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1,3-Benzenediboronic Acid

    • Product Name 1,3-Benzenediboronic Acid
    • Alias 1,3-Benzenediyldiboronic acid
    • Einecs 807-715-2
    • 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
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    Specifications

    HS Code

    634083

    Productname 1,3-Benzenediboronic Acid
    Casnumber 14443-80-2
    Molecularformula C6H8B2O4
    Molecularweight 165.75
    Appearance White to off-white solid
    Meltingpoint 285-290°C (decomposition)
    Smiles B(O)Oc1cccc(B(O)O)c1
    Solubility Soluble in water and alcohols
    Purity Typically >97%
    Storagetemperature Store at 2-8°C
    Synonyms 1,3-Phenylenediboronic acid
    Density Approx. 1.24 g/cm³
    Ecnumber 238-418-6

    As an accredited 1,3-Benzenediboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,3-Benzenediboronic Acid is packaged in a 25-gram amber glass bottle with a tamper-evident cap and chemical safety labeling.
    Shipping 1,3-Benzenediboronic Acid is shipped in tightly sealed containers to prevent moisture and air exposure. It is packed in accordance with relevant chemical safety regulations, labeled appropriately, and cushioned to avoid breakage. Shipping is typically via certified carriers, compliant with local and international hazardous materials guidelines, ensuring safe and secure delivery.
    Storage 1,3-Benzenediboronic Acid should be stored in a tightly sealed container, protected from moisture, air, and direct sunlight. Keep in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Store at room temperature unless specified otherwise by the manufacturer. Proper labeling and secondary containment are recommended to prevent accidental exposure or spills.
    Application of 1,3-Benzenediboronic Acid

    Applications of 1,3-Benzenediboronic Acid in Industrial Manufacturing

    1,3-Benzenediboronic acid plays a key role as a functional building block in several specialized downstream manufacturing environments. Our direct production knowledge and ongoing support with industrial partners enable reliable integration for advanced synthesis and large-scale processes. Below we present primary application scenarios backed by current commercial-scale usage and strict adherence to industry-specific standards.

    1. Pharmaceutical Intermediate Synthesis for API Production

    In pharmaceutical intermediate manufacturing, 1,3-benzenediboronic acid serves as a pivotal coupling partner in constructing biaryl motifs through Suzuki-Miyaura cross-coupling. This application is essential in producing structurally complex active pharmaceutical ingredients, where high purity and traceability remain paramount. It enters the synthesis pipeline during the targeted formation of C–C bonds, directly impacting molecular design and synthetic route efficiency in API manufacturing for antihypertensive agents and oncology therapeutics.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monographs for APIs (Ph. Eur.)
    • US FDA 21 CFR Part 210/211
    • Chinese Pharmacopoeia 2025 Edition (ChP)

    Typical usage ratio

    • 0.05–0.15 molar equivalents relative to halogenated reactant; adjustment based on reaction yield and impurity profile in pilot batches.

    Downstream process integration

    • Introduced directly in general or high-throughput Suzuki coupling steps under nitrogen with controlled temperature and moisture-sensitive handling; post-coupling purified via crystallization or preparative chromatography.

    Final product types

    • Intermediate biaryl pharmaceutical compounds
    • Active pharmaceutical ingredients (e.g., angiotensin receptor blockers, kinase inhibitors)
    • Advanced drug substance intermediates for fill-finish plants

    2. Electronic Materials: OLED and Organic Semiconductor Manufacturing

    Major electronic manufacturing facilities employ 1,3-benzenediboronic acid in the assembly of organic light-emitting diodes and related organic semiconductors. It enables the formation of high-performing π-conjugated frameworks via cross-coupling polymerizations. The compound enters as a monomeric or comonomeric species, with stoichiometry and sequence critical to charge transport and device efficiency. Downstream, it forms the foundation of electroluminescent and semiconductive layers for advanced display technologies.

    Industry compliance standards

    • JEDEC Solid State Technology Association Standards (JESD)
    • IPC-6012 Qualification and Performance Specification for Rigid Printed Boards
    • IATF 16949 Quality Management System (for electronics supply chain)
    • RoHS 3 (EU 2015/863) restriction compliance

    Typical usage ratio

    • 5%–25% by monomer feed in polymerization steps, precisely adjusted according to molecular weight targets and end-group capping requirements.

    Downstream process integration

    • Dispersed in anhydrous organic solvents for controlled polymerizations, typically under argon and Pd catalysis, with subsequent in-line fractionation and purification to prevent electronic trap formation in final films.

    Final product types

    • OLED emissive and conductive layer polymers
    • Organic field-effect transistor (OFET) active materials
    • Fluorescent and phosphorescent small molecules for display and lighting applications

    3. Fine Chemical Synthesis of Biaryl Agrochemical Actives

    Producers of advanced agrochemical intermediates integrate this raw material in biaryl bond formation for herbicides and fungicides, targeting stability, activity, and environmental profile optimization. It is crucial during Suzuki coupling and other palladium-catalyzed transformations where batch traceability and compositional consistency must meet agro-sector safety and global regulatory demands. Each synthesis batch undergoes tailored optimization to balance cost, throughput, and downstream formulating considerations.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001 for Chemical Manufacturing
    • European Commission Regulation (EC) No 1107/2009 for Plant Protection Products
    • China National Standard GB 2763 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 0.08–0.20 molar equivalents per coupling reaction, modified based on target active concentration and synthesis scale.

    Downstream process integration

    • Added during core C–C coupling for biaryl segment assembly, then routed through solvent exchange, crystallization, and micronization; process incorporates inline analytical verification for residual boron species.

    Final product types

    • Technical-grade biaryl herbicide intermediates (e.g., azole- or pyrazole-based actives)
    • Fungicide building blocks with improved soil stability
    • Agrochemical pre-formulations for further blending

    4. Specialty Polymer Modification and Custom Material Development

    In advanced material R&D and specialty plastics production, 1,3-benzenediboronic acid functions as a bifunctional linker for tailor-made functional polymers. Manufacturers deploy it to introduce boronate crosslinking points in networks that modify surface properties or tune solubility and thermal performance. Entry points in the polymer synthesis sequence are selected according to desired network density and intended end-use, such as membrane casting, sensing elements, or specialty coatings.

    Industry compliance standards

    • ISO 14001 Environmental Management System for polymer production
    • REACH (EC) No 1907/2006 Registration, Evaluation, Authorisation and Restriction of Chemicals
    • ASTM D883 Standard Terminology Relating to Plastics
    • UL 94 Flammability Standard (as applicable to final product safety testing)

    Typical usage ratio

    • 1–10 mol% of the total monomer content, with adjustments determined by required crosslink density and mechanical performance targets.

    Downstream process integration

    • Dispensed into homogeneous polymerization or co-polymerization steps; often dissolved in mixed solvents and heated under inert atmosphere prior to shape casting or extrusion.

    Final product types

    • Modified polyesters and polyarylenes with boronate functionalities
    • Networked polymer films and membranes for separation technology
    • Smart coatings and functionalized thermoplastics
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