Dianoged-inj 100mg EPF

£40.00

Pharmaceutical-grade Methandienone 100 mg/mL injectable (Euro Prime Farmaceuticals Dianoged-inj analytical standard). Complete clinical and analytical profile for licensed anti-doping, forensic, and research laboratories. Purity ≥99.5%, full verification package. Strictly not for human use or sale.

Dianoged-inj 100mg EPF
Dianoged-inj 100mg EPF
£40.00

Dianoged-inj 100 mg/mL by Euro Prime Farmaceuticals (EPF) is one of the highest-concentration oil-based injectable methandienone formulations currently documented in European forensic seizures and WADA casework. This analytical reference standard exactly replicates the original EPF high-potency composition and is supplied exclusively to licensed institutions for LC-MS/MS method validation, high-dose metabolite profiling, stability studies, and forensic comparison. Purity ≥99.5% independently confirmed by third-party ISO/IEC 17025 laboratories using HPLC, GC-MS, NMR, and FTIR.

  • Appearance: Clear, deep golden to amber viscous oily solution
  • Concentration: 100 mg/mL methandienone
  • Molecular Formula: C20H28O2
  • Molecular Weight: 300.44 g/mol

Dianoged-inj 100 mg EPF — Clinical & Pharmaceutical Reference Guide

Introduction

Dianoged-inj 100 mg/mL from Euro Prime Farmaceuticals (EPF) represents the ultra-high-strength evolution of injectable methandienone (methandrostenolone) in the modern European underground laboratory landscape. By doubling the concentration of standard injectable Dianabol while maintaining oil-based solubility, this formulation produces a uniquely intense pharmacokinetic and metabolite profile in research models. Authenticated reference material is indispensable for anti-doping laboratories, law-enforcement forensics, and academic researchers studying high-dose 17α-alkylated steroid administration, prolonged metabolite detection, and parenteral delivery systems.

Key Features & Scientific Relevance

  • Purity ≥99.5% independently verified by ISO/IEC 17025-accredited third-party laboratories
  • Exact replication of original Euro Prime Farmaceuticals Dianoged-inj 100 mg/mL high-potency formula
  • Primary ultra-high-strength injectable methandienone reference in current WADA and European forensic screening
  • Complete analytical data package (CoA, 1H/13C-NMR, LC-MS/MS, GC-MS, HPLC chromatograms) included
  • Supplied exclusively to institutions holding valid controlled-substance registration

This clinical profile of Dianoged-inj 100 mg EPF is the definitive resource for regulated high-concentration injectable methandienone analytics.

Product Specifications

  • Active Compound: Methandienone (17β-hydroxy-17α-methylandrosta-1,4-dien-3-one)
  • Brand: Dianoged-inj (Euro Prime Farmaceuticals – EPF)
  • Strength: 100 mg/mL
  • Typical Vehicle: Miglyol 840, benzyl benzoate, benzyl alcohol (high-solubility carrier system)
  • CAS Number: 72-63-9
  • Molecular Formula: C20H28O2
  • Molecular Weight: 300.44 g/mol
  • Structural Classification: 17α-methylated anabolic-androgenic steroid; C17-α alkylated, high-potency oil-based injectable
  • Appearance: Clear deep golden to amber viscous solution

These parameters are identical to the original EPF high-strength manufacturing specification.

Applications & Usage

Licensed laboratories utilize this reference standard for:

  • Validation of ultra-sensitive LC-MS/MS methods at elevated methandienone concentrations
  • Direct forensic comparison of seized high-potency Euro Prime Farmaceuticals preparations
  • Stability and forced-degradation studies of concentrated oil-based 17α-alkylated steroids
  • Pharmacokinetic research involving high-dose parenteral methandienone administration
  • Quality-control calibration in accredited contract analytical organizations

All use must occur under approved controlled-substance protocols.

Purity & Analytical Testing

Every batch undergoes comprehensive third-party characterization including:

  • High-Performance Liquid Chromatography (HPLC) with PDA/UV detection
  • Gas Chromatography-Mass Spectrometry (GC-MS)
  • Nuclear Magnetic Resonance (1H-NMR and 13C-NMR)
  • Fourier-Transform Infrared Spectroscopy (FTIR)
  • Residual solvent and heavy-metal screening per ICH guidelines

Certificate of Analysis confirms ≥99.5% purity and absence of related impurities such as 17-epimethandienone or unreacted precursors.

Safety & Handling Guidelines

Methandienone is a Schedule III (US) / Class C (EU) controlled substance. Handle only under fume hood wearing nitrile gloves, safety goggles, and laboratory coat. Store upright at 15–30 °C, protected from light, in a locked, access-restricted cabinet. Disposal must follow hazardous-waste and controlled-substance destruction regulations.

Secure & Confidential Distribution for Institutions

Material is released solely to verified license holders in plain, unmarked, tamper-evident packaging compliant with IATA dangerous-goods requirements. No external labeling reveals contents. Analytical documentation is delivered via secure encrypted portal with mandatory chain-of-custody records.

Why Choose This Reference Material?

  • Exact match to Euro Prime Farmaceuticals Dianoged-inj 100 mg/mL ultra-high-potency formulation
  • Full analytical data package supplied with every lot
  • Trusted by leading European and international anti-doping and forensic laboratories
  • Meets or exceeds ISO/IEC 17025 and GMP reference-standard specifications

Legal & Safety Disclaimer

Dianoged-inj 100 mg EPF reference standard is intended exclusively for analytical, forensic, research, and educational purposes within licensed facilities. It is not for human or veterinary use, not for resale as a medicinal product, and not available to individuals. Possession requires valid controlled-substance authorization. All local, national, and international regulations must be strictly observed.

FAQ Section

What is Dianoged-inj 100 mg EPF?

Dianoged-inj is a premium European-brand 100 mg/mL ultra-high-strength oil-based injectable formulation of Methandienone manufactured by Euro Prime Farmaceuticals (EPF), supplied only as an analytical reference standard.

Is high-concentration injectable methandienone regulated?

Yes, it is classified as Schedule III in the United States, Class C in the EU, and strictly regulated worldwide.

How is pharmaceutical-grade purity verified?

Purity is independently confirmed using HPLC, GC-MS, NMR, and FTIR by accredited laboratories; results are documented in the Certificate of Analysis.

How should Dianoged-inj 100 mg reference material be stored?

Store at 15–30 °C, protected from light, in a secure, access-restricted location compliant with controlled-substance regulations.

Who is authorized to acquire this analytical standard?

Only licensed analytical laboratories, forensic units, academic institutions, and pharmaceutical organizations holding appropriate controlled-substance registration may possess this material.

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