Hydrocortisone Acetate

• Formula: C₂₃H₃₂O₆
• Molecular weight: 404.4966
• IUPAC Standard InChI: InChI=1S/C23H32O6/c1-13(24)29-12-19(27)23(28)9-7-17-16-5-4-14-10-15(25)6-8-21(14,2)20(16)18(26)11-22(17,23)3/h10,16-18,20,26,28H,4-9,11-12H2,1-3H3/t16-,17-,18-,20+,21-,22-,23-/m1/s1 Copy

  
• IUPAC Standard InChIKey: ALEXXDVDDISNDU-MCHRFJOXSA-N Copy
• CAS Registry Number: 50-03-3
• Chemical structure:
  This structure is also available as a 2d Mol file
• Stereoisomers:
  • Pregn-4-ene-3,20-dione,11beta,17alpha,21-trihydroxy-,21 acetate
• Other names: Hydrocortisone 21-acetate; Pregn-4-ene-3,20-dione, 21-(acetyloxy)-11,17-dihydroxy-, (11β)-; Abbocort; Aceto-Cort; Bambicort; Berlison F; Biocortar; Carmol HC; Chemysone; Collusul-HC; Compound F acetate; Cortacream; Cortaid; Cortef acetate; Cortell; Cortes; Corticosterone, 17-hydroxy-, 21-acetate; Cortifoam; Cortisol acetate; Cortisol, 21-acetate; Cortril acetate; Cortril acetate-AS; Eye-Cort; Fernisone; Hycortole acetate; Hydrin-2; Hydrocortisat; Hydrocortistab; Hydrocortone acetate; Hydrosone; Hydroxycorticosterone acetate; Hysone-A; HA; Isopto-Hydrocortisone; Lanacort; Mysone; Pabracort; Pregn-4-ene-3,20-dione, 11β,17,21-trihydroxy-, 21-acetate; Resicort; 11β,17α-Dihydroxy-21-acetoxypregesterone; 17α-Hydrocorticosterone-21-acetate; 17α-Hydroxycorticosterone acetate; 17-Hydroxycorticosterone acetate; 17-Hydroxycorticosterone-21-acetate; 21-Acetoxy-11β,17α-dihydroxypregn-4-ene-3,20-dione; Acetate-AS; NSC 741; Pregn-4-ene-3,20-dione, 21-(acetoxy)-11,17-dihydroxy-, (11-β)-; Anusol-HC; CaldeCort; Colifoam; Colofoam; Cordes; Efcolin; Hc45; Hydrocal; Lenirit; Sigmacort; Sintotrat; Velopural; 11,17-Dihydroxy-3,20-dioxopregn-4-en-21-yl acetate, (11β)-; Wycort; Proctocort; 11β,17α,21-Trihydroxypregn-4-ene-3,20-dione 21-acetate; 21-Acetoxy-11β,17-dihydroxypregn-4-en-3,20-dione; 21-Acetoxy-11β,17-dihydroxypregn-4-ene-3,20-dione
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• Information on this page:
  • Phase change data
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: William E. Acree, Jr., James S. Chickos

Enthalpy of fusion

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Cenuse and Meltzer, 1997
Cenuse, Z.; Meltzer, V., DSC characterization of drugs containing cyclopentanophenanthrene nucleus, An. Univ. Bucuresti. Chimie, 1997, 6, 101. [all data]

Regosz, Chmielewska, et al., 1994
Regosz, A.; Chmielewska, A.; Pelplinska, T.; Kowalski, P., Prediction of the solubility of steroid hormones, Pharmazie, 1994, 49, 5, 371. [all data]

Notes

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• Symbols used in this document:
  

  ΔfusH

  Enthalpy of fusion

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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