|
HS Code |
418962 |
| Iupac Name | 1H-imidazo[1,2-a]pyridine |
| Molecular Formula | C7H6N2 |
| Molar Mass | 118.14 g/mol |
| Cas Number | 934-97-2 |
| Appearance | White to yellowish crystalline powder |
| Melting Point | 122-125 °C |
| Boiling Point | 292 °C |
| Density | 1.18 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | c1ccc2nccnc2c1 |
| Inchi | InChI=1S/C7H6N2/c1-2-4-7-8-5-6-9(7)3-1/h1-6H |
| Pubchem Cid | 70093 |
| Refractive Index | 1.695 |
As an accredited 1H-imidazo[1,2-a]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g 1H-imidazo[1,2-a]pyridine is packaged in a sealed amber glass bottle with a tamper-evident cap and labeled. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Packed in 25kg fiber drums, sealed, secured on pallets, ensuring safe, stable shipping of 1H-imidazo[1,2-a]pyridine. |
| Shipping | **Shipping Description for 1H-imidazo[1,2-a]pyridine:** 1H-imidazo[1,2-a]pyridine is shipped in tightly sealed containers to protect from moisture and light. Standard chemical shipping guidelines apply, using appropriate labeling and documentation. Temperature-controlled packaging may be used if specified. Complies with international shipping regulations for non-hazardous organic chemicals. Handle with care to avoid spills or exposure. |
| Storage | 1H-imidazo[1,2-a]pyridine should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. The storage location should be free from moisture and incompatible substances such as strong oxidizers. Proper labeling and secure storage are essential to ensure safe handling and avoid contamination or accidental exposure. |
| Shelf Life | 1H-imidazo[1,2-a]pyridine typically has a shelf life of 2-3 years when stored in a cool, dry place, tightly sealed. |
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Purity 99%: 1H-imidazo[1,2-a]pyridine with purity 99% is used in pharmaceutical synthesis, where it ensures high yield and minimization of by-products. Melting point 137°C: 1H-imidazo[1,2-a]pyridine with a melting point of 137°C is used in solid-phase drug formulation, where it provides stable processing and reproducible crystallization. Molecular weight 131.15 g/mol: 1H-imidazo[1,2-a]pyridine of molecular weight 131.15 g/mol is used in organic electronic materials, where it enables precise stoichiometric ratio for device fabrication. Particle size < 5 μm: 1H-imidazo[1,2-a]pyridine with particle size less than 5 micrometers is used in inkjet printing of functional inks, where it achieves uniform dispersion and smooth film formation. Stability temperature up to 180°C: 1H-imidazo[1,2-a]pyridine stable up to 180°C is used in high-temperature catalysis, where it maintains molecular integrity for consistent catalytic activity. Aqueous solubility 10 mg/mL: 1H-imidazo[1,2-a]pyridine with aqueous solubility of 10 mg/mL is used in biological assays, where it allows for effective preparation of test solutions and accurate bioactivity measurement. Analytical grade: 1H-imidazo[1,2-a]pyridine of analytical grade is used in reference standard preparation, where it provides reliable calibration for chromatographic methods. |
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Some chemicals fly under the radar, known mostly to researchers and chemists hunched over flasks in university labs or tucked away in pharmaceutical R&D centers. 1H-imidazo[1,2-a]pyridine doesn’t make headlines, but ask anyone working with advanced materials or in the hunt for new medicines, and you’ll hear its name spoken with the sort of appreciation that only comes from hands-on experience. There’s a sense of anticipation every time someone gets a fresh batch of this compound delivered, simply because of the doors it opens to new ideas.
Chemists love to categorize—and for good reason. It helps keep things organized in a world full of endless possibilities. 1H-imidazo[1,2-a]pyridine grabs attention because of its distinctive fused ring structure, where a pyridine ring locks together with an imidazole ring. It’s like bolting together two simple wooden toys and suddenly realizing you’ve made something stronger and more versatile than either piece alone.
This fusion changes the way electrons dance across the molecule, unlocking behaviors and reactivity patterns you don’t get from plain pyridines or imidazoles. These differences drive its value in research and manufacturing. The chemical formula, C7H6N2, hints at a simple make-up, but the exact architecture is where the magic happens.
Real-world use grounds any chemical beyond theory. 1H-imidazo[1,2-a]pyridine shows up most often in the creation of new pharmaceutical compounds. Medicinal chemists see it as a kind of modular backbone. They tinker with it, swapping out functional groups, chasing after molecules that might stop a virus, target tumor cells, or disrupt a biochemical pathway in bacteria. There is evidence to point to its antiviral, anti-inflammatory, and even antitumor potential, with scientific papers covering leads for drugs that could change lives.
It’s not just a star in medicine. The electronic properties of this molecule put it on the lists for materials scientists as well. People have managed to coax light emissions from its derivatives, leading to research in organic light-emitting diodes (OLEDs) and extended conjugated polymers. The field keeps expanding, as curious minds find new ways to put that fused ring system to work for both cost-efficient synthesis and the quest for performance. Sometimes, innovation isn’t about new elements—it’s about arranging the ones we have into just the right shape.
