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6-Bromonicotinic Acid

    • Product Name 6-Bromonicotinic Acid
    • Alias 6-Bromo-3-pyridinecarboxylic acid
    • Einecs 212-333-4
    • 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

    374286

    Cas Number 33252-79-6
    Molecular Formula C6H4BrNO2
    Molecular Weight 202.01 g/mol
    Iupac Name 6-bromopyridine-3-carboxylic acid
    Appearance White to off-white powder
    Melting Point 210-213 °C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Chemical Structure BrC5H3N(CO2H)
    Smiles C1=CC(=NC=C1C(=O)O)Br
    Inchi InChI=1S/C6H4BrNO2/c7-5-2-1-4(6(9)10)3-8-5/h1-3H,(H,9,10)
    Storage Temperature Room temperature
    Pka 3.7 (carboxylic acid group)
    Synonyms 6-Bromo-3-pyridinecarboxylic acid

    As an accredited 6-Bromonicotinic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 6-Bromonicotinic Acid, 25g: Supplied in an amber glass bottle with screw cap, labeled for laboratory use and hazard warnings.
    Shipping 6-Bromonicotinic Acid is shipped in tightly sealed containers compliant with safety regulations for hazardous chemicals. Packaging ensures chemical stability and prevents leakage. Shipping is conducted by certified carriers, usually under ambient conditions, with clear labeling and documentation. Specialized handling instructions and material safety data sheets (MSDS) accompany each shipment for safe transport and receipt.
    Storage 6-Bromonicotinic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases and oxidizing agents. Protect it from moisture, heat, and direct sunlight. Ensure proper labeling and keep the storage area free from ignition sources. Always follow local regulations and safety guidelines for chemical storage.
    Application of 6-Bromonicotinic Acid

    Applications of 6-Bromonicotinic Acid in Industrial Manufacturing

    6-Bromonicotinic acid supports critical synthesis routes in specialized chemical manufacturing. Below, we detail its true-to-market applications across high-value downstream sectors, focusing on specific compliance norms, formulation ratios, industrial integration stages, and final product types delivered by industry end-users.

    1. Pharmaceutical Intermediate in Pyridine-Based API Synthesis

    This compound acts as a building block during the multi-step synthesis of advanced pharmaceutical intermediates, especially in pyridine-derived drug development. Its functionalized aromatic ring supports the preparation of target molecules through nucleophilic aromatic substitution and cross-coupling reactions, directly impacting purity and process reproducibility for small-molecule APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) synthesis grade specifications
    • 21 CFR Part 211 – FDA Current Good Manufacturing Practice (cGMP) for Finished Pharmaceuticals
    • USP-NF validation for process intermediates

    Typical usage ratio

    • As a coupling partner, typically 0.8 to 1.2 mole equivalents relative to complementary reactants, with exact ratios adjusted for reaction yield optimization and residual impurity control

    Downstream process integration

    • Feeding into Suzuki-Miyaura or Buchwald-Hartwig cross-coupling steps after initial purification and drying; incorporated directly into reactor vessels under nitrogen atmosphere

    Final product types

    • Pyridine-linked kinase inhibitors
    • Antiviral formulation intermediates
    • Respiratory therapy active substances
    • Central nervous system (CNS) drug ingredients

    2. Agrochemical Active Ingredient Precursor

    Manufacturers use this halogenated pyridine derivative in the synthesis of advanced crop protection compounds, particularly as a substrate for introducing tailored substituents required for target-specific activity in select herbicides and fungicides. Its chemical reactivity enables streamlined manufacturing routes and product traceability under agro-sector audit norms.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical material
    • ISO 9001:2015–certified quality control across the synthesis chain
    • EU REACH Registration for chemical safety compliance
    • OECD Test Guidelines for environmental and toxicological assessment

    Typical usage ratio

    • Application as a key intermediate at 1.0 mole equivalent versus downstream alkyl- or arylating agents; batch scales of 5%–15% by weight based on overall active ingredient output, selectively increased for reaction yields over 90%

