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Methyl 2-Chloro-6-Methylpyridine-4-Carboxylate

    • Product Name Methyl 2-Chloro-6-Methylpyridine-4-Carboxylate
    • Alias Methyl 2-chloro-6-methylisonicotinate
    • Einecs EINECS 696-215-3
    • 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

    211800

    Product Name Methyl 2-Chloro-6-Methylpyridine-4-Carboxylate
    Cas Number 884494-14-0
    Molecular Formula C8H8ClNO2
    Molecular Weight 185.61 g/mol
    Appearance White to off-white solid
    Melting Point 71-75°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Storage Conditions Store at room temperature, away from moisture and light
    Smiles COC(=O)C1=CC(=NC(=C1)Cl)C
    Inchi InChI=1S/C8H8ClNO2/c1-5-3-6(8(11)12-2)4-10-7(5)9/h3-4H,1-2H3
    Synonyms Methyl 2-chloro-6-methylisonicotinate

    As an accredited Methyl 2-Chloro-6-Methylpyridine-4-Carboxylate 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, sealed with a screw cap, labeled with the chemical name, formula, hazard warnings, and batch number.
    Shipping The chemical **Methyl 2-Chloro-6-Methylpyridine-4-Carboxylate** is securely packaged in sealed containers compliant with safety regulations. It is shipped via ground or air transport with appropriate labeling and documentation. Temperature and handling precautions are observed to prevent contamination, leaks, or exposure during transit. Delivery tracking and material safety data are included.
    Storage Methyl 2-Chloro-6-Methylpyridine-4-Carboxylate should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents. Ensure proper labeling and restrict access to authorized personnel. Store at room temperature unless otherwise specified by the manufacturer or safety data sheet (SDS).
    Application of Methyl 2-Chloro-6-Methylpyridine-4-Carboxylate

    Applications of Methyl 2-Chloro-6-Methylpyridine-4-Carboxylate in Industrial Manufacturing

    As a direct manufacturer, we supply methyl 2-chloro-6-methylpyridine-4-carboxylate to a defined set of intermediates and transformation routes within the fine chemicals sector. This compound's unique structure and reactivity allow its targeted application in pharmaceutical synthesis, agrochemical formulation, specialty chemical intermediates, and advanced material modification. The following sections detail how industrial customers integrate this intermediate into production flows, in line with compliance requirements, validated usage ratios, and resulting product classes.

    1. Pharmaceutical API Intermediate Production

    Our material serves as a key intermediate in the synthesis of selective pharmaceutical active pharmaceutical ingredients (APIs), especially those involving pyridine-based scaffolds. Customers utilize its reactivity in amide coupling and heterocycle modifications, supporting the manufacture of antihypertensive agents, new-generation antibacterial drugs, and CNS-active pharmaceutical molecules. Our manufacturing batches are dosed to precise levels according to process needs, and support full traceability for regulated drug substance manufacture.

    Industry compliance standards

    • Good Manufacturing Practice (GMP, ICH Q7 and EU GMP Part II)
    • US FDA 21 CFR Parts 210/211 (for API processes)
    • ICH Q3A/B guidelines for impurities
    • Pharmacopoeial references: USP/NF, Ph. Eur., JP (as raw material specification guidance)

    Typical usage ratio

    • 0.5–1.8 molar equivalents per targeted intermediate, adjusted for target yield and reaction step conversion; optimization based on impurity control and scalability studies in route development.

    Downstream process integration

    • Charged directly into amidation or cyclization vessels post-purification, or fed by continuous pumps in flow chemistry setups.
    • Quality-checked prior to integration through HPLC purity and residual solvent analysis.

    Final product types

    • Active pharmaceutical ingredients such as anti-infectives, antihypertensives, neurological disorder treatment agents.
    • Pharmaceutical intermediates for registered drugs undergoing clinical or commercial scale-up.

    2. Agrochemical Active Compound Synthesis

    Methyl 2-chloro-6-methylpyridine-4-carboxylate is widely adopted as a building block for the synthesis of herbicide and insecticide actives containing pyridine motifs. Its stability enables precise incorporation into N-heterocyclic active compounds via ester cleavage and further functionalization. Downstream users in agrochemical sectors rely on its defined impurity profile for large-batch consistency and regulatory compliance for both end-use and export markets.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) pesticide specification guidelines
    • ISO 9001 quality management for agrochemical ingredient traceability
    • Regulation (EC) No 1107/2009 (for registration, evaluation, and authorization of plant protection products in the EU)
    • EPA 40 CFR Parts 150–189 (U.S. agrochemical requirements)

    Typical usage ratio

    • 5–15% by weight of total batch in the synthesis stage, with final concentration determined by desired backbone structure of the target compound and required yield-to-cost balance during scale-up.

