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HS Code |
964522 |
| Cas Number | 15862-07-4 |
| Molecular Formula | C6H2Cl2N2 |
| Molecular Weight | 173.00 g/mol |
| Iupac Name | 2,6-dichloropyridine-4-carbonitrile |
| Synonyms | 2,6-Dichloro-4-cyanopyridine |
| Appearance | White to pale yellow crystalline solid |
| Melting Point | 97-100°C |
| Boiling Point | 319°C |
| Density | 1.49 g/cm³ |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=NC(=C1Cl)Cl)C#N |
| Inchi | InChI=1S/C6H2Cl2N2/c7-4-1-5(3-9)2-6(8)10-4/h1-2H |
As an accredited 2,6-dichloropyridine-4-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100-gram package of 2,6-dichloropyridine-4-carbonitrile comes in a sealed, amber glass bottle with a secure screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed in 20′ FCL with moisture protection, properly labeled drums or bags, meeting chemical transport regulations. |
| Shipping | 2,6-Dichloropyridine-4-carbonitrile is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous chemical and should be handled in compliance with local and international transport regulations. Ensure proper labeling and documentation, and store in a cool, dry place during transit to prevent degradation or accidental exposure. |
| Storage | 2,6-Dichloropyridine-4-carbonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and avoid excessive heat. Ensure proper labeling and restrict access to trained personnel. Follow all relevant safety guidelines and local regulations for chemical storage. |
| Shelf Life | 2,6-Dichloropyridine-4-carbonitrile typically has a shelf life of 2–3 years when stored in a cool, dry, tightly sealed container. |
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Purity 99%: 2,6-dichloropyridine-4-carbonitrile with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimized impurities. Particle size 20 µm: 2,6-dichloropyridine-4-carbonitrile with particle size of 20 micrometers is used in catalyst preparation, where it enables greater surface area and uniform reactivity. Melting point 133°C: 2,6-dichloropyridine-4-carbonitrile with melting point of 133°C is used in agrochemical formulation, where stable thermal properties support controlled processing conditions. Molecular weight 190.00 g/mol: 2,6-dichloropyridine-4-carbonitrile with molecular weight of 190.00 g/mol is used in heterocyclic compound synthesis, where precise stoichiometry enhances reaction control. Stability temperature 75°C: 2,6-dichloropyridine-4-carbonitrile stable up to 75°C is used in pigment manufacturing, where maintained stability prevents decomposition during thermal processing. Water content ≤0.5%: 2,6-dichloropyridine-4-carbonitrile with water content less than or equal to 0.5% is used in electronic material development, where reduced moisture prevents hydrolysis and ensures device reliability. Residual solvent ≤200 ppm: 2,6-dichloropyridine-4-carbonitrile with residual solvent below 200 ppm is used in advanced material engineering, where low solvent residues improve safety and regulatory compliance. Chromatographic purity ≥98%: 2,6-dichloropyridine-4-carbonitrile with chromatographic purity of at least 98% is used in fine chemical research, where high analytical purity supports reproducible research outcomes. Storage under inert atmosphere: 2,6-dichloropyridine-4-carbonitrile stored under inert atmosphere is used in sensitive organic synthesis, where protection from oxidation ensures chemical integrity. Bulk density 0.6 g/cm³: 2,6-dichloropyridine-4-carbonitrile with bulk density of 0.6 g/cm³ is used in custom formulation blends, where controlled density aids accurate dosing and mixing efficiency. |
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Every chemical tells a story by how it’s made, where it’s used, and the people relying on its consistency. 2,6-Dichloropyridine-4-carbonitrile belongs to that family of building blocks the industry values for their reliability and versatility. We’ve shaped our manufacturing on customer feedback: purity matters, and so does the way the product handles in a busy plant. The model our clients use most clocks in at over 99% purity, and it stays stable during shipping, even when weather goes from humid to dry and back again. Working with this compound means seeing its subtle differences compared to less chlorinated or unsubstituted pyridines.
In any manufacturing plant, efficiency isn’t just a buzzword—it’s what lets teams turn orders around without delay. When we began producing 2,6-dichloropyridine-4-carbonitrile at scale, adjustments to filtration and drying cut down impurities that often cause wasted man-hours downstream. A clean batch gives researchers and production managers exactly what they hoped for—predictable behavior in their next steps, whether in pharmaceuticals, crop protection, or specialty colorants.
For the people mixing reagents in the reactor or measuring batch yields, there’s little tolerance for surprises. Aromatic nitriles sound simple on paper, but a few stray organic acids or unstable byproducts can tank a synthesis or wreck a catalyst bed. For years, we traced every off-spec batch to its cause, down to nuances like trace moisture in raw materials or slight variations in chlorination timing. Over time, the tweaks add up: now, moisture content stays below 0.3%, and we routinely check for residual solvents down to parts-per-million. This doesn’t just help meet specifications; it means a plant manager can plan with confidence.
