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Metenolone

CAS No.
153-00-4
Chemical Name:
Metenolone
Synonyms
metenolone;Methenolon;METHENOLONE;Metenolone base;Methenolone Base;Metenolone Acetat;Methenolone Tablet;Metenolone Chemical;Metenolone USP/EP/BP;Methenolone, 1.0 mg/mL
CBNumber:
CB8335436
Molecular Formula:
C20H30O2
Molecular Weight:
302.46
MDL Number:
MFCD00273128
MOL File:
153-00-4.mol
MSDS File:
SDS
Last updated:2024-05-16 17:35:26

Metenolone Properties

Melting point 149.5-152°; mp 160-161° (Popper)
alpha D +58.9°
Boiling point 430.4±45.0 °C(Predicted)
Density 1.084±0.06 g/cm3(Predicted)
pka 15.08±0.70(Predicted)
CAS DataBase Reference 153-00-4(CAS DataBase Reference)
FDA UNII 9062ZT8Q5C
ATC code A14AA04

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS08,GHS07
Signal word  Danger
Hazard statements  H351-H302-H362-H360
Precautionary statements  P201-P202-P281-P308+P313-P405-P501-P264-P270-P301+P312-P330-P501-P201-P260-P263-P264-P270-P308+P313
DEA Controlled Substances CSCN: 4000
CSA SCH: Schedule III
NARC: No

Metenolone price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth Carbosynth FM32216 Methenolone 153-00-4 10mg $125 2021-12-16 Buy
Biosynth Carbosynth FM32216 Methenolone 153-00-4 50mg $350 2021-12-16 Buy
AHH MT-16693 Methenolone 98% 153-00-4 0.05g $446 2021-12-16 Buy
Product number Packaging Price Buy
FM32216 10mg $125 Buy
FM32216 50mg $350 Buy
MT-16693 0.05g $446 Buy

Metenolone Chemical Properties,Uses,Production

Originator

Primobolan ,Schering ,W. Germany,1961

Uses

Methenolone is an anabolic steroid. This is a controlled substance.

Definition

ChEBI: Methenolone is a 3-hydroxy steroid. It has a role as an androgen.

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

Metenolone Preparation Products And Raw materials

Metenolone Suppliers

Global( 70)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Yanxi Chemical Co., Ltd.
+8617531190177 peter@yan-xi.com China 5858 58
Nantong Guangyuan Chemicl Co,Ltd
+undefined17712220823 admin@guyunchem.com China 615 58
hebei hongtan Biotechnology Co., Ltd
+86-86-1913198-3935 +8617331935328 sales03@chemcn.cn China 970 58
Hubei XinRunde Chemical Co., Ltd.
+8615102730682 bruce@xrdchem.cn CHINA 566 55
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293 sales@sdzschem.com China 2930 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29815 58
Hebei Miaobian Biotechnology Co., Ltd
+8617733850068 CHINA 967 58
Qiuxian Baitai New Material Co., LTD
+8618330912755 sale2@hbyalin.com China 1658 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471 sales@sarms4muscle.com China 10473 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490 info@gihichemicals.com China 49979 58

View Lastest Price from Metenolone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
 Metenolone base pictures 2024-10-31 Metenolone base
153-00-4
US $30.00 / kg 1kg 98% 2000kg hebei hongtan Biotechnology Co., Ltd
Metenolone base pictures 2024-10-31 Metenolone base
153-00-4
US $30.00 / kg 1kg 98% 2000kg hebei hongtan Biotechnology Co., Ltd
Metenolone pictures 2024-10-25 Metenolone
153-00-4
US $0.00-0.00 / kg 1kg 0.99 10 tons Hebei Yanxi Chemical Co., Ltd.
  • Metenolone base pictures
  • Metenolone base
    153-00-4
  • US $30.00 / kg
  • 98%
  • hebei hongtan Biotechnology Co., Ltd
  • Metenolone pictures
  • Metenolone
    153-00-4
  • US $0.00-0.00 / kg
  • 0.99
  • Hebei Yanxi Chemical Co., Ltd.
(5S,8R,9S,10S,13S,14S,17S)-17-hydroxy-1,10,13-triMethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3H-cyclopenta[a]phenanthren-3-one METHENOLONE metenolone 1(5-ALPHA)-ANDROSTEN-1-BETA-METHYL-17-BETA-OL-3-ONE 1,5ALPHA-ANDROSTEN-1-METHYL-17BETA-OL-3-ONE 17beta-hydroxy-1-methyl-5alpha-androst-1-en-3-one MethenoloneAcetate434-05-9/Base 17b-Hydroxy-1-methyl-5a-androst-1-en-3-one 1-Methyl-D1-androsten-17b-ol-3-one 5a-Androst-1-en-3-one, 17b-hydroxy-1-methyl- (6CI, 7CI, 8CI) Androst-1-en-3-one, 17-hydroxy-1-methyl-, (5a,17b)- (9CI) 17-Hydroxy-1,10,13-trimethyl-4,5,6,7,8,9,10,11,12,13, 14,15,16,17-tetradecahydro-cyclopenta[a]phenanthren-3-one 5a-Androst-1-en-3-one, 17b-hydroxy-1-methyl- Androst-1-en-3-one, 17-hydroxy-1-methyl-, (5a,17b)- Metenolone Chemical (5S)-17-hydroxy-1,10,13-trimethyl-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one Methenolone, 1.0 mg/mL 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 Androst-1-en-3-one, 17-hydroxy-1-methyl-, (5α,17β)- Metenolone USP/EP/BP 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 1(5α)-ANDROSTEN-1β-METHYL-17β-OL-3-ONE Metenolone base Methenolone Acetate, Primobolan 25mg Tablets Methenolone Acetate, Primobolan 50mg Tablets 153-00-4 Intermediates & Fine Chemicals Pharmaceuticals Finished Steroid and Hormone Steroids Steroid and Hormone