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Ibuproxam (CAS 53648-05-8)

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Alternate Names:
2-(4-Isobutylphenyl)-propiohydroxamic acid
CAS Number:
53648-05-8
Molecular Weight:
221.3
Molecular Formula:
C13H19NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Ibuproxam is used to relieve pain and reduce inflammation. It works by inhibiting the production of prostaglandins, which are chemicals that cause pain and inflammation. Ibuproxam is a derivative of ibuprofen and has similar pharmacological properties. It is a white crystalline powder that is sparingly soluble in water. Ibuproxam is used to study the mechanisms of inflammation and pain. Its chemical structure and mode of action are utilized for understanding the biochemistry of inflammation and pain. Ibuproxam is used as a reference standard in analytical chemistry to test the purity of other NSAIDs.


Ibuproxam (CAS 53648-05-8) References

  1. Effects of the host cavity size and the preparation method on the physicochemical properties of ibuproxam-cyclodextrin systems.  |  Mura, P., et al. 1999. Drug Dev Ind Pharm. 25: 279-87. PMID: 10071820
  2. Comparative study of ibuproxam complexation with amorphous beta-cyclodextrin derivatives in solution and in the solid state.  |  Mura, P., et al. 2002. Eur J Pharm Biopharm. 54: 181-91. PMID: 12191690
  3. Thin layer chromatographic resolution of some 2-arylpropionic acid enantiomers using L-(-)-serine, L-(-)-threonine and a mixture of L-(-)-serine and L-(-)-threonine-impregnated silica gel as stationary phases.  |  Aboul-Enein, HY., et al. 2003. Biomed Chromatogr. 17: 325-34. PMID: 12884398
  4. Enantiomeric resolution of some 2-arylpropionic acids using L-(-)-serine-impregnated silica as stationary phase by thin layer chromatography.  |  Aboul-Enein, HY., et al. 2003. J Pharm Biomed Anal. 32: 1055-9. PMID: 12899993
  5. Contact and photocontact allergy to ketoprofen: clinical and experimental study.  |  Mozzanica, N. and Pigatto, PD. 1990. Contact Dermatitis. 23: 336-40. PMID: 2151373
  6. Wetting Kinetics: an Alternative Approach Towards Understanding the Enhanced Dissolution Rate for Amorphous Solid Dispersion of a Poorly Soluble Drug.  |  Verma, S. and Rudraraju, VS. 2015. AAPS PharmSciTech. 16: 1079-90. PMID: 25672820
  7. Mangosteen pericarp extract embedded in electrospun PVP nanofiber mats: physicochemical properties and release mechanism of α-mangostin.  |  Sriyanti, I., et al. 2018. Int J Nanomedicine. 13: 4927-4941. PMID: 30214198
  8. Anti-inflammatory therapy for preventing stroke and other vascular events after ischaemic stroke or transient ischaemic attack.  |  Coveney, S., et al. 2020. Cochrane Database Syst Rev. 5: CD012825. PMID: 32392374
  9. Concomitant Use of NSAIDs or SSRIs with NOACs Requires Monitoring for Bleeding.  |  Lee, MT., et al. 2020. Yonsei Med J. 61: 741-749. PMID: 32882758
  10. `Risk of cardiovascular disease associated with febuxostat versus allopurinol use in patients with gout: a retrospective cohort study in Korea.  |  Jeong, H., et al. 2023. Rheumatol Int. 43: 265-281. PMID: 36346443
  11. ROS-lowering doses of vitamins C and A accelerate malignant melanoma metastasis.  |  Kashif, M., et al. 2023. Redox Biol. 60: 102619. PMID: 36774779
  12. Anti-inflammatory, analgesic and ulcerogenic properties of S-(+)-ibuproxam, racemic ibuproxam-beta-cyclodextrin and S-(+)-ibuproxam-beta-cyclodextrin.  |  Bole-Vunduk, B., et al. 1996. J Pharm Pharmacol. 48: 1153-7. PMID: 8961164
  13. Compatibility study between ibuproxam and pharmaceutical excipients using differential scanning calorimetry, hot-stage microscopy and scanning electron microscopy.  |  Mura, P., et al. 1998. J Pharm Biomed Anal. 18: 151-63. PMID: 9863953

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ibuproxam, 100 mg

sc-471430
100 mg
$156.00