Piperidine is an organic compound with the molecular formula (CH2)5NH. This heterocyclic amine consists of a six-membered ring containing five methylene bridges (–CH2–) and one amine bridge (–NH–). 2403-88-5, formula is C9H19NO, Name is 2,2,6,6-Tetramethyl-4-piperidinol. It is a colorless liquid with an odor described as objectionable, and typical of amines. Recommanded Product: 2,2,6,6-Tetramethyl-4-piperidinol.
Hosoya, Kazuki;Yenchit, Saranya;Tadokoro, Yuta;Oya, Kei;Iwamori, Satoru research published 《 Improved singlet oxygen detection sensitivity in electron spin resonance using a spin-trap agent incorporated into a water-soluble polymer film》, the research content is summarized as follows. 2,2,6,6-Tetramethyl-4-piperidinol (TEMP) is a spin-trap agent for ESR (ESR) that is usually employed in solution However, in this study, TEMP is mixed with hydroxypropyl methylcellulose (HPMC) to form a film for the detection of singlet oxygen in vacuo. The ESR intensity achieved is 3.3 times higher than that for a previously reported polyvinyl alc. film. Furthermore, the diffusion of singlet oxygen into HPMC is shown to follow Fick’s law, having a diffusion coefficient of ≈2.5 x 10 -8 cm2 s-1.
Recommanded Product: 2,2,6,6-Tetramethyl-4-piperidinol, 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., 2403-88-5.
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem