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.

Description

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 body’s post-cycle recovery process.

Key Specifications

Ā Active Compound: Clomiphene Citrate (Clomid)

Ā Chemical Formula: C26 H28 CINO • 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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