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2,6-Dichloropyridine-4-Carboxaldehyde

    • Product Name 2,6-Dichloropyridine-4-Carboxaldehyde
    • Alias 2,6-Dichloroisonicotinaldehyde
    • Einecs 217-937-5
    • 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

    952753

    Chemical Name 2,6-Dichloropyridine-4-Carboxaldehyde
    Cas Number 87629-67-2
    Molecular Formula C6H3Cl2NO
    Molecular Weight 176.00
    Appearance White to light yellow crystalline powder
    Melting Point 87-91°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Smiles C1=C(C(=NC(=C1Cl)Cl)C=O)
    Inchi InChI=1S/C6H3Cl2NO/c7-5-1-4(3-10)2-6(8)9-5/h1-3H
    Synonyms 2,6-Dichloro-4-formylpyridine
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 2,6-Dichloropyridine-4-Carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle features a white screw cap, amber glass for light protection, hazard labeling, chemical name, and manufacturer information.
    Shipping 2,6-Dichloropyridine-4-Carboxaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. Packaging adheres to international transport regulations for hazardous materials. The containers are clearly labeled and cushioned to minimize breakage during transit. Temperature and handling instructions are provided to ensure safe and compliant delivery.
    Storage 2,6-Dichloropyridine-4-carboxaldehyde should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizers. Keep the container tightly closed and protected from light and moisture. Store in a chemically resistant container, properly labeled, and ensure access is limited to trained personnel. Avoid prolonged exposure to air and direct sunlight.
    Application of 2,6-Dichloropyridine-4-Carboxaldehyde

    Applications of 2,6-Dichloropyridine-4-Carboxaldehyde in Industrial Manufacturing

    Our factory-grade 2,6-Dichloropyridine-4-Carboxaldehyde finds critical utilization in specialized chemical synthesis sectors. We serve direct downstream industries where our material’s selectivity, reactivity, and regulatory traceability are key for scalable production and high-value end markets.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers apply our compound as a core intermediate for developing key heterocyclic scaffolds in antihypertensive, anti-inflammatory, and antiviral drug APIs. This raw material drives the condensation and cyclization reactions producing pharmacologically active compounds under cGMP conditions. Its controlled reactivity and low impurity levels allow for consistent downstream yield and batch reproducibility in regulated API environments.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP / Ph. Eur. General Chapters for impurities and residual solvents
    • FDA 21 CFR Parts 210 & 211 (GMP)
    • China Pharmacopoeia standards for intermediates in regulated APIs

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to main amine or hydrazine reactant (formula-specific and adjusted for side-reactions and yield optimization)

    Downstream process integration

    • Dosed into stepwise heterocyclic condensation, typically after initial precursor ring closure
    • Controlled addition at 40–90°C under inert or oxygen-free atmosphere
    • Subsequent purification by crystallization or preparative chromatography to isolate the pure intermediate

    Final product types

    • Pyridine-based antihypertensive drug APIs
    • Antiviral agent intermediates (pyridine-derivatives)
    • Anti-inflammatory bulk actives
    • Specialty generic API intermediates

    2. Agrochemical Precursor Manufacturing

    Leading agrochemical companies utilize this compound as an essential building block in the synthesis of fungicide, herbicide, and insecticide actives containing substituted pyridine motifs. The molecule’s dual chloro and aldehyde substituents enable targeted functionalization via Grignard or nucleophilic addition, producing robust and field-stable actives that address resistance and regulatory residue constraints.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Registration (EC/1907/2006)
    • SANCO/221/2000 Good Laboratory Practice
    • ISO 9001:2015 for agrochemical production QC

    Typical usage ratio

    • 1–1.4 molar equivalent to active pyridine core (ratio optimized for specific pesticide structure and cyclization step)

    Downstream process integration

    • Introduced after core substrate activation and prior to heterocyclic ring fusion
    • Reaction temperature range: 55–110°C in presence of controlled base or Grignard reagent
    • Followed by halogenation or further side-chain modification, then crude product isolation

    Final product types

    • Pyridine-derived herbicides (e.g., picolinic acid-based actives)
    • Broad-spectrum systemic fungicide raw ingredients
    • Residual-reducing insecticide intermediates
    • Seed treatment technicals for large-acreage application

    3. Specialty Dye and Pigment Intermediate Production

    Industrial pigment and specialty dye manufacturers select this pyridine compound for direct ring-substitution, facilitating controlled syntheses of high purity azo and heteroaromatic chromophores. The dual chlorine and aldehyde functional groups allow step-growth polymerization or condensation, opening the route for custom molecular dye engineering with targeted colorfastness and high thermal stability for plastics and coatings.