Pyridine derivatives have become essential in medical research, pesticide development, and advanced materials. Each variant, though, has its quirks. 2,6-dichloropyridine-4-carbonitrile handles a set of roles that simpler pyridines or those substituted elsewhere cannot match. Two chlorine atoms on the six and two positions close off points of reactivity, giving the molecule a temperament better suited for modern syntheses that need defined, reproducible results. The nitrile group at the four position opens doors—literally and figuratively—to further transformations, acting as a launching pad for a range of functionalization steps.
Colleagues in agricultural R&D tell us they value this specific substitution pattern for creating more robust crop protection agents. Some of these agents stay intact long enough to perform in the field, thanks to that unique chemistry. Our own technical staff recognizes how the distinctive reactivity aids in selective coupling, cyclization, or reductive processes—routes not easily managed with less hindered isomers.
Factories learn the hard way that changing batches or suppliers midstream leads to headaches—reactivity shifts, side reactions follow, yields drop. As manufacturers, we take pride in creating a batch process for 2,6-dichloropyridine-4-carbonitrile that runs the same year after year. We rely on our own reactor controls, our filtration methods, our crystallization know-how, not generic third-party protocols. Every improvement comes from direct experience, not theory.
Technical teams from partner companies often send samples from their spent catalyst beds or final products back to our lab. Sometimes an uptick in a trace impurity gives them trouble downstream. Whether it’s HPLC, GC-MS, or NMR, our lab staff matches those blips in their product to steps in our own process. More than once, this feedback loop led us to refine our workup or switch suppliers for a single solvent, all based on hard data. We see this as a responsibility: clean product isn’t just about compliance—it saves someone else hours of rework or troubleshooting.
No manufacturer escapes the realities of scale-up and logistics. 2,6-dichloropyridine-4-carbonitrile isn’t produced in tiny lots: kilogram runs feed into multi-ton operations, and sudden changes in demand ripple through the supply chain all the way from the raw materials to end use. Production managers need packaging that keeps out moisture and dust, and everything must move in certified drums that stand up to global transit.
Maintaining this delicate chain depends on real forecasting—not just for the primary compound, but for the raw ingredients and processing aids, too. Shortages halfway around the globe cause prices to spike or batches to get delayed, but long-term agreements with chemical suppliers keep our lines humming. During the pandemic, logistics snarls were the rule, not the exception. Instead of waiting for things to improve, we worked with freight forwarders for custom temperature control and kept extra inventory in bonded warehouses, even when it cut into margins. Reliable supply matters more than shaving a few cents off per kilo.
Purity looks simple on a certificate, but its importance stretches past numbers on a page. For 2,6-dichloropyridine-4-carbonitrile, specs like chloride content, water, and organic residuals translate directly to yields and quality at the next step. Pharmaceutical chemists reach for this molecule when planning syntheses of advanced intermediates and API scaffolds. Lower impurities mean fewer purification steps, stronger batch-to-batch reproducibility, and regulatory confidence.
We once worked with a partner scaling up a new agrochemical where the trace presence of halogenated byproducts caused off-notes in their final formulation. Chasing down the cause, we adjusted the quenching sequence in our process and deepened the vacuum drying stage. That fix, minor in the scope of daily operations, bumped acceptance rates and shortened their downstream QC cycle. Lessons like these show how the minutiae of upstream chemistry, sometimes overlooked, set the tone for every user past the factory gate.
Chemical manufacturing means accountability—to the team, the wider community, and the environment. Chlorinated pyridine derivatives carry their own hazards. Decades ago, plant workers handled open systems with minimal protection; that era has passed, and the legacy is clear. Direct experience teaches us not just to box up waste streams or post a few warning labels, but to design enclosed handling, monitored air, and strict spill response from the ground up.
Our senior operators learned the hard way that even tightly closed centrifuges can leak, and quality assurance doesn’t work as an afterthought. We layer in safety training and ask our newest hires to shadow veterans not just at the controls, but in sample prep, cleaning, and loading docks. Regulations drive some of this—our market reach depends on REACH registration, consistent GHS labeling, and maintaining audit-ready records. Real-world discipline goes beyond paperwork. When an accident nearly happened in a tanker transfer due to miscommunication between shifts, root-cause analysis led to color-coded valves, punch-list checks, and mandatory signoffs. Every improvement comes from collective memory.
Academic research can sometimes miss the questions industry users need answered: What happens if the solvent contains more than 0.5% water? How sensitive is the downstream amination to minor byproducts? What shelf life matters in real conditions? We collect data not just during pilot runs, but also from feedback after months in storage or those phone calls from customers who discover drummed material after the expiration date.
Our direct experience shows that 2,6-dichloropyridine-4-carbonitrile with high purity and low secondary chloride performs better than the technical grade version commonly sold by traders. When used as a building block for pharmaceutical pyridine analogues, residual acidity in the compound leads to deactivation of catalysis—sometimes cutting yields by 30-40%. These are not theoretical risks. Users count on homogeneity from drum to drum, so we test every ton for isomer content, residual organics, and particle size distribution. The more consistency at our plant, the fewer headaches for the people downstream.
