Halotestin 5 mg
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- Halotestin 5 mg
- Brand: Magnus Pharmaceuticals
- Content: 100 tablets | 5 mg per tablet
- Manufactured in: Europe
Product Overview
Halotestin 5 mg provides fluoxymesterone, a potent 17--alkylated, 9-fluoro androgenic steroid with roughly 5 the androgen-receptor (AR) affinity of testosterone. It’s a gold standard in strength-focused AAS research, particularly for muscle-performance modeling, neural drive stimulation, and non-estrogenic lean-mass retention.
Its small 5 mg dosing allows precision micro-administration in both low- and high-resolution sampling models. With ~100% oral bioavailability and a mean half-life of 9 hours, Halotestin is ideal for acute PK/PD trials involving strength output, aggression, and hormonal modulation—without estrogen conversion.
Key Research Highlights
Explosive strength modeling: ~5 AR binding vs. testosterone supports peak-force output studies
Zero aromatisation: No estrogenic conversion — ideal for lean-gain without gynecomastia risks
Neural & aggression activation: Reported increases in CNS stimulation and workout aggression
Hepatic monitoring required: High risk of cholestatic jaundice and liver stress beyond 20 mg/day
WADA S1 banned: Any exposure yields a positive anti-doping result
Suggested Laboratory Applications
Androgen-receptor pathway modeling
Non-estrogenic strength gain simulations
Lean muscle maintenance in caloric-restriction studies
CNS aggression and neural drive research
Hepatotoxicity and cholestasis mechanism analysis
Technical Specifications
| Field | Data |
|---|---|
| Chemical Name | Fluoxymesterone |
| Chemical Formula | C<sub>20</sub>H<sub>29</sub>FO<sub>3</sub> |
| Synonyms | Halotestin; Ultandren; 9-Fluoro-11,17-dihydroxy-17-methyl-androst-4-en-3-one |
| Molecular Weight | 336.45 g/mol |
| CAS Number | 76-43-7 |
| Half-life (oral) | ~9 hours; peak plasma at ~1–2 h |
| PubChem Benefits | strength, neural drive, estrogen-mediated effects |
Main Risks
Cholestatic liver injury, mood swings, HDL/LDL, hypertension
Total Active Compound
500 mg fluoxymesterone per carton (5 mg 100 tablets)
Shelf-life
36 months (manufacturer specification)
Detection Window
7 days; LC-MS/MS detects long-term urinary metabolites
PubChem-Supported Research Insights
Fluoxymesterone increases maximal force output and lean-muscle density
Its non-aromatising structure eliminates estrogenic effects, such as fluid retention or gynecomastia
Stimulates androgen-driven CNS activity for enhanced aggression and neural activation
Documented use in androgen deficiency and ER+ cancer studies
Any fluoxymesterone exposure is a guaranteed WADA S1 violation
Documented Research Side Effects
Hepatocellular injury and cholestatic jaundice in extended protocols
Dyslipidaemia (HDL, LDL), acne, aggression, and hypertension
Elevated liver enzymes, especially >20 mg/day or 2+ weeks of use
Confirmed doping risk — banned across all tested competitive levels
Handling & Compliance
For Research Use Only — Not for human or veterinary useStore at 20–25°C, protect from light and moisturePurchase confirms qualified researcher statusListed on WADA Prohibited List S1 — any exposure triggers a positive test
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Package:100 tablets | 5 mg per tablet
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CAS Number:76-43-7
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Molecular formula:C<sub>20</sub>H<sub>29</sub>FO<sub>3</sub>
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Country of manufacture:Europe