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2-Chloropyridine-4-Carboxylic Acid Tert-Butyl Ester

    • Product Name 2-Chloropyridine-4-Carboxylic Acid Tert-Butyl Ester
    • Alias tert-Butyl 2-chloroisonicotinate
    • Einecs 617-158-4
    • 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

    697756

    Productname 2-Chloropyridine-4-Carboxylic Acid Tert-Butyl Ester
    Molecularformula C10H12ClNO2
    Molecularweight 213.66 g/mol
    Casnumber 139280-41-6
    Appearance White to pale yellow solid
    Purity Typically ≥ 97%
    Storageconditions Store at 2-8°C, protect from light and moisture
    Solubility Soluble in organic solvents such as dichloromethane, ethyl acetate
    Smiles CC(C)(C)OC(=O)c1ccnc(c1)Cl
    Inchi InChI=1S/C10H12ClNO2/c1-10(2,3)14-9(13)7-4-5-12-8(11)6-7/h4-6H,1-3H3
    Synonyms Tert-Butyl 2-chloroisonicotinate

    As an accredited 2-Chloropyridine-4-Carboxylic Acid Tert-Butyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Chloropyridine-4-Carboxylic Acid Tert-Butyl Ester comes in a sealed, 25-gram amber glass bottle with a secure cap.
    Shipping **Shipping Description:** 2-Chloropyridine-4-Carboxylic Acid Tert-Butyl Ester is shipped in tightly sealed, chemical-resistant containers, clearly labeled with hazard and handling information. The package is cushioned to prevent breakage and transported under ambient conditions unless otherwise specified. Compliance with regional chemical shipping regulations and appropriate documentation is ensured for safe delivery.
    Storage 2-Chloropyridine-4-carboxylic acid tert-butyl ester should be stored in a tightly sealed container, protected from moisture and light. Keep in a cool, dry, and well-ventilated area, away from heat and incompatible substances such as strong acids or bases. Label clearly and avoid prolonged exposure to air to prevent decomposition. Store at room temperature unless otherwise specified by the supplier.
    Application of 2-Chloropyridine-4-Carboxylic Acid Tert-Butyl Ester

    Applications of 2-Chloropyridine-4-Carboxylic Acid Tert-Butyl Ester in Industrial Manufacturing

    As a manufacturer specialized in the production of 2-chloropyridine-4-carboxylic acid tert-butyl ester, we support multiple advanced chemical synthesis processes across regulated industries. The following sections outline the principal industrial application scenarios for this intermediate, covering precise compliance frameworks, formulation practices, end-use integration stages, and common final goods for each downstream field.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    This compound serves as a protected pyridine carboxylate source in multi-step syntheses for certain APIs, including selected kinase inhibitors and CNS-targeted drugs. Downstream pharmaceutical customers incorporate it during early to mid-stage coupling and condensation reactions for heterocyclic core assembly within regulated manufacturing environments prioritizing strict impurity control and batch traceability.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • U.S. FDA regulation 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) for intermediates
    • ICH Q3A/B guidelines for residual solvents and impurities

    Typical usage ratio

    • 0.9–1.2 molar equivalents relative to target pyridine coupling partners; quantities are adjusted according to target yield and byproduct minimization required in each specific API route.

    Downstream process integration

    • Integrated during the amidation or ester hydrolysis step following halogen-metal exchange or in situ deprotection, after initial ring activation and before final catalyst addition or protection group removal.

    Final product types

    • Small molecule kinase inhibitors
    • Neuroactive heterocycles for CNS therapies
    • Oncology precursor compounds
    • Research-stage drug development intermediates

    2. Agrochemical Active Ingredient Production

    Major producers in the crop protection sector utilize this ester as a nitrogen-containing building block for pyridine-derived herbicide and fungicide actives. The raw material enters syntheses where alkoxycarbonyl functional groups enable downstream cyclizations and controlled chlorination steps while maintaining purity compliant with agricultural chemical standards.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 Quality Management (for process controls)
    • REACH Regulation (EC) No 1907/2006 preregistration and notification for substances used in agriculture
    • OECD Guidelines for the Testing of Chemicals—Residual Purity

    Typical usage ratio

    • Used at 0.75–1.3 stoichiometric equivalents depending on intended cyclization efficiency and the nature of functional group transformations in each downstream molecule.

    Downstream process integration

    • Added to reactors following initial halogenation of precursor pyridine or after first-step methylation, typically before condensation and before the introduction of phosphorus oxychloride or base-catalyzed hydrolysis.

    Final product types

    • Pyridine-based herbicide technical concentrates
    • Fungicidal active ingredient intermediates
    • Formulated crop protection actives with site-specific delivery
    • Seed treatment agents (technical grade)

    3. Specialty Chemical Synthesis for Electronic Materials

    Manufacturers in the electronics chemical sector apply this ester as a protected intermediate within custom syntheses for pyridine derivatives used as charge transport or coordination ligands in photoresist resins and OLED/LC polymer blends. Its tert-butyl ester group stabilizes sensitive intermediates during prolonged batch reactions, compliant with trace metal and residual halide limitations for advanced materials.

    Industry compliance standards

    • IEC 62474: Material Declaration for Products of and for the Electrotechnical Industry
    • Restriction of Hazardous Substances (RoHS) Directive 2011/65/EU
    • ISO 9001 Quality Management (for traceability and batch release)
    • Internal QC protocols for semiconductor-grade purity

    Typical usage ratio

    • 0.2–0.6 parts by weight per 1 part functionalized pyridine precursor; ratio fine-tuned based on required degree of esterification and final ligand or monomer design.

    Downstream process integration

    • Charged into high-purity glass-lined reactors after in situ base pre-treatment; enters mid-synthesis as a nucleophilic component during ligand functionalization or ester transfer reactions prior to final purification and thermal deblock.

    Final product types

    • OLED charge transport material precursors
    • Photoresist resin building blocks
    • Pyridine-based ligands for advanced polymers
    • High-purity intermediates for microelectronics chemicals

    4. Fine Chemical Intermediate for Dye and Pigment Manufacture

    Producers of high-performance dyes employ this intermediate for constructing complex pyridine-based chromophores. It is chosen for its compatibility with diazotization and azo coupling pathways, where tert-butyl ester protection withstands harsh acid/base conditions encountered in pigment core assembly, ensuring batch reproducibility and color consistency in end products.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for industrial dyes
    • ISO 9001:2015 and ISO 14001:2015 Environmental Management
    • ETAD code of good practice for pigment manufacture
    • OEM batch testing for pigment residue and purity

    Typical usage ratio

    • Employed at 0.5–1.0 molar equivalents depending on the complexity of the final pigment structure and targeted chromatic properties; adapted for both lab-scale development and large-batch synthesis.

    Downstream process integration

    • Introduced after the initial diazotization of aniline/pyridine derivatives and before final azo coupling or thermal deprotection; typically enters at the intermediate pigment formation or high-temperature condensation stage.

    Final product types

    • Pyridine-based organic pigments
    • Special application dyes for technical fiber coloration
    • UV-stable tint masterbatches
    • Chromophore intermediates for automotive and plastics sectors
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