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. Related Products of 533-73-3
Pandard, Justine;Pan, Na;Ait-Yahiatene, Eric;Grimaud, Laurence;Lemaitre, Frederic;Guille-Collignon, Manon research published 《 From FFN Dual Probe Screening to ITO Microdevice for Exocytosis Monitoring: Electrochemical and Fluorescence Requirements》, the research content is summarized as follows. In this work, four different new fluorescent false neurotransmitters (FFN) probes were synthesized to contribute to the rationale of the FFN design. Their electroactive and spectroscopic properties were investigated. Hence, the optimal excitation and emission wavelengths (from 344 to 393 nm and 423 to 474 nm, resp.) make these probes adapted to fluorescence microscopy. Moreover, their electroactivity were demonstrated to occur at relatively low oxidation potentials for three of them (I, II and III: 0.26, 0.25 and 0.30 V vs. Ag/AgCl, resp.) and at 0.74 V vs. Ag/AgCl for IV on carbon fiber electrodes. However, epifluorescence observations evidenced that the new designed FFN with the best spectroscopic and electrochem. properties (III) did unfortunately not accumulate into secretory vesicles of model BON N13 cells. It thus confirms that V is currently the best “bioelectrofluorescent” compromise. This is why total internal fluorescence reflection microscopy measurements were then studied with the model V and BON N13 cells. Beyond the choice of the appropriate FFN, other anal. requirements are needed. As a consequence, the features of the transparent and conducting indium tin oxide (ITO) microdevice for coupled amperometry-fluorescent measurements were investigated and optimized in terms of effects on the electrochem. performances and reusability. These results pave the way for future coupled investigations of exocytosis with the FFN-ITO device association
Related Products of 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