Synthesis of [3H]cyfluthrin
For the elucidation of the distribution and biotransformation of Cyfluthrin in tse‐tse flies the tritium‐labelled compound was needed. A brominated precursor was dehalogenated with tritium gas using a special noble metal catalyst to give the desired [3H]Cyfluthrin. The labelling position was confirm...
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Veröffentlicht in: | Journal of labelled compounds & radiopharmaceuticals 1993-10, Vol.33 (10), p.949-955 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | For the elucidation of the distribution and biotransformation of Cyfluthrin in tse‐tse flies the tritium‐labelled compound was needed. A brominated precursor was dehalogenated with tritium gas using a special noble metal catalyst to give the desired [3H]Cyfluthrin. The labelling position was confirmed by 3H‐NMR spectroscopy. After synthesis and purification, the [3H]Cyfluthrin obtained showed a specific activity of 23.7 Ci/ mmol (877 GBq/mmol). |
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ISSN: | 0362-4803 1099-1344 |
DOI: | 10.1002/jlcr.2580331009 |