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4-Butylphenylboronic Acid

    • Product Name 4-Butylphenylboronic Acid
    • Alias 4-Butylbenzeneboronic acid
    • Einecs 628-123-2
    • 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

    976214

    Productname 4-Butylphenylboronic Acid
    Casnumber 5122-95-2
    Molecularformula C10H15BO2
    Molecularweight 178.04
    Appearance White to off-white solid
    Meltingpoint 110-114°C
    Boilingpoint No data available
    Solubility Slightly soluble in water; soluble in common organic solvents
    Purity Typically ≥97%
    Storagetemperature Store at 2-8°C
    Smiles CCCCc1ccc(B(O)O)cc1
    Inchikey FJOMFJQAHXHUOQ-UHFFFAOYSA-N

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

    Packing & Storage
    Packing The 25g 4-Butylphenylboronic Acid is supplied in a sealed amber glass bottle with a screw cap and safety labeling.
    Shipping 4-Butylphenylboronic Acid is shipped in tightly sealed containers to prevent moisture exposure. It is packed according to hazardous material regulations, clearly labeled, and cushioned to prevent breakage. Shipping is done via ground or air, ensuring compliance with all safety and chemical transport guidelines for safe and secure delivery.
    Storage 4-Butylphenylboronic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect the chemical from moisture and direct sunlight. Store at room temperature or as recommended by the manufacturer, and ensure the storage area is clearly labeled and accessible only to trained personnel.
    Application of 4-Butylphenylboronic Acid

    Applications of 4-Butylphenylboronic Acid in Industrial Manufacturing

    Our capabilities as a dedicated manufacturer enable us to supply 4-Butylphenylboronic Acid (4-BPBA) for multiple specialized sectors. This compound plays critical roles in key industrial and scientific applications, particularly those requiring precision in organic synthesis, advanced pharmaceuticals, and innovative materials. Below we detail proven, field-validated downstream scenarios, emphasizing application methodology, real compliance requirements, and the finished goods our partners reliably produce.

    1. Pharmaceutical Intermediate Synthesis for Antidiabetic Agents

    4-BPBA serves as a crucial building block in the Suzuki coupling step during the large-scale synthesis of active pharmaceutical ingredients (APIs) for second-generation antidiabetic therapies, including certain DPP-4 inhibitors. The compound’s arylboronic functionality enables selective cross-coupling, helping downstream partners achieve high-purity intermediates required for regulatory approval in major pharma markets.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • EU EudraLex Volume 4, Part II GMP
    • Chinese Pharmacopeia (CP), as applicable for export APIs

    Typical usage ratio

    • 1.05–1.25 molar equivalents relative to halide substrate; adjusted to minimize unreacted boronic acid and control side-products during coupling

    Downstream process integration

    • Metered addition into the Suzuki cross-coupling reactor after pre-catalyst and base charging; followed by aqueous workup, purification via column or crystallization, and final conversion to regulated API form

    Final product types

    • Pharmaceutical APIs for oral antidiabetic medications (e.g., DPP-4 inhibitors such as linagliptin intermediates)
    • High-value pharmaceutical intermediates for contract manufacturing organizations (CMOs)

    2. Fine Chemical Synthesis for OLED Material Intermediates

    In the electronics and optoelectronic sector, 4-BPBA acts as a key arylating agent in the synthesis of high-purity organic functional materials, notably those used in light-emitting layers for OLED (Organic Light Emitting Diode) displays and lighting. The compound’s butyl substituent helps improve molecular solubility and thermal characteristics of downstream emissive molecules.

    Industry compliance standards

    • International Electrotechnical Commission (IEC) 62341 OLED Standards
    • ISO 9001:2015 Quality Management for Electronic Materials
    • IEC QC 080000 for hazardous substance process management
    • RoHS Directive 2011/65/EU adherence for downstream OEMs

    Typical usage ratio

    • 0.85–1.10 equivalents per aryl halide, based on solubility and molecular design of targeted OLED intermediates; tightly controlled to reduce byproduct formation

    Downstream process integration

    • Introduced in palladium-catalyzed cross-coupling stage in batch reactors; post-reaction, intermediates isolated through solvent precipitation or chromatographic separation before further functional group modifications

    Final product types

    • OLED emitter and hole transporting material intermediates
    • Functional aryl building blocks for novel display technologies

    3. Agrochemical Research Intermediates for Crop Protection

    Several major agrochemical producers employ this raw material to construct advanced aromatic structures for new-generation fungicide and herbicide intermediates. Its use centers on introducing hydrophobic phenyl moieties into candidate molecules, which can enhance membrane affinity and bioavailability for the final active ingredient.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides (including JMPR evaluation)
    • ISO 9001:2015 for quality control of agrochemical precursors
    • REACH Registration (EU) for precursor chemical usage
    • US EPA 40 CFR Part 172 for experimental use permits

    Typical usage ratio

    • 0.95–1.15 molar equivalents per target halogenated aromatic; levels optimized case-by-case to maximize coupling efficiency and purity for pre-commercial agrochemical intermediates

    Downstream process integration

    • Charged to jacketed reactors for Suzuki–Miyaura reactions, often followed by extraction and continuous distillation, then forwarded to structure-activity relationship (SAR) screening teams

    Final product types

    • Key intermediates for novel crop protection agents (pre-patent registration)
    • Lead compound libraries evaluated in field test plots

    4. Specialty Polymer Synthesis for Advanced Resins

    Manufacturers of specialty polymers and resins apply the boronic acid derivative to introduce adjustable hydrophobic/aromatic segments in advanced resin formulations. These high-performance materials are in demand for coatings and engineered plastics requiring precise thermal, chemical, or mechanical properties.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for resin production and environmental management
    • ASTM D638 and D790 for mechanical property validation in polymer composites
    • UL 94 for flammability compliance of plastic resins
    • REACH (EC 1907/2006) registration obligations for downstream material safety in the EU

    Typical usage ratio

    • 0.5–2.0% by weight relative to total monomer feed; adjusted based on desired chain length and targeted glass transition temperature (Tg) parameters

    Downstream process integration

    • Added during copolymerization via Boronic esterification or Suzuki-Polycondensation, allowing for homogeneous mixing and controlled block segment architecture, followed by pelletizing or solution casting

    Final product types

    • Advanced thermoset and thermoplastic resins for electronic encapsulation
    • High-performance coatings for aerospace substrates
    • Engineering plastics with tailored barrier properties
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