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HS Code |
345062 |
| Chemical Name | 1H-Pyrrolo[3,2-b]pyridine |
| Cas Number | 38748-32-2 |
| Molecular Formula | C7H6N2 |
| Molecular Weight | 118.14 |
| Iupac Name | 1H-pyrrolo[3,2-b]pyridine |
| Appearance | White to off-white solid |
| Melting Point | 71-73 °C |
| Boiling Point | 313 °C |
| Density | 1.23 g/cm³ (20 °C) |
| Solubility In Water | Slightly soluble |
| Smiles | c1ccc2nccnc2c1 |
| Inchi | InChI=1S/C7H6N2/c1-2-6-7(3-1)8-4-5-9-6/h1-5,8H |
| Pubchem Cid | 10345 |
| Flash Point | 142.4 °C |
| Refractive Index | 1.653 |
As an accredited 1H-Pyrrolo[3.2-b]pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1H-Pyrrolo[3,2-b]pyridine is supplied in a 25g amber glass bottle with a tightly sealed cap and clear hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL container can load approximately 12,000 kg of 1H-Pyrrolo[3,2-b]pyridine, packed in 25 kg fiber drums or bags. |
| Shipping | 1H-Pyrrolo[3,2-b]pyridine is shipped in tightly sealed containers to prevent moisture exposure and contamination. The package complies with all relevant chemical transportation regulations, including labeling and documentation. The chemical is typically shipped at ambient temperature, unless otherwise specified, ensuring safe and secure delivery to laboratories and research facilities. |
| Storage | Store **1H-Pyrrolo[3,2-b]pyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Handle under inert atmosphere if sensitive to air or moisture. Follow all relevant safety and regulatory guidelines for hazardous organic chemicals. |
| Shelf Life | 1H-Pyrrolo[3,2-b]pyridine typically has a shelf life of 2-3 years when stored in a cool, dry, airtight container. |
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Purity 98%: 1H-Pyrrolo[3.2-b]pyridine with purity 98% is used in medicinal chemistry research, where it ensures reproducible synthetic yield and high biological activity. Melting point 92 °C: 1H-Pyrrolo[3.2-b]pyridine featuring a melting point of 92 °C is used in pharmaceutical formulation development, where it provides enhanced processability and stable compound integration. Molecular weight 118.14 g/mol: 1H-Pyrrolo[3.2-b]pyridine with a molecular weight of 118.14 g/mol is used in small molecule library synthesis, where it enables accurate mass balance and reliable analytical characterization. Particle size <10 μm: 1H-Pyrrolo[3.2-b]pyridine with particle size below 10 μm is used in solid-state drug delivery research, where it offers improved dissolution rates and uniform dispersion. Stability temperature up to 180 °C: 1H-Pyrrolo[3.2-b]pyridine stable up to 180 °C is used in high-temperature reaction screening, where it maintains chemical integrity and consistent reactivity. Water content <0.5%: 1H-Pyrrolo[3.2-b]pyridine with water content below 0.5% is used in moisture-sensitive chemical syntheses, where it prevents hydrolysis and degradation of active species. |
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Anyone who’s ever worked on a small molecule synthesis or spent time reading the newer pharmaceutical patents will have seen the curious name 1H-Pyrrolo[3,2-b]pyridine. It doesn’t exactly roll off the tongue, but in today’s fine chemical market, this compound tells a real story about changing demands, innovative pathways, and some honest challenges with both supply and use.
There are reasons this compound gets people talking. The fusion of pyrrole and pyridine in its structure opens up a range of possibilities. Medicinal chemists are constantly hunting for heterocycles that tweak biological activity just the right way, and this one fits the bill. In workshops and conferences, standing over an HPLC or in a planning meeting, you’ll often find someone mentioning it, usually because its small changes lead to big differences in activity or selectivity.
Having worked both at the bench and in project teams, I’ve found that what really matters for customers is not just whether a building block exists, but what makes it matter over all the others cramped into the catalogue. For me, grappling with product choices means weighing purity, batch-to-batch reliability, and even honestly looking at the routes used to make the stuff in the first place.
Most sources that sell 1H-Pyrrolo[3,2-b]pyridine offer it at high purity, typically over 98%. This isn’t just a number to put on a certificate of analysis—if you’ve ever struggled through late nights at the prep column because of a mystery signal on the NMR, you know why purity rates matter, especially in an era of trace analysis and chronic over-regulation. For those making research batches, anything less than clean material makes downstream reactions unpredictable, risking waste of time and precious intermediates.
Boiling point and melting point data show up in technical sheets, but in the lab, few people refer to those unless you’re troubleshooting a new scale-up or suspicious decompositions. In my own experience, more folks care about solubility. This product dissolves well in polar solvents like DMF and DMSO, plus it can go into standard organics with a little warming. Handling is straightforward on the bench—there’s a faint drift to the smell, which should alert you, but it isn’t particularly nasty compared to similar nitrogen heterocycles. Maintain good air flow, as anyone who’s inhaled an unfortunate noseful of alkaloid can tell you, and basic PPE covers most scenarios.
