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HS Code |
505098 |
| Iupac Name | 2,5-dichloro-1H-imidazo[4,5-b]pyridine |
| Molecular Formula | C6H2Cl2N3 |
| Molecular Weight | 188.01 |
| Cas Number | 188595-46-0 |
| Smiles | Clc1nc2nccc2c(Cl)n1 |
| Appearance | Solid |
| Solubility | Slightly soluble in organic solvents |
| Pubchem Cid | 24897987 |
| Synonyms | 2,5-Dichloroimidazo[4,5-b]pyridine |
As an accredited 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 10 grams of 1H-imidazo[4,5-b]pyridine, 2,5-dichloro-, tightly sealed with a tamper-evident cap. |
| Container Loading (20′ FCL) | 20′ FCL container loading for 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- ensures secure, efficient, and compliant bulk chemical shipment. |
| Shipping | 1H-imidazo[4,5-b]pyridine, 2,5-dichloro-, is shipped in tightly sealed containers, protected from moisture and light. The chemical is handled according to hazardous material regulations, with appropriate labeling and documentation. Transportation follows international guidelines for hazardous chemicals, ensuring safety and compliance during transit to prevent spills or contamination. |
| Storage | 1H-imidazo[4,5-b]pyridine, 2,5-dichloro-, should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong acids, bases, and oxidizing agents. Always follow appropriate chemical storage protocols and ensure the container is clearly labeled. |
| Shelf Life | 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- is typically stable for 2–3 years when stored in a cool, dry, dark place. |
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Purity 98%: 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting Point 226°C: 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- with a melting point of 226°C is used in high-temperature organic synthesis, where it allows for stable reaction conditions. Stability Temperature up to 180°C: 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- with stability temperature up to 180°C is used in medicinal chemistry research, where it maintains molecular integrity during compound screening. Molecular Weight 188.01 g/mol: 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- at a molecular weight of 188.01 g/mol is used in agrochemical development, where precise molecular targeting enhances bioactivity. Particle Size ≤10 μm: 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- with a particle size less than or equal to 10 μm is used in controlled-release formulation studies, where uniform dispersion improves release kinetics. Assay ≥99%: 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- with an assay of 99% or higher is used in analytical reagent preparation, where high chemical purity provides reliable analytical results. Solubility in DMSO 50 mg/mL: 1H-imidazo[4,5-b]pyridine, 2,5-dichloro- with solubility in DMSO at 50 mg/mL is used in solution-phase screening, where it enables high-concentration dosing for biological assays. |
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Every batch of 1H-imidazo[4,5-b]pyridine, 2,5-dichloro-, runs through our reactors with close attention to every parameter. Years of chemical synthesis experience have taught us that small changes in temperature, pressure, or raw material quality will translate into big difference at the user’s end. Research groups and commercial production teams both want a material that is robust through all kinds of downstream steps. Our focus is to supply it at a purity that does not create surprises in process development or scale-up.
This compound stands out with a molecular structure that pharmaceutical chemists have found reliable for building kinase inhibitors, anti-viral scaffolds, and advanced agrochemical cores. Our own pilot chemists have run it through a wide range of conditions: high throughput screening libraries, medicinal chemistry expansion, custom analog synthesis. With repeated use, it’s clear that the two chlorine atoms at the 2 and 5 positions grant useful electronic properties. Unlike the single-chlorinated or unsubstituted analogs, the dichloro version opens more options for selective functionalization—something we’ve seen time and time again in both our labs and those of customers.
Users working with heterocycles anticipate headaches—especially those handling imidazopyridines or other bicyclic systems. Our manufacturing methods keep the material stable and non-hygroscopic. Chemists pouring out samples in gloveboxes or on the bench report dry, consistent powder, free-flowing and simple to weigh out. That comes from extensive process control early in synthesis, then close attention to drying and packaging. It might sound simple, but anyone who’s worked with sticky, clumpy heterocycles realizes what a difference it makes in day-to-day laboratory work.
For our small-scale collaborators, the 2,5-dichloro derivative lets them skip extra purification steps. By holding the impurity profile close to the limits seen in published syntheses, side-products don’t creep up at chromatography or in prep HPLC. That means less time staring at streaky plates, less solvent waste, and fewer head-scratching troubleshooting sessions during route optimization. More than one customer has remarked how much they appreciate that less time goes to cleaning up their own work after the raw material supplier.
We’ve produced nearly every variant of imidazo[4,5-b]pyridine in the book: unsubstituted, mono-halogenated, electron-donating, electron-withdrawing. The differences become striking during purification and reaction optimization. The dichloro- analog, particularly at the 2 and 5 positions, brings a unique balance between reactivity and stability. Chlorine deactivates certain positions on the ring and blocks unwanted side-reactions—valuable when you’re running selective couplings or late-stage derivatization.
Project teams aiming to introduce further substitution, such as Suzuki or Buchwald-Hartwig couplings, find the dichloro framework much more predictable compared to the mono-chloro analogs. Where mono-halogenated rings sometimes give mixture-prone outcomes, the 2,5-dichloro pattern delivers localized reactivity—the sort of thing you might miss just by reading a synthetic route, but recognize instantly once you scale a ten-gram reaction.
Making high-purity dichloro imidazopyridine costs more than the simpler versions and requires specific control at each halogenation stage. Our production engineers spend extra time confirming selectivity, as partial chlorination gives rise to isomeric impurities that can shadow in NMR and later confound bioassay work. We created our protocols from scratch after several customer complaints about unreliable supply from other vendors—sticky batches, off-color powders, misplaced peaks in LCMS. Long experience has taught us that investing in this compound’s synthesis pays off for every stakeholder.
Pharmaceutical discovery moves fast and expects suppliers to keep up. Whether the end user is hunting activity against a new target or crafting a focused SAR campaign, interruption at the building-block stage loses weeks or months that can’t be replaced. Medicinal chemistry teams want every gram to be exactly as expected: pure, consistent, and easily handled.
Several clients who develop kinase inhibitors asked us to ramp up supply of the 2,5-dichloro imidazopyridine once their early hits came back promising. Some of them shared their data under confidentiality, and we tracked how variations in our own material influenced their yields and purity after derivatization steps. Bringing these lessons back to our own floor, we improved drying cycles, tweaked solvent systems, and tightened in-process controls. This isn’t just quality-speak—it shows up as smoother batch-to-batch performance for the medicinal chemists downstream, and fewer headaches during hit expansion.
We’ve also supported customers shifting between milligram library synthesis and larger runs to feed animal studies or advanced screening campaigns. Scale-up brings its own set of challenges. Dusting off our own kilo-scale prep notes, we know that bulk synthesis amplifies every little hiccup from the lab. Our approach gives a powder that dissolves smoothly, handles without caking, and remains shelf-stable during extended storage.
It’s not all pharma: the same core finds paths into agricultural chemicals and advanced materials. The substitution pattern of 2,5-dichloro benefits agrochemical researchers who want metabolic blocking or environmental resilience. Bench scientists have described how the unique electronic properties compared to other halogenated imidazopyridines led to improved performance in crop protection leads. Several agrochemical partners requested custom pack sizes for field-ready formulation trials; our packaging team worked with them to deliver exactly what matched their workflow, all without introducing moisture or contamination from bulk transfer.
Material scientists occasionally approach us to run development batches for specialty coatings, sensors, or optoelectronics. Some of these projects require trace impurity control much tighter than what’s demanded in pharmaceutical applications—solvent residues, heavy metals, and halide byproducts matter at the parts-per-million level. We adjusted our purification scheme and raw material handling accordingly. Building enough flexibility to handle these wide-ranging applications has improved our own processes year after year.
Compared to certain pyridine derivatives, 2,5-dichloro imidazopyridine resists clumping and maintains a dry powdery texture over months of storage. Based on our retention samples going back several years, properly sealed drums or bottles show little physical change and retain full reactivity in follow-up reactions in external and internal trials. High humidity and temperature will increase the risk of gradual discoloration, as noticed in a few extreme test cases, but basic ambient storage and sealed packaging have proven reliable.
Every user knows the frustration of opening a long-stored chemical only to find an off-color, tacky mess. By re-running dozens of retention samples and stress testing under hot warehouse conditions, we’ve minimized these problems. A lot of traditional compounds in this family tend to attract water once opened or broken down, especially lower-chlorinated versions or those with alkyl substitutions; the dichloro version proves much more robust in that regard.
On several contract manufacturing projects, we watched how researchers integrated our 2,5-dichloro imidazopyridine at different points in their broader syntheses. In one notable project—a client scaling up late-stage analogs ahead of IND submission—the upstream supplier delivered material with a slightly different melting point and subtle spectral impurities. The project threatened to bog down as every following step became unpredictable. After a quick exchange of technical data, we adapted by overhauling our halogenation process, stepped up final purification, and delivered new material on a tight timeline. The client not only rescued their process but ended up extending their program based on the successful data package.
Direct conversations with medicinal, agro, and material scientists have helped us fine-tune every aspect—particle size, flow characteristics, packing options, impurity reporting. It’s a feedback loop that continually pulls us beyond textbook specifications, into the realm of real working chemistry. That shared problem-solving defines our approach—chemistry for chemists, built on trial, adjustment, and honest reporting.
Industry is demanding not just quality, but real effort to minimize environmental impact and improve supply reliability. For 2,5-dichloro imidazopyridine, we’ve evolved our process away from traditional chlorinating agents known for producing persistent waste or halogenated byproducts difficult to dispose of. By investing in more selective halogenation methods and closed-loop solvent recovery, fewer waste drums leave our facility, and downstream users receive cleaner, safer material.
Process intensification has given us a more reproducible yield and allows for flexible batch sizes—handy for both research and commercial users. Several times, unexpected orders have landed on our production schedule for sudden scale-up. Thanks to modular reactor trains and a well-drilled operations team, we now meet accelerated turnaround without having to loosen quality standards. This wasn’t always the case—older setups limited us to fixed batch sizes and inevitably delayed important projects. Through continuous investment and real-world necessity, our system now meets the kind of demand industrial chemistry expects.
Every chemical manufacturer claims high purity and reliability, but only regular feedback from downstream chemists separates real success from empty promises. Several times a year, we rerun side-by-side tests—our own product against major international suppliers. Our analytical team compares LCMS, NMR, melting point, and colorimetric data. We pay extra attention to trace impurities below regulatory thresholds, since after several close calls at customer labs, those minute differences often make or break high-precision biological or physical experiments.
Analytical reproducibility stands out as a make-or-break metric. Each batch of dichloro imidazopyridine receives cross-checked NMR and GC-MS evaluation against a library of retained samples. If anything drifts from established benchmarks, we remove the batch from release. That avoids the all-too-common downstream headaches and false starts seen from suppliers treating QC as a checklist, rather than a problem-prevention system.
On at least two occasions, external customers sent us advanced analytical data on coupled products—data that revealed subtle differences invisible on basic spectrometry. Reviewing these findings, we built them into our own internal protocols. Instead of treating QC as an endpoint, it’s now a living system that grows alongside new research demands. Our goal is that no customer—no matter how advanced their analytical capabilities—finds surprises in our material.
Recent disruptions in global logistics put the spotlight on the weakest links in supply. We saw first-hand how delays from upstream raw material sectors translated into frustration at the end of research lines. After a particularly rough season, we re-sourced baseline chemicals from multiple regions and invested in a local backup production setup. That resilience means steady supply, even while global markets stumble. Users planning multi-month, multi-kilo development cycles appreciate knowing their inventory won’t dry up at a critical moment—a peace of mind that can’t be measured in a spec sheet.
Smaller customers have sometimes struggled to order less-than standard commercial quantities from global players; our warehouse model enables delivery in both standard packs and custom increments. This reduces excess waste, storage burdens, and keeps cash flow smoother for academic and startup clients who can’t tie up budgets on large, single-use lots.
What sets a real manufacturer apart from intermediaries is the day-to-day, batch-by-batch adjustment. Problems and solutions learned on our own shop floor translate into real improvement for end users. Through close attention to customer results, careful material science, and regular in-house experimentation, every shipment of 2,5-dichloro imidazopyridine reflects our commitment to building practical, robust, and trustworthy chemistry.
The compounds we make are more than catalog entries or case numbers. Every bottle, every drum, and every process scale reflects years of challenge, failure, and creative solution. Our dichloro imidazopyridine has moved through countless hands—students synthesizing their first analog, experienced process chemists scaling ten kilos at a time, agronomists trialing new crop protection agents. Each user brings a new use, a new challenge, and more feedback—feedback that continues to shape the compound we deliver.
Chemistry is always evolving, and so must those who make the building blocks. By staying grounded, honest, and closely linked to actual user experience, we continue to provide material that doesn't just meet the paperwork but actually helps progress meaningful science.