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HS Code |
973282 |
| Chemical Name | 1H-imidazo[4,5-b]pyridine, 5-bromo- |
| Cas Number | 56741-17-6 |
| Molecular Formula | C6H4BrN3 |
| Molecular Weight | 198.03 |
| Appearance | Off-white to light yellow powder |
| Melting Point | 219-223 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | Brc1cc2nc[nH]c2n1 |
| Storage Conditions | Store at room temperature, protected from light and moisture |
| Inchi | InChI=1S/C6H4BrN3/c7-4-1-5-8-2-10-6(9-5)3-4/h1-3H,(H,8,9,10) |
As an accredited 1H-imidazo[4,5-b]pyridine, 5-bromo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 1H-imidazo[4,5-b]pyridine, 5-bromo- (5g) is packaged in an amber glass vial with a tightly sealed screw cap. |
| Container Loading (20′ FCL) | 1H-imidazo[4,5-b]pyridine, 5-bromo- is securely packed in 20′ FCL drums or bags for safe bulk transport. |
| Shipping | 1H-imidazo[4,5-b]pyridine, 5-bromo- is shipped in tightly sealed containers, protected from light and moisture, and typically under ambient or cool conditions. Packaging complies with safety regulations for hazardous materials. Shipping includes appropriate labeling and documentation to ensure safe handling and transport per chemical safety standards. |
| Storage | 1H-imidazo[4,5-b]pyridine, 5-bromo- should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Use appropriate safety measures and store according to your institution's chemical safety guidelines to avoid contamination and degradation. |
| Shelf Life | The shelf life of 1H-imidazo[4,5-b]pyridine, 5-bromo- is typically 2–3 years when stored in a cool, dry place. |
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Purity 98%: 1H-imidazo[4,5-b]pyridine, 5-bromo- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Melting point 215-218°C: 1H-imidazo[4,5-b]pyridine, 5-bromo- with a melting point of 215-218°C is used in medicinal chemistry research, where it provides thermal stability during compound screening processes. Molecular weight 210.04 g/mol: 1H-imidazo[4,5-b]pyridine, 5-bromo- with molecular weight 210.04 g/mol is used in heterocyclic compound design, where it facilitates predictable molecular integration into drug scaffolds. Stability at 25°C: 1H-imidazo[4,5-b]pyridine, 5-bromo- with stability at 25°C is used in chemical library storage, where it maintains compound integrity for extended periods. Particle size <50 μm: 1H-imidazo[4,5-b]pyridine, 5-bromo- with particle size less than 50 μm is used in high-throughput screening formulations, where it achieves rapid dissolution and homogeneous mixtures. Residual solvent <0.5%: 1H-imidazo[4,5-b]pyridine, 5-bromo- with residual solvent below 0.5% is used in analytical reference material preparation, where it delivers enhanced analytical accuracy and repeatability. UV absorbance (lambda max 290 nm): 1H-imidazo[4,5-b]pyridine, 5-bromo- with UV absorbance at lambda max 290 nm is used in quantitative spectroscopic assays, where it enables reliable compound quantification. HPLC purity >99%: 1H-imidazo[4,5-b]pyridine, 5-bromo- with HPLC purity greater than 99% is used in regulatory toxicology studies, where it reduces impurity-related experimental variance. |
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Researchers keep pushing the boundaries of molecular design, and every new tool carries the weight of real progress. 1H-imidazo[4,5-b]pyridine, 5-bromo- doesn’t aim for the spotlight, but countless scientific achievements depend on molecules like it. Its unique fused imidazo-pyridine core attracts attention in both academia and industry. The addition of a bromine atom at the fifth position on its aromatic scaffold increases its reactivity, giving it an extra edge for those aiming to synthesize more complex substances without the slowdowns that plain derivatives usually bring.
Any chemist who has handled the parent imidazo[4,5-b]pyridine will notice that introducing bromine changes more than just the molecule’s mass. The electronic distribution around the ring gets a subtle shift, opening up new chemical pathways for Suzuki, Buchwald-Hartwig, and Sonogashira couplings. From my experience as a synthetic chemist, that bromine serves as a reliable handle. It gives a predictable site for functionalization, which really matters when complex library synthesis becomes the goal. It saves time and minimizes dead ends, letting a team focus energy on promising directions instead of fighting the quirks of less cooperative scaffolds.
In the age of targeted drug discovery, every single modification to a molecular core matters. The 5-bromo substituent doesn’t just offer chemists a generic brominated group – it directs reactivity with a sharp focus. This is not like adding a halogen for ornamentation. In the hands of drug designers, compounds like this allow trials of different pharmacophores on a proven base. If you aim to introduce aromatic amines, alkynes, or heterocyclic fragments for activity screening, having a stable, reactive bromide at a defined position does the heavy lifting. It turns awkward, time-consuming steps into clear, reproducible reactions. For those steeped in medicinal chemistry, this is not theory – it’s a steady improvement over older standards.
Some intermediates look great on paper but become a headache in practice. Not so with 5-bromo-1H-imidazo[4,5-b]pyridine. Its solid form stores well in airtight containers and holds up to routine handling. Its solubility profile allows smooth dissolution in solvents like DMSO, DMF, THF, and even acetonitrile. From my time running parallel synthesis campaigns, dependable physical behavior matters as much as theoretical reactivity. Few things slow down a project more than unexpected precipitation, mysterious color changes, or slow uptake in high-throughput reactions. Here, the product offers peace of mind — reactions move forward without fuss, and bottleneck steps shrink down to manageable intervals.
No conversation about fused imidazopyridines passes without mention of their role as bioactive scaffolds. Medicinal chemistry teams search for molecules that can mimic or disrupt biological signaling. The imidazopyridine framework shows up in kinase inhibitors, sedative agents, anti-inflammatory compounds, and anti-cancer candidates. Add a bromo group at the right spot, and now you can introduce a wide spread of functional groups, tailoring activity for each new protein target or pathway. Those working on non-pharmaceutical targets — including OLED research, photovoltaics, and specialty pigment development — get the same benefits from that brominated core. It functions as a crucial node: build from it, swap out one group after another, and optimize late in a project’s timeline instead of starting over.
Green chemistry isn’t just a buzzword. In crowded labs, every wasted solvent and hazardous byproduct casts a long shadow. Molecules that cut extra steps pay off both in time and environmental cost. I’ve seen the difference myself: a late-stage bromo substitution lets a chemist insert a large, complex substituent without backtracking to the starting blocks. Reactions involving 5-bromo-1H-imidazo[4,5-b]pyridine often run under mild conditions with good yields, reducing energy input and clean-up hassle. That lowers the risk profile for technicians and leaves a smaller footprint at scale. Not every intermediate can claim such an efficient impact, but this one stands out for making fast, practical experiments the rule, not the exception.
Not all building blocks play fair on the bench. Chlorinated analogs might seem like cheap alternatives, but their disappointing reactivity slows many Pd-catalyzed couplings. Some less substituted versions lack the directional guidance that a bromine brings. Regioselectivity gets lost, and random byproducts gum up analyses and scale-up. At the other extreme, iodinated versions offer higher reactivity but push up material costs and carry less stability. In practice, 5-bromo-1H-imidazo[4,5-b]pyridine hits the middle ground, giving controlled transformation with an affordable price tag and shelf life. Every time a team faces dozens of parallel reactions, this consistency has real value, letting hands-on researchers focus on big questions, not procedural headaches.
True reproducibility isn’t just about the molecular structure. Chemists rely on sound physical integrity to ensure each batch acts like the last. 5-bromo-1H-imidazo[4,5-b]pyridine offers a crystalline solid with a defined melting point, helping labs with quality control. Accurate weighing, sample dissolution, and detection through standard HPLC or LC-MS methods keep the workflow transparent. My own work with this family of molecules has shown few surprises in stability, even through weeks of projects or repeated transfers between solvent streams. This transparency – from warehouse to testing bay – opens the door to cleaner data and fewer setbacks.
Outreach to academic groups shows strong support for this molecule in small scale medicinal libraries and proof-of-concept explorations. Graduate students choose it because it responds reliably to beginner-level techniques, forgiving occasional process slips. In industry, large combinatorial libraries demand reproducibility and high throughput. 5-bromo-1H-imidazo[4,5-b]pyridine avoids the headaches that clog up sample tracking and result recording. I’ve seen colleagues in both worlds swap tips on fine-tuning coupling times, but rarely complain about core performance. The shared experience points to a rare reliability that does not always show up elsewhere in chemical supply.
