Methenolone acetate Struktur

17β-Hydroxy-1-methyl-5α-androst-1-en-3-onacetat

Bezeichnung:17β-Hydroxy-1-methyl-5α-androst-1-en-3-onacetat

CAS-Nr434-05-9

Englisch Name:Methenolone acetate

CBNumberCB8446910

SummenformelC22H32O3

Molgewicht344.49

MOL-Datei434-05-9.mol

Synonyma

17β-Hydroxy-1-methyl-5α-androst-1-en-3-onacetat

17β-Hydroxy-1-methyl-5α-androst-1-en-3-onacetat physikalisch-chemischer Eigenschaften

Schmelzpunkt	138-139°
Siedepunkt	419.57°C (rough estimate)
Dichte	1.0906 (rough estimate)
Brechungsindex	1.5000 (estimate)
storage temp.	Store at -20°C
Löslichkeit	DMSO : ≥ 3.6 mg/mL (10.45 mM)
Aggregatzustand	Solid
Farbe	White to Off-White
InChI	InChI=1/C22H32O3/c1-13-11-16(24)12-15-5-6-17-18-7-8-20(25-14(2)23)21(18,3)10-9-19(17)22(13,15)4/h11,15,17-20H,5-10,12H2,1-4H3/t15-,17-,18-,19-,20-,21-,22-/s3
InChIKey	PGAUJQOPTMSERF-MQEWATRANA-N
SMILES	[C@]12([H])CC[C@]3(C)[C@]([H])(CC[C@@]3([H])[C@]1([H])CC[C@@]1([H])CC(=O)C=C(C)[C@]21C)OC(=O)C \|&1:0,4,6,10,12,16,24,r\|
CAS Datenbank	434-05-9(CAS DataBase Reference)

Gefahreninformationscode (GHS)

Methenolone acetate Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung
Methenolone acetate (Brand name: Primobolan) is a synthetic, orally active anabolic-androgenic steroid and dihydrotestosterone (DHT) derivative. It can be used for the treatment of bone marrow disease and anemia. Methenolone acetate is known for its higher therapeutic efficiency and lower hepatic toxicity compared with its 17 alpha- alkylated analogs. However, it is frequently abused in human sports because of its capability of increasing muscle strength as well as promoting performance and aggressiveness. It is capable of enhancing performance in racehorses.
Chemische Eigenschaften
White Solid
Originator
Primobolan ,Schering ,W. Germany,1961
Verwenden
Methenolone acetate is an anabolic steroid. This is a controlled substance.
Definition
ChEBI: Methenolone acetate is a steroid ester.
Manufacturing Process
8.42 ml of methyl iodide are slowly added dropwise at room temperature with stirring in a nitrogen atmosphere to 3.067 g of magnesium turnings and 107 ml of absolute ether. After about 30 minutes, 185 ml of absolute tetrahydrofuran are slowly introduced and then liquid is distilled off until a boiling point of 62°C is reached. After cooling to room temperature, 613 mg of cuprous chloride are added and then 10 g of ?1,4,6-androstatrien-17β-ol-3- one-17-acetate in 110 ml of tetrahydrofuran slowly introduced. After 30 minutes reaction time, the whole is cooled to 0C, the excess of Grignard reagent decomposed with saturated ammonium chloride solution, the product diluted with ether and the aqueous phase separated. The ethereal phase is washed consecutively with aqueous sodium thiosulfate solution, saturated ammonium chloride solution and water. It is dried over sodium sulfate and evaporated to dryness under vacuum. The residue is dissolved in 40 ml of pyridine and 20 ml of acetic anhydride and the solution kept for 16 hours at room temperature. It is then stirred into ice water and the precipitate filtered with suction, dried and recrystallized from isopropyl ether. 1α-Methyl-?4,6- androstadien-17β-ol-3-one-17-acetate is obtained. MP 156°C to 157°C; [α]D25 = -33.8° (in CHCl3; c = 0.9). Yield 65-70% of the theoretical.
4.67 g of 1α-methyl-?4,6-androstadien-17β-ol-3-one-17-acetate are dissolved in 273 ml of methanol and, after the addition of 350 mg of 10% palladium on calcium carbonate catalyst, hydrogenated until 1 mol equivalent of hydrogen has been taken up. After filtering off the catalyst, the solution is treated with 150 ml of 2N-hydrochloric acid and evaporated under vacuum to about 1/3 of the volume. The whole is then diluted with water and extracted with ether. The ethereal solution is washed with water until neutral, dried over sodium sulfate and evaporated. The crude product is heated on a steam bath for 90 minutes in 10 ml of pyridine and 10 ml of acetic anhydride. Extraction with ether is then carried out and the ethereal phase washed until neutral with water. The crude crystalline 1α-methyl-?4-androsten-17β-ol-3-one-17- acetateobtained after drying and evaporation of the solution, melts at 122°C to 129°C. Yield 98% of the theoretical.
1α-Methyl-?4-androsten-17β-ol-3-one-17-acetate when purified by recrystallization from isopropyl ether melts at 138°C to 139°C.
Therapeutic Function
17β-Hydroxy-1β-methyl-5α-androst-l-ene-3-one acetate
Einzelnachweise
Ho, Emmie N. M., et al. "Metabolic studies of methenolone acetate in horses." Analytica Chimica Acta 540.1(2005): 111-119.
https://en.wikipedia.org/wiki/Metenolone_acetate

Methenolone acetate Upstream-Materialien And Downstream Produkte

17β-Hydroxy-1-methyl-5α-androst-1-en-3-onacetat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

434-05-9, Methenolone acetate Verwandte Suche:

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