同位素 ›› 2010, Vol. 23 ›› Issue (4): 206-210.DOI: 10.7538/tws.2010.23.04.0206

• 特约专栏:稳定同位素制备及应用技术 • 上一篇    下一篇

13C,15N3-盐酸氨基脲合成方法的优化

王伟;杜晓宁;刘占峰;李良君;宋明鸣;李杰   

  1. 上海化工研究院,上海200062
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2010-11-20 发布日期:2010-11-20

Study on Synthesis of 13C, 15N3-Semicarbazide Hydrochloride

WANG Wei;DU Xiao-ning;LIU Zhan-feng;LI Liang-jun;SONG Ming-ming;LI Jie   

  1. Shanghai Research Institute of Chemical Industry, Shanghai 200062, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2010-11-20 Published:2010-11-20

摘要: 采用13C,15N2双标记尿素和15N2标记水合肼为原料,经回流反应一步合成13C,15N3-盐酸氨基脲。通过单因素考察和正交实验对13C,15N3-盐酸氨基脲的合成工艺进行优化,得到最优反应条件为:15N2-水合肼与13C,15N2-尿素的进料摩尔比为1.4∶1,加热温度为135 ℃,反应时间为4.5 h。采用此优化合成条件单步合成反应收率>90%,13C,15N3-盐酸氨基脲纯度≥98%,13C丰度≥97%,15N丰度≥99%。结果显示,该方法具有反应周期短,产物收率高,后处理简便易行等优点。

关键词: 13C,15N双标记, 盐酸氨基脲, 合成

Abstract: The 13C,15N2 doubly labeled Urea and 15N2 labeled Hydrazine hydrate were used as raw materials, and 13C,15N3-SEM·HCl was synthesized by a direct one-step synthesis which based on the reflux reacting. The reaction conditions of 13C,15N3 labeled semicarbazide hydrochloride were mainly investigated by the experiment designs, like singlefactor design and orthogonal design. The following optimized conditions were obtained as follow: the mole ratio 15N2-N2H4 to 13C,15N2-urea was 1.4∶1, the reaction temperature was 135 ℃, the reaction time was 4.5 h, and the yield of 13C,15N3 labeled semicarbazide hydrochloride was above 90%, the purity ≥98%, the abundance of 13C ≥97%, the abundance of 15N ≥99%. This technology had many advantages, like short production cycle, high yield and sample later-processing.

Key words: 13C, 15N doubly labeling, SEM•, HCl, synthesis