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HS Code |
874187 |
| Chemical Name | 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile |
| Molecular Formula | C9H6N4O2 |
| Molecular Weight | 202.17 |
| Cas Number | 1373609-24-7 |
| Appearance | Solid (typically crystalline powder) |
| Solubility | Sparingly soluble in water, soluble in DMSO and methanol |
| Iupac Name | 6-hydroxy-4-methoxy-1H-pyrazolo[1,5-a]pyridine-3-carbonitrile |
| Pubchem Cid | 139855470 |
| Storage Conditions | Store at room temperature, away from moisture and light |
| Smiles | COc1c(O)nc2c(n1)cccn2C#N |
| Inchi | InChI=1S/C9H6N4O2/c1-15-8-7(14)12-9-5(4-10)2-3-11-6(8)9/h2-3,14H,1H3 |
As an accredited 6-Hydroxy-4-methoxypyrazolo[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 | Amber glass bottle containing 5 grams of 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile, labeled with hazard warnings and batch information. |
| Container Loading (20′ FCL) | 20′ FCL container loads approximately 12 metric tons, securely packed in fiber drums or cartons, moisture-protected, suitable for chemical transport. |
| Shipping | This chemical, 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile, is securely packaged and shipped in compliance with standard regulations for laboratory chemicals. It is sealed in a chemical-resistant container, protected from moisture and light, and delivered via trackable courier with appropriate labeling, safety documentation, and handling instructions to ensure safe transit. |
| Storage | Store 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile in a tightly sealed container, protected from light and moisture. Keep at room temperature, ideally in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Ensure proper labeling and avoid prolonged exposure to air. Follow appropriate safety protocols and consult the material safety data sheet (MSDS) for further handling and storage information. |
| Shelf Life | Shelf life of 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile is typically 2 years when stored in a cool, dry place. |
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Purity 98%: 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product quality. Melting point 205°C: 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile at melting point 205°C is used in solid-state drug formulation, where it provides enhanced thermal stability during processing. Particle size <10 µm: 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile with particle size under 10 µm is used in nanoparticle drug delivery systems, where it improves dissolution rate and bioavailability. Solubility in DMSO 20 mg/mL: 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile with solubility in DMSO at 20 mg/mL is used in in vitro screening assays, where it enables homogeneous solutions for reliable activity testing. Moisture content <0.5%: 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile with moisture content below 0.5% is used in sensitive API manufacturing, where it prevents hydrolytic degradation and extends product shelf life. Stability temperature up to 120°C: 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile stable up to 120°C is used in high-temperature synthesis processes, where it maintains compound integrity and performance. UV absorbance λmax 315 nm: 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile characterized by UV absorbance at λmax 315 nm is used in analytical method development, where it allows precise quantification of sample concentration. |
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Every batch of 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile that leaves our facility starts in a heated stainless-steel reactor about the size of a small truck. We have watched this molecule become a staple in synthetic chemistry, especially among researchers aiming to develop new pharmaceuticals and advanced intermediates. Chemists across custom synthesis and discovery programs ask for it by name, chasing its unique reactivity and molecular profile. With each run, our team adapts production practices to actual customer feedback, not just textbook routes or accepted literature yields. We learned early on that subtle control over solvent choices or pH tweaking during cyclization can drastically shift impurity levels and reproducibility.
Our motivation stems from seeing bottlenecks and pain points familiar to any chemist: cost, time, and batch-to-batch consistency. During scale-up, we faced the usual dilemma of exotherm management and side-product control. Classic procedures in the public domain often stop short of full characterization or process safety review. We noticed competing products suffered from single-spot TLC acceptance, so we pushed for tighter HPLC standardization as a policy. By tracking both yield and downstream impurity profiles, we help our clients avoid not only regulatory headaches but unexpected isolates during their own downstream modifications.
