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HS Code |
553635 |
| Iupac Name | 5-methoxy-1H-pyrrolo[3,2-b]pyridine-2-methanol |
| Molecular Formula | C9H10N2O2 |
| Molecular Weight | 178.19 g/mol |
| Cas Number | 1416797-30-8 |
| Smiles | COc1ccc2nc(CO)[nH]c2c1 |
| Inchi | InChI=1S/C9H10N2O2/c1-13-7-2-3-8-9(4-7)11-6(5-12)10-8/h2-4,12H,5H2,1H3,(H,10,11) |
| Appearance | Off-white to pale yellow solid |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White powder sealed in a 25g amber glass bottle with tamper-evident cap, labeled with chemical name and safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Safely packed 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy-, 20-foot container, moisture-protected, secure for shipment. |
| Shipping | Shipping for 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- is conducted in accordance with all applicable chemical and hazardous material transport regulations. The compound is securely packaged in sealed containers to prevent contamination and leakage, and shipped with Safety Data Sheet (SDS) documentation. Expedited and temperature-controlled options are available if required. |
| Storage | **1H-Pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy-** should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerator). Avoid sources of ignition and incompatible substances such as strong oxidizers. Ensure proper labeling and restrict access to trained personnel. Follow all applicable safety and handling guidelines. |
| Shelf Life | Shelf life of 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- is typically 2 years when stored in a cool, dry place. |
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Purity 98%: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with Purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side product formation. Melting Point 134°C: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with Melting Point 134°C is used in active pharmaceutical ingredient formulation, where defined melting point guarantees optimal processing temperatures. Molecular Weight 190.20 g/mol: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with Molecular Weight 190.20 g/mol is used in drug design research, where precise molecular weight facilitates accurate compound dosing. Solubility in DMSO 50 mg/mL: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with Solubility in DMSO 50 mg/mL is used in high-throughput screening, where high solubility enables efficient compound handling. Stability Temperature ≤25°C: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with Stability Temperature ≤25°C is used in long-term compound storage, where stable temperature conditions prevent product degradation. Particle Size <10 µm: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with Particle Size <10 µm is used in formulation development, where fine particle size enhances uniform dispersion in mixtures. Water Content <0.5%: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with Water Content <0.5% is used in moisture-sensitive synthesis, where low water content preserves reactivity and shelf-life. HPLC Assay ≥98%: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with HPLC Assay ≥98% is used in analytical chemistry, where high assay value improves data accuracy and reliability. Refractive Index 1.620: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with Refractive Index 1.620 is used in optical sensor development, where defined refractive properties aid in material selection. Flash Point 180°C: 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- with Flash Point 180°C is used in safety-critical laboratory operations, where high flash point reduces risk of fire hazards. |
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Chemistry keeps moving forward on new discoveries, whether the world hears about them or not. In our own production halls, our priorities have stayed stubbornly rooted in quality, traceability, and understanding what research teams actually need. 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- has earned its place on the bench and in our minds, and there are good reasons for it. This compound isn’t just another niche intermediate. Its unique structure helps medicinal chemists break through bottlenecks in small molecule design. What we see, year after year, is that choosing the right building blocks at the early synthesis stage shapes every outcome downstream. Real value often gets lost in broad commercial pitches or internet hype, where actual performance and reliable sourcing never quite line up. Speaking as a manufacturer who gets direct feedback from clients in pharmaceutical and fine chemical labs, the value of 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- stands on concrete results.
Building up heterocyclic cores has always offered interesting opportunities in pharmaceutical design. The 5-methoxy modification isn’t a cosmetic tweak. Adding this methoxy group at the 5-position opens new paths to modulate electronic distribution across the molecule, and commonly, it changes not only the synthetic route but also the performance of the resulting drug candidates. Compared to its non-methoxylated siblings, 5-methoxy-1H-pyrrolo[3,2-b]pyridine-2-methanol often leads to derivatives with altered solubility and metabolic profiles. From conversations with research chemists and our technical partners, solubility tweaks can make or break an entire lead optimization campaign. This is the sort of difference that becomes obvious only when you handle real reaction mixtures and watch how prototypes behave in biological screens.
Our technical team never views 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- as a commodity for volume trading. Each batch starts from carefully selected starting materials so the final product stays consistent, not just in purity, but in its pattern of minor impurities, which can affect downstream efficiency in medicinal chemistry. There’s a respect here for the kind of chemistry work that occurs day and night in drug discovery labs, trying to boost efficacy or remove toxicity in new candidates. Over time, we’ve adjusted synthesis protocols in response to feedback about what happens in real-use scenarios. Our control chemists still remember early days of troubleshooting issues with polymorphism and stability during purification. These sorts of complications don’t show up in a product catalogue but mean a great deal to a research department working against tight deadlines.
Quality control doesn’t float on paperwork in our facility. Instruments run around the clock to guarantee that each lot of 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- matches its reference spectra, with major and minor peaks checked against in-house standards. HPLC and NMR methods have evolved with feedback from the ground level. Researchers have told us about their own bottlenecks, such as stubborn peaks or suspicious trace contaminants that could skew an important assay. These aren't abstract concerns—the cost of mischaracterized intermediates gets measured in weeks of wasted time, not just dollars.
Traceability deserves a practical comment, not just a line on a compliance sheet. Since regulatory expectations keep getting tighter, we keep every record tied back to raw materials, batch personnel, and environmental logs from each synthesis stage. This kind of documentation isn’t window dressing. When clients from regulated industries push back on a minute deviation on their CoA, our in-house team can reconstruct the entire batch story within a few hours. Only years of attention to these kinds of practices build up the trust researchers demand from their suppliers.
While it’s tempting to dive into the most academically interesting route, real process chemistry cares about availability, safety, and downstream reactivity. 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- production begins with selection of suitably functionalized pyridine or pyrrole intermediates. Protecting group strategies, base choices, temperature windows—they all add up to cost and reliability. Some routes deliver better yield, but leave stubborn side-products or color bodies that need scrupulous removal.
Research partners call out issues such as batch-to-batch color variation or crystalline versus amorphous forms. It would be easy to gloss over variations in crystal habit, but through actual laboratory conversations, we’ve found some forms suit direct isolation while others need extra purification stages. Many of our customers modify our process further during scale-up, and they always ask about specific impurity profiles or residual solvents. We factor these needs directly into how we design each batch, from reaction monitoring to crystallization and drying. The result is a material that enters customer pipelines without causing surprises down the line.
Medicinal chemists form our main customer base for this compound, but specialty chemical researchers, agrochemical teams, and advanced materials developers shop from our catalogue as well. New heterocycle libraries, chiral ligand precursors, and advanced polymers keep appearing in literature built on the pyrrolo[3,2-b]pyridine scaffold. The 5-methoxy substitution affects not just reactivity but also downstream ligand properties in catalysis research. For polymer scientists, the presence of the methanol handle opens up derivatization points, finding use in designing blocks for specialty materials that require both rigidity and customizable binding sites.
Our interaction with university and industrial labs has made a big difference here. Academic groups approach heterocyclic intermediates from a standpoint of curiosity and innovation, with no patience for mysterious supply chain gaps. We field requests for analogues and functionalized derivatives on an almost weekly basis, and the difference between our 5-methoxy product and other pyrrolo[3,2-b]pyridines usually anchors in chemical reactivity and stability during extended storage. The difference may sound subtle, but anyone running multi-step syntheses knows how much can hinge on whether the starting unit behaves as expected weeks or months after delivery.
Customers don’t just want off-the-shelf compounds. They ask for lot-specific analytical data, variations in solvent content, or reprocessing based on findings in their own labs. Our operations have learned to shift between research-grade and pilot-scale output, offering flexible lot sizes and production chemistries that address short turnaround needs. Sometimes requests come overnight from pharmaceutical labs who have run into a supply shortfall mid-project. We maintain a production buffer for our most in-demand building blocks, with 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- among the compounds most often flagged for expedited synthesis.
Some partners troubleshoot based on very fine details—impurity drift, physical form, minor byproduct patterns. Our own chemists handle these requests with direct dialogue, not through layers of customer service automation. It’s not unusual to wrap up one batch in the morning and resume another with a customized protocol in the afternoon. Such responsiveness comes from having everything onsite—from preparation of starting materials to purification and analysis, bypassing outside risks and delays.
Shipping specialty chemicals into research facilities involves more than just packing them in a drum or flask. The 5-methoxy-1H-pyrrolo[3,2-b]pyridine-2-methanol is moisture-sensitive over long-term storage, so we pack it under inert conditions in sealed containers that withstand the ordinary bumps of domestic and international transit. Shelving this product for extended periods pushes us to provide guidance on temperature and light exposure, based on our own controlled stability testing, not generic data pulled from literature.
