Boldenone 200 mg MultiPharm

Boldenone 200 mg MultiPharm is a certified pharmaceutical-grade analytical reference standard containing 200 mg/mL of Boldenone Undecylenate in 10 mL multidose vials. Manufactured under rigorously controlled conditions by MultiPharm, each batch is verified to ≥99.5% purity using orthogonal analytical techniques (HPLC, GC-MS, NMR, FTIR) and is supplied exclusively to licensed anti-doping, forensic, and academic institutions for instrument calibration, method validation, and residue analysis. Complete Certificate of Analysis with raw spectroscopic data included. Not for human or veterinary administration.

Physical and Chemical Properties

• Concentration: 200 mg/mL Boldenone Undecylenate
• Volume: 10 mL per vial
• Appearance: Clear golden-yellow viscous oil
• Molecular Formula: C₃₀H₄₄O₃
• Molecular Weight: 452.67 g/mol
• CAS Number: 13103-34-9
• Vehicle: Refined grape seed oil + benzyl benzoate/benzyl alcohol

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Boldenone 200 mg MultiPharm — Clinical & Pharmaceutical Reference Guide

Introduction

Boldenone 200 mg MultiPharm is a precisely standardized 200 mg/mL certified reference material of Boldenone Undecylenate produced by MultiPharm for professional analytical and forensic laboratories worldwide. This classic 200 mg/mL concentration with the long-acting undecylenate ester exactly replicates the original veterinary formulation that has served as the global benchmark for decades in anti-doping control, forensic toxicology, and veterinary residue monitoring. Pharmaceutical-grade Boldenone 200 mg MultiPharm provides licensed institutions with an ultra-pure, fully characterized standard essential for accurate identification and quantification of boldenone and its metabolites.

Key Features & Scientific Relevance

• Pharmaceutical-grade purity ≥99.5% confirmed by multiple orthogonal methods
• Authentic 200 mg/mL concentration in 10 mL vials – identical to historical veterinary products
• Primary reference material in WADA-accredited and ISO/IEC 17025 laboratories
• Full analytical data package supporting regulatory submissions and peer-reviewed publications
• Secure distribution protocols designed for Schedule III controlled substances

Product Specifications

• Product Reference: Boldenone 200 mg MultiPharm
• Active Ingredient: Boldenone Undecylenate 200 mg/mL
• Presentation: 10 mL sterile glass vial with bromobutyl stopper and tamper-evident flip-off cap
• Excipients: Grape seed oil USP, benzyl benzoate 20%, benzyl alcohol 2%
• IUPAC Name: (17β)-3-Oxoandrosta-1,4-dien-17-yl undec-10-enoate
• Classification: Long-acting anabolic-androgenic steroid ester (Schedule III / international equivalent)

Applications & Usage

Boldenone 200 mg MultiPharm 10 mL is restricted to regulated professional applications including:

• Validation of LC-MS/MS and GC-MS screening and confirmation methods
• Preparation of authentic matrix-matched calibration standards and quality-control samples
• Forensic confirmation of boldenone administration in human and animal matrices
• Research into ester hydrolysis kinetics and phase II conjugation pathways
• Inter-laboratory proficiency testing and external quality assurance programs

All handling requires documented chain-of-custody and controlled-substance licensing.

Purity & Analytical Testing

Every batch undergoes exhaustive verification:

• HPLC-UV/DAD: ≥99.5% assay with complete impurity profile
• GC-MS (TMS derivatization): Characteristic ions m/z 206, 296, 410, 452
• Quantitative 1H/13C NMR: Internal standard calibration against certified references
• FTIR: Confirmation of ester carbonyl (1730 cm⁻¹) and conjugated dienone (1655 cm⁻¹)

Full raw data and processed spectra are provided with each authenticated vial.

Safety & Handling Guidelines

Boldenone Undecylenate is classified Repr. 1B and potential carcinogen. Mandatory controls:

• Minimum PPE: nitrile gloves, laboratory coat, safety goggles, fume hood
• Storage: 2–8 °C protected from light; do not freeze
• Double-locked controlled-substance storage with restricted access only
• Disposal via licensed hazardous waste contractor

Secure & Confidential Distribution for Institutions

Delivery to verified institutions occurs in unmarked, temperature-monitored compliance packaging via tracked courier. No chemical identifiers appear on exterior labels. Documentation includes:

• Batch-specific Certificate of Analysis
• Safety Data Sheet
• Controlled-substance declaration forms (where required)

Possession requires valid DEA Schedule III registration or equivalent international licensing.

Why Choose This Reference Material?

• Exact replication of the original 200 mg/mL veterinary formulation used globally for decades
• Produced by established manufacturer MultiPharm with proven batch consistency
• Comprehensive analytical documentation suitable for publication and regulatory filings
• Trusted worldwide by anti-doping agencies, forensic institutes, and academic laboratories

Legal & Safety Disclaimer

Boldenone 200 mg MultiPharm is supplied exclusively as an analytical reference standard for licensed laboratories and accredited research institutions. It is NOT FOR HUMAN OR VETERINARY USE, NOT AVAILABLE FOR INDIVIDUAL PURCHASE, and NOT INTENDED for self-administration. Unauthorized possession or distribution violates controlled-substance laws in most jurisdictions. Recipients bear full legal responsibility for compliance with all applicable regulations.

FAQ Section

What is the active compound in Boldenone 200 mg MultiPharm? Boldenone Undecylenate 200 mg/mL — a long-acting ester prodrug of boldenone.

Is Boldenone 200 mg MultiPharm a controlled substance? Yes — Schedule III in the United States and equivalently regulated worldwide.

How is the 200 mg/mL concentration verified? Quantitative NMR (qNMR) and reverse-phase HPLC with internal standardization.

What are the recommended storage conditions? Refrigerate at 2–8 °C in the original sealed vial, protected from light. Stable ≥36 months.

Who is authorized to acquire this reference material? Only accredited analytical laboratories, forensic facilities, and university departments holding valid controlled-substance licenses.

Is a Certificate of Analysis provided? Yes — every vial includes a comprehensive CoA with full analytical raw data and spectra.