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

    • Product Name: 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro-
    • Chemical Name (IUPAC): 5-fluoro-7H-pyrrolo[2,3-b]pyridine-2-carboxylic acid
    • CAS No.: 153034-86-3
    • Chemical Formula: C8H5FN2O2
    • 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.
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    Specifications

    HS Code

    301578

    Chemical Name 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro-
    Molecular Formula C8H5FN2O2
    Molecular Weight 180.14 g/mol
    Cas Number 1442651-08-6
    Appearance Solid
    Solubility Soluble in DMSO, low solubility in water
    Purity Varies; typically ≥97%
    Smiles C1=CC2=NC(=C(C=C2N=C1)F)C(=O)O
    Inchi Key OBYGULJAVGWDDS-UHFFFAOYSA-N
    Storage Conditions Store at room temperature, away from light and moisture
    Synonyms 5-Fluoro-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid

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

    Packing & Storage
    Packing The chemical is packaged in a 5-gram amber glass bottle with a tamper-evident cap and clearly labeled with hazard and identification information.
    Container Loading (20′ FCL) 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro-: 20′ FCL container loaded with securely packaged drums, compliant with chemical transport regulations.
    Shipping Shipped in secure, tightly sealed containers to prevent contamination and exposure, 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- is handled according to chemical safety regulations. Packaging complies with international transport standards, often including secondary containment and hazard labeling, with expedited delivery in temperature-controlled conditions if sensitivity or stability require.
    Storage Store 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- in a tightly sealed container, away from moisture, light, and incompatible substances in a cool, dry, and well-ventilated area. Keep at room temperature or as specified by the supplier. Ensure proper labeling and access restricted to trained personnel. Avoid exposure to heat and sources of ignition.
    Shelf Life The shelf life of 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- is typically 2–3 years under proper storage conditions.
    Application of 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro-

    Purity 98%: 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- with purity 98% is used in pharmaceutical intermediate synthesis, where enhanced reaction yield and product consistency are achieved.

    Melting Point 212-216°C: 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- with melting point 212-216°C is used in high-temperature formulation processes, where stable processing conditions are maintained.

    Molecular Weight 180.13 g/mol: 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- with molecular weight 180.13 g/mol is used in targeted drug design, where precise molecular compatibility is ensured.

    Particle Size <50 µm: 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- with particle size under 50 µm is used in solid dosage form production, where improved compound dispersion is achieved.

    Stability Temperature up to 120°C: 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- with stability temperature up to 120°C is used in chemical storage applications, where long-term compound integrity is preserved.

    Water Content ≤0.5%: 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- with water content no greater than 0.5% is used in moisture-sensitive synthesis pathways, where hydrolysis risks are minimized.

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    Certification & Compliance
    More Introduction

    1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro-: Manufacturing Perspective

    Understanding the Chemical: A Closer Look from the Factory Floor

    In today’s chemical manufacturing space, 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- stands apart because of its unique heterocyclic framework and the strategic substitution at the five position. Real work with this molecule always starts from sourcing the best raw materials, which means strict inspection of every shipment of pyridine and fluoroacetic acid arriving at our plant. The specificity of this compound’s structure, with fluorine placed for precise influence on electronic properties, shapes how each batch comes together and how it delivers value across the pharmaceutical and advanced materials sectors.

    Our chemists invest long hours ensuring every small step in the multi-stage synthesis gets the attention it demands, because any shortcut means risking purity or structure. Through tailored conditions—just the right solvent system, pressure, and temperature profile—we achieve optimal yields. Experience teaches that off-the-shelf general reagents or rushed shortcuts always lead to costly clean-up or rejects. With this carboxylic acid, every time a reaction reaches completion, we verify not just with thin-layer chromatography but also check against reference spectra, confirming proper fluorine incorporation and correct ring closure. Every step matters, because many of our client partners rely on absolute reproducibility between different production batches.

    Specification and Quality with an Eye for Detail

    This product doesn’t leave our gates unless it exceeds at least 98% HPLC purity, passing a suite of organoleptic and instrumental tests. Experience shows that even a half-percent variance in byproducts like unreacted pyridine or regioisomeric impurities can undermine downstream pharmaceutical synthesis. Handling and isolating the product requires close attention— from vacuum-assist filtration to air-tight drying— because the compound picks up moisture, and slight decomposition soon follows.

