Copper ibuprofenate

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Copper ibuprofenate
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Anhydrous
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Monohydrate
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R = (CH3)2CHCH2C6H4CH(CH3)-
Names
IUPAC name
bis[2-(4-isobutylphenyl)propionato]copper(II)
Identifiers
3D model (JSmol)
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  • InChI=1S/4C13H17O2.2Cu/c41-9(2)8-11-4-6-12(7-5-11)10(3)13(14)15;;/h44-7,9-10H,8H2,1-3H3;;/q4*-3;2*+6
    Key: HEFOJHHJEKPEDO-UHFFFAOYSA-N
  • c0cc(CC(C)C)ccc0C(C)C-OCu+2(OC-C(C)c0ccc(CC(C)C)cc0)OC-C(C)c0ccc(CC(C)C)cc0
Properties
C52H68Cu2O8
Molar mass 948.200 g·mol−1
Appearance Blue Powder
Density 1.299 g/cm3[1]
Slightly soluble
Solubility in isopropanol Slightly soluble
Related compounds
Related compounds
Copper aspirinate

Ibuprofen

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Copper ibuprofenate is a coordination complex consisting of copper(II) and the conjugate base of ibuprofen. The compound is prepared by the reaction of sodium ibuprofenate with copper(II) sulfate.[2][3]

Copper ibuprofenate adopts a typical Chinese lantern structure, as seen for many transition metal carboxylate complexes. X-ray crystallography reveals a polymer with a bonding motif very similar to that of copper(II) trifluoroacetate.[1]

It has been suggested that copper complexes of anti-inflammatory drugs are more active than the parent drug[4] and produce fewer gastrointestinal side-effects.[5] In 2008, a United States patent was issued for the utilization of ibuprofenate complexes (including copper ibuprofenate) as a wood preservative.[6]

References

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