library.onepin.app/masteron-propionate-drostanolone-propionate Peptide Education Library
Education only, not medical advice 21+ Every dose is an example to finalize with a licensed provider
Hormonal Anabolic-Androgenic SteroidFDA-approved medicineControlled substance

Masteron Propionate (Drostanolone Propionate)

Drostanolone Propionate · Mast P

100mg EOD – 100 mg IM EOD (every other day) or E3D
InjectableDHT DerivativeNon-AromatizableShort-Ester

Drostanolone propionate, marketed historically as Masteron, is an injectable anabolic-androgenic steroid derived from dihydrotestosterone (DHT). It was originally developed in the 1950s and used medically from the early 1960s for treatment of advanced breast cancer in women, based on its mild anti-estrogenic and anti-aromatase properties. The propionate ester is short, with a plasma half-life of approximately 2-3 days, requiring injections every other day or every third day for stable blood levels.

Quick Start
Route
IM (intramuscular)
Start low
100mg IM
Frequency
EOD (every other day) or E3D
Timing
No fasting required

Inject EOD given the 2-3 day half-life. Always pair with a testosterone base. Excellent syringe compatibility with other oil-based AAS - can be combined with test propionate, trenbolone acetate, or NPP in the same injection for reduced pin count.

Start here. Every protocol below is ordered lowest-first. Begin at the smallest effective dose, hold about a week to assess tolerance, and step up only if needed.

Tiered Protocols · lowest first
Conservative start
100mg EOD · IM (intramuscular) · EOD (every other day) or E3D
conservative starter
100mg EOD
EOD (every other day) or E3D
Expert
Pre-Contest Hardener
100 mg · IM · Every other day
human clinical trial · Historical breast-cancer literature 1968-1982 (e.g. PMID 5068714, PMID 6293073); DROLBAN NDA 012936
HISTORICAL CANCER THERAPY, NOT A PHYSIQUE DOSE. Drostanolone propionate was genuinely FDA-approved (DROLBAN, Eli Lilly) for palliative treatment of advanced metastatic breast cancer in postmenopausal women; that approval was WITHDRAWN in April 1994. The population matters: those women had little endogenous sex-hormone production and the risk-benefit calculus was cancer palliation. VIRILIZATION was a clinically important adverse effect. The exact original label dose is not retrievable from the accessible record, and the widely repeated figures circulate mainly on vendor and forum pages. Schedule III controlled substance; no modern trial exists.
100 mg
Every other day
01

How it works

Drostanolone binds the androgen receptor (AR) with moderate affinity and drives protein synthesis and nitrogen retention, with a strong preference for lean tissue. As a DHT derivative, it does not aromatize to estrogen and has no intrinsic estrogenic activity.

A distinctive feature of drostanolone is its mild aromatase-inhibition effect - it competes at the aromatase enzyme with other aromatizable androgens (testosterone, methandrostenolone), reducing estrogen conversion from those compounds. This is why it is often added to a testosterone cycle as a mild AI alternative. It also displaces testosterone from sex-hormone binding globulin (SHBG), raising free testosterone.

Unlike 17-alpha-alkylated orals, drostanolone is injectable and not hepatotoxic in the classical sense. It still suppresses endogenous testosterone production via HPT-axis feedback, though less aggressively than 19-nor compounds. A testosterone base is standard.

02

What to expect

Early
Days 1–7

First 1-2 weeks: subtle drying effect and mild strength improvement. Libido often improves (free testosterone rise from SHBG displacement).

Mid
Weeks 2–4

Weeks 3-5: peak hardness and conditioning effect visible, especially in sub-10% body fat. Vascularity noticeably increases.

Later
Weeks 4–12

Weeks 6-10: sustained gains, diminishing return beyond 10 weeks. Side-effect burden mostly androgenic (skin, hair). Cycle off to reset.

03

Evidence

HumanPresent
AnimalPresent
In-vitroPresent

References for this compound are being re-checked against their source records. We are not showing them until each one is confirmed to support the claim it sits under.

04

Side effects & safety

Commonly reported

  • Accelerated hair loss in genetically predisposed users
  • Oily skin and acne (androgenic effect)
  • Suppression of endogenous testosterone (dose-dependent)
  • Lipid shift (HDL drop, LDL rise)
  • Injection site discomfort (short ester, frequent injections)

Less common & notes

  • Increased aggression or libido, mood changes, elevated blood pressure, minor cardiovascular markers.
  • Women: significant virilization risk at any meaningful dose - generally contraindicated in women except for historical breast cancer use under strict medical supervision.
  • Rare: severe lipid shifts, cardiac strain with prolonged high-dose cycling, psychological effects.
05

Pharmacokinetics

Illustrative plasma concentration · 12 d
Half-life
2-3 days
Peak · Tmax
1-2 days

Post-injection

Elimination
7-10 days
Bioavailability
~100%

IM (oil depot)

Duration of action
2-3 days

Per injection - supports EOD or E3D dosing

Clearance

Hepatic metabolism. Renal excretion of metabolites.

Storage. Store at controlled room temperature (20-25°C / 68-77°F). Protect from light. Oil-based solution - do not refrigerate or freeze. Draw with a larger gauge needle and inject with a smaller one (18G draw, 23-25G inject). Keep out of reach of children and in a locked location - Schedule III controlled substance in the United States.

06

Regulatory status

Schedule III controlled substance in the United States under the Anabolic Steroids Control Act of 1990. Originally FDA-approved (brand name Masteron, Syntex) for advanced breast cancer in women - discontinued in the late 1990s. Possession or distribution without a valid prescription is a federal offense in the United States. Classified similarly in most international jurisdictions.

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The guide & community

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