2,4-dichloropyridine-3-carbaldehyde

    • Product Name: 2,4-dichloropyridine-3-carbaldehyde
    • Chemical Name (IUPAC): 2,4-dichloropyridine-3-carbaldehyde
    • CAS No.: 79473-92-6
    • Chemical Formula: C6H3Cl2NO
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    821519

    Chemicalname 2,4-dichloropyridine-3-carbaldehyde
    Molecularformula C6H3Cl2NO
    Molecularweight 176.00 g/mol
    Casnumber 119711-68-3
    Appearance Light yellow crystalline powder
    Meltingpoint 49-52 °C
    Density 1.48 g/cm3 (approximate)
    Solubility Slightly soluble in water; soluble in organic solvents such as DMSO, methanol
    Purity Typically ≥98%
    Storageconditions Store in a cool, dry place, tightly closed container
    Smiles C1=CN=C(C(=C1Cl)C=O)Cl
    Inchi InChI=1S/C6H3Cl2NO/c7-5-1-4(3-10)6(8)9-2-5/h1-3H

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, tightly sealed with a screw cap, labeled with chemical name, formula, hazard symbols, and handling instructions.
    Container Loading (20′ FCL) 20′ FCL container loads approximately 12 metric tons of 2,4-dichloropyridine-3-carbaldehyde, packed in 25 kg fiber drums or bags.
    Shipping 2,4-Dichloropyridine-3-carbaldehyde should be shipped in tightly sealed containers to prevent leakage, with proper labeling as a hazardous chemical. It must be packaged according to local and international regulations, including protection from moisture and incompatible substances. Ensure transport by qualified carriers with documentation, and compliance with UN, IATA, or DOT guidelines.
    Storage 2,4-Dichloropyridine-3-carbaldehyde should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers. Keep the container in a cool, dry, and well-ventilated area, ideally in a dedicated chemical storage cabinet. Ensure it is clearly labeled and handled only by trained personnel using appropriate personal protective equipment.
    Shelf Life Shelf Life: 2,4-Dichloropyridine-3-carbaldehyde is stable for at least 2 years if stored in a cool, dry, sealed container.
    Application of 2,4-dichloropyridine-3-carbaldehyde

    Purity 99%: 2,4-dichloropyridine-3-carbaldehyde with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal byproduct formation.

    Melting Point 92°C: 2,4-dichloropyridine-3-carbaldehyde with melting point 92°C is used in heterocyclic compound preparation, where predictable phase transition facilitates controlled reactions.

    Molecular Weight 176.0 g/mol: 2,4-dichloropyridine-3-carbaldehyde with molecular weight 176.0 g/mol is used in agrochemical research, where precise formulation supports consistent experimental results.

    Moisture Content <0.5%: 2,4-dichloropyridine-3-carbaldehyde with moisture content below 0.5% is used in fine chemical processes, where low water content avoids hydrolysis and degradation.

    Flash Point 110°C: 2,4-dichloropyridine-3-carbaldehyde with flash point 110°C is used in specialty chemical manufacturing, where safe handling conditions are maintained during processing.

    Stability Temperature up to 60°C: 2,4-dichloropyridine-3-carbaldehyde with stability temperature up to 60°C is used in controlled storage environments, where product decomposition is minimized.

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    Certification & Compliance
    More Introduction

    2,4-Dichloropyridine-3-carbaldehyde: Experience, Reliability, and Performance in Every Batch

    A Substance with a Specialized Purpose

    Day in and day out, our workshops handle the production of 2,4-dichloropyridine-3-carbaldehyde with a clear understanding of its critical function across diverse chemical industries. In over ten years of continuous manufacture, we've learned this molecule isn’t the sort of building block that gets much front-page attention. Instead, it quietly shapes the backbone of advanced syntheses in pharmaceuticals, crop protection, and specialty materials. Our perspective comes from close proximity to the process floor, not from boardrooms or third-party market chatter. Factory hands, lab supervisors, and QC specialists know its value follows directly from how it’s produced, cleaned, handled, and packaged.

