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HS Code |
821072 |
| Chemical Name | 2-(1H-Pyrazol-3-yl)pyridine |
| Molecular Formula | C8H7N3 |
| Molecular Weight | 145.16 g/mol |
| Cas Number | 886365-45-5 |
| Appearance | off-white to pale yellow solid |
| Melting Point | 95-98°C |
| Solubility In Water | Slightly soluble |
| Smiles | c1ccc(nc1)c2c[nH]nn2 |
| Inchi | InChI=1S/C8H7N3/c1-2-4-7(9-5-1)8-3-6-10-11-8/h1-6H,(H,10,11) |
As an accredited 2-(1H-Pyrazol-3-Yl)Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 5 grams, white label with chemical name, structure, CAS number, hazard pictograms, and supplier logo. |
| Shipping | 2-(1H-Pyrazol-3-yl)pyridine is shipped in tightly sealed containers, protected from light and moisture. It is handled as a laboratory chemical under standard precautions. Packaging complies with chemical transport regulations; if classified as non-hazardous, it ships at ambient temperature. Documentation includes appropriate labeling and Safety Data Sheet (SDS). |
| Storage | 2-(1H-Pyrazol-3-yl)pyridine should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Ensure proper labeling and limit access to trained personnel. Handle under a fume hood if dust or vapors are generated. |
Applications of 2-(1H-Pyrazol-3-Yl)Pyridine in Industrial ManufacturingAs a direct manufacturer of 2-(1H-Pyrazol-3-Yl)Pyridine, we supply this specialty heterocycle to key industries where it acts as a valuable intermediate for high-value products. This material's reactivity and coordination capability support advanced molecular design and performance requirements in each application area below. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical companies deploy 2-(1H-Pyrazol-3-Yl)Pyridine as a core structure in the synthesis of kinase inhibitors and certain neuroactive agents. Medicinal chemists utilize its pyridine-pyrazole motif in scaffold hopping to build advanced molecular libraries. Downstream, this intermediate enters multi-step synthesis, often via Suzuki coupling or condensation, where it attaches to functionalized halides or boronic acids. Process chemists adjust the charge between 5–15%, varying input with respect to conversion efficiency, yield, and subsequent step demands. Final APIs containing this motif proceed to strict regulatory validation in clinical and commercial scale-up environments. Industry compliance standards
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2. Ligand Building Block in Homogeneous CatalysisChemical process development teams in fine chemical and API production use 2-(1H-Pyrazol-3-Yl)Pyridine to construct N,N-bidentate and pincer ligands for homogeneous catalysts. These ligands optimize transition metal complex activity and selectivity for hydrogenation, carbonylation, and C–C bond formation. Formulators typically apply 1–4 mol% loading when assembling ligand–metal complexes, though this ratio is tuned based on substrate reactivity and catalyst stability in each process. By adopting this heteroaromatic, manufacturers enhance efficiency in continuous and batch transformations, improving product throughput and selectivity. Industry compliance standards
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3. Building Block for Agrochemical Discovery and SynthesisMajor agrochemical firms integrate 2-(1H-Pyrazol-3-Yl)Pyridine into the discovery and development of novel crop protection agents. Synthetic chemists exploit the molecule's aromatic reactivity in coupling and annulation reactions, often at a ratio of 10–20% based on lead optimization workflows. The compound serves as a key intermediate in producing potential herbicides and fungicides with improved target affinity and metabolic stability. Downstream production incorporates this material through direct N-arylation or amidation, forming new active molecules tested in bioefficacy trials. Industry compliance standards
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4. Electronic Material Precursor for OLED and Optoelectronic ApplicationsSpecialty materials producers exploit the electronic features of 2-(1H-Pyrazol-3-Yl)Pyridine to build advanced optoelectronic molecular precursors. R&D teams utilize this molecule for synthesizing electron-transport and hole-blocking layers within OLED devices. During formulation, manufacturers add 3–12% of the compound to reaction feeds for synthesizing custom ligands or emitter complexes. Downstream stages incorporate this material in vacuum deposition-grade intermediates or as a ligand for metal complexes, supporting high-brightness, stable device fabrication. Industry compliance standards
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Some molecules never leave the test stage, but 2-(1H-Pyrazol-3-Yl)Pyridine has proven itself in real-world synthesis lines for years. At our facility, this compound, often referenced by its CAS number in research circles, is a staple among heterocyclic intermediates. Every batch rolling from our reactors goes through rigorous testing, not just for purity but for its consistent response in downstream chemistry. Chemists crafting novel pharmaceuticals, agrochemical researchers working on crop protection scaffolds, and those in the material sciences all request this compound for a reason: it delivers reliability where it matters most—scale-up work.