    Downstream process integration

    • Dosed into stepwise Mannich or Grignard reactions following in-house or on-site halogen exchange; forms part of conversion to final active ingredient by direct modification of the bromine functional group

    Final product types

    • Herbicide intermediates for cereals and broadleaf crops
    • Fungicidal actives for seed treatment and foliar sprays
    • Pyridine-based insecticidal technical concentrates

    3. Building Block for Organic Electronic Material Synthesis

    Producers utilize this intermediate within the specialty chemicals sector to generate core monomers for organic semiconductors, photoconductors, and light-emitting molecule development, where precise functionalization determines stability and charge-transport performance. Its bromo-moiety facilitates high-yield C–C and C–N bond formation under controlled, high-purity conditions.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances) Directive compliance for electronic materials
    • ISO 14001:2015 Environmental Management Systems
    • REACH Annex XIV authorization as applicable for downstream use
    • UL Yellow Card certification for final product safety

    Typical usage ratio

    • Used at 1.05–1.10 equivalents relative to stannylated, boronated, or aminated co-reactants, with loading fine-tuned to minimize byproduct formation and post-purification waste

    Downstream process integration

    • Introduced at monomer coupling stages via catalytic palladium-mediated processes under anhydrous, oxygen-controlled atmosphere in bench- to pilot-scale reactors

    Final product types

    • OLED (organic light-emitting diode) emitter and host molecules
    • P-type and n-type organic semiconductors
    • Organic photovoltaic absorber components

    4. Intermediate for Specialty Dye and Pigment Manufacture

    The compound operates as a key intermediate in dye and pigment synthesis, where its bromine substituent enables customized ring substitutions and extension, allowing downstream manufacturers to achieve desired solubility, lightfastness, and color tone in high-value specialty colorants for critical industrial coatings and printing inks.

    Industry compliance standards

    • EN 71-3:2019 (Safety of toys — migration of certain elements, applicable to pigments in children’s products)
    • ISO 18451-1:2015 (Pigments and extenders — Terminology)
    • REACH Annex XVII for restricted substances in finished colorants
    • APEO-free and heavy metal-free requirements for final products (industry self-regulation)

    Typical usage ratio

    • Intermediate charged at 0.9–1.1 molar equivalents in sequential substitution and fusion reactions, with percentage by mass determined by targeted chromophore output and downstream mixing batch size

    Downstream process integration

    • Feeding to multistep synthesis after initial deprotection, often under acid or base catalysis, then batch-blended with co-intermediates; isolation under crystallization/precipitation protocols

    Final product types

    • High-stability inkjet printer pigments
    • Precision textile dye intermediates
    • Automotive and industrial coatings pigments
    • Thermal and photochromic specialty dyes

    5. Ligand Source in Metal Complex Catalyst Production

    Chemical processors rely on this compound for synthesis of custom nitrogen-containing ligands that serve as coordination agents in homogeneous and heterogeneous metal catalyst systems. Its position-specific bromine atom supports direct arylation and subsequent ligand derivatization, impacting catalytic efficiency and selectivity in fine chemical manufacturing.

    Industry compliance standards

    • ISO 9001:2015 for consistent catalyst intermediate traceability
    • Responsible Care Global Charter for product stewardship in catalyst production
    • Compliance with local chemical handling and storage directives (e.g., OSHA 1910.119 in the US)
    • RoHS evaluation for eventual downstream use in electronics-related catalysis

    Typical usage ratio

    • Usually applied at 1.0–1.3 equivalents in ligand-coupling steps, adjusted based on ligand-chain length and required donor atom density

    Downstream process integration

    • Charged to batch reactors in early ligand synthesis; processed further via amination, alkylation, and purification steps before complexation with metal centers

    Final product types

    • Palladium and platinum complex catalysts
    • Nickel-catalyzed cross-coupling agents
    • Functionalized bipyridine or terpyridine ligands for research and industrial catalysis
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