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HS Code |
116927 |
| Chemical Name | 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- |
| Molecular Formula | C6H2BrFN2 |
| Molecular Weight | 201.00 g/mol |
| Cas Number | 406273-11-2 |
| Appearance | Off-white to light brown solid |
| Melting Point | 104-107°C |
| Solubility | Soluble in organic solvents such as DMSO and DMF |
| Smiles | N#Cc1cccc(Br)n1F |
| Inchi | InChI=1S/C6H2BrFN2/c7-5-1-2-4(8)10-6(5)3-9 |
| Pubchem Cid | 10196280 |
As an accredited 2-Pyridinecarbonitrile, 6-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 containing 25 grams of 2-Pyridinecarbonitrile, 6-bromo-3-fluoro-, tightly sealed with a screw cap for safety. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed in 20-foot containers, using proper chemical drums or bags to prevent spillage, contamination, and damage. |
| Shipping | 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- is shipped in tightly sealed containers, protected from light and moisture. The packaging meets hazardous material regulations, ensuring safe transportation. Handle with gloves and protective equipment. Shipping is by approved carriers in accordance with local, national, and international chemical transport guidelines to prevent spillage, damage, or contamination. |
| Storage | **2-Pyridinecarbonitrile, 6-bromo-3-fluoro-** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and properly labeled. Protect from direct sunlight and moisture. Use appropriate safety measures (gloves, goggles) when handling to avoid inhalation or contact with skin and eyes. |
| Shelf Life | The shelf life of 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- is typically 2 years, stored in a cool, dry, sealed container. |
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Purity 98%: 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and low impurity levels in target compounds. Melting point 82°C: 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- featuring a melting point of 82°C is used in custom organic synthesis processes, where it provides predictable solid-state behavior for controlled crystallization. Molecular weight 213.01 g/mol: 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- at a molecular weight of 213.01 g/mol is used in agrochemical research, where its precise mass enables accurate stoichiometric calculations in formulation development. Stability temperature up to 120°C: 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- with stability up to 120°C is used in high-temperature reaction conditions, where it maintains structural integrity and minimizes decomposition. Particle size <50 microns: 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- with particle size below 50 microns is used in fine chemical manufacturing, where enhanced dispersibility leads to improved reaction uniformity and product performance. Solubility in DMF: 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- demonstrating high solubility in DMF is used in solution-phase synthesis, where it allows for homogeneous reaction mixtures and efficient product isolation. HPLC purity ≥99%: 2-Pyridinecarbonitrile, 6-bromo-3-fluoro- with HPLC purity of 99% or greater is used in medicinal chemistry applications, where trace contamination is minimized and reproducibility is maximized. |
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Working directly with heterocyclic chemistry, we understand how the subtle interplay of molecular structure and purity can steer outcomes in complex syntheses. One compound that stands apart in our catalog is 2-pyridinecarbonitrile, 6-bromo-3-fluoro-. Over years of developing and scaling specialty pyridines, our experience highlights the transformative value these fine chemicals deliver in modern research and manufacturing.
Our 2-pyridinecarbonitrile, 6-bromo-3-fluoro-, produced at controlled scales in our own reactors, features careful batch monitoring and consistent traceability. This compound, with the molecular formula C6H2BrFN2, combines a bromo group at the 6-position with a fluorine at the 3-position, plus the functional group of a nitrile at the 2-position. As a manufacturer, producing this molecule requires tight control over process parameters, particularly during halogenation and subsequent cyanation steps.
Customers and collaborators often approach us with the same question: Why choose this substituted pyridine variant over a simpler or less decorated analog? The answer lies in how the specific patterning of bromine and fluorine atoms, together with the nitrile handle, lets the molecule serve as a highly versatile intermediate. These modifications unlock regioselective reactivity, serve as anchor points for cross-coupling, and tune the electronic environment of the ring system with finesse.
Producing 2-pyridinecarbonitrile, 6-bromo-3-fluoro- calls for precision throughout each phase. Rigorous purification by column chromatography or preparative HPLC consistently ensures high purity—essential for both academic and industrial chemists chasing reproducible results downstream. Every batch is monitored by NMR, mass spectrometry, and HPLC. Here in the plant, spot checks for common residual metallics, GC screening for potential solvent carryover, and periodic in-depth stability trials form the backbone of our quality program.
Due to the delicate balance required during halogen introduction and cyanation, we’ve refined our synthetic route to minimize byproducts and optimize yields. Over time, subtle tweaks—like temperature ramp rates or alternative bases—proven in our pilot facility have migrated into our main production lines. As a result, we typically achieve batch purities around 98% or greater by HPLC, and we actively seek feedback from long-term buyers who use this product in downstream transformations.
Through conversations with technical directors and R&D labs, we’ve learned exactly how this compound earns its keep. The bromo and fluoro positions are neither random nor purely academic; these functionalities open doors for cross-coupling, nucleophilic aromatic substitution, and late-stage diversification. The nitrile at the 2-position gives medicinal chemists another handle for further elaboration, including conversion to amidines, tetrazoles, amides, or primary amines.
In medicinal chemistry, scientists leverage 2-pyridinecarbonitrile, 6-bromo-3-fluoro- as a scaffold for kinase inhibitor discovery or as a building block for CNS-active heterocycles. Small tweaks in the pyridine ring electronics—down to the atom—often spell the difference between inactive and breakthrough molecules, and we’ve had the opportunity to listen firsthand as our clients explain how our material feeds into their programs. Custom syntheses using our compound have led to library expansions, allowing SAR exploration along both the bromo and fluoro axes. We have witnessed a surge in requests from agrochemical project teams aiming to build more environmentally conscious crop protection molecules, where the fine control over substitution patterns proves essential to tuning both activity and persistence.
Trustworthy supply is critical. Many users cite that some third-party offerings occasionally suffer from lot-to-lot inconsistency or unreliable documentation. Since every production run takes place on our premises, all characterization data, CoAs, and references trace back to our in-house analytics. This means our partners receive both a rigorous product and the story behind its synthesis, available for deeper audit or regulatory review.
Not every pyridinecarbonitrile meets the rigorous standards demanded by modern targets. Simple analogs—lacking bromine or fluorine—sometimes fail to deliver the same chemical latitude. For instance, fluorine at the 3-position provides potent leverage in metabolic stability, often mediating dramatic improvements in pharmacokinetics. Medicinal chemists who have used basic 2-pyridinecarbonitrile frequently report improved selectivity and binding affinity after incorporation of bromine or fluorine at key ring sites.
The bromo group serves as an optimal handle for Suzuki, Buchwald-Hartwig, or Stille cross-couplings. Some clients originally invested in more common chloro analogs but switched after hitting stubborn regioselectivity hurdles or sluggish reaction rates. Bromine strikes a better balance between reactivity and stability than chlorine, especially in high-throughput campaigns. Having both functionalities present in the same molecule empowers users to explore broader Structure-Activity Relationship spaces with fewer synthetic steps, a detail that rarely escapes the attention of teams under tight timelines or budgets.
Compared against 2-pyridinecarbonitrile alone, the 6-bromo-3-fluoro- variant allows users to traverse new synthetic territory. The dual halogenation pattern means that parallel cross-coupling campaigns can run from a single precursor, saving time and cost. Notably, one of our long-standing customers in Japan developed an innovative library of anti-infectives by sequentially exploiting both halogens, highlighting how this single intermediate can catalyze exploratory work previously requiring a half-dozen customized starting points.
Such differences don’t always show up in summary tables. As manufacturers, every time we generate this product, our staff notice the aroma, the solubility profile, and operational quirks compared with less decorated pyridines. Highly substituted pyridines sometimes foam more, absorb differently on silica, and demand unique handling during crystallization. Over the years, we’ve built these lessons into our manufacturing SOPs, translating direct observation into better batch reproducibility and faster fill-and-finish operations. Our warehouse crew still points out how the storage stability and lower caking tendency make this compound less fussy compared to more polar analogs.
Manufacturing fine chemicals like 2-pyridinecarbonitrile, 6-bromo-3-fluoro- rarely unfolds perfectly on the first take. Each change in reagent source or small process tweak can have unexpected downstream impacts. Early on, we encountered yield drops tied to subtle pH swings during workup. Through cycle-after-cycle improvements, data-logging, and operator training, these hurdles turned into lessons and then protocols. Consistency now stems from deep process control and cumulative know-how.
Trace impurities, such as residual halides or solvent fragments, used to present seasonal variability. Once we isolated the root causes—detailed off-shift operator logs helped here—extra filtration steps and slight temperature nudges solved what once seemed perpetual. Today, our QA team routinely batches out purities high enough to support both research and early clinical or agro use without the last-minute reprocessing often required by bulk-oriented suppliers.
Scaling this molecule from flask to plant demanded real-world creativity. Analytics alone couldn’t always pinpoint where unwanted byproducts hid. Only by running semiworks campaigns and charting every anomaly did we uncover the critical mix and hold times that prevent side reactions. In our sector, knowledge acquisition rarely travels in a straight line; we often learn more fixing a batch than through any textbook example. Each production run feeds experience back into our continuous improvement cycles, benefiting future batches and long-term customer trust.
Ensuring stability and ease of handling stands as a daily concern in our plant. With 2-pyridinecarbonitrile, 6-bromo-3-fluoro-, we found that sealed amber containers and inert gas backfilling during packaging retain product integrity throughout long shipments. We’ve field-tested these protocols after watching early samples degrade when left in poorly sealed jars. Feedback from both Europe and US partners guided us toward containers that stand up to repeated opening and recapping.
We encourage open communication with every order. Many process chemists report that our material dissolves quickly in standard solvents and survives ambient shipping better than rivals. On the rare occasion of clumping or color drift, customer input returns straight to the production floor, where QA and synthesis teams make rapid corrections. Unlike a trading house, direct manufacturing means we own root cause diagnosis and have authority to make process or packaging changes for any recurring issue.
Demand for transparent documentation runs high. Each lot ships with a full analytical package, compiled by our in-house lab. Notarized NMR spectra, HPLC traces, and detailed synthesis routes remain available to any regulatory body or customer audit, supporting not just compliance but open science. Many small labs have shared their gratitude for this support when regulatory review cycles stress their resources.
Decades spent in synthesis reveal the dual pressures of efficiency and safety. Embracing sustainable chemistry means more than switching solvents or chasing green checklists. With this nitro-bromo-fluoro pyridine, all spent reaction streams undergo on-site neutralization, halide recycling, and exhaust monitoring. This industry still faces difficulties with the disposal of halogenated waste, and we continually adapt with both mechanical upgrades and chemist retraining.
Colleagues across the industry share worries over large-scale halogen introduction or management of cyanation byproducts. While the risks persist, upstream engineering—such as contained reaction vessels and improved local scrubbing—reduces exposure risks and protects both staff and community. Transparency on these challenges builds trust with downstream partners, who increasingly want assurance that production won’t compromise health or environment. We’ve responded by opening our plant doors for regular third-party review, welcoming scrutiny as a driver for real progress.
Suppliers face rising stakeholder demand for lifecycle data, not just product performance. By building out cradle-to-gate carbon tracking and conducting regular internal audits, we equip our partners to meet their own sustainability goals. We view these measures not as cost centers, but as investments in both operational resilience and long-term relationships.
As synthetic tasks grow more demanding, collaboration between chemists and producers becomes ever more vital. Off-the-shelf chemicals only go so far. Time and again, users come back seeking modifications: higher-scale custom runs, switchups in crystallization solvents, or altered particle size distributions for automated dosing equipment. With each request, we see what sets direct manufacturing apart—responsiveness, process transparency, and a sense of shared purpose.
More than one medicinal chemistry team credits faster hit-to-lead progress to access to variants made on our line, rather than struggling with non-reproducible material from resellers. In the synthetic crop protection space, project managers rely on our continuity of supply for scale-up campaigns that stretch over years and regulatory cycles. These partnerships not only foster innovation but ensure no project gets derailed by a lost recipe or supply chain hiccup.
Direct lines of communication often let us catch problems before they reach the bench. For instance, we’ve adjusted drying parameters after learning that automated weighing robotics on a customer’s bottling line choked on fine particles. These iterative improvements feed back into our product—and ultimately deliver better value to end-users.
Every successful run of 2-pyridinecarbonitrile, 6-bromo-3-fluoro- tells a story about chemistry, commitment, and curiosity. From the earliest attempts with small flasks and endless TLC plates, to the present day’s multi-kilo reactors, our team sees this product not as a static commodity, but as a living part of hundreds of research narratives worldwide.
No two requests look alike. Some call for multi-step documentation for clinical trial supply. Others want advice blending this pyridine with rare coupling partners or guidance on long-term storage for regulatory filing. By staying close to the bench and valuing each conversation—positive or negative—we continue adapting our approach to fit how real people use our chemistry in the real world.
Inventiveness remains built into our process DNA. The technical staff, many of whom hold years of bench chemistry experience, keep a direct connection to both the practicalities and the possibilities of these compounds. Their feedback loops into everything: raw material evaluation, process modification, even the rhythms of reactor maintenance and solvent recycling. Long nights troubleshooting a stubborn batch translate to smoother runs in the future—not just for us, but for every customer downstream.
Manufacturing fine chemicals for applied research and industry rewards those who pay attention to detail. Experience has taught us that no shortcut can match disciplined process control. With 2-pyridinecarbonitrile, 6-bromo-3-fluoro-, our journey continues to be shaped by evolving applications, constant problem-solving, and honest exchanges with the people who rely on what we make.
In a landscape filled with resold, relabeled drums and fading batch histories, we believe hands-on production, transparent documentation, and open dialogue stand out as true markers of trust. The future of chemical manufacturing will keep raising the bar—but as long as synthetic innovation depends on building blocks like this one, we expect to keep learning, improving, and delivering results batch after batch.
For scientists needing a differentiated, well-characterized intermediate to push their latest project forward, 2-pyridinecarbonitrile, 6-bromo-3-fluoro- offers a bridge between theory and tangible results—supported by the processes, people, and perspective of a manufacturer committed to real-world outcomes.