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2,6-Dichloropyridine-4-Carbonyl Chloride

    • Product Name 2,6-Dichloropyridine-4-Carbonyl Chloride
    • Alias 2,6-Dichloroisonicotinoyl chloride
    • Einecs 254-511-3
    • 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
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    Specifications

    HS Code

    714241

    Product Name 2,6-Dichloropyridine-4-Carbonyl Chloride
    Cas Number 635-23-4
    Molecular Formula C6H2Cl3NO
    Molecular Weight 210.45 g/mol
    Appearance White to off-white solid
    Melting Point 60-63 °C
    Density 1.72 g/cm³ (estimated)
    Solubility Reacts with water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CC(=NC(=C1Cl)C(=O)Cl)Cl
    Inchi InChI=1S/C6H2Cl3NO/c7-3-1-4(8)10-6(2-3)5(9)11/h1-2H

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

    Packing & Storage
    Packing The 25g of 2,6-Dichloropyridine-4-Carbonyl Chloride is securely packaged in a sealed amber glass bottle with safety labeling.
    Shipping 2,6-Dichloropyridine-4-Carbonyl Chloride is shipped in tightly sealed containers under cold and dry conditions. It should be handled as a hazardous material, with appropriate hazard labeling and documentation. Transportation must comply with local, national, and international regulations for corrosive, toxic chemicals to ensure safe and compliant delivery.
    Storage 2,6-Dichloropyridine-4-carbonyl chloride should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong bases and oxidizers. The container must be tightly closed and clearly labeled, made from material resistant to corrosive chemicals. Use secondary containment to prevent spills and ensure the storage area is equipped for handling hazardous chemicals.
    Application of 2,6-Dichloropyridine-4-Carbonyl Chloride

    Applications of 2,6-Dichloropyridine-4-Carbonyl Chloride in Industrial Manufacturing

    2,6-Dichloropyridine-4-carbonyl chloride serves as a critical intermediate in complex organic synthesis for diversified downstream sectors. Our direct manufacturing experience has revealed its widespread use in regulated industries requiring stringent compliance, defined process controls, and precise formulation practices. The following sections outline detailed application scenarios, including standards, dosage guidance, integration points, and the main classes of finished products realized by end-users of this intermediate.

    1. Pharmaceutical API Synthesis (Pyridine-bearing Compounds)

    In the pharmaceutical sector, many drug manufacturers incorporate this raw material as an acylating agent for producing active pharmaceutical ingredients (APIs) involving substituted pyridine frameworks. Our facility supplies multi-ton quantities to GMP-compliant API plants using batch or continuous synthesis routes, particularly in the manufacture of targeted anticancer, anti-inflammatory, and anti-infective molecules containing halogenated pyridinyl moieties.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Directive 2003/94/EC and PIC/S GMP PE009 guidelines
    • USP/NF, Ph. Eur., and JP pharmacopoeia reference monographs (as applicable to downstream APIs)
    • US FDA 21 CFR 211: Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • 0.85–1.10 mol per mol of amine or alcohol functional group in the coupling reaction; can be adjusted to 1.15 mol to drive specific amidation/acylation steps where excess reagent improves conversion efficiency.

    Downstream process integration

    • Charged during acylation or condensation step following initial pyridine skeleton assembly; typically dissolved in high-purity acetonitrile or DMF under inert atmosphere, monitored by HPLC for endpoint determination; spent reagent is neutralized post-reaction prior to workup.

    Final product types

    • Oral and parenteral APIs featuring dichloropyridinyl structures (e.g., novel kinase inhibitors, third-generation cephalosporins, anti-tubercular compounds)
    • Regulatory starting materials for multi-step small-molecule therapeutics

    2. Agrochemical Active Ingredient Manufacturing

    Leading crop protection chemical firms rely on this raw material as a coupling agent to construct substituted pyridine motifs found in herbicides and systemic insecticides. Industrial-scale syntheses benefit from its reactivity profile in the preparation of advanced intermediates and target compounds used in pest management, requiring adherence to strict chemical quality, purity, and impurity profile specifications.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • REACH Regulation (EC) No 1907/2006 (for use in EU markets)
    • ISO 9001:2015 Quality Management Systems as required for agrochemical supply chains
    • EPA FIFRA Guidelines (for US market registration of actives)

    Typical usage ratio

    • 0.90–1.25 mol per mol of nucleophile substrate (based on scale and excess management); increased excess (up to 1.30) applied in flow systems to maximize yield in persistent side-reactions.

