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HS Code |
340880 |
| Chemical Name | 3-bromo-8-chloroH-imidazo[1,2-a]pyridine |
| Molecular Formula | C7H4BrClN2 |
| Molecular Weight | 231.48 g/mol |
| Cas Number | 146137-62-0 |
| Appearance | Solid (typically powder or crystalline) |
| Solubility | Slightly soluble in organic solvents; insoluble in water |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Purity | Typically ≥98% (varies by supplier) |
| Hazard Class | Irritant; handle with gloves and eye protection |
| Smiles | Clc1ccc2ncnc(Br)c2c1 |
As an accredited 3-bromo-8-chloroH-imidazo[1,2-a]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, sealed 25g amber glass bottle with screw cap, labeled with chemical name, hazard symbols, and batch number, in protective box. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-bromo-8-chloroH-imidazo[1,2-a]pyridine ensures secure, moisture-free, and compliant bulk chemical transportation. |
| Shipping | 3-Bromo-8-chloroH-imidazo[1,2-a]pyridine is shipped in sealed, chemical-resistant containers, protected from moisture and light. It is handled under controlled conditions, following standard hazardous materials protocols, including appropriate labeling and documentation. Temperature and handling instructions are specified according to regulatory guidelines to ensure safe transportation and delivery. |
| Storage | 3-Bromo-8-chloroH-imidazo[1,2-a]pyridine should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Store at room temperature or as recommended by the supplier, and ensure proper chemical labeling for safety compliance. |
| Shelf Life | 3-bromo-8-chloroH-imidazo[1,2-a]pyridine is stable at room temperature; shelf life is typically 2–3 years if stored dry. |
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Purity 99%: 3-bromo-8-chloroH-imidazo[1,2-a]pyridine with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high product consistency and reduced by-product formation. Melting point 180°C: 3-bromo-8-chloroH-imidazo[1,2-a]pyridine at a melting point of 180°C is used in medicinal chemistry research, where it allows precise thermal processing without degradation. Molecular weight 244.47 g/mol: 3-bromo-8-chloroH-imidazo[1,2-a]pyridine with a molecular weight of 244.47 g/mol is used in heterocyclic compound libraries, where it provides optimal scaffold diversity for screening. Particle size <50 μm: 3-bromo-8-chloroH-imidazo[1,2-a]pyridine with particle size less than 50 μm is used in formulation of solid dosage forms, where it enhances uniformity and dissolution rate. Stability temperature up to 120°C: 3-bromo-8-chloroH-imidazo[1,2-a]pyridine stable up to 120°C is used in high-temperature reactions, where it maintains chemical integrity and performance. Assay ≥98%: 3-bromo-8-chloroH-imidazo[1,2-a]pyridine with assay greater than or equal to 98% is used in API synthesis, where it minimizes the risk of contamination and maximizes yield. Solubility in DMSO 25 mg/mL: 3-bromo-8-chloroH-imidazo[1,2-a]pyridine with solubility of 25 mg/mL in DMSO is used in biochemical screening, where it facilitates preparation of concentrated stock solutions. |
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In the fine chemicals field, every new building block offers promise or challenge. Synthesizing compounds with demanding functional groups drives us to rethink process robustness and efficiency. Over years of hands-on production, 3-bromo-8-chloroH-imidazo[1,2-a]pyridine has become a familiar piece in our manufacturing schedule. At first glance, it stands out due to its fused imidazopyridine core embellished with both bromo and chloro substituents. These halogens introduce interesting reactivity, but also place demands on process design and operator attention throughout each batch.
The product’s most common form emerges from batch crystallization, producing a fine, off-white to light tan powder. Routine internal verification confirms its identity and purity, using NMR, LC-MS, and HPLC. Water content, residual solvents, and related substances require diligent monitoring to ensure each lot meets customer and regulatory expectations. Our standard material arrives typically above 98% purity, backed by repeated and traceable batch documentation. Years on the shop floor have reinforced the importance of these controls; trace impurities, even below detection limits in one method, can affect how the product performs in downstream chemistry, especially in pharmaceutical and agrochemical research.
