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Hydroquinone CAS#123-31-9

Hydroquinone CAS#123-31-9
Iupac Name:benzene-1,4-diol
CAS No.: 123-31-9
Molecular Weight:110.11064
Introduction:
Hydroquinone (C6H6O2) is a phenolic organic compound belonging to the class of aromatic hydrocarbons with hydroxyl functional groups. It exists at room temperature as a white to off-white crystalline solid with a mild, characteristic odor. The compound is known for its ability to undergo oxidation, often turning brown upon exposure to air or light due to the formation of quinone derivatives. It is moderately soluble in water and highly soluble in organic solvents such as ethanol and ether, which facilitates its use in various chemical and industrial applications.

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PRODUCT DESCRIPTION

PropertyValue
Density1.3±0.1 g/cm³
Boiling Point286.0±0.0 °C at 760 mmHg
Melting Point172-175 °C (lit.)
Molecular FormulaC₆H₆O₂
Molecular Weight110.111
Flash Point141.6±14.4 °C
Exact Mass110.036781
PSA40.46000
LogP0.64
Vapour Density3.81 (vs air)
Vapour Pressure0.0±0.6 mmHg at 25°C
Index of Refraction1.612
StabilityStable. Combustible. Incompatible with strong oxidizing agents, strong bases, oxygen, ferric salts. Light and air-sensitive. Discolours in air.
Water Solubility70 g/L (20 °C)
Use and Manufacturing

1 DefinitionChEBI: A benzenediol comprising benzene core carrying two hydroxy substituents para to each other.

2 General DescriptionLight colored crystals or solutions. May irritate the skin, eyes and mucous membranes. Mildly toxic by ingestion or skin absorption.

3 Produe MethodThere are three current manufacturing processes for HQ:oxidative cleavage of diisopropylbenzene, oxidation of aniline,and hydroxylation of phenol.Diisopropylbenzene is air oxidized to the intermediatediisopropylbenzene bishydroperoxide. This hydroperoxideis purified by extraction and reacted further to formhydroquinone. The purified product is isolated by filtrationand packaged. The process can be almost entirely closed,continuous, computer-controlled, and monitored.HQcan also be prepared by oxidizing aniline to quinone inthe presence of manganese dioxide and sulfuric acid.p-Benzoquinone is then reduced to HQ using iron oxide.The resulting hydroquinone is crystallized and dried.The process occurs in a closed system.HQis also manufactured by hydroxylation of phenol usinghydrogen peroxide as a hydroxylation agent. The reaction iscatalyzed by strong mineral acids or ferrous or cobalt salts.

4 Purification MethodsCrystallise quinol from acetone, *benzene, EtOH, EtOH/*benzene, water or acetonitrile (25g in 30mL), preferably under nitrogen. Dry it under vacuum. [Wolfenden et al. J Am Chem Soc 109 463 1987, Beilstein 6 H 836, 6 IV 5712.] Hydroquinone Preparation Products And Raw materials Preparation Products

5 UsageUse as photographic reducer and developer; as reagent in the determination of small quantities of phosphate; as antioxidant. Depigmentor

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