Oxidative degradation of fentanyl in aqueous solutions of peroxides and hypochlorites was written by Qi, Lihong;Cheng, Zhenxing;Zuo, Guomin;Li, Shanmao;Fan, Qiping. And the article was included in Defence Science Journal in 2010.Category: amides-buliding-blocks This article mentions the following:
Fentanyl widely used in clinics as practices is potentially utilized as an incapacitant in countering terrorism and its analogs would be used as an addictive drug, so the degradation of these compounds need to be investigated for protecting environment and human health. The degradation of fentanyl was examined in a series of oxidant aqueous solutions The degradation pathways of fentanyl in the oxidant solution are discussed according to all products identified by GC/MS and LC/MS. In the experiment, the researchers used many compounds, for example, N,N-(Ethane-1,2-diyl)bis(N-acetylacetamide) (cas: 10543-57-4Category: amides-buliding-blocks).
N,N-(Ethane-1,2-diyl)bis(N-acetylacetamide) (cas: 10543-57-4) belongs to amides. In primary and secondary amides, the presence of N–H dipoles allows amides to function as H-bond donors as well. Thus amides can participate in hydrogen bonding with water and other protic solvents; the oxygen atom can accept hydrogen bonds from water and the N–H hydrogen atoms can donate H-bonds. Ionic, or saltlike, amides are strongly alkaline compounds ordinarily made by treating ammonia, an amine, or a covalent amide with a reactive metal such as sodium.Category: amides-buliding-blocks
Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics