Bromonordiazepam Blister – 10x 2.5mg

Buy Bromonordiazepam Blister – 10 × 2.5mg – High‑Purity Analytical Reference Pellets for Professional Laboratory Use

Overview

Buy Bromonordiazepam Blister – 10 × 2.5mg (7‑Bromo‑5‑phenyl‑1,3‑dihydro‑1,4‑benzodiazepin‑2‑one) is a structurally characterized benzodiazepine derivative supplied in blister‑sealed units (10 × 2.5 mg) for precision analytical, forensic, and calibration‑standard applications.

The blister packaging ensures dose stability, moisture control, and sample traceability, supporting GLP (Good Laboratory Practice) and ISO 9001‑level research protocols.

⚠️ For laboratory, scientific, and forensic research only. Not for therapeutic or human use.

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Chemical Identity

• Chemical Name: 7‑Bromo‑5‑phenyl‑1,3‑dihydro‑1,4‑benzodiazepin‑2‑one
• Synonyms: Bromonordiazepam, Norflurazepam, Desalkylflurazepam
• Chemical Formula: C15H10BrN2O
• Molecular Weight: 329.16 g/mol
• CAS Number: 28910‑91‑0
• Chemical Class: Halogenated benzodiazepine amide derivative
• Formulation: Pellets, 2.5 mg each; 10 units per blister
• Purity: ≥ 99.0 % (HPLC verified)
• Appearance: White to off‑white solid pellets
• Stability: 24 months under controlled conditions

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Applications Across Chemistry Disciplines

Organic & Inorganic Chemistry

• Representative of amide‑substituted aromatic heterocycles, ideal for electronic delocalization and bond character analysis.
• Serves as a model compound for studying C–Br activation, amide resonance, and fusion‑ring tautomerism.
• The bromo‑phenyl moiety facilitates palladium‑ and nickel‑catalyzed cross‑coupling experiments (Suzuki, Stille, Ullmann reactions).
• The coordinated amide oxygen and bromine atoms enable ligand interaction studies in inorganic complexation research.

Chemical Biology

• Utilized as a benchmark compound for non‑biological phase I metabolism modelling (oxidative N‑dealkylation and hydroxylation simulations).
• Helps study chemical properties governing membrane partitioning, lipophilicity, and hydrogen bond propensity without biological testing.
• Contributes to computational enzyme pathway modeling to predict metabolite structures and stability factors.

Computational Chemistry

• Reference for DFT, HF, and semi‑empirical molecular‑orbital computations, especially for halogenated aromatics.
• Commonly used to analyze HOMO–LUMO gap energy, dipole moment distribution, and polarizability indices.
• A standard in molecular dynamics and conformational energy surface calculations for multicyclic benzodiazepines.
• Feeds data into QSAR/QSPR training sets and AI‑driven chemical property prediction systems.

Environmental Chemistry

• Serves as a reference standard for trace benzodiazepine analysis in water, sediment, and soil samples.
• Applied in wastewater pollutant profiling, bioassay correlation, and photodegradation kinetic studies.
• Suitable for validating LC–MS/MS identification of halogenated organic pollutants and metabolites.
• Supports carbon–halogen degradation pathway research in oxidative advanced treatment processes (AOP).

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Laboratory Equipment & Consumables

Recommended Instruments

• HPLC / UPLC: Purity and identity verification
• LC–MS/MS: Molecular mass and fragment ion confirmation
• FTIR: Amide C=O stretch (1650 cm⁻¹); C–Br absorption (~600 cm⁻¹)
• ¹H / ¹³C NMR: Structural confirmation and aromatic shift analysis
• DSC/TGA: Thermal stability and pellet integrity profiling

Essential Consumables

• Analytical grade methanol and acetonitrile for sample dilution.
• Amber HPLC vials with PTFE caps to prevent light/solvent degradation.
• Desiccant pouches for sample preservation.
• Laboratory balances (precision 0.1 mg) and micropipettes for accurate weighing and dosing.
• PPE: nitrile gloves, anti‑static lab coat, and safety goggles for handling classified reference compounds.

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Regulation & Safety

Regulatory Status

• Classified for research and analytical use only.
• Distribution in some regions may require special authorization or controlled substance licensing.
• Compliance with DEA, ECHA, REACH, and local chemical handling regulations is mandatory.

GHS Hazard Classification (Indicative)

⚠️ Harmful if swallowed (Category 4)
⚠️ Causes mild skin/eye irritation (Category 2A/2B)
⚠️ Potential aquatic chronic toxin (Category 3)

Safety Guidelines

• Handle in fume hood with adequate ventilation.
• Prevent contact with oxidizers or acid anhydrides.
• Dispose of unused samples through approved hazardous waste channels (EPA 40 CFR standard).
• Supplied with complete Safety Data Sheet (SDS) and Certificate of Analysis (CoA) for traceability and compliance.

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Chemical Informatics Integration

• Canonical SMILES: Brc1ccc2c(ccc(n2)C(=O)NCCN)
• Molecular Descriptors Available: MW, TPSA, log P, dipole moment, H‑bond donor/acceptor count.
• Compatible Software: ChemAxon, RDKit, KNIME, Open Babel, Schrödinger.
• Data Export: SDF, MOL, InChI, and JSON formats for LIMS integration.
• Supports: FAIR Data principles in chemical informatics databases and computational chemistry workflows.

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Analytical Characterization Summary

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Storage & Shelf Life

• Store in a cool (15–25 °C), dry place away from direct light.
• Keep in sealed blister format until use to avoid oxidation and moisture ingress.
• Stable for up to 24 months when stored under recommended conditions.

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SEO Optimized Keywords

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