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HS Code |
830002 |
| Productname | 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile |
| Casnumber | 69045-84-7 |
| Molecularformula | C6HCl2FN2 |
| Molecularweight | 191.00 |
| Appearance | White to off-white solid |
| Meltingpoint | 78-81°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents (e.g. DMSO, DMF) |
| Storagecondition | Store in a cool, dry place; keep container tightly closed |
| Synonyms | 2,6-Dichloro-5-fluoronicotinonitrile |
| Smiles | C1=C(C(=NC(=C1Cl)C#N)Cl)F |
| Inchi | InChI=1S/C6HCl2FN2/c7-4-1-5(9)6(8)11-3(4)2-10 |
As an accredited 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed 100-gram amber glass bottle, clearly labeled with product name, CAS number, hazard symbols, and handling instructions. |
| Container Loading (20′ FCL) | 20′ FCL can load approximately 8–10 MT of 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile, packed in 25 kg fiber drums. |
| Shipping | **Shipping Description:** 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Appropriate hazard labeling is applied, and all relevant chemical safety regulations and documentation for transport—such as safety data sheets—are included to ensure safe handling during transit. |
| Storage | Store **2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep away from sources of ignition and moisture. Label the container clearly and handle with suitable personal protective equipment (PPE) such as gloves and safety goggles. Follow appropriate storage guidelines for hazardous chemicals. |
| Shelf Life | Shelf life of 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile is typically 2-3 years if stored in a cool, dry place. |
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Purity 99%: 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal side product formation. Melting point 76°C: 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile with melting point 76°C is used in agrochemical production processes, where stable handling and precise formulation are required. Molecular weight 207.01 g/mol: 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile with molecular weight 207.01 g/mol is used in specialty chemical manufacturing, where compatibility with downstream reaction pathways is enhanced. Particle size <50 μm: 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile with particle size below 50 μm is used in advanced material research, where improved dispersion and reactivity offer superior end-product uniformity. Stability temperature up to 120°C: 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile with stability temperature up to 120°C is used in high-temperature catalytic applications, where thermal integrity maintains reaction efficacy. |
Competitive 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile prices that fit your budget—flexible terms and customized quotes for every order.
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Experience stands out as the best teacher on our production floor. Over years of manufacturing complex heterocycles, we’ve put 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile through its paces at scale. This compound forms an essential part of the toolkit for building advanced agrochemical and pharmaceutical molecules. From batch reactors to pilot plants, meeting exacting customer standards comes down to purity, reproducibility, and yield—and this intermediate delivers consistent results that users in demanding sectors recognize straight away.
Inside our facilities, we handle lots of halogenated pyridine series substances. This particular compound—known in our shop as model SF-DCFPCN—features both chlorine and fluorine subsituents on the pyridine ring, as well as a nitrile functional group at position three. These structural traits mean it performs certain coupling and substitution reactions that more basic pyridines can’t achieve. In the daily process routine, we run the reaction under strictly monitored conditions, paying close attention to moisture control, solvent quality, and downstream purification. Customers rely on the product’s sharp melting point and a narrow impurity profile for their next steps, not just in theory, but batch after batch.
Every container we ship reflects hundreds of careful laboratory and full-scale production trials. Our most requested product grade comes as a pale white crystalline solid, with purity typically not less than 98 percent by high-performance liquid chromatography. We document trace levels of dichlorinated or monofluorinated impurities and flag any deviation from the standard spectrum, drawing on regular NMR and GC-MS checks. Moisture content, a hidden enemy in sensitive reactions, is kept below 0.2 percent. For our long-term partners in pesticide and pharmaceutical synthesis, these tight specs translate directly into higher process yields and reduced off-specification waste. The compound’s stability during long-distance transport gives downstream users peace of mind, especially for high-volume orders moving across different continents or climates.
Dialing in the right building block goes beyond a quick catalog search. Over the past decade, our partners have shifted toward more halogenated and functionalized heterocycles as regulatory pressure mounts and patent lifecycles tighten. The dual halogenation plus nitrile arrangement in 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile lets medicinal chemists and crop protection researchers construct a wider array of target molecules with fewer synthetic steps. In practical terms, this means less waste, lower raw material costs, and shorter cycle times between idea and product launch. Synthetic chemists particularly value the reactivity difference between the fluorine and the two chlorine atoms, enabling flexible selective substitutions that save months of route scouting. The nitrile group at position three extends the range of possible transformations—amidation, reduction, cyclization—that are needed in real-world product pipelines.
Shifting from laboratory to industrial production of halogenated pyridines surfaced more hurdles than textbooks let on. In our plants, we faced significant challenges with byproduct management, solvent selection, and control of exotherms, especially during the halogenation and cyanation steps. Over time, investments in in-line analytical monitoring and process automation let us clamp down on run-to-run variability. We gather feedback from users who spot trace byproducts in their own trials; each comment loops back to our QC process. Waste treatment infrastructure grew as production scaled, especially to handle halogenated streams safely. We rebuilt scrubber systems, trained team leads on swift response, and fine-tuned the sequence of additions so that heat release never catches the crew off guard. Years of batch records have shaped a process that minimizes offcuts and keeps tight control not just at the final crystallization but from the first charge onward.
