MIT-10MG

$65.00

Chemical Information and Compositions of MIT-10MG

For researchers, biochemists, and wholesale distributors, the molecular structure of MIT-10MG is a fascinating study in extreme anabolic potency driven by structural double-bond engineering.

Official Chemical Nomenclature

  • Chemical Name: 17α-methyl-5α-androst-1-en-3-one-17β-ol
  • Chemical Formula: C20H30O2
  • Molecular Weight: 302.45 g/mol
  • CAS Number: 5292-25-1

Structural Composition Breakdown

MIT-10MG is a derivative of Dihydrotestosterone (DHT). Its structural architecture features two critical modifications that elevate it from a weak androgen to an atomic mass builder:

  1. The 1-ene (Double Bond at Carbon 1): This is the most crucial structural feature. The addition of a double bond between carbons 1 and 2 is the same modification that differentiates Primobolan (Methenolone) from standard DHT. This 1-ene group profoundly protects the molecule from degradation by the 3α-hydroxysteroid dehydrogenase (3α-HSD) enzyme in skeletal muscle. While DHT is instantly deactivated in muscle, MIT-10MG survives intact, allowing it to bind aggressively to the androgen receptor and drive massive protein synthesis.
  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 the source of the compound’s notorious hepatotoxicity. The liver recognizes the 17aa structure as foreign and struggles to process it, leading to severe cholestasis and enzyme transaminase spills.
  3. 5-Alpha Reduced: Because it is a DHT derivative, MIT-10MG is already 5-alpha reduced. It cannot be converted by the 5-alpha reductase enzyme into a more potent androgen. It binds to the androgen receptor in its inherent state.

Physical and Chemical Properties

  • State at Room Temperature: Solid (Crystalline Powder)
  • Color: White to off-white
  • Solubility: Practically insoluble in water; freely soluble in organic solvents such as DMSO, ethanol, chloroform, and ethyl oleate.
  • Melting Point: Approximately 140°C to 145°C.

Pharmacokinetics

  • Route of Administration: Oral
  • Half-Life: The biological half-life of MIT-10MG is estimated to be between 6 to 9 hours. This 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: MIT-10MG possesses an anabolic rating of 910 to 1000 and an androgenic rating of 100 to 220 (relative to methyltestosterone). Testosterone, for comparison, is 100/100. This massive skew toward anabolism explains why MIT-10MG builds muscle so rapidly and aggressively.
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