Shin, Yong-Uk team published research in Separation and Purification Technology in 2022 | 533-73-3

HPLC of Formula: 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.

In general, the hydroxyl group makes alcohols polar. 533-73-3, formula is C6H6O3, Because of hydrogen bonding, alcohols tend to have higher boiling points than comparable hydrocarbons and ethers. HPLC of Formula: 533-73-3

Shin, Yong-Uk;Lim, Jihun;Hong, Seungkwan research published 《 Integrating electrochemical oxidation and flow-electrode capacitive deionization for enhanced organic degradation and perchlorate removal in high salinity waters》, the research content is summarized as follows. This study aimed to assess the application of an electrochem. oxidation (ECO) and flow-electrode capacitive deionization (FCDI) sequential hybrid process for the treatment of high-concentration ions, organic pollutants (i.e., humic acid, alginate, benzoic acid, phenol, and 4-chlorophenol), and marine algae. The ECO system led to the rapid generation of reactive chlorine species (RCS) via anodic oxidation of the boron-doped diamond (BDD) electrode under optimum current in the NaCl-based feed solution, which caused the reduction of total organic carbon (TOC) and the degradation of algae cells. However, the formation of undesirable byproducts (i.e., toxic perchlorate) was triggered by direct electrolysis. Concurrently, the optimal operational conditions of the FCDI system were evaluated based on the monitoring of process performance according to various parameters (i.e., applied voltage, electrode mass loading, electrolyte concentration in the flow electrode, feed solution concentration, and adsorption/desorption phase operation). Finally, the superiority of the ECO-FCDI hybrid process was confirmed and clearly demonstrated via the effective decomposition of organic compounds and the complete removal of toxic perchlorate byproduct together with the effect of deionization. To the best of our knowledge, this work is the first to develop and apply the ECO-FCDI integrated process for the removal of a broad spectrum of pollutants (including both organics and ions) and to attain successful desalination.

HPLC of Formula: 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