    Industry compliance standards

    • OEKO-TEX Standard 100 for harmful substances in colorants
    • GHS/CLP (EC No 1272/2008) for chemical hazard classification
    • EN 71-3: Toy Safety (colorant limits)
    • ISO 18314-1 for colorimetric analysis in industrial pigments

    Typical usage ratio

    • 5–15% by weight in azo or polyaromatic synthesis batch (varies by target chromophore type)

    Downstream process integration

    • Added post-diazonium coupling or in nucleophilic aromatic substitution reactions
    • Enables branching or terminus functionality in pigment molecules
    • Refined through multiple precipitation and filtration steps prior to downstream blending

    Final product types

    • High-performance heterocyclic dyes for plastics
    • Automotive-grade pigments with UV stability
    • Textile colorants meeting colorfastness testing
    • Electronic display color filter raw materials

    4. Advanced Electronic Materials Precursor

    Producers of advanced electronic materials apply this dichloropyridine derivative as a highly selective intermediate for synthesizing electron-transporting materials, OLED small molecules, and specialty liquid crystals. Its planar structure and functional positions are exploited during Suzuki or Buchwald–Hartwig couplings, yielding defined heterocyclic systems that support fine-tuned electronic properties and device reliability.

    Industry compliance standards

    • JEDEC Standard JESD243 for material purity in semiconductors
    • IEC 61249-2-21: Halogen-Free Electronic Substrates
    • IPC-4101D: Base Materials for High-Performance Printed Boards
    • RoHS Directive 2011/65/EU

    Typical usage ratio

    • 2–7% by weight in functional monomer feeds (ratio varies based on desired charge mobility and polymer backbone length)

    Downstream process integration

    • Charged during Suzuki, Stille, or amination coupling reactions after monomers pre-purification
    • Processed under rigorously controlled anhydrous and inert atmospheres from 80–130°C
    • Post-reaction, intermediates are directed to vacuum distillation and purity assessment

    Final product types

    • OLED emitter and hole-transporting compounds
    • Specialty organic semiconductors
    • High-performance liquid crystals for advanced displays
    • Optoelectronic device component materials (powders and purified solutions)

    5. Custom Polymer Modifier Synthesis

    Custom polymer and resin formulators incorporate this carboxaldehyde-substituted pyridine as a reactive chain-linking agent or functional group anchor, increasing the rigidity, chemical resistance, or site selectivity of engineering plastics and resins. The aldehyde group provides a reactive handle for condensation or crosslinking, allowing for tailored material properties and niche technical applications in elastomers and advanced adhesives.

    Industry compliance standards

    • ISO 9001:2015 for quality control in polymers
    • REACH Annex XVII (restrictions on monomers and additives)
    • ASTM D256: Impact resistance (relevant for modified plastics)
    • FDA 21 CFR 177.1810 (polymers for indirect food contact, where applicable)

    Typical usage ratio

    • 0.5–3% by weight relative to base polymer (adjusted for molecular weight and degree of modification required)

    Downstream process integration

    • Blended in melt or solvent phase prior to polymerization
    • Incorporated at reactive extrusion step for industrial-scale resin modification
    • Post-addition, undergoes curing or copolymerization with the bulk monomer feed

    Final product types

    • Engineering plastics with enhanced chemical resistance
    • Thermoset resins for electrical insulation
    • High-strength adhesives for automotive applications
    • Special order polymeric coatings for corrosion-prone environments
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    Certification & Compliance
    More Introduction

    2,6-Dichloropyridine-4-Carboxaldehyde: A Reliable Choice for Specialty Synthesis

    Introducing Our Commitment to Purity and Consistency

    Every chemist knows the difference that a high-quality starting material brings to a challenging synthesis. From our position as a direct manufacturer, we pay attention to every stage in the preparation of 2,6-Dichloropyridine-4-Carboxaldehyde. Instead of relying on intermediaries, we manage sourcing, reaction control, and purification ourselves. Each lot receives close monitoring for homogeneity, targeted impurity levels, and verified moisture content. Chemists in agrochemical, pharmaceutical, and functional materials labs have come to rely on this approach because it directly impacts yield and downstream impurity profiles.

    Over the years, we’ve worked side by side with R&D specialists and plant engineers. Their requests often center on three demands: minimal batch-to-batch variation, documented residual solvent data, and compatibility with both pilot and production-scale protocols. Most synthesis routes for 2,6-Dichloropyridine-4-Carboxaldehyde involve chlorination strategies, but small changes in temperature, solvent order, or reaction timing produce significant effects on product color, trace contaminants, and even solubility. Through hands-on optimization and close analytics, our team has narrowed these variations and regularly meets the demanding specifications major firms require.

