Description
Buy Trenbolone Acetate Powder Online | Secured Tracked Logistics EU
Order High-Purity Trenbolone Acetate Powder for Laboratory Research
Technical Specifications & Product Identification Data
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- Systematic IUPAC Nomenclature: [(10R,13R,17R)-13-methyl-3-oxo-2,6,7,8,14,15,16,17-octahydro1H-cyclopenta[a]phenanthren-17-yl] acetate
- Standard CAS Registry Number: 10161-34-9 (Raw Base Ester Form)
- Molecular Formula: C₂₀H₂₄O₃ (Refined Unadulterated Powder Form)
- Exact Molar Mass: 312.41 g/mol
- Physical Presentation: Pale yellow to dense yellow crystalline homogenous powder
- Structural Classification: Nandrolone-derived 19-nor (19-demethyl) anabolic steroid analogue featuring three conjugated double bonds across the core ring system and a short acetate ester linked at the 17-beta position.
Theoretical Pharmacology & Documented Adverse Effects
Legal Status & European Regulations
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- European Union: Severely penalized and scheduled under anti-doping acts and medicine safety frameworks across all Member States. Distribution, unauthorized wholesale logistics, and possession of bulk powder matrices outside licensed clinical medical operations face severe criminal prosecution under EU law.
- United Kingdom: Monitored as a Class C controlled substance under the Misuse of Drugs Act 1971, making any form of unauthorized commercial importing, manufacturing, or distribution entirely illegal.
- 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 an ultra-potent 19-nor anabolic derivative, exposure to Trenbolone Acetate powder carries critical cardiovascular and neurological dangers. Documented adverse reactions include severe cardiac hypertrophy, renal strain, extreme lipid imbalances, and profound psychomotor agitation.
Trenbolone Acetate lacks a carbon atom at the 19th position (making it a 19-nor compound) and features a triple-bond backbone system that drastically accentuates its receptor affinity. Furthermore, it incorporates a short, rapid-clearing two-carbon acetate ester tail, whereas Testosterone Enanthate uses a longer seven-carbon enanthate chain to retard clear-out kinetics.
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.
