Maleic anhydride

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Maleic anhydride[1]
Maleic anhydride
Maleic anhydride-3d.png
IUPAC name Furan-2,5-dione
Identifiers
InChI InChI=1/C4H2O3/c5-3-1-2-4(6)7-3/h1-2H
InChIKey FPYJFEHAWHCUMM-UHFFFAOYAP
Standard InChI InChI=1S/C4H2O3/c5-3-1-2-4(6)7-3/h1-2H
Standard InChIKey FPYJFEHAWHCUMM-UHFFFAOYSA-N
CAS number [108-31-6]
EC number 203-571-6
RTECS UE5950000
ChemSpider 7635
SMILES
Properties
Chemical formula C4H2O3
Molar mass 98.06 g/mol
Appearance White crystals
Density 1.48 g/cm3
Melting point

52.8 °C, 326 K, 127 °F

Boiling point

202 °C, 475 K, 396 °F

Solubility in water Reacts
Structure
Hazards
Material safety data sheet (MSDS) MSDS at J. T. Baker
EU classification Corrosive (C)
R-phrases Template:R22, Template:R34, Template:R42/43
S-phrases Template:S2, Template:S22, Template:S26,
Template:S36/37/39, Template:S45
NFPA 704
NFPA 704.png
 
 
 
 
Flash point 102 °C
Related compounds
Other acid anhydrides Succinic anhydride
Other compounds Maleic acid
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)

Maleic anhydride (cis-butenedioic anhydride, toxilic anhydride, dihydro-2,5-dioxofuran) is an organic compound with the formula C4H2O3. In its pure state it is a colourless or white solid with an acrid odour.

Maleic anhydride was traditionally manufactured by the oxidation of benzene or other aromatic compounds. As of 2006, only a few smaller plants continue to use benzene; due to rising benzene prices, most maleic anhydride plants now use n-butane as a feedstock:

2 CH3CH2CH2CH3 + 7 O2 → 2 C2H2(CO)2O + 8 H2O

Characteristic reactions

The chemistry of maleic anhydride is very rich, reflecting its ready availability and bifunctional reactivity.

  • It hydrolyzes, producing maleic acid, cis-HO2CCH=CHCO2H. With alcohols, the half-ester is generated, e.g., cis-HO2CCH=CHCO2CH3.
  • Maleic anhydride is a potent dienophile in Diels-Alder reactions.
  • Maleic anhydride (MA) is an excellent ligand for low-valent metal complexes, examples being Pt(PPh3)2(MA) and Fe(CO)4(MA).

References

  1. Merck Index, 11th Edition, 5586.

External links

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