolysis of [ 11C]cyanate to [ 11C]carbonate, a possible side reaction, was found to proceed at a rate of 0.010 ± 0.001 min −1 at 113°C.</abstract><cop>Oxford</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>3980120</pmid><doi>10.1016/0020-708X(85)90229-7</doi><tpages>4</tpages></addata></record>
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ispartof The International journal of applied radiation and isotopes, 1985-02, Vol.36 (2), p.141-144
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subjects Aliphatic compounds
Carbon Radioisotopes
Chemistry
Chromatography, High Pressure Liquid
Cyanides - metabolism
Exact sciences and technology
Organic chemistry
Preparations and properties
Urea - chemical synthesis
title Use of 11C as a tracer for studying the synthesis of [ 11C]urea from [ 11C]cyanide
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