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用于高效液相色谱法定量分析化学不稳定卤代化合物的三苯甲基烷基化柱前衍生化方法的开发

Development of a Triphenylmethyl Alkylation Pre-Column Derivatization Method for HPLC Quantitative Analysis of Chemically Unstable Halogenated Compounds.

作者信息

Lu Jianwu, Shi Yinfei, Ye Xiaoxia, Yuan Shun, Yang Xiaolong, Sun Xun, Wu Taizhi

机构信息

National Key Laboratory of Lead Druggability Research (NKLLDR), Shanghai Institute of Pharmaceutical Industry, China State Institute of Pharmaceutical Industry, 285 Gebaini Road, Shanghai 201203, China.

Department of Natural Medicine, School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai 201203, China.

出版信息

ACS Omega. 2024 Mar 19;9(13):15311-15319. doi: 10.1021/acsomega.3c09982. eCollection 2024 Apr 2.

Abstract

The primary limitations of the quantitative analysis of thermally labile halogenated compounds by traditional gas chromatography (GC) are the inadequacy of identifying the insufficiently volatile impurity (often with a high boiling point) and the difficulty in obtaining a standard substance with a reliable standardized assay. Taking the 4-(Chloromethyl)-5-methyl-1,3-dioxol-2-one (DMDO-Cl, ) as an example, we reported a triphenylmethanamino-derivatization method to overcome the challenges of the assay determination of such species. During the quantification of , the presence of GC-undetectable polymeric impurity poses a critical challenge in assessing the material quality. Moreover, the standard substance of is not available on the market due to its inherent instability during storage and handling, further complicating the quantitative analysis. In this work, a precolumn HPLC-UV derivatization method based on triphenylmethanamino-alkylation was developed to quantitatively analyze . The resulting derivative exhibits excellent crystallinity and superior physical and chemical stability and possesses effective chromophores for UV detection. The conversion from analyte to derivative demonstrates desirable reactivity and purity, facilitating quantitative analysis using the external standard method. The chemical derivatization-chromatographic detection method was optimized and validated, demonstrating its high specificity, good linearity, precision, accuracy, and stability. This method offers a valuable alternative to the general quantitative NMR (qNMR) detection technique, which exhibits reduced specificity in the presence of increased levels of impurities in compound .

摘要

传统气相色谱法(GC)对热不稳定卤代化合物进行定量分析的主要局限性在于,难以鉴定挥发性不足的杂质(通常沸点较高),且难以获得具有可靠标准化测定的标准物质。以4-(氯甲基)-5-甲基-1,3-二氧戊环-2-酮(DMDO-Cl)为例,我们报道了一种三苯甲烷氨基衍生化方法,以克服对此类物质进行测定的挑战。在对DMDO-Cl进行定量时,气相色谱无法检测到的聚合物杂质的存在,对评估材料质量构成了重大挑战。此外,由于其在储存和处理过程中固有的不稳定性,DMDO-Cl的标准物质在市场上无法获得,这进一步使定量分析复杂化。在这项工作中,开发了一种基于三苯甲烷氨基烷基化的柱前高效液相色谱-紫外衍生化方法,用于对DMDO-Cl进行定量分析。所得衍生物表现出优异的结晶性以及卓越的物理和化学稳定性,并拥有用于紫外检测的有效发色团。从分析物DMDO-Cl到衍生物的转化显示出理想的反应活性和纯度,便于使用外标法进行定量分析。对化学衍生化-色谱检测方法进行了优化和验证,证明了其高特异性、良好的线性、精密度、准确度和稳定性。该方法为通用定量核磁共振(qNMR)检测技术提供了一种有价值的替代方法,在化合物中杂质水平增加时,qNMR检测技术的特异性会降低。

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