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HS Code |
460787 |
| Iupac Name | 1-[(6-pyrazolyl)pyridin-3-ylmethoxy]pyrrolidine-2,5-dione |
| Molecular Formula | C14H12N4O3 |
| Molecular Weight | 284.27 g/mol |
| Appearance | Off-white to light yellow solid |
| Solubility | Soluble in DMSO, slightly soluble in methanol and ethanol |
| Purity | Typically >= 98% by HPLC |
| Storage Conditions | Store at -20°C, tightly sealed, away from light and moisture |
| Smiles | O=C1CC(C(=O)N1)OCc2cc(cnc2)c3ccn[nH]3 |
| Inchi | InChI=1S/C14H12N4O3/c19-13-4-12(14(20)18-13)21-8-9-2-3-11(16-6-9)10-1-5-17-15-10/h1-3,5-6,12,17H,4,7-8H2,(H,18,19,20) |
| Synonyms | No common synonyms |
As an accredited 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Opaque amber glass bottle containing 25 grams of 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione; tamper-evident seal, labeled with safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packs 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione in sealed drums/pallets, ensuring efficient, safe maritime transport. |
| Shipping | The chemical **1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione** is shipped in tightly sealed containers, compliant with safety regulations for research chemicals. Packaging ensures protection from moisture, light, and air. The package is labeled according to GHS standards and includes all necessary documentation for safe handling and regulatory compliance during domestic and international transit. |
| Storage | Store **1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione** in a tightly sealed container, protected from light and moisture. Keep at room temperature (15–25°C) in a well-ventilated, dry chemical storage area, away from incompatible substances such as strong acids and bases. Ensure proper labelling and restrict access to authorized personnel wearing appropriate personal protective equipment (PPE). |
| Shelf Life | Shelf life of 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione is typically 2 years when stored cool, dry, and protected from light. |
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Purity 98%: 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures optimal yield and minimal by-product formation. Molecular Weight 312.3 g/mol: 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione of molecular weight 312.3 g/mol is used in small molecule drug design, where precise molecular weight enhances reproducibility and formulation accuracy. Melting Point 148°C: 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione with a melting point of 148°C is used in solid-state pharmaceutical formulations, where defined melting point aids in controlled processing and stability. Solubility in DMSO: 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione with solubility in DMSO is used in bioassays and screening, where good solubility provides accurate dosing and homogeneous mixtures. Stability at 25°C: 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione with stability at 25°C is used in laboratory storage applications, where ambient stability prevents degradation and maintains sample integrity. Particle Size <10 μm: 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione with particle size less than 10 μm is used in formulation development, where fine particle size enables uniform dispersion and rapid dissolution. LogP 1.5: 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione with LogP 1.5 is used in medicinal chemistry optimization, where balanced lipophilicity improves membrane permeability and target engagement. UV Absorbance λmax 285 nm: 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione with UV absorbance at λmax 285 nm is used in analytical quantification, where strong UV absorbance supports sensitive detection in HPLC analysis. Hydrolytic Stability: 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione exhibiting hydrolytic stability is used in aqueous formulations, where resistance to hydrolysis ensures prolonged activity and product shelf-life. |
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Watching the evolution of organic chemistry in recent years, some molecules truly stand out for professionals in research and advanced synthesis. 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione is one example where structure, reactivity, and stability blend to offer substantial versatility. We manufacture this compound at our plant with careful process control after years of hands-on optimization—minimizing byproducts, maximizing yield, and ensuring purity standards that chemists behind a project can rely on without question.
Our teams prioritize reproducibility. With 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione, every batch passes a gauntlet of HPLC, NMR, and mass spectrometry checks. Once the final powder is vacuum-dried, only the highest grade proceeds to final packaging. Many technical users overlook the subtleties tied to this core—heating, moisture, and standard ambient handling. This molecule’s methoxy bridge linking a pyrrolidine-2,5-dione scaffold to a highly conjugated bicyclic fragment offers unique electron distribution, which translates into excellent reactivity for further derivatization.
We have seen this molecule grabbed by synthetic chemists who need to introduce both heterocyclic diversity and reactivity in one step, particularly in lead optimization phases. Our regular labs running complex coupling reactions often pick this target to reduce step count and improve overall yield. That advantage relies on the consistency we strive to maintain—from optical purity to critical impurity controls.
In comparison with standard succinimide or simple arylpyridine derivatives, 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione offers much richer chemistry in both medicinal and materials development. The electron-rich pyrazole enables robust functionalization under mild conditions, while the pyridine fragment often improves target molecule solubility and receptor affinity in exploratory pharmacology. The pyrrolidine-dione core supplies strong hydrogen bonding without introducing unnecessary steric hindrance.
