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2-Chloro-3-Pyridylboronic Acid

    • Product Name 2-Chloro-3-Pyridylboronic Acid
    • Alias 2-Chloro-3-pyridinylboronic acid
    • Einecs 410-480-7
    • 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

    965499

    Chemical Name 2-Chloro-3-Pyridylboronic Acid
    Cas Number 875447-36-6
    Molecular Formula C5H5BClNO2
    Molecular Weight 157.36 g/mol
    Appearance White to off-white solid
    Melting Point 190-195°C (decomposes)
    Purity Typically ≥97%
    Smiles B(C1=C(C=CN=C1)Cl)(O)O
    Inchi InChI=1S/C5H5BClNO2/c7-4-2-1-3-8-5(4)6(9)10/h1-3,9-10H
    Solubility Soluble in DMSO, slightly soluble in water
    Storage Conditions Store at 2-8°C, away from light and moisture

    As an accredited 2-Chloro-3-Pyridylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, tightly sealed with a screw cap; features hazard labeling, chemical name, purity, and supplier information.
    Shipping 2-Chloro-3-pyridylboronic acid is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is classified under standard chemical shipping regulations and should be handled as a potentially hazardous material. Appropriate labeling, documentation, and compliance with local and international transport guidelines ensure safe and secure delivery.
    Storage **2-Chloro-3-pyridylboronic acid** should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry, well-ventilated area, ideally under inert gas such as nitrogen. Avoid contact with strong oxidizers and bases. Store the chemical at room temperature or as recommended by the supplier, and ensure proper labeling for safety and easy identification.
    Application of 2-Chloro-3-Pyridylboronic Acid

    Applications of 2-Chloro-3-Pyridylboronic Acid in Industrial Manufacturing

    2-Chloro-3-pyridylboronic acid serves key roles as a boron-containing building block in advanced chemical synthesis. Our in-plant quality oversight ensures consistent performance in all downstream sectors. Below, we detail the primary industrial application scenarios where this material anchors value-added transformations, including specific regulatory, formulation, integration, and product considerations for each.

    1. Pharmaceutical Active Ingredient Synthesis

    Leading pharmaceutical manufacturers incorporate this compound during Suzuki-Miyaura cross-coupling to construct complex heteroaromatic frameworks required in next-generation APIs. Tight process control and documentation support regulatory submissions and batch traceability, safeguarding patient safety and developer compliance during the transition from R&D to scale production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211 (US cGMP)
    • European Pharmacopoeia monographs as applicable to the final API
    • JP, USP regulatory registration pathways where relevant

    Typical usage ratio

    • 0.8%–2.5% by weight of total reaction mass (stoichiometry adjusted according to the target aryl halide and catalyst turnover)

    Downstream process integration

    • Charged into reaction systems during the Suzuki coupling stage post-halide activation; often introduced simultaneously with palladium catalyst and suitable base; precise dosing regulated via in-line flow or batch addition control systems

    Final product types

    • Small-molecule kinase inhibitors
    • Pyridyl-based antiviral agents
    • Intermediates for central nervous system therapeutics

    2. Crop Protection Agrochemical Intermediates

    Major agrochemical innovation relies on selective coupling reactions using pyridylboronic acids as core intermediates in the synthesis of new-generation herbicides and insecticides. In these facilities, advanced adherence to supply chain quality and recorded traceability supports the stringent stewardship demanded by global crop protection regulations and the increasing trend toward low-residue active substances.

    Industry compliance standards

    • FAO/WHO Technical Guidelines on Pesticide Specification & Quality Control
    • ISO 9001:2015 certified manufacturing process
    • REACH registration for European market entry
    • China ICAMA registration requirements for domestic-use intermediates

    Typical usage ratio

    • 1.0–2.5% of total batch weight, calculated against the active intermediate output; actual ratio varies by the number of aryl couplings required in the synthetic route

    Downstream process integration

    • Fed into catalytic reactors for aryl–aryl or aryl–alkyl coupling reaction stages, followed by quenching and extraction for intermediate isolation in multipurpose synthesis lines

    Final product types

    • Nitrogen heterocycle herbicide intermediates
    • Insecticide precursors utilizing pyridyl scaffolding
    • Seed treatment fungicide building blocks

    3. OLED Display Material Synthesis

    Specialty electronics material manufacturers leverage the compound within Suzuki couplings to build functionalized pyridine-based ligands or polymers for organic light-emitting diode (OLED) device layers. Strict material purity, low metal residue, and defined particle sizing are integral at this stage due to the impact on electronic performance and device reliability in consumer and industrial displays.

    Industry compliance standards

    • JEITA Display Device Material Cleanliness Specifications
    • IEC 62471 (for photobiological safety in finished OLED displays)
    • RoHS Directive 2011/65/EU for restriction of hazardous substances in electronics
    • Internal panel manufacturer quality benchmarks

    Typical usage ratio

    • 0.3–1.5% by weight in the monomer or small molecule feed for targeted ligand assembly; ratio tuned for the specific electronic function and molecular design

    Downstream process integration

    • Added during the fine chemical precursor synthesis phase, prior to purification and polymerization, in controlled atmosphere reactors to suppress residual catalyst and moisture pickup

    Final product types

    • Pyridine-based OLED emitting layer monomers
    • Electron transport materials for flat panel displays
    • Intermediate ligands for solution-processable display inks

    4. Specialty Fine Chemical Research and Custom Synthesis

    Contract synthesis service providers and fine chemical producers incorporate this advanced boronic acid as a selective transformation agent during project-specific pilot syntheses. Documentation aligns with both customer project protocols and national environmental safety mandates, particularly for custom chemicals entering global distribution channels.

    Industry compliance standards

    • ISO 9001:2015 quality management system
    • Globally Harmonized System (GHS) for Working Chemical Classification, Labeling, and SDS documentation
    • OECD Principles of Good Laboratory Practice (GLP) for regulated research synthesis
    • Applicable regional chemical substance notifications (e.g., TSCA, REACH pre-registration)

    Typical usage ratio

    • 0.5–3.0% per target molecule formation; adjusted depending on target compound complexity and run scale from gram to kilogram quantities

    Downstream process integration

    • Applied in the coupling phase of multi-step syntheses, either in batch reactor or flow chemistry setups, with formulations adapted per end-use performance objectives or structural requirements

    Final product types

    • Custom aryl-pyridine motif compounds for pharma studies
    • Special-purpose organic building blocks for advanced material design
    • Research-grade reference substances and screening libraries
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