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HS Code |
795968 |
| Iupac Name | 2-(Imidazo[1,2-a]pyridin-3-yl)acetic acid |
| Molecular Formula | C10H8N2O2 |
| Molecular Weight | 188.18 g/mol |
| Cas Number | 117660-13-2 |
| Appearance | White to pale yellow solid |
| Melting Point | 216-218 °C |
| Solubility In Water | Slightly soluble |
| Chemical Structure | C1=CN2C=CN=CC2=NC1CC(=O)O |
| Smiles | OC(=O)CC1=CN2C=CN=CC2=NC1 |
| Inchi | InChI=1S/C10H8N2O2/c13-10(14)6-8-5-12-9-3-1-2-4-7(9)11-8/h1-5H,6H2,(H,13,14) |
As an accredited Imidazo[1,2-a]pyridine-3-aceticacid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Imidazo[1,2-a]pyridine-3-acetic acid, 10g: Supplied in a sealed amber glass bottle with tamper-evident cap and detailed labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packs Imidazo[1,2-a]pyridine-3-aceticacid in drums or bags, maximizing space, ensuring safe chemical transport. |
| Shipping | Imidazo[1,2-a]pyridine-3-acetic acid is shipped in tightly sealed containers to prevent contamination or moisture absorption. It should be transported in compliance with all regulatory guidelines for laboratory chemicals, ensuring proper labeling and documentation. Store and ship at ambient temperature, away from sunlight, heat, and incompatible substances to maintain product integrity. |
| Storage | Imidazo[1,2-a]pyridine-3-acetic acid should be stored in a cool, dry, and well-ventilated area, away from heat or ignition sources. Keep the container tightly closed and protected from moisture and direct sunlight. Store the chemical in a clearly labeled container, separated from incompatible substances such as strong oxidizing agents. Follow standard laboratory safety practices and consult the SDS for detailed storage guidelines. |
| Shelf Life | Imidazo[1,2-a]pyridine-3-acetic acid typically has a shelf life of 2-3 years if stored tightly sealed, cool, and dry. |
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Purity 98%: Imidazo[1,2-a]pyridine-3-aceticacid with 98% purity is used in pharmaceutical intermediate synthesis, where high chemical reliability ensures reproducible batch outcomes. Melting point 155°C: Imidazo[1,2-a]pyridine-3-aceticacid at melting point 155°C is used in medicinal compound formulation, where precise thermal processing prevents degradation. Molecular weight 189.19 g/mol: Imidazo[1,2-a]pyridine-3-aceticacid with molecular weight 189.19 g/mol is used in structure-activity relationship studies, where accurate dosing enables consistent bioactivity assessment. Stability temperature 120°C: Imidazo[1,2-a]pyridine-3-aceticacid with stability temperature 120°C is used in high-temperature reaction environments, where thermal resistance maintains compound integrity. Particle size <10 μm: Imidazo[1,2-a]pyridine-3-aceticacid with particle size less than 10 μm is used in tablet manufacturing, where uniform dispersion supports optimal drug release rates. Water solubility 5 mg/mL: Imidazo[1,2-a]pyridine-3-aceticacid at water solubility 5 mg/mL is used in injectable formulations, where increased solubilization enhances bioavailability. HPLC assay 99%: Imidazo[1,2-a]pyridine-3-aceticacid with HPLC assay 99% is used in analytical reference standards, where high assay purity guarantees accurate quantification. Residual solvent <0.1%: Imidazo[1,2-a]pyridine-3-aceticacid with residual solvent less than 0.1% is used in active pharmaceutical ingredient production, where minimal impurities ensure regulatory compliance. |
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In the industrial synthesis arena, few building blocks have found as much traction as imidazo[1,2-a]pyridine derivatives. Imidazo[1,2-a]pyridine-3-aceticacid stands out for its clarity of reactivity and versatility in both pharmaceutical and fine chemical pathways. Over the years, our team has worked hands-on from kilo-lab to full-scale production, gaining an intimate perspective that books alone rarely capture. We have seen this compound anchor numerous innovative projects, both straightforward and challenging. These are the experiences that shape our approach to not just making, but really understanding its value to fellow chemists and engineers.
This compound carries the molecular formula C10H8N2O2, offering a fused bicyclic system that merges electron richness with discrete points of functionalization. The crystalline powder often appears off-white to pale yellow. Production at our site adheres to high-purity benchmarks - typically over 98.5% by HPLC - and moisture content tests remain stringent to fend off hydration issues in storage or downstream protocols.
The stability, both thermal and oxidative, means it handles scale-up stress well. From bench trials up to metric ton quantities, particle size distribution can be tuned through careful milling. Throughout several hundred batches for custom and catalog orders, this consistency has cut processing stoppages compared with less rigorously controlled alternatives. Each drum is traceable to its manufacturing lot. We preserve full analytical records, including NMR, IR, LC-MS, and elemental analysis, so end-users see the real molecular fingerprint before it ever enters their reactors.
As straightforward as an aromatic heterocycle might seem, subtle differences in synthesis routes lead to trade-offs in yield, impurity profile, and residual reagents. Our facility still uses glass-lined reactors for intermediates prone to base hydrolysis, avoiding stainless steel at critical junctures. We dedicate a separate crystallization suite for imidazo[1,2-a]pyridine-3-aceticacid, away from highly basic or sulfur-containing lines, because we have noticed trace cross-contamination can undermine not only analytical specs but also downstream pharmacology screens. These lessons emerged from direct troubleshooting after several customers detected outliers years ago with off-the-shelf material. Since then, we have not seen those issues resurface.
Understanding how minor impurities interact later in synthetic sequences guides our process design philosophy. We don’t take shortcuts around isolation or control points, since even legally compliant product may fail to deliver on its scientific promise if overlooked. This is especially true for customers working at the interface of medicinal chemistry and scale-up, where flaky performance can derail months of work.
Many industrial and academic partners rely on this compound as a scaffold for kinase inhibitor design, CNS-active agents, and rare disease candidate libraries. Its combination of structural rigidity and well-placed nitrogen atoms makes it a favorite for late-stage functionalization. Early in our history, a midsize biotech came to us with solubility concerns while modifying the acetic acid tail to introduce different esters. By working collaboratively to tune particle size and drying conditions, we reduced aggregation problems they previously faced using unoptimized batches from standard commercial sources.
The carboxylic acid handle provides a gateway into robust coupling strategies. Peptide mimicry, amide formation, and Suzuki-Miyaura couplings have all been reliably reported. In our technical follow-ups, researchers frequently mention fewer side reactions and less byproduct formation when starting from our material versus some of the lower-purity imports. As a result, they gain additional flexibility for SAR (structure-activity relationship) campaigns or rapid analog generation without constant purification headaches.
The landscape of imidazo[1,2-a]pyridine chemistry today is broad. Still, imidazo[1,2-a]pyridine-3-aceticacid pulls ahead from more conventional carboxylic acid derivatives due to its discrete substitution pattern. Not all isomers behave equally. For example, 2-carboxylic acid variants or their methyl ester relatives invite different reactivity due to ring electronics, sometimes undermining cyclization yields or selectivity in multistep synthesis.
What we produce avoids the viscosity and tack common in similar alkylated or halogenated analogs. This quality proves beneficial where automated solid-dispensing equipment or parallel synthesis arrays are standard practice. We have supplied high-throughput screening teams who struggled with inconsistent flow rates from materials sourced through less experienced vendors. In direct side-by-side trials customers confirmed smoother operation with our batches, saving time and labor costs.
Our compound also resists thermal discoloration more effectively than comparable heteroaromatic acids. A customer working on high-temperature amide couplings reported stabilized yields and color, with fewer decomposition products, when switching to our supply. The reduced introduction of colored impurities into downstream compounds pays dividends in the purification and analytical stages.
Real-world handling counts for more than spec sheets will ever tell. We committed to packaging practices that safeguard integrity: triple-layer barrier bags, nitrogen flushing, and tamper-evident seals as standard, not as upgrades. These procedures grew out of feedback from customers encountering caking or hydrolysis when using basic polybags during long haul shipments.
Our workers run through rigorous glove-box and hood protocols, especially in the drying and milling rooms. Dispatchers understand that moisture pick-up, even as low as 0.1%, can throw off a subsequent solid-phase coupling or result in an erroneous melting point. Regular hands-on training ensures leaks and warehouse lapses stay rare. That level of care does not come from compliance pressure, but from company pride and the belief that every batch leaving our plant should reflect both technical mastery and respect for the end user.
Maintaining trust means more than distributing a single batch analysis. Our internal review layers begin with in-process monitoring and extend through QC release, with cross-checks by two separate analytical teams. Trends across many lots have revealed that HPLC alone misses certain low-level UV-absorbing fragments, so we commit to running supplemental LC-MS screens whenever possible—informed by our own in-house discoveries of rare extraneous spots during customer troubleshooting projects.
Every batch is linked to employee sign-off logs and archived with comprehensive traceability. Over time, the company’s focus pivoted from simply “meeting spec” to documenting repeat performance. Sometimes this means production or QA staff spend extra hours digging into minor anomalies. Those extra checks have caught micro-level impurities from minor changes in reactor agitation or pH near the finish—issues that never surface in mass-market production.
Such attention to detail brings tangible benefits. We have seen large pharma clients report longer shelf-life and more reproducible results in their hands compared to material of similar stated purity from other origins. In one case, a failure analysis traced a formulation inconsistency not to synthetic pathway divergence, but to a different manufacturer’s lack of consistent drying technique. Since then, the scientist leading that project has requested only our batches for critical work.
Waste minimization and safer chemistry have always shaped our factory upgrades. Imidazo[1,2-a]pyridine-3-aceticacid synthesis in our plant now generates one-third less solvent waste compared to protocols used in many smaller contract labs. The switch to closed filtration systems and low-solvent crystallizations has protected our workplace and neighboring environment alike.
Rather than chase expedient one-off production runs, our engineers target steady output with routine solvent recovery and dedicated waste neutralization. These aren’t abstract targets or public relations talking points but direct responses to regulatory audits and limits on plant emissions. Our team recognizes that it is not enough to make reliable molecules; we carry a duty to craft them mindfully, without passing long-term burdens to communities or future chemists.
We continue reevaluating raw material sources for their own environmental footprints, and have begun working with suppliers on greener alternatives for certain starting materials, while fully validating the impact of any change before scaling up.
Researchers and process chemists who call upon our material know that questions reach an internal chemist, not just an operator reading from a script. Experienced hands are ready to talk through real syntheses, not just dispense paperwork. Whether customers want to scale from grams to kilos or need custom drying, our flexibility stems from direct experience managing similar projects ourselves.
We also welcome returning data, sharing in troubleshooting, and providing second opinions for challenging transformations. Over the years, many methods and improvements have grown out of these partnerships. One recent example involved a client searching for better conversion and purity in a late-stage amidation; after a few rounds exchanging material samples and technical notes, they documented a 12% yield improvement by adopting tweaks we used at scale. This kind of engagement doesn’t show up in sales statistics, but it does in long-term relationships and in acknowledgments when projects finally hit publication or market approval.
Plenty of imidazo[1,2-a]pyridine-3-aceticacid now fills catalogs and online marketplaces, sometimes at a fraction of the price. The industry has learned, sometimes the hard way, that “on paper” results rarely tell the whole picture. Our plant’s raw material traceability and process discipline routinely catch inconsistencies—be it a change in solvent grade from an upstream source, atmospheric moisture swings, or micro-extraneous residues from hastily cleaned vessels.
Customers switching back and forth between vendors have commented on the time lost revalidating processes when unforeseen variables sneak in with bulk imports. Our own data show that batch-to-batch consistency not only streamlines regulatory filings but also saves time otherwise lost to root cause investigations and repeated rework. For researchers making high-value targets or clinical candidates, this reliability can mean staying ahead in a fast-moving competitive field.
The story of imidazo[1,2-a]pyridine-3-aceticacid on our lines still grows. Ongoing R&D trials explore safer, less wasteful oxidants for key steps, and more efficient crystallization protocols that further reduce energy and time per batch. Senior chemists lead process improvement sprints every quarter, always in conversation with customer feedback about new problems arising in real applications.
Partnerships with academic groups and innovation consortia keep us sharp. They push for better selectivity, easier late-stage modification, and more sustainable routes. Whether optimizing catalyst routines or refining drying protocols, we continue to view each challenge as a learning opportunity, never just another order to fill.
From a manufacturer’s standpoint, each kilogram of imidazo[1,2-a]pyridine-3-aceticacid tells a story not just of technical accomplishment but of ongoing responsibility to quality, scientific integrity, and community well-being. Our practices, honed through many years of hands-on production and troubleshooting, reflect a deep understanding of not just molecular science but the real-world needs and concerns of those who advance it.
The changes we adopt today in process control, environmental responsibility, and technical support flow directly from our experience and commitment to every user of this vital scaffold. As challenges and applications evolve, so do our methods, always with an eye toward trust, transparency, and better science.