Clomid 50 mg
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- Clomid 50 mg
- Brand: Magnus Pharmaceuticals
- Content: 50 tablets | 50 mg per tablet
- 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
Hypogonadism and HPG-axis recovery modeling
Fertility pathway stimulation and spermatogenesis studies
Post-cycle hormonal normalization
Estrogen feedback suppression simulations
PCT protocols for anabolic steroid models
Technical Specifications
| Field | Data |
|---|---|
| Chemical Name | Clomiphene Citrate (E/Z stereoisomer mixture) |
| Chemical Formula | CHClNO + CHO CHClNO·CHO |
| 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
Increases LH and FSH via ER modulation at hypothalamic level
Improves serum testosterone in hypogonadal models
Enhances fertility parameters: count, motility, morphology
Supports hormonal balance post-anabolic cycles
Detectable in anti-doping screens — listed on WADA S4
Documented Research Side Effects
Transient blurred vision and light sensitivity
Mood fluctuations and hot flashes
Lipid profile changes (HDL/LDL imbalance)
Testicular or ovarian enlargement with extended use
Rare thrombo-embolic events
Handling & Compliance
For Research Use Only — Not for human or veterinary administrationStore at 15–25°C, protect from light and moisturePurchase confirms qualified researcher statusListed on WADA Prohibited List S4 — any exposure may trigger a positive test
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Package:50 tablets | 50 mg per tablet
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CAS Number:50-41-9
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Molecular formula:C₂₆H₂₈ClNO + C₆H₈O₇ → C₃₂H₃₆ClNO₈·C₆H₈O₇
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Country of manufacture:Europe
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Half-life:~50 hours