    Downstream process integration

    • Added in closed-system reactors during chlorination or condensation process after formation of core structure; precise addition monitored via in-line FTIR or GC assay to reduce formation of unwanted side-products; process validated by scale-up trials before commercial batch production.

    Final product types

    • Systemic herbicides and insecticides containing 2,6-dichloropyridinyl moieties (e.g., pyridinecarboxamide derivatives)
    • Concentrated wettable powder and emulsifiable concentrate agrochemical formulations for field application

    3. Specialty Polymer and Resin Synthesis

    Advanced material manufacturers utilize this compound as a monomer building block in producing high-performance engineering resins or specialty polyamides that exhibit enhanced thermal stability and chemical resistance. The selectivity and reactivity allow incorporation into polymer matrices where precise molecular control is paramount, especially in electronic, automotive, and membrane applications.

    Industry compliance standards

    • ISO 9001:2015 for polymer and resin production quality management
    • RoHS Directive 2011/65/EU (as regards restricted substances in electronics)
    • ASTM D256 and D638 for end-use mechanical and thermal property validation
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), EC No 1907/2006

    Typical usage ratio

    • 10–23 wt% relative to total monomer content, depending on targeted molecular weight and required performance properties; ratios fine-tuned by viscosity, chain extension, and end-group analysis.

    Downstream process integration

    • Introduced in step-growth polymerization reactors during the condensation of diamines and diacyl chlorides; intermediate purification steps maintain end-capping integrity; monitored by GPC and FTIR for chain length and structural incorporation.

    Final product types

    • High-performance specialty polyamides and resins for automotive electronics housings, sensor encapsulation, and membrane filtration elements
    • Polymeric intermediates for further composite material integration

    4. Chemical Intermediate for Advanced Dyes and Pigment Synthesis

    Leading colorant producers apply this compound as an acyl chloride intermediate in synthesizing complex pyridine-based chromophores and specialty pigments used for technical textiles, plastics, and specialty coatings. Its integration enables introduction of unique electron withdrawing groups, enhancing finished pigment stability and solubility for demanding end-use environments.

    Industry compliance standards

    • Oeko-Tex Standard 100 (for textile dye safety, where relevant)
    • ISO 9001:2015 for dye and pigment production
    • Registration under EU REACH (EC No 1907/2006) for dyestuff intermediates
    • DIN EN 12880/12881 for pigment and dye extractables and leachables (as required by some customers)

    Typical usage ratio

    • 5–17 wt% relative to the principal dye intermediate; adjustments made depending on bath formulation and dye purity needs.

    Downstream process integration

    • Added during acylation steps in multi-stage dye intermediate synthesis; usually introduced after initial condensation of aromatic precursors; monitored by TLC or HPLC to confirm complete conversion before isolation and purification.

    Final product types

    • Technical textile dyes and pigments with pyridine modifications for improved light and wash fastness
    • Pigment dispersions and masterbatches for high-performance plastics and coatings

    5. Intermediate for Electronic and Photoactive Materials

    Manufacturers in the electronics and photonics sectors integrate this raw material in the synthesis of photoactive compounds and functionalized pyridine derivatives for use in OLED, photovoltaic, and display panel components. Its high purity and narrow impurity profile enable predictable reactivity for critical optoelectronic precursors, supporting fabrication of next-generation devices.

    Industry compliance standards

    • IPC-4101 for base materials used in printed circuit boards
    • ISO 14001:2015 Environmental Management (for photonic/electronic chemical production sites)
    • RoHS 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • REACH EC No 1907/2006 (for commercialization of photoactive intermediates)

    Typical usage ratio

    • 2–9 mol% relative to core aromatic or heteroaromatic backbone, based on photophysical design and required quantum efficiency; strict control exercised during formulation trials.

    Downstream process integration

    • Fed into etherification or acylation stages during the synthesis of electron-transporting molecules; tightly controlled via microreactor or pilot loop to ensure batch-to-batch reproducibility; product QC confirmed by NMR and mass spectrometry.

    Final product types

    • Electron transport materials and hole-injection layers for OLED/PLED displays
    • Sensitizers and acceptors in dye-sensitized or organic solar cells
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    Certification & Compliance
    More Introduction

    Introducing 2,6-Dichloropyridine-4-Carbonyl Chloride: A Perspective from the Manufacturer’s Plant Floor

    Direct Insights into Production, Use, and Differentiation

    From the moment the raw pyridine starts its transformation beneath the lights of our chemical plant, 2,6-Dichloropyridine-4-Carbonyl Chloride stands out as one of the more challenging and valuable intermediates we produce. Our team always treats compounds like this with a blend of respect and precision—experience teaches that exact handling and a strict attention to process detail mean everything when you chase purity at scale.

    We synthesize 2,6-Dichloropyridine-4-Carbonyl Chloride from dichlorinated pyridine, following a multi-stage pathway involving chlorination and acyl chloride formation. Maintaining stringent exclusion of moisture, and carefully controlling temperature and reagent addition rate, we avoid forming byproducts. The result is a product with a clear yellow crystalline appearance, known among our technicians for its distinct, slightly pungent odor and its reactivity under controlled handling. After filtration and distillation, we test every batch for purity by HPLC and GC. Over the years, our team’s experience helps us reliably keep impurities below 0.5%, with custom tuning available for more demanding synthesis routes.

    Model, Specifications, Physical Aspects

    Our most requested model typically offers a purity above 99%, with particle sizes optimized for ease of transfer in both batch and continuous synthesis setups. The melting point falls between 65 and 68°C—this range tells a lot to those working in custom fine chemical synthesis, hinting at both grain quality and integrity through transport. Moisture content remains low by drying under vacuum, usually well below 0.2%, which directly helps minimize hydrolysis risks at downstream reactors.

    The compound’s molecular structure—pyridine ring with chlorines at positions 2 and 6, and the reactive carbonyl chloride group at position 4—confers significant reactivity. Early in our manufacturing career, it became obvious that even slight deviations in ring chlorination or side-chain formation lead to pronounced changes in both processability and compatibility with downstream reactions. Consistent care at each step gives our carbonyl chloride a sharper performance edge compared to those blended outside of a controlled, single-source facility. Our dedicated clamping and venting lines, alongside monitored small-scale reactors for each lot, minimize the contamination risks that sometime crop up in less vigilant settings.

    Direct Uses in the Field—What We’ve Seen Work

    This compound rarely leaves our facility for a simple or low-value function. Its main life unfolds as a central intermediate in the synthesis of pharmaceutical building blocks, especially those needing precise activation at the pyridine core. One of our product’s strongest points is its ability to serve as a highly selective acylating or chlorinating agent, latching onto amines or alcohols where conventional acyl chlorides bring too much collateral reactivity. Chemists at several of our longtime client firms have praised its performance when constructing heterocyclic scaffolds for active pharmaceutical ingredients, often describing how its distinct chemical backbone allows for a clean coupling—a crucial attribute in large-scale active substance preparations, where purity means both efficacy and regulatory compliance.

    In the agrochemical sector, manufacturers often favor our version for introducing a pyridine scaffold into new crop protection molecules. It proves itself during the stepwise attachment of complex substituents—yielding higher final product mass with fewer purification cycles. We’ve seen companies working in dye and specialty polymer synthesis harness this product’s robustness and stability when applied to activating hard-to-derivatize aromatic systems.

    Many production teams we supply report that the finer grain and greater homogeneity of our crystalline material supports seamless charging into automated reactors and metering systems. Early in our process improvement efforts, our technical staff switched drying and packaging protocols to minimize fines and dust generation, which pays off particularly in closed-system transfers. That kind of operational reliability often dictates whether or not a kilo-lab or full-scale plant can keep pace with product launches or scale-ups—based on feedback from teams running everything from benchtop trials to multi-ton reactors.

