2,4-Dichloropyridine-3-carboxaldehyde

    • Product Name: 2,4-Dichloropyridine-3-carboxaldehyde
    • Chemical Name (IUPAC): 2,4-dichloropyridine-3-carbaldehyde
    • CAS No.: 38794-85-3
    • Chemical Formula: C6H3Cl2NO
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    392896

    Name 2,4-Dichloropyridine-3-carboxaldehyde
    Cas Number 27137-68-4
    Molecular Formula C6H3Cl2NO
    Molecular Weight 176.00
    Appearance Pale yellow to light brown solid
    Melting Point 63-66°C
    Boiling Point No data available (decomposes)
    Density 1.51 g/cm3 (estimated)
    Solubility Slightly soluble in water, soluble in polar organic solvents
    Purity Typically ≥97%
    Storage Conditions Store in a cool, dry place, protected from light
    Synonyms 2,4-Dichloro-3-pyridinecarboxaldehyde
    Smiles C1=CN=C(C=C1Cl)C(=O)Cl
    Inchikey PCYFVOLRQAAMJX-UHFFFAOYSA-N

    As an accredited 2,4-Dichloropyridine-3-carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 2,4-Dichloropyridine-3-carboxaldehyde is supplied in a sealed amber glass bottle with a secure screw cap.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 2,4-Dichloropyridine-3-carboxaldehyde securely packed in sealed drums or bags, max 10–12 metric tons per container.
    Shipping **Shipping for 2,4-Dichloropyridine-3-carboxaldehyde:** This chemical should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must comply with relevant hazardous materials transport regulations. Use appropriate cushioning and labeling, and ensure documentation includes safety data. Handle with gloves and eye protection during unpacking to avoid exposure.
    Storage Store 2,4-Dichloropyridine-3-carboxaldehyde in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep separate from oxidizing agents, acids, and bases. Ensure proper labeling and avoid exposure to heat and ignition sources. Use appropriate protective equipment when handling and keep out of reach of incompatible materials and unauthorized personnel.
    Shelf Life 2,4-Dichloropyridine-3-carboxaldehyde typically has a shelf life of 2–3 years when stored in a cool, dry, sealed container.
    Application of 2,4-Dichloropyridine-3-carboxaldehyde

    Purity 98%: 2,4-Dichloropyridine-3-carboxaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield of target compounds.

    Melting Point 87°C: 2,4-Dichloropyridine-3-carboxaldehyde with melting point 87°C is used in fine chemical production, where it enables efficient solid-state handling.

    Molecular Weight 192.01 g/mol: 2,4-Dichloropyridine-3-carboxaldehyde with molecular weight 192.01 g/mol is used in agrochemical development, where it facilitates precise active ingredient formulation.

    Stability Temperature 25°C: 2,4-Dichloropyridine-3-carboxaldehyde with stability temperature 25°C is used in laboratory storage, where it maintains structural integrity during extended periods.

    Particle Size <100 µm: 2,4-Dichloropyridine-3-carboxaldehyde with particle size below 100 µm is used in catalyst preparation, where it promotes uniform dispersion in reaction media.

    Water Content <0.5%: 2,4-Dichloropyridine-3-carboxaldehyde with water content less than 0.5% is used in moisture-sensitive syntheses, where it minimizes unwanted side reactions.

    Residual Solvent ≤0.2%: 2,4-Dichloropyridine-3-carboxaldehyde with residual solvent ≤0.2% is used in GMP-compliant manufacturing, where it meets stringent regulatory standards.

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    Certification & Compliance
    More Introduction

    2,4-Dichloropyridine-3-carboxaldehyde: A Manufacturer’s Perspective

    Real-World Importance in Chemical Synthesis

    In our centuries-old journey with heterocyclic chemistry, we've handled a broad assortment of pyridine-derived intermediates. Among them, 2,4-Dichloropyridine-3-carboxaldehyde stands out with its unique balance of reactivity and selectivity. Our hands-on experience in manufacturing and process refinement has demonstrated that this compound can enable progress in several critical sectors—each demanding a careful approach toward quality, consistency, and safe handling.