From experience, we know small differences in synthesis—temperature swings, solvent grades, subtle tweaks in pH—can mean the difference between a workable intermediate and an unusable by-product mess. Our technicians never cut corners here. The structure of 2-(1H-Pyrazol-3-Yl)Pyridine seems straightforward, but routes with different starting materials, or tweaks to cyclization conditions, easily change impurity profiles. Our route delivers a clean compound because we don’t just monitor the obvious peaks on a chromatogram—we track the ones others tend to ignore, too. This matters for anyone making kinase inhibitors, nitrogen-containing ligands or anything sensitive to trace contaminants.
Once our product leaves quality control, there’s no going back. Every kilogram shows a clearly measured melting point, matches a sharp NMR pattern, and finishes off with a purity above 98%—verified using more than one method, not just HPLC. We’ve tried lower specs in the past for cost reasons, but the headache it brings on customer lines is never worth it. Most requests focus on the powder form because it dissolves evenly in polar organic solvents, but we’ve also supplied this molecule recrystallized to meet stricter requirements for instructor-led labs and analytical standards.
We package and store the material with moisture protection, because 2-(1H-Pyrazol-3-Yl)Pyridine can pick up ambient water over time. Water content skews yield, especially in metal-catalyzed couplings. We ship with freshly dried product whenever possible. Our storage tests prove that vacuum-sealed bottles, packed in airtight drums, perform well through a multi-month supply chain. We guarantee this with real aging data, not theory.
Our customers keep finding uses I couldn’t have predicted. It started as an intermediate for certain cancer therapeutics—serving as an anchor ring for chiral synthesis and bidentate ligands. Then came the requests from crop science teams, who matched its core scaffold to bioactive leads controlling resistant fungal strains in cereals and vegetables. Custom synthesis companies often mention its compatibility with cross-coupling reactions—especially Suzuki and Buchwald-Hartwig protocols. In our own pilot work, it has helped build even larger, more complex heterocycles, reducing the overall step count.
Years of fielding technical questions taught us that the moment a customer asks about “stubborn side reactions,” it usually means an impurity or water issue. We share not just our data but details on purification tricks—such as the right drying agent blends or proper base selection—directly out of our own development notebooks. Our approach draws from batch observations, scale-up hiccups, and even issues seen with overworked solvent recovery systems. Anyone can recite theoretical reactivity, but direct troubleshooting comes only from many runs and hands-on failures.
From the manufacturer’s eye, 2-(1H-Pyrazol-3-Yl)Pyridine stands apart from other similar building blocks, such as plain pyridine derivatives or unsubstituted pyrazoles. Its defining trait isn’t just the fused nitrogen system, but the relative ease of selective functionalization at positions that tend to foul up in other systems. We’ve run comparison studies with analogs lacking the pyrazole or changing its positioning; the differences in reactivity and product yields can be enormous. This core permits cleaner introduction of advanced motifs, reducing the need for later purification steps.
The dual heteroaromatic scaffold can coordinate transition metal centers in a way that plain pyridines or pyrazoles can’t. This feature attracts the attention of catalyst developers looking to create new, robust ligand systems. In one collaboration, we supplied this molecule for use in C-H activation protocols, where the product’s geometry let chemists skip otherwise required chelation steps, saving time and cuts on waste streams. These achievements never show up in the sales sheet, but they drive repeat orders for those in the know.
Manufacturing isn’t about theoretical yields—it’s about what comes through in the drum. One headache we’ve solved relates to product isolation. In the early days, our first crystallization approach resulted in fine powders prone to static and clumping, gumming up filling lines and frustrating everyone. By adjusting evaporation profiles and adding gentle agitation at the right moment, we overcame this, creating a product with improved handling and reduced operator frustration. It sounds minor, but nobody wants downtime caused by a sticky intermediate.
Handling aromatics prone to light-induced degradation taught us to package under reduced light and step up batch documentation. A surprising number of complaints about “off-target color” or “strange odor” have their roots in subtle processing gaps, not shipping delays. We reinforce this message to every operator joining our team: treat each batch as if you’ll run the next step yourself. The right attitude downstream saves us from returns upstream.
Specifying 2-(1H-Pyrazol-3-Yl)Pyridine alongside dozens of other nitrogen heterocycles has shown us how a single atom shift transforms reactivity. Customers familiar with standard building blocks—like 2,2’-bipyridine or 1H-pyrazole—sometimes wonder if a cheaper compound will deliver the same results. Our own bench trials quickly shut down this hope; the electronic distribution and bond angles in this pyrazolylpyridine lead to faster coupling and better yields in most cases. Where scalability matters, we can often eliminate a purification column or avoid a protecting group, shaving hours off production.