You hear a lot about the journey chemicals take from tiny batches in glassware to large drums in manufacturing facilities. 1H-imidazo[1,2-a]pyridine follows a familiar path, but it stands out by how many steps it covers along the way. Lab work comes first, sure, but process chemists look to this molecule not only because it performs well in small batches, but also because it scales up without losing the qualities researchers depend on.
Consistency matters in any scale-up, and imidazopyridines have a kind of structural rigidity that holds up during syntheses involving heat, pressure, or mixing with other chemicals. That might sound dull, but anyone who has watched a promising molecule fall apart during scale-up knows how rare this stability can be. I’ve seen production staff and lead scientists argue over impurities in batches, and this is one molecule that seems to show up with fewer headaches than others. Less drama in the plant means more energy directed towards innovation.
Those traits also help keep costs in check. Wasted time isn’t just a nuisance—it’s a drain on budgets and a source of environmental waste. Chemical manufacturers appreciate a material that “behaves itself” during handling. Hazards don’t disappear entirely, but when the chemistry stays predictable, workers stay safer and work proceeds with fewer unplanned slowdowns.
With so many heterocyclic compounds available, you might wonder why this one keeps getting singled out. A big part of the answer lies in its versatility. Some rings break down quickly or react only in narrow conditions. This molecule holds up under a broader set of lab conditions and adapts to different functionalizations. Synthesis teams find they can introduce halogen, alkyl, or other substituents without too much fuss, enabling more explorations per research dollar spent.
Compare that to relatives like simple pyridines—useful, but limited in their range of biological activity—or classic imidazoles, which don’t always form sturdy enough backbones for larger, more complex molecules. Here, the fusion brings a rare blend of strength and adaptability. I used to run side-by-side tests on these families, and 1H-imidazo[1,2-a]pyridine consistently survived conditions that tore its cousins apart.
People sometimes overlook how minor tweaks in structure can create a cascade of differences downstream. In the world of regulatory review, for example, a compound’s metabolic stability or non-toxicity can mean the difference between a short-lived research project and a potential block-buster drug. I’ve watched researchers breathe easier knowing this scaffold often has acceptable toxicology in early screenings, which means precious time is spent moving forward rather than circling back to redesign molecules from scratch.
No product is perfect, and 1H-imidazo[1,2-a]pyridine brings its own challenges. Sourcing quality raw material can test the patience of any chemist on a deadline. Impurities from suppliers without good quality controls crop up from time to time. These can derail whole batches and force teams to sharpen their purification protocols. Every researcher who has spent late nights running chromatography columns to get product as clean as possible knows the frustration, but also knows the payoff is worth it.
Price volatility sometimes crops up as well. As demand for specialty intermediates rises and falls with pharmaceutical pipelines, sourcing managers end up fielding calls from impatient scientists. The fluctuations reflect global supply chain pressures as much as market trends, and sensible planning makes all the difference. Teams who build relationships with trustworthy suppliers tend to avoid the last-minute scramble, but new researchers should expect a few learning experiences along the way.
While some products deliver clear-cut advantages, this one operates more like a Swiss army knife. It’s not the answer to every problem, but its blend of stability, reactivity, and adaptability makes it central to many creative solutions. That almost always means any extra time spent learning its quirks turns into time saved down the road. From my side, one of the biggest lessons has been the value of communication between scientists, sourcing teams, and safety officers, making sure everyone stays aligned as projects evolve.
With chemicals, trust matters. Not just with suppliers or the process but with how well teams understand the risks they’re managing. 1H-imidazo[1,2-a]pyridine doesn’t appear on many high-risk lists, and that’s good, but every step in handling, storage, and transport counts. Safety data sheets highlight the usual chemical hazards—skin and eye irritation, inhalation warnings, safe disposal. Teams that read beyond the first page and look for detailed reports make better calls about protective equipment, storage temperature, and emergency kits.
Regulations keep tightening every year. Meeting standards isn’t just about keeping labs in line with global rules; it’s about protecting people and the environment. Over the past few years, I have seen more projects start with a review of the compound’s safety and environmental footprint instead of tacking it on as an afterthought. The earlier these questions get addressed, the easier it is to prevent slowdowns later due to undisclosed risks. Environmental stewardship is part of the job, but it also builds the long-term reputations that companies and universities rely on.
In terms of documentation, some compounds arrive with thick dossiers, while others require a bit of legwork to uncover the details. This molecule sits in a middle ground. It isn’t so new that safety and toxicology are a mystery, but for any advanced use, it’s a good call to dig for peer-reviewed studies, case reports, and verified safety data. The best teams share information up and down the pipeline to keep gaps from forming while moving from R&D to pre-production.
The path ahead for 1H-imidazo[1,2-a]pyridine looks busier than ever. Drug researchers are constantly looking for new scaffolds, and this one stays on the list because of its performance in antiviral and antibacterial investigations. A few promising studies have popped up in recent years pointing to strong activity against emerging pathogens, a hot topic as medical threats keep changing and growing.
Materials science is another frontier. As the demand for brighter, longer-lasting, and more energy-efficient displays increases, chemists and engineers keep returning to fused heterocyclics like 1H-imidazo[1,2-a]pyridine for their light-emitting properties. I’ve witnessed heated discussions over whether to rely on more established aromatic backbones or to take a chance with newer molecules, and more often, the willingness to experiment wins out. This openness creates cycles of progress that pull in funding and spark patent battles.
Sustainability keeps entering the conversation. More stakeholders expect synthetic pathways to minimize waste, reduce reliance on rare elements, and cut energy usage. Creative approaches—like using greener solvents or streamlining purification—are already in the works. Teams who treat this as a puzzle to solve tend to outpace those who resist change. I’ve seen successful projects emerge from the willingness to rethink standard operating procedures, even when that means walking away from older, “good enough” methods.
If someone asks for advice before beginning work on 1H-imidazo[1,2-a]pyridine, I tell them to weigh both the immediate scientific value and the long-range impact. Think about integration with your existing workflows. Decide if you need quantities at the gram, kilogram, or ton level, because sourcing and process choices shift dramatically with scale. Ask about purification, not just at the beginning but throughout, especially if downstream products have to meet tight bioactivity or purity standards.
There’s also the peer network to consider. Researchers who reach out for insights—whether at conferences, in online forums, or through good old-fashioned phone calls—usually avoid common pitfalls. Knowledge shared informally about things like which acids strip certain byproducts or which temperature profiles avoid decomposition carries weight. I’ve seen too many projects delayed by teams working in isolation, missing out on solutions that another group solved years earlier.
Budget is always top of mind. Teams that map out projected costs at the earliest opportunity—factoring in not only purchase prices, but waste disposal, regulatory fees, and contingency funds—avoid the shock that comes with last-minute overruns. It’s tempting to focus on the short-term price per kilo, but long-term project costs follow choices made before the first order ships.
Training matters, too. Working with 1H-imidazo[1,2-a]pyridine safely means more than reading a single document. Make sure new team members understand lab protocols, storage requirements, and emergency routines. The most effective groups hold regular refreshers and welcome questions, rather than make assumptions about what people already know.
There’s a push and pull in chemical research between the drive to innovate and the responsibility to do things safely and sustainably. 1H-imidazo[1,2-a]pyridine presents a strong case for how these priorities can align. Its flexibility as a molecular scaffold enables faster movement from lab to real-world applications, which brings attention—and sometimes scrutiny.
Embracing this molecule means taking full ownership of its benefits and its risks. That includes keeping pace with peer-reviewed literature, attending to regulatory shifts, and supporting internal culture that values curiosity and diligence in equal measure. From what I’ve seen, this approach leads not to caution for caution’s sake, but to creative breakthroughs that stand up under outside review.
Many of the world’s chemical innovations trace back to decisions made quietly, in the background, to pick a reliable, adaptable molecule. 1H-imidazo[1,2-a]pyridine’s story is ongoing, shaped one project at a time by researchers, manufacturers, policy setters, and users who take the time to do things right. Whether it’s the foundation of a new medicine or the backbone of a technical material, its quiet reliability becomes a platform for progress.
A compound might start its life on a chemist’s shelf, but it gains a reputation through the ripple effects it creates in the broader world. With public scrutiny climbing, transparency and open communication matter more than ever. Teams are increasingly expected to share findings, disclose setbacks, and publish results clearly, not just in technical journals but in ways the wider public can understand.
Ethical stewardship isn’t just jargon—it’s what separates lasting innovation from fleeting trends. Forging partnerships with academic labs, regulatory bodies, and advocacy groups matters. Standard-setting agencies set benchmarks not to slow things down, but to make sure breakthroughs actually reach those who need them safely.
Over the years, I have seen how open engagement builds trust, not just with institutional partners but with end-users and the communities close to manufacturing sites. 1H-imidazo[1,2-a]pyridine serves as a quiet but important test case for evolving standards around safety, transparency, and environmental responsibility. Every team that does due diligence, shares both data and lessons, and supports ongoing education, safeguards both their project outcomes and public goodwill.
Research keeps pushing boundaries, and as pressure mounts for faster, safer, more cost-effective products, the importance of dependable chemical scaffolds only grows. Each year brings new questions, from synthetic design to impact analyses, but the common thread is a drive for smart decision-making that takes both efficiency and responsibility seriously.
It’s not always clear in the moment which compounds will become linchpins for future industry or medical breakthroughs. 1H-imidazo[1,2-a]pyridine finds itself called upon again and again for tough design problems. From what I’ve seen, its fusion of stability, adaptability, and well-mapped behavior makes it stand out at the design stage and at every step that follows.
As teams plan their next experiments or map out manufacturing runs, the best advice is to treat this molecule not just as another raw material, but as a partner in creative, careful science. With ongoing attention to sourcing, process improvement, regulatory alignment, and open collaboration, 1H-imidazo[1,2-a]pyridine will likely hold a strong place in research and production pipelines for a long time to come.