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HS Code |
717404 |
| Chemical Name | 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid |
| Cas Number | 1341086-94-1 |
| Molecular Formula | C9H8N2O2 |
| Molecular Weight | 176.17 |
| Appearance | Solid |
| Purity | Typically >98% |
| Solubility | Soluble in DMSO, DMF |
| Storage Conditions | Store at 2-8°C |
| Smiles | Cn1cc2ccc(C(=O)O)nc2n1 |
| Inchi | InChI=1S/C9H8N2O2/c1-11-4-7-3-8(9(12)13)5-10-6(7)2/h3-5H,1H3,(H,12,13) |
As an accredited 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5g amber glass vial, sealed with a red cap, and labeled with compound details and safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid, sealed drums, moisture-protected, compliant with chemical transport regulations. |
| Shipping | 1-Methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid is shipped in sealed, airtight containers to prevent contamination and moisture exposure. It is typically transported at ambient temperature unless otherwise specified. Appropriate labeling and documentation, in accordance with relevant chemical and safety regulations, are included to ensure safe and compliant delivery. |
| Storage | Store 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container clearly labeled and protected from moisture. Follow all relevant safety and chemical hygiene protocols for storage and handling. |
| Shelf Life | Shelf life of 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid is typically 2 years if stored cool, dry, and protected from light. |
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Purity 98%: 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid with Purity 98% is used in pharmaceutical intermediate synthesis, where high purity enables efficient downstream reactions. Melting Point 225°C: 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid with Melting Point 225°C is used in high-temperature catalysis studies, where thermal stability allows for robust experimental protocols. Particle Size ≤10 µm: 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid with Particle Size ≤10 µm is used in fine chemical formulation, where small particle size promotes homogeneous dispersion. Stability Temperature up to 180°C: 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid with Stability Temperature up to 180°C is used in organic electronics manufacturing, where thermal resilience ensures material integrity during device fabrication. Molecular Weight 188.18 g/mol: 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid with Molecular Weight 188.18 g/mol is used in medicinal chemistry research, where precise molecular mass facilitates accurate dosage calculations. HPLC Assay ≥99%: 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid with HPLC Assay ≥99% is used in analytical reference standards, where verified composition supports reliable calibration. |
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Working in synthesis day after day, few chemical compounds stand out for both versatility and reliability the way 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid does. Behind the tongue-twister of a name sits an essential scaffold that helps chemists pursue a range of demanding projects. Our team dedicates significant attention to this molecule, seeing first-hand how its chemical backbone survives the practical challenges that occur from bench to kilogram scale.
Crystalline, off-white, and consistent in texture, the compound offers a molecular formula of C9H8N2O2. This structure carves out a solid place in pyrrolopyridine chemistry. We monitor every batch for purity using NMR and HPLC; we insist on levels above 98% purity because stray impurities can disrupt downstream applications or even push reactions off course. Moisture content drops below 0.5% due to tight control in our drying rooms, and we routinely check for heavy metals to ensure safe handling in any sensitive synthesis.
The melting point holds steadily in the 186–189°C range. This window proves helpful for both verification and process monitoring. Repeated experience shows sharp melting behavior, which hints at good batch-to-batch consistency. From pH tolerance during dissolution to solubility trends in polar and non-polar solvents, our process chemists collect and test these samples constantly, building a record that gives our partners and researchers better control over reaction conditions.
Our journey with this acid started years ago, right at the laboratory scale. We learned quickly that irregular parameters could lead to unwanted byproducts. Staying attentive to such fine details, we have steadily scaled up to pilot batches and full commercial volumes, tweaking and rehoning our process with each run. Using only reclaimed solvents that undergo a dual-filtration process, we lower environmental burdens while ensuring product quality. Safety remains at the core of our operation; supervisors monitor reaction temperatures and stirring rates at all hours because early signs of runaway exotherms should never be missed.
Handling this compound, we see the importance of dust minimization. Any powder, even a stable one like this, presents risks if inhaled or left to accumulate unseen. Each filling station comes equipped with local exhaust and barriers to control exposure without bottlenecking production volume. Drum liners and moisture barriers serve well, but above all, experienced workers spot potential problems before they occur. This blend of automation and human vigilance prevents costly loss and upholds high safety standards.
We categorize our 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid under production codes that follow internal traceability rules. Each batch comes mapped against its unique record, logging every solvent charge, every pH adjustment, and every quality checkpoint. No corners get cut; a failed test at the final specification means a hard stop, not a rerun through a filter press to salvage off-spec material. We let only fully compliant, specification-matched lots into inventory. Our model offers a well-defined content of active acid, with minimal residual solvents and only trace organic byproducts—much lower than industry averages.
Packing options remain flexible. Over the years, we learned not every client needs large drums, so we developed lines for smaller bottles or vacuum-sealed bags. Packaging gets chosen by looking at the moisture susceptibility of acidic nitrogen compounds—a lesson we learned after one rainy season, which taught us about the dangers of even short periods of exposure.
Every chemist who works with nitrogen-rich heterocycles faces hurdles—not every precursor dissolves or reacts the way we hope. This compound manages to bridge several tough gaps. Medicinal chemists lean on it as a fragment for kinase inhibitor research, thanks to the aromatic stability and ease of modification at both carboxylic and methyl positions. Others see the value in the basic nitrogen atom, which offers points for metal coordination or nucleophilic substitutions.
We work closely with process review teams who refine synthetic routes, transitioning from exploratory reactions to robust pilot schemes. Many report smooth amide-bond formation when coupling our acid with a range of amines by using carbodiimide methods, with high conversion rates and fewer side products. Those in the agrochemical field have told us that the compound enables stable intermediates, especially during the stepwise incorporation of halogen functionality. The functional group compatibility gained from the pyridine and pyrrole ring combination leads to broader selectivity in downstream steps—a key reason the molecule maintains popularity in hit-to-lead and optimization campaigns.
For those choosing among pyrrolopyridine family members, subtle differences in substitution patterns influence both reactivity and practical handling. Some try 1-methyl-1H-pyrrolo[2,3-b]pyridine without the carboxyl adornment at the 5-position, but miss out on the direct route to amide or ester derivatives. The carboxylic acid group not only serves as a versatile anchor; it also increases the water solubility just enough to ease the workup and purification steps that trip up competing heterocycles. From experience, pyridine-based acids with substitutions elsewhere on the ring show lower yields in peptide coupling and more side reactions during halogenation attempts.
Standard benzoic acids or indole carboxylic acids offer alternatives, but these lack the nitrogen pattern that makes our compound stand out both electronically and in coordination chemistry. Many customers enter trials with generic pyrrole acids; our team often gets contacted only after those options force difficult separations or fail to deliver the selectivity needed. The methyl group, present at the 1-position, adjusts electron density without making the core scaffold too reactive. This leads to more reliable steps and cleaner endpoints.
We initially thought demand would center around basic research, but reality showed opportunities in process chemistry, medicinal exploration, and even pigment development. The stability of the compound enables storage under standard conditions, so synthetic teams can keep a reserve for months. Formulation groups appreciate that our acid doesn’t migrate or interact with stabilizers, keeping both pharmaceuticals and other specialty chemicals within tight specification windows.
Our regular clients report that, compared with other scaffolds in their libraries, this compound offers a nearly plug-and-play presence in heterocyclic chemistry pipelines. Whether intended for final product or as a key intermediate, it brings a level of reproducibility critical to scale-up. We have observed that fewer cleaning cycles are required in the reactor systems after runs with this acid, in contrast to higher-resin carboxylates and many fused aromatic scaffolds. Less fouling, fewer risk points—that saves labor and enables faster turnaround between batches.
Customers ask about the best containers for long-term storage. We recommend sealed fluoropolymer bottles for shipments that may see wide temperature swings, based on thermal cycling tests we ran over the past two winters. Kraft-lined drums work for larger lots, especially if customers need to weigh out material in stages. Silica gel sachets or vacuum-tight seals further suppress ambient moisture creep, which, left unchecked, could spoil reactivity. Each strategy gets developed from our own baseline in the factory—nothing leaves our dock without us being confident it will arrive as we intend.
Lessons learned from smaller batches help guide every transport cycle. We noticed that improper sealing led to acid crystallization at the mouth of containers during storage in humid regions. Now, our workflow includes a second round of inspections for external powdering or lump formation. Although the acid resists deliquescence, subtle breakdown over time can create handling headaches if left unmonitored. Our commitment involves not just delivering the substance, but making sure clients encounter ideal working conditions, batch after batch.
