Parwaz Khan, Aftab Aslam team published research in Journal of Industrial and Engineering Chemistry (Amsterdam, Netherlands) in 2021 | 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., Formula: C6H6O3

Formula: C6H6O3, In chemistry, an alcohol is a type of organic compound that carries at least one hydroxyl functional group (−OH) bound to a saturated carbon atom. 533-73-3, name is Benzene-1,2,4-triol, An important class of alcohols, of which methanol and ethanol are the simplest examples, includes all compounds which conform to the general formula CnH2n+1OH.

Parwaz Khan, Aftab Aslam;Singh, Pardeep;Raizada, Pankaj;Asiri, Abdullah M. research published 《 Converting Ag3PO4/CdS/Fe doped C3N4 based dual Z-scheme photocatalyst into photo- Fenton system for efficient photocatalytic phenol removal》, the research content is summarized as follows. In this work, a dual Z-scheme Ag3PO4/CdS/Fe-g-C3N4 (AP/CdS/FeCN) photocatalyst was prepared by precipitation- deposition method. AP/CdS/FeCN photocatalyst was converted into the heterogenous photo-Fenton system with the addition of H2O2. The synergistic coupling between AP/CdS/FeCN and H2O2 resulted in enhanced for phenol degradation, with a rate constant of constant 6.2 x 10-4 s-1, which is 1.31 and 1.61 times than that of AP/CdS/FeCN and Fe2O3/H2O2. The enhancement in photodegradation was attributed to (i) more regeneration of Fe2+ ions, (ii) enhanced visible light absorption, (iii) elevated redox potential due to more hydroxyl radical′ s formation, and (iv) low Fe leaching in the reaction solution As indicated by EIS, PL, and trapping experiments, photoinduced CB electrons of g-C3N4 and CdS were transferred entirely to Fe3+ to regenerate Fe2+ ions to accelerate the Fenton cycle. In comparison to the conventional Fe2O3/H2O2 Fenton process, Fe ion leaching in AP/CdS/FeCN/H2O2 catalytic system was almost negligible. It confirmed strong chem. interaction of Fe3+ with g-C3N4. AP/CdS/FeCN/H2O2 displayed significant catalytic efficacy and firmness for five successive catalytic cycles. Moreover, the AP/CdS/FeCN/H2O2 nanocomposite exhibited substantial mineralization perfomance for other phenolic pollutants. The results demonstrate that AP/CdS/FeCN/H2O2 catalytic system has the potential for water purification

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., Formula: C6H6O3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts