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4-Nitrophenylboronic Acid Pinacol Ester

    • Product Name 4-Nitrophenylboronic Acid Pinacol Ester
    • Alias 4-Nitrophenylboronic acid pinacol ester
    • Einecs 410-610-2
    • 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

    705009

    Productname 4-Nitrophenylboronic Acid Pinacol Ester
    Casnumber 210407-02-2
    Molecularformula C12H16BNO4
    Molecularweight 249.08
    Appearance Pale yellow solid
    Meltingpoint 84-88 °C
    Purity Typically ≥98%
    Storagetemperature 2-8 °C
    Solubility Soluble in organic solvents such as DMSO, chloroform, and dichloromethane
    Synonyms 4-Nitrophenylboronic acid pinacol ester; (4-nitrophenyl)boronic acid pinacol ester
    Boilingpoint Decomposes before boiling
    Smiles B(c1ccc(cc1)[N+](=O)[O-])OC(C)(C)C(C)(C)O

    As an accredited 4-Nitrophenylboronic Acid Pinacol Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 5-gram amber glass bottle with a screw cap, clearly labeled with chemical name, warnings, and safety information.
    Shipping 4-Nitrophenylboronic Acid Pinacol Ester is shipped in tightly sealed containers to prevent moisture exposure and contamination. It is packed with appropriate labeling according to chemical safety regulations and shipped at ambient temperature as a non-hazardous material. All handling complies with local and international transport guidelines to ensure safe and secure delivery.
    Storage 4-Nitrophenylboronic Acid Pinacol Ester should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of moisture. Keep the container tightly closed and store at room temperature or as recommended by the manufacturer. It should be protected from incompatible substances such as strong oxidizing agents. Always follow standard chemical storage protocols.
    Application of 4-Nitrophenylboronic Acid Pinacol Ester

    Applications of 4-Nitrophenylboronic Acid Pinacol Ester in Industrial Manufacturing

    4-Nitrophenylboronic acid pinacol ester serves as a key organoboron intermediate for cross-coupling reactions in pharmaceutical, agricultural, and materials research. Our plant-grade material is designed for strict formulation requirements and industrial process integration. Below are major downstream industries utilizing this compound in their continuous and batch production environments, with precise attention to compliance, formulation, process sequence, and finished goods portfolio.

    1. Active Pharmaceutical Ingredient (API) Synthesis — Suzuki Coupling Intermediates

    Innovator and generic pharmaceutical manufacturers engage this boronic ester as a coupling partner for synthesizing heterocyclic scaffolds and biaryl structures in cardiovascular, oncological, and neuroscience drugs. Strict traceability governs the handling, and the material enters high-throughput or campaign-based synthesis routes, providing electron-rich fragments essential in regulated finished medicines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP—EudraLex Volume 4
    • US FDA 21 CFR Part 210/211
    • Japanese Pharmacopoeia raw material standards for intermediates

    Typical usage ratio

    • 0.80–1.20 equivalents relative to halogenated partner in Suzuki-Miyaura reactions; exact quantity aligns with process yield control and impurity profile management.

    Downstream process integration

    • Charged at the coupling step following the activation of halogenated aromatics, under palladium catalysis; controlled temperature (80–100°C) and inert atmosphere within glass-lined or stainless reactors.

    Final product types

    • Pharmaceutical intermediates for antihypertensive and anticancer agents (e.g., Valsartan, Imatinib derivatives)
    • Regulated API pathway intermediates containing biaryl moieties

    2. Agrochemical Active Ingredient Synthesis

    Manufacturers use the compound in the synthesis of advanced agrochemical scaffolds, particularly for selective herbicides and fungicides containing aryl or heteroaryl linkages. Its precise reaction profile helps maintain batch-to-batch consistency critical for large-scale crop protection chemical campaigns.

    Industry compliance standards

    • FAO/WHO Recommended Specifications for Plant Protection Products
    • ISO 9001:2015 for process control and traceability
    • EU Regulation (EC) No 1107/2009 for pesticide active substances

    Typical usage ratio

    • 0.90–1.10 equivalents in cross-coupling reaction steps; adjusted based on targeted conversion and minimization of process by-products.

    Downstream process integration

    • Added in the coupling phase after halide substrate preparation on multipurpose synthesis lines, utilizing Pd- or Ni-catalysis in solvent-controlled environments.

    Final product types

    • Intermediates for triazole-based fungicide actives
    • Precursors to aryl-substituted pyrazole insecticides
    • Biaryl core herbicide raw materials

    3. Electronic and Display Materials — OLED Intermediate Production

    In advanced display manufacturing, this boronic ester enables the synthesis of electron transport and emissive layer molecules for OLED (Organic Light Emitting Diode) panels. Downstream integration centers on purity and minimal metal contaminant profiles, essential to the reproducibility and electrical performance of the final device.

    Industry compliance standards

    • JEITA Standard for OLED raw materials
    • IEC 62679-3-1 for flat panel display materials assessment
    • ISO 9001:2015 for QC and traceability

    Typical usage ratio

    • 1.00–1.15 equivalents referenced to the aryl halide core; tightly controlled to optimize film-forming characteristics and reduce electronic defects.

    Downstream process integration

    • Dispensed during the Suzuki coupling of emitter and host molecules in dry, oxygen-free solutions with low-metal catalysts, supporting both pilot and commercial synthesis batch scales.

    Final product types

    • OLED host and emitter molecules for display pixels
    • Small-molecule blue and green light-emitting units
    • Hole/electron transport material intermediates

    4. Specialty Chemical Synthesis — Analytical Reagents Production

    Analytical chemical companies formulate diagnostic and calibration reagents using this pinacol ester for site-selective biaryl construction. Stringent lot traceability supports applications in colorimetric, fluorometric, and sensor solutions, often requiring high analytical purity and low boron residue.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • ISO/IEC 17025 for chemical analytics
    • REACH Registration (EC No 1907/2006) for commercialized chemicals within Europe

    Typical usage ratio

    • 0.95–1.05 equivalents, set according to reaction kinetics in analytical marker production, accounting for downstream purification efficiency.

    Downstream process integration

    • Introduced during selective coupling to generate nitrophenyl or biaryl structures for fluorophore and chromophore backbones, followed by HPLC or LC-MS purification to meet reagent grade standards.

    Final product types

    • HPLC and LC-MS calibration standards
    • Colorimetric assay reagents
    • Fluorescent chemical sensors for environmental and biomedical monitoring

    5. Fine Chemical Manufacturing — Liquid Crystal Intermediate Synthesis

    Producers of display-grade liquid crystal materials apply this compound in Suzuki-based construction of rigid biphenyl and nitrophenyl cores. This ensures consistent batch properties and alignment essential for high-resolution displays and performance-critical applications.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronic chemical content control
    • ISO 9001:2015 for dense phase production lines
    • JEITA guidelines for liquid crystal raw materials

    Typical usage ratio

    • 1.00–1.25 equivalents based on target molecular framework and impurity profile; minor ratio changes reflect purity requirements for optical performance.

    Downstream process integration

    • Dosed at the Suzuki-coupling step to construct tailored biphenyl and aryl-ether subunits critical for liquid crystal phase behavior, immediately followed by column chromatographic refinement and microfiltration.

    Final product types

    • Liquid crystal intermediates for TFT-LCD and OLED applications
    • High-purity biphenyl and terphenyl building blocks
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