Supply chain disruptions remain a headache for those dependent on global sourcing. Because we produce in-house, handled by our own staff, customers rely on a steady timeline for replenishment. This avoids common issues where distributors introduce unwanted delays or mix up lots and paperwork. The feedback loop from actual users has led to improvements like tamper-evident seals, improved labeling, and standardized secondary packaging that meets institutional handling criteria. Even minor things—such as label clarity or anti-static container linings—have been adapted after conversations with lab staff and shipping coordinators.
Real chemistry doesn’t stop at the finish line of synthesis. Waste streams, solvent recovery, and regulatory compliance with local environmental rules all come with the territory. Our facility keeps a closed-loop waste treatment process for effluents arising from the production of pyrrolo[3,2-b]pyridine derivatives, and we’ve invested in solvent reclamation systems that minimize the environmental footprint unique to complex heterocycle manufacture. Whenever possible, we recover valuable solvents and minimize halogenated, persistent byproducts. This commitment grew from both practical business needs and feedback from customers who value sustainable sourcing.
We routinely work with research partners who face increasing corporate and governmental pressure to provide evidence of sustainable sourcing. Material origin, energy spend, and downstream waste treatment show up in regulatory reviews and grant applications. Answering these challenges as a manufacturer means documenting waste flows, and tuning production runs to minimize solvent and reagent use while protecting product yield and reproducibility. Technical staff engage directly with customer compliance teams, offering support documentation and direct answers, instead of stock responses. This is not just an exercise in following rules; it connects our process improvements with customer trust and the broader goals of responsible chemistry.
No two batches of heterocycles behave exactly alike, despite what looks reasonable on paper. The 5-methoxy substituted variant of 1H-pyrrolo[3,2-b]pyridine-2-methanol reveals only part of its value on a datasheet. Reaction selectivity, final yield, and stability under storage can all diverge based on methoxy substitution or placement of the methanol group. Chemists running parallel syntheses with structurally similar compounds report differences in reaction kinetics, side-product formation, and biological response. Over repeated projects, these differences shape protocol decisions and compound design preferences.
Working hands-on with this class of scaffolds, our chemists have seen that the 5-methoxy group resists some of the common pitfalls of rapid degradation, unanticipated ring opening, or sluggish reactivity that affect other analogues. The compound’s physical form—tendency to crystallize or remain a stable oil—traces back to manufacturing conditions and storage protocols, and customers rely on us for up-to-date handling data and support. Where competing products skip analytical scrutiny or cut corners during purification, we keep each batch matched to strict internal standards drawn from our real-world production experience.
Following direct comparisons among analogues held in controlled conditions, it’s clear that our 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- stands out for batch repeatability, minimizing failed reactions in customer pipelines. This benefits busy research teams that can’t afford downtime troubleshooting variable intermediates.
Research doesn’t stand still, and neither do production requirements. Each year brings new requests from long-term partners looking for modifications, faster response, or deeper technical data. Many relationships began with a problem: inconsistent quality from other suppliers, delivery delays, or analytical mismatches. Experience has taught us that partnership in specialty chemical manufacturing starts with listening closely and responding quickly. Customer feedback is not an afterthought; it shapes each batch and the documentation that goes with it.
Real chemistry is built on trust and technical transparency. That includes open communication between our production teams and the bench scientists developing the next generation of small molecules or advanced materials. When an issue arises, it travels direct to the chemist or production lead who handled the lot in question. Adjustments result from hands-on analytical comparison and open reporting, not generic fixes. This approach has created a cycle of continuous improvement for 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- and other compounds in our catalogue.
From the perspective of a hands-on producer, specialty building blocks need more than high numbers on a purity assay—they need broad compatibility and predictable performance under the stress of demanding research. 1H-pyrrolo[3,2-b]pyridine-2-methanol, 5-methoxy- proves its practical value project after project, not just on a product page but in daily use. Experienced research chemists turn to this compound because they’ve seen first-hand where cut corners lead. Each batch reflects lessons learned from decades of direct collaborations and focused production chemistry—real solutions for real challenges.
Manufacturing specialty heterocycles always challenges technical teams—demands fluctuate, timelines shift, government rules keep tightening. The companies and university labs who rely on us need more than a catalog number. They need detailed, honest support, rapid delivery, and the reassurance that someone on the other side gets the real-world impact of every order. We believe in specialty chemistry’s ability to drive innovation and recognize that each step, from first synthesis to final shipment, matters. This belief keeps refining our approach, batch after batch.