戊唑钠的纯度分析及副产物分离

Xinyi Li, Yuangang Xu, Jianxin Zhou, Tianyang Hou, Ze Xu, Pengcheng Wang, Ming Lu
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引用次数: 0

摘要

作为合成大多数高能五唑化合物的重要中间体,五唑钠的反应体系复杂,副产物多,但没有合适的HPLC分析方法。在研究五唑钠水溶液紫外吸收峰的基础上,成功建立了五唑钠的高效液相色谱纯度分析方法,并验证了该方法的灵敏度、准确性和重复性。当检测波长为192nm,色谱柱为Agilent WondaSil C18 Superb(4.6×250mm,5μm),流动相为95%水和5%乙腈混合溶液,流速为0.8ml/min,分析时间为8min,样品量为1μL,柱温为40°C,得到五唑钠的液相图谱。分析结果表明,五唑钠的保留时间为3.76 min,在0.3068–0.3288 g/L范围内呈良好的线性关系。线性方程为y=-217447.64+835837.85x,相关系数R2为0.99997,具有良好的灵敏度、准确性和重复性。此外,对合成五唑钠的三种副产物进行了简单分离。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Purity analysis and by-product separation of pentazole sodium

Purity analysis and by-product separation of pentazole sodium

As an important intermediate in the synthesis of most energetic pentazole compounds, the reaction system of sodium pentazole is complex and has many by-products, but there is no suitable HPLC analysis method. Based on the study of ultraviolet absorption peak of sodium pentazole aqueous solution, the HPLC purity analysis method of sodium pentazole was successfully established and its sensitivity, accuracy and repeatability were verified. When the detection wavelength was 192 nm, the chromatographic column was Agilent WondaSil C18 Superb (4.6 × 250 mm, 5 μm), the mobile phase was 95% water and 5% acetonitrile mixed solution, the flow rate was 0.8 ml/min, the analysis time was 8 min, the sample size was 1 μL and the column temperature was 40 °C, a liquid phase map of sodium pentazole was obtained. The analysis results showed that the retention time of pentazole sodium was 3.76 min, and showed a good linear relationship in the range of 0.3068–0.3288 g/L. The linear equation is y = -217447.64+835837.85x, the correlation coefficient R2 is 0.99997, and it has good sensitivity, accuracy and repeatability. In addition, three by-products from the synthesis of sodium pentazole were simply separated.

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