Wu, Zhifang team published research in New Journal of Chemistry in 2022 | 533-73-3

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., COA of Formula: C6H6O3

In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 533-73-3, formula is C6H6O3, Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble. COA of Formula: C6H6O3

Wu, Zhifang;Fu, Wencai;Xu, Huixia;Zheng, Rui;Han, Fangjie;Liang, Zhishan;Han, Dongfang;Han, Dongxue;Li, Fenghua;Niu, Li research published 《 A simple preparation method of in situ oxidized titanium carbide MXene for photocatalytic degradation of catechol》, the research content is summarized as follows. Photocatalytic systems have been widely applied to treat the highly toxic and refractory aromatic sewage water pollution problem. However, the development of highly active and excellent durability photocatalysts has always been the long-term challenge for water pollution control. In this work, a kind of MXene (MX) Ti3C2-TiO2 composite has been successfully fabricated by in situ oxidation using a simple method. The removal efficiencies of MX-TiO2(200) for catechol (CC) were up to 92% under simulated sunlight radiation for 90 min, with a rate constant k of 0.0243 min-1. Compared with pristine MX Ti3C2, such a Ti3C2-TiO2 composite remarkably accelerated the formation rates of O2– and OH due to its metallic nature and large sp. surface area, which further accelerates the migration of photogenerated carriers (generated by TiO2) to Ti3C2. The activity of the MX-TiO2(200) did not show noticeable variation after 5-times recycling. A possible Schottky barrier electron transfer mechanism for MX-TiO2 composite degradation of catechol pollutants was further proposed. The MX-TiO2(200) composite developed in this study exhibits great potential as an ideal photocatalyst for application in phenolic pollutant wastewater treatment.

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., COA of Formula: C6H6O3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts