Date published: 2026-4-20

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Triamcinolone acetonide (CAS 76-25-5)

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Alternate Names:
Aristoderm; Kenalone, Solodelf
Application:
Triamcinolone acetonide is an inhibitor of IgE-dependent release of histamine
CAS Number:
76-25-5
Molecular Weight:
434.50
Molecular Formula:
C24H31FO6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Triamcinolone acetonide is an antiinflammatory steroid that inhibits the IgE-dependent release of histamine. This is done by human basophils and the growth of NEL-M1 human melanoma cells. It possesses potent anti-inflammatory, immunosuppressive, and anti-allergic properties. Triamcinolone acetonide is derived from the combination of triamcinolone, a steroid hormone, and acetic acid.


Triamcinolone acetonide (CAS 76-25-5) References

  1. A risk-benefit assessment of intranasal triamcinolone acetonide in allergic rhinitis.  |  Gawchik, SM. and Saccar, CL. 2000. Drug Saf. 23: 309-22. PMID: 11051218
  2. Isolating triamcinolone acetonide particles for intravitreal use with a porous membrane filter.  |  Nishimura, A., et al. 2003. Retina. 23: 777-9. PMID: 14707826
  3. Triamcinolone acetonide in ocular therapeutics.  |  Jermak, CM., et al. 2007. Surv Ophthalmol. 52: 503-22. PMID: 17719372
  4. Intraocular sustained-release delivery systems for triamcinolone acetonide.  |  Mansoor, S., et al. 2009. Pharm Res. 26: 770-84. PMID: 19184374
  5. Evaluation of diffusion of triamcinolone acetonide from the distal interphalangeal joint into the navicular bursa in horses.  |  Boyce, M., et al. 2010. Am J Vet Res. 71: 169-75. PMID: 20113224
  6. Pharmacokinetics of triamcinolone acetonide for the treatment of macular edema.  |  Yilmaz, T., et al. 2011. Expert Opin Drug Metab Toxicol. 7: 1327-35. PMID: 21790508
  7. [Triamcinolone acetonide without solvents].  |  Martínez Rubio, M., et al. 2012. Arch Soc Esp Oftalmol. 87: 320-3. PMID: 23021229
  8. Microemulsion containing triamcinolone acetonide for buccal administration.  |  Padula, C., et al. 2018. Eur J Pharm Sci. 115: 233-239. PMID: 29414307
  9. The Role of Excipients in the Stability of Triamcinolone Acetonide in Ointments.  |  van Heugten, AJP., et al. 2018. AAPS PharmSciTech. 19: 1448-1453. PMID: 29450828
  10. Resistance band training after triamcinolone acetonide injection for subacromial bursitis: A randomized clinical trial.  |  Zhu, P., et al. 2021. J Rehabil Med. 53: jrm00140. PMID: 33043381
  11. Nanodelivery of triamcinolone acetonide with PLGA-chitosan nanoparticles for the treatment of ocular inflammation.  |  Xing, Y., et al. 2021. Artif Cells Nanomed Biotechnol. 49: 308-316. PMID: 33739906
  12. Dose identification of triamcinolone acetonide for noninvasive pre-corneal administration in the treatment of posterior uveitis using a rapid, sensitive HPLC method with photodiode-array detector.  |  Khan, MS., et al. 2022. Biomed Chromatogr. 36: e5264. PMID: 34653273
  13. Suprachoroidal Space Triamcinolone Acetonide: A Review in Uveitic Macular Edema.  |  Fung, S. and Syed, YY. 2022. Drugs. 82: 1403-1410. PMID: 36018461
  14. Triamcinolone acetonide. A review of its pharmacological properties and therapeutic efficacy in the management of allergic rhinitis.  |  Jeal, W. and Faulds, D. 1997. Drugs. 53: 257-80. PMID: 9028745

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Triamcinolone acetonide, 50 mg

sc-205872
50 mg
$57.00

Triamcinolone acetonide, 250 mg

sc-205872A
250 mg
$152.00