Medroxyprogesterone acetate
- Formula: C24H34O4
- Molecular weight: 386.5244
- IUPAC Standard InChI: InChI=1S/C24H34O4/c1-14-12-18-19(22(4)9-6-17(27)13-21(14)22)7-10-23(5)20(18)8-11-24(23,15(2)25)28-16(3)26/h13-14,18-20H,6-12H2,1-5H3/t14?,18-,19+,20+,22-,23+,24-/m0/s1
- IUPAC Standard InChIKey: PSGAAPLEWMOORI-MRIZVWMHSA-N
- CAS Registry Number: 71-58-9
- Chemical structure:
This structure is also available as a 2d Mol file - Stereoisomers:
- Other names: Pregn-4-ene-3,20-dione, 17-(acetyloxy)-6-methyl-, (6α)-; Pregn-4-ene-3,20-dione, 17-hydroxy-6α-methyl-, acetate; Depo-Provera; Depomedroxyprogesterone acetate; Depot-medroxyprogesterone acetate; Farlutin; Gestapuran; Lutopolar; Lutoral; Metigestrona; MAP; MPA; Oragest; Perlutex; Prodasone; Progestalfa; Progevera; Provera; Proverone; Repromix; Sirprogen; U 8839; Veramix; 17α-Acetoxy-6α-Methylprogesterone; 17α-Hydroxy-6α-methylprogesterone acetate; 6α-Methyl-17α-hydroxyprogesterone acetate; 6α-Methyl-17-acetoxyprogesterone; (6α-Pregn-4-ene-3,20-dione, 17-(acetyloxy)-6-methyl-; Depcorlutin; Depo-Promone; Deporone; DMPA; DP150; Nadigest; Nidaxin; Progesterone, 17-hydroxy-6α-methyl-, acetate; Promone-E; Supprestral; 17α-Acetoxy-6-α-methylpregn-4-ene-3,20-dione; 17α-Hydroxy-6α-methylpregn-4-ene-3,20-dione acetate; 17-Acetoxy-6α-methylprogesterone; 6α-Methyl-17α-acetoxypregn-4-ene-3,20-dione; 6α-Methyl-17α-acetoxyprogesterone; 6α-Methyl-4-pregnene-3,20-dion-17α-ol acetate; (6α)-17-(Acetyloxy)-6-methylpreg-4-ene-3,20-dione; Depo-mpa; 17-Hydroxy-6-α-methylpregn-4-ene-3,20-dione acetate; Medroxyacetate progesterone; Metipregnone; NSC-26386; Progesterone, 17α-hydroxy-6α-methyl-, acetate; Provera dosepak; Curretab; Cycrin; 17-Hydroxy-6α-methylpregn-4-en-3,20-dione acetate; Amen; Clinovir; Depo-clinovir; Farlutal; G-Farlutal; Hysron; Sodelut G; 6-Methyl-3,20-dioxopregn-4-en-17-yl acetate, (6α)-; Progeston; 17α-Hydroxy-6α-methyl-4-pregnene-3,20-dione 17-acetate; 6α-Methyl-17R-hydroxyprogesterone acetate; 6α-Methyl-17α-acetoxy-Δ4-pregnene-3,20-dione; Depo-Ralovera; Ralovera; Hematrol; Aragest; Asconale; Colirest; Medroprogesterone acetate; Medroxyprogesterone 17-acetate
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Gas Chromatography
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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: NIST Mass Spectrometry Data Center, William E. Wallace, director
Van Den Dool and Kratz RI, non-polar column, temperature ramp
| Column type | Active phase | I | Reference | Comment |
|---|---|---|---|---|
| Capillary | Ultra-2 | 2947. | Daeseleire, de Guesquiere, et al., 1991 | 25. m/0.2 mm/0.33 μm, He, 5. K/min, 280. C @ 10. min; Tstart: 200. C |
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.
Daeseleire, de Guesquiere, et al., 1991
Daeseleire, E.; de Guesquiere, A.; van Peteghem, C.,
Derivatization and gas chromatographic-mass spectrometric detection of anabolic steroid residues isolated from edible muscle tissue,
J. Chromatogr., 1991, 562, 1-2, 673-679, https://doi.org/10.1016/0378-4347(91)80617-L
. [all data]
Notes
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- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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