Halotestin (Fluoxymesterone) 10mg
$100.00
Halotestin supplies 50 oral tablets of high-purity Fluoxymesterone standardized at 10 mg per tablet. Packaged in a secure amber pill bottle, this potent 9\alpha-fluoro-substituted androgen is widely evaluated in laboratory research for its profound effect on central nervous system activation, strength signaling, and non-aromatizing androgen receptor binding. Strictly for laboratory research use only.
Halotestin provides high-purity Fluoxymesterone standardized at 10 mg per tablet (50 tablets per bottle). Fluoxymesterone is an extremely potent halogenated derivative of methyltestosterone, modified at the 9\alpha-fluoro and 11\beta-hydroxy positions to maximize androgenic activity while resisting aromatization and metabolic breakdown.
This oral research compound is extensively studied in biochemical and physiological models for its rapid impact on erythrocyte production, neuromuscular drive, and androgen receptor saturation without estrogenic conversion. The bottle features signature Core Peptides branding and layout for clear cataloging and dose verification.
Key Specifications
Ā Active Compound: Fluoxymesterone (Halotestin)
Ā Chemical Formula: \text{C}_{20}\text{H}_{29}\text{FO}_{3}
Ā Molecular Weight: 336.44\text{ g/mol}
Ā Dosage / Strength: 10 mg per tablet
Ā Quantity: 50 Tablets per Bottle
Ā Brand/Manufacturer: Core Peptides
Ā Formulation: Oral Tablets
Ā Classification: 17$\alpha$-Alkylated Oral Androgen / Research Compound
Dosage & Research Protocol Guidelines
Ā Experimental Standard Dosage: In advanced endocrine evaluation models, standard research protocols analyze daily dosage ranges between 10 mg and 20 mg (1 to 2 tablets).
Ā Administration Frequency: Due to its active half-life of approximately 9.5 hours, daily administration is typically divided into morning and afternoon doses to maintain steady plasma concentration.
Ā Research Model Duration: Experimental observation periods are generally restricted to 3 to 4 weeks maximum due to 17$\alpha$-alkylated hepatic parameters and rapid HPTA suppression dynamics.
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