Verma, Neha team published research in ChemPhotoChem in 2021 | 533-73-3

Recommanded Product: Benzene-1,2,4-triol, 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.

With respect to acute toxicity, simple alcohols have low acute toxicities. Doses of several milliliters are tolerated. 533-73-3, formula is C6H6O3, For pentanols, hexanols, octanols and longer alcohols, LD50 range from 2–5 g/kg (rats, oral). Ethanol is less acutely toxic.All alcohols are mild skin irritants. Recommanded Product: Benzene-1,2,4-triol

Verma, Neha;Ananthakrishnan, Rajakumar research published 《 Boosted Charge Transfer Efficacy of an All-Solid-State Z-Scheme BiOI-CD-CdS Photocatalyst for Enhanced Degradation of 4-Nitrophenol and Oxidation of Benzyl Alcohol under Visible Light**》, the research content is summarized as follows. Recently, utilization of solar light for chem. reactions has become a popular approach. Inspired by nature, we fabricated a ternary system, BiOI-CD-CdS, which is more durable and shows multiple photocatalytic applications. The incorporated carbon dots (CD) serve as a solid-state electron mediator and Z-scheme facilitator. The material was employed for photooxidative degradation of 4-nitrophenol (a pollutant) and selective oxidation of benzyl alc. into the corresponding aldehyde in an acetonitrile medium. In this study, 10 wt % BiOI-CD-CdS (denoted as 10 wt % BCC) shows the highest photocatalytic performance compared to the individual semiconductors BiOI and CdS, and gave a degradation rate constant (k) of 12.67×10-3 min-1 (4-nitrophenol), which is 17.5 times and 6.5 times higher than its individual components. Moreover, the catalyst offers a 90 % conversion of benzyl alc. to benzaldehyde with high selectivity (98 %). Directed by mechanistic insight, the charge transfer process was observed between BiOI and CdS, where CD serves as an electron mediator/charge separator. The radicals formed by the photocatalysis are superoxide (O2.-), hydroxyl radicals (.OH), and holes (h+). The intermediates and mechanistic pathways were traced using HPLC, GC-MS, and EPR studies. Moreover, the work demonstrated a smart strategy for designing a ternary Z-scheme photocatalytic system, which could be useful for environmental decontamination and selective organic transformation under visible light.

Recommanded Product: Benzene-1,2,4-triol, 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