Boldenon 250mg Ice Pharmaceuticals

Boldenon 250mg Ice Pharmaceuticals is a high-concentration (250 mg/mL) certified analytical reference standard of Boldenone Undecylenate supplied in 10 mL vials exclusively for licensed analytical, forensic, and research laboratories. Each batch is verified to ≥99.5% purity by orthogonal methods (HPLC, GC-MS, NMR, FTIR) and includes a full Certificate of Analysis with raw data. Intended solely for instrument calibration, method validation, anti-doping testing, and residue analysis. Not for human or veterinary administration.

Physical and Chemical Properties

• Concentration: 250 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 with benzyl benzoate and benzyl alcohol

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Boldenon 250mg Ice Pharmaceuticals — Clinical & Pharmaceutical Reference Guide

Introduction

Boldenon 250mg Ice Pharmaceuticals is a precisely manufactured 250 mg/mL Boldenone Undecylenate certified reference material designed specifically for professional analytical and forensic applications. The 250 mg/mL concentration, combined with the long-acting undecylenate ester, mirrors formulations frequently encountered in both historical veterinary products and contemporary illicit sources, making it an indispensable standard for anti-doping laboratories, national forensic services, and academic research groups worldwide. Pharmaceutical-grade Boldenon 250mg Ice Pharmaceuticals provides licensed institutions with an ultra-pure, fully characterized reference for accurate qualitative and quantitative analysis of boldenone and its metabolites.

Key Features & Scientific Relevance

• Pharmaceutical-grade purity ≥99.5% confirmed by multiple independent analytical techniques
• 250 mg/mL strength in convenient 10 mL vials for high-level calibrators and fortified samples
• Primary reference material in WADA-accredited laboratories and ISO/IEC 17025 facilities
• Comprehensive analytical data package supporting regulatory submissions and publications
• Secure, compliance-focused handling and distribution for Schedule III controlled substances

Product Specifications

• Product Reference: Boldenon 250mg Ice Pharmaceuticals
• Active Ingredient: Boldenone Undecylenate 250 mg/mL
• Presentation: 10 mL sterile glass vial with rubber stopper and tamper-evident flip-off cap
• Excipients: Grape seed oil USP, benzyl benzoate 20–25%, benzyl alcohol 2%
• Chemical Name: (17β)-3-Oxoandrosta-1,4-dien-17-yl undec-10-enoate
• Classification: Long-acting anabolic-androgenic steroid ester (Schedule III / equivalent)

Applications & Usage

Boldenon 250mg Ice Pharmaceuticals 10 mL is used exclusively in regulated environments for:

• Validation of ultra-sensitive LC-MS/MS and GC-MS detection methods
• Preparation of matrix-matched quality-control and calibration standards
• Forensic confirmation of boldenone administration in human and animal matrices
• Research into ester hydrolysis and phase II metabolic pathways
• Proficiency testing and external quality assurance programs

All activities require documented chain-of-custody and controlled-substance licensing.

Purity & Analytical Testing

Each batch undergoes exhaustive characterization:

• HPLC-UV/DAD: ≥99.5% assay with full impurity profile
• GC-MS (after derivatization): Diagnostic ions m/z 206, 296, 410, 452
• 1H/13C NMR: Complete structural assignment against certified reference spectra
• FTIR: Confirmation of ester and conjugated dienone functional groups

Full raw data and processed results are supplied with every authenticated vial.

Safety & Handling Guidelines

Boldenone Undecylenate is classified as reproductive toxicant Category 1B and potential carcinogen. Required controls include:

• PPE: nitrile gloves, laboratory coat, safety goggles, fume hood ventilation
• 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 plain, 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 250 mg/mL concentration replicates real-world samples for authentic matrix studies
• Unmatched analytical documentation for regulatory and peer-reviewed work
• Superior batch-to-batch consistency critical for long-term research
• Trusted globally by anti-doping agencies, forensic institutes, and university laboratories

Legal & Safety Disclaimer

Boldenon 250mg Ice Pharmaceuticals is provided strictly 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 under any circumstances. Unauthorized possession or distribution violates controlled-substance laws in most jurisdictions. Recipients accept full responsibility for compliance with all applicable regulations.

FAQ Section

What is the active compound in Boldenon 250mg Ice Pharmaceuticals? Boldenone Undecylenate 250 mg/mL — a long-acting ester prodrug of boldenone.

Is Boldenon 250mg Ice Pharmaceuticals regulated? Yes — Schedule III in the United States and equivalently controlled worldwide.

How is the 250 mg/mL concentration confirmed? Quantitative NMR (qNMR) and HPLC with internal standardization against certified references.

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

Who may legally acquire this reference material? Only accredited analytical laboratories, forensic facilities, and university departments with valid controlled-substance licensing.

Is documentation provided with each vial? Yes — every vial includes a comprehensive Certificate of Analysis with full analytical raw data.