|
HS Code |
828921 |
| Chemical Name | 3,5-Difluoropyridine-2-carbonitrile |
| Molecular Formula | C6H2F2N2 |
| Molecular Weight | 140.09 g/mol |
| Cas Number | 183865-19-8 |
| Appearance | White to off-white solid |
| Melting Point | 67-70°C |
| Solubility | Soluble in common organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=NC(=C1F)C#N)F |
| Inchi | InChI=1S/C6H2F2N2/c7-4-1-5(8)10-6(2-4)3-9 |
| Synonyms | 2-Cyano-3,5-difluoropyridine |
| Storage Temperature | Store at room temperature |
As an accredited 3,5-Difluoropyridine-2-carbonitrile 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 3,5-Difluoropyridine-2-carbonitrile, sealed with a tamper-evident cap and labeled for laboratory use. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 3,5-Difluoropyridine-2-carbonitrile securely packed in 25kg/drum, 9 tons (approx. 360 drums) per container. |
| Shipping | 3,5-Difluoropyridine-2-carbonitrile is shipped in tightly sealed containers, protected from moisture and light. It is transported in compliance with relevant chemical and hazardous material regulations. Handling requires appropriate labeling and documentation, with provisions for safe storage and spill response during transit to ensure stability and avoid contamination or accidental release. |
| Storage | 3,5-Difluoropyridine-2-carbonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep the chemical away from incompatible substances such as strong oxidizers. Ensure proper labeling and avoid exposure to moisture. Use suitable chemical storage cabinets and follow all relevant safety guidelines for hazardous chemicals. |
| Shelf Life | 3,5-Difluoropyridine-2-carbonitrile has a shelf life of at least 2 years when stored in a cool, dry, airtight container. |
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Purity 98%: 3,5-Difluoropyridine-2-carbonitrile with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal reaction yield and reduced by-product formation. Melting Point 49–52°C: 3,5-Difluoropyridine-2-carbonitrile with a melting point of 49–52°C is used in agrochemical development, where controlled melting point allows precise formulation processing. Stability Temperature up to 60°C: 3,5-Difluoropyridine-2-carbonitrile with stability temperature up to 60°C is used in high-temperature organic synthesis, where thermal stability maintains compound integrity during reactions. Particle Size <10 μm: 3,5-Difluoropyridine-2-carbonitrile with particle size below 10 μm is used in catalyst preparation, where fine particle size enhances surface reactivity and dispersion. Moisture Content ≤0.5%: 3,5-Difluoropyridine-2-carbonitrile with moisture content ≤0.5% is used in electronics chemicals manufacturing, where low moisture prevents unwanted hydrolysis and preserves product properties. Assay ≥99%: 3,5-Difluoropyridine-2-carbonitrile with assay ≥99% is used in custom chemical synthesis, where high assay ensures chemical accuracy and reproducibility in multi-step syntheses. |
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Every batch of 3,5-Difluoropyridine-2-carbonitrile reflects our commitment to purposeful design and process rigor at the plant level. This compound, recognized for its dual fluorine atoms at the 3 and 5 positions and the carbonitrile functional group at the 2 position, plays a distinctive role in fine chemical synthesis. In years of operation, our team has seen demand trends carry this compound from research-scale specialties to consistently requested intermediates for agrochemical, pharmaceutical, and specialty material development.
We produce this molecule under controlled environments with processes refined through practical experience—decisions shaped by actual outcomes on our floor, not only on paper. Customers rely on our consistency, underscored by in-house documentation of batch homogeneity, and robust analytical oversight. Modern spectroscopic methods, including HPLC and NMR, guide batch approvals. There is no substitute for walking past vessels and trusting our team’s hands-on approach; we have learned that inspection at every critical juncture outperforms theoretical risk assessment.
3,5-Difluoropyridine-2-carbonitrile leaves our facility with a minimum purity of 98%, as established by internal audits and external collaborators’ feedback. The appearance can range from off-white to pale yellow crystalline solid; this variation owes to lot-to-lot raw material nuances, but we’ve learned how subtle color differences correlate more with synthesis scale than performance in downstream reactions. Moisture is managed through high-efficiency drying and sealed packaging, as hydrolysis risks can compromise the carbonitrile moiety.
Each container is checked for appropriate sealing and uniform distribution so researchers—whether scaling early process samples or larger, production-size batches—do not wrestle with caking, unplanned contamination, or uneven packing. Packaging choices, such as amber glass for photolabile customers, are available based on decades of feedback from hands-on practitioners.
