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6-Chloro-2-Methyl-3-Nitropyridine

    • Product Name 6-Chloro-2-Methyl-3-Nitropyridine
    • Alias 6-Chloro-2-methyl-3-nitro-pyridine
    • Einecs 629-040-8
    • 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

    168026

    Productname 6-Chloro-2-Methyl-3-Nitropyridine
    Casnumber 151181-55-2
    Molecularformula C6H5ClN2O2
    Molecularweight 172.57 g/mol
    Appearance Yellow to brown crystalline solid
    Meltingpoint 79-82°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and DMF
    Smiles CC1=NC=C(C(=C1)[N+](=O)[O-])Cl
    Inchi InChI=1S/C6H5ClN2O2/c1-4-8-3-5(7)6(2-4)9(10)11/h2-3H,1H3
    Storageconditions Store at room temperature, in a cool, dry place

    As an accredited 6-Chloro-2-Methyl-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 6-Chloro-2-Methyl-3-Nitropyridine, labeled with hazard symbols, product, and batch information.
    Shipping 6-Chloro-2-Methyl-3-Nitropyridine is shipped in sealed, chemically resistant containers. It is handled according to hazardous material regulations, labeled appropriately, and protected from moisture and light. Transport complies with international and local chemical safety guidelines, ensuring secure packaging to prevent leaks, spills, or contamination during transit.
    Storage Store 6-Chloro-2-Methyl-3-Nitropyridine in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Segregate from incompatible substances such as strong oxidizers and bases. Use secondary containment to prevent spills and ensure proper personal protective equipment is worn when handling.
    Application of 6-Chloro-2-Methyl-3-Nitropyridine

    Applications of 6-Chloro-2-Methyl-3-Nitropyridine in Industrial Manufacturing

    6-Chloro-2-Methyl-3-Nitropyridine serves as a critical building block in numerous fine chemical and pharmaceutical synthesis chains. Our manufacturing experience shows its integration is especially valued in sectors where stringent regulatory compliance, controlled process parameters, and precise formulation impact downstream product quality.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    This pyridine derivative functions among the initial core intermediates in multi-step manufacturing of targeted APIs such as anti-infective, cardiovascular, and oncological compounds. Its chloro-nitro configuration supports selective substitution reactions, providing crucial scaffolds for advanced heterocyclic actives. Pharmaceutical plants carry out nucleophilic aromatic substitution or reduction under controlled conditions, following GMP-compliant protocols, with real-time QC for impurity profiles and residual solvents.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) – ICH Q7A
    • European Pharmacopoeia (Ph. Eur.) for intermediates
    • US FDA 21 CFR Part 210/211 (for API route stages)
    • Chinese Pharmacopoeia standards for ingredient traceability

    Typical usage ratio

    • Ranges from 1.0 to 1.5 molar equivalents per target molecule.
    • Ratios frequently adjusted based on impurity controls and step yield optimization.
    • Purity specification: ≥98% (HPLC).

    Downstream process integration

    • Introduced during Stage II–IV of multi-step synthesis.
    • Employed for halo/nitro-pyridine ring closure, followed by hydrogenation or substitution.
    • Reaction conditions closely regulated for temperature and pH to ensure selectivity.

    Final product types

    • Active pharmaceutical ingredients: antimalarial drugs, kinase inhibitors, antivirals.
    • Advanced drug intermediates for contract manufacturing organizations (CMO) use.

    2. Agrochemical Active Substance Production

    Chloro-nitro-methyl-pyridine compounds play a significant role in the manufacture of crop protection and pest control actives. Downstream formulators leverage the selective nitration and halogen reactivity to introduce key functional groups into insecticides, fungicides, and herbicides. Batch synthesis and continuous processing lines require strict control of residual impurities in line with global agricultural regulations to ensure safety margins.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001-certified production SOPs
    • China National Food Safety Standard for Maximum Residue Limits (GB 2763)

    Typical usage ratio

    • 0.95 to 1.2 moles per mole of target compound in initial condensation steps.
    • Adjusted to maintain less than 0.5% unresolved starting material.
    • Purity: ≥97% for crop chemical synthesis.

    Downstream process integration

    • Added to the halogenation or coupling reaction stages of active ingredient manufacture.
    • Commonly used in pyridine ring derivatization leading to sulfonylurea or triazole classes.
    • Process includes solvent extraction, crystallization, and flash drying.

    Final product types

    • Technical grade pesticides: insecticides, herbicides, fungicides.
    • Crop protection formulation intermediates for global agrochemical brands.

    3. Specialty Dye and Pigment Precursors

    Selective halogen and nitro substitution patterns in this molecule meet formulation needs of specialty dyes and pigments industries. Fine chemical manufacturers rely on precise molar ratios during aromatic ring functionalization to create photostable, high-yield colorants for plastics, fiber, and ink industries. Downstream partners require assurance on solvent residue and uniform batch color intensity that meet export and environmental standards.

    Industry compliance standards

    • European Union REACH Regulation for industrial dyes
    • OEKO-TEX® Standard 100 (textile applications)
    • EN 71-3 (Safety of toys – migration of certain elements)
    • US EPA Toxic Substances Control Act (TSCA) inventory checks

    Typical usage ratio

    • 0.85 to 1.1 molar equivalents for mono-azo pigment synthesis.
    • Batch adjustments depend on target chromophore and intensity grade.
    • Purity: ≥98% required for high-purity color formulations.

    Downstream process integration

    • Feeds into condensation or coupling reactions.
    • Employed in coupling steps before azo dye formation or as a ring-modifier for anthraquinone pigments.
    • Process incorporates inline NIR analysis for consistency.

    Final product types

    • High-purity industrial dyes for plastic resins
    • Specialty pigments for coatings, printing inks, and textile colorants

    4. Electronic and Liquid Crystal Intermediate Manufacturing

    The unique electronic configuration of this pyridine derivative suits its use as a precursor in the synthesis of liquid crystal compounds, electro-active materials, and advanced intermediates used in the production of OLED displays and high-performance electronic materials. Strict impurity control and particle size monitoring are implemented to prevent electrical degradation in end-use electronic applications. Batch traceability forms a core part of our supply quality documentation.

    Industry compliance standards

    • RoHS Directive (EU) 2011/65/EU for hazardous substances
    • IEC 61249-2-21 for halogen-free requirements in electronics
    • JEITA (Japan Electronics and Information Technology Industries Association) purity guidelines
    • ISO 9001:2015 (for electronic chemical production)

    Typical usage ratio

    • Application-specific ratios: generally 1.0 ± 0.05 equiv in core-forming reactions for liquid crystal units.
    • Higher precision required for charge-transport material synthesis.
    • Purity specification: 99% min for low conductive residue electronic materials.

    Downstream process integration

    • Used in the Suzuki or Buchwald–Hartwig coupling reactions during liquid crystal molecule creation.
    • Integrated prior to final condensation or cyclization stages for electronic material precursors.
    • Process involves ultrafiltration, particle screening, and solvent-free handling where required.

    Final product types

    • High purity liquid crystal materials for TFT and OLED displays
    • Charge transport agents for photoconductors in copier/printer applications
    Free Quote

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