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Determination of Enantiomeric Purity of 2-Piperidinemethanamine by HPLC Combined With Pre-Column Derivation

机译:HPLC结合柱前衍生测定2-哌啶甲胺的对映体纯度

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A new HPLC method has been developed and validated for determination of enantiomeric purity of 2-piperidinemethanamine within a short run time of less than 10 min. The method was based on pre-eolumn derivation of 2-piperidinemethanarnine with 3,5-dinitrobenzoie acid and complete separation of enantiomers has been achieved on a CHI-DMB analytical column (250 mm x 4.6 mm) using n-hexane: ethanol (85:15 v/v) as mobile phase at a flow rate of 1,0 mL min~(-1) under UV photodiode-array detector detection. Then the effects of mobile phase and temperature on enantioselectivity were further evaluated. The method was validated with respect to precision, accuracy, linearity, limit of detection (LOD), limit of quantification (LOQ) and robustness. The recoveries were between 99.1 and 102.3 % with percentage relative standard deviation less than 1.17 %. The LOD and LOQ for first enantiomer were 13.7 and 46.3 μg mL~(-1) and for second enantiomer were 15.2 and 51.4 μg mL~(-1), respectively. This method is expected to be accurate, stable, rapid and sensitive for determination of the enantiomeric purity of 2-piperidinemethanamine in bulk samples.
机译:已开发出一种新的HPLC方法,并已验证了该方法可在不到10分钟的短时间内测定2-哌啶甲胺的对映体纯度。该方法基于2-哌啶甲胺与3,5-二硝基苯甲酸的柱前衍生,在CHI-DMB分析柱(250 mm x 4.6 mm)上,使用正己烷:乙醇(85,85)实现了对映体的完全分离。在紫外光电二极管阵列检测器检测下,以1,0 mL min〜(-1)的流速作为流动相:15 v / v)。然后进一步评估了流动相和温度对映体选择性的影响。该方法在精度,准确度,线性,检测限(LOD),定量限(LOQ)和鲁棒性方面得到了验证。回收率在99.1%至102.3%之间,相对标准偏差百分比小于1.17%。第一对映体的LOD和LOQ分别为13.7和46.3μgmL〜(-1),第二对映体的LOD和LOQ分别为15.2和51.4μgmL〜(-1)。预期该方法对于测定大批量样品中2-哌啶甲胺的对映体纯度是准确,稳定,快速和灵敏的。

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