Description
Buy Testosterone Enanthate Powder Online | Secured Tracked Logistics EU
Order High-Purity Testosterone Enanthate Powder for Laboratory Research
Technical Specifications & Product Identification Data
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- Systematic IUPAC Nomenclature: [(10R,13R,17R)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] heptanoate
- Standard CAS Registry Number: 315-37-7 (Raw Base Ester Form)
- Molecular Formula: C₂₆H₄₀O₃ (Refined Unadulterated Powder Form)
- Exact Molar Mass: 400.60 g/mol
- Physical Presentation: Fine white to off-white crystalline, slightly waxy homogenous powder
- Structural Classification: Anabolic-androgenic steroid derivative featuring a heptanoate (enanthate) fatty acid ester linked at the 17-beta-hydroxyl position of the core cyclopentanoperhydrophenanthrene structure to prolong clear-out clearance kinetics.
Theoretical Pharmacology & Documented Adverse Effects
Legal Status & European Regulations
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- European Union: Heavily restricted, regulated, or classified as controlled prescription-only substances or scheduled narcotics across all EU Member States. National drug acts—such as Germany’s Arzneimittelgesetz (AMG) anti-doping updates and equivalent legislation in France and the Netherlands—strictly criminalize unauthorized production, possession, or distribution outside authorized pharmaceutical manufacturing loops.
- United Kingdom: Classified as a Class C controlled substance under the Misuse of Drugs Act 1971, subject to strict criminal enforcement for unauthorized importing or commercial distribution infrastructure.
- Shipping Policy: Orders addressed to private residential zip codes or unauthorized territories will be delivered securely and discretely at you risk and responsibility
Authorized Research Use & Safety Warning
Frequently Asked Questions (FAQ)
As a potent androgen receptor ligand, exposure to raw Testosterone Enanthate powder can cause deep cardiovascular strain, severe lipid imbalances, suppression of the natural hypothalamic-pituitary-gonadal axis, and severe hepatotoxicity if basic containment barriers collapse.
The addition of the seven-carbon enanthate ester chain changes the molecule’s overall lipophilicity profile. This structural modification slows down the clearance kinetics during laboratory tissue assays, allowing for prolonged analytical observation of receptor binding stability compared to unesterified raw testosterone base.
No. This compound is synthesized and handled strictly as an analytical reference standard. It is not approved for human or veterinary consumption, and any such application is completely illegal and carries life-threatening health and legal consequences.
