| Identification | More | [Name]
Methenolone acetate | [CAS]
434-05-9 | [Synonyms]
1(5-ALPHA)-ANDROSTEN-1-BETA-METHYL-17-BETA-OL-3-ONE ACETATE
17b-hydroxy-1-methyl-5alpha-androst-1-en-3-one acetate
METENOLONE ACETATE
METHENOLONE ACETATE
17-(acetyloxy)-1-methyl-,(5-alpha,17-beta)-androst-1-en-3-on
17-beta-hydroxy-1-methyl-5-alpha-androst-1-en-3-onacetate
17-beta-hydroxy-1-methyl-5-alpha-androst-1-en-3-oneacetate
nibal
premobolan
primobolan
primobolone
primonabol
sh567
sh567a
sq16496
17b-Hydroxy-1-methyl-5a-androst-1-en-3-one acetate
1-Methyl-17b-hydroxy-5a-androst-1-en-3-one acetate
1-Methyl-17b-hydroxy-5a-androst-1-en-3-one-17b-acetate
1-Methyl-5a-androst-1-en-17b-ol-3-one acetate
5a-Androst-1-en-3-one, 17b-hydroxy-1-methyl-, acetate (6CI, 8CI) | [EINECS(EC#)]
207-097-0 | [Molecular Formula]
C22H32O3 | [MDL Number]
MFCD00864181 | [Molecular Weight]
344.49 | [MOL File]
434-05-9.mol |
| Questions And Answer | Back Directory | [Preparation]
In a dry reaction flask, metenolone and acetic anhydride were mixed. Pyridine was then slowly added to the reaction mixture as an acid-binding agent and reaction solvent. The resulting reaction mixture was vigorously stirred at room temperature. The reaction progress was monitored by TLC or gas chromatography. After the starting material metenolone had completely reacted, the reaction mixture was slowly poured into an ice-water mixture. The reaction system was extracted multiple times with an organic solvent. All organic layers were combined and dried on anhydrous sodium sulfate. The desiccant was removed by filtration, and the resulting filtrate was concentrated under vacuum to remove volatile organic solvents. The residue was purified by silica gel column chromatography to obtain Methenolone acetate. |
| Chemical Properties | Back Directory | [Melting point ]
138-139° | [Boiling point ]
419.57°C (rough estimate) | [density ]
1.0906 (rough estimate) | [refractive index ]
1.5000 (estimate) | [storage temp. ]
Store at -20°C | [solubility ]
DMSO : ≥ 3.6 mg/mL (10.45 mM) | [form ]
Solid | [color ]
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 DataBase Reference]
434-05-9(CAS DataBase Reference) |
| Questions and Answers (Q&A) | Back Directory | [Description]
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. | [References]
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
|
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Originator]
Primobolan ,Schering ,W. Germany,1961 | [Uses]
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 |
|
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Jinan Putubio Tech Co., Ltd.
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+86 (531) 8099-2215 |
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