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2,6-Dichloro-3-Nitropyridine

    • Product Name 2,6-Dichloro-3-Nitropyridine
    • Alias 2,6-Dichloro-3-nitro-pyridine
    • Einecs 242-617-7
    • 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
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    Specifications

    HS Code

    136679

    Chemicalname 2,6-Dichloro-3-Nitropyridine
    Molecularformula C5H2Cl2N2O2
    Molecularweight 193.99 g/mol
    Casnumber 82034-46-6
    Appearance Yellow to light brown solid
    Meltingpoint 85-89 °C
    Solubility Soluble in organic solvents like dichloromethane and ethanol
    Purity Typically ≥98%
    Smiles Clc1cccc(Cl)n1[N+](=O)[O-]
    Storagetemperature Store at 2-8 °C
    Iupacname 2,6-dichloro-3-nitropyridine

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2,6-Dichloro-3-Nitropyridine, sealed with a tamper-evident cap and labeled with hazard warnings.
    Shipping 2,6-Dichloro-3-nitropyridine is shipped in tightly sealed containers, protected from moisture and incompatible substances. It is typically packaged according to regulations for hazardous chemicals, with appropriate hazard labels. Transportation must ensure stability, prevent leaks, and comply with local, national, and international safety guidelines for toxic and potentially environmentally hazardous substances.
    Storage **2,6-Dichloro-3-Nitropyridine** should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizing or reducing agents. Keep away from heat, sparks, and open flames. Store under inert atmosphere if possible, and clearly label the storage container. Use appropriate chemical safety storage cabinets.
    Application of 2,6-Dichloro-3-Nitropyridine

    Applications of 2,6-Dichloro-3-Nitropyridine in Industrial Manufacturing

    As an established producer of 2,6-Dichloro-3-Nitropyridine, we supply this advanced pyridine derivative to leading industry players across several tightly defined downstream sectors. Below, we detail the primary application domains where this intermediate achieves commercial-scale integration, with concrete reference to regulatory environments, formulation practices, technical process roles, and finished products manufactured by our customers.

    1. Pharmaceutical Intermediate for Anti-Infective Synthesis

    Major pharmaceutical manufacturers incorporate 2,6-Dichloro-3-Nitropyridine as a core synthetic building block during the multi-stage preparation of select active pharmaceutical ingredients (APIs), such as certain nitropyridine-derived antimicrobials and anti-tuberculosis agents. Its specific substitution pattern critically enables late-stage chlorination and nitration reactions, producing intermediates that feed directly into API finalization steps.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP) – ICH Q7
    • Ph. Eur. — European Pharmacopoeia monographs for APIs
    • United States Pharmacopeia (USP) regulatory guidance
    • China Pharmacopoeia for registered pharmaceutical intermediates

    Typical usage ratio

    • Utilization at 0.8–1.2 molar equivalents relative to target API core scaffold; precise quantity adjusted by route-specific stoichiometry and process control yield.

    Downstream process integration

    • Introduced during mid- or late-stage intermediate formation in stepwise synthesis, typically via controlled nucleophilic aromatic substitution or heterocycle derivatization—prior to deprotection, coupling, or crystallization steps in API manufacturing.

    Final product types

    • Anti-mycobacterial drugs (e.g., nitropyridine quinoline-type compounds)
    • Second-generation nitroaromatic anti-infectives
    • Other regulated pharmaceutical actives dependent on substituted chloropyridine intermediates

    2. Crop Protection Active Ingredient Synthesis

    Agricultural chemical manufacturers utilize this raw material in the synthesis of select chlorinated pyridine-based herbicides and fungicides. Its electron-withdrawing nitro and chloro groups facilitate downstream cyclization and halogenation routes without introducing off-target reactivity often observed with less substituted pyridine isomers.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System (for agrochemical production)
    • REACH Annex VIII registration for advanced intermediates in Europe
    • China Pesticide Registration (ICAMA)

    Typical usage ratio

    • 0.5–1.0 mol per active ingredient batch, often determined by targeted yield, downstream purity specifications, and functionalization requirements tied to the final molecule’s regulatory dossier.

    Downstream process integration

    • Enters after primary pyridine backbone formation, supporting specific halogenation, ring closure, or nitration steps within continuous or batch production lines, prior to active ingredient isolation and formulation blending.

    Final product types

    • Selective pre-emergence herbicides for broadleaf weed control
    • Pyridine-based fungicides with systemic activity
    • Custom-formulated crop protection compounds registered by local authorities

    3. Fine Chemical Synthesis for Electronic Material Intermediates

    Electronics material producers employ this compound as a tailored intermediate for synthesizing advanced nitrogen-containing heterocyclic structures utilized in the formulation of specialty dyes, liquid crystal intermediates, and functional OLED materials. Its unique substitution facilitates metalation and cross-coupling reactions required for high-purity, functional end-products.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System (electronic chemicals)
    • RoHS Directive 2011/65/EU for downstream electronic applications
    • IECQ QC 080000 (Hazardous Substance Process Management)
    • National standards for electronic and optoelectronic intermediates (GB50397, China)

    Typical usage ratio

    • Applied at 0.95–1.05 molar equivalents depending on chain length and substitution requirements; ratios adjusted for optimal color fastness or luminescence efficiency in dyes and display precursor production.

    Downstream process integration

    • Reacts as a coupling partner during Suzuki, Buchwald-Hartwig, or direct arylation steps performed under controlled inert atmosphere synthesis; timing is aligned with strict purity and trace residue monitoring before downstream functionalization.

    Final product types

    • Pyridine-based electronic dyes for semiconductor photolithography
    • Precursors for liquid crystal display (LCD) materials
    • OLED emitter and transport molecule intermediates

    4. Custom Synthesis of Specialty Chemical Building Blocks

    Chemical synthesis and contract manufacturing organizations demand this pyridine derivative for the preparation of rare building blocks, such as nitrochlorinated heterocycles, that serve as key precursors for patent-protected agrochemical leads, specialty monomers, and advanced research reagents. Its reactivity profile supports precise multi-step functionalization with minimized byproduct development at industrial scale.

    Industry compliance standards

    • ISO 9001:2015 for custom synthesis QC management
    • Confidential Disclosure Agreement (CDA) protocols for patented project work
    • Hazardous Materials Regulations (49 CFR, US DOT) for intermediate storage/transport
    • REACH intermediate authorization (where required in EU)

    Typical usage ratio

    • 1.0–1.3 equivalents per reaction, adjusted according to substrate reactivity and complexity of target moiety; scale-up campaigns may modify excess ratios for downstream purification efficiency.

    Downstream process integration

    • Introduced in regioselective halogen exchange, nitration, and metal-catalyzed assembly reactions typically in small to mid-scale reactors for batch or continuous pilot plant operation, preceding further derivatization or functional group interconversion.

    Final product types

    • Custom nitropyridine intermediates for product innovation
    • Nitrochlorinated monomer building blocks for performance polymer synthesis
    • Specialty reagents for contract research and process development
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