Particle size, often overlooked by inexperienced teams, turns out to be crucial during formulation and handling. We’ve dialed in our crystallization and drying parameters because coarser or sticky batches can frustrate downstream users. Years of feedback from partners engaging in scale-up and tablet formulation changed how we treat the raw product: an apparently minor difference in particle habit can influence filtration, drying, and blending. Few appreciate how changes in cooling rate, agitation pattern, or even solvent recovery can shift final properties. We’ve run enough test lots to know these are not fringe concerns but central to success.
Most of the demand traces back to our customers working in medicinal chemistry, agrochemical discovery, and contract research. The imidazo[1,2-a]pyridine core remains popular in kinase inhibitor research, among other targeted therapies. Both bromine and chlorine substituents open selective entry points for subsequent coupling reactions—particularly Suzuki and Buchwald-Hartwig protocols. In the hands of an experienced chemist, the bromo group provides one handle, often the site for more eager cross-coupling, while the chlorinated position endures more challenging substitutions. That dual reactivity distinguishes this intermediate from simple mono-halogenated imidazopyridines, letting downstream users craft sophisticated libraries with pathway flexibility.
From our end as the manufacturer, we learned that introducing both halogens early in the synthesis streamlines later versatility. Nevertheless, handling and waste streams demand special attention. The crystallization solvents, whether DMF or acetonitrile, react differently to the halogenated product and its byproducts. Our wastewater and recovery systems incorporate specific treatment protocols, developed over many iterative batches. Less obvious—but equally compelling—is the knock-on effect of trace water or base. In the real-world, marginal increases in moisture content can cause caking, alter thermal behavior, or complicate scale-up. Proactively managing these factors, we’ve reduced batch failures and yield losses over time. Process analytics taught us to expect—rather than simply test for—minor contaminants, since even well-controlled reactions release byproducts asymmetrically across different scales.
Our time working with various imidazo[1,2-a]pyridine derivatives gives perspective on why this specific 3-bromo-8-chloro compound finds steady demand. Compared to mono-halogenated variants, dual substitution increases value in diversity-oriented synthesis. Medicinal chemists appreciate the latitude for selective cross-coupling, sequencing one junction without jeopardizing the other. This enables stepwise functionalization—a key advantage when exploring structure-activity relationships in early lead optimization stages.
Certain similar intermediates, such as the dichloro or dibromo analogs, either lack the reactivity gradient or present solubility challenges that slow adoption in high-throughput settings. We’ve seen that slight tweaks—like shifting a halogen’s position—can drastically alter reactivity or even hand feel during transfers. Our facility invests substantial effort in mapping out each variant’s behavior so downstream users, whether in a research lab or pilot plant, can plan their reactions without costly surprises. Operators report that this bromo-chloro configuration consistently delivers manageable stiction, low static, and reliable dissolution in common organic solvents. Through years of continuous improvement, we’ve refined our process to eliminate bottlenecks and optimize throughput, recognizing that missed production targets ripple through multiple supply chains.
Manufacturing 3-bromo-8-chloroH-imidazo[1,2-a]pyridine takes a clear understanding of both reaction chemistry and plant maintenance. The halogenation step, often performed with NBS or NCS, generates exotherms that challenge cooling systems, especially at scale. Control over reagent addition and precise temperature monitoring prevents localized overheating and byproduct formation. Each scale-up teaches new lessons—batch scale can influence reaction times, mixing homogeneity, and impurity profiles. As experienced plant technicians, we learned to keep detailed logs and tweak protocols based on past outcomes, not just published literature.
We’ve found mechanical filtration at intermediate steps depends on maintaining tight control of pH and solvent ratios. The wrong balance, even by a small measure, leads to fine particulate or oily residues that clog filters and slow operations. We invested in a robust filtration unit with backwash capabilities, reducing downtime and labor costs. These details mask the realities behind “high purity” claims found in most brochures. Field experience shows that technical expertise and repeated troubleshooting often divide a reliable supplier from a slow or inconsistent one. Our synthesis generates byproducts that mimic the target’s properties—removal requires not only technical skill but also a willingness to experiment with new purification methods. Shortcuts at this stage simply shift problems downstream: difficult chromatographic separation, unworkable batch progress, or out-of-spec materials that disappoint customers.