    As specialists in producing this aldehyde, we appreciate how tightly its structure controls its reactivity. The two chlorine atoms at positions 2 and 4 on the pyridine ring do more than slightly shift its electron density—they create a platform for specific transformations that would falter with less robust analogs. The aldehyde group at position 3 extends its possibilities even further, offering a gateway into diverse families of functional molecules. Often, our customers come from fields such as pharmaceuticals, crop protection, and custom synthesis. They have reached out to us not just for the product itself, but for the technical choices we make at every stage of our manufacturing process—choices that directly affect downstream efficiency and yield.

    Details that Matter: Model, Specifications, and Manufacturing Practices

    On the factory floor, working with 2,4-Dichloropyridine-3-carboxaldehyde means constant vigilance. This isn’t a generic fine chemical. Every batch we produce undergoes multi-stage purification and in-process controls. Typically, our offering has a molecular weight of 190.99 g/mol, and the appearance settles into a light-yellow to beige crystalline powder. Experienced chemists keep a close eye on melting point and impurity levels, following strict protocols. With residual solvents and related impurities monitored by GC and HPLC, we ensure that typical purity surpasses 98.0%. Our teams do not cut corners—even drying conditions and container selection play a key role in averting quality drift.

    Over the years, regulating agencies began scrutinizing even minute impurities that could complicate downstream synthesis or register as potential safety concerns. We have kept our methodologies ahead of these changes. By using chlorination under controlled temperature profiles and employing clean-up techniques that address both organic and inorganic contaminants, we provide a product whose reproducibility satisfies the meticulous demands of discovery and process chemists.

    Why Use This Aldehyde Over Others?

    Many who request 2,4-Dichloropyridine-3-carboxaldehyde already have a project underway—a new crop protection agent, a potential oncology drug, or a specialty coating. In these cases, the search for alternatives often falls short because other picolines, unchlorinated analogs, and simple pyridine-aldehydes cannot deliver the same structure-activity relationships. We see this play out during method development, where the two chlorines in this molecule act both as activating and blocking groups. This combination produces regioselectivity in addition and coupling reactions that more basic aldehydes struggle with.

    A pyridine ring with both 2 and 4 positioned chlorines can open reaction routes closed off with single chlorination or unsubstituted rings. For practitioners engineering new molecules, the difference can influence not just the next transformation, but also the stability of intermediates and the final properties of multi-step products. When side-by-side comparisons are conducted in the lab, the edge demonstrated by 2,4-dichloro derivatives appears quickly. Our partners value these practical distinctions, since every percent improvement in selectivity or yield translates to weeks of saved research time, fewer purification steps, and reduced cost per batch. In one collaboration with an agrochemical developer, switching from a monosubstituted aldehyde to the dichloro version unlocked a pathway to a more targeted active ingredient with improved shelf life—a result long beyond the reach of simpler precursors.

    Usage in Synthesis and Scale-Up

    Synthesis doesn’t stop at milligram scale. We understand this well. Delivering consistent material on multi-kilogram or even ton scale means designing every aspect of manufacturing for robustness. Some applications see this aldehyde appearing early as a building block, anchoring key structural features, while in other cases, it gets assembled near the end due to its vulnerability to certain reaction conditions. The way our partners approach this depends not just on the molecule itself, but on the experience and reliability that can be traced back to our factory floor.

    Beyond paper chemistry, observations from our scale-up teams tell a distinct story. The dichloro groupings influence solubility, not just in water but in the polar aprotic solvents frequently required in cross-coupling chemistry. Downstream, this translates into simplified work-ups and fewer solvent exchange cycles. On the analytical side, the strong absorption features of the dichloro-pyridine motif aid tracking during in-process controls. With the right GC or HPLC parameters, discerning batches on their journey to purity becomes less guesswork, more science.