    Downstream process integration

    • Used as a precursor in ester hydrolysis steps, or as a coupling substrate for halogen exchange in N-heterocyclic synthetic routes, typically under controlled temperature and solvent systems.

    Final product types

    • Active herbicidal agents based on pyridine derivatives
    • Insecticide actives targeting soil and foliar pests
    • Agrochemical concentrates used for formulation of field-ready agro products

    3. Specialty Chemical Intermediate for Dye and Pigment Synthesis

    Industrial dye manufacturers exploit this compound’s methyl and chloro substitution pattern to create pyridine-containing azo and heterocyclic colorants. These specialized molecules feature in high-performance printing inks and textile dyes, where structural fidelity and predictable reactivity underpin product reproducibility and application fastness. Our controlled process minimizes cross-contaminants to match color chemistry requirements.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for registration and safe handling
    • Oeko-Tex Standard 100 (for textile applications requiring tested tolerated chemicals)
    • ISO 9001:2015 for specialty chemicals traceability
    • Specific exporter or end-market chemical inventories (TSCA, ENCS for U.S., Japan markets)

    Typical usage ratio

    • 3–8% by mass in pigment molecule synthesis, tailored to reaction pathway and chromophore yield; adjusted during pilot scale-up for desired shade and purity.

    Downstream process integration

    • Direct input into condensation-azo or nucleophilic aromatic substitution reactions in dye manufacturing reactors.

    Final product types

    • Nitrogen-containing azo dyes for textile applications
    • High-saturation pigments for industrial and specialty coatings
    • UV-stable colorants for plastics and synthetic fibers

    4. Intermediate for Electronic Material Modification

    Producers of advanced electronic materials use this compound for tailoring functionalized pyridine residues within organic semiconductors and charge transport enhancers. The halogenated structure enables selective cross-coupling and further functionalization needed in OLED layers and printed electronics. Purity, trace elements, and absence of interfering residuals are essential for electrical performance and device reliability.

    Industry compliance standards

    • IEC 62474 (material declaration for the electrical and electronics industry)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001 (environmental management, especially for electronics-grade chemicals)
    • Internal semiconductor supplier quality agreements

    Typical usage ratio

    • 1–4% weight in precursor blends, based on polymer backbone design and electronic property optimization; defined by R&D evaluation and pilot-scale test runs for conductivity and stability.

    Downstream process integration

    • Incorporated in solution-phase synthesis of functional monomers, or utilized directly in palladium-catalyzed coupling steps for building conjugated systems.

    Final product types

    • Pyridine-modified monomers for organic electronic thin films
    • Charge-transport enabling agents in OLED devices
    • Specialty resins and additives for advanced printed electronic substrates

    5. Crop Protection Intermediate for Fungicide Synthesis

    Fungicide manufacturers source our compound as a key intermediate for the creation of pyridine-based fungicidal actives. Its chemical structure enables access to potent molecules via regioselective halogen substitution and methyl-directed transformation. Production runs meet the trace impurity and residual halogen content needed for downstream registration and efficacy requirements in finished field applications.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (relevant to environmental safety of new fungicides)
    • FAO/WHO International Code of Conduct for Pesticide Management
    • ISO 17025 (for batch traceability and analytical validation in agrochemical labs)
    • National pesticide registration requirements (e.g., China, Brazil, EU, U.S. EPA)

    Typical usage ratio

    • 6–20% by mole in base synthesis processes, modified according to the target backbone for the pyridine fungicide group and desired crop-specific activity level.

    Downstream process integration

    • Direct loading into halogen exchange and nucleophilic substitution batch reactors, with temperature and solvent profile adapted to control regioselectivity and limit byproduct formation.

    Final product types

    • Systemic and contact fungicides for cereals, fruits, and vegetable protection
    • Seed treatment compositions containing pyridine-active molecules
    • Pre-mixed formulations for agronomy market supply chains
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