Clomid 50 mg
$60.00
Clomid 50 mg is a research-grade oral tablet formulation engineered for high-purity laboratory applications. Each bottle contains 50 tablets of HPLC-verified Clomiphene Citrate, third-party tested to guarantee purity exceeding 99% and manufactured in the USA under strict quality standards. Formulated specifically for research evaluating selective estrogen receptor modulation, GnRH pathway stimulation, and LH/FSH secretion cascades, this product is strictly intended for research use only.
Clomid 50 mg provides high-purity, laboratory-verified research tablets manufactured under strict quality control standards in the USA. Formulated with 50 mg of pure Clomiphene Citrate per tablet a non-steroidal selective estrogen receptor modulator (SERM) this product is engineered for maximum accuracy and reproducibility in biochemical, endocrine, and reproductive biology research examining hypothalamic-pituitary-gonadal (HPG) axis dynamics, gonadotropin stimulation, and estrogen receptor occupancy.
Clomid, or Clomiphene Citrate, finds widespread use among bodybuilders as an integral component of their post-cycle therapy (PCT) regimen, aimed at facilitating recovery after a steroid cycle. Operating as an anti-estrogen compound, Clomid plays a crucial role in reinstating hormonal equilibrium by obstructing estrogen receptors in targeted tissues. This action triggers the release of follicle-stimulating hormone and luteinizing hormone, fostering the natural production of testosterone. This, in turn, helps prevent muscle loss and contributes to the bodyās post-cycle recovery process.
Key Specifications
Ā Active Compound: Clomiphene Citrate (Clomid)
Ā Chemical Formula: C26 H28 CINO ā¢ C6H8O7
Ā Molecular Weight: 598.1 g/mol
Ā Concentration: 50 mg per tablet
Ā Quantity: 50 Tablets
Ā Purity Standard: Exceeds 99% (Third-Party HPLC & Mass Spectrometry Verified)
Ā Formulation: Solid Oral Research Tablets
Ā Origin: Manufactured in USA
Ā Classification: Research Use Only
Primary Research Applications
Ā Hypothalamic Estrogen Receptor Antagonism: Clomiphene competes with endogenous estrogen for binding sites in the hypothalamus, blocking negative feedback and serving as a critical tool to study GnRH pulse frequency upregulation.
Ā Gonadotropin Secretion (LH & FSH Dynamics): Widely utilized in rodent and cell culture models to measure downstream pituitary release of Luteinizing Hormone (LH) and Follicle-Stimulating Hormone (FSH).
Ā Endogenous Testosterone & Steroidogenesis Pathways: Extensively researched in endocrinology protocols to evaluate testicular Leydig cell activation and intratesticular testosterone synthesis following pituitary gonadotropin release.
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Key Specifications
Ā Active Compounds: Sermorelin (GHRH 1-29) & GHRP-2 (Pralmorelin)
Ā Blend Ratio / Concentration: 5 mg Sermorelin + 5 mg GHRP-2 (10 mg total per vial)
Ā Chemical Formulas: \text{C}_{149}\text{H}_{246}\text{N}_{44}\text{O}_{42} (Sermorelin) / \text{C}_{45}\text{H}_{55}\text{N}_{9}\text{O}_{6} (GHRP-2)
Ā Purity Standard: Exceeds 99% (Third-Party HPLC Verified)
Ā Formulation: Sterile Lyophilized Powder
Ā Origin: Manufactured in USA
Ā Classification: Research Use Only
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Ā Dual-Mechanism GH Secretion Synergy: Combines GHRH receptor stimulation (Sermorelin) with ghrelin/growth hormone secretagogue receptor (GHS-R) binding (GHRP-2) to analyze supra-additive pituitary growth hormone pulsatility.
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Ā Metabolic Rate & Lipid Oxidation: Investigated in body composition models to assess lipolysis mechanisms, visceral fat metabolism, and recovery dynamics following cellular stress.
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