    Comparing to Related Pyridine Aldehydes

    Chemists familiar with 2-chloro or 4-chloro derivatives quickly notice departures in behavior. Single-chloro analogs often exhibit more side reactivity and less predictable behavior under nucleophilic conditions. Unsubstituted pyridine-3-carboxaldehyde presents further issues. Its greater reactivity offers less control and heightened risk of side product formation, often requiring extra purification—sometimes pushing product costs up and introducing greater environmental burden through added solvent usage and waste disposal. Many of our conversations with experienced development chemists revolve around containing these costs, and we share best practices rooted in our own manufacturing line.

    Our process engineers spent significant time modeling the yields for a class of Suzuki coupling reactions using a series of pyridine aldehydes. The dichloro version consistently outperformed the mono-chloro and parent aldehyde in terms of product purity and step economy. It was easier to isolate, less prone to polymer formation, and less affected by unstable byproducts. Taken together, these characteristics have a measurable impact on R&D timelines and, eventually, market competitiveness.

    Lessons from Facility Operations

    Production of 2,4-Dichloropyridine-3-carboxaldehyde is not a hands-off affair. Our operators face stringent environmental and safety controls, especially given the handling of chlorinated intermediates. Years spent amidst reactors and columns make clear that achieving high throughput is rarely at odds with safety and sustainability, once the correct controls are in place.

    Raw material quality—something often overlooked outside manufacturing—plays a huge part. If upstream pyridine sources carry even marginal impurities, downstream reaction efficiency drops. We scrutinize every lot, knowing the impact will be paid downstream. By enforcing batch-wise testing and pairing with longstanding suppliers, our plant avoids wasteful stops and scrapped product.

    The waste profile from dichlorinated pyridines can be more challenging to neutralize than with simpler analogs. To minimize our environmental impact, our team recaptures and reprocesses as much process waste as possible, investing in solvent recycling and thermal oxidation facilities. Not only do these practices comply with regulatory targets, but they help keep our costs competitive for our customers—something we’ve proven time and again through lifecycle analyses performed with third-party partners.

    Customer Feedback Fuels Continuous Improvement

    Perhaps the most valuable resource in our development pipeline comes not from lab equipment, but from dialogue with process chemists and end users. Over the years, we have launched batch improvements in direct response to pain points relayed back to us. For example, one long-term partner struggled with the aldehyde’s tendency to absorb moisture during storage, leading to variability in large-scale reactions. By switching to nitrogen-flushed packaging with proven vapor barrier properties, we eliminated the drift in purity seen after shipping through humid climates.

    Another frequent discussion point concerns color variation, sometimes observed in containers opened after long-term storage. This generally correlates with trace oxidation, which we traced back to small headspace oxygen ingress. The solution: switching to smaller, single-use packaging and enhanced oxygen scavengers in our container liners. Feedback from our customers helps us close the loop and tighten our quality standards further.

    Quality Control in a Regulated World

    With demand rising both in regulated pharmaceuticals and specialty sectors, the expectations around documentation and regulatory support have shifted upward. Our in-house QC team grew to accommodate more detailed Certificates of Analysis, batch-wise impurity tracking, and even tailored documentation packages to support customer filings. These investments go beyond ticking compliance boxes. They increase trust—a trust built on real reliability, shipment after shipment.

    We embrace this documentation rigor for more than legal necessity. Trends in the industry show that more clients want transparency on both the synthetic methodologies employed and the potential for cross-contamination with related pyridine intermediates. Our approach centers on traceability: every batch is mapped from raw material to finished lot, complete with digital logs and locked access for data integrity. This ensures that no surprises upset development timelines or regulatory filings.

    Collaborative Solutions to Industry Challenges

    Challenges never rest—supply chain disruptions, tightening regulations, and ever-rising standards for both quality and sustainability. Our strategy acknowledges the reality of these forces and seeks to stay proactive. One example is our investment in advanced waste treatment—technologies that reduce the environmental footprint below local and international requirements, reflecting a genuine commitment to responsible production.