Molecular structure sets 2,6-dichloropyridine-4-carbonitrile apart, and with it comes practical impact. The di-chlorination pattern alters both solubility and reactivity, which shapes everything from solvent choice to compatibility with downstream catalysts. Users often compare compounds like 3,5-dichloropyridine-4-carbonitrile or simpler pyridine-4-carbonitrile, expecting interchangeable behavior—but lab results consistently show otherwise. Side chain reactions crop up, or crystallization fails, when the subtle balance of electron withdrawing effects and steric hindrance shifts.
This specific substitution also means engineers can predict stability better, which aids both large batch storage and use in sensitive applications. Shelf life extends, and off-color degradation rarely appears compared to monosubstituted relatives. We’ve had feedback from the electronics manufacturing sector touting improved throughput and fewer filter clogs when swapping in our standardized batches of 2,6-dichloropyridine-4-carbonitrile for formulations originally based on less pure competitors. These improvements get noticed in the numbers, but just as much in lowered downtime and fewer troubleshooting calls.
Minimizing environmental footprint sometimes seems at odds with scaling up production. Years ago, disposal of chlorinated byproducts meant costly high-temperature incineration or specialized waste hauling. Through in-house R&D, we developed a method to recycle process water after rigorous phase separation and activated carbon treatment. The result: cutting water discharge by more than half over the span of three years and reducing hazardous waste shipments.
The compound itself isn’t especially volatile, but because it carries acutely hazardous labels, safe storage requires precision. Each drum gets an airtight liner, and storage areas remain under negative pressure with alarmed vapor detectors. These aren’t decorative measures—they result from decades of lessons in loss prevention and incident reporting. Protecting our plant team and the communities nearby shapes how we select every containment system, right down to drum seals and forklift routes.
Markets change. New synthesis routes emerge, and regulations tighten worldwide. We’ve updated our plant control system numerous times, frequently retraining both veteran and newly hired staff. One major improvement included adding inline NMR for faster release testing, reducing lot approval times from days to hours. These aren’t just for show; the improvements go straight to customers, who notice shorter lead times and more predictable product.
Sometimes clients approach us with a new downstream application that pushes the product into unfamiliar territory—emerging OLED precursors, specialty pigments, or pilot-scale clinical candidates. Rather than stick to old specs, we invest in process optimization runs and detailed impurity mapping, drawing on all the process data we’ve collected over decades. This direct partnership speeds up innovation and builds trust.
Collaboration no longer follows a straight path from supplier to customer. We interact with regulatory teams, academic researchers, formulation chemists, environmental officers, and shipping specialists—sometimes all on the same day. Certificates of analysis now include far more than residual solvents or melting point; customers want confirmation of heavy metal absence, identity confirmation by NMR, and trace impurity tracking across multiple lots. Meeting these new expectations means investing in robust data systems and transparent communication.
We once partnered with a research team pursuing green chemistry alternatives for halogenated aromatic intermediates. Their proposed routes cut energy usage by almost a third, but presented real-world trade-offs in yield and scalability. By sharing in-plant trial results, analytical troubleshooting, and practical lessons on waste handling, both sides developed a more realistic perspective. The final result wasn’t perfect, but the process opened new territory, especially for applications where sustainability is top priority.
At the foundation of our production lies not just stainless steel or computer automation but real people. Everyone from chemical engineers, analytical chemists, warehouse staff, to maintenance workers plays a hand in each batch of 2,6-dichloropyridine-4-carbonitrile. The feedback that lands on a supervisor’s desk, whether a leak report or a new client requirement, shapes tomorrow’s product every bit as much as any SOP or technical drawing.
Unlike commodity chemicals, specialty organics like ours interact with the real world in detail: irregular delivery routes, customs hurdles, evolving applications, shifting client standards. Prompt response means the difference between a line running or a project stalling. We don’t outsource these questions to generic support desks. Instead, plant supervisors and technical staff work directly with customer teams, often analyzing new questions late at night when a hiccup emerges from a supplier on another continent. The personal pride and professional satisfaction from every successful batch extends beyond the plant gates—through every product, every customer, every end-user.
2,6-Dichloropyridine-4-carbonitrile, at a glance, may appear just another entry in a chemical catalogue. Our experience producing this compound at scale tells a richer story—a specialized building block with hard-won reliability, technical versatility, and a manufacturing tradition that’s grown alongside the science of modern chemistry. The lessons from every ton produced don’t just rest on paper, they’re written in the day-to-day realities of plant management, market changes, regulatory challenges, and customer trust.
For every kilo leaving our facility, our promise extends beyond purity on a certificate. Each batch reflects our commitment to the people molding innovations, advancing science, and solving the everyday challenges of modern manufacturing. It’s chemistry built from experience, refined with every question, and delivered with practical respect for what’s at stake.