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.

ANDROXINE 50mg ALPHA PHARMA

  • 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. ANDROXINE 50mg ALPHA PHARMA

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. ANDROXINE 50mg ALPHA PHARMA

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. ANDROXINE 50mg ALPHA PHARMA

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. ANDROXINE 50mg ALPHA PHARMA

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