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The area of the qualifier eCl@ss maintaining a kind of production Phenol on the B2B-Portal www.bridge2b.net
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CAS 108-95-2
EINECS/EILINCS/NLP 203-632-7
IUCLID HPVC428
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In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of a hydroxyl group-OH bonded directly to an aromatic hydrocarbon group. - Look up phenol in Wiktionary, the free dictionary. - Phenols can have two or more hydroxy groups bonded to the aromatic rings in the same molecule. The simplest examples are the three benzenediols, each having two hydroxy groups on a benzene ring.
Its cellular uptake is both rapid and passive due to its lipophilic character, and signs of systemic toxicity develop soon after exposure. Phenol's main target organs are the liver and kidney. It may also effect the respiratory and cardiovascular systems. - In the molten state, it is a clear, colourless liquid with a low viscosity. It is soluble in most organic solvents, and solubility is limited in aliphatic solvents. Phenol's solubility. In water is limited at room temperature, above 68C it is entirely water soluble.
Owing to the fact that acetone is miscible with water it serves as an important solvent in its own right, typically as the solvent of choice for cleaning. Which is 19 0 in comparison to phenol with a pKa of 10 0 However, this similarity of acidities of phenol and acetone enol is not observed in the gas phase, and is due to the fact that the difference of solvation energies of the deprotonated acetone enol and phenoxide almost exactly offsets the experimentally observed gas phase acidity difference.
Phenol, also known as carbolic acid, is an organic compound with the chemical formula C6H5OH. It is a white, crystalline solid. This functional group consists of a phenyl, bonded to a hydroxyl-OH. - Edit Properties Phenol is appreciably soluble in water, with about 8 3 g dissolving in 100 ml 0 88 M. - Edit Acidity It is slightly acidic: the phenol molecule has weak tendencies to lose the H+ ion from the hydroxyl group, resulting in the highly water-soluble phenolate anion C6H5O, called phenoxide anion.
Background on phenol, including its physical properties. - This page looks at the structure and physical properties of phenol very old name: carbolic acid. - Giving a structure rather like this: The donation of the oxygen's lone pair into the ring system increases the electron density around the ring. That makes the ring much more reactive than it is in benzene itself. That is explored in another page in this phenol section. It also helps to make the-OH group's hydrogen a lot more acidic than it is in alcohols.
Phenol, also known as carbolic acid, is an organic compound with the chemical formula C6H5OH. - Properties Phenol is appreciably soluble in water, with about 8 3 g dissolving in 100 mL 0 88 M. - It is a reactive molecule. Acidity It is slightly acidic: the phenol molecule has weak tendencies to lose the H+ ion from the hydroxyl group, resulting in the highly water-soluble phenolate anion C6H5O, called phenoxide anion. Smith, Michael B. March, Jerry 2007, Advanced Organic Chemistry: Reactions, Mechanisms, and Structure 6th ed.
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