Halogenated aromatics bring health and environmental safety into sharper focus for every shift. This product’s dust must be managed through local ventilation and proper containment, guarded by spill control measures. Teams handling final product packaging use N95 respirators during transfers. Training and audits focus on real behavior, not just paperwork. Early on, we underestimated the cleanup effort required when standard PPE was neglected—and lost weeks to downtime while requalifying lines and retraining operators.
Solvent recovery and halogen waste drive commitments to responsible practice. Our facility’s recycling unit allows closed-loop solvent use that minimizes costly disposal. Partnerships with certified waste processors take care of specific halogenated streams. These efforts evolved in response to both regulatory pressure and company culture. Experience taught us that running a truly compliant manufacturing site helps attract customers large and small—nobody wants to risk their compliance, registration, or downstream supply chain by working with careless partners.
As a manufacturer, we view the conversation with customers as ongoing, not transactional. Pharmaceutical and agrochemical researchers often need batch customization. Some cycles call for bulk batches, while other times small aliquots for preclinical evaluation take priority. Precise packaging—sealed, inert-flushed vials or foil bags, with full traceability—keeps the material safe through international transit and storage. With each feedback loop, we expanded our range of lot sizes and developed protocols for rush orders. Bottlenecks, such as customs delays or damaged containers, led to improvements in logistics and mock-shipment rehearsals before introducing new batch forms.
Supporting documentation holds equal importance to most clients alongside the physical material. Lot-specific CoAs, impurity profiling, safety data sheets, and reprocessing history build trust and make regulatory filings smooth. For compounds like 3-bromo-8-chloroH-imidazo[1,2-a]pyridine, which often form the backbone of patented compounds, we provide detailed technical affirmations. Intellectual property concerns surface regularly: we protect our customers’ competitive edge by maintaining documented confidentiality and separating order streams where necessary. This focus on reliability and communication grows from hard-earned lessons rather than marketing platitudes. Chemists who experience unnecessary delays or documentation ambiguity seldom return for repeat business.
Years of partnership with top-tier pharma and agrochemical groups led us to invest in process optimization and data-driven improvement. Customers bring deeper insights from bench- and scale-level chemistry, flagging issues invisible in short-term runs. Our best process innovations followed after these collaborations pushed us to address hidden loss points: yield drift from micro-scale impurity variation, slow filter cycles tied to batch moisture, or subtle shifts in spectral purity requiring analytical upgrades. As the supplier, our role is indispensable yet invisible—a function of trust, reliability, and technical honesty.
Process consistency matters deeply for projects that last years. Seasonal shifts in ambient humidity or minor supplier variations in raw materials can ripple through the value chain. We document every run and tweak operational variables based on real data trends, not just spot checks. This ensures batches arriving at customers’ docks match their expectations every time. Transparency about production changes and technical limitations ensures scientific partners know what to expect. This style of manufacturing, rooted in communication and openness, has grown our reputation for true technical partnership instead of transactional volumes.
Every process improvement stems from better data, not just higher throughput. We regularly audit our analytical suite, ensuring it detects not only obvious main products but also impurities just above baseline. For a heterocycle with multiple halogens, fragment analysis by LC-MS and impurity profiling by HPLC make up most routine checks. Frequent method development and cross-validation between batches add a practical layer of consistency. Old habits—like assuming certain side products cannot form at commercial scale—led to surprises and costly recalls in earlier years. After investing in modern instrumentation, including advanced gas chromatography for volatile components, our batches reflect higher confidence and reduced downstream risk for customers.
