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HS Code |
623246 |
| Chemical Name | 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- |
| Molecular Formula | C6H2BrFN2 |
| Molecular Weight | 201.0 g/mol |
| Cas Number | 883546-41-4 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Solubility | Slightly soluble in common organic solvents (e.g., DMSO, methanol) |
| Smiles | C1=CC(=NC=C1Br)C#N |
| Inchi | InChI=1S/C6H2BrFN2/c7-5-1-6(9-3-5)2-4-8/h1,3H |
| Synonyms | 5-Bromo-3-fluoropyridine-2-carbonitrile |
| Hazard Statements | May cause irritation to skin, eyes, and respiratory tract |
As an accredited 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed with a screw cap, labeled clearly, containing 25 grams of 2-Pyridinecarbonitrile, 5-bromo-3-fluoro-. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- is securely packed, ensuring safe transport and minimal contamination risks. |
| Shipping | **Shipping Description:** 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- is shipped in sealed, chemical-resistant containers, under ambient conditions unless otherwise specified. The package is clearly labeled with hazard and handling instructions in compliance with DOT/IATA regulations. Avoid exposure to heat, direct sunlight, and incompatible substances. Ensure delivery through authorized carriers with appropriate documentation. |
| Storage | 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizers. Keep the storage area clearly labeled and secure. Avoid excessive heat or open flames, and ensure good laboratory safety practices are followed when handling and storing this chemical. |
| Shelf Life | The shelf life of 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- is typically 2-3 years when stored properly in a cool, dry place. |
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Purity 98%: 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures product consistency and minimizes side reactions. Molecular weight 215.01 g/mol: 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- at molecular weight 215.01 g/mol is applied in agrochemical research, where precise molecular control aids in structure-activity relationship studies. Melting point 75°C: 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- with a melting point of 75°C is utilized in organic synthesis, where defined phase transition enables easy handling and formulation. Stability temperature up to 120°C: 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- stable up to 120°C is used in high-temperature catalytic processes, where thermal resistance maintains compound integrity. Particle size <50 micron: 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- with particle size less than 50 micron is applied in fine chemical production, where reduced particle dimensions optimize dissolution rate and reactivity. |
Competitive 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- prices that fit your budget—flexible terms and customized quotes for every order.
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Operating on the factory floor and moving tons of specialty chemicals each month, we get a close-up look at compounds that rarely make headlines. Most chemists, bench or industrial, know some pyridine derivatives, but the blend of a bromine at the 5-position and a fluorine at the 3-position changes reactivity in a way you can measure and trust over repeated syntheses. We see 2-Pyridinecarbonitrile, 5-bromo-3-fluoro-, known among researchers for its reliability in substitution schemes and its responsiveness as an intermediate in pharmaceutical and agrochemical labs. Our own experience producing this material—batch after batch—has shown that the true value lies in its predictable performance in cross-coupling and nucleophilic aromatic substitution, opening doors to new heterocycles, specialty ligands, and building blocks for core bioactive molecules.
Specifications for material sound dry on paper, but choosing the right model means choosing a consistent outcome from development to pilot to full scale production. At our core facility, most orders specify material in the range of 98% to 99% HPLC purity, often confirmed by a 1H NMR and mass spec for the heavier users who care about by-products and subtle lot-to-lot differences. Most requests are for a fine powder, pale to light brown, and our team’s focus on drying and packaging keeps moisture content under 0.5%. This lets our customers run reactions without headaches due to hydrolysis or side formation, especially when scaling up from grams to kilos. The bromine sits at the C5 position, making it more reactive toward Suzuki or Buchwald-Hartwig couplings than similar pyridinecarbonitriles. The fluorine on C3 subtly shifts reactivity, steering substitution to sites favored in drug analogs and advanced material precursors. With each drum leaving the line, we have built feedback loops with researchers to keep solubility, particle size, and purity within tight limits so reaction outcomes stay reproducible from the first trial to routine batches.
Nothing replaces time in the lab. As a manufacturer, we watch our partners run early-stage research through process validation; their feedback shapes where and how we improve. Most get drawn to this compound for its versatility—medicinal chemists rely on the bromo group for straightforward palladium-catalyzed couplings, while process chemists appreciate the reduced need for careful base selection due to the fluorine's influence. We have seen teams in pharmaceutical development use this intermediate to construct complex scaffolds for kinase inhibitors, drawing praise for the consistent handling and batch reproducibility. In crop science, the electron-withdrawing effects of both the cyano and fluoro groups make certain herbicidal analogs possible, leading to improved metabolic stability in field applications. With every synthesis plant that moves from flask to reactor, control over reactivity, yield, and color profile becomes more important than abstract theoretical benefits. We respond by keeping spectral libraries up-to-date and acting on customer experience—never leaving them to troubleshoot solo.