I spent years at a CRO where our bread and butter was custom synthesis for drug discovery teams. In those years, one theme stuck out: unusual heterocycles started to take over from the standard indoles and pyridines. 1H-Pyrrolo[3,2-b]pyridine proved to be a hit as a core scaffold for kinase inhibitors. You see the patterns show up in patent libraries from big companies, especially in oncology and anti-inflammatory research. Some fragments based on this framework bind with higher selectivity, or make better hydrogen bond partners, than their simpler analogs.
It’s not just about binding affinity or buzzword synergy; the way this compound fits into combinatorial libraries allows for rapid generation of analogs without wringing hands over reaction incompatibility. You can plug this heterocycle into most Buchwald-Hartwig or Suzuki couplings. That means fewer headaches and more flexibility. Some of my colleagues have told me about dropping it into a sequence just to fill out an SAR map, later finding out that this led to their lead compound. Those stories drive home the point: one scaffold can change the course of a whole project.
Formulation scientists care about more than just activity, though. The metabolic stability of these systems sometimes surprises even the cautious ones. The extra nitrogen atoms can make the molecule more (or less) susceptible to oxidation, and sometimes lead to altered ADME profiles. When your team has six months and a shrinking budget, that small metabolic twist often makes the difference between success and being cut.
Let’s be honest: If you’re not the chemist in the plant making it, you probably care less about the technicalities of synthesis routes. From a broad market standpoint, though, 1H-Pyrrolo[3,2-b]pyridine stands in contrast to more common heterocycles because of the routes used to prepare it. The bulk of what’s out there starts with straightforward cyclization reactions, often involving substituted pyridines or furan rearrangements. Those steps have their own hazards, but scale reasonably well, which keeps costs under control for research-scale orders.
At larger scale, regulatory and purity challenges pile up. The worldwide shift towards increased environmental scrutiny means that sources based in countries with stricter emission controls tend to cost more. Solvents like DMF, used in some syntheses, now get flagged for environmental monitoring. In Europe, the REACH directives shape a lot of what suppliers can and cannot do. Companies with robust environmental certifications are at an edge here, both in cost and long-term sustainability. From my time working with global sourcing teams, I know how keeping track of yearly regulatory updates is almost a second job beside the chemistry itself.
Transport and import of specialty chemicals has its own snag. While not a particularly hazardous substance, 1H-Pyrrolo[3,2-b]pyridine’s packaging needs to withstand extended transit over widely varied temperatures without degradation. Small changes in packaging design or impurities introduced during storage can lead to frustrating batch failures for customers—a real pain point, especially if your project budget is on the line.
Why would someone choose this compound over more standard building blocks like indole or regular pyridines? The answer isn’t always straightforward. I’ve sat through enough design meetings to hear fresh graduates suggesting standard motifs, only to watch more experienced team members nudge the conversation toward less common frameworks. 1H-Pyrrolo[3,2-b]pyridine brings a different electron density distribution, which actually can matter in protein-ligand interactions.
If you’re looking for increased rigidity in your scaffold, this compound offers a fused system that holds its conformation better than plain pyridine. That plays a big role in structure-based drug design, where small tweaks can help investigators clean up conformational entropy problems or pack into a tight active site. With the structure easily amenable to halogenation, sulfonation, or other functionalizations, it provides a means of controlled diversification that stands out from older scaffolds known for being tricky to functionalize or less tolerant to reaction conditions.
While some will say “a ring is a ring,” the switch from indole to pyrrolo[3,2-b]pyridine has, in real trials, led to differences in solubility and bioavailability for certain candidate drugs. As a synthetic chemist who’s transferred plenty of methods from paper to production, I’ve seen yields jump or crash based solely on the electronics of the ring system chosen. The fused system is less prone to certain side reactions seen with open-ring analogs. That means more reliable chemistry, less troubleshooting, and better project timelines.
Shortcutting long trial-and-error periods is always the dream. With 1H-Pyrrolo[3,2-b]pyridine, the main opportunity comes from its position as a proven scaffold—one with track records in kinase inhibitor development, antiviral screening, and even in the newer crop of CNS-targeted drugs. There’s enough precedent in the literature to give medicinal chemists both confidence and caution.
Risk doesn’t mean “danger” in the dramatic sense. In this market, risk usually looks like inconsistent supply, unexpected purity problems, or regulatory hurdles that delay a launch. During the pandemic, disrupted international shipping hit just-in-time inventories hard, and this was one of several heterocyclic stocks that ran low in some places. Teams that preemptively qualified alternate vendors weathered those storms—something I’ve advised on, after seeing too many close calls in my own projects.
