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Triamcinolone acetonide EP impurity E

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Triamcinolone acetonide EP impurity E, >98%

CAS No. : [1524-86-3]

Synonyms : 1,2-Dihydrotriamcinolone acetonide; 9-Fluoro-16α,17-(isopropylidenedioxy)cortico sterone; 11β,16α,17α,21-Tetrahydroxy-9α-fluoropregn-4-ene-3,20-dione 16,17-acetonide; (11β, 16α)-9-Fluoro-11,21-dihydroxy-16,17-[(1-methylethylidene)bis(oxy)]pregn-4-ene-3,20-dione; 9-Fluoro-11β,21-dihydroxy-16α,17-(1-methylethylidenedioxy)pregna-4-ene-3,20-dione

IUPAC Name : (6aS,6bR,7S,8aS,8bS,11aR,12aS,12bS)-6b-Fluoro-7-hydroxy-8b-(2-hydroxyacetyl)-6a,8a,10,10-tetramethyl-1,2,5,6,6a,6b,7,8,8a,8b,11a,12,12a,12b-tetradecahydro-4H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-4-one

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25MGRequest A Quote
In Stock  Estimated to ship on 20 September 2026
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Chemical Properites
Mol. Formula :
C24H33FO6
Mol. Weight :
436.52
Appearance :
Pale brown solid
Melting Point :
Not available
Solubility :
MeOH
For Laboratory research use only, not for drug, household or other uses.

Applications : This is an impurity of Triamcinolone acetonide, that inhibits fibroblast growth factor (bFGF)-induced proliferation of retinal endothelial cells, reduces chondrocyte viability leading to cartilage destruction, and activates anti-inflammatory macrophages. Triamcinolone acetonide is also used to study diseases like atopic dermatitis.

References : Spandau U. H. M. et al.: British journal of ophthalmology, 89(6), 745-747, 2005; Euppayo T. et al.: In Vitro Cellular & Developmental Biology-Animal., 52(7), 723-735, 2016; Siebelt M. et al.: Arthritis research & therapy., 17(1), 1-13, 2015; Jensen J. M. et al.: Acta Dermato-Venereologica., 93(5), 515-519, 2013; Zhen X. et al.: Int. J. Biol Sci., 16(13), 2382-2391, 2020.

Storage : Keep container tightly closed under nitrogen or argon and refrigerate for long-term shelf life.

Caution : In case of contact with skin or eyes, rinse immediately with plenty of water and seek medical advice. Wear suitable protective clothing and gloves.

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