Description
Clomid 50 mg
Brand: Magnus Pharmaceuticals
Content: 50 tablets | 50 mg per tablet
Price: €29
Manufactured in: Europe
🧪 Product Overview
Clomid 50 mg delivers clomiphene citrate, a well-studied oral selective estrogen receptor modulator (SERM) designed for hormonal recovery, fertility research, and post-cycle therapy (PCT) studies. By suppressing estrogen’s negative feedback on the hypothalamic–pituitary–gonadal (HPG) axis, clomiphene promotes an increase in luteinising hormone (LH), follicle-stimulating hormone (FSH), and endogenous testosterone levels.
Each film-coated tablet contains 50 mg of clomiphene citrate, with a long elimination half-life (~50 hours) supporting once-daily dosing. It has shown consistent benefits in restoring sperm quality, modulating testosterone:estrogen ratios, and reversing anabolic-induced hormonal suppression. Listed under WADA S4, oral exposure remains a doping liability.
✅ Key Research Highlights
HPG-axis revival:
50 mg/day raised LH and serum testosterone within 4–6 weeks in male hypogonadism studies [PMC]
Fertility support:
Improved sperm concentration and motility in oligozoospermic men [PMC]
PCT utility:
Widely used in post-anabolic steroid cycles to normalize hormonal ratios [Swolverine]
Oral convenience:
~50-hour elimination half-life allows for simple once-daily administration [PubChem, MedlinePlus]
Anti-doping risk:
Listed under WADA S4 — highly detectable; recent bans confirm risk even at low exposure [WADA, The Sun]
🧬 Suggested Laboratory Applications
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Hypogonadism and HPG-axis recovery modeling
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Fertility pathway stimulation and spermatogenesis studies
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Post-cycle hormonal normalization
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Estrogen feedback suppression simulations
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PCT protocols for anabolic steroid models
📊 Technical Specifications
| Field | Data |
|---|---|
| Chemical Name | Clomiphene Citrate (E/Z stereoisomer mixture) |
| Chemical Formula | C₂₆H₂₈ClNO + C₆H₈O₇ → C₃₂H₃₆ClNO₈·C₆H₈O₇ |
| Synonyms | Clomid; Omifin; Serophene; CC; 2-(p-(2-chloro-1,2-diphenylethenyl)phenoxy)-N,N-diethylethanamine |
| Molecular Weight | 405.96 g/mol (free base); 598.09 g/mol (citrate salt) |
| CAS Number | 50-41-9 |
| Half-life | ~50 hours |
| Detection Window | High detectability — anti-doping flags expected |
| Documented Benefits | ↑ LH/FSH, ↑ testosterone, improved sperm count, PCT recovery |
| Main Risks | Visual issues, mood swings, lipid changes, hot flashes |
| Total Active Compound | 2,500 mg per carton (50 mg × 50 tablets) |
| Shelf-life | 36 months (manufacturer specification) |
❄️ PubChem-Supported Research Insights
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Increases LH and FSH via ER modulation at hypothalamic level
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Improves serum testosterone in hypogonadal models
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Enhances fertility parameters: count, motility, morphology
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Supports hormonal balance post-anabolic cycles
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Detectable in anti-doping screens — listed on WADA S4
⚠️ Documented Research Side Effects
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Transient blurred vision and light sensitivity
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Mood fluctuations and hot flashes
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Lipid profile changes (HDL/LDL imbalance)
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Testicular or ovarian enlargement with extended use
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Rare thrombo-embolic events
🧯 Handling & Compliance
For Research Use Only — Not for human or veterinary administration
Store at 15–25 °C, protect from light and moisture
Purchase confirms qualified researcher status
Listed on WADA Prohibited List S4 — any exposure may trigger a positive test
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