4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile

    • Product Name: 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile
    • Chemical Name (IUPAC): 4,6-dibromo-1H-pyrazolo[1,5-a]pyridine-3-carbonitrile
    • CAS No.: 356783-16-9
    • Chemical Formula: C8H3Br2N3
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    913956

    Productname 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile
    Casnumber 1330565-11-1
    Molecularformula C8H3Br2N3
    Molecularweight 319.94
    Appearance Solid
    Purity Typically ≥98%
    Solubility Slightly soluble in DMSO, DMF
    Storagetemperature Store at 2-8°C
    Synonyms 6,4-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile
    Smiles C1=CN2C(=NC=C(C2=N1)Br)C#NBr
    Inchikey WGXIVNFIQJODPC-UHFFFAOYSA-N

    As an accredited 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25g of 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile supplied in a sealed amber glass bottle with tamper-evident cap.
    Container Loading (20′ FCL) 20′ FCL container loading for 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile: Securely packaged, maximizing space efficiency and preventing contamination.
    Shipping Shipping of **4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile** is carried out in tightly sealed containers, compliant with chemical transport regulations. The material is typically packaged with cushioning to prevent breakage and labeled appropriately with hazard information. Temperature control and handling precautions are observed to ensure safe and secure delivery.
    Storage Store 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Ensure the storage area is clearly labeled and access is limited to trained personnel. Follow all relevant safety protocols and local regulations for hazardous chemicals.
    Shelf Life 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile is stable for at least two years if stored in a cool, dry place.
    Application of 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile

    Purity 98%: 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal by-product formation.

    Melting Point 230°C: 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile with a melting point of 230°C is used in high-temperature organic reactions, where it offers thermal stability and process reliability.

    Particle Size <10 µm: 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile with particle size less than 10 µm is used in solid dispersion formulations, where it improves dissolution rate and uniformity.

    Moisture Content <0.5%: 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile with moisture content below 0.5% is used in moisture-sensitive syntheses, where it prevents hydrolytic degradation and maintains compound integrity.

    Storage Stability 24 Months: 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile with a storage stability of 24 months is used in chemical stock management, where it ensures long-term usability and consistent performance.

    Molecular Weight 289.95 g/mol: 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile with molecular weight 289.95 g/mol is used in custom heterocycle assembly, where it allows precise stoichiometric calculation for scalable synthesis.

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    Certification & Compliance
    More Introduction

    Introducing 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile: The Chemical Backbone for Next-Generation Synthesis

    Leading the Way with Molecular Precision

    At our lab, every batch of 4,6-Dibromo-pyrazolo[1,5-a]pyridine-3-carbonitrile reflects years of experience on the manufacturing floor, not just in theory but in daily practice. The molecule—often referred to by its model number, DBPP-3CN—brings together a balance of reactivity and stability seldom found in heterocyclic intermediates. The compound's structure, defined by two strategically placed bromine atoms and a cyano group at the 3-position, pushes the boundaries for chemists working on the synthesis of pharmaceutical compounds, agrochemicals, and organic electronics.

    The Drive Behind Manufacturing This Compound

    Many years operating reactors, optimizing purification, and studying reaction mechanisms firsthand have taught us where bottlenecks appear and how inventive tweaks to a molecule's backbone might reduce downstream waste or streamline conversions. A few decades ago, options for pyrazolo[1,5-a]pyridine derivatives were narrower. Chemists working at the interface of drug design craved new building blocks—ones robust enough to handle grueling multi-step syntheses and compatible with diverse coupling techniques. We developed our process for DBPP-3CN to address these gaps, drawing from iterative improvements in bromination and cyanation sequence management.

    How 4,6-Dibromo Differentiates Itself

    The arrangement of the bromine atoms at the 4 and 6 positions earns DBPP-3CN its spot in advanced research pipelines. Experienced medicinal chemists will recognize how this arrangement unlocks far more selective cross-coupling pathways than the more common mono-brominated variants. The difference plays out at the lab bench: cross-coupling yields are higher, purification is easier, and the by-product profile is cleaner. Our technicians routinely report less chromatographic tailing—a welcome relief on busy shift days.

    The 3-carbonitrile motif pushes versatility further. Cyano groups often serve as both synthetic handles and key functional motifs, acting as precursors for a range of downstream transformations: amides, tetrazoles, and more. This duality sets DBPP-3CN apart from non-cyano analogues, making it a strong candidate for programs spanning medicinal, agricultural, and high-performance materials chemistry.

    Working with Our Product: Real-World Considerations

    A major driver behind customer preference for our DBPP-3CN rests with its physical properties. Unlike some fine chemicals, DBPP-3CN presents as an off-white to beige solid, offering manageable dusting tendencies. Our own operators appreciate the reduced risk of airborne particulate—something often mentioned by process safety teams. The compound typically shows good solubility in polar aprotic solvents, including DMF and DMSO. We reached this level through persistent tweaking of crystal forms and tight control over the final drying process.

    Our controlled process parameters mean customers can avoid headaches linked to batch-to-batch variability. As a manufacturer, we believe these seemingly small production details matter a great deal once the compound enters a high-throughput workflow. Not having to double-check melting points or suspect pH swings saves laboratory time and maintains project timelines—an advantage pointed out to us by more than one project chemist over the years.

    Applications Shaped by Manufacturing Knowledge

    In pharmaceutical R&D, researchers searching for new kinase inhibitors or CNS candidates have been quick to embrace DBPP-3CN as a pivot point for structure diversification. The dibromo scaffold offers reliable anchoring for Suzuki or Buchwald–Hartwig couplings, letting chemists attach aryl or amine groups selectively at either the 4 or 6 position before or after further functionalization of the nitrile. Our familiarity with these pathways comes directly from trials in custom synthesis campaigns. We have seen how strategic use of this compound can shorten timelines in early-stage library synthesis.

    In crop protection, our direct conversations with application labs revealed the demand for molecular frameworks carrying both strong electron-withdrawing and halogen features. DBPP-3CN fits neatly into new classes of fungicides and insecticides, where halogen placement forms the basis for improved activity or better metabolic profiles. Here, scalable access to material with controlled purity and traceability cannot be stressed enough. We take particular pride in our ability to trace batches from the reactor to the client’s bench—no mixed lots, no surprises.

    Even in electronic materials, the rigid, planar core of pyrazolo[1,5-a]pyridine supports charge mobility pathways, and bromination provides exit points for further tuning of photophysical properties. A few years back, engineers in the OLED field asked for grams to prototype organic light-emitting layers; they noted the importance of the cyano group for balancing electron affinity, which determined both color purity and operational stability.

    Specification Decisions Drawn from the Factory Floor

    Early trials led us to offer DBPP-3CN with a minimum purity of 98%, confirmed by both HPLC and NMR. Lower grades occasionally find use in bulk agricultural synthesis, but experience showed us that maintaining this high spec prevents downstream failures during scale-up—especially in pharma and electronics applications. Achieving this threshold meant investing in column technology that gives sharp separations, making sure side products like unreacted precursors or mono-brominated impurities stay below 1%. This level of control is rarely found outside original manufacturers and is a cornerstone of our supply assurance.

    Customers sometimes ask about options for higher purities or special formulations. Over the years, we have produced material up to 99.5% on custom request, especially for those running long stability studies or developing analytical standards. We recommend vacuum-sealed packaging to protect from moisture ingress, as repeated studies have shown trace hydrolysis can slightly shift the melting range. Tank infrared dryers and glovebox packaging lines came at a real cost, but the return shows up not just in technical specs but in customer trust.

    Learning from Process Improvements and Challenges

    Making DBPP-3CN isn’t trivial. The bromination step can lead to safety concerns due to exothermic behavior, so we rely on jacketed reactors with precision temperature control. Our engineering staff have tested and installed automatic quench protection, which eliminated the occurrence of runaway temperatures. Scaling up, we discovered that poor agitation could form dead zones in the vessel, leading to localized overbromination and unwanted isomers. It took a redesign of our stirring system and a bit of hands-on troubleshooting to maintain reliable selectivity.

    A major concern at the post-synthesis stage involves filtration and drying. Early batches encountered fine filtration problems due to the compound’s crystalline size distribution. We upgraded to a multi-stage filtration train, combining depth media with fine mesh screens, ensuring clear separation and minimizing waste. An ongoing dialogue with our downstream users taught us that trace solvents in the final product could cause headaches during subsequent reactions. Now, we keep residual solvents below 500 ppm, as confirmed by routine GC analysis.

    Why Original Manufacturing Matters

    Purchasing directly from producers makes a difference. Over the past decade, too many customers have returned with stories of product sourced from trading channels where key data never matched reality, and inconsistent purity grounded entire projects. Our in-house analytics mean each shipment includes a batch-specific report—one our own process chemists review, not a faceless quality desk offsite. Feedback cycles with R&D teams help us tweak later runs, often long before problems grow large enough to affect outcomes.

    The ability to control source and documentation stands out as a big reason researchers keep coming to the original factory. We manage everything onsite, from initial weigh-in of starting materials to final closing of drums. If a customer has questions about an impurity or a shift in melting range, our technical leads know the answer, because most times, they ran the batch themselves. Real-world manufacturing isn’t about ticking boxes; it’s about knowing what actually leaves the plant and how it’ll behave in your specification.