Counterfeit and off-spec material is a real issue with specialty chemicals. Research teams need to partner with trusted suppliers with transparent traceability, ideally audited regularly. This isn’t just a regulatory checkbox—it keeps projects safe from batch failures and lost time. Tools like NMR and LC-MS, combined with robust purchasing policies, go a long way towards preventing problems before they reach the flask.
Trust grows over time. In drug discovery or materials research, those who work with 1H-Pyrrolo[3,2-b]pyridine and similar compounds learn quickly which suppliers deliver on their claims and which struggle to meet the bar. Transparency matters more these days, as both environmental and human safety expectations sharpen. I’ve watched relationships between R&D labs and their suppliers deepen as teams swap detailed spectral data, audit findings, and feedback about performance. If you’re buying significant quantities, don’t hesitate to dig for independent analytical data—more suppliers are willing to share this now than even five years ago.
From the other end, producers investing in better manufacturing controls gain a real edge. Providing full traceability, adapting to new green chemistry guidelines, and regularly updating customers on process changes build real-world credibility. Companies that ignore these shifts end up chasing regulatory tailwinds and risk being cut from critical supply lists.
Laboratory users, especially in pharmaceutical settings, have the right to demand not only COAs, but also safety and traceability assurances. As a user, I always check for a batch-specific analytical run with HPLC, NMR, and LC-MS, not simply a generic printout. My projects have run on tight deadlines, and delays due to hidden impurities or paperwork have always been more expensive than confirming details up front.
Each year, stricter environmental laws and new supply chain vigilance ramp up the pressure. The chemistry community can’t rely only on tradition or what’s “always worked.” Production methods for 1H-Pyrrolo[3,2-b]pyridine using sometimes controversial solvents like DMF or DMSO now come under greater scrutiny, and waste management practices are being watched more closely. Many suppliers are working to implement less toxic processes, both due to internal company values and external regulatory demands.
For me, a big part of E-E-A-T compliance in this space now means working with suppliers who can deliver detailed environmental metrics alongside technical ones. Several procurement departments with which I’ve worked now ask for solvent usage breakdowns, environmental impact statements, or even carbon footprint profiles per product batch. This extends trust, supports transparency, and signals real environmental engagement.
Global regulations shape both cost and availability. European REACH registration, for instance, can add significant lead time or cost to certain shipments, while import/export controls on specialty chemicals from Asia can throw wrenches into supply chains. Anyone who remembers the 2017 crackdown on Chinese fine chemical plants knows the upheaval sudden regulatory pressure can bring to pricing and lead times.
No product, no matter how useful, arrives without a list of potential headaches. If you’re considering 1H-Pyrrolo[3,2-b]pyridine for your lab, there are a few practical strategies that help smooth the bumps in the road.
First, always budget extra time for sourcing—especially for large or time-sensitive projects. Contingency plans can save weeks. In my own work, having at least two pre-vetted vendors for every key building block got us through some tough international shipping delays.
Second, demand full batch analytics. Suppliers offering full NMR and chromatogram data up front reduce your risk of receiving off-spec batches, which in turn keeps downstream chemistry on schedule. Some will even arrange for custom purification on request, which may cost more but saves time in the end.
Third, keep an eye on pre-registration and regulatory status. A good practice in recent years—especially with compounds used in pharma—has been to request details about REACH registration or other compliance records before committing to large batch purchases. This reduces risk of shipment holds or recalls.
Fourth, don’t overlook the importance of small-scale pilot runs. If your route calls for higher loadings or late-stage introduction of 1H-Pyrrolo[3,2-b]pyridine, do a test on multi-gram scale first. This allows troubleshooting with your chemistry team in case you run into unexpected reactivity or solubility concerns.
1H-Pyrrolo[3,2-b]pyridine isn’t just a chemical curiosity, and its value won’t disappear with a fad. The industry’s move toward more diverse, functionally rich heterocycles means interest is likely to increase, driven by both big pharma’s hunger for novel structures and the ever-growing toolkit of medicinal chemists.
Sustainability will guide the next chapter. As the industry moves towards more responsible manufacturing, customers will watch not just prices, but also environmental claims and verified supply chain practices. Having worked in teams that built business cases around green chemistry transitions, I’ve seen firsthand the value good environmental stewardship adds—not just in compliance, but in attracting clients who share those values.
In my circles—analytical chemists, R&D project leads, formulation experts—everyone agrees that trust, transparency, and adaptability shape the future. The more everyone along the chain shares experience, data, and feedback, the better the market becomes for users and suppliers alike.
Sometimes progress in chemistry comes from something as simple as a new skeleton for building molecules. 1H-Pyrrolo[3,2-b]pyridine stands as proof that innovation isn’t always flashy—sometimes it’s as much about careful synthesis, solid supply relationships, and lessons learned at the bench. It pays to listen to those who have wrestled with both failed routes and spectacular successes. From what I’ve seen, investing in reliability, transparency, and solid data cuts through the noise and gives teams the edge to do their best science, whether that’s pushing a drug from idea to IND, or building the technology of tomorrow.