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毛细管气相色谱法测定欧芹中扑草净及其降解产物

Capillary gas chromatographic determination of prometryn and its degradation products in parsley.

作者信息

Bardalaye P C, Wheeler W B

出版信息

J Assoc Off Anal Chem. 1985 Jul-Aug;68(4):750-3.

PMID:4030649
Abstract

Residue analysis of the herbicide prometryn (2,4-bis(isopropylamino)-6-methylthio-1,3,5-triazine) is widely known, but an analytical method for determining its metabolities or degradation products in addition to the parent chemical has not yet been reported in the literature. The procedure reported here is for the extraction and determination of prometryn and 2 metabolites, 2-amino-4-isopropylamino-6-methyl-thio-1,3,5-triazine and 2,4-diamino-6-methylthio-1,3,5-triazine, in parsley. Crops were extracted with 2-propanol followed by concentration of the extract and partitioning with a minimum amount of hexane in the presence of a large excess of water to remove most of the green pigment. The aqueous phase was divided into 2 equal halves: (A) One-half portion was partitioned with dichloromethane in the presence of saturated sodium chloride solution, the dichloromethane phase was separated, and the aqueous phase was discarded. The organic solvent was evaporated, and the contents were reconstituted in petroleum ether before prometryn analysis. (B) The other half was made slightly alkaline with ammonium hydroxide solution and was partitioned with ethyl acetate in the presence of saturated sodium chloride solution. The ethyl acetate phase was concentrated, centrifuged to remove any turbidity, and analyzed for the 2 metabolities above. Fused silica capillary gas chromatography (GC) with nitrogen-phosphorus (N-P) detection was used for quantitation. The limit of detection was 0.05 mg/kg for all the compounds examined. Recoveries from fortified parsley samples ranged from 59 to 73% at fortification levels of 0.05 to 1.0 mg/kg.

摘要

除草剂扑草净(2,4-双(异丙基氨基)-6-甲硫基-1,3,5-三嗪)的残留分析广为人知,但文献中尚未报道除母体化合物外测定其代谢物或降解产物的分析方法。本文报道的方法用于提取和测定欧芹中的扑草净及其两种代谢物,即2-氨基-4-异丙基氨基-6-甲硫基-1,3,5-三嗪和2,4-二氨基-6-甲硫基-1,3,5-三嗪。用2-丙醇提取作物,然后浓缩提取物,并在大量水存在下用最少的己烷进行分配,以去除大部分绿色色素。水相分为两等份:(A)一半在饱和氯化钠溶液存在下用二氯甲烷分配,分离出二氯甲烷相,弃去水相。蒸发有机溶剂,在进行扑草净分析前将内容物用石油醚复溶。(B)另一半用氢氧化铵溶液调至微碱性,并在饱和氯化钠溶液存在下用乙酸乙酯分配。浓缩乙酸乙酯相,离心去除任何浑浊物,并分析上述两种代谢物。采用带氮磷(N-P)检测的熔融石英毛细管气相色谱(GC)进行定量。所有检测化合物的检测限为0.05 mg/kg。在0.05至1.0 mg/kg的加标水平下,加标欧芹样品的回收率为59%至73%。

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