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3,5-Dichloropyridine

    • Product Name 3,5-Dichloropyridine
    • Alias 3,5-Dichloro-pyridine
    • Einecs 217-336-6
    • 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

    268264

    Chemicalname 3,5-Dichloropyridine
    Casnumber 626-01-7
    Molecularformula C5H3Cl2N
    Molecularweight 148.99
    Appearance Colorless to pale yellow liquid
    Boilingpoint 211-213°C
    Meltingpoint 15-18°C
    Density 1.37 g/cm3
    Purity Typically ≥98%
    Solubility Soluble in organic solvents, slightly soluble in water
    Flashpoint 97°C
    Refractiveindex 1.567

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

    Packing & Storage
    Packing The 3,5-Dichloropyridine is supplied in a 100g amber glass bottle, tightly sealed with a screw cap and labeled for laboratory use.
    Shipping 3,5-Dichloropyridine is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. Packaging complies with regulations for hazardous chemicals. Transport is usually by ground or air, with appropriate hazard labeling and documentation. Handling requires safety measures to prevent leaks, spills, or exposure. Always follow local and international shipping guidelines.
    Storage 3,5-Dichloropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition. Keep it out of direct sunlight and separate from incompatible substances such as strong oxidizers and acids. Ensure proper labeling and restrict access to authorized personnel. Use appropriate secondary containment to prevent spills or leaks.
    Application of 3,5-Dichloropyridine

    Applications of 3,5-Dichloropyridine in Industrial Manufacturing

    As a committed manufacturer of 3,5-Dichloropyridine, we supply bulk quantities of this key intermediate to innovative customers in several specialty sectors. Below, we detail its industrial-scale applications, referencing recognized compliance standards, refined incorporation protocols, production process roles, and finished goods utilized across select downstream markets.

    1. Pharmaceutical Active Ingredient Synthesis

    3,5-Dichloropyridine serves as a critical building block for producing pharmaceutical intermediates, particularly for anti-infective and oncology drugs. Its chlorinated pyridine structure enables direct functionalization in heterocyclic compound synthesis. Leading API manufacturers incorporate our material in the first or mid-stage coupling steps to construct complex heterocyclic scaffolds, with precise batchwise addition governed by process safety, impurity profile, and scalability requirements for regulated drug substances.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) Synthesis Guidelines
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia ChP 2020 (applicable synthesis protocols)

    Typical usage ratio

    • 10–30% of total reactant mass in primary heterocyclic coupling stages, precise ratio depends on API route and targeted yield versus byproduct suppression

    Downstream process integration

    • Introduced at Stage 1 or 2 as a core pyridine ring donor in multi-step synthesis of API intermediates; batch or continuous addition in solvent-controlled environments with in-process control of halide content and trace residuals

    Final product types

    • Second- and third-generation cephalosporin antibiotic intermediates
    • Heterocyclic kinase inhibitor intermediates for oncology APIs
    • Specialty anti-tubercular drug compounds

    2. Agrochemical Active Ingredient Manufacture

    Chemical crop protection manufacturers employ 3,5-Dichloropyridine in synthesizing key intermediates for herbicides, fungicides, and insecticides. Its dichloro substitution pattern delivers strong nucleophilic reactivity, supporting downstream conversion into protective molecules for field applications. Quality assurance labs monitor the introduction of our material at early condensation and substitution stages to ensure consistency in active ingredient yield and halogen control for established agrochemical formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for Agrochemical Synthesis
    • REACH Regulation (EC) No 1907/2006 for European markets
    • Chinese GB/T 1604-2001 Agrochemical Manufacturing Standards

    Typical usage ratio

    • 5–22% of the total weight in initial condensation or halogen-exchange steps, ratio determined by molecule target (e.g., pyridine-based herbicides or pyrazole fungicides) and yield optimization

    Downstream process integration

    • Added in primary condensation as the chlorine-donating pyridine component during intermediate construction; monitored via in-process chromatography to control impurity formation

    Final product types

    • Pyridine-containing herbicide technical concentrates (e.g., picolinafen intermediates)
    • Fungicide intermediates for strobilurin class products
    • Building blocks for neonicotinoid insecticides

    3. Dye and Specialty Pigment Synthesis

    Our 3,5-Dichloropyridine plays a role in the advanced formulation of organic dyes and specialty pigments, supplying electron-withdrawing functionality for pyridine-based chromophore development. Colorant producers integrate our compound in halogenation and ring modification stages to impart shade stability, lightfastness, and process color uniformity, governed by strict regulatory checks and purity validation from the initial batch scale to continuous production.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textiles (related to colorant safety)
    • EN 71-3 for colorant use in toys and consumer goods
    • ISO 9001 for pigment and dye manufacturing quality assurance
    • RoHS Directive 2011/65/EU (where pigments are used in electronics)

    Typical usage ratio

    • 8–15% of total dye-pigment precursor mass; the actual portion is balanced according to target chromophore intensity and batch scale-up reproducibility parameters

    Downstream process integration

    • Employed in ring chlorination and substitution as a precursor before azo- or anthraquinone coupling reactions; incorporated during temperature-controlled blending in solvent or fused salt media

    Final product types

    • Pyridine-based textile dyes with high color fastness
    • Halogen-resistant synthetic pigments for coatings and inks
    • UV-stable dyes for plastics and specialty polymers

    4. Electronic and Liquid Crystal Material Synthesis

    Specialty electronics materials manufacturers utilize 3,5-Dichloropyridine to synthesize advanced intermediates essential for liquid crystal displays (LCDs) and certain organic semiconductors. The chemical’s dichloro ring system permits regioselective derivatization and supports the fabrication of high-purity, high-performance functional monomers. Quality and yield remain closely monitored through robust QC procedures, as the purification and precise dosing of intermediates defines the final device’s electrical and optical characteristics.

    Industry compliance standards

    • ISO 9001 and IATF 16949 for electronic material manufacturing quality systems
    • RoHS compliance (lead, mercury, cadmium, hexavalent chromium control)
    • IEC 61249-2-21 for halogen-free base materials (where required)
    • Japanese Industrial Standards (JIS) for electronics chemicals

    Typical usage ratio

    • 2–12% input based on the specific liquid crystal or precursor molecule, with the range adjusted for functional performance and downstream polymerization efficiency

    Downstream process integration

    • Added during initial monomer synthesis or halide exchange in liquid crystal precursor production; solution blending under inert conditions followed by high-purity distillation

    Final product types

    • Biphenyl-based liquid crystal monomers
    • Intermediate components for TFT-LCD panel fabrication
    • Functionalized aromatic compounds for organic electronic devices
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