    Model and Specification Details Shaped by Real-World Needs

    Direct feedback from chemists drives every revision and adjustment in our product spec. A typical 2,6-Dichloropyridine-4-Carboxaldehyde lot reaches >99% purity by HPLC, with clarity in residue profiles and low ppm-level chlorinated impurities. For users who need more granular data, we run supplementary GC-MS analyses and can adapt testing frequency for custom agreements. We never default to generic trace impurity reports. Instead, each certificate reflects real batch data for nitrosamine risk, residual sulfur, and even volatile breakdown products observed during long-term storage.

    Our technical staff avoid the lure of "one size fits all." They focus on solvent residues, particle size distribution, and packaging options because chemists have distinct needs. Some users in the pharmaceutical line value small, amber glass bottles to protect from light-induced breakdown, while pilot plant teams often request drum lots with tamper-evident sealing to reduce cross-contamination. For multi-ton users, reusable stainless containers cut waste and lower total lifecycle cost. The format adapts to the need, but without sacrificing control over critical product properties.

    Comparison with Other Chloropyridine Derivatives

    Within the chloride-substituted pyridine family, 2,6-Dichloropyridine-4-Carboxaldehyde stands out for its balance of reactivity and selectivity. This compound features two electron-withdrawing chloro groups, which limit overreaction in sensitive couplings, and a carboxaldehyde at the para position, giving access to diverse downstream chemistry. Many chemistries turn to more common dichloropyridines or even mono-substituted analogues; these lack the distinctive balance between aromatic stability and functionalization potential that our customers pursue here.

    Other compounds with single substitutions or with chloro groups at the 3 and 5 positions bring different behavior in cross-coupling, condensation, and reductive amination sequences. For example, a 2,3-dichloro substituent profile often activates the ring, making it more susceptible to nucleophilic attack, but this increases risk of side-product formation during scale-up. The 2,6 arrangement, combined with the aldehyde group at the 4 position, offers a favored stability window for reactions demanding high selectivity. These distinctions only become more marked in continuous-flow settings or when raw material costs pressure large-scale processes.

    Understanding Usage in Research and Manufacturing

    For our customers, the real measure of this product lies in its performance during difficult sequence steps. 2,6-Dichloropyridine-4-Carboxaldehyde enters advanced synthetic pathways, often as a core-building block for kinase inhibitors, crop protection agents, and dye intermediates. The molecule's symmetry and electronic effects guide regioselective transformations in heterocycle assembly, while the presence of the aldehyde opens entry points for diverse condensation reactions. Many clients use it to construct fused bicyclic scaffolds, where control over starting material purity and particle behavior matters as much as the stoichiometry.

    Scale-up teams in fine chemicals often point to the reactivity window of our material as a benefit. They’ve reported more predictable reaction profiles compared to older supply batches from the global market's less-regulated streams. The difference emerges at higher substrate concentrations, where sensitive coupling steps can go off path due to hidden residual organics or abnormal distribution of particle size. These process hazards cost weeks in cleaning, de-bottlenecking, and validation time, and our own plant has seen and solved these with careful process engineering at source.

    Practical Challenges, Solutions, and Our Perspective

    Handling a chlorinated heteroaromatic with an aldehyde group poses its own set of problems. Moisture absorption can degrade product and force the formation of trimerized side chains, making storage and shipment especially tricky in high-humidity regions. We solved this through investment in low-moisture packaging, now tracked by batch-specific validation data. Instead of just warning about shelf-life, we deliver lots already validated for two-year stability in sealed form.

    Process engineers need reactivity profiles with fewer unknowns. Stray metallic contaminants from upstream chlorination and workup lines often trigger failed downstream reactions or regulatory flags, risking both safety and IP issues. Our plant reconfigured its column and vessel linings to food-grade standards and overhauled water quench steps, yielding lower trace metal content without need for downstream scavenging.

    Shipping requirements continue to grow, especially for export. We invest annually in hazardous goods compliance, and our team publishes direct shipping guidelines customized for each customer’s receiving and storage constraints. This reduces waste, delay at port, and regulatory snagging at customs inspection, while lowering total land transport cost. Our logistics team has real-world experience managing the paperwork and preparing regulatory files for major markets in East Asia, the US, and Europe, so consignments move with fewer surprises.

    Supporting Research and Large-Scale Operations

    Researchers value predictable performance. They cite batch records, supporting technical data, and traceability as reasons for repeat orders. When critical experiments run on small-scale syntheses, a product grade with consistent properties means fewer failed reactions, improved reproducibility, and expedited scale-up. We’ve contributed technical support to projects moving from milligram screens into pilot reactors, and shared how collectors, driers, and transfer processes need tuning as volumes increase. Several pharma partners describe smoother validation runs and matched impurity profiles when using our lots, outpacing older stocks purchased through indirect traders.

