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9-Phenanthracenylboronic Acid

    • Product Name 9-Phenanthracenylboronic Acid
    • Alias 9-Phenanthreneboronic acid
    • Einecs 606-146-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    641179

    Chemical Name 9-Phenanthracenylboronic Acid
    Molecular Formula C14H11BO2
    Molecular Weight 222.05 g/mol
    Cas Number 851276-94-8
    Appearance White to off-white solid
    Melting Point 250-254 °C
    Purity Typically >98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store in a cool, dry place, keep container tightly closed
    Smiles B(C1=CC2=CC=CC=C2C3=CC=CC=C13)(O)O

    As an accredited 9-Phenanthracenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 1-gram quantity of 9-Phenanthracenylboronic Acid is supplied in a sealed amber glass vial with a secure screw cap.
    Shipping 9-Phenanthracenylboronic Acid is shipped in tightly sealed containers, protected from moisture and light. It is handled as a stable solid under standard conditions. Shipping complies with all chemical safety regulations, and packaging ensures minimal exposure during transit. Appropriate labeling and documentation accompany each shipment for secure and compliant delivery.
    Storage 9-Phenanthracenylboronic acid should be stored in a cool, dry, well-ventilated area, away from moisture, direct sunlight, and incompatible substances such as strong oxidizers. The container must be tightly sealed to prevent hydrolysis and contamination. Store the chemical at room temperature or as specified by the supplier, and always follow standard laboratory safety and chemical storage protocols.
    Application of 9-Phenanthracenylboronic Acid

    Applications of 9-Phenanthracenylboronic Acid in Industrial Manufacturing

    As the original manufacturer of 9-Phenanthracenylboronic Acid, we focus on supporting advanced chemical synthesis applications. This compound’s unique aromatic boronic structure enables it to serve key roles across several sectors, most notably in fine chemicals, OLED intermediates, pharmaceutical research, and specialty organic materials. Each area listed below represents an established downstream industry path where large-scale consumers employ this raw material in specific, process-dependent roles under strict regulatory and quality frameworks.

    1. OLED Material Synthesis for Flat Panel Displays

    Leading display manufacturers rely on 9-Phenanthracenylboronic Acid as a pivotal coupling component in the design and scale-up of blue light-emitting materials for high-performance OLED screens. The compound enters Suzuki–Miyaura cross-coupling reactions to construct rigid, extended π-conjugated systems required for emitter molecules exhibiting deep blue chromaticity, thermal stability, and high quantum efficiency. Downstream partners integrate the material within their internal development cycles for OLED display panels conforming to both television and mobile device requirements.

    Industry compliance standards

    • RoHS 2 Directive (EU 2011/65/EC) for hazardous substances in electronics
    • IEC 62321 analytical methods for regulated substances
    • JEITA self-regulation guidelines on organic electronic materials
    • ISO 14001 for environmental management in chemical processing

    Typical usage ratio

    • 1.5%–4.5% w/w relative to total molar substrate in the emitter layer precursor batch, adjusted according to performance tuning of the emitter molecule

    Downstream process integration

    • Incorporation during the Suzuki–Miyaura cross-coupling step to introduce boron-linked phenanthrene motifs, followed by purification and formulation as part of emitter or host material development

    Final product types

    • Blue OLED emitter compounds
    • Small-molecule hosts for OLED pixel architectures
    • Patterned OLED display units for mobile, television, and automotive segments

    2. Pharmaceutical Intermediates for API Synthesis

    9-Phenanthracenylboronic acid serves as a boron-source building block in the modular construction of complex polycyclic aromatic intermediates used for oncology and advanced central nervous system (CNS) active pharmaceutical ingredient research pipelines. Customers apply it in pharmaceutical facilities specializing in protected boronate derivatives for further diversification, en route to patented drug candidates under GMP conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. (European Pharmacopoeia) standards for chemical purity
    • 21 CFR Part 211 cGMP for Finished Pharmaceuticals
    • USP <823> for radiolabelled drug synthesis (if isotopic labelling involved)

    Typical usage ratio

    • 0.8%–2.5% w/w, based on the specific API intermediate target and reaction stoichiometry; chemists tailor charge according to yield optimization protocols

    Downstream process integration

    • Added as a limiting substrate during palladium-catalyzed cross-coupling reactions for biaryl scaffold assembly in the API intermediate structural motif formation

    Final product types

    • Polycyclic aromatic pharmaceutical intermediates
    • Advanced building blocks for clinical candidate libraries
    • Synthetic reference compounds for impurity profiling

    3. Specialty Organic Semiconductors and Sensor Materials

    Producers of organic semiconductors and photonic sensor substrates incorporate 9-Phenanthracenylboronic Acid when designing conjugated frameworks that offer improved charge carrier mobility and environmental robustness. This compound is introduced during solution-processable conjugated polymer or small-molecule synthesis that targets specific photoelectronic device layers with demanding performance criteria.

    Industry compliance standards

    • IPC-4101 for organic electronic substrate materials
    • REACH (EC 1907/2006) for raw material registration and use in specialty chemicals
    • ISO 9001 for quality management systems in functional material processing
    • IEC 62899 for printed electronics technical requirements

    Typical usage ratio

    • 1.0%–3.0% molar ratio against main chain monomers in the formulation, fine-tuned per polymerization and small-molecule design

    Downstream process integration

    • Dosed during Suzuki-coupling or Miyaura borylation step for backbone extension and introduction of functional boronic motifs, followed by post-synthetic purification and device ink formulation

    Final product types

    • Organic thin-film transistor (OTFT) layers
    • Photodetector pixel arrays
    • Molecular sensor active matrices for chemical and bio-sensing devices

    4. Dye and Fluorescent Probe Chromophore Construction

    Chemical manufacturers and research labs utilize 9-Phenanthracenylboronic Acid as a key coupling partner when assembling rigid organic chromophores for analytical dyes and near-UV/visible fluorescent probes. Its unique polycyclic scaffold enables the preparation of highly emissive, photostable derivatives useful in life sciences and materials diagnostics, where strict control of purity and batch reproducibility is essential.

    Industry compliance standards

    • ISO 17034:2016 for reference material producer competence (for analytical-grade dyes)
    • GLP (Good Laboratory Practice) for analytical reagent manufacturing
    • EN 71-3 Safety of Toys–Migration of Certain Elements (for dyes in children's product testing)
    • Spectroscopic grade criteria set by end-user specification sheets

    Typical usage ratio

    • 0.5%–2.2% w/w relative to overall chromophore synthesis batch, with adjustments for targeted emission wavelength and quantum yield parameters

    Downstream process integration

    • Added in the initial cross-coupling synthesis step to generate substituted phenanthrene backbone, with subsequent purification before probe or dye formulation and quality control

    Final product types

    • Fluorescent biochemical probes for microscopy
    • High-performance analytical laboratory dyes
    • Spectral calibration standards for optical equipment
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