    Setting Ourselves Apart from Other Suppliers

    Chemical supply chains follow a crowded landscape. Traders and repackagers meet some needs, but those further downstream risk running into unspecific paperwork, mixed product, or, worse, counterfeit or degraded lots. In contrast, our facility runs 24/7 for core customers, with each lot tied by serial to raw materials checked against internal documentation. Last year alone, we scrapped three entire runs rather than risk sending out-of-spec material—a painful decision financially, but the kind of choice a manufacturer makes to uphold commitments.

    Many end users have come to rely on the uniform batch-to-batch characteristics we deliver. Unlike distributed product, which may be stored under unpredictable conditions, our logistics protocol ensures controlled temperature and humidity from factory to warehouse. This approach isn’t easy, but the alternative—variability in reactivity, unpredictable side-band peaks in NMR, sluggish dissolution times—ends up costing far more in wasted development hours and failed scale-ups.

    Feedback as a Driver of Process Innovation

    Partnerships with large pharmaceutical and agrochemical firms have pushed us to upgrade raw material sourcing protocols and analytical calibration. A contract synthesis client pointed out years ago that minor residuals of iron or copper could poison certain catalysts. From this, we introduced inline metal scavenging and periodic trace metals quantification by ICP-MS. It’s one thing to run spot checks; it’s entirely another to hardwire continuous improvement into production.

    Direct customer feedback also inspired us to introduce standardized 1 kg, 5 kg, and 20 kg pack sizes, matching the most common R&D and pilot batch needs. Smaller pilot-scale users wanted better handling; our packaging team designed PTFE-lined caps to stop ingress from even persistent atmospheric moisture, as moisture-sensitive reactions performed by some clients demanded zero tolerance for water uptake.

    Pushing Boundaries in Product Development

    The breadth of applications for DBPP-3CN continues to expand as research teams push for molecules with tight, precise functions. A couple of years back, a team developing ligands for new chelation resins discovered that small tweaks in both the bromine and cyano placement changed metal-binding selectivity. That work would have languished using less pure or inconsistently produced material. Likewise, an academic group studying fluorescence tagging prioritized our high-purity batches because their probes’ quantum yields depended on minimal background signals.

    Some innovations originate internally. Our technical group regularly tests reaction routes for transforming DBPP-3CN to biaryls, amides, or even fused polycyclic compounds. Lessons learned in these small-scale demos feed directly back into process tweaks. By keeping technical and production teams under one roof, we ensure the learning cycle repeats quickly, without red tape.

    Benefits Backed by In-House Experience

    Every production run tells a story. Sometimes, issues show up unexpectedly—an odd batch color, a faint off-odor, a minor shift in crystalline habit. Drawing on decades of in-house know-how, the team investigates every new blip, correlating data from NMR, IR, and HPLC with conditions logged during synthesis. This diligence feeds back into our training system for new hires, who learn firsthand that “close enough” rarely is.

    High specification on DBPP-3CN, in our view, means more than a number on a datasheet. It reflects a commitment not just to analytical thresholds, but to understanding how those numbers translate into better downstream transformations, less operator intervention, and more predictable results for every scientist relying on our work at each step of their research.

    Adapting to Evolving Regulatory and Market Needs

    As global regulations tighten on halogenated intermediates, tracking and documentation grow ever more important. Our compliance team stays current with relevant import, export, and storage standards. This vigilance emerged from practical experience—years ago, missed paperwork delayed shipments and cost research timelines dearly. Now, automated monitoring of documentation and lot-specific archiving mean that when a customer’s regulatory auditor asks for full traceability, everything is ready at hand—no rework, no panicked calls to third parties.

    Sustainability also influences our DBPP-3CN production. Facing growing demand to reduce downstream environmental impact, we invested in closed-loop solvent recovery and emissions scrubbing. Operator training emphasizes not just safety, but minimizing waste at every stage—earned lessons from our own early days, sorting through heavy drums of spent solvents and seeing the cost, both environmental and economic, of not planning ahead.

    What Sets the Manufacturer's Perspective Apart

    Our expertise doesn't come from a brochure. It comes from sleepless nights troubleshooting crystallization issues, from years on the line adjusting stir rates and feed schedules, from direct dialogue with the scientists using our product in their daily grind. We've been there: waiting for the HPLC to confirm a clean peak, scrapping material when an impurity sneaks above tolerance, celebrating when a downstream coupling works perfectly thanks to a high-integrity starting material.

    DBPP-3CN may look like another reagent on paper, but in practice, its value stems from countless hours spent understanding how every small choice in manufacturing ripples out into a customer’s success. With every bottle, drum, or truckload, we stake a reputation earned not through clever marketing, but through the daily discipline of doing the job right, every time.