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HS Code |
411963 |
| Chemicalname | 6-Bromo-8-chloroimidazo[1,2-a]pyridine |
| Molecularformula | C7H4BrClN2 |
| Molecularweight | 231.48 g/mol |
| Casnumber | 573762-49-5 |
| Appearance | Light yellow to brown solid |
| Solubility | Slightly soluble in DMSO, DMF, and methanol |
| Smiles | C1=CN2C=NC=C2C(=C1Br)Cl |
| Inchi | InChI=1S/C7H4BrClN2/c8-5-1-2-11-6(3-5)4-7(9)10-11/h1-4H |
| Iupacname | 6-bromo-8-chloroimidazo[1,2-a]pyridine |
| Purity | Typically ≥ 95% (as specified by most suppliers) |
| Storagetemperature | 2-8°C (refrigerated) |
As an accredited 6-Bromo-8-chloroimidazo[1,2-a]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial containing 5 grams of 6-Bromo-8-chloroimidazo[1,2-a]pyridine, securely capped, with hazard and identification label affixed. |
| Container Loading (20′ FCL) | 20′ FCL loaded with securely packed drums of 6-Bromo-8-chloroimidazo[1,2-a]pyridine, meeting safety and international shipping standards. |
| Shipping | 6-Bromo-8-chloroimidazo[1,2-a]pyridine is shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent contamination or moisture absorption. It is handled following all relevant safety guidelines and regulations, including proper labeling and documentation, and is typically shipped via ground or air freight with hazardous material precautions as required. |
| Storage | Store **6-Bromo-8-chloroimidazo[1,2-a]pyridine** in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and clearly labeled. Avoid exposure to moisture or extreme temperatures. Use suitable chemical-resistant containers, and follow all relevant safety and handling guidelines as specified in the compound’s SDS. |
| Shelf Life | 6-Bromo-8-chloroimidazo[1,2-a]pyridine is stable for at least two years when stored cool, dry, and protected from light. |
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Purity 98%: 6-Bromo-8-chloroimidazo[1,2-a]pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures reproducible bioactive molecule formation. Melting Point 156°C: 6-Bromo-8-chloroimidazo[1,2-a]pyridine with melting point 156°C is used in high-temperature coupling reactions, where thermal stability prevents decomposition. Molecular Weight 246.48 g/mol: 6-Bromo-8-chloroimidazo[1,2-a]pyridine of molecular weight 246.48 g/mol is used in lead compound optimization studies, where precise stoichiometry enhances reaction efficiency. Stability Temperature up to 120°C: 6-Bromo-8-chloroimidazo[1,2-a]pyridine with stability temperature up to 120°C is used in medicinal chemistry research, where stability under assay conditions maintains compound integrity. Particle Size <20 µm: 6-Bromo-8-chloroimidazo[1,2-a]pyridine with particle size less than 20 µm is used in solid-state formulation development, where fine particle size improves dissolution rate. Water content <0.5%: 6-Bromo-8-chloroimidazo[1,2-a]pyridine with water content below 0.5% is used in moisture-sensitive syntheses, where low hygroscopicity minimizes side reactions. Residual solvent <100 ppm: 6-Bromo-8-chloroimidazo[1,2-a]pyridine with residual solvent under 100 ppm is used in GMP-compliant drug manufacturing, where minimal impurities satisfy regulatory requirements. |
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Every chemist in our production lab knows the challenges that come with finding the right heterocyclic scaffold. It’s rarely as simple as picking a material off the shelf; the pathway demands predictability, proven purity, and a level of consistency to satisfy both development and scale-up. Over the years, 6-Bromo-8-chloroimidazo[1,2-a]pyridine has emerged on our own workbenches as a backbone for innovative synthesis, showing up wherever medicinal and agrochemical research calls for precision.
We run a tightly controlled process to ensure reproducibility. No shortcuts or compromises. From raw precursor selection to the reaction controls, our facility leans into years of real-world feedback. Every batch follows validated steps, refining them through input from synthetic teams and scaling engineers. Chemists in our plant turn out purity levels well above 98 percent because trace contaminants undermine downstream chemistry and project timelines. The end product comes in off-white to pale yellow crystalline solids, which speaks to both chemical strength and practical handling.
Purity makes or breaks these intermediates. Without strict control on halogen substitution and byproduct removal, anything built from this scaffold loses reliability. We routinely analyze samples by HPLC and NMR, tracking the smallest impurities. Customers working in drug discovery or pesticide development have voiced how cleanliness at this stage shapes their results—not just laboratory runs, but regulatory submissions and upscaling. Moisture must sit below 0.5 percent, and each shipment includes a detailed analysis so researchers stay fully informed.
This compound acts as a pivotal building block for heterocyclic chemistry. Medicinal chemists reach for it to construct kinase inhibitors, antivirals, or more exploratory compound libraries. Agrochemical innovators employ it to build pest-control scaffolds with high selectivity. What stands out to our team is the degree of transformation flexibility—its 6-bromo and 8-chloro positions invite cross-coupling, especially Suzuki and Buchwald-Hartwig reactions. These substitutions often serve as hooks for introducing functional diversity, expanding the chemical space accessible from a single intermediate.
Over the last decade, synthetic teams across the pharmaceutical, crop science, and materials science industries have emphasized reliability over flamboyant claims. Our own projects routinely demand careful scale-ups from gram to multi-kilo lots. Clients want the peace of mind that a batch from six months ago reacts just like the one arriving today—no unknowable side reactions or uninvited isomers. Practical feedback from these real projects has taught us to focus on process consistency, from filtration to packing, to preserve the properties customers expect. We know that when an intermediate fails, whole syntheses grind to a halt. Every factory decision, from solvent selection to drying technique, answers to the same standard: proven downstream performance, not just theoretical purity.
In the global pool of pyridine derivatives, most candidates offer either versatility or reactivity—but rarely both at once without trading off shelf stability or handling. 6-Bromo-8-chloroimidazo[1,2-a]pyridine stands out for striking a balance. Its dual halogenation gives chemists two unique points for modification, supporting sequential or orthogonal transformations. Fewer options offer this level of directed synthesis without complicating purification or triggering instability. Dorfman and Makarov (published synthetic methodologies) have both exploited this intermediate for rapid analog generation, achieving yields that less robust pyridine backbones can’t match. For the ultimate user, this means more structure-activity relationship data with less route complexity.
Seasoned staff will tell newcomers to keep these halogenated intermediates shielded from unnecessary moisture and sunlight. In the lab, we've found simple desiccators or well-sealed drums maintain quality over the months needed for large synthesis programs. Aggressive oxidation risks decomposition, so each facility run emphasizes careful handling. Waste minimization matters, too. We recover and recycle solvents using modern reprocessing columns, building cleaner production and safer environments. Waste streams are evaluated on a batch-by-batch basis. This attention to detail isn't dictated by regulation alone—it’s how process chemists avoid the headaches downstream that come with contamination or material loss.
Marketing decks lean heavily on broad claims, but it’s our experience inside the production suite that determines what counts. Some researchers insist on 99.5 percent purity, but that extra step hammers overall yield and cost. In practice, we've learned 98-99 percent often delivers the precise reactivity medicinal and agrochemical discoveries require, without introducing hidden inefficiencies. Teams working at the bench benefit most from accurate, transparent analytics over pie-in-the-sky promises. Our reports don’t just check the right regulatory boxes; they report actual impurity profiles so chemists can plan—no matter if it’s for regulatory filing or a first round of SAR synthesis.
Many fail to appreciate the gulf between tens of grams and hundreds of kilograms. Within our manufacturing blocks, adjustments to crystallization, temperature ramp rates, and filtrate handling all reflect lessons from real campaigns. New employees learn quickly that maintaining crystal habit—without introducing hard-to-remove fines—pays dividends in downstream operations such as dissolution or further coupling. By standardizing our drying and packaging, the material flows smoothly into automated handling systems—critical for pilot plant or high-throughput pharma labs. The logistics team works closely with production, flagging any sensory changes in physical form, color, or particle size before a drum hits the outbound dock.
Commodity chemical suppliers often disappoint research teams who expect unwavering supply. No one feels the pain of halted R&D more than in-house chemists. Years of actual shortages have taught us to keep raw ingredient contracts diversified, invest in vertical integration where possible, and pin inventory plans to seasonal demand cycles. Experienced buyers in the pharma world tell us unplanned delays lose months of lead time; anticipating these risks sets our strategy. We've built redundancy into reactors and staffing to guarantee continued production, even during market turbulence or unforeseen logistics storms.
Over time, it’s the regular exchanges with client project leaders and their feedback that shape our process design. Sometimes simple tweaks—more secure drum seals, minor milling adjustments, changes in drying time—yield significant improvements to day-to-day usability at the bench. An early pharma customer once flagged that a small, persistent impurity was complicating a downstream step. Our process chemists dove back into the synthesis, identifying extraction tweaks that eliminated the offender without raising cost or lead time. We treat these lessons as cumulative, building a long-term playbook that benefits every customer, not just the one raising the flag.
No responsible manufacturer ignores their footprint. Our compliance team meets regularly to evaluate process risk, hazardous waste minimization, and worker safety under evolving standards. Every batch run includes data review for emissions, energy use, and water consumption. Incentives for plant managers reward waste minimization and near-miss reporting because experience tells us that a single careless incident can upend years of trust. From chemistries selected to process design, we scrutinize every step for sustainability. Solvent recovery shields both our margins and our environmental record. Downstream users often signal their appreciation through repeat orders, citing both product quality and environmental due diligence as non-negotiable requirements.
Chemical R&D never stands still. Our process teams stay plugged into academic bulletins and patent news, adapting methods as new synthetic routes or process intensifications earn peer validation. Last year, implementing a new catalyst reduced side-product formation by 15 percent—a change only validated through careful, batch-wise trials. Our philosophy privileges tried-and-true chemistry, balancing the excitement of new methods with the dependability required for critical-path intermediates. Researchers concerned with downstream stability or reactivity find our approach aligns with their own: evolutionary change, not reckless leaps, serves both output and innovation.
Start-ups and university labs operate with leaner resources but place ambitious demands on intermediates like 6-Bromo-8-chloroimidazo[1,2-a]pyridine. Early engagement with these groups unearths application trends—recently, a focus on new antiviral candidates and crop-protection molecules with higher resistance thresholds. By supporting custom modifications or supplying small-lot splits for preclinical work, we've watched promising ideas scale into globally significant programs. Relationships built on small wins today foster larger partnerships as new compounds clear each milestone in their path to the market.
In our own R&D group, the first trial with this intermediate took on the synthesis of a novel kinase inhibitor. The team noted smooth reactivity and clean NMR signals, pointing to efficient coupling at the bromo and chloro positions. Early skepticism about shelf stability faded as materials held integrity through the entire campaign, outlasting more traditional imidazopyridines under identical conditions. The learning: robust intermediates translate to fewer headaches in days packed with deadlines.
One production campaign showed unexpected difficulties with post-reaction work-up, as water-soluble side products risked carryover into the main fraction. The solution combined tighter pH control during extraction and an optimized, staged wash—fixed not by theory, but by practical repetition and insistence from staff on the ground. Issues like these reinforce an open feedback loop between operators and process chemists, sharpening process resilience and cutting back costly rework. Every lesson carries forward, protecting subsequent batches and customer targets alike.
Trust between chemical supplier and user outlasts any single transaction. Several multi-year projects began with a few grams sent for feasibility study; as their confidence in batch purity and reproducibility grew, these partnerships deepened. Our logistics office maintains regular communications, aligning delivery schedules to ease warehouse overflow for customers forecasting big campaigns. Our plant chemists understand that every late drum is not just a logistical miss but a potential risk to a long chain of research. Turning out 6-Bromo-8-chloroimidazo[1,2-a]pyridine with integrity anchors these collaborations in mutual reliability.
We notice an uptick in requests for masked substituents or difunctional halogen patterns even more complex than what this intermediate offers. While our core process stays focused, R&D teams probe routes to unlock new analogs, testing catalyst tolerance and seeking greener solvents. Where possible, we pilot new approaches for existing customers, providing supporting analytical data and guidance. Internal discussions revolve around process scale, regulatory acceptance, and novel application spaces in fine chemicals and specialty materials. Staying active means more than just manufacturing; it involves anticipating the changing needs of leading edge chemists worldwide.
6-Bromo-8-chloroimidazo[1,2-a]pyridine has earned its stripes on our production line because it outperforms competitors in both stability and transformation efficiency. Clear process documentation, batch-to-batch reproducibility, and on-time logistics support our partners from discovery kick-off to regulatory submission. By centering our methodology on the facts from daily production and honest dialogue with our clients, we strengthen everyone’s ability to bring new molecules from idea to reality. Every drum shipped reflects our commitment, not to generic claims, but to the standards set by chemists in the world’s most demanding laboratories.
It’s not enough to produce a quality material in isolation. Our company takes pride in learning from every interaction, whether it’s a big pharma client scaling for clinical trials or a university startup making their first analog library. We invest in staff training, build redundancy into our supply chain, and open doors to technical troubleshooting as routine practice. Industry calls for more than raw materials—it calls for trust, partnership, and continuous technical innovation. For all of us in chemical manufacturing, each improvement made with 6-Bromo-8-chloroimidazo[1,2-a]pyridine marks progress for the entire field.