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再探N-亚硝基二乙醇胺。

N-Nitrosodiethanolamine revisited.

作者信息

Andersen J R, Batsberg W, Carlsen L, Egsgaard H, Larsen E, Senning A, Senning A

出版信息

Biomed Mass Spectrom. 1980 May;7(5):205-10. doi: 10.1002/bms.1200070506.

Abstract

N-nitrosodiethanolamine is believed to be a weakly carcinogenic chemical, and as it occurs widely--in consumer products for example--it may constitute a significant hazard to humans. However, the chemical evidence concerning the identity, purity and properties of N-nitrosodiethanolamine is incomplete, and this casts some doubt on the basis of the current interest in this substance. In the present paper a purification procedure of synthetic N-nitrosodiethanolamine based on high-performance liquid chromatography is given. Other fractionation procedures such as gas liquid chromatography, ambient pressure column chromatography and distillation are shown to be inadequate. The purity and identity of purified N-nitrosodiethanolamine is established by means of electron impact and field ionization mass spectrometry, including metastable defocusing and collision induced decomposition techniques. Furthermore, 1H and 13C nuclear magnetic resonance and, to a lesser extent, infrared and ultraviolet spectroscopy are used. Deuterium labelled analogues of N-nitrosodiethanolamine and the parent diethanolamine are employed in rationalizing the results obtained.

摘要

N-亚硝基二乙醇胺被认为是一种弱致癌化学物质,由于它广泛存在——例如在消费品中——它可能对人类构成重大危害。然而,关于N-亚硝基二乙醇胺的身份、纯度和性质的化学证据并不完整,这使得目前对该物质的关注缺乏依据。本文给出了基于高效液相色谱法的合成N-亚硝基二乙醇胺的纯化程序。结果表明,气液色谱法、常压柱色谱法和蒸馏法等其他分馏程序并不适用。纯化后的N-亚硝基二乙醇胺的纯度和身份通过电子轰击和场电离质谱法确定,包括亚稳散焦和碰撞诱导分解技术。此外,还使用了1H和13C核磁共振,以及程度较低的红外和紫外光谱。N-亚硝基二乙醇胺和母体二乙醇胺的氘代类似物被用于解释所得结果。

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