Hydrocortisone
- Formula: C21H30O5
- Molecular weight: 362.4599
- IUPAC Standard InChI: InChI=1S/C21H30O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h9,14-16,18,22,24,26H,3-8,10-11H2,1-2H3/t14-,15-,16-,18+,19-,20-,21-/m1/s1
- IUPAC Standard InChIKey: JYGXADMDTFJGBT-NDNUHCHRSA-N
- CAS Registry Number: 50-23-7
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Stereoisomers:
- Other names: Hydroxycortisone; Pregn-4-ene-3,20-dione, 11,17,21-trihydroxy-, (11β)-; Cortisol; anti-Inflammatory hormone; Cobadex; Cort-Dome; Cortanal; Cortef; Cortenema; Corticreme; Cortifan; Cortiment; Cortispray; Cortonema; Cortril; Dihydrocostisone; Domolene-HC; Efcorbin; Epiderm H; Esiderm H; Ficortril; Genacort; Heb-Cort; Hidro-Colisona; Hycort; Hycortol; Hycortole; Hydrasson; Hydro-Adreson; Hydrocorticosterone; Hydrocortisone alcohol; Hydrocortisyl; Hydrocortone; Hytone lotion; HC; Incortin-H; Kendall's Compound F; NSC 10483; Optef; Otosone-F; Permicort; Polcort H; Reichstein's Substance M; Scheroson F; Signef; Tarcortin; Texacort lotion 25; Topicort; Traumaide; 11β-Hydroxycortisone; 17α-Hydroxycorticosterone; 17-Hydroxycorticosterone; 4-Pregnen-11β,17α,21-triol-3,20-dione; Aeroseb HC; Ala-Scalp; Alacort; Barseb HC; Cetacort; Cleiton; Compound F; Compound F (kendall); Cortisol alcohol; Cortolotion; Cortoxide; Cremesone; Delacort; Dermacort; Dermolate; Efcortelan; Efcortelin; Eldecort; Eldercort; Epicort; Fiocortril; H-Cort; Hydro-colisona; Hydrocortisone free alcohol; Hydrocortistab; Hytone; Incortin-hydrogen; Komed HC; Maintasone; Pregn-4-ene-3,20-dione, 11β,17,21-trihydroxy-; Proctocort; Rectoid; 11β-Hydrocortisone; 11β,17α,21-Trihydroxy-4-pregnene-3,20-dione; 11β,17α,21-Trihydroxypregn-4-ene-3,20-dione; 11β,17,21-Trihydroxypregn-4-ene-3,20-dione; 4-Pregnene-11β,17α,21-triol-3,20-dione; Acticort; CaldeCort Spray; Lacticare-HC; Nutracort; Penecort; 11,17,21-Trihydroxypregn-4-ene-3,20-dione, (11β)-; 11β,17,21-trihydroxyprogesterone; Dioderm; Anflam; Dermocortal; Zenoxone; U 1851; Medicort; Mildison; 11Beta,17,21-trihydroxy progesterone; Cor-Tar-Quin (Salt/Mix); Cort-Quin (Salt/Mix); Cortisporin (Salt/Mix); Drotic (Salt/Mix); Neo-Cort-Dome (Salt/Mix); Nystaform-HC (Salt/Mix); Otalgine (Salt/Mix); Otic-Neo-Cort-Dome (Salt/Mix); Otobiotic (Salt/Mix); Otocort (Salt/Mix); Pediotic Suspension (Salt/Mix); Racet (Salt/Mix); Vioform-Hydrocortisone (Salt/Mix); VoSol HC (Salt/Mix); Vytone (Salt/Mix); Alphaderm (Salt/Mix)
- Permanent link for this species. Use this link for bookmarking this species for future reference.
- Information on this page:
- Other data available:
- Options:
Phase change data
Go To: Top, References, Notes
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
| ΔfusH (kcal/mol) | Temperature (K) | Reference |
|---|---|---|
| 8.566 | 486. | Regosz, Chmielewska, et al., 1994 |
References
Go To: Top, Phase change data, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
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
Go To: Top, Phase change data, References
- Symbols used in this document:
ΔfusH Enthalpy of fusion - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
- The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
- Customer support for NIST Standard Reference Data products.