Journal of the American Chemical Society, 132(31), 10741-10747 (2010-08-05)
Azodicarboxamides (R(2)NCON=NCONR(2)) are shown to act as new templates for the assembly of unprecedented azo-functionalized hydrogen-bond-assembled [2]rotaxanes. Moreover, these binding sites can be reversibly and efficiently interconverted with their hydrazo forms through a hydrogenation-dehydrogenation strategy of the nitrogen-nitrogen bond. This
Catalytic oxidation of hydrazodicarboxamide to azodicarboxamide by oxygen.
Kaszonyi A, et al.
J. Mol. Catal., 80(3), L13-L17 (1993)
Fourier transform infrared spectrometry (FTIR) for qualitative and quantitative analysis of azodicarboxamide and its potential impurities.
Otte X, et al.
Analytica Chimica Acta, 355(1), 7-13 (1997)
Fourier transform infrared spectrometry (FTIR) for qualitative and quantitative analysis of azodicarboxamide and its potential impurities.
We recently demonstrated that azodicarbonamide is an immunosuppressive compound that inhibits calcium mobilization in T lymphocytes. In this study, we show that azodicarbonamide prevents the progression of human CD4+ T lymphocytes into the G1 phase of the cell cycle, inhibits
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