| Identification | More | [Name]
Hydroxyprogesterone acetate | [CAS]
302-23-8 | [Synonyms]
17-(acetyloxy)-pregn-4-ene-20-dione
17-ap
20-dione,17-hydroxy-pregn-4-ene-acetate
acetoxyprogesterone
prodoxacetate
u5533
17A-HYDROXYPROGESTERONE 17-ACETATE
17A-HYDROXYPROGESTERONE 17-ACETATE VETRA
17-alpha-Hydroxylprogesterone
17α-acetoxy-4-pregnene-3,20-dione
17α-hydroxyprogesterone 17-acetate
HYDROXYPROGESTERONE, 17a-(RG)
17a-Acetoxyprogesterone
17a-Hydroxy-4-pregnene-3,20-dione acetate
17a-Hydroxyprogesterone acetate
Hydroxyprogesterone acetate
17α-Hydroxylprogesterone acetate
17α-Acetoxy-4-pregnene-3,20-dione, 17α-Acetoxyprogesterone, 17α-Hydroxy-4-pregnene-3,20-dione 17-acetate, 4-Pregnen-17α-ol-3,20-dione acetate
17α-Acetoxypregn-4-ene-3,20-dione | [EINECS(EC#)]
206-119-6 | [Molecular Formula]
C23H32O4 | [MDL Number]
MFCD00021156 | [Molecular Weight]
372.5 | [MOL File]
302-23-8.mol |
| Chemical Properties | Back Directory | [Melting point ]
249-250°C | [Boiling point ]
421.94°C (rough estimate) | [density ]
1.0415 (rough estimate) | [refractive index ]
1.4433 (estimate) | [storage temp. ]
Sealed in dry,2-8°C | [solubility ]
Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Sparingly) | [form ]
neat | [Water Solubility ]
1.01mg/L at 20℃ | [λmax]
241nm(EtOH)(lit.) | [BRN ]
2227870 | [InChI]
InChI=1S/C23H32O4/c1-14(24)23(27-15(2)25)12-9-20-18-6-5-16-13-17(26)7-10-21(16,3)19(18)8-11-22(20,23)4/h13,18-20H,5-12H2,1-4H3/t18-,19+,20+,21+,22+,23+/m1/s1 | [InChIKey]
VTHUYJIXSMGYOQ-KOORYGTMSA-N | [SMILES]
C1(=O)C=C2[C@](C)(CC1)[C@]1([H])[C@]([H])([C@@]3([H])[C@@](CC1)(C)[C@@](OC(C)=O)(C(=O)C)CC3)CC2 | [CAS DataBase Reference]
302-23-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R40:Limited evidence of a carcinogenic effect.
R48:Danger of serious damage to health by prolonged exposure. | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 2811 6.1/PG 2
| [WGK Germany ]
3
| [RTECS ]
TU5074000
| [HS Code ]
29372390 |
| Hazard Information | Back Directory | [Chemical Properties]
Off-White Solid | [Uses]
An impurity in steroid drug Megestrol acetate (M208050). | [Synthesis]
The general procedure for the synthesis of the target compound (CAS: 4134-58-1) using the compound (CAS: 83984-86-5) as starting material was as follows: the diester (51 g, melting point 192-196°C) was dissolved in a solvent mixture of 1.4 liters of technical grade xylene and 510 ml of cyclohexanone. Water was removed from the system by distillation (250 ml of distillate was collected). Subsequently, aluminum isopropoxide (51 g) dissolved in 210 ml of xylene was added dropwise to the reaction system over a period of 5 minutes under slow distillation conditions, and distillation was continued for 45 minutes (another 210 ml of distillate was collected). Upon completion of the reaction, the mixture was rapidly cooled, the reaction was quenched by the addition of an ice-water mixture, and the remaining solvent was removed by steam distillation. The resulting solid product was collected by filtration and dried. The crude product was extracted using hot acetone and subsequently recrystallized by acetone to give 40.7 g (86% yield) of 17α-acetoxy-progesterone with a melting point of 240-243 °C. The melting point of the further purified sample was raised to 243-247 °C. *The 2% yield of the raw material is equivalent to 78.95%. | [References]
[1] Patent: EP1359154, 2003, A1. Location in patent: Page/Page column 16; 28; 30; 32
[2] Journal of the American Chemical Society, 1956, vol. 78, p. 820,823 |
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