Our company philosophy emphasizes both efficiency and safety but increasingly centers on sustainability. As regulations tighten, we focus more effort on reducing both solvent use and waste generation, especially during workup. Process optimization teams regularly revisit older methods, redesigning extraction or recrystallization conditions to recover excess reagent and minimize water consumption. Capturing solvent vapors back into the main supply loop produces real savings across a year’s worth of production cycles.
Our experience with 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid led to refinement of our reactor cleaning protocols, lowering rinse times and cutting solvent consumption nearly in half. We also moved to UV-transparent plastic drums after discovering that colored resins interacted with some trace nitrogen byproducts over long storage. Adopting this change cut returns and improved yield consistency in the labs of our largest customers.
Every compound tests a chemist’s patience at some stage, and this carboxylic acid is no exception. We overcame early crystallization issues by redesigning agitation during precipitation. Grain size matters, especially for large-scale drying—too fine, and dust control systems get overwhelmed; too coarse, and drying times increase, potentially trapping solvent within the lattice. Frequent in-process sampling keeps particle distribution within manageable bounds, a direct response to lessons learned scaling up piped cooling and adjusting solvent influx.
Shipping logistics make or break a smooth handoff. One misstep in customs can expose sensitive acids to unfavorable environmental conditions, so all carriers are briefed about the risks of temperature fluctuations and moisture ingress. We take packing cues straight from our own R&D storage studies, matching every route with the best available container system. This avoids “just good enough” shortcuts that might work for cheaper, less critical materials. Such attention to detail reflects the experience of dozens of shipments and complaints addressed, rather than just compliance requirements.
Those shopping intermediates from traders or third-party sources often encounter gaps in documentation or questionable quality. By owning the process end-to-end, we maintain control from sourcing raw materials to packing finished product. Each sample gets grounded in our traceability files, so research groups and commercial clients can trace performance or problems right back to specific batches and see which protocol applied at the time. Problems get handled by those with hands-on context, not just by flipping through paper logs. Manufacturing in-house lets us test alternate crystallization solvents or reaction times, refining the acid’s profile with direct feedback from actual users.
On one occasion, a major customer reported issues with catalyst residue in a finished pharmaceutical intermediate, traced all the way back to residual metals in the acid’s feeding stream. We responded not with paperwork, but by modifying our metal-screening protocol, swapping out glassware types, and closing feedback loops between QA and production. Such turnaround—driven by our chemists, engineers, and QA team—would never happen if we had outsourced major steps or left troubleshooting to outside agencies removed from daily plant operations.
Chemists often design elegant syntheses that work well at the flask level. Real-world scale magnifies challenges in heat dissipation, phase separation, and mixing. We move between the theoretical and practical, fine-tuning the handling of 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid so research translates directly to the pilot line. Lessons from crystallization become new batch records; feedback from clients updates our process SOPs. Some labs want minimal solvent residues, others prioritize particular crystal size distributions. We respond by adjusting grinding and screening lines, selecting between analytical and preparative chromatography for troublesome lots.
With decades in the chemical trade, we have built a network of scientists, forklift operators, analytical chemists, and sales coordinators who each add perspective to the process. Chemists might chase purity, but operators notice how powders pour, how packed drums swell under temperature, and how packaging survives rough handling in freight. We listen to both sides—cross-department collaboration prevents headaches downstream, especially when a detail as small as liner thickness can mean the difference between smooth dispensing and the need to spend hours cleaning up fine powder leaks.
Our experience manufacturing 1-methyl-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid shaped both our company outlook and our processes. Time and again, we see that small changes—whether tighter process windows, a different agitator blade, or an extra check at packaging—compound to make dramatic differences in quality and user satisfaction. The compound’s unique combination of chemical features and physical reliability keeps our teams focused on incremental improvements, driven by direct communication with users rather than distant market trends. For chemists pushing the boundaries across pharmaceutical, agrochemical, or specialty applications, our acid stands as a trusted building block, proven not through buzzwords but by results in the lab and factory. This reliability emerges from experience, constant learning, and a respect for each challenge encountered and solved.