Our deep bench in process development makes a visible difference when customers ask for tweaks—say, modifications to particle size or solvent residue levels. Rather than outsourcing small-scale customizations, our teams tune parameters in house, then validate each pilot run side by side with our customers’ requirements. Around the plant, workers see every kilogram as evidence of skill built on practice: managing dust, minimizing moisture pick-up, and ensuring seamless switching between product campaigns.
Most of the requests for 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile come from downstream innovation. Agrochemical formulators often need high-purity intermediates to develop next-generation active ingredients aimed at resistant species. The fine details of halogen placement shape both product performance and regulatory approval, especially for compounds targeting pests with tough metabolic resistance. We’ve seen this intermediate chosen not because of historical precedent but due to the unique balance of electronic and steric effects offered by the combined chloro and fluoro groups. This selectivity grants synthetic chemists an edge when tackling rare or hard-to-reach scaffolds.
On the pharmaceutical side, drug discoverers order this intermediate for use in exploratory syntheses and late-stage lead optimization. Its chemical backbone appears in various kinase inhibitors, CNS agents, and anti-infective candidates. The easily modified nitrile is attractive for constructing amide and other nitrogenous scaffolds needed in modern drug molecules. In real-world processes, chemists replace the chlorine atoms in a stepwise, controlled fashion, often leveraging the difference in their reactivity to maximize yield and selectivity. The fluorine atom, meanwhile, adjusts electron density and metabolic stability, helping fine-tune how the resulting molecule interacts with biological targets. We work closely with process chemists to adjust our manufacturing output based on which derivative they are chasing—sometimes with only days’ lead time between their specification and our next campaign launch.
We often receive questions about substitution: could another halogenated pyridine fill the same slot? Our long production record makes the answer clear. Ordinary dichloro- or difluoro-pyridinecarbonitriles can’t replicate the same coupling yields, especially where selectivity in nucleophilic aromatic substitution matters. The spatial arrangement of two chlorines and one fluorine on this molecule’s core ring delivers a distinctive blend of reactivity and downstream flexibility. For some processes, users have swapped in 2,6-dichloro-3-pyridinecarbonitrile or 5-chloro-2-fluoro-3-pyridinecarbonitrile, only to see lower yields or more byproducts in the final API stage. In crop protection, subtle changes in halogen pattern lead to shifts in field performance and breakdown profiles, which regulatory authorities scrutinize closely. Years of process troubleshooting confirm that the right intermediate cuts both cost and risk by reducing the number of purification steps needed down the line.
Physical behavior on the plant floor also matters. Unlike some closely related molecules, this compound exhibits excellent bulk stability and resists clumping or decomposition even during prolonged storage in variable humidity conditions. During shipping, the crystalline material remains free-flowing, with few instances of caking or dusting. By contrast, derivatives with fewer halogen atoms often require extra drying or more robust containment to keep quality up and hazards down. This operational reliability keeps our customers’ lines moving with fewer slowdowns and less material loss in handling and weighing.
Decades spent refining the manufacturing process for 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile have convinced our team that consistency is the real differentiator. It’s easy to underestimate the difference incremental improvements make until a process runs at hundreds of kilograms per shift. Every production batch teaches fresh lessons—from raw material sourcing in global markets to final checks as containers leave our warehouse. By keeping most critical operations in house, we guard every step from contamination, mislabeling, or errant residues that can expand QC time downstream.
Improvement never stops. Each year, new safety regulations and downstream reporting requirements prompt us to invest in documentation and auditing. Our analytical teams test not just for ordinary contaminants, but for extremely low levels of regulated substances. Training cycles for all team members help reinforce the connection between standard work and customer impact: precision in humidity monitoring, oversight in solvent recovery, clean handoffs at every shift. We encourage field reports from long-term partners who experience issues outside typical scenarios—smaller anomalies often signal process drift before the lab even detects it. Formal root cause analysis, paired with boots-on-the-ground observation, forms the backbone of our response to any hiccup, big or small.
Greater industry scrutiny on environmental impact and sustainability means we can’t rely on yesterday’s process. Our teams continue to refine waste treatment, recycle solvent streams, and explore greener synthetic routes. Some pilots have replaced legacy solvents with lower-toxicity alternatives, cutting secondary pollutant output by measurable margins. We redesign process steps to reduce halogenated byproduct load and regularly consult with third parties—industry chemists, engineering experts, and regulatory specialists—on safer, more sustainable practices. Responsible halogen management has become a core part of shop-floor culture, not just a compliance box to tick. Tracing every kilogram from start to finish, we back up our claims with continuous monitoring and third-party audits on demand.
Our long partner relationships with leading agrochemical and fine pharma firms drive us to view stewardship as a shared effort. We provide transparency not only in technical specs but in how raw materials are sourced, how waste is disposed of, and how process controls evolve with new best practices. When our clients develop new products or shift regulatory filings, we stand ready to adapt our intermediate to minimize both environmental and operational risk. Progress in fine chemical synthesis only happens through partnership—upstream expertise feeding the downstream pipeline, from our reactors to their innovations in the field or clinic.
Each order we send out for 2,6-Dichloro-5-fluoro-3-pyridinecarbonitrile carries with it the combined knowledge and hard work of a team dedicated to craftsmanship in chemical production. This compound anchors itself as more than just a stop along the supply chain. Every process detail—tight specifications, careful handling, responsiveness to customer change—shapes the reliability, accessibility, and performance of the next breakthrough agrochemical or pharmaceutical product lurking around the corner. Our doors stay open to partners who value not just a product, but a relationship built on decades of hands-on experience and a commitment to better chemistry, run after run.