    What Sets This Molecule Apart

    Our factories have processed a range of pyridine derivatives, each with their quirks. The aldehyde function at the 3-position on the 2,4-dichloropyridine ring magnifies reactivity and makes it a preferred option in designing new heterocyclic scaffolds. Most typical chloropyridines carry substitutions that only affect where they bolt onto a molecular framework. By introducing the carbaldehyde group, this product allows chemists a direct handle for condensation, nucleophilic addition, or cyclization. The result is a path to compounds that simpler dichloropyridines cannot yield, including intermediates vital to research and active pharmaceutical ingredients.

    Over the years, we’ve manufactured and shipped many tons of standard 2,4-dichloropyridine and 3,5-dichloropyridine. The inclusion of the carbaldehyde group at the 3-position creates a difference that’s hard to spot by eye but makes all the difference in a chemist’s hands. Other related substances, like 2,6-dichloropyridine or plain 2,4-dichloropyridine, may serve well for halogen exchange, cross-coupling, or substitution work. Still, they lack the functional group reactivity needed for condensation reactions or for building specialized rings. That difference lets this particular aldehyde deliver what the others cannot: versatility in formulating more complex molecules.

    Consistency and Traceability in Production

    Within our facilities, purity targets don’t just exist on paperwork; they’re hard-won through precise orchestration. Consistent yields and reproducibility set apart a reputable chemical manufacturer. We pursue purity levels above 98 percent—measured using both gas chromatography and NMR—because even small amounts of unreacted pyridines, chlorinated byproducts, or oxidized aldehydes will compromise downstream syntheses. The aldehyde group brings distinct sensitivity; it can undergo reactions with ambient oxygen, trace amines, and even basic silica. These risks shine a spotlight on raw material control and equipment cleaning. One unnoticed contaminant, and the downstream implications can echo across an entire production run.

    Our teams have learned not to cut corners on nitrogen blanketing through transfer, storage, and packaging pipelines. Aldehydes, especially those set into dichloropyridine backbones, don’t tolerate exposure as stoically as other intermediates. During the years when we piloted our synthesis method, we moved from open glass-lined kettles to closed reactors and monitored headspace chemistry with greater vigilance. Each improvement tightened our control over byproducts and water content. No two lots ever come out identical, but experience tells us which process points to watch closely. We calibrate every vessel and recirculate solvents multiple times before introducing critical raw materials. Our customers—often research divisions for major pharmaceutical firms—demand traceable batch records. They rely on the assurance that impurity profiles remain both predictable and minimal.

    Specifications: Experience as a Guide

    Lab protocols can read like checklists, but on the factory floor, every parameter connects to months or years of observation. For this aldehyde, our target purity aligns with 98 percent minimum by area normalization. Moisture content shows up frequently in inquiries from process chemists, and we maintain Karl Fischer titrations to keep levels below 0.5 percent by weight. Chloride residue, residual solvents, and trace related substances fill out the rest of the specification sheet. But numbers only tell part of the story—texture, color consistency, and odor all inform a technician’s first impression of batch quality. The yellow-to-brown crystalline powder—never clumped, never sticky—speaks to careful drying and precise control of end-point quenching.

    We’ve learned that shipping has its own lessons. Even if a material clears analytical hurdles, physical handling can cause subtle changes: static charge buildup, trace oxidation, or caking under humid conditions. Over time, we moved away from fiber drums and now use carefully lined stainless vessels or HDPE containers with moisture absorbers. Every detail, right down to the foil seals and tamper-evident packaging, carries echoes of what we’ve seen in real-world incidents and near misses.

    Where Customers Put It to Work

    Customers approach us with project requirements that stretch across industries. Pharmaceutical research, agrochemical intermediates, and advanced polymer synthesis—each application brings its own constraints and ambitions. Within the pharma sector, the aldehyde group’s reactivity unlocks routes to elaborate heterocycle formation and condensation with primary amines or hydrazines. These steps lay the groundwork for everything from antiviral agents to kinase inhibitors, and our partners frequently mention that competing materials never quite match the conversion efficiency or side-product stability of our batches.

    Agrochemical teams care about not just yield but about repeatability. One field chemist once described it succinctly: with consistent product, their syntheses run “on rails”—unexpected results vanish, and unnecessary troubleshooting steps disappear. Consistency isn’t just about brand trust: it’s the difference between one-off success and systematic, scalable deployment in process chemistry. For our clients targeting new herbicide, pesticide, or fungicide prototypes, the 2,4-dichloro motif combines with the carbaldehyde to set off a new round of molecular design, improving biological activity and selectivity.

    In materials science, new classes of polymers and advanced materials frequently start with these sorts of reactive building blocks. The aldehyde group brings functional handles for cross-linking or for attaching further electronic and photoactive units. Technicians have told us how subtle changes—trace water percentages, lot-to-lot color shifts—translate to macroscopic changes in material properties. Those stories shape how we approach both QC and continuous process improvement.

    Subtle Differences, Practical Implications

    Chemists may lump many pyridine derivatives together at first glance, but details in substitution and reactivity craft the line between success and failure in multistep synthesis. Our work with 2,4-dichloropyridine-3-carbaldehyde reinforces this at every step. Compared against related molecules like 2,4-dichloropyridine or 3,5-dichloropyridine, the carbaldehyde group keeps the molecule highly reactive—especially attractive when designing condensation steps or building blocks for multi-ring targets.

    We handle requests for related substances such as 2,6-dichloropyridine or aldehyde-free variants, which often serve customers optimizing for lower cost or reduced reactivity in bulk synthesis. Still, only the aldehyde-bearing derivative lends itself as flexibly to the kind of reductive amination, imine formation, or extension chemistry needed for the most demanding pharmaceutical or specialty polymer applications. It’s not just about reactivity; the presence of the aldehyde affects physical stability, solubility in polar and semi-polar solvents, and the need for careful exclusion of water or base during storage.

    Making the right match between molecule and use comes down to how closely the supplier understands not just what they sell, but why each minor structural change matters. Our continued direct contact with end users has illustrated this lesson time and again—failed syntheses trace back to hidden variables like stabilizer residue, trace isomer presence, or physical crystal form differences, each one able to sideline a complex project. Only by knitting together manufacturing experience, feedback from customers, and a willingness to revisit old protocols do we manage to sharpen the product to users’ actual needs.

    Challenges Met in Production and Delivery

    Production of aldehyde-containing pyridines doesn’t allow for shortcuts. From raw materials (chloropyridine isomers, reagents for Vilsmeier-Haack or similar formylation steps, and specialty solvents) to finished product, every phase courts its own risks and learning curves. Over the years, our teams have adapted old bench chemistry to safe, large-scale systems. Early problems—overchlorination, incomplete hydrolysis, or post-reaction polymer formation—forced us to refine in-line monitoring, invest in more robust agitation equipment, and plan for rapid downstream isolation.

    A major concern during isolation involves water contaminants. Even a few tenths of a percent of water lead to hydrolysis or dissolves away tiny but important product fractions. We've wrestled with this reality since the early runs, increasing our in-process Karl Fischer tests and rotating storage drums faster to minimize exposure time. Shipping through summer months revealed new concerns with aldehyde stability and color changes. Simple solutions, such as double-sealing and temperature logging, grew from direct responses to customer feedback and real shipment issues. Materials handled with callousness react in kind; crystals wilt, surface moisture collects, and the chemistry downstream turns unpredictable.

    We see growing pressure from downstream users for more transparency in carbon footprint and regulatory documentation. Technology teams increasingly want a view into starting material sources, emissions controls, and minimized waste. Aldehyde chemistry doesn’t always leave a small mark: from use of chlorinated solvents to energy-intensive distillation and drying. Our approach includes maximizing recycle rates of solvents, switching to lower impact desiccants, and working with trusted raw material suppliers for quality documentation and chain-of-custody assurance. Some buyers ask for LCA-type data, and while not every plant has the luxury of automated reporting, we maintain transparent and honest accounting, accepting audits and sharing findings with technical and commercial staff alike.

