IUPAC Name
2-Benzofuran-1,3-dione
Cas Number
85-44-9
HS Code
2917.35.00
Formula
C8H4O3
Appearance
Fine White Powder
Common Names
Isobenzofuran-1,3-dione
Packaging
25 KG PE bag, 1,250 KG Falcon Bag
Phthalic anhydride, with the chemical formula C6H4(CO)2O, acts as the anhydride of phthalic acid and represents a significant commercial form of this acid. It stands as a pioneering example of the widespread use of a dicarboxylic acid anhydride, playing a crucial role in industrial chemistry. Particularly, it is instrumental in the extensive production of plasticizers for plastics, contributing to the estimated global production volume of about 3 million tonnes annually in 2000.
Manufacturing Process:
Discovered by Auguste Laurent in 1836, contemporary synthesis of phthalic anhydride employs various methods, including the oxidation of naphthalene or ortho-xylene. These processes involve vanadium pentoxide (V2O5) as the active oxidant, playing a pivotal role in multiple steps and being regenerated by molecular oxygen. Starting from o-xylene, the oxidation reaction is run at about 320–400 °C and has the following stoichiometry:
C6H4(CH3)2 + 3 O2 → C6H4(CO)2O + 3 H2O
The reaction proceeds with about 70% selectivity. About 10% of maleic anhydride is also produced: C6H4(CH3)2 + 7.5 O2 → C4H2O3 +4 H2O + 4 CO2
Phthalic anhydride and maleic anhydride are recovered by distillation by a series of switch condensers.
The naphthalene route (the Gibbs phthalic anhydride process or the Gibbs–Wohg naphthalene oxidation reaction), a process whose use has declined in compared to the o-xylene route, has the following mechanism:
Phthalic anhydride can also be prepared from phthalic acid by simple dehydration.
Phthalic anhydride, with the chemical formula C6H4(CO)2O, acts as the anhydride of phthalic acid and represents a significant commercial form of this acid. It stands as a pioneering example of the widespread use of a dicarboxylic acid anhydride, playing a crucial role in industrial chemistry. Particularly, it is instrumental in the extensive production of plasticizers for plastics, contributing to the estimated global production volume of about 3 million tonnes annually in 2000.
Manufacturing Process:
Discovered by Auguste Laurent in 1836, contemporary synthesis of phthalic anhydride employs various methods, including the oxidation of naphthalene or ortho-xylene. These processes involve vanadium pentoxide (V2O5) as the active oxidant, playing a pivotal role in multiple steps and being regenerated by molecular oxygen. Starting from o-xylene, the oxidation reaction is run at about 320–400 °C and has the following stoichiometry:
C6H4(CH3)2 + 3 O2 → C6H4(CO)2O + 3 H2O
The reaction proceeds with about 70% selectivity. About 10% of maleic anhydride is also produced: C6H4(CH3)2 + 7.5 O2 → C4H2O3 +4 H2O + 4 CO2
Phthalic anhydride and maleic anhydride are recovered by distillation by a series of switch condensers.
The naphthalene route (the Gibbs phthalic anhydride process or the Gibbs–Wohg naphthalene oxidation reaction), a process whose use has declined in compared to the o-xylene route, has the following mechanism:
Phthalic anhydride can also be prepared from phthalic acid by simple dehydration.
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