← Back to Compounds
injectableanabolic

Dihydroboldenone

DHB1-Testosterone1-Test Cyp1-Test
200
Anabolic Ratio
100
Androgenic Ratio
4d
Half-Life

A non-aromatizing injectable anabolic steroid (DHT derivative of Boldenone). Provides lean, dry gains similar to Primobolan but with stronger anabolic potency. Known for severe post-injection pain (PIP). Very limited human clinical data exists.

Mechanism of Action

Binds androgen receptors directly — already 5α-reduced so no further reduction occurs. Does not aromatize into estrogen. Exhibits strong androgen receptor affinity and drives protein synthesis in skeletal muscle. Moderate erythropoiesis stimulation. The 1-dehydro modification increases anabolic selectivity over the parent Boldenone molecule.

Dihydroboldenone molecule
Molecular structure

Typical Dosing

200 mg
low / week
350 mg
moderate / week
500 mg
high / week

⚠ Warning Flags

  • ZERO human clinical data — all evidence is preclinical or anecdotal
  • Notorious for severe post-injection pain (PIP)
  • Does not aromatize — requires a testosterone base for estrogen support
  • No estrogen = no neuroprotection or cardioprotection from this compound alone

Effect Profile

Muscle Protein Synthesis
7High
Nitrogen Retention
7High
Strength Gains
7High
Red Blood Cell Production
6Moderate
Fat Loss
5Moderate
Glycogen Storage
5Moderate
Recovery Speed
6Moderate
Collagen Synthesis
4Low

Side Effect Profile

Hormonal Suppression
7High
Estrogenic Effects
1Minimal
Androgenic Effects
5Moderate
Cardiovascular Strain
5Moderate
Liver Stress
1Minimal
Insulin Resistance
2Minimal
Mood Changes
3Low
Prostate Risk
4Low

Research Studies

Androgens and Anabolic Agents: Chemistry and Pharmacology

Vida JA · 1969

Classified 1-testosterone (DHB) as a highly anabolic compound with favorable tissue selectivity relative to testosterone.

Pharmacology of anabolic steroids

Kicman AT · 2008

PubMed

Reviews structure-activity relationships of AAS including 1-dehydro modifications that increase anabolic selectivity.

Structural characteristics of anabolic androgenic steroids contributing to binding to the androgen receptor and to their anabolic and androgenic activities

Fragkaki AG et al. · 2009

PubMed

Confirms strong androgen receptor binding affinity of 1-testosterone derivatives.