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ProhormoneResearch

Masteron Enanthate

MAS-ter-on en-ANth-ate

Research profile · How we handle evidence

Category

Prohormone

Compound type

Phase / Status

Research

Controlled substance

Standard Dose

400-600mg weekly

As directed

Half-life

8-10 days

Plasma elimination

Route(s)

OR / IN / TO

Oral, Injectable or Topical

Research Stage

Status Unknown

Research phase not specified; exercise appropriate caution.

Overview

If you see Masteron Enanthate discussed online, it is usually the longer-acting (enanthate) ester of drostanolone. Because it is DHT-derived, it is not designed to aromatize into estrogen the way some other steroids can. That said, "no estrogen conversion" does not mean "no risk": androgenic side effects (for example acne or hair shedding in people who are genetically prone) and changes to blood lipids have been reported with androgen exposure. Any use outside approved medical indications is educational only and should be treated as investigational, with a clinician involved for risk assessment.

Plain-language summary

If you see Masteron Enanthate discussed online, it is usually the longer-acting (enanthate) ester of drostanolone. Because it is DHT-derived, it is not designed to aromatize into estrogen the way some other steroids can. That said, "no estrogen conversion" does not mean "no risk": androgenic side effects (for example acne or hair shedding in people who are genetically prone) and changes to blood lipids have been reported with androgen exposure. Any use outside approved medical indications is educational only and should be treated as investigational, with a clinician involved for risk assessment.

Administration Routes

  • Oral
  • Injectable
  • Topical

Also known as

Mast EMast EnthMasteron EnanthateDrostanolone EnanthateLong MastDrost E

Mechanisms

1

DHT-derived anabolic steroid

Detailed mechanism

Masteron Enanthate is drostanolone conjugated with the heptanoate (enanthate) ester at the C-17 hydroxyl, forming a depot that releases free drostanolone over 8-10 days as esterases in serum and tissue hydrolyze the ester bond. The liberated drostanolone, a 2-methyl DHT derivative, binds the androgen receptor to activate anabolic gene programs in skeletal muscle while being structurally incapable of aromatization due to the absence of an aromatizable C-19 angular methyl group. The longer release profile relative to the propionate ester allows twice-weekly injections to maintain stable plasma concentrations, but the extended depot also means that androgenic side effects and HPG axis suppression persist well past the final injection, with detectable drug remaining for several weeks.

Safety

Side effects

  • Hair loss
  • Acne
  • Cholesterol issues
  • Virilization in women

Reported benefits

  • Muscle hardening
  • No estrogen conversion
  • Good for cutting

Safety profile

Consult medical professional before use

Clinical trials

See research status

Structure

View 3D structure

Verified structure

Masteron Enanthate

Exact 2D structure can be rendered from a PubChem-backed canonical SMILES string.

Verified via PubChemMatched by casNumber
Source: PubChemLookup: 13425-31-5InChIKey ZNYZYASFVYLKPE-SRGKWKMDSA-N
Chemical Formula
C27H44O3
Molecular Weight
416.6 g/mol
CAS Number
13425-31-5
InChIKey
ZNYZYASFVYLKPE-SRGKWKMDSA-N

Stack Context

No stack data available.

References

  1. 1

    Drostanolone Enanthate - PubChem Compound Record (NLM)

    View source
  2. 2

    Drostanolone (PIM 901) - WHO International Programme on Chemical Safety, absorption and ester-related pharmacology (INCHEM)

    1993

    View source
  3. 3

    Drostanolone propionate pharmacokinetics and detection in urine (PubMed)

    1990

    View source
  4. 4

    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.