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HS Code |
908563 |
| Chemical Name | 5,6-Dichloro-3-pyridinecarbonitrile |
| Molecular Formula | C6H2Cl2N2 |
| Molecular Weight | 173.00 g/mol |
| Cas Number | 4318-56-3 |
| Appearance | White to light yellow solid |
| Melting Point | 123-127 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(N=C1C#N)Cl)Cl |
| Inchi | InChI=1S/C6H2Cl2N2/c7-5-1-4(3-9)2-10-6(5)8/h1-2H |
| Storage Conditions | Store at room temperature, keep container tightly closed |
As an accredited 5,6-Dichloro-3-pyridinecarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle, sealed, labeled “5,6-Dichloro-3-pyridinecarbonitrile,” with hazard symbols and batch number displayed. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Typically 14–16 metric tons of 5,6-Dichloro-3-pyridinecarbonitrile packed in 25 kg fiber drums. |
| Shipping | 5,6-Dichloro-3-pyridinecarbonitrile is typically shipped in tightly sealed containers to prevent moisture and contamination. It should be packaged according to regulatory standards for hazardous materials, with clear labeling. Transport requires temperature control, away from incompatible substances, and compliance with relevant safety and environmental regulations for chemical shipping. |
| Storage | Store 5,6-Dichloro-3-pyridinecarbonitrile in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible substances. Keep the container tightly closed, clearly labeled, and protected from physical damage. Store away from strong oxidizing agents. Use appropriate chemical storage cabinets if available, and ensure access is restricted to trained personnel. |
| Shelf Life | 5,6-Dichloro-3-pyridinecarbonitrile is stable under normal storage conditions; recommended shelf life is at least two years if kept sealed. |
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Purity 98%: 5,6-Dichloro-3-pyridinecarbonitrile with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting Point 108°C: 5,6-Dichloro-3-pyridinecarbonitrile with a melting point of 108°C is used in agrochemical formulation, where it facilitates precise processing and formulation stability. Particle Size <10 microns: 5,6-Dichloro-3-pyridinecarbonitrile with particle size below 10 microns is used in catalyst manufacturing, where it enables efficient dispersion and reaction rates. Moisture Content <0.5%: 5,6-Dichloro-3-pyridinecarbonitrile with moisture content less than 0.5% is used in electronic chemical synthesis, where it minimizes impurity incorporation and degradation risks. Storage Stability at 25°C: 5,6-Dichloro-3-pyridinecarbonitrile with storage stability at 25°C is used in long-term inventory management, where it maintains chemical integrity and usability over extended periods. |
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In the chemical manufacturing industry, every compound has its own story—one shaped by years of research, production challenges, and the evolving needs of the sectors we serve. Among the products that keep us constantly reaching for a higher standard is 5,6-Dichloro-3-pyridinecarbonitrile, sometimes referenced by its chemical abbreviation. Methods of synthesis and purification have evolved alongside market demand, but the commitment at its core remains identical: deliver chemistry that meets the modern world’s real needs.
As a producer, we don’t just look at 5,6-Dichloro-3-pyridinecarbonitrile as a stock code or a catalog entry. Each batch reflects choices about raw material sourcing, reaction conditions, and environmental responsibility. The appeal of this compound lies not in a generic role as a building block, but in its track record supporting pharmaceutical and agrochemical pipelines.
The molecule itself stands apart from other pyridinecarbonitriles. The two chlorine atoms located at the 5 and 6 positions give it a distinct profile, creating opportunities for targeted reactivity. Compared with mono-chloro variants or those modified at other positions, this version demonstrates better performance in some coupling reactions, allowing researchers and manufacturers to push synthesis in directions that offer results, not just theory.
From a production standpoint, synthesizing this compound presents a few challenges. Consistency matters. We control temperature profiles and manage purification with care, drawing on both experienced staff and refined equipment. Maintaining the right level of residual moisture and minimizing isomeric byproducts is not just a checkbox; quality impacts the next link in supply chains, sometimes with millions of dollars at stake.
We tailor the material’s physical form to fit user need—not out of habit, but from listening to long-term customers in formulation labs. Crystalline powders help with automatic dosing, so we put effort into controlling particle size. When specific purity grades become relevant—usually above ninety-nine percent, measured by HPLC—we run extra steps. We apply our own analytical results and listen to feedback, pushing for improvements batch after batch.
Those who work in agricultural technology or small-molecule drug synthesis see the value of a compound like 5,6-Dichloro-3-pyridinecarbonitrile every day. For larger-scale crop science, it serves as a precursor to several classes of pesticides and herbicides. Its structure enables efficient downstream substitution, helping chemists build more complex molecules with improved selectivity. The pharmaceutical sector relies on it as an intermediate in research projects and scale-up campaigns where positional selectivity and manageable leaving groups simplify the synthetic pathway.
Such versatility explains why demand remains steady, even as regulatory scrutiny on chloroarene intermediates has increased. There’s no shortcut in developing alternatives with the same balance of cost, reactivity, and downstream compatibility. Stakeholders keep returning to this compound for its tried-and-true output. For some processes, the choice is driven by how effectively it moves lab-scale yields to full-scale reactors.
Directly comparing 5,6-Dichloro-3-pyridinecarbonitrile with other halogenated pyridines, the distinctions clarify pretty fast. Position matters: substitution at 5 and 6 changes electron distribution, which in turn shifts how follow-up reactions behave. This can reduce steps, minimize required reagents, and improve reproducibility. That doesn’t mean it suits every process, but where it fits, competitors rarely match the blend of performance and predictability that comes from this arrangement.
Producing high-purity halogenated intermediates brings its share of difficulties. Chlorinated pyridines have a reputation for generating byproducts, sometimes requiring tricky purification. As manufacturers, we became familiar with optimizing crystallization and developing better solvent recovery practices. Any residual impurities complicate scale-up for our clients, so we keep detailed batch records and maintain a focus on repeatability.
Environmental responsibility pushes us to reduce chlorinated waste streams. Over years of experience, we improved separation techniques and found ways to recycle more process water. Our plant operators spot minor deviations faster, using in-house spectroscopic tools. We believe that incremental improvements over hundreds of batches guard against upset conditions and protect supply.
Maintaining consistency in this compound supports customers attempting multi-step syntheses. Some pharmaceutical clients submit tough specs, and often require additional documentation. We facilitate that by keeping process controls tight, providing traceable COA results, and reviewing analytical logs with chemists and QA staff together.
Most new requests for 5,6-Dichloro-3-pyridinecarbonitrile originate from R&D teams who already know what downstream application they want. Their work sets innovation in motion, but a glitch in a batch can stall entire campaigns. We worked hand-in-hand with development chemists during early pilot projects, seeing firsthand how detection of a single polar impurity could wreck a reaction sequence. Those lessons pushed us to refine filtration, invest in higher-sensitivity analytics, and upgrade drying steps beyond what generic industry specs would demand.
On the other side of the spectrum, price matters. Bulk customers in agrochemicals look at input costs every fiscal quarter. They depend on competitive rates, so we optimize every yield-cutting bottleneck. We traced solvent use, improved reactor utility efficiency, and continually look for greener auxiliaries which don’t compromise overall efficiency. Rather than move costs around by skimping on input quality, our goal has always been to minimize waste, streamline handling, and supply a consistent product that supports downstream process stability.
End users set standards, not the other way around. In some contexts, a 97 percent assay fits the bill, while others insist on trace analysis of individual isomers or regulated limits on chlorinated byproducts. We adapt; our facilities are set up to meet different purity targets without over-driving the costs for everyone else. Some want fine powders for automated dispensing, which means extra effort in milling and dust control. Others use the material in pelletized form for easier manual handling. Both bring their own complications—static build-up, hygroscopic behavior—so we build feedback loops with our customers to resolve practical bottlenecks before they cause real downtime.
Testing goes beyond batch release. We set up ongoing stability evaluations to monitor shelf-life and make sure repacked product behaves reliably, especially for international shipment and cross-season storage. No one likes finding out mid-process that a compound picked up moisture in transit.
Multinationals sometimes send their own teams to audit our techniques. We don’t consider this an intrusion; rather, it’s a validation of the efforts invested by our process chemists and QA staff. Being transparent has helped us stay on supplier lists, get involved early in route selection conversations, and even influence how new synthetic targets are planned.
