Zhang, Liangliang team published research on Applied Catalysis, B: Environmental in 2021 | 2403-88-5

Related Products of 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., 2403-88-5.

Piperidine structural motif is present in numerous natural alkaloids. These include piperine, which gives black pepper its spicy taste. This gave the compound its name. 2403-88-5, formula is C9H19NO, Name is 2,2,6,6-Tetramethyl-4-piperidinol. Other examples are the fire ant toxin solenopsin, the nicotine analog anabasine of tree tobacco (Nicotiana glauca), lobeline of Indian tobacco. Related Products of 2403-88-5.

Zhang, Liangliang;Wang, Kai;Yu, Luying;Luo, Kaijie;Guo, Shaopeng;Chen, Hong;Li, Xiang;Chen, Yonghang;Yu, Xin;Qian, Yajie;Liu, Yanbiao;Xue, Gang research published 《 Why does sludge-based hydochar activate peroxydisulfate to remove atrazine more efficiently than pyrochar》, the research content is summarized as follows. Sludge-derived hydrochar (HC) and pyrochar (PC) by hydrothermal and pyrolytic treatments were compared their peroxydisulfate (PDS) activation capacities toward atrazine (ATZ) removal. The HC alone induced lower ATZ removal than PC alone. However, ATZ removal was significantly enhanced in HC/PDS system rather than in PC/PDS system. ATZ removal via adsorption was very low, and singlet oxygen (1O2) primarily contributed to its removal, independently on the PDS addition Compared to HC, PC possessed stronger electron transfer capacity, exhibiting a higher ATZ removal. After PDS addition, humic substances (HS) in HC (36.3 ± 2.4 mg/g) played a decisive role in enhanced ATZ degradation: PDS excited HS to a triplet state (3HS*); then, PDS and 3HS* together yielded more 1O2. Meanwhile, 3HS* accelerated electron transfer on HC surface. Thus, more electrons were transferred from AZT to 1O2. However, function of small amount of HS in PC (1.5 ± 0.2 mg/g) could be ignored.

Related Products of 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., 2403-88-5.

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem