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<article article-type="research-article" dtd-version="1.3" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">chemicallytech</journal-id><journal-title-group><journal-title xml:lang="en">Fine Chemical Technologies</journal-title><trans-title-group xml:lang="ru"><trans-title>Тонкие химические технологии</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2410-6593</issn><issn pub-type="epub">2686-7575</issn><publisher><publisher-name>MIREA – Russian Technological University (RTU MIREA).</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">chemicallytech-274</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CHEMISTRY AND TECHNOLOGY OF MEDICINAL COMPOUNDS AND BIOLOGICALLY ACTIVE SUBSTANCES</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ХИМИЯ И ТЕХНОЛОГИЯ ЛЕКАРСТВЕННЫХ ПРЕПАРАТОВ И БИОЛОГИЧЕСКИ АКТИВНЫХ СОЕДИНЕНИЙ</subject></subj-group></article-categories><title-group><article-title>Analysis of difenacoum in rodenticide compositions containing derivatives coumatetralyl</article-title><trans-title-group xml:lang="ru"><trans-title>Анализ дифенакума в родентицидных композициях, содержащих производные куматетралила</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Носикова</surname><given-names>Л. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Nosikova</surname><given-names>L. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра химии и технологии редких и рассеянных элементов, наноразмерных и композиционных материалов им. К.А. Большакова, доцент</p></bio><email xlink:type="simple">kochchem@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кочетов</surname><given-names>А. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Kochetov</surname><given-names>A. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Испытательная аналитическая лаборатория, химик-аналитик</p></bio><email xlink:type="simple">vorfolomeeva.e.v@yandex.ru</email><xref ref-type="aff" rid="aff-2"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Московский технологический университет (Институт тонких химических технологий), 119571, Москва, пр-т Вернадского, д. 86</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Moscow Technological University (Institute of Fine Chemical Technologies), 86, Vernadskogo pr., Moscow 119571</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>ЗАО «МЕТТЭМ-Технологии, Балашиха, 143900</institution><country>Россия</country></aff><aff xml:lang="en"><institution>«METTEM-Technology», 3, Parkovaya str., Balashikha, 143900</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2015</year></pub-date><pub-date pub-type="epub"><day>28</day><month>12</month><year>2015</year></pub-date><volume>10</volume><issue>6</issue><fpage>88</fpage><lpage>95</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Nosikova L.A., Kochetov A.N., 2015</copyright-statement><copyright-year>2015</copyright-year><copyright-holder xml:lang="ru">Носикова Л.А., Кочетов А.Н.</copyright-holder><copyright-holder xml:lang="en">Nosikova L.A., Kochetov A.N.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.finechem-mirea.ru/jour/article/view/274">https://www.finechem-mirea.ru/jour/article/view/274</self-uri><abstract><p>The possibility of simultaneous determination of the title compounds and coumatetralyl derivatives (coumatetralyl, flocumaphen and brodifacoum) in rodenticide means was considered. The conditions of direct analytical determination and stages of preparation were adapted, which will provide determination of the isomeric composition of difenacoum in rodenticide compositions. Using less polar mobile phases on the basis of acetonitrile is preferable as compared to mixtures on the basis of methanol. Conditions allowing the separation of enantiomers with the limit of sensitivity of the method for difenacoum level 0.0002% were found, which allows to monitor the content of more active trans isomers of the title compound both in the original rodenticide substances and in the end poisoned baits. Implementation of the analytical stage of the determination of the isomeric composition of difenacoum involves the use of simpler equipment due to the implementation of the isocratic mode afterwards.</p></abstract><trans-abstract xml:lang="ru"><p>Рассмотрены возможности одновременного определения в родентицидных средствах титульного соединения и производных куматетралина (куматетралил, флокумафен и бродифакум). Адаптированы условия проведения непосредственно аналитического определения и стадии пробоподготовки, обеспечивающие определение изомерного состава дифенакума в родентицидных композициях. Использование менее полярных подвижных фаз на основе ацетонитрила предпочтительнее смесей на основе метанола. Подобраны условия, при которых достигается разделение энантиомеров при пределе чувствительности метода для дифенакума на уровне 0.0002%, что позволяет осуществлять мониторинг содержания более активных транс- изомеров для титульного соединения как в исходных родентицидных субстанциях, так и в конечных отравленных приманках. Реализация аналитической стадии определения изомерного состава дифенакума сопряжена с использованием аппаратурно более простого оборудавания оборудования за счет реализации изократического режима элюирования</p></trans-abstract><kwd-group xml:lang="ru"><kwd>дифенакум</kwd><kwd>родентициды</kwd><kwd>куматетралил</kwd><kwd>ОФ ВЭЖХ</kwd></kwd-group><kwd-group xml:lang="en"><kwd>difenacoum</kwd><kwd>rodenticide</kwd><kwd>coumatetralyl</kwd><kwd>flocoumafen</kwd><kwd>brodifacoum</kwd><kwd>RF-HPLC</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Jung J.-C., Park O.-S. // Molecules. 2009. V. 14. P. 4790-4803.</mixed-citation><mixed-citation xml:lang="en">Jung J.-C., Park O.-S. // Molecules. 2009. V. 14. P. 4790-4803.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">O`Connor J.A. // Research. 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