    Direct Comparisons—Our Product Versus Alternatives

    Over years of manufacturing, we’ve regularly benchmarked our 2,6-Dichloropyridine-4-Carbonyl Chloride against both imported and domestic alternatives. A core difference lies in the control we exert over chlorination degree and side-product suppression. Slight excesses of other chlorinated pyridine isomers, especially 2,4- or 3,5-substituted forms, often slip into third-party batches, and those isomers tend to introduce significant process headaches downstream—incompatible reactivity, unexpected off-colors, difficulties in analytical separation of target molecules. Because our plant manages both the chlorinated pyridine and carbonylation steps under one roof, we close off nearly all possibilities for cross-contamination, delivering single-isomer, high-purity lots batch after batch.

    Competitors who cannot guarantee single-source origin sometimes end up blending batches from a mix of reactors or even different facilities, chasing inventory targets rather than chemical integrity. To a procurement officer, the price tag might look attractive for a short while, but we regularly hear from frustrated chemists and plant technical managers who’ve spent days troubleshooting unexpected gelation, filtration clogs, or loss of yield—costs that can far outweigh a price difference measured in cents per gram.

    On another front, particle size uniformity, moisture content, and the ability to offer custom packing matter a great deal in practice. From years of listening to customers and watching the changes that ripple through global chemical supply chains, our team learned that a poorly blended batch can create persistent flow issues, with fines gumming up pneumatic transfer lines or larger chunks requiring manual intervention. Because we manufacture and package everything under strict climate control, the risk of variable particle size or lump formation drops to near zero.

    Addressing Common Production Challenges

    Producing 2,6-Dichloropyridine-4-Carbonyl Chloride at scale has its share of operational hurdles—ones that often separate seasoned manufacturers from opportunistic resellers. Maintaining high purity through multiple chlorination and substitution steps requires both proven reaction designs and real-time monitoring. Minor process drifts can lead to heavier halogenation or the birth of structurally similar impurities that can escape coarse analytical screens. Investing in robust in-line monitoring, and training operators to look for subtle color or odor changes—these simple insights, taken from years of “plant-floor living,” play the biggest factor in keeping our chemical clean and consistent.

    Moisture is the enemy of any acid chloride. We run all post-reaction handling, drying, and packing in a dedicated dry room equipped with continuous humidity monitoring. Years ago, we learned that even a few extra minutes exposed to humid air can turn high-value acid chloride into a sticky, hydrolyzed mess—resulting in dangerous venting and, worse, unworkable product down the line. So, airtight drums, heavy-gauge lined bags, and “just-in-time” filling procedures now come standard in our shop, not merely as a box to check but as the product of hard field lessons.

    Transportation also plays a crucial, often undervalued role. Recrystallized product can cake or degrade in standard containers. We specify temperature- and moisture-stabilized transit for longer journeys and regularly ship out cold packs or anti-static liners for batches headed to high-humidity regions. We’ve seen this investment pay off especially well for customers with long, cross-ocean supply chains. Their feedback always highlights the clear reduction in handling trouble and station downtime compared with lower-tier suppliers.

    A final word about regulatory and safety considerations—genuine chemical manufacturers live with these every day. As a chlorinated pyridine derivative, this product falls into several restricted shipping classes under international dangerous goods codes. Every member of our logistics team undergoes regular training, and all labeling meets the specific requirements for both export and domestic shipments. Not all suppliers invest here, but cutting corners can mean delays, legally forced returns, or, in some cases, damaged freight. We’ve worked closely with both government inspectors and third-party auditors to streamline this process, giving customers fewer headaches and smoother compliance reporting.

    The Human Factor Behind the Production Line

    Our tenured plant operators and synthesis chemists make all the difference in the successful manufacturing of sophisticated intermediates like 2,6-Dichloropyridine-4-Carbonyl Chloride. Many have spent decades learning the sensory cues of a stable batch—watching the color transition of crude mother liquors, listening to the sizzle as the carbonyl is introduced, and smelling for that faint, sharp note that signals the reaction has progressed. This collective knowledge, built through both training and long hours spent next to the reactors, guides us every day.

