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2,5,6-Tribromo-3-Methylpyridine

    • Product Name 2,5,6-Tribromo-3-Methylpyridine
    • Alias 3-Methyl-2,5,6-tribromopyridine
    • Einecs 242-487-1
    • 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

    317813

    Iupac Name 2,5,6-Tribromo-3-methylpyridine
    Molecular Formula C6H4Br3N
    Molecular Weight 345.83 g/mol
    Cas Number 118971-26-3
    Appearance Off-white to light brown solid
    Melting Point 75-80°C
    Solubility Slightly soluble in solvents like DMSO or DMF
    Purity Typically ≥98%
    Smiles CC1=NC(=C(C(=C1)Br)Br)Br
    Inchi InChI=1S/C6H4Br3N/c1-3-2-4(7)6(9)5(8)10-3/h2H,1H3
    Storage Conditions Store in a cool, dry place

    As an accredited 2,5,6-Tribromo-3-Methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, tightly sealed, labeled "2,5,6-Tribromo-3-Methylpyridine," with hazard symbols and chemical details displayed.
    Shipping 2,5,6-Tribromo-3-Methylpyridine is shipped in tightly sealed containers, protected from moisture and light. The packaging complies with relevant chemical safety regulations for hazardous materials. Transport is arranged via certified carriers, and documentation, including the Safety Data Sheet (SDS), accompanies the shipment to ensure safe handling and regulatory compliance throughout transit.
    Storage 2,5,6-Tribromo-3-methylpyridine should be stored in a tightly sealed container, away from incompatible materials such as strong oxidizers and bases. Keep it in a cool, dry, well-ventilated area, protected from light and moisture. Store at room temperature and label the container clearly. Follow all standard laboratory safety procedures, including proper personal protective equipment (PPE).
    Application of 2,5,6-Tribromo-3-Methylpyridine

    Applications of 2,5,6-Tribromo-3-Methylpyridine in Industrial Manufacturing

    Our in-house produced 2,5,6-Tribromo-3-Methylpyridine is a specialty pyridine derivative that functions as an essential intermediate across several sectors. The sections below describe its established roles and process value in targeted downstream manufacturing fields, with each scenario detailing industrial compliance, application-specific formulation, integration method, and types of finished goods by actual producers.

    1. Agrochemical Intermediate for Pyridine-Based Herbicides

    This material provides a brominated pyridine nucleus central to the synthesis of modern selective herbicide actives. Major agrochemical groups require it during the preparation of pyridine derivatives used in broadleaf and grass weed management for cereal and oilseed crops. Downstream formulators standardize inclusion based on target yield and metabolic pathway specificity, leveraging its precise reactivity pattern to build active ingredients with improved environmental fate and crop safety.

    Industry compliance standards

    • FAO/WHO Specification for Plant Protection Products (primary reference for intermediates and actives)
    • ISO 9001:2015 Quality Management for chemical synthesis plants
    • REACH Annex II for registration and environmental assessment in the EU
    • U.S. EPA 40 CFR Part 158 for pesticide registration supporting documentation

    Typical usage ratio

    • 15–25% of total core intermediates in the synthesis batch, calculated per mole ratio to the next functionalization step; adjustment depends on final product yield targets and required reaction selectivity.

    Downstream process integration

    • Added as a starting material in bromination-coupling steps; conversion to tetrazole-substituted or carboxylic acid derivatives performed via condensation or metal-catalyzed substitution stages.

    Final product types

    • Pyridine-based post-emergence herbicide actives (e.g., pyroxsulam, aminopyralid)
    • Custom-formulated herbicide technical concentrates
    • Granular ready-to-use crop protection agents

    2. Pharmaceutical Intermediate in Respiratory API Manufacture

    Leading active pharmaceutical ingredient (API) manufacturers employ this compound as a key intermediate in synthesizing substituted pyridine scaffolds for respiratory drug substances. Inhaled corticosteroid analogs and antitussive agents utilize its tribrominated framework to introduce defined regioselectivity and halogen patterning, critical to downstream bioactivity and pharmacokinetic profile optimization. Process chemists reference pharmacopeial and ICH guidelines to ensure the intermediate’s purity and traceability through every stage.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guidance for APIs
    • USP–NF, EP, and JP monographs for relevant pyridine intermediates
    • FDA 21 CFR Part 210 & 211 for processing and batch controls
    • WHO GMP for pharmaceutical manufacturing sites

    Typical usage ratio

    • Varies from 10–22% of the total reaction substrate mass in multistep API synthesis; optimized in pilot trials based on yield and impurity profile.

    Downstream process integration

    • Stagewise addition post-halogenation, serving as a core building block for heterocyclic coupling and subsequent amination or esterification, depending on API structure.

    Final product types

    • Intermediates for inhaled corticosteroids
    • Custom respiratory drug actives
    • Cough suppressant bulk substances for formulation

    3. Building Block for Electronic Chemical Synthesis (OLED Materials)

    Manufacturers of advanced display and lighting materials rely on this tribrominated pyridine for its controlled electron-withdrawing and halogen-rich structure when synthesizing OLED (organic light-emitting diode) emitting layer precursors. It introduces site-specific bromine atoms, crucial to improving charge transfer and photostability in the final compound. Industry QC teams validate material quality using electronics-grade standards and evaluate bromine placement by HPLC and NMR before moving to polymerization or cross-coupling stages.

    Industry compliance standards

    • IEC 60424-1 for chemical raw material traceability in electronics
    • RoHS Directive (EU) for controlled substances in electronics intermediates
    • IPC-4101C: Qualification and performance specification for base materials
    • ISO 14001:2015 Environmental Management for specialty chemical plants

    Typical usage ratio

    • 0.5–8% by weight in the pre-polymerization step, with proportions defined by desired emission wavelength and charge transport properties in the resulting OLED precursor.

    Downstream process integration

    • Introduced at the heteroaryl cross-coupling stage for construction of polycyclic aromatic or phosphorescent emitter frameworks; typically processed via Suzuki, Buchwald, or Stille couplings.

    Final product types

    • OLED blue, green, and red emitter layer chemicals
    • Small-molecule charge transport layers for display panels
    • Next-generation organic semiconductor precursors

    4. Intermediate for Industrial Dyes and Pigments

    The chemical’s bromine content and methylpyridine ring position make it a preferred intermediate for specialty dye and pigment syntheses. Pigment manufacturers introduce it in controlled steps to achieve precise molecular architectures, optimizing properties such as color fastness and light stability for textile, plastic, and specialty ink applications. Regulatory scrutiny over residual brominated compounds requires careful QC and batch documentation.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemical safety (residual content/release)
    • EN 71-3:2019 for safety of toys (applies to pigments for plastic and printing)
    • ISO 9001:2015 and ISO 14001:2015 for pigment chemical process control
    • China GB 18582-2020 (Indoor decorative paint materials)

    Typical usage ratio

    • 2–12% of formulation batch, set according to target chromophore structure and required thermal/UV resistance of the pigment product.

    Downstream process integration

    • Added at the condensation or cyclization stage after initial pyridine functionalization, followed by bromine-bleaching or azo coupling with pigment base compounds.

    Final product types

    • High-performance textile dyes
    • Specialty pigments for plastics and polymer composites
    • UV-resistant inkjets and packaging dyes
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