Boldenon 250mg Ice Pharmaceuticals

Boldenon 250mg Ice Pharmaceuticals is a pharmaceutical-grade analytical reference standard containing 250 mg/mL of Boldenone Undecylenate in a 10 mL multidose vial. Manufactured under rigorously controlled conditions, each batch is verified to ≥99.5% purity using orthogonal analytical techniques (HPLC, GC-MS, NMR, FTIR) and is supplied exclusively to licensed institutions for instrument calibration, method validation, anti-doping control, and forensic toxicology. Full Certificate of Analysis and raw spectroscopic data accompany every vial. Not for human or veterinary use.

Physical and Chemical Properties

• Concentration: 250 mg/mL Boldenone Undecylenate
• Volume: 10 mL per vial
• Appearance: Clear, golden-yellow viscous oily solution
• Molecular Formula: C₃₀H₄₄O₃
• Molecular Weight: 452.67 g/mol
• CAS Number: 13103-34-9
• Vehicle: High-purity grape seed oil + benzyl benzoate/benzyl alcohol

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Boldenon 250mg Ice Pharmaceuticals — Clinical & Pharmaceutical Reference Guide

Introduction

Boldenon 250mg Ice Pharmaceuticals is a high-concentration (250 mg/mL) certified reference material of Boldenone Undecylenate specifically formulated for professional analytical and forensic laboratories. The 250 mg/mL strength, combined with the long-chain undecylenate ester, replicates formulations historically encountered in both veterinary medicine and illicit markets, making it an essential standard for anti-doping laboratories, national forensic institutes, and reference-material collections worldwide. Pharmaceutical-grade Boldenon 250mg Ice Pharmaceuticals provides licensed professionals with an ultra-pure, fully characterized tool for accurate identification and quantification of boldenone and its metabolites in complex biological samples.

Key Features & Scientific Relevance

• Pharmaceutical-grade purity ≥99.5% confirmed by multiple orthogonal methods
• 250 mg/mL concentration in 10 mL vials – ideal for preparation of high-level calibrators and fortified samples
• Critical reference standard in WADA-accredited and ISO/IEC 17025 laboratories
• Complete analytical data package supporting regulatory submissions and peer-reviewed research
• Secure handling and distribution protocols designed for Schedule III controlled substances

Product Specifications

• Product Reference: Boldenon 250mg Ice Pharmaceuticals
• Strength: Boldenone Undecylenate 250 mg/mL
• Presentation: 10 mL sterile glass vial with bromobutyl stopper and tamper-evident seal
• Excipients: Refined grape seed oil USP, benzyl benzoate 20–25%, 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 / equivalent)

Applications & Usage

Boldenon 250mg Ice Pharmaceuticals 10 mL is restricted to regulated professional settings including:

• Development and validation of ultra-sensitive LC-MS/MS and GC-MS methods
• Preparation of high-concentration quality-control samples and calibration curves
• Forensic confirmation of boldenone administration in human and animal samples
• Research into ester hydrolysis kinetics and glucuronide/sulfate conjugation
• External quality assurance schemes and proficiency testing programs

All procedures require documented chain-of-custody and appropriate licensing.

Purity & Analytical Testing

Every batch is exhaustively characterized:

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

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

Safety & Handling Guidelines

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

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

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 package includes:

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

Possession requires valid DEA Schedule III registration or international equivalent.

Why Choose This Reference Material?

• Exact 250 mg/mL concentration matches emerging illicit-market trends for authentic matrix studies
• Unparalleled analytical documentation suitable for publication and regulatory filings
• Superior batch-to-batch consistency essential for longitudinal research
• Trusted globally by anti-doping agencies, forensic institutes, and academic laboratories

Legal & Safety Disclaimer

Boldenon 250mg Ice Pharmaceuticals 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 ingredient in Boldenon 250mg Ice Pharmaceuticals? Boldenone Undecylenate 250 mg/mL — a long-acting ester of 1-dehydrotestosterone.

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

How is the 250 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.