Methasteron (Superdrol)

$35.00

Chemical Information and Compositions of Methasteron (Superdrol)

For researchers, biochemists, and wholesale distributors, the molecular structure of Methasteron (Superdrol) is the foundation of its pharmacological profile. Understanding its composition is vital for analytical testing, formulation, and predicting its behavior in biological systems.

Official Chemical Nomenclature

  • Chemical Name: Methyldrostanolone; 2α,17α-dimethyl-5α-androstane-3α,17β-diol; 17β-hydroxy-2α,17α-dimethyl-5α-androstan-3-one
  • Chemical Formula: C21H34O2
  • Molecular Weight: 318.49 g/mol
  • CAS Number: 3381-88-2

Structural Composition Breakdown

Methasteron (Superdrol) is a direct derivative of Drostanolone (Masteron), which is itself a derivative of Dihydrotestosterone (DHT). However, specific structural alterations transform Masteron’s mild nature into Superdrol’s atomic potency:

  1. The 2α-Methyl Group: The addition of a methyl group at the 2-alpha position is the defining characteristic of Methasteron (Superdrol). This structural addition profoundly protects the steroid from metabolic degradation via 3α-hydroxysteroid dehydrogenase (3α-HSD), an enzyme that normally breaks down DHT derivatives in skeletal muscle. By blocking this enzyme, the 2α-methyl group allows the steroid to survive long enough in the muscle tissue to exert massive anabolic effects, drastically increasing its potency compared to its parent compound, Masteron.
  2. 17-Alpha Alkylation (17aa): To survive oral ingestion and bypass first-pass hepatic metabolism, a methyl group is added at the 17th carbon position. While this allows the pill to remain bioavailable in the bloodstream, it is also the source of the compound’s severe hepatotoxicity (liver stress), a trait common to all 17aa oral steroids but particularly aggressive in Methasteron (Superdrol).
  3. 5α-Reduced Structure: Because it is a DHT derivative, Methasteron (Superdrol) is already “5-alpha reduced.” This means the enzyme 5-alpha reductase cannot alter it further in the body. It cannot convert into a more androgenic metabolite in the skin or prostate. It binds directly to the androgen receptor in its inherent form.

Physical and Chemical Properties

  • State at Room Temperature: Solid (Fine Crystalline Powder)
  • Color: White to off-white
  • Solubility: Practically insoluble in water; soluble in organic solvents such as DMSO, ethanol, methanol, and chloroform.
  • Melting Point: Approximately 120°C to 122°C.

Pharmacokinetics

  • Route of Administration: Oral
  • Half-Life: The biological half-life of Methasteron (Superdrol) is estimated to be between 6 to 8 hours. This relatively short half-life necessitates a dosing protocol of twice daily to maintain stable and steady blood plasma levels, preventing peaks and troughs that can exacerbate side effects.
  • Anabolic/Androgenic Ratio: Methasteron (Superdrol) boasts an anabolic rating of 400 and an androgenic rating of 20 (relative to methyltestosterone). Testosterone, for comparison, is 100/100. This massive 20:1 anabolic-to-androgenic ratio in vitro explains why Methasteron (Superdrol) produces such dramatic muscle hypertrophy with relatively fewer androgenic side effects (like hair loss or severe acne) compared to highly androgenic steroids like Halotestin or Trenbolone.
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