Industrially, piperidine is produced by the hydrogenation of pyridine, usually over a molybdenum disulfide catalyst: C5H5N + 3 H2 → C5H10NH. 2403-88-5, formula is C9H19NO, Name is 2,2,6,6-Tetramethyl-4-piperidinol. Pyridine can also be reduced to piperidine via a modified Birch reduction using sodium in ethanol. Recommanded Product: 2,2,6,6-Tetramethyl-4-piperidinol.
Wen, Meiting;Ren, Li;Zhang, Jingyan;Jiang, Jingang;Xu, Hao;Guan, Yejun;Wu, Peng research published 《 Designing SAPO-18 with energetically favorable tetrahedral Si ions for an MTO reaction》, the research content is summarized as follows. The silicon (Si) site location in silicoaluminophosphate zeolites has significant influences on their acidic and catalytic properties. Herein, AEI analog silicoaluminophosphates with controlled tetrahedral silicon centers (T sites) were synthesized using specially designed amines as expected organic structure-directing agents (OSDAs). DFT calculations show that the OSDAs with different electronegativity can direct Si atoms into the T sites with more favorable energy advantages. Their catalytic performances in a methanol-to-olefin (MTO) reaction also reflected that OSDAs controlled the Si location in the framework, and the T3 sites had better performance than T1 sites. This finding provides evidence that OSDAs are capable of guiding the Si ions into more favorable T sites, achieving desirable catalytic properties as solid acid catalysts.
2403-88-5, 2,2,6,6-Tetramethyl-4-piperidinol(TEMPO) is a useful research compound. Its molecular formula is C9H19NO and its molecular weight is 157.25 g/mol. The purity is usually 95%.
TEMPO is an intermediate used in the preparation of Piperidinyloxy free radical derivatives.
TEMPO is an organic compound that acts as a radical scavenger. It is stable in the presence of water and air and can be used for the inhibition of bacterial growth. TEMPO reacts with reactive intermediates to form non-reactive substances and terminate chain reactions. This process is optimal at temperatures between 0°C and 40°C and pH values between 3.5 and 7.5. TEMPO has been shown to inhibit the growth of bacteria by reacting with reactive molecules such as amines, chlorides, or low energy radicals in aqueous solution. TEMPO also has genotoxic activity that inhibits DNA synthesis in bacterial cells through oxidation of guanine residues on DNA molecules., Recommanded Product: 2,2,6,6-Tetramethyl-4-piperidinol
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem