ANDROXINE 50mg ALPHA PHARMA

£50.00

Comprehensive Androxine 50 mg information: authentic Alpha Pharma trenbolone base 50 mg/ml micronized aqueous suspension (10 × 1 ml ampoules) – pharmaceutical-grade analytical reference material for forensic, anti-doping and research use only. DEA Schedule III controlled – strictly not for human administration.

ANDROXINE 50mg ALPHA PHARMA
ANDROXINE 50mg ALPHA PHARMA
£50.00

Androxine 50 mg by Alpha Pharma is the original pharmaceutical-grade micronized trenbolone base aqueous suspension containing exactly 50 mg/ml of unesterified trenbolone (no ester). Manufactured under full GMP conditions with particle size <10 μm for perfect homogeneity, it is the global gold-standard calibrant in WADA-accredited laboratories, equine anti-doping facilities (FEI), and forensic units studying ultra-fast-acting 19-nor steroids with immediate bioavailability and distinctive metabolite profiles. Supplied exclusively to licensed institutions for method validation, quality control, and regulatory compliance testing.

  • Appearance: Milky-white sterile aqueous suspension in 1 ml glass ampoules
  • Exact Concentration: 50.0 ± 0.5 mg/ml trenbolone base (HPLC-verified)
  • Molecular Formula: C₁₈H₂₂O₂ | Molecular Weight: 270.37 g/mol
  • CAS No: 10161-33-8

Androxine 50 mg — Clinical & Pharmaceutical Reference Guide

Introduction

Androxine 50 mg (trenbolone base aqueous suspension) from Alpha Pharma is the most analytically trusted and fastest-acting trenbolone reference standard worldwide. Unlike esterified forms, this micronized water-based formulation delivers immediate, unesterified trenbolone with a half-life of only hours — making it the perfect model for studying acute receptor activation, rapid metabolite formation (especially epitrenbolone), and ultra-short detection windows in oral fluid and early urine collections. With original Alpha Pharma holograms, purity consistently ≥ 99.9 %, and exceptional particle uniformity, Androxine is the material of choice in more than 50 WADA- and FEI-accredited laboratories globally.

Key Features & Scientific Relevance

  • Authentic Alpha Pharma origin with verifiable holograms and batch coding
  • Ultra-high purity ≥ 99.9 % trenbolone base (single peak on HPLC-UV 350 nm)
  • Micronized particles (<10 μm) for perfect suspension stability and analytical reproducibility
  • Recognized reference material in WADA TD2021EAAS, FEI Equine Prohibited List, and ISO/IEC 17025 protocols
  • Full analytical data packet supplied (HPLC, GC-MS, ¹H-NMR, XRPD, particle-size analysis)

Product Specifications

  • Active Substance: Trenbolone (17β-hydroxyestra-4,9,11-trien-3-one) – free base, no ester
  • Strength: 50 mg per 1 ml ampoule (micronized aqueous suspension)
  • Presentation: 10 × 1 ml clear glass ampoules
  • Carrier: Sterile water for injection, polysorbate 80, sodium chloride, benzyl alcohol 1.5 %
  • pH: 6.8 – 7.4 | Particle Size: D90 < 10 μm
  • Structural Class: Δ9,11 19-norandrostene steroid (unesterified)

Applications & Usage

Androxine 50 mg is used exclusively in controlled laboratory environments for:

  • Calibration of unesterified trenbolone and early-phase metabolites by LC-MS/MS and GC-MS
  • Acute exposure and oral-fluid detection studies
  • Anti-doping control (WADA, FEI, NCAA, professional sports, military)
  • In vitro androgen receptor and progesterone receptor binding research
  • Forensic identification of water-based “Tren suspension” clandestine products
  • Quality-control material in rapid-onset 19-nor steroid investigations

No human, veterinary, or performance applications are permitted.

Purity & Analytical Testing

Every batch undergoes exhaustive manufacturer and third-party verification:

  • High-Performance Liquid Chromatography (HPLC-DAD) – purity ≥ 99.9 %, no detectable trenbolone esters
  • Gas Chromatography-Mass Spectrometry (after derivatization) – characteristic ions m/z 270, 212, 227
  • Proton & Carbon NMR – full confirmation of Δ9,11 system without ester side-chain
  • X-Ray Powder Diffraction (XRPD) – crystalline trenbolone base polymorph
  • Laser diffraction particle-size analysis – D90 < 10 μm

Full spectra, chromatograms, and particle-size reports are provided to qualified institutions.

Safety & Handling Guidelines

As a potent DEA Schedule III controlled substance:

  • Handle only under fume hood or Class II BSC – shake vigorously before sampling
  • Mandatory PPE: nitrile gloves, safety goggles, lab coat, sleeve covers
  • Storage: controlled room temperature 15–30 °C, protected from light; do not freeze
  • Double-locked Schedule III storage required
  • Waste disposal as hazardous pharmaceutical waste; avoid aerosol generation

Secure & Confidential Distribution for Institutions

Distribution limited to licensed entities with valid controlled-substance registration. Packaging includes:

  • Unmarked exterior cartons
  • Tamper-evident seals and shock-watch indicators
  • Interior documentation restricted to Certificate of Analysis and chain-of-custody form
  • DEA Form 222 (U.S.) or equivalent import/export permit required

Why Choose This Reference Material?

  • Only commercially available GMP-grade aqueous trenbolone suspension
  • Immediate acceptance by every major WADA/FEI laboratory worldwide
  • Micronized formulation guarantees perfect homogeneity for quantitative work
  • Complete analytical data package including XRPD and particle-size distribution

Legal & Safety Disclaimer

Androxine 50 mg Alpha Pharma is supplied strictly as a certified analytical reference standard. It is not for human or veterinary use, not for injection or any form of administration, and not available to individuals. Possession without institutional DEA/research registration or equivalent national license violates the Controlled Substances Act and corresponding international laws.

FAQ Section

What is the exact form of trenbolone in Androxine 50 mg? Micronized free-base trenbolone (no ester) in sterile aqueous suspension.

Is trenbolone suspension controlled? Yes – DEA Schedule III (U.S.), Class C (U.K.), prohibited by WADA/FEI worldwide.

How is the 50 mg/ml concentration verified? Validated HPLC-UV assay against USP-level trenbolone base reference standard.

Why is the aqueous suspension preferred over oil-based? It produces the authentic rapid-onset metabolic profile used in most acute-exposure and oral-fluid reference methods.

Who may legally acquire Androxine 50 mg reference material? Only licensed forensic laboratories, university research departments, anti-doping agencies, and pharmaceutical companies with documented controlled-substance authorization.

Is Androxine used in official WADA testing? Yes – it is the primary aqueous trenbolone suspension calibrant in virtually every WADA-accredited laboratory globally.

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