Feedback from customers feeds directly into our next improvement cycles. One team developing kinase inhibitors ran into trace metal residue from a competing supplier’s product, which we traced to inadequate washing and not fully optimized separation steps. By sharing our own QA methods—metals analysis, evaluation by ICP-MS, and careful water wash profiles—we helped customers troubleshoot faster than through standard support channels. This kind of open exchange doesn’t happen when a product launches from a trader or is moved between warehouses without connection to those making it day after day.
Accountability starts on our shop floor and ends with customer success stories. When researchers call in saying a downstream coupling failed, our technical team asks the questions only another hands-on chemist would: What was the base? What was the water content? Did the product clock in at expected optical rotation? Many of our answers come from problems we solved in our own scale-ups, not from a script. We maintain internal logs of every reported problem, not to cover ourselves, but to guide process tweaks for future batches. Openness about small hiccups has built repeat trust clients rely on.
Our technical sheets back decisions with results from internal and customer-driven evaluations. Product certifications aren’t just regulatory hurdles; they mirror practical batch reproducibility. If a major manufacturer of specialized ligands or a pharma pilot plant flags a concern, we run both fresh and retained samples for side-by-side checks, sharing all spectra with the client. There's no skipping steps or hiding behind generalized responses. What matters gets discussed openly, leading both manufacturers and clients toward continual process improvement.
Some buyers get tempted by cheaper imports with looser specs, thinking a quick chromatography can rescue a dirty batch. We’ve run head-to-head tests with lots pulled straight from these sources—often finding variances in water, unknown fluorescing spots under TLC, or low-mass byproducts invisible to routine QC. On the manufacturer side, we know exactly where each run started and ended, and how each process shift from reactor to drying affects final fitness for use.
We’ve taken the time to document long-term stability, because some supply chains stretch months or cross hemispheres before their contents finally reach the user’s bench. It’s the difference between keeping R&D workflows smooth and dealing with months of delays when a batch turns up unusable. Over the years, we’ve heard all the creative workarounds—from re-extraction to costly repurifications—when something simple like water content or packaging technique would have eliminated the problem at the source. We refine each detail for the next shipment.
We didn’t always get it right from the start. Early shipments in less protective containers sometimes attracted complaints about color drift or caking. After a few rounds of this, we switched fully to inert sealed packaging and augment every outgoing box with sample packets for validation by the receiver. This step, born from our own trial and error, has cut back on confusion and sped up qualification at the customer site.
Gas chromatography, mass spectrometry, and full NMR panels now back every outgoing lot—because cutting analytical corners boomerangs as field complaints. Before, rushed loads might have left small peaks unexamined; those days are gone. We fix standards not by what’s cheapest or easiest, but by what survived our own lab stress tests. All this means trace-level purity, accurate consistent specifications, and fast answers when questions arise.
Proximity to both bulk and small-scale customers gave us practical perspective on logistics. Large volume users depend on regular, reliable delivery patterns, while research groups want freshness and smaller aliquots. We diversified container formats and adjust batch schedules to prevent long pre-shipment storage. Simple, hands-on tweaks like these save headaches later, especially in international shipments facing customs and climate swings.
Our chemists regularly visit both customer sites and partner university labs. Direct dialogue revealed recurring worries: batch-to-batch variability, unexpected impurities, inconsistent documentation, and lack of hands-on support when reactions stall. We take these seriously because we’re stakeholders, too. Our own team runs trial syntheses, stress tests different lots using sensitive palladium- and copper-catalyzed protocols, and even push product through analyzers meant to spot stability drift during long sea freight.
Each insight folds back into practical action. We changed purification solvents after field reports tied faint odor issues to precursor traces. That shift didn’t appear on any official document, but it made downstream processes more robust. Responding to feedback formed our standard practice, not just an afterthought.
Looking back on years of real batch failures, customer hotlines, successful production improvements, and solved logistics headaches, we see every shipment of 2-(1H-Pyrazol-3-Yl)Pyridine as proof that behind-the-scenes hands-on work means more than polish at the sales end. The knowledge comes not from copying generic product specs, but from learning at the bench and scaling up lessons batch by batch.
This is how our company’s experience shapes what you receive: not a faceless powder, but a reliably engineered chemical ready for tomorrow’s synthesis. Real manufacturing means using every field report, technical slip, and proven solution to refine every gram that ships. We bring that experience to every bottle, every drum, and every conversation—starting at the reactor, ending in the customer’s hands, and always looking for the next practical step forward.