Rather than relying on theoretical purities and supplier datasheets, our labs run each batch through full NMR, LC-MS, and residual solvent analyses. Inquiries often focus on water content and residual contaminants—ranging from starting material remnants to trace inorganic salts. Through trial, we optimized a post-reaction crystallization step that improves not only purity readings but also stockroom shelf stability. Users appreciate receiving a product that resists caking and shows less tendency to degrade under ambient moisture. The light tan powder we pack today wouldn’t have passed our first year’s quality thresholds, which lagged due to old drying cabinet practices. Technicians who physically bottle each kilogram have streamlined packaging designs that keep the material clean for long-haul transport.
We have moved past the era of “assay on request.” Instead, every shipment comes with recent lot data: typically showing purity above 98% by HPLC, residual solvents below industry cutoffs, and moisture readings matching the true shelf tolerances seen in medchem and process labs. Keeping up with tightening customer QC expectations, we maintain an internal, ever-evolving reference panel from multiple lots for cross-comparison. Talking directly to research chemists, we hear that their own characterization needs often exceed regulatory minimums, a reality we embrace rather than push back against.
Clients from pharmaceutical research and agrochemical start-ups order this compound as a key intermediate in heterocycle libraries and structure-activity relationship (SAR) campaigns. The hydroxy and methoxy group placement, combined with the cyano substitution, opens a variety of selective transformations—allowing for functionalization at either position with relative chemoselectivity. Process chemists like its leaving group profile in nucleophilic substitutions, while medicinal chemistry teams report it tolerates a range of coupling partners. Its performance stands out during steps where keeping side reactions in check means the difference between weeks of troubleshooting or a clean progression in a route.
Many off-the-shelf pyrazolopyridine derivatives lack reliable supply chains at commercial scale or show inconsistent analytical performance when subjected to downstream transformations. Our batch notes highlight when a customer’s project requires uncharacteristically high reactivity or sensitivity. Individual lots may be matched and referenced directly with the researcher’s own analytical criteria. Feedback loops between supplier and bench chemist build trust and save substantial calendar time.
Manufacturing 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile taught us to spot surface-level differences that have outsized downstream effects. Take for example the difference between crude precipitation and controlled crystallization: We’ve seen what happens when rundown material, poorly dried or not properly filtered, derails subsequent reactions. Researchers in pharmaceutical labs reported higher pressure drops during filtration and unexplained yield loss when using uncontrolled grades. So, we doubled down on post-processing rigor, often exceeding the standards common in routine heterocycle manufacturing.
While several catalogues list seemingly interchangeable analogues, side-by-side analytical work demonstrates not all are identical in terms of stability or reactivity. Some competitors supply darker, impure lots that develop color or decomposition on standing. We rarely see these issues now, having isolated and removed the causes years ago: metal-catalyzed decompositions, solvent incompatibilities, and batch aging under warehouse conditions. Typical bystanders in the compound’s class struggle with hydrolysis sensitivity; our product features increased shelf stability through specific solvent removal and neutral pH storage. Regular feedback from medchem groups confirmed our lots dissolved more cleanly in common solvents, cutting prep time and waste disposal costs.
Another difference comes from adaptability to different project scales. Larger synthesis runs require more robust in-process sampling and often need ongoing feedback direct from operators rather than just quality control paperwork. We don’t mind taking extra time to record and communicate subtle process shifts because these can be make-or-break details for the end-user. A real difference is felt not in theoretical purity lines but in the frictionless continuation from delivery to use, especially across multinational sites.
Over years, our operators gained fluency in how 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile behaves through every process stage. During batch reactions, viscosity changes pinpoint optimal endpoint detection, more so than color alone. We learned to re-dry and re-analyze any material up for shipment, as seasons and ambient humidity dramatically alter the flow and compressibility of a batch.
Equipment fouling, a notorious headache, occurred regularly until we refined the filtration and solvent swap protocol. Instead of barrel scraping, we switched filter media type and updated agitation speeds. This improved consistency—not just by assay but also in actual, measured throughput. By analyzing failed batches, we stopped future losses and cut plant waste. Staff in final QC labs became adept at rapidly flagging outlier lots and communicating root-cause findings to shift supervisors before shipment.
During customer visits and audits, we have real, transparent conversations about what to expect from our process. Some clients require milligram-scale samples pulled fresh during campaign planning. Others, already familiar with our track record, trust that our shipments will match expectations based on direct, ongoing communication. We believe “off the shelf” shouldn’t mean “off the standards.” If a product batch deviates from prior expectations, our door stays open for dialogue, and we routinely supply additional characterization to ensure alignment with project goals.