Judging differences between this compound and other pyridinecarbonitriles, many researchers focus on where halogenation occurs. Over time we've confirmed that replacing the C5 hydrogen with bromine makes the molecule primed for cross-coupling, yet preserves enough stability for long shelf life under standard packaging. The fluorine atom makes a difference not just in reaction routes, but in the downstream properties of finished molecules—improving bioavailability in some pharma candidates, for example, due to increased lipophilicity or metabolic resistance. When our process engineers discuss batches of 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- with their colleagues handling 3-cyano-5-bromopyridine or even 2-pyridinecarbonitrile without halogenation, they talk about reaction times, the need for cryogenic conditions, or the way product isolation changes at scale. Lessons from dozens of campaigns show that the specific substitution pattern of the bromo and fluoro groups saves time during clean-up, reduces column chromatography where possible, and leads to fewer headaches with environmental controls—an underrated but crucial factor in larger manufacturing runs.
Our stakeholders—lab chemists, process researchers, and operations managers—demand more than a certificate of analysis. Each kilogram of 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- we produce reflects processes continuously tuned by actual end users. Questions about shelf life and air sensitivity pop up regularly. We design the packing setup to prevent degradation, with moisture-barrier liners, nitrogen flushes, and tamper seals. Throughout the supply chain, accuracy in weights, purity, and even labeling become non-negotiable, not because of regulations alone, but from repeated lessons earned through delays, rework, and troubleshooting requests. Our QC teams revisit NMRs and chromatograms from every lot, reporting directly to production leads if they see even subtle changes in by-product profiles. Chemists count on these details to avoid last-minute surprises that ruin weeks of work. Over the years, our biggest improvements haven’t come from buying fancier instruments or adding more paperwork, but from honest conversations about the realities of scale-up, storage, and the ripple effect a single out-of-spec batch can cause in a clinical supply chain.
Differences in performance stand out most in step reactions—especially where chemo- or regioselectivity matters. Large molecule synthesis can falter if an intermediate responds unpredictably. We have records of clients who compared our 5-bromo-3-fluoro pyridinecarbonitrile with similar derivatives made abroad or by distributors who relabel and repackage. The number of failed runs drops sharply for customers sourcing material direct from our facility, a pattern traced back to tighter control of raw materials and continuous improvement on feedback from those running late-night reactions on tight deadlines. Our own technical staff regularly test competing samples, focusing not only on purity per se but how each batch interacts with ligands, solvents, and bases common in modern syntheses. No two sources produce material exactly alike, but our production strategy irons out batch-to-batch variability so projects can be planned with confidence, whether the user is making five grams for late discovery or hundreds of kilos for an IND campaign.
The chemistry itself is not novel—what matters is what users can do with it. As an actual manufacturer, our job doesn’t stop at producing high-purity powder. We pay attention to those anecdotal details coming from the field—cases where a batch’s particle size helped or hindered filtration, or subtle changes in color hinted at incomplete reactions upstream. Our team schedules regular debriefs with clients from laboratories and process plants to review what worked and where issues cropped up. Minor changes in crystal habit or polymorph can steer performance in sometimes unpredictable ways, so feedback loops remain open. The more we know about use practices in biotech, pharma, and specialty materials, the faster we can adjust reactor conditions, drying protocols, or blending steps to serve evolving needs.
We see firsthand that raw material uniformity forms the backbone of successful patented syntheses. When customers run high-pressure reactors or flow chemistry setups, consistency in melting point and handling properties reduces operator risk and equipment downtime. For instance, teams exploring Suzuki couplings with our 5-bromo-3-fluoro intermediate often report improved yields or selectivity compared to older versions sourced without close manufacturing oversight. That comes not from luck, but through lean manufacturing steps designed to remove process drift and human error at every stage. Trust develops as reaction troubleshooting points back to design of experiment, not errors in raw materials.
From an engineering standpoint, scale brings new variables. Packing lines and reactor prep require tight control over powder flow, clumping, and electrostatic properties. Experience has shown us that tweaking drying times and sieving methods improves downstream handling in robotic feeders and manual scoops alike. We respond in kind, working closely with operations teams to fine-tune micro-details—eliminating unnecessary fines, preventing bridging in hoppers, and streamlining recharging between runs. This sounds basic, but years of field data and site visits prove that real-world bottlenecks rarely show up in the R&D phase, only once hundreds of liters move through reactors on a timeline and under cost constraints.
