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. , Related Products of 533-73-3
Witkowski, Bartlomiej;Jain, Priyanka;Gierczak, Tomasz research published 《 Aqueous chemical bleaching of 4-nitrophenol brown carbon by hydroxyl radicals; products, mechanism, and light absorption》, the research content is summarized as follows. The reaction of hydroxyl radicals (OH) with 4-nitrophenol (4NP) in an aqueous solution was investigated at pH = 2 and 9. The molar yield of the phenolic products quantified was ca. 0.2 at pH = 2 and 0.4 at pH = 9. The yield of 4-nitrocatechol (4NC) was higher at pH = 9. At the same time, a lower number of phenolic products was observed at pH = 9 due to irreversible reactions of some phenols formed at pH > 7. Mineralization investigated with a total organic carbon (TOC) analyzer showed that after 4NP was completely consumed, approx. 85% of the organic carbon remained in the aqueous solution Moreover, as inferred from the TOC measurements and the molar yields of the phenols formed, 65% of the organic carbon that remained in the aqueous solution was attributed to the non-aromatic products. The light absorption of the reaction solution between 250 and 600 nm decreased as a result of the OH reaction with 4NP. However, the 4NP solution showed a noticeable resistance to the chem. bleaching reaction investigated due to the formation of light-absorbing byproducts. This phenomenon effectively prolongs the timescales of the chem. bleaching of 4NP by OH by a factor of 3-1.5 at pH 2 and 9, resp. The exptl. data acquired indicated that both photolysis and the reaction with OH can be important processes for the removal of light-absorbing organic compounds from cloud water particles containing 4NP.
Related Products of 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., 533-73-3.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts