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HS Code |
340651 |
| Product Name | ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate |
| Molecular Formula | C10H9BrN2O2 |
| Molecular Weight | 269.09 g/mol |
| Appearance | solid |
| Solubility | soluble in organic solvents such as DMSO, DMF |
| Smiles | CCOC(=O)c1cn2cc(Br)cnc2n1 |
| Inchi | InChI=1S/C10H9BrN2O2/c1-2-15-10(14)6-7-5-13-9-8(11)3-4-12-9(7)13/h3-6H,2H2,1H3 |
| Storage Temperature | Store at 2-8°C |
| Synonyms | Ethyl 3-bromoimidazo[1,2-a]pyridine-5-carboxylate |
| Usage | Intermediate in pharmaceutical synthesis |
As an accredited ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25-gram amber glass bottle with a secure screw cap and clearly labeled hazard symbols and details. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL):** Securely packed drums or fiberboard boxes, palletized and shrink-wrapped, maximizing capacity for safe, efficient bulk shipment. |
| Shipping | **Shipping Description:** Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate is shipped in tightly sealed, chemically resistant containers under ambient conditions. The package is clearly labeled with hazard information. Shipments comply with local and international transport regulations for laboratory chemicals, ensuring secure handling to prevent spills, exposure, and degradation during transit. |
| Storage | **Storage for ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate:** Store the compound in a tightly sealed container, protected from light and moisture, at room temperature (15–25°C). Keep in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Ensure proper chemical labeling and containment to avoid exposure. Follow all laboratory chemical safety protocols during handling and storage. |
| Shelf Life | Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate is stable for at least 2 years when stored tightly sealed at 2–8°C. |
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Purity 98%: Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal impurity formation in active compound production. Melting point 143°C: Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate with melting point 143°C is used in medicinal chemistry research, where precise melting point enables reproducible compound isolation and handling. Molecular weight 281.08 g/mol: Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate with molecular weight 281.08 g/mol is used in drug design studies, where defined mass supports accurate molecular modeling and pharmacokinetic calculations. Stability temperature up to 80°C: Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate with stability temperature up to 80°C is used in automated synthesis platforms, where thermal stability aids in consistent product output during prolonged reactions. Particle size <40 μm: Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate with particle size <40 μm is used in solid dosage form development, where fine particle size improves dissolution rate and homogeneity in formulation processes. HPLC grade: Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate HPLC grade is used in analytical reference standard preparation, where high analytical quality allows for precise quantification and method validation. |
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Standing on the production floor and seeing the daily transformation of starting materials into advanced intermediates drives a certain appreciation for well-designed specialty chemicals. Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate has become a familiar presence in our reactors, a smartly built heterocyclic compound that opens doors in synthetic and medicinal chemistry. Our experience as the manufacturer shapes the approach we take to guarantee both consistency and flexibility, because the research and industrial applications rarely wait for unreliable supply or questionable purity.
Drawing on a decade of process refinement, we developed scalable routes to ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate—CAS number, if you need it, will come up in downstream documents—but for our team, this molecule presents as a robust, off-white crystalline solid with a moderate shelf life and reliable stability under standard lab storage. The structure bridges a bromo-substituted imidazopyridine core and an ester group. This combination brings a balance of reactivity and processability that isn’t easily matched by generic halogenated heterocycles or more sensitive analogs.
The unique substitution pattern makes it especially valuable when preparing functionalized, fused-ring systems. Over the years, we’ve seen an uptick in requests from teams developing kinase inhibitors, anti-infective agents, and custom ligand scaffolds. Most notably, the bromo position at the three-position is no accident—our R&D chemists prioritized it for optimized cross-coupling performance. Compared to parent imidazopyridine esters without the bromo group or with a substituent shifted elsewhere, our version opens C–C and C–N coupling routes that flow more smoothly under Buchwald-Hartwig, Suzuki, and Stille protocols.
Every batch carries the result of trial and error, persistent QC, and honest feedback from partners in pharmaceuticals, contract research organizations, and advanced materials labs. We never underestimate the cost of failed syntheses at late stages. That’s why the focus has always included rigorous monitoring of assay and water content, avoidance of residual palladium, and particle size control, as filtration and recrystallization outcomes can shift based on these, even at scales above 100 kg.
Unlike bulk aromatic esters or generically functionalized pyridines sourced through traders, ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate that comes directly from the originating producer gives tighter control over finer details: batch-to-batch color, solubility in mixed solvents, and carryover of trace impurities (like unreacted starting material or side-product regioisomers). Years back, when we transitioned from flask synthesis to continuous-flow protocols, several early partners saw their own productivities jump. They attributed it to the increased reproducibility and higher confidence that the intermediate would behave the same, time after time.
Some customers ask for milligram samples to support fragment library synthesis. Others receive drums fit for ongoing API research. Our process operators—many of whom have handled the same intermediates for years—know which tweaks cut delays at crystallization or filtration. Their knowhow helps us deliver on project commitments.
The technical team watches for sharp melting points, clarity of NMR spectra, and confirmation from HPLC or GC where appropriate. Customers working on downstream halogen-metal exchange, lithiation, or transition metal-catalyzed coupling need assurance that trace water and residual acid or base are well managed, since these easily jeopardize sensitive building block chemistry.
We routinely offer purity above 98% by HPLC, with supplementary data on water content by Karl Fischer and options for custom particle milling. Not every lab finds the default 50-200 microns ideal, so by speaking directly to process chemists, we avoid headaches later due to inconsistent filtration rates or poor slurry handling.
Another aspect that sets this compound apart stems from our in-house environmental controls. Several downstream users discovered that traces of chlorinated solvents or heavy-metal contaminants in bromo-heterocycles can interfere with scale-up or regulatory filings. By handling solvent recovery and purification under one roof, we drive out these risks. Not every supplier builds that margin for safety into their process, but for us, it saves both us and our customers from repeated qualification rounds.
After watching countless projects progress from screening hits through to scale-up, we notice project teams often begin with a broader set of bromo- or iodo-substituted imidazopyridines, only to settle on the ethyl 3-bromo variant for practical reasons. The ethyl ester group, compared to methyl or bulkier esters, allows just enough hydrolytic reactivity for route planning in both medicinal and process chemistry. Isopropyl and tert-butyl esters don’t always offer the same combination of reactivity and crystallinity.
As for the bromo at the 3-position, it’s far from arbitrary. Other substitution patterns (like 2- or 6-bromo) show divergent selectivity or decompose under typical coupling conditions. The electron distribution and steric accessibility of our featured compound lets chemists reach for a wider palette of transformations, from direct arylation to elaboration by nucleophilic aromatic substitution—capabilities less accessible in the more crowded or electron-rich analogs.
Labs chasing cost reduction sometimes ask if cheaper, lower-purity bromo-imidazopyridines work just as well. Our hands-on experience says otherwise. Small changes in impurity profile snowball into unpredictable side products and stubborn purification steps. Particularly during lead optimization, losing time or raw material to reprocessing or repeated chromatography bites much deeper than the modest material cost difference.
Years in the chemical plant teach practical safety lessons that flow right into our choices around packaging and shipment. Bromo-heterocyclic esters may not top the hazard lists, but care prevents dust formation and accidental exposure during both charging and sampling. By listening to customer feedback, we moved to heavy-weight polyethylene liners and robust drums—simplifying transfer in both small and bulk lots. This minimizes breakage and exposure compared to the older, thinner-walled containers often seen circulating among distributors.
Stability also features in user feedback. Our product rests comfortably in cool, dry storage for extended periods, without rapid uptick in acid or color formation. But for customers running long projects, we also provide guidance on intermediate repurification or transfer of open containers. These practical, field-driven pointers act as insurance against frustrating downtime should anyone encounter a clogged line or off-specification batch.