    Industrial plants operating on multi-ton scales raise different priorities. Energy cost, waste minimization, and regulatory compliance dictate much of their purchasing discussion. By refining both our synthesis and purification steps, we've optimized yields and cut hazardous byproduct formation. Less off-gassing in drying, fewer insolubles in reactor transfers, and lower demand for post-process cleanup translates into operational savings downstream. In our own operations, changing temperature profiles and solvent systems reduced both effluent load and batch time, which we share transparently with partners keen to deepen their own process data pool.

    Product Evolution and Working with Chemists

    No chemical manufacturing protocol holds forever, and we keep product evolution close to chemists’ needs. Customer feedback has driven our investments in real-time analytics and greater batch control. In the past, customers flagged abnormal melting points after long-haul shipment or sample exposure. To address this, we built quality checkpoints into every stage, tracking physical properties and monitoring product appearance through storage trials. Any drift outside tight bounds now triggers a process review or, if needed, reprocessing rather than shipment.

    We integrate automation into select parts of our manufacturing to reduce handling error, particularly during hazardous or repeat-sensitivity tasks such as final filtration and packaging. This technological investment pays off: better control over trace contaminant pickup, improved reproducibility, and faster response to custom requests. At the same time, chemists have the freedom to request modifications, whether to meet new trace impurity guidelines, accommodate changes in their downstream chemistry, or enable regulatory clearance for a new drug program.

    Global Supply Security and Reliable Logistics

    Supply disruptions hit hardest when project deadlines draw near. Over decades, we've learned that buffer stocks and deep integration with transport partners make as much difference as chemistry does. While global shipping strains, we keep multiple domestic and foreign warehouses supplied to prevent single-point failure. For critical partners running continuous operations, our team provides direct scheduling for just-in-time replenishments, reducing capital tied up in inventory while keeping line stoppages at bay.

    Customs compliance and documentation complexity require attention to detail and proactive management. Our logistics specialists stay current on global chemical transport regulations and advise on changing documentation standards in destination countries. We've published and updated comprehensive SDS in multiple languages, prepared VOC and REACH dossiers, and accompany shipments with pre-checked technical and hazard documents. This close engagement directly translates into fewer customs delays and safer, more transparent handling at customer sites.

    Environmental Responsibility and Adaptability

    Large-scale chloropyridine production can carry environmental burdens. We actively pursue process efficiencies to lower energy consumption and waste generation. Effluent treatment and solvent recovery facilities at our main site have reduced chemical load to local water supplies, drawing on years of dialogue with our local community and regulatory bodies. Compliance has moved beyond simply meeting emission ceilings; now, we aim to surpass local norms, setting a positive example in the region.

    Waste recycling, especially of solvents and byproducts, reduces our direct environmental impact and provides a cost offset, which we share with large-volume partners through competitive pricing strategies. Green chemistry is moving from concept to necessity, and our leadership continually audits process streams, invests in byproduct valorization, and shares best practices with industry forums. We've shown that supporting sustainability stands as the practical, long-term solution that allows all sides—manufacturer, customer, and neighbor—to benefit.

    Future Directions Shaped by Industry and Science

    As industry demand patterns shift, so do the expectations for raw materials. Our close partnerships with pharmaceutical and agrochemical researchers suggest that new applications for our 2,6-Dichloropyridine-4-Carboxaldehyde are on the way, including in catalytic chemistry and materials science. These users demand tailored impurity profiles, more documentation supporting regulatory submissions, and continuous improvement in product processing. We welcome such challenges and treat direct engagement with users as both opportunity and necessity.

    Process safety receives our ongoing focus, with safety audits not just for compliance but for better response to new hazards from scale-up or evolving technologies. Our manufacturing and technical support teams share incident learnings with partners to help prevent accidents and improve site safety across the sector. This open channel delivers solutions ahead of new regulations rather than reacting after avoidable setbacks.

    The Value of Experience and Hands-On Manufacturing

    Supplying 2,6-Dichloropyridine-4-Carboxaldehyde involves more than just producing and selling a molecule. Every process improvement, technical tweak, and new equipment purchase stems from direct feedback and daily engagement with working chemists. Years of batch records and real-world performance data have shaped our product's journey. We recognize that every lot carries the weight of someone’s experiment, someone’s production schedule, and in the end, someone’s trust.

    Our commitment as a manufacturer goes far beyond cost competition. By driving specification improvements, investing in staff training, and leveraging technology, we maintain control from raw materials to final shipment. As customers blend this compound into more advanced applications, we remain a source of technical insight, stewardship, and innovation. Each new synthetic challenge met with our product strengthens our understanding of its true value in the marketplace of ideas and solutions.