    Why Direct Experience Matters

    What distinguishes manufacturers from resellers, traders, and generic distributors springs from proximity—knowledge built not from repeating catalog claims but from living through real production cycles, process breakdowns, customer complaints, and problem-solving. Every batch of 2,4-dichloropyridine-3-carbaldehyde we have produced reflects years of effort, ongoing process improvement, and stubborn attention to detail. Our R&D chemists have shifted purification protocols with each new set of impurities encountered; our plant managers tweak batch sizes or cycle times in response to energy cost or demand fluctuations.

    A handful of buyers will visit our plants for direct qualification. They spend a day observing not just the reactor rooms, but raw material offloading and containerization steps. They ask questions impossible to answer from standard specification sheets—about trace isomer controls, dust minimization in the filling room, or the energy source for our drying lines. Their demanding gaze keeps us honest. What always surprises these technical evaluators is not just the instrumentation or material cleanliness but the accumulated know-how captured by line supervisors and technicians—what to check after storms, how to handle jamming equipment, which alarms signal real risk. There’s no substitute for local knowledge, and oral culture courses through every shift change.

    This approach—personal, responsive, detail-rich—doesn’t come from market research or templated online guidance. It’s born of learning the material’s quirks and knowing how minor missteps multiply into loss, hassle, and wasted hours for the customer. It keeps our teams alert even once the product leaves the gate, sustaining dialogue long after the sale—fielding questions on batch differences, supporting trouble-shooting in custom synthesis, and recording lessons that roll back into improved methods and safer operations.

    Responding to Shifting Demands and Innovations

    As regulatory standards, technology, and market expectations shift, we adapt both formula and process for 2,4-dichloropyridine-3-carbaldehyde. Sometimes this involves a push for higher purities, as new downstream chemistry becomes more sensitive to trace impurities. Other times, customers innovate and request consistent polymorph distribution, better stability under UV light, or pilot-scale samples that anticipate regulatory testing. Feedback loops—where our product quality feeds into a customer’s own manufacturing tweaks—prompt improvements not just for individual batches but for long-term strategy. Being both close to the process and flexible enough to accommodate changes means troubleshooting never stops, and neither does learning.

    Supply chain changes in recent years—trade restrictions, tighter environmental rules, and more demanding end-use approvals—have shifted the way we source key reagents. These challenges force direct investment in supplier relationships and secure, long-term contracts. Experience has shown that even a single change in a second-tier raw material or reagent can echo back through the reaction to affect yield, purity, and downstream performance. Making those links visible and closing information gaps with users lays the groundwork for more productive partnerships.

    Innovation also comes as markets demand safer and more sustainable chemistry. We have reduced use of halogenated solvents, increased recovery rates of reaction media, and evaluated continuous flow synthesis methods to reduce waste and lower per-unit energy costs. At the lab scale, new analytical methods deliver earlier warning of side product formation or color drift. This attentiveness delivers a product that better matches user needs and keeps us ahead of compliance requirements—practices learned from problem-solving as much as from regulatory mandates.

    Our Promise: Honest Work, Real Value

    Supplying 2,4-dichloropyridine-3-carbaldehyde isn’t about chasing hype or ticking boxes on a compliance form. It is about meeting the plain but demanding needs of chemical researchers and process engineers with a molecule they can trust batch to batch, shipment to shipment. Claims about purity or reactivity mean little if not backed by willingness to expose real process data, batch histories, and direct responses to actual user problems. Our teams take pride in offering not just a product but the support, troubleshooting, and constant improvement born from standing beside our material every day.

    For our customers—whether developing a new drug candidate, scaling up for a pilot agrochemical run, or launching a novel smart material—the difference comes down to supply you can bet your project on. That reliability only arises when the manufacturer stands behind the laboratory bench, on the process floor, and on the receiving dock, watching out for the details that make science possible. That’s the promise we deliver in every drum and every report: experience, responsiveness, and a determination to help you do your best work, starting at the molecular level.