Contact with hundreds of process chemists, both in pharma and materials research, shapes our sense of where ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate fits the evolving landscape. Libraries of kinase inhibitors now increasingly rely on fused heterocycles as core scaffolds. This compound finds itself not only as a building block but sometimes as a transformer, enabling shift to completely new chemical space by enabling late-stage diversification.
Recently, requests have expanded beyond conventional medicinal chemistry. Several battery materials teams explored the bromo-imidazopyridine skeleton for use in organic electronic intermediates. Even though these efforts remain at the prototype stage, the technical demands challenge us to push further on trace purity—especially with respect to halide residuals and transition metal contaminants—because those features now affect device performance and downstream warranty costs.
Our ongoing dialog with academic labs and contract manufacturers also surfaces new problems to solve. Often, short-notice delivery requests or custom quantities require nimble scheduling and flexible packaging. Our production scheduling didn’t always allow for this in the past, but by dedicating part of the plant to rapid response orders, we now meet these needs without derailing larger project timelines.
Sustainability in chemical manufacturing isn't just about ticking a box. Early on, waste reduction and recovery mattered mainly for cost. Now we see both regulators and downstream partners looking for evidence of solvent reuse, minimization of off-spec discharge, and greener alternatives to hazardous reagents. Our method now recycles over eighty percent of the organic solvent load, lowering both environmental burden and overhead while maintaining reliable, year-round output.
For customers preparing documentation for regulatory submission, provenance matters. Full traceability from raw materials through to final product batches anchors confidence. In cases where downstream intermediates require detailed impurity mapping—whether by LC/MS, NMR, or ICP—we collaborate directly with customer QA teams to close data gaps before they threaten to delay a launch.
The regulatory landscape also generates rapid change: restrictions on hazardous substances, new guidelines for impurity profiling, and evolving good manufacturing practice standards. With every update, our technical and quality teams adapt methods, often ahead of schedule, to smooth the handoff from research to preclinical to commercial supply.
Supplying specialty intermediates like ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate requires more than posting a catalog entry or quoting a spec sheet. The real hurdles show up during tech transfer, scale-up, and the unpredictable stages of product launch. Over the years, we’ve fielded last-minute changes in batch sizes, late requests for custom packaging, and unanticipated analytical support. Where others rely on stockholders or third-party warehouses, our direct production model minimizes confusion, slashes shipping times, and keeps control in the hands that actually know the material.
Chemists rely on reliable supply—unexpected batch irregularities, subpar purity, or mishandling upend careful project plans. By maintaining clear channels between our plant, R&D, and customer-facing teams, we’ve built a pattern of rapid response. If a customer stumbles into an unforeseen technical issue, we draw on firsthand experience to adjust delivery or offer troubleshooting. This feedback loop, born from day-to-day collaboration rather than template-driven service, beats purely transactional supplier relationships.
Unexpected regulatory changes and supply chain disruptions remain constant threats. Directly manufacturing and warehousing our own inventory gave us the buffer to weather recent cross-border transport bottlenecks. Instead of scrambling through intermediaries, we maintained rhythm in delivery, helping projects move forward even as logistics snarled up across industries.
Ethyl 3-bromoH-imidazo[1,2-a]pyridine-5-carboxylate is more than a line item or a fleeting trend. It reflects years of process improvements, hands-on production, and honest engagement with chemists who solve real-world problems. Its characteristics—clean reactivity profile, high lot-to-lot consistency, and tailored handling support—make the difference between failed batches and smooth progression in everything from drug discovery to new materials exploration.
For those working in specialty synthesis, time pressures and cost constraints never let up. By staying pragmatic, responsive, and rigorous about the outcomes our chemical enables, we continually fine-tune both what we make and how we deliver it. Every kilogram represents a partnership between the bench and the plant, guided by a shared drive to build something better in the lab and at scale.