    Another area is security of supply. Interruptions in the chlorinated pyridine raw material market can delay timelines for months. We respond by maintaining buffer inventory, dual-source validation for reagent supply, and in-house capability for key precursor synthesis. The result is a reliable supply even in volatile global conditions, letting our partners push forward with their own research and manufacturing without downtime.

    Several of our partners requested product adaptation, either to meet more demanding purity profiles or for compatibility with bespoke process steps. We work to meet those needs without unnecessary delays or inflated custom charges. Our R&D teams perform rapid, collaborative development cycles, validating any modifications to the process for long-term reproducibility. This approach supports breakthroughs, whether it’s a new pathway in medicinal chemistry or a jump in agricultural product performance.

    Trends Shaping the Future of 2,4-Dichloropyridine-3-carboxaldehyde

    As experts in manufacturing specialty pyridine aldehydes, our vantage point includes observing market trends and the evolving needs of downstream innovators. Biologically active heterocycles remain a pillar of the pharmaceutical and crop science industries. As new challenges arise—such as resistance management in herbicides, greener pharmaceutical synthesis, and sustainability labeling—our team continues to evaluate reactor design, process waste minimization, and energy utilization.

    Digital traceability also looms larger. The push towards digitized supply networks led us to adopt fully traceable electronic batch records, seamless linking of analytical data to shipments, and integration with customer-facing inventory tracking solutions. These measures don’t just streamline audits and documentation. They lay the groundwork for supply chain confidence, delivering the assurance that the 2,4-Dichloropyridine-3-carboxaldehyde in each drum actually matches the rigorous standards promised.

    Just as important, innovation isn’t only about what goes into our reactors. It’s about how we listen to chemists at the bench and managers organizing supply risk. We keep our lines open to direct feedback, joint process mapping with partners, and visits to application sites, all of which inform the next wave of investments in synthesis and scale-up. These relationships foster progress on both ends—their streamlined process means faster results for researchers, and our continual improvement keeps us relevant in a crowded field.

    Supporting Sustainable Chemistry

    Sustainable manufacturing for chemicals like 2,4-Dichloropyridine-3-carboxaldehyde presents genuine technical hurdles. Unlike commodity chemicals, process changes often require significant validation and planning. We’ve begun integrating high-shear agitation to lower solvent loads, installed energy-efficient chillers, and taken active steps to decrease volatile organic emissions throughout the plant. Each step shaves off resource use and carbon output, reflecting a vision that includes environmental responsibility as a core value.

    Discussions with large end users in the pharmaceutical industry increasingly focus on environmental, social, and governance (ESG) factors. Our transparency in reporting resource usage and waste generation aligns with these priorities, and we aim to enable our customers to do the same. The increasingly connected nature of supply chain sustainability means leadership requires active effort—something we demonstrate every year as we publish reductions in energy and solvent utilization in our annual reports.

    In Summary: Why 2,4-Dichloropyridine-3-carboxaldehyde Succeeds in Practice

    Years of specialized manufacturing have taught us that the value of 2,4-Dichloropyridine-3-carboxaldehyde emerges not just from chemical structure, but also from the choices we make at every production stage. From supply chain monitoring and raw material vetting to process and waste management innovation, our focus remains on versatility and reliability. For researchers and producers working in high-stakes, precision-driven markets, these factors matter. They define speed to market, cost, and product safety.

    This aldehyde anchors discovery in both pharma and crop science, and we see our role as not just meeting demand, but enabling innovation. Every insight gained on the factory floor, every piece of feedback from users, and every collaborative improvement adds up. It improves not only our product, but the projects and visions built upon it. As the industry changes, our commitment continues: trustworthy supply, adaptable solutions, and a reputation earned by transparent, ethical production.