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ProhormoneApproved

Masteron (Drostanolone)

MAS-ter-on

Research profile · How we handle evidence

Category

Prohormone

Compound type

Phase / Status

Approved

FDA approved (brand name Drostanolone). Discontinued in US but available internationally. Still used in veterinary medicine.

Standard Dose

200-400mg weekly (injectable), 25-50mg daily (oral)

2-3x weekly (injectable), once daily (oral)

Half-life

2-3 days (propionate), 10-12 days (enanthate)

Plasma elimination

Route(s)

OR

Oral

Research Stage

Market Approved

Regulatory approval granted; post-market monitoring ongoing.

Overview

Drostanolone is typically discussed as a late-cycle or 'drying' agent because it is DHT-derived and does not convert to estrogen. However, it can still affect lipids, hormones, and hair follicles in susceptible individuals, and it carries general risks associated with androgen exposure. If you are considering any use, use medical supervision and avoid relying on informal dosing practices.

Plain-language summary

Drostanolone is typically discussed as a late-cycle or 'drying' agent because it is DHT-derived and does not convert to estrogen. However, it can still affect lipids, hormones, and hair follicles in susceptible individuals, and it carries general risks associated with androgen exposure. If you are considering any use, use medical supervision and avoid relying on informal dosing practices.

Administration Routes

  • Oral

Also known as

MastMast PMast PropMasteronDrostanolone PropionateDPThe HardenerDrost

Mechanisms

1

DHT-derived anabolic steroid - binds androgen receptors, has mild anti-estrogenic properties. Already 5-alpha-reduced so it can't convert to estrogen.

Detailed mechanism

Drostanolone is a 2-methyl derivative of dihydrotestosterone (DHT) esterified at C-17 for injectable depot formulations, making it intrinsically resistant to aromatization because it lacks the C-19 methyl group required for CYP19A1 substrate recognition. It binds the androgen receptor with moderate affinity, promoting anabolic gene transcription in muscle (actin, myosin, IGF-1) while simultaneously competing with estradiol for binding at the estrogen receptor alpha in a partial antagonist capacity - the mechanistic basis for its mild anti-estrogenic reputation in users stacking with aromatizing compounds. The 2-methyl substitution also partially retards 5-alpha reduction, extending biological activity, though androgenic effects on scalp follicles (via local DHT) and sebaceous glands remain clinically relevant in genetically susceptible individuals.

Safety

Side effects

  • Hair loss (it's DHT-derived - accelerates MPB)
  • Acne and oily skin
  • Testosterone suppression
  • May lower HDL cholesterol
  • Prostate enlargement
  • Injection site pain (enanthate)

Reported benefits

  • Hard, dry, vascular muscle appearance
  • Zero water retention
  • Mild anti-estrogenic effects
  • Preserves muscle during extreme cutting
  • Pre-contest favorite
  • No estrogen-related side effects

Safety profile

Well-characterized safety profile from extensive clinical use and trials.

Clinical trials

Completed clinical trials leading to FDA or regulatory approval.

Structure

Verified structure

Masteron (Drostanolone)

No exact public structure match was confirmed, so the app will render a formula-backed illustration.

Formula-backed
C20H28O2312.46 g/molCAS 521-12-03 element fingerprint
Chemical Formula
C20H28O2
Molecular Weight
312.46 g/mol
CAS Number
521-12-0

Stack Context

Stacks with

Testosterone EnanthateWinstrolAnavarTrenbolone

References

  1. 1

    Drostanolone propionate pharmacokinetics and detection in urine (PubMed)

    1990

    View source
  2. 2

    Drostanolone (PIM 901) - WHO International Programme on Chemical Safety pharmacological profile (INCHEM)

    1993

    View source
  3. 3

    Adverse Effects of Anabolic-Androgenic Steroids: A Literature Review (PMC)

    2021

    View source

This profile summarizes research literature for education only. It is not medical advice, and it does not diagnose, treat, or recommend a dose. Consult a qualified professional before changing a protocol.

Research-driven insights.Evidence-based decisions.