Producing halogenated and nitrile-containing chemicals carries safety and environmental responsibilities. Our team operates with a boots-on-the-ground mentality—recognizing that proper waste management, engineering controls, and exposure prevention keep our colleagues, customers, and communities safer. By using closed charging systems and real-time process analytics, we reduce off-gassing, minimize spills, and improve first-pass yields. Small adjustments around solvent recovery and waste stream management, learned over years of full-scale campaigns, have lowered both operational costs and environmental footprint.
Handling and shipping these materials requires more than meeting regulatory markers. We’ve learned the extra mile—monitoring drum weights to the gram, tamper sealing pallets, and running cold-chain logistics for especially sensitive batches—prevents returns, wasted time, and downstream contamination far more effectively than post-failure root cause analysis ever could. Teams on the front line of chemical manufacturing benefit from established hazard communication, regular safety drills, and design input for container geometry and labeling. No single checklist covers every use scenario, but our philosophy prioritizes ongoing dialogue and rapid-response technical support. Relationships with our clients run deep because we listen when things go wrong, not just when orders are placed.
Modern R&D environments in pharma, crop science, and material chemistry demand full transparency from their partners. Having walked these factory lines, our leadership understands that trust grows through traceability, not just certificates. Each lot carries its full genealogy, including exact supplier records for starting materials, names of plant operators, and test data from every reactor run. Investigators and quality teams have open access to batch histories, not redacted summaries, so troubleshooting can move from symptom to root cause without hidden gaps. Years of working through customer audits and regulatory reviews have taught us that cutting corners or papering over deviations never ends well for anyone involved.
Users building molecular libraries for drug discovery know that even a one percent impurity can create weeks of confusion in assay data or mislead screening platforms. Drawing on direct production data, we back every lot of 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- with validated analytical support, open raw chromatograms, and method details so researchers don’t find themselves guessing at silent contaminants. It’s not about marketing—it's about preventing avoidable delays, steering clear of costly reformulations, and earning long-haul loyalty from innovation-driven partners who expect more than a transactional supplier relationship.
Experience on both the chemical production line and in customer laboratories shapes how we approach business. We don’t treat intermediates like generic commodities. The insights we gain serve long-term process improvement, feedback-driven upgrades, and investment in talent who know both synthesis and scale-up. When a customer offers observations about reaction homogeneity, post-run clean-up, or crystallization quirks, those details cycle into process control documents—not just for regulatory box-checking, but to hone a product that stands out on the merits. Our digital infrastructure records audit trails, complaint resolutions, and special requests for future batches, so that history translates into continuous performance upgrades. Engagements at technical conferences, plant visits, and customer review sessions provide fresher data than any market survey ever could.
We encourage researchers to connect early and often, asking the tough questions about spectral quality, reactivity deviations, and even container ergonomics. Through these partnerships, we build documentation and protocols that hold water in the real world, not just on spreadsheets. Sourcing directly from the production source, rather than a distributor or trading house, reduces the risk of relabeling or extended supply chains, where traceability suffers and batch history blurs. The aim remains clear: support innovation in synthesis, conserve time and resources, and turn promising molecules from concept into reliable, scalable, and regulatory-auditable reality.
Decades at the bench and in the plant reveal the truest value of reliable chemical intermediates. 2-Pyridinecarbonitrile, 5-bromo-3-fluoro- earns its keep because it adapts to both discovery phase and commercial scale environments with seldom-seen versatility. Whether users focus on drug scaffold elaboration, crop protection leads, or new material development, the similarities and differences with other pyridinecarbonitriles go far beyond a line in a catalog. Direct feedback from those running the reactions, plus relentless attention to shipment, storage, and batch-to-batch reproducibility, shape how this compound is made and delivered.
Every order, every drum, tells a story built through collaboration, listening, and shared learning. This compound holds a steady place in chemical development pipelines because production, packaging, and technical support evolve to meet the rigor of real research—not just compliance-driven form filling. The unique halogenation pattern streamlines modern coupling and substitution strategies, while the manufacturer's involvement ensures that researchers stay equipped with a material that tackles today’s synthesis challenges and tomorrow’s scale-up needs. Our doors stay open to the next generation of problems, confident that open, honest feedback keeps this and every product on a continuous improvement path.