Department of Occupational and Environmental Health, University of Iowa, Iowa City, IA, United States.
Environ Int. 2010 Nov;36(8):835-42. doi: 10.1016/j.envint.2010.02.011. Epub 2010 Apr 10.
Diazomethane is a highly explosive and toxic gas routinely employed for the quantitative and clean derivatization of phenols. We investigated the commercially available trimethylsilyldiazomethane in the presence of diisopropylethylamine as a safe, non-explosive and less-toxic alternative using six phenolic polychlorinated biphenyls as model analytes and fluoro-tagged analogues as internal standards. We compared yields and derivatization times of each method employing a liver microsomal extract as a real matrix. Steric hindrance and electronic properties of the analytes were also investigated. The alternative method afforded equal to higher derivatization yields with increased reaction times, up to 100 min, while explosion and toxic exposure risks were minimized and cost efficiency was increased above 25%. These findings demonstrate that non-explosive trimethylsilyl diazomethane produces comparable derivatization results to the dangerous diazomethane under the conditions studied.
叠氮化甲烷是一种高爆炸和有毒气体,常用于定量和清洁衍生酚类物质。我们研究了在二异丙基乙胺存在下商业上可获得的三甲基硅基叠氮甲烷,将其作为一种安全、非爆炸和低毒性的替代品,使用六种酚类多氯联苯作为模型分析物,并使用氟标记类似物作为内标。我们比较了每种方法的产率和衍生化时间,使用肝微粒体提取物作为真实基质。还研究了分析物的空间位阻和电子性质。替代方法在增加反应时间的情况下提供了相等或更高的衍生化产率,最高可达 100 分钟,同时最小化了爆炸和有毒暴露的风险,并提高了 25%以上的成本效益。这些发现表明,在研究条件下,非爆炸的三甲基硅基叠氮甲烷产生与危险的叠氮甲烷相当的衍生化结果。