We rely heavily on continuous feedback loops: not just static customer surveys, but candid phone calls, shared chromatograms, and “what went wrong” post-mortems. Researchers ask about dissolution profiles or batch-to-batch color drifts, so we track these physical traits alongside analytical data. Our stock does not leave the warehouse unless it survives practical tests seen in actual labs—whether direct addition to high-throughput screening or integration into gram-scale flow reactors.
Real-world chemistry differs from controlled conditions. We field inquiries every month from clients troubleshooting downstream step yields, often discovering that their other supplier’s lots secretly contained unreacted precursors or moisture that frustrated scale-up. Sharing lessons gained with each run, we exchange not only lot numbers but workarounds and troubleshooting expertise. Our average client may buy just a kilo at a time, but the depth of technical support often mimics that of long-term industrial partnerships.
This approach flows from viewing each synthesized lot as a record of improvement, not just a product moving down a pipeline. Whether a kilo or a hundred grams, we prioritize communication across our own ranks and with our customers. The result has been repeat business with leading innovation teams, whose confidence derives from proven chemical consistency, not just formatted assurance sheets.
Every year brings a new wave of challenges for specialty chemical producers. Our process chemists routinely revise synthetic steps as fresh data emerges from the literature or the customer end. Small changes—such as switching suppliers for starting materials or adjusting water content during isolation—ripple across batches unless managed with discipline. Laboratory staff still tracks each modification in live process notebooks, keeping lessons current and accessible for comparison as the regulatory and customer environments shift.
Market trends in pharmaceutical research increasingly call for advanced heterocycles, and the feedback cycle continues to shorten. Many of the chemists we work with now operate in virtual teams scattered around the globe, so tight tolerance for batch consistency and crystal form matters more than ever. We don’t cut corners on purity or packing, knowing backlogs and failed experiments cost more than any possible savings on in-process controls.
As the variety of applications grows, we field technical questions on everything from solvent system optimization to endpoint detection for functional conversions. We see that well-synthesized and well-characterized 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile helps drive projects efficiently forward—whether for developing kinase inhibitors, novel ligands, or other advanced intermediates. In the rapidly evolving world of chemical innovation, useful heterocycles are not fungible commodities, and our shop puts that belief into practice every day.
Making pyrazolopyridine-based building blocks looks simple on paper. In daily practice, controlling for repeatable conversion, avoiding side-reactions, and minimizing contamination from solvents or processing aids turns out to be the true measure of expertise. Staff turnover and equipment upgrades bring new techniques and surprises, but the principles stay the same—each small adjustment in the process can spell success or headache for our customers. Our team runs cross-training to catch slips and promote a culture where staff spot and fix irregularities independently.
The chemical producer’s world keeps moving, ready or not, as regulation tightens and new application fields emerge. We keep detailed lot histories, not for paperwork alone but to support meaningful problem-solving for each inquiry. Our senior technicians often serve as liaisons to end users, passing along troubleshooting tips that prevent unnecessary downtime. Whether confronting questions about trace metals, filtration rates, or optimum solvent removal, we lean on practical knowledge built over years. Chemistry grows from collaboration, and no packaged bottle should be a mystery to its user.
The story of 6-Hydroxy-4-methoxypyrazolo[1,5-a]pyridine-3-carbonitrile in our plant reflects a larger truth about manufacturing specialty heterocycles: building a successful product takes much more than ticking boxes on a specification sheet. Putting real effort into post-synthesis processing, analytical confirmation, and preventive process controls pays dividends not just for our customers’ results but for our own stability as a chemical producer. We meet chemists at eye level—with transparency, direct feedback, and a commitment to sustainable progress.
As chemists ourselves, we know what frustrates and what sparks ideas in discovery programs. We strive to partner with those advancing pharmaceutical innovation, not just as a supplier but as a technical resource. In the end, our pride comes not from quantity shipped but from clean progress at the bench—where actual science gets done, plans move forward, and time rarely stands still.