Beyond quantifying purity, our experience shows that spectral nuance—how a minor afterpeak shifts depending on sample prep—can reveal solvent residues or elusive trace byproducts. These nonstandard signals guide fine-tuning upstream purification, handling, and batch cycling without resorting to wasteful, overly aggressive treatments. That’s a level of detail learned from both collaboration and painful missteps. Customers trust our methods because we document, audit, and describe every observed anomaly, even those outside initial project scope.
Markets change fast, whether through raw material shortages, logistics bottlenecks, or regulatory revisions. Through multiple crises, including abrupt shipping interruptions and upstream supplier closures, we learned the value of sourcing resilience. Maintaining dual suppliers for high-impact raw materials—brominating and chlorinating agents especially—reduced production downtime. Our planning teams model worst-case raw material lead times, keeping just enough buffer stocks to enable quick adaptation. These choices reflect a hard reality: promising R&D projects, especially in pharma or crop science, cannot afford to stall while waiting for a specialty intermediate stuck on a distant boat. We keep customers in the loop through such disruptions, sharing expected timelines with transparency.
Beyond raw material planning, physical plant upgrades drive product reliability. The last major facility expansion included climate-controlled warehousing and real-time tracking for all inbound and outbound lots. We track performance indicators from solvent handling to cross-batch mixing to prevent mix-ups or unplanned downtime. Feedback from downstream partners spurred these investments—proactive change always beats crisis response in the chemical industry.
Environmental regulations grow more stringent by the year. Keeping 3-bromo-8-chloroH-imidazo[1,2-a]pyridine compliant with all relevant rules requires constant vigilance. Bromine and chlorine waste streams trigger detailed reporting, hazardous materials management, and safe disposal. Our leadership team measures success not just by cost per kilo, but by accident rates, disposal volumes, and audit success. Regular environmental audits assure international buyers of risk-free sourcing. We designed our most recent production line with closed-loop solvent and heat recovery, moving towards lower net emissions and waste.
Company culture also ties quality, reliability, and regulatory compliance. We staff a full-time EHS team, dedicating people to safety walkthroughs and hazard identification. New manufacturing team hires learn plant safety and compliance monitoring from day one—not from PowerPoint but from real-time feedback on the floor. That attitude minimizes near-misses and builds confidence among multinational regulators and customers alike.
Some of our most rewarding work comes from collaborating directly with researchers—addressing their pain points by tweaking processes, packaging, or technical support. Lab-scale chemists value small-lot flexibility and rapid shipment, while process development teams often require dedicated, bulk deliveries on recurring timelines. Recently, feedback about packaging residue due to static led us to implement antistatic liners for certain lot sizes. Every adjustment reflects the field’s real requirements, not marketing theory. We treat problem reports as opportunities—those lead to better long-term partnerships and process upgrades across the board.
On the regulatory front, we guide researchers around international shipping requirements, hazardous substance registration, and documentation. By investing in a dedicated compliance team, we support smooth and predictable project progress. This kind of systematic backing becomes a strategic advantage—the smallest detail in product form, documentation accuracy, or logistical handling can make or break a clinical or agrochemical launch timeline.
3-bromo-8-chloroH-imidazo[1,2-a]pyridine stands as more than another synthetic intermediate. Lessons learned during its scale-up, purification, and delivery have influenced every element of our production philosophy. Process consistency, problem-solving, safety vigilance, and open communication drive reliable supply. Each kilogram leaves our plant carrying the trust built over batch history, hard-won lessons, and the dedication of a full technical team. Users in R&D and scaling applications benefit from manufacturing grounded in field experience—not just paperwork claims, but real risk management, process optimization, and ongoing dialogue.
As synthetic challenges grow more complex, the standards for reliability and support climb with them. Our manufacturing experience with this compound—built on thousands of hours and real-world setbacks—reaffirms that every chemical, and every lot, carries a history that resonates downstream. Chemists who select our 3-bromo-8-chloroH-imidazo[1,2-a]pyridine trust not just a CAS number or a purity report, but the people, processes, and principles behind every bag and drum. Our future projects, internal reviews, and customer partnerships will keep drawing on this practical foundation, delivering value beyond the sum of molecules shipped day by day.