Bromazolam Light Pellets 3mg

Buy Bromazolam Light Pellets  3mg Online

Buy Bromazolam Light Pellets  3mg (8‑bromo‑1‑methyl‑6‑phenyl‑4H‑[1,2,4]triazolo[4,3‑a][1,4]benzodiazepine) is a triazolobenzodiazepine derivative designed as a stable organic analytical standard.
The 3 mg “Light Pellet” formulation is developed for rapid dissolution, low matrix interference, and optimized mass accuracy in analytical and computational chemistry applications.

Each pellet achieves ≥ 99.0 % HPLC purity, with homogeneous weight distribution for quantitative assay calibration, spectroscopic validation, and theoretical studies in chemical informatics.

⚠️ For laboratory, forensic, and analytical research only. Not for human consumption or clinical use.

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Chemical Identity

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Applications Across Chemistry Disciplines

Organic & Inorganic Chemistry

• The triazole and diazepine fusion provides an excellent case study for heterocyclic stability and π‑electron conjugation.
• The bromo substitution on the aryl ring enables exploration of C–Br activation in cross‑coupling reactions (Suzuki, Heck, and Buchwald–Hartwig mechanisms).
• Used as a model compound for investigating electrophilic aromatic substitution, halogenation kinetics, and hydrogen‑bonded transition states.
• In inorganic chemistry, the heterocyclic nitrogens serve as simulated ligand donor sites in metal–ligand complexation studies.

Chemical Biology

• Utilized for structure‑activity relationship (SAR) studies of non‑biological analogues of GABA_A modulators.
• Ideal for predictive modeling of lipophilicity, log P/log D, and pKa in virtual screening without bioassay testing.
• A reactive framework for understanding amide–azole interactions and proton transfer dynamics in chemical biophysics.
• Benchmark compound for machine‑learning datasets on benzodiazepine ring reduction and drug‑like property estimation.

Computational Chemistry

• Facilitates DFT and MLHF optimizations, yielding valuable electronic and molecular orbital data.
• Used as a model for MEP (Electrostatic Potential Map), HOMO–LUMO gap, and charge distribution analyses.
• Included in MD and ab initio simulations for multi‑ring heteroaromatic stability profiling.
• Supports QSPR modelling and QSAR training datasets for AI‑assisted chemical prediction engines.

Environmental Chemistry

• Serves as an internal standard for LC–MS/MS and GC–MS wastewater and river water analysis.
• Included in studies on degradation kinetics, oxidative persistence, and soil absorption coefficients (Koc, Kow).
• Used for developing calibration curves in environmental monitoring of benzodiazepine residues.
• Facilitates evaluations of AOP (Advanced Oxidation Processes) efficiency under UV and catalytic conditions.

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Laboratory Equipment & Consumables

Recommended Instrumentation

• HPLC/UPLC: Purity and retention factor validation.
• LC–MS/MS: Mass identification (m/z ≈ 370 for [M + H]⁺).
• FTIR: C=O stretch (≈ 1655 cm⁻¹) and C–Br bond (≈ 600–630 cm⁻¹).
• ¹H/¹³C NMR: Used to confirm structure and ring fusion patterns.
• DSC/TGA: Examination of melting and thermal stability parameters.

Essential Consumables

• HPLC Solvents: acetonitrile, methanol, DMSO, and chloroform (analytical grade).
• Glassware: amber vials, PTFE‑lined caps to prevent oxidation/light exposure.
• Instruments: precision microbalances (± 0.1 mg) and graded pipettes for solution quantification.
• PPE: nitrile gloves, anti‑fog safety goggles, lab coat, and adequate ventilation in fume hood.

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Regulation & Safety

Regulatory Status

• Supplied exclusively for research and analytical testing; not approved for pharmaceutical applications.
• Controlled distribution policy applies in some jurisdictions (consult local legislation).
• Compliant with European REACH, GHS, and chemical data handling standards.

Indicative GHS Classification

⚠️ Harmful if swallowed (Category 4)
⚠️ Causes eye irritation (Category 2A)
⚠️ Toxic to aquatic life (Category 3)

Safety Handling Guidelines

• Manage in fume hood under controlled conditions.
• Prevent contact with oxidizers and strong acids.
• Dispose via licensed organic waste contractors per EPA and OECD chemical protocols.
  - Delivered with Safety Data Sheet (SDS) and Certificate of Analysis (CoA) for traceability.

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Chemical Informatics Integration

• Canonical SMILES: Cn1c2cc(Br)ccc2n2ncc(c12)c3ccccc3
• Descriptors Available: Molecular Weight, TPSA, Dipole Moment, log P, Hydrogen Bond Donors/Acceptors.
• Software Compatibility: ChemDraw, RDKit, Open Babel, KNIME, Schrödinger, ChemAxon, and Biovia.
• Fully formatted for integration into LIMS and FAIR‑compliant databases.
• Provides structure‑property files in SDF, MOL, CSV, and JSON formats.
• Useful for cheminformatics AI modelling and data standardization across multi‑disciplinary datasets.

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Analytical Characterization Summary

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Storage & Stability

• Store below 25 °C, in dry, light‑protected conditions.
• Keep sealed within original amber vials until use.
• Avoid UV exposure and oxidizing environments.
• Shelf life: ≥ 24 months (quality maintained under GLP storage).

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SEO Optimized Keywords

Bromazolam Light Pellets 3 mg, analytical grade Bromazolam, triazolobenzodiazepine reference compound, heterocyclic bromo standard, research grade Bromazolam pellets, computational chemistry model molecule, benzodiazepine reference standard, QSAR dataset compound, environmental LC–MS standard, chemical informatics reference, forensic research standard.