    From the manufacturer’s point of view, maintaining consistently high bulk density and fine, uniform crystalline form matters just as much as purity. In many research and development labs, ease of weighing and solubility behaviors play a key role. Crystals of this carboxylic acid pack reliably into containers, which avoids static clumping or loss during transfer. We know customers prefer a dry, free-pouring product. Over time, the nuances in appearance—shades and glints in the powdered material—can signal issues in crystallization or residual solvents, so every shift’s operator stays attentive to the smallest color deviation or stickiness. That vigilance pays back, since the final user doesn’t want batch-to-batch surprises.

    Why the 5-Fluoro Group Matters in Application

    The addition of a fluorine atom to the basic pyrrolo[2,3-b]pyridine-2-carboxylic acid core alters both chemical reactivity and biological properties, supporting a range of tailored applications. In practice, fluorine enhances metabolic stability and alters polarity, expanding the toolbox for medicinal chemists developing kinase inhibitors or other small-molecule therapeutics. Our facility regularly receives inquiries from researchers testing drug-like analogues featuring fluorine substitutions. They point to the improved enzyme selectivity and better pharmacokinetic profiles compared to non-fluorinated counterparts. We see these effects reflected in repeat orders coming from global biotech clients seeking leads for safer, more potent therapies.

    Outside drug development, the compound also proves valuable in modern materials science. Specifically, the electronic effects from the fluorine addition can tune absorption and emission behaviors of sensor materials. Some electronics manufacturers source our 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- for inclusion in organic semiconductors, leveraging its predictable structure in device fabrication. Again, batch consistency and structural precision drive real-world performance; any misplacement of the fluorine or ring-opening impurities can undermine subsequent product stability or function. We continue to refine our quality control process, combining classic structural elucidation techniques and new inline spectroscopy to catch even trace deviations before shipment.

    Genuine Manufacturing Challenges

    Scaling up from grams to multi-kilogram production means learning from each cycle. Early in our work with this compound, scale-up brought out previously hidden bottlenecks—especially how water content in intermediate steps impacts overall yield. In small flasks, it’s easier to dry solvents and monitor reaction progress; in a 500-liter vessel, even a few milliliters stray water means starting troubleshooting. Sometimes production slows or stalls, not from lack of expertise, but from humidity rises or subtle catalyst deactivation, issues that never show up in theoretical process descriptions. That’s why continuous investment in better drying methods, purpose-built filtration equipment, and on-the-fly analytical checks has become critical. Every batch teaches new lessons, and peer review between shifts has helped avoid costly downtime or wasted runs.

    Safety is never background noise. Fluorinated intermediates, while not as reactive as some, demand extra attention in venting systems and waste processing. Each unit operator here knows that even trace atmospheric release can corrode ductwork or trigger alarms, so every reaction runs with redundant scrubbers and monitored pressure drops. Strict adherence to PPE and regular equipment audits keeps the team confident in every shift. It is never about shortcuts or hoping problems stay hidden. Honestly, sharing near-misses and rolling out team-based improvement plans each quarter has built real resilience in our operation.

    Comparisons—How 5-Fluoro- Differs from Similar Compounds

    Many manufacturers, including us, work with a portfolio of pyrrolo[2,3-b]pyridine derivatives. Adding a fluorine at position five changes not only reactivity but downstream application potential. By comparison, the non-fluorinated 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid serves as a starting point for agrochemical intermediates, but lacks the needed stability for advanced pharma research. Halogenated variants like the 5-chloro or 5-bromo analogues offer better leaving group chemistry, but usually introduce more bulk and less precise electronic effects. Through regular data sharing with technical teams, we’ve recorded higher cell permeability and improved activity with the fluoro group over these heavier halogens—advantages seen clearly in screening assays and biological testing.

    Other fluorinated heterocycles exist, of course. What sets this structure apart is both the core rigidity and the delicate balance between synthetic accessibility and potent biological properties. Compounds bearing fluorine at alternative locations on the ring tend to show very different reactivity, with some positions giving unpredictable side products or harder-to-separate isomers. The five-position addition achieves a desirable mix of heightened metabolic resilience—Defunct structures quickly degrade in bioassays, while this compound sees much slower breakdown and more consistent assay results. Researchers have flagged this benefit repeatedly, sending performance feedback that helps us refine our synthesis and handling to match real lab demands.

