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2-Fluoro-5-Bromo-3-Methylpyridine

    • Product Name 2-Fluoro-5-Bromo-3-Methylpyridine
    • Alias 2-Fluoro-5-bromo-3-picoline
    • Einecs 841-321-5
    • 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

    623424

    Product Name 2-Fluoro-5-Bromo-3-Methylpyridine
    Molecular Formula C6H5BrFN
    Molecular Weight 190.02 g/mol
    Cas Number 1186140-04-2
    Appearance Colorless to pale yellow liquid
    Boiling Point 206-208°C
    Density 1.66 g/cm³
    Purity Typically ≥97%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC1=C(C=CN=C1Br)F
    Inchi InChI=1S/C6H5BrFN/c1-4-2-3-9-6(8)5(4)7
    Refractive Index n20/D 1.565

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

    Packing & Storage
    Packing 100g of 2-Fluoro-5-Bromo-3-Methylpyridine is packaged in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 2-Fluoro-5-Bromo-3-Methylpyridine is shipped in tightly sealed, chemical-resistant containers to prevent contamination and leakage. It is transported under ambient conditions, labeled according to regulatory guidelines for hazardous materials. Ensure handling by trained personnel, and store in a cool, dry place away from incompatible substances during transit.
    Storage Store 2-Fluoro-5-Bromo-3-Methylpyridine in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling and restrict access to trained personnel. Follow all relevant safety, environmental, and regulatory guidelines for hazardous chemicals.
    Application of 2-Fluoro-5-Bromo-3-Methylpyridine

    Applications of 2-Fluoro-5-Bromo-3-Methylpyridine in Industrial Manufacturing

    2-Fluoro-5-Bromo-3-Methylpyridine serves as an advanced key intermediate for numerous chemical manufacturing sectors. Its unique pyridine-based structure and dual halogenation support downstream synthesis of complex molecules, specifically where high selectivity and functional group tolerance are required. Below are targeted industrial application fields where this material integrates directly into specialized production processes.

    1. Pharmaceutical Intermediate for Antineoplastic Agents

    Multistage synthesis in the pharmaceutical industry uses this compound as a building block for specialty heterocyclic scaffolds, supporting the discovery and mass production of next-generation antineoplastic drugs. Medicinal chemists employ it to construct advanced pyridine motifs in kinase inhibitors and related therapeutics, enabling controlled introduction of fluoro and bromo groups at specific positions. In these applications, the compound enters early or mid-stage synthesis, undergoes cross-coupling and substitution, and proceeds further to elaborate bioactive structures with precise purity profiles required for pharmaceutical use.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and EP monographs for intermediate registration
    • FDA 21 CFR Part 210/211 for process validation and traceability
    • EU REACH registration (when shipped/used in EU markets)

    Typical usage ratio

    • 0.5–2.5 molar equivalents relative to target heterocycle; specific ratio depends on substitution pattern and scale of batch size

    Downstream process integration

    • Reacted via Suzuki or Buchwald–Hartwig cross-coupling in a controlled environment under palladium catalysis
    • Integrated in Step 1 or 2 for molecular core construction, prior to final deprotection or crystallization

    Final product types

    • Small molecule antineoplastic APIs (protein kinase and tyrosine kinase inhibitors)
    • Batch intermediates for oncology active pharmaceutical ingredients
    • Pre-registered advanced pharmaceutical intermediates (APIs-in-progress)

    2. Agrochemical Synthesis for Herbicide Actives

    Crop protection compound developers use this pyridine derivative as a precursor for building halogenated heterocycles in advanced herbicides. The molecule is introduced into synthetic routes to access key intermediates that set up substitution for phenoxyalkyl and urea herbicidal actives. Downstream blending involves strict process controls to ensure correct incorporation of the fluoro and bromo functionalities, which directly impact the selectivity and environmental stability of the final formulated herbicides.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical manufacturing
    • FAO/WHO Specifications for Plant Protection Products (active ingredient identity and purity)
    • Globally Harmonized System (GHS) labelling and hazard communication
    • EU Regulation (EC) No 1907/2006 (REACH) for agricultural chemicals

    Typical usage ratio

    • Typically 0.8–1.3 molar equivalents in herbicide precursor pathway; adjusted to minimize byproduct formation

    Downstream process integration

    • Engaged in halogen-metal exchange reactions followed by nucleophilic substitution
    • Used during early intermediate formation before coupling to aromatic linkers or cyclization

    Final product types

    • Selective herbicide active ingredients (pyridine-based herbicidal molecules)
    • Crop protection intermediates for further formulation
    • Technical-grade and emulsifiable concentrate (EC) agrochemicals

    3. Electronic Chemicals for Liquid Crystal Materials

    Manufacturers in the display and electronics industry incorporate this compound for the synthesis of high-purity liquid crystal intermediates owing to its dual halogen substituted pyridine structure. The electronic-grade synthesis demands precise control of impurities to ensure high optical clarity and stability. This raw material is introduced as a coupling node for aryl-pyridine or alkyl-pyridine linkage formation, subsequently yielding target compounds with tunable mesogenic properties critical for the final performance of display panels.

    Industry compliance standards

    • IEC 62474 Reporting for substances in electronic products
    • RoHS Directive 2011/65/EU restrictions for hazardous substances
    • ASTM D5630 for purity and residue testing
    • Customer-specific panel manufacturer QC protocols

    Typical usage ratio

    • 1.00 molar equivalent for core mesogen synthesis; range maximizes end-product liquid crystal purity

    Downstream process integration

    • Participates in Grignard or metal-catalyzed coupling as the heterocyclic source
    • Step-integration prior to functionalization with alkyloxy or cyano groups for mesogenic alignment

    Final product types

    • High-stability liquid crystal mixtures for TFT-LCD panels
    • OLED and LC display material intermediates
    • Optoelectronic grade specialty chemicals

    4. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Dye and pigment formulators leverage this halogenated pyridine as a core intermediate for specialty colorant molecules. The dual halogen and methyl groups allow precise downstream hydrolysis, amination, or coupling to deliver unique color properties, stability, and solubility profiles. Industrial dye syntheses require tight control over raw material ratios and integration timing to achieve high tint strength and reproducible chromaticity in final pigments or dye preps for high-value coatings, inks, and plastics.

    Industry compliance standards

    • ISO 9001 and ISO 14001 for chemical plant quality and environmental control
    • REACH registration and notification for specialty dye substances
    • GHS-compliant hazardous substance communication
    • Oeko-Tex Standard 100 (for textile-related dyes if applied)

    Typical usage ratio

    • 0.6–1.1 molar equivalents, determined by azo or anthraquinone dye backbone requirements

    Downstream process integration

    • Introduced during primary condensation with diazonium salts or anilines
    • May be used at pre-coupling or post-coupling step depending on target pigment architecture

    Final product types

    • Specialty pigments for high-durability and high-chroma coatings
    • Textile and paper dye intermediates
    • Technical-grade colorants for printing inks and plastics
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