Other pyridine intermediates exist, but few line up with the range of reactivity, substitution pattern, and physical stability that this compound brings to the bench. For those working on halogen exchange, the 5,6 positions tend to yield more predictable substitution compared with analogs halogenated at positions 2 or 4. In practice, this means fewer surprises mid-reaction and less waste in purifying the target. Mono-chloro analogs on the market have their place, but dual substitution steps open synthetic doors that single substitution can’t easily match.
Our regular feedback shows that clients notice these performance differences. In pilot-scale or plant-scale projects, small tweaks based on the precise location of halogens influence both final yields and impurity profiles. This advantage gets amplified as users scale up, turning lab success into commercial production where every percentage point counts.
For projects requiring more complex transformations, the dichloro compound can be used to introduce further substitutions or coupling partners, supporting the synthesis of heterocyclic scaffolds that mono-chloro or non-chlorinated analogs can’t achieve as efficiently. We believe these properties account for the sustained attention this molecule receives in chemical literature, as well as in real-world process development.
There is no shortcut to understanding what it takes to manufacture a specialty intermediate like 5,6-Dichloro-3-pyridinecarbonitrile. Our operators have spent years tuning reactor loading, adjusting agitation speeds, and documenting the effect of small temperature shifts. For us, every process tweak becomes another datapoint supporting better yields and more predictable product for our customers.
Mistakes can be costly. Over the years, we experienced everything from blocked filters to inadvertent batch oxidations. Recovering from these setbacks means learning fast. We train each new technical recruit on previous incidents, run simulations on pilot rigs, and invest in robust cleanup procedures to handle both routine and rare events. No process remains static, and sharing process improvements internally has driven much of our reliability as a supplier.
Delivering to multiple countries requires more than just good intentions. We learned to anticipate customs issues around import and export controls, to comply with changing regulatory standards for controlled chemicals, and to revise documentation the moment local authorities updated requirements. This hands-on learning helped keep our product flowing even during periods of tight regulation and increased scrutiny during quality audits.
Batch releases involve more than checking boxes. We apply both in-line QC checks and regular off-line analysis, verifying not only the typical impurity trace but also the physical attributes that influence real handling conditions in customer sites. When a new batch fails to crystalize at a desired rate, or if a cross-contamination risk is spotted, every member of the technical team gets involved—reviewing possible root causes, adjusting next batch conditions, and making sure corrective actions stick.
We’ve handled unexpected surges in demand driven by new research, as well as abrupt cancellations due to regulatory shifts. The production schedule flexes to match reality. Resilience means holding buffer stocks when possible, lining up alternate sources of raw materials, and certifying secondary vendors to keep feedstock supply uninterrupted.
We prioritize frequent engagement with regular customers, seeking feedback on their latest process issues. Some reach out after seeing an uptick in gelation or crystallization anomalies; some point out subtle changes in powder flow. Every insight shapes our operational decisions and technology upgrades.
Sustainability moves from buzzword to responsibility, especially with compounds that demand responsible chlorine handling and effluent treatment. We introduced solvent recovery steps, supported staff training on safe handling of chlorinated intermediates, and interfaced with local authorities to support proper waste treatment. Beyond regulatory compliance, we see direct gains in reducing cost and improving operator safety.
The quest for better process efficiency drives continuous review of every dollar spent on utility consumption, labor, and waste management. Close attention to technical journals, and frequent exchanges with research partners, keeps our methods current. New reactor coatings, improved agitation systems, and more selective crystallization seeding agents have all entered our plant setup in response to challenges unique to this product.
As a specialty chemical manufacturer, we rely on practical knowledge as much as specifications. Customer applications drive our attention to details—particle size, moisture stability, and scalability become as important as the base assay. Every metric receives ongoing scrutiny and real-world testing, not just theoretical projection. Our long-term engagements with innovators in agrochemicals and pharmaceuticals help us see each batch as a step in real problem-solving, rather than just a number on a spreadsheet.
For those who depend on reliable, consistent chemical intermediates, we welcome open dialogue, onsite visits, and honest problem reporting. The journey from basic material synthesis to customer process success is one we continue to build collaboratively.
5,6-Dichloro-3-pyridinecarbonitrile endures as a practical solution to specific synthetic challenges. Our role as a manufacturer means embracing every difficulty in the pursuit of increasingly high standards. Each order reflects both our commitment and the trust placed in our hands by end users who expect nothing less.