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首页> 外文期刊>Journal of separation science. >Simultaneous determination of flupyradifurone and its two metabolites in fruits, vegetables, and grains by a modified quick, easy, cheap, effective, rugged, and safe method using ultra high performance liquid chromatography with tandem mass spectrometry
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Simultaneous determination of flupyradifurone and its two metabolites in fruits, vegetables, and grains by a modified quick, easy, cheap, effective, rugged, and safe method using ultra high performance liquid chromatography with tandem mass spectrometry

机译:改进的快速,简便,廉价,有效,坚固而安全的方法同时使用超高效液相色谱-串联质谱法同时测定水果,蔬菜和谷物中的氟吡呋喃及其两种代谢物

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摘要

An effective analytical method for the simultaneous determination of a novel insecticide flupyradifurone and its two metabolites was developed using ultra high performance liquid chromatography with tandem mass spectrometry coupled with a quick, easy, cheap, effective, rugged, and safe procedure. The three target compounds were extracted with acetonitrile and cleaned up with octadecylsilane, and were separated successfully between 1.9 and 3.1 min using an HSS T3 chromatographic column connected to an electrospray ionization source. All the matrix-matched samples at three fortified levels (0.01, 0.05, and 0.5 mg/kg) provided satisfactory recoveries in the range of 70.3-116.5% with relative standard deviations below 18.6%. The limits of quantitation were 10 g/kg for flupyradifurone and difluoroethylamino-furanone and 100 g/kg for 6-chloronicotinic acid. The limit of quantification of flupyradifurone was far below the maximum residue limit in the USA. The method is of great significance for establishing maximum residue limits in China.
机译:建立了一种同时测定新型杀虫剂氟吡呋喃及其两种代谢物的有效分析方法,该方法采用串联质谱联用的超高效液相色谱结合快速,简便,廉价,有效,坚固耐用和安全的程序。三种目标化合物用乙腈萃取并用十八烷基硅烷纯化,并使用连接至电喷雾电离源的HSS T3色谱柱在1.9至3.1分钟之间成功分离。三种强化水平(0.01、0.05和0.5 mg / kg)的所有基质匹配样品在70.3-116.5%的范围内提供令人满意的回收率,相对标准偏差低于18.6%。氟吡呋喃酮和二氟乙基氨基呋喃酮的定量限为10 g / kg,6-氯烟酸的定量限为100 g / kg。氟吡呋喃酮的定量限远低于美国的最大残留限。该方法对建立中国最大残留限量具有重要意义。

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