Metenolone CAS 153-00-4

Introduction:Basic information about Metenolone CAS 153-00-4, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Metenolone Basic information

Product Name:Metenolone
Synonyms:Methenolone Base;Methenolone Tablet;(5α,17β)-17-Hydroxy-1-Methylandrost-1-en-3-one;1-Methyl-5α-androst-1-en-17β-ol-3-one;1-Methyl-Δ1-androsten-17β-ol-3-one;Methenolon;Metenolone Acetat;(5S,8R,9S,10S,13S,14S,17S)-17-hydroxy-1,10,13-trimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
CAS:153-00-4
MF:C20H30O2
MW:302.46
EINECS:205-812-0
Product Categories:Intermediates & Fine Chemicals;Pharmaceuticals;Finished Steroid and Hormone;Steroids;Steroid and Hormone
Mol File:153-00-4.mol

Metenolone Chemical Properties

Melting point 149.5-152°; mp 160-161° (Popper)
alpha D +58.9°
Boiling point 430.4±45.0 °C(Predicted)
pKa15.08±0.70(Predicted)
density 1.084±0.06 g/cm3(Predicted)
CAS DataBase Reference153-00-4(CAS DataBase Reference)

Safety Information

DEA Controlled SubstancesCSCN: 4000
CSA SCH: Schedule III
NARC: No

Metenolone Usage And Synthesis

OriginatorPrimobolan ,Schering ,W. Germany,1961
UsesMethenolone is an anabolic steroid. This is a controlled substance.
DefinitionChEBI: Methenolone is a 3-hydroxy steroid. It has a role as an androgen.
Manufacturing Process8.42 ml of methyl iodide are slowly added dropwise at room temperature withstirring in a nitrogen atmosphere to 3.067 g of magnesium turnings and 107ml of absolute ether. After about 30 minutes, 185 ml of absolutetetrahydrofuran are slowly introduced and then liquid is distilled off until aboiling point of 62°C is reached. After cooling to room temperature, 613 mgof 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 30minutes reaction time, the whole is cooled to 0C, the excess of Grignardreagent decomposed with saturated ammonium chloride solution, the productdiluted with ether and the aqueous phase separated. The ethereal phase iswashed consecutively with aqueous sodium thiosulfate solution, saturatedammonium chloride solution and water. It is dried over sodium sulfate andevaporated to dryness under vacuum. The residue is dissolved in 40 ml ofpyridine and 20 ml of acetic anhydride and the solution kept for 16 hours atroom temperature. It is then stirred into ice water and the precipitate filteredwith 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 dissolvedin 273 ml of methanol and, after the addition of 350 mg of 10% palladium oncalcium carbonate catalyst, hydrogenated until 1 mol equivalent of hydrogenhas been taken up. After filtering off the catalyst, the solution is treated with150 ml of 2N-hydrochloric acid and evaporated under vacuum to about 1/3 ofthe volume. The whole is then diluted with water and extracted with ether.The ethereal solution is washed with water until neutral, dried over sodiumsulfate and evaporated. The crude product is heated on a steam bath for 90minutes in 10 ml of pyridine and 10 ml of acetic anhydride. Extraction withether is then carried out and the ethereal phase washed until neutral withwater. The crude crystalline 1α-methyl-?4-androsten-17β-ol-3-one-17-acetateobtained after drying and evaporation of the solution, melts at 122°Cto 129°C. Yield 98% of the theoretical.
1α-Methyl-?4-androsten-17β-ol-3-one-17-acetate when purified byrecrystallization from isopropyl ether melts at 138°C to 139°C.
Therapeutic Function17β-Hydroxy-1β-methyl-5α-androst-l-ene-3-one acetate

Metenolone Preparation Products And Raw materials

Raw materialsMagnesium-->Hydrogen-->Iodomethane
Preparation Products1β-Methyl-17β-hydroxy-5α-androstane-3-one
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