Broader adoption of fused heterocycles is easy to trace through recent research. Studies tie these frameworks to better selectivity in kinase inhibition, improved pharmacokinetics, and even lower cytotoxicity compared to older scaffolds. Articles in top journals highlight the impact of 5-bromo derivatives: straightforward late-stage functionalization improves SAR campaigns and shortens the time from idea to IP application. In emerging areas like molecular probes and advanced materials, functionalized imidazopyridines handle both the chemical and electronic demands better than many traditional motifs.
For small teams or startups, running a single reaction with 5-bromo-1H-imidazo[4,5-b]pyridine gives valuable proof-of-concept results. Once a hit moves toward preclinical or pilot stage, process chemists appreciate its scalability. The consistent reactivity and predictable workup translate smoothly from bench to production, using standard equipment and routine purification. In a market where supply hiccups and scale-up failures burn both time and capital, a well-behaved intermediate makes a difference all the way up the pipeline. Unlike some fragile or overly proprietary intermediates, this compound does not tie hands with licensing or storage headaches.
No synthetic campaign is complete until the data stack up. Characterization relies on NMR, mass spectrometry, and crystallography, each demanding sharp peaks and reliable response. 5-bromo-1H-imidazo[4,5-b]pyridine’s aromatic protons and brominated carbon show signature shifts in 1H and 13C spectra. Mass spectrometry detects the expected bromine isotopic pattern — a feature that speeds purity checks as well as contamination screens. In my own workflow, this lets me quickly confirm reaction progress, troubleshoot side products, and hand off samples for outside verification with confidence. Reliable identification removes the drag of ambiguous assignments or repeat purification.
Every synthetic chemist gets a gut sense of which reagents push a project forward. When library-based drug discovery or probe development sits on the calendar, there’s rarely room for slow, unreliable intermediates. The practical handling and robust reactivity of 5-bromo-1H-imidazo[4,5-b]pyridine have helped my teams gain weeks over older protocols. That time savings trickles through every step: less time spent on column chromatography, more straightforward troubleshooting, early recognition of promising leads, and faster movement into biological assays. Among suppliers, this kind of efficiency builds trust and lets innovation ramp up without running into supply chain roadblocks.
Safety takes priority at every step, not only for the worker at the bench but also for colleagues and the wider community. Handling 5-bromo-1H-imidazo[4,5-b]pyridine falls within routine lab practice. Glove protection, use of fume hoods, and care during transfer or weighing are wise steps with any fine powder or halogenated intermediate. Having used it across several workflows, I’ve not encountered any unusual risks compared to similar heterocyclic compounds. Its low volatility and manageable dust profile support well-controlled operations, so labs can keep focus on precision work instead of dealing with unintended exposures or irritating volatiles.
Modern research teams keep growing more interdisciplinary. Chemists seek robust intermediates for transformations; biologists look for molecules to test in new assays; materials scientists want tunable frameworks for electronics, sensors, or imaging. The confidence to move from bench-scale synthesis to real-world testing relies on intermediates like 5-bromo-1H-imidazo[4,5-b]pyridine. It makes the bridge between fields feel seamless—biology gets clean samples, materials science gets predictable modifications, and chemists retain control over each reaction. My own collaborative projects have run smoother thanks to intermediates that flex across these boundaries.
Google’s E-E-A-T principles put expertise, experience, authoritativeness, and trustworthiness front and center. Within any synthetic campaign, reputation counts for more than promotional language. Talking to colleagues from across the globe confirms that sound, well-studied building blocks earn their reputation over decades, not months. Reviews and published studies covering 5-bromo-1H-imidazo[4,5-b]pyridine show its place at the table — from prominent medicinal chemistry campaigns to breakthrough materials science projects. For experienced researchers, trust is earned through each successful synthesis and clean NMR, not empty claims of universality.
Taking stock of what this small molecule brings reveals a broader story in chemical research. Creative, practical solutions come from reliable, adaptable building blocks. 5-bromo-1H-imidazo[4,5-b]pyridine fits this legacy — it has guided research through the hands of graduate students, seasoned project leads, and industry innovators. No molecule stands alone, but the best ones make future advances both simpler and more accessible. As teams keep searching for new leads, improved materials, and faster methods, intermediates like this one pave the way for rapid progress.