We have supplied 3,5-Difluoropyridine-2-carbonitrile to teams working on advanced heterocyclic scaffolds, preparing pyridine-based fungicides, and developing next-generation medicinal chemistry pathways. In process development, we’ve watched this compound prove its worth during Suzuki coupling, nucleophilic aromatic substitution, and subsequent transformations. Chemists working with this intermediate frequently pursue targets such as substituted pyridines, fluorinated pyrimidines, and complex ring systems for drug programs or target-specific crop protection agents.
Feedback loops between our process engineers and customer R&D units have been vital. Issues like scaling exothermic steps or unexpected byproduct formation often trace back to fine adjustments in pressure control or the order of reactant addition. Sharing those operational lessons with users has cut hours of troubleshooting—more than any datasheet tweak ever could. Many clients have remarked on improvements in downstream yield and purity when swapping from older, less consistent supplies to ours, especially during critical alkylation or reduction steps.
Solubility in common laboratory solvents remains straightforward, with the compound dissolving in chloroform, DMSO, and acetonitrile. Some customers have asked about alternative, greener solvents: Our field experience suggests that the molecule’s robust pyridine ring and nitrile group retain their character across a fair range of polar aprotic environments, though we always encourage small-scale validation when new process solvents are proposed.
Chemicals like 3,5-Difluoropyridine-2-carbonitrile require a blend of prediction and ground-level troubleshooting. Our operations evolved to handle exothermicities and oxidative sensitivity well before larger market demand appeared. Plant utilities—ventilation, chilled circulation systems, and real-time vapor monitoring—arose from one too many sticky reactor incidents. Our priority, forged by past line shutdowns, centers on maintaining tight environmental control from synthesis to packaging.
We prefer precision through regular calibration of weighing instruments and online sensors, checked by humans who recognize the faintest discrepancy in measured values versus expected reactivity. Unexpected foaming or solubility during workup sometimes signaled a tank’s service interval or a subtle change in a key raw material. We’ve learned that ignoring these weak signals often leads to reprocessing, lost hours, and wasted energy. Sooner or later, this approach yields less photo- and thermo-degradation in finished product—and better results for our customers’ syntheses.
3,5-Difluoropyridine-2-carbonitrile stands apart from many of its analogs. The positional fluorination impacts electron density on the ring, directly shaping reactivity during subsequent synthetic steps. Chemists in the field often report increased selectivity in cross-coupling or aromatic substitution due to this unique substitution pattern. The carbonitrile group at the 2 position invites further functionalization, enabling access to a variety of derivatives without introducing additional ring activation elsewhere.
In comparison, mono-fluorinated or non-fluorinated pyridine nitriles often display less predictable results under translational catalysis or amination routes. The double fluorination at 3 and 5 influences both product stability and downstream modification potential. Our own comparative batches, run for contract research groups, have underlined these points—all while highlighting the challenges presented by similar compounds on handling (such as 2,3-difluoropyridine-5-carbonitrile) that may show higher volatility or less controlled crystallization.
From the first pilot runs, our team tracked how different end-uses handled these differences. Agrochemical and pharmaceutical groups repeatedly chose our 3,5-difluorinated compound for its cleaner profile in late-stage development, stating longer shelf life and less demand for additional purification. This fits with our QC findings: The dual fluorination confers both chemical and physical stability, reducing the formation of isomeric byproducts during storage and synthesis, unlike analogs with alternate halogen placement.
Direct communication with downstream partners steered us away from single-solvent solutions for washing or extraction. Some of the earliest purification hurdles disappeared only after multi-solvent protocols—no substitute for process trials that test theory at scale.
Batch management success depends on more than the reaction itself; downstream handling and shipment require equal care. We run repeated checks on temperature sensitivity during transit, particularly through variable climates, after several hard-won lessons involving stress cracking and unexpected moisture ingress. Each time a minor packaging tweak prevented a bigger loss, our team internally catalogued the fix and reported it into subsequent production rounds.
Feedback from laboratory and pilot-plant users led us to introduce tamper-evident seals and revisit dry box requirements, as compounding humidity in poorly conditioned storerooms can degrade product over months. Our approach includes providing straightforward documentation—not just what a regulator needs, but also relevant handling notes that come out of real use. Customers shared back insights that proved invaluable, such as the ideal time window between opening and full consumption, or the benefits of immediate inert gas backfilling for longer-term storage.
We believe packaging does not just protect a product—it safeguards research momentum. One delayed trial due to compromised material can upend weeks of schedules and budgets, a lesson we learned in partnership with process development chemists working toward regulatory approval. Responding to these demands, our packaging evolution includes customizable lot sizes, careful moisture monitoring, and robust outer containers for extended shipment durations.
Operating a chemical manufacturing plant means fielding a spectrum of questions around environmental management and regulatory compliance. For compounds like 3,5-Difluoropyridine-2-carbonitrile, every improvement in waste reduction or solvent recycling comes from observing actual outcomes, sometimes after an avoidable spike in disposal costs or new regulatory guidance. Our team learned from local authorities on fugitive emissions reporting and quickly instituted monitoring for points in our synthesis that risked minor raw material loss.
Daily reality includes monitoring stack emissions, upgrading scrubbing units for halogenated vapor capture, and evaluating every process change for downstream impacts. When we shifted one synthesis step to a lower temperature, not only did the batch consistency improve, but the lab’s ventilation needs eased and solvent losses dropped. These are not theoretical advantages—they come out of measuring, adjusting, and trying again until improvement shows in both inspection logs and lowered energy bills.
Certification from national and international agencies followed improvements made on the floor, not the other way around. Our team regularly reviews new compliance standards, learning which production tweaks can cut both risk and overhead without increasing lead times for demanding R&D programs.
Researchers and manufacturers share a common goal: reliable, reproducible outcomes. In close partnerships with external scientists, our team often participates in problem-solving beyond mere supply logistics. Hands-on troubleshooting has refined recommendations around storage temperature, inert atmosphere handling, and preferred solvent systems that match our own plant-side findings.
We’ve taken part in round-table discussions on expanding synthetic utility for 3,5-Difluoropyridine-2-carbonitrile, where knowledge exchange led directly to improved catalyst loads or elimination of unnecessary salt washes. These suggestions stem from ongoing observation, not external literature alone. For example, one collaborative feedback loop led us to introduce flame-sealed containers for highly sensitive compound sub-lots, speeding up intake qualification at the user’s site by days, not hours.
Our team also offers insight on competitive testing against other intermediates. With a clear understanding of how different substituents interact in cyclization or oxidation stages, we can guide process choices that reduce overall material loss and shrink timelines.
Manufacturing 3,5-Difluoropyridine-2-carbonitrile is never a static operation. Our process logs cover more than a decade of continuous improvement, analyzing both successful runs and early mistakes. We learned about batch contamination not from customer complaints, but often before material left our site, leading to new filtration and centrifuge protocols. Temperature excursions in early summers led to staggered production scheduling and investment in cooling redundancy. Each lesson shapes a tradition of operational vigilance.
Repeat customers recognize the value of this consistency. Some have shifted entire research pipelines or product launches to rely on our supply, crediting a lower rate of requalification or reanalysis—a claim we don’t take lightly, as it reflects years of measuring reaction outcomes and product stability profiles in real use.
Achieving this reliability hinges on frequent, honest communication channel between plant floor, analytical lab, and clients in production or discovery units. Direct observations—what works and what delays progress—inform not only in-house improvements but also shape the best practices our customers take away to their own processes.
Amid evolving market conditions or raw material fluctuations, we lean on a blend of data-driven vigilance and hands-on experience. Inventory planning, buffer stocks, and alternate sourcing appeared in our operations not by policy decree, but from actual shrinkage events or supply breakdowns. Our chemists see market pressure not as a disruption, but a challenge for continuous ingenuity.
Our credibility grows through experience, not only by meeting formal standards but by anticipating research and manufacturing needs. Each request—whether an urgent single kilogram for a pilot project or multi-ton consignments for a drug expansion—receives attention informed by years spent watching actual impacts. From exacting release criteria to lessons learned through hands-on troubleshooting, our reputation connects to outcomes in actual chemistry, not theory.
Technical support lines are staffed by chemists who use our own products. Site visits and customer audits do more than check boxes; they call attention to day-to-day realities, highlighting bottlenecks or suggesting incremental fixes before they become persistent issues. Trust, in our experience, grows not from big promises but from small, regular demonstrations of reliability, technical competence, and transparent discussion of risks.
Customers have remarked that our practical advice—warnings about solvent compatibility, tips for long-term sample retention, or strategies for scale-up—has proven valuable when compared to the generic guidance sometimes offered by traders or non-specialist suppliers. This is a result of having synthesized, stored, and shipped the chemical ourselves, tracking how every tweak impacts both analytical outcomes and customer workflows.
3,5-Difluoropyridine-2-carbonitrile deserves more than generic handling. As originators and ongoing stewards of its production, our outlook is rooted in real-world learning. Improvements spring from feedback, mistakes, and the drive to keep processes reliable amid shifting requirements and increasingly complex end uses. Supporting chemists as they innovate means not only producing a pure, stable intermediate, but backing it with contextual knowledge earned from years on the plant floor and through direct engagement with those advancing science at the bench.
Every order reflects a shared investment: we recognize not only your trust, but the cost in time and opportunity tied to a well-made batch. We continue to build on that understanding, refining process, upgrading quality, and advocating for your success at every step—knowing that new applications and greater expectations will challenge us to produce even more reliable outcomes down the line.