Simple alcohols are found widely in nature. Ethanol is the most prominent because it is the product of fermentation, a major energy-producing pathway. 533-73-3, formula is C6H6O3, Other simple alcohols, chiefly fusel alcohols, are formed in only trace amounts. More complex alcohols however are pervasive, as manifested in sugars, some amino acids, and fatty acids. , Name: Benzene-1,2,4-triol
Dai, Yuxuan;Wang, Yuting;Zuo, Gancheng;Kong, Jijie;Guo, Yang;Sun, Cheng;Xian, Qiming research published 《 Photocatalytic degradation mechanism of phenanthrene over visible light driven plasmonic Ag/Ag3PO4/g-C3N4 heterojunction nanocomposite》, the research content is summarized as follows. Visible light driven plasmonic Ag/Ag3PO4/g-C3N4 heterojunction nanocomposite with regular morphol. was prepared via a modified facile method. The two-dimensional ultrathin g-C3N4 nanosheet is uniformly wrapped on the surface of Ag3PO4 nanopolyhedron. A charge transfer bridge was built between Ag3PO4 nanopolyhedron and g-C3N4 nanosheet due to the reduction of Ag nanoparticles. This structure can inhibit the recombination of photogenerated electron-hole pairs and promote the transfer of photogenerated carriers, so as to produce more active species for participating in the photocatalytic reaction. In addition, the surface plasmon resonance (SPR) of appropriate Ag nanoparticles enhanced the absorption and utilization of visible light. Compared with Ag3PO4 and Ag/Ag3PO4, Ag/Ag3PO4/g-C3N4 showed higher photocatalytic activity. Under visible light irradiation, the degradation rate of phenanthrene (PHE) was 0.01756 min-1, which was 3.14 times and 2.38 times that of Ag3PO4 and Ag/Ag3PO4, resp. After four cycles of photocatalytic reaction, the Ag/Ag3PO4 /g-C3N4 photocatalyst still maintained high photocatalytic activity. The active sites of PHE were predicted by Gaussian simulation calculation and combined with intermediate products identification of GC-MS, the possible degradation pathway of PHE was speculated. This research has reference significance for the construction of plasmonic heterojunction photocatalyst in the field of environmental pollution remediation.
533-73-3, Benzene-1, 2, 4-triol, also known as hydroxyhydroquinone or 1, 2, 4-benzenetriol, belongs to the class of organic compounds known as hydroxyquinols and derivatives. Hydroxyquinols and derivatives are compounds containing a 1, 2, 4-trihydroxybenzene moiety. Benzene-1, 2, 4-triol is soluble (in water) and a very weakly acidic compound (based on its pKa). Outside of the human body, benzene-1, 2, 4-triol can be found in tea. This makes benzene-1, 2, 4-triol a potential biomarker for the consumption of this food product.
Benzene-1,2,4-triol is a benzenetriol carrying hydroxy groups at positions 1, 2 and 4. It has a role as a mouse metabolite.
1,2,4-Benzenetriol is a metabolite of benzene.
1,2,4-Benzenetriol is an intermediary metabolite of benzene that is present in roasted coffee beans. It is mutagenic and it causes cleaving of DNA single strands by the generation of reactive oxygen species.
1,2,4-Benzenetriol is a reactive molecule that has been shown to have hydrogen bonding interactions with copper chloride. It has been proposed as an inhibitor of methyltransferase, which is involved in the synthesis of methionine. Studies have shown that 1,2,4-Benzenetriol can also inhibit iron homeostasis and transfer reactions. The x-ray diffraction data for this compound shows that it forms a complex with the hydroxyl group. This complex is stabilized by hydrogen bonding interactions with the hydroxylic proton of the 1,2,4-benzenetriol molecule. 1,2,4-Benzenetriol has been shown to be toxic to HL-60 cells and K562 cells at concentrations greater than 5 mM. It has also been found to be effective against chlorogenic acids and other compounds in energy metabolism studies at concentrations between 0.5 and 2 mM., Name: Benzene-1,2,4-triol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts