1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo-

    • Product Name: 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo-
    • Chemical Name (IUPAC): 5-bromo-7H-pyrrolo[2,3-b]pyridine-3-carboxylic acid
    • CAS No.: 1209457-77-5
    • Chemical Formula: C8H5BrN2O2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    579144

    Iupac Name 5-Bromo-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid
    Molecular Formula C8H5BrN2O2
    Molecular Weight 241.045 g/mol
    Cas Number 877399-52-3
    Appearance Off-white to yellow solid
    Smiles C1=CN=C2C(=C1)C(=NC2)C(=O)OBr
    Inchi InChI=1S/C8H5BrN2O2/c9-5-2-6-7(10-3-5)4(1-11-6)8(12)13/h1-3H,(H,12,13)
    Solubility Soluble in DMSO, slightly soluble in water
    Chemical Class Pyrrolopyridine carboxylic acid derivative

    As an accredited 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 1-gram amber glass vial with a secure screw cap, labeled with product name and safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo-: Secure bulk packaging for safe international chemical transport.
    Shipping Shipping for **1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo-** involves secure packaging in compliance with chemical safety regulations. This compound is typically shipped in sealed containers, labeled according to hazardous material guidelines, and transported via certified carriers. Shipping documentation will include safety data sheets (SDS) and relevant hazard classifications.
    Storage 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- should be stored 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 tightly closed when not in use and avoid exposure to moisture. Proper labeling and storage in accordance with local regulations are recommended.
    Shelf Life Shelf life of **1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo-** is typically 2–3 years if stored cool, dry, and protected from light.
    Application of 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo-

    Purity 98%: 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity incorporation.

    Melting point 223°C: 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- with a melting point of 223°C is used in high-temperature reaction protocols, where it provides enhanced thermal stability during cyclization steps.

    HPLC grade: 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- of HPLC grade is used in research analytical studies, where it guarantees accurate compound quantification and reproducible chromatographic results.

    Molecular weight 253.04 g/mol: 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- with a molecular weight of 253.04 g/mol is used in medicinal chemistry programs, where it facilitates precise stoichiometric calculations for lead optimization.

    Particle size <50 µm: 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- with particle size below 50 µm is used in solid dispersion formulations, where it promotes homogeneous blending and enhanced dissolution rates.

    Storage stability 24 months at 2-8°C: 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- with 24 months storage stability at 2–8°C is used in bulk chemical storage, where it maintains consistent reactivity and minimizes degradation over time.

    Water solubility <0.1 mg/mL: 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- with water solubility less than 0.1 mg/mL is used in organic solvent-based extractions, where it prevents premature precipitation during process development.

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    Certification & Compliance
    More Introduction

    Introducing 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo-: A Manufacturer’s Perspective

    A Commitment to Consistency in Chemical Production

    Over the years, we have seen the methods for preparing heterocyclic carboxylic acids shift from unpredictable batch reactions to specialized controlled syntheses. Our recent work with 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo-, has pushed us to double down on both process control and traceability. We synthesize this compound starting from well-documented raw materials and maintain a chain of custody for every input. Our chemists routinely audit yields, pH levels, and impurity profiles, giving us control over what might otherwise introduce batch-to-batch variation. This stands out among similar five- and six-membered ring compounds where inconsistent supply chains have led to hiccups for downstream users.

    Why We Care About Purity and Crystal Habit

    Many manufacturers overlook subtle differences in crystal habit and surface area, but these affect everything from filtration times to solubility in research-scale operations. From the grinding mills to the drying ovens, we monitor not just what comes out, but even what sticks to the walls of our equipment. You might be surprised how a tiny amount of residual moisture can affect both sample handling and analytical reproducibility. With this carboxylic acid, we’ve seen that a stable, free-flowing powder not only expedites research but also plays a big part in minimizing waste during transfers and scale-up to pilot production.

    Bromination and Its Implications

    Bromination brings unique reactivity to the backbone of this pyrrolopyridine acid. The 5-bromo position means the molecule can serve as a handle for Suzuki cross-coupling and other palladium-catalyzed transformations, but these reactions demand extremely pure starting material. We observed that low levels of inorganic halide byproducts could ruin an entire sequence, clogging columns and impacting catalyst turnover. Through in-line monitoring and real-time halide sensing, our operations team can assure that each lot conforms closely to targeted halogen balance. These process checks let our partners start their own syntheses with confidence, removing a common frustration experienced with less stringently-produced heterocycles.

    Solubility, Handling, and Storage: Lessons from the Floor

    Once, we handled a custom lot with a much broader particle size distribution that stuck together and resisted redissolution during sample preparation. Our technical staff designed a post-synthesis milling step to produce a predictable, fine powder, reducing time spent by our customers breaking up clumps. In our experience, too, this compound displays solid shelf stability if kept away from direct light and humidity. Competing acids sometimes arrive to end users as sticky, compacted cakes that risk cross-contamination, something we avoid by tamper-evident, poly-sealed packaging directly from our filling line.

    Applications in Synthesis and Discovery

    Structure-activity relationship programs in the pharmaceutical industry routinely incorporate the 1H-pyrrolo[2,3-b]pyridine core. The carboxylic acid function at the three position, paired with a bromine at the five, positions the molecule well for rapid diversification—both by direct amidation and through cross-coupling. One research group reported a more than 30 percent increase in library throughput after switching to our grade because they spent less time repeating failed coupling reactions. We’ve seen this acid chosen over isomeric pyridine or pyrrole carboxylic acids especially for its ready further derivatization, a point of difference amplified by its controlled reactivity profile.

    Supporting Analytical Needs

    We recognize the role of trace elemental analysis, especially as end users push boundaries with catalytic and bioconjugation reactions. It is routine for us to provide ICP-MS and NMR spectra on each batch, not just because customers demand it, but because our own process improvements rely on knowing exactly what impurities are present. In one case, a spike in trace potassium identified a flaw in one of our supply lines, leading to a plantwide check of our washing systems—a change that improved overall product quality, not just for this acid, but across several of our heterocyclic lines.

    How Our Processes Shape Research Outcomes

    From weighing and dissolving small lots to multi-kilogram process runs, our operators see firsthand how consistency translates to uptime and throughput downstream. Several research teams we work with have reported faster method development after implementing our powders, citing lower baseline drift and less need for extensive sample prep. These findings resonate with our own test work, where tighter control over starting material enabled us to identify hidden mechanistic details in cross-coupling and condensation reactions. The difference between a well-controlled 5-bromo acid and a run-of-the-mill analog doesn’t appear on a typical certificate of analysis, but shows itself in the daily workflow of bench scientists who use it.

    Why Form, Not Just Purity, Matters

    Form influences not only how easily a chemist can weigh out a dose, but also how reliably data can be reproduced. Overly fine powders produced static buildup and led to weighing errors until we optimized the milling step. Coarser grades from other sources sometimes introduced longer dissolution times, which delayed analysis or led to non-uniform concentrations during automated liquid handling. Our approach to size and morphology optimization draws on field feedback as much as on analytical lab results. There is no off-the-shelf recipe for this—every run and every input feedstock shape our process.

    Addressing Challenges in Downstream Synthesis

    In conversation with process chemists, we’ve learned some pyrrolopyridine acids can form trace N-oxides during storage. We’ve instituted light-shielded packaging and worked with cap manufacturers to improve seal integrity, greatly reducing occurrence of degradation products. Our in-house studies found no measurable N-oxide formation across a 12-month shelf life under typical laboratory conditions, unlike other substituted acids in this class, which often required pre-use purification steps. This saves significant time in high-throughput screening and QC, keeping focus on forward reactions, not re-purification.

    Differentiating from Common Analogs

    Other heterocyclic carboxylic acids, even those with halogen substituents, can mismatch in reactivity or compatibility with catalytic systems. For example, we have compared 5-chloro and 5-bromo versions in standard Suzuki couplings and found that the bromo analog proceeds at lower catalyst loadings and under milder conditions—findings also echoed in published data. Our production method also specifically limits trace polysubstituted byproducts and heavy metal contaminants, which can be particularly problematic in pharmaceutical and agrochemical R&D settings. Where off-pattern side reactions occur frequently with lower quality supplier products, our compound repeatedly achieves the desired selectivity, reducing rework and troubleshooting on the part of the end user.

    Sustainability Practices and Responsible Sourcing

    Our facility sources brominating agents from ISO-audited partners. Over the last five years, we have developed solvent recovery systems for the mother liquors, cutting solvent waste by more than 40 percent. We use in-line monitoring to minimize reagent excess and reduce hazardous waste, a practice that distinguishes our operation from many bulk producers who still rely on oversized batch additions. Part of our commitment extends to providing transparent disclosures for customers working under green chemistry mandates, including detailed breakdowns of process solvent use and cycle times. Our own audits have uncovered improvements ranging from raw material supply down to packaging substrate, each narrowing the environmental footprint associated with every gram shipped.

    User Experience From Lab to Pilot Scale

    Smaller, exploratory labs often value consistency above all, since a failed reaction can mean both lost time and materials. Our capacity to provide both gram and multi-kilogram lots without variance lets us partner closely with both discovery and process teams. Researchers scaling syntheses beyond 100 g benefit from reliable powder flow and quick re-dissolution, avoiding the kinds of headaches that come from non-uniform particle size or inconsistent crystallization habits which we have witnessed with alternate suppliers.

    Meeting Regulatory and Documentation Needs

    Regulatory traceability plays a bigger role today than it did a decade ago. Synthetic chemists and QA professionals rely on robust documentation to support compound qualification. We generate detailed batch histories, impurity profiles, and retest intervals, providing evidence backed by archived samples, not just raw data printouts. Recent requests from partners in Europe and North America led us to improve our documentation of trace elemental and organic impurities, surpassing even prevailing ICH guidelines for research-use materials.

    Collaborative Improvement Based on Real-World Feedback

    Routine interaction with academic and industrial research groups has taught us that open communication about observed anomalies, even minor ones, can drive continual improvement. One customer noted minor inconsistencies in melting point over several deliveries, prompting us to adjust milling temperatures and improve the timing of crystallization steps. We implemented these charges plant-wide, which led to measurably tighter melting range and reduced out-of-spec batches, a success directly traceable to end user feedback.

    Future Opportunities and Process Innovation

    We keep a close watch on the needs of medicinal chemists and process engineers pursuing the next wave of heterocycle-based compounds. Market trends point to increased demand for well-documented starting materials that streamline library synthesis and automated high-throughput screening. By continually refining purity, form, and trace byproduct levels, we anticipate needs that once caught procurement teams off guard. Our in-house analytics and deep process knowledge put us in a position to supply novel analogs with the same level of documentation and control expected from core products.

    Engaging Directly With Scientists and Technical Teams

    Direct feedback from the field often gives us a fuller picture than in-house QC tests alone. By speaking to chemists running pilot reactions and screening new coupling protocols, we see how minor changes in form or impurity content can have cascading consequences on throughput or data reliability. One team reported that switching to a less controlled supplier introduced unexpected side reactions, only resolved after reverting to our standard lots. Their experience matches our internal findings: process details matter at every stage, not just at the analytical endpoint.

    How Our History Shapes Product Quality

    Our experience spans thousands of metric tons across the chemical spectrum, and every tweak to process or scale informs how we approach specialty acids like 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo-. From day one, we have avoided shortcuts and quick process changes that might offer short-term gain at the cost of downstream risk. This philosophy helps us deliver product that is not just analytically clean, but easy to handle and reliable to use, even in strict regulatory or sensitive research settings.

    Continuous Improvement as a Core Value

    Unlike standard commodity producers, we do not settle for recipes that merely ‘meet spec’. Our staff invests heavily in process development and field trials, bringing feedback from chemists all over the globe back to the production floor. We view every batch as a potential lesson in efficiency, quality, or process safety. As a result, our products, including the 5-bromo acid, evolve over time, staying aligned with the precise requirements of leading research and production labs.

    Final Thoughts: Value Behind Every Batch

    Manufacturing 1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid, 5-bromo- goes beyond meeting specifications. Every container carries the weight of accumulated process knowledge, rigorous quality checks, and feedback from thousands of end users. The result is more than just a raw material; it is a foundation for innovation in discovery, synthesis, and product development. For those building new molecules, designing cleaner routes, or scaling up efficient processes, the difference brought by thoughtful, experienced manufacturing teams cannot be overstated.