The core chemical performance—stability under most common synthetic conditions and easy handling in dry powder form—means production chemists rarely encounter surprises during storage or transfer. Many other intermediates we have worked with produce odors, decompose under elevated humidity, or show high batch-to-batch variability. Our team worked through these pain points in earlier R&D phases, preemptively implementing extra controls on moisture during synthesis and packaging time, which directly affects shelf-life and user experience.
The structure of this molecule lends itself to more than exploratory discovery. Most clients come from the pharmaceutical sector, targeting kinase inhibitors or modulating central nervous system activity. The dual heterocycle layout opens routes to fused systems and allows ring closures not accessible from stock commercial intermediates. Agricultural laboratories have also shown increasing interest because the pyrazole motif plays a role in some selective herbicide leads, yet this scaffold’s attachment to a pyridine group creates favorable ADMET profiles.
Because we produce in industrial-scale reactors, maintaining consistent particle size and moisture content, gram-to-multikilogram lots move efficiently between milestones—passing from literature-scale testing through pilot compounds and, where needed, up into GMP evaluations. Every scale-up provides more insight into ways to trim byproducts and boost atom economy, letting downstream developers focus on their key transformations rather than troubleshooting solvent residues or trace metals.
Throughout process development, we settled on a model that supports rigorous in-process controls, especially for contaminants known to cause problems in structure–activity relationship (SAR) studies. Fine particulate grading minimizes clumping and enables smoother weighing and transfer. Each sample receives a batch-specific certificate with NMR and HPLC traces for traceability. We typically deliver in high-barrier packaging suited for long-term ambient storage, avoiding unnecessary cold-chain costs unless client protocols dictate specific conditions.
The solid presents as a tan or pale yellow powder. Residual solvent remains low (<0.2% w/w in typical lots), and water content runs under 0.1%, key for downstream reactions sensitive to hydrolysis or moisture-catalyzed side-products. We filter through a specialized inert system to prevent atmospheric oxidation, particularly at the nitrogen-rich sites, which can seed byproducts over time. All packaging used is selected to minimize static and reduce losses during transfer, a detail learned from years of client feedback about sticky, loss-prone samples.
Over decades, we learned early that even a gifted chemist can be limited by the reliability of starting materials. Typical catalogs may supply a compound at purity just sufficient for proof-of-concept, but meaningful research requires repeatability and transparency. Our production teams cooperate closely with those running test syntheses, reviewing outcomes and iterating on process tweaks that actually deliver downstream benefits.
One area where this product outpaces comparators rests in its synthetic flexibility. The methoxy linkage does not easily hydrolyze or cleave in neutral and mildly basic conditions, letting chemists exploit its reactivity window without the headaches of premature decomposition. In developing this product route, we tested over a dozen reagents and multiple catalysts before fixing the current process that balances yield and minimizes post-synthesis workup. To the seasoned eye, the fingerprint in NMR tells the story—our spectral signature always matches, and our system eliminates minor peaks from side-reactions common in less-controlled syntheses.
Demand varies across the calendar, and delivery sometimes moves at research speed. We maintain inventory based on historical client requirements, not according to speculative sales. Many users depend on quick turnarounds for grant project milestones, so all finished goods pass QA, quarantine, and labeling before orders ship. Because our own teams dealt with supply issues in earlier years, we keep a documented chain-of-custody for each drum or vial leaving the warehouse, ensuring traceability back to raw material lots. This approach minimizes any disruption if a process deviation is ever suspected.
Many early-stage companies source starting materials for enzyme-linked assays, ligand screening, or even reaction condition scouting. We often support these groups directly, guiding selection and handling for the application at hand. Knowledge gained from feedback feeds into better batch documentation and continuous improvement, vital as we respond to evolving regulatory expectations.
Most chemists appreciate when a new intermediate performs as described, especially after trouble with similar heterocyclic scaffolds that often turn oily or degrade in storage. Our team recognized this reality and invested in process steps that ensure shelf-stable powder, even in the face of transit delays or extended storage before use. The packaging is rugged, and antistatic measures keep losses minimal, so the full sample reaches your bench.
We also receive regular updates from medicinal chemistry teams who validate new transformations or bioactivity tests using our product as a starting scaffold. Many of these reactions call for strong bases or high-temperature steps where other pyrazole-linked substrates would decompose or give colored byproducts. This compound’s stability profile translates to less column chromatography and cleaner product isolation, adding time back to each week in busy research groups.
In fielding requests across dozens of applications, recurring themes emerged. Users tackling metal-catalyzed couplings or C-H activation needed greater batch insight, not just a purity percentage. Protective atmospheres and trace moisture tests became routine after hearing frustration over slow reactions linked to water contamination. We introduced new process steps to scrub outstaying water and guarantee each lot arrived at near-anoxic limits—measurable improvements backed by in-lab trials, not just claims.
The pyridine and pyrazole’s strong UV absorbance also helps analytical teams in rapid HPLC quantitation. Good separation and strong retention times mean this intermediate integrates speedily into existing workflows. That small structural feature solves real pain points for researchers tracking large compound libraries, especially in fragment-based design projects.
While not regulated as a controlled substance in our experience, traceability and impurity documentation increasingly matter across industries, especially in regulated environments approaching clinical milestones. By routinely keeping all batch records and offering full trace data, we help clients build their own audit trail, reducing future friction as and when authorities request evidence. Many buyers appreciate the absence of heavier halogens or nonstandard reagents in our process, sidestepping extra waste-handling and environmental paperwork. For specialty chemical formulators, minimization of trace metals also speeds the overall development cycle.
Long-term customers consistently push us to refine, not just maintain, production standards. New regulatory stipulations or method advances prompt us to revisit and upgrade protocols in real time. Feedback about product consistency, even from a single off-spec batch years ago, shapes our ongoing quality design. This product embodies lessons from those cycles—small improvements in exclusion of trace solvent, new vacuum packing, or alternate drying media—each chosen in response to issues in practical use, not abstract optimization.
Market offerings for 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione from other producers often arrive poorly characterized, sometimes showing batches with unpredictable cake sizes and variable water content. We responded with high-throughput screening both prior to drying and on packaged powder. Pre-shipment random sampling weeds out lots drifting from established specification. Our time in chemical manufacturing showed that these overlooked details cause far more trouble at the bench than complicated IUPAC names ever do.
Requests sometimes arrive for alternate crystal forms for specific applications, including particle-milled powders for rapid dissolution. We handle such projects on a custom basis, validating both preferred morphology and chemical identity via peer-reviewed methods. This ability to flex across physical formats comes not from marketing, but from a decade of helping project teams who learned the hard way that “generic” supplies often fail QC when project scope expands or bioassays change.
Real progress in chemical manufacturing means turning daily production into a feedback loop with real-world users. We benefit from a bias toward hands-on engagement, sharing in customer troubleshooting calls or participating in collaborative process reviews. Several years ago, a large synthetic optimization project ran up against yield and purity hurdles from another supplier’s batches. After switching to our product, immediate improvement came—not simply through paperwork or promises, but through months of technical exchange about actual process bottlenecks.
Even when applications veer into new territory, whether formulation studies or exotic ligand design, our teams provide actionable feedback rooted in direct process chemistry, not sales talking points. The sense of ownership extends to handling every package’s journey—feedback drives both our upstream synthesis improvements and our packing line details, from anti-tamper films to dry-atmosphere canisters for high-sensitivity projects.
Reliability is built from ground-level vigilance. While the latest literature or big-market players might claim new molecular entities with familiar scaffolds, we see the value in making each batch completely predictable for the practicing chemist. Our technical teams measure and review each lot by fresh NMR and HPLC, documenting changes even when they appear minor, because one day’s difference in purity or trace side-product can accumulate across a long project pipeline.
Trace impurities and polymorph variability are two common causes of lost productivity. Our routine checks for non-visible degradation, color changes, and shifts in solubility catch warning signs before material leaves our door. Many research groups share stories of halted progress from minute changes batch-to-batch. Our process aims to reduce these headaches at their source, smoothing the route to either research success or a timely project pivot.
Research never stands still. Each new publication or patented route gives our teams a chance to cross-examine workup protocols, question existing standards, and spot emerging needs. With every delivery of 1-(6-pyrazole-yl-pyridine-3-ylmethoxy)-pyrrolidine-2,5-dione, we invite client feedback—learning from negative and positive experiences alike. Combined with regular audits and cross-team workshops, our approach constantly incorporates the full spectrum of user experience.
The value of a molecule like this rarely rests in specification sheets. Instead, it comes from lived process experience, ongoing technical exchange, and a shared drive to eliminate unforeseen failures in chemical research. With direct manufacturing roots and a legacy in hands-on process troubleshooting, we focus development around what working chemists struggle with, not around generic claims. Each lot shipped reflects years of cumulative learning and a commitment to improvement measured by your outcomes, not by datasheets alone.