    End-User Experiences—Feedback that Shapes Manufacturing

    Customer insight has shaped much of our process design. Early shipments pointed to trace carryover of metal catalyst residues; rapid feedback from a pharmaceutical partner led us to include extra steps for fine filtration and chelation. Once, an academic partner developing a kinase inhibitor library reported crystallization issues due to microscopic over-dryness, leading us to revisit our air-handling protocol to retain just enough process moisture during final isolation. These adjustments don’t happen by chance. Every lesson gets logged, and teams work through options together to refine operating protocols, always looping back client observations over to the process chemists and quality teams before embedding improvements in our SOPs.

    Researchers using this acid as a precursor for active pharmaceutical ingredient (API) development often share their experience with scale, noting how reactivity holds up under higher concentrations without unwanted oligomerization or byproduct formation. That predictability saves time and enables rapid project cycling, something we aim to safeguard with every production run. Industrial customers emphasize handling ease—no one wants to spend extra hours breaking up clumped product with a spatula or running repeat dissolutions trying to adjust for solubility swings. We test every drum, verifying not just purity but also flow properties, sharing test run data with the technical service teams supporting end users worldwide.

    Solutions to Persistent Issues

    Rather than standard fixes, we approach each challenge as a partnership problem-solving effort. Tech transfer never happens in a vacuum—our scientists and operators talk directly with end users to address persistent humidity uptake, suggesting storage in sealed, argon-flushed drums and demonstrating simple transfer tools that eliminate static buildup. Where solvent selection causes headaches, our R&D group prepares parallel solubility profiles under real-world conditions, sharing these data so customers can switch carriers with confidence.

    Some issues arise from regulatory shifts, with new guidelines in certain regions affecting how residual solvents or heavy metals are quantified. Every such change prompts us to re-examine analytical techniques in the QA lab, investing in improved instrument calibration and better third-party reference standards to close the loop. Communication goes beyond compliance; when a change in guidance affects product release or documentation, we hold internal cross-disciplinary briefings to work through implications before anything leaves the warehouse. That lets us act as real partners with clients, not just suppliers who hand off generic certificates of analysis and walk away.

    Environmental Stewardship and Responsibility

    Fluorinated organic compounds, by nature, require extra focus on waste and emissions handling. No production campaign is considered finished here until residual mother liquors and washings have been neutralized and disposed of following best practices. We run wet scrubbing for vent gases, and verify water discharges for fluorine content daily against both local and international guidelines. Every reactor operator receives environmental training and recognizes the importance of strict adherence to handling protocols.

    Over the last five years, upgrades to solvent recovery systems have driven down process losses by over 40%. This saves real money in operations, but more importantly, lowers our environmental impact considerably. Many chemical plants let old procedures linger—hoping regulators don’t look closely. We instead welcome visits from third parties, openly sharing our safety records and recent improvements, believing that visible stewardship creates better investment in the business, stronger team morale, and more committed partner relationships across the supply chain.

    Continuous Improvement and Industry Perspective

    Staying ahead in the fine chemicals industry means blending institutional knowledge with a readiness to adapt to new challenges as they arise. Annual reviews of all production data, side-by-side with recent literature and regulatory updates, keep our entire team current. Experienced operators mentor new hires through real production cycles rather than abstract desk training. This builds tacit knowledge—being able to tell from a slight shift in product hue or dissolve speed if something in upstream chemistry has changed, far ahead of a failed lab report. Skill isn’t just a credential here—it takes hands-on repetition, day in and day out.

    Customers want the latest version of every product, so we proactively redesign steps whenever efficiency, environmental, or safety considerations shift. For this 5-fluoro derivative, current process monitoring includes real-time reaction tracking using IR and NMR, with in-process corrective measures logged and reviewed weekly. Regular feedback from sales and technical support flows directly into process improvement meetings.

    In the broader market, demand for fluorinated heterocycles continues to rise, especially as pharma and advanced materials partners move away from older, less sustainable reagents. The proven value of 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- rests on our ability to consistently meet or beat user needs, which means investing in both people and infrastructure. Technological upgrades—like digitized batch tracking and improved real-time release analytics—remain ongoing, guided by both customer expectation and our internal learning curve.

    Final Thoughts from Direct Manufacturing Experience

    Producing 1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid, 5-fluoro