Selakjani, Peyman Pouresmaeel team published research in International Journal of Adhesion and Adhesives 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

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. , Formula: C6H6O3

Selakjani, Peyman Pouresmaeel;Dorieh, Ali;Pizzi, Antonio;Shahavi, Mohammad Hassan;Hasankhah, Amir;Shekarsaraee, Sara;Ashouri, Marzieh;Movahed, Sogand Ghafari;Abatari, Mohadese Niksefat research published 《 Reducing free formaldehyde emission, improvement of thickness swelling and increasing storage stability of novel medium density fiberboard by urea-formaldehyde adhesive modified by phenol derivatives》, the research content is summarized as follows. Notwithstanding the enormous benefits of medium d. fiberboard, free formaldehyde emission and low water resistance are the significant disadvantages to reducing their application. In this research, phenolic compounds such as phenol, 1,2,4-trihydroxy benzene (hydroxyquinol), and 4-tert-Bu catechol in various amounts were added to an industrial-grade liquid urea-formaldehyde polymer in an attempt to alleviate these defects. Medium d. fiberboard panels were manufactured from the modified urea-formaldehyde resins. The panels’ phys. and mech. properties, such as thickness swelling, water absorption, formaldehyde emission, modulus of rupture, modulus of elasticity, and internal bond strength were then investigated. The results showed that the free formaldehyde emission contents for the modified composite panels ranged from 25.4% to 50.1% lower than for the unmodified panel. Also, the lowest and highest levels of thickness swelling occurred with the medium d. fiberboard panels bonded with UF-P1 and the unmodified urea-formaldehyde, resp. The results clearly showed that the urea-formaldehyde polymer’s storage capacity increased substantially with the addition of phenolic derivatives The produced novel medium d. fiberboard results can be said to substantially lower environmental and health hazards associated with these materials and have a beneficial effect on the water transport characteristics exhibited by these materials. Consequently, this research may play a role as a useful stepping-stone for solving the fundamental problems of medium d. fiberboard production industries.

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