434-05-9

  • Product Name:Methenolone Acetate
  • Molecular Formula:C22H32O3
  • Purity:99%
  • Molecular Weight:
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Product Details

Methenolone Acetate 434-05-9 supplier, in stock, low price

  • Molecular Formula:C22H32O3
  • Molecular Weight:344.494
  • Vapor Pressure:5.54E-08mmHg at 25°C 
  • Melting Point:138-139° 
  • Refractive Index:1.536 
  • Boiling Point:441.2 °C at 760 mmHg 
  • Flash Point:189.9 °C 
  • PSA:43.37000 
  • Density:1.1 g/cm3 
  • LogP:4.69600 

434-05-9 Usage

Methenolone acetate is a synthetic anabolic-androgenic steroid that acts as a potent androgen and has been marketed as a treatment for inoperable breast cancer.  It can be used for the treatment of bone marrow disease and anemia. Metenolone acetate is a long-acting anabolic steroid with weak androgenic properties. It is capable of enhancing performance in racehorses.

 

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-/m0/s1

434-05-9 Relevant articles

Development and validation of RP-HPLC method for analytical characterization of the anabolic steroid Methenolone acetate in food supplements

Diana Tzankova , Alexandrina Mateeva , Javor Mitkov , Lily Peikova , Maya Georgieva

, Pharmacia 69(1): 151–155

A necessity of the health risk associated with their unregu-lated usage requires development of suitable fast and precise methods for their evaluation. The obtained result lead us to the conclusion that the identified in the label Methenolone acetate is found as im-purity rather than as a main constituent.

LC-MS/(MS) confirmatory doping control analysis of intact phase II metabolites of methenolone and mesterolone after Girard's Reagent T derivatization

Yiannis S. Angelis, Argyro G. Fragkaki, Polyxeni Kiousi, Panagiotis Sakellariou, Christophoros Christophoridis

, Drug Testing and Analysis 2023

For the evaluation of the proposed protocols, urine samples from methenolone and mesterolone excretion studies were analyzed against at least one sample from a different excretion study.

434-05-9 Process route

17β-acetoxy-1-methyl-androsta-1,4-dien-3-one
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17β-acetoxy-1-methyl-androsta-1,4-dien-3-one

3-oxo-1-methyl-5α-androst-1-en-17β-yl acetate
434-05-9

3-oxo-1-methyl-5α-androst-1-en-17β-yl acetate

Conditions
Conditions Yield
With thallium(III) nitrate trihydrate; In diethylene glycol dimethyl ether; for 24h; Ambient temperature;
8%
17β-Hydroxy-1-methyl-Δ<sup>1</sup>-5α-androstenon-(3)-acetat
434-05-9,49566-70-3,79732-38-0

17β-Hydroxy-1-methyl-Δ1-5α-androstenon-(3)-acetat

Conditions
Conditions Yield
2'-Pyrazolino-4'.3':1.2-androstanol-(17β)-on-(3)>, 1.)saures Al2O3 / CCl4, 2.)Acetnhydrid / Pyridin;
 

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    17β-acetyloxy-1-methyl-2-<(phenylthio)methyl>-5α-androst-1-en-3-one

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