    We keep communication lines wide open between quality assurance, production, and shipping. If a batch deviates from standard specifications—even by a fraction—everyone in the loop gets an immediate update. This multidisciplinary approach, rooted in genuine teamwork, does more for traceability and real-time decision-making than any automated system on its own. Our customers often remark on the level of transparency and detail in our COA paperwork and batch documentation.

    Feedback from Downstream Users

    Some of the best improvements we’ve made over the years stem directly from close conversations with chemists and production managers who use our acid chlorides. Early on, one large pharmaceutical customer documented reduced crystallizer fouling and faster downstream purifications thanks to the consistent purity of our batch. Their technical feedback led us to invest in a better final-filtration system and adopt a slightly tighter exclusion window on minor impurities, a change that has since become a key selling point.

    Similarly, agrochemical clients reported that denser, more uniform batches reduced the time staff spent loading and charging material, especially when running semi-automated pilot units. Their observations helped drive our shift to high-integrity inner bags and low-static liners, reducing both waste and technician exposure. In a field like fine chemicals, customer-led tweaks mean everything—the supplier-client relationship is more like a partnership than a spot-market transaction.

    Environmental Considerations

    Making chlorinated intermediates such as 2,6-Dichloropyridine-4-Carbonyl Chloride requires attention to environmental controls—something we never downplay while developing or scaling up a process. The chlorination steps generate hydrochloric acid off-gas and, on occasion, minor chlorinated organic waste. Our facility operates dedicated scrubber systems and batch-level containment to capture and neutralize emissions. Regular wastewater monitoring and investment in solvent recovery units also help reduce both environmental impact and operating costs.

    We constantly push for greener process improvements, including aligning solvent systems with best-available chemistry and exploring in-process recycling for wash solvents and byproducts. Adopting these approaches reduces both waste treatment loads and external costs for users looking to satisfy their own “green chemistry” mandates. Chemical manufacturing, in practice, always balances process yield, batch turnaround, and environmental stewardship. Teams that ignore one for the sake of the other rarely last; years in the trade have proven this point to us beyond doubt.

    Supply Chain Resilience and Reliability from the Manufacturer’s View

    The global fine chemicals market moves quickly, and keeping product available through shifting demand, shipping challenges, and regulatory changes draws directly on our long-term plant management expertise. Unlike trading houses, as the direct source, we carry both raw material inventory and finished lots, so customers rarely experience gaps. If a global event creates raw material shortages, we can reschedule production runs and adjust operational focus, coordinating directly with plant teams instead of relaying messages through layers of intermediaries.

    Over the past regulatory cycles, some traditional feedstock sources have fluctuated in quality or reliability. Our solution has been to work only with vetted suppliers, audit them personally, and keep a network of backup options for every single critical raw component. This redundancy sometimes costs more up front, but experience shows it’s the only way to guarantee smooth, uninterrupted delivery—especially for high-stakes projects in pharma or crop protection where missing a timeline means much more than inconvenience.

    Every day, our production and quality teams review batch histories, customer feedback, and global supply signals. We’ve found that this direct, “boots-on-the-ground” approach builds far more confidence among major users than glossy brochures or sales promises ever could.

    Summary of Key Differentiators

    Ultimately, the real distinctions with our 2,6-Dichloropyridine-4-Carbonyl Chloride come from a combination of disciplined process control, plant-scale integration, and a commitment to end-user realties. Hands-on manufacturing control, from in-house synthesis of dichloropyridine through to carbonylation and final packaging, lets us keep both purity and performance at a level hard to match for loosely coordinated suppliers or cross-blended material.

    From raw material intake to the last packed drum, we focus on detail and direct communication—between our own teams, with our customers, and with the regulators who oversee the industry. This constant, iterative feedback cycle means that we possess both the technical know-how and the operational agility to keep product flowing and standards high.

    In chemical manufacturing, talk is cheap—only consistent performance and integrity over years build trust. Our commitment shows itself batch after batch, not just in technical numbers but in the real-world results reported back by those who rely on our products to keep their own operations running. This is what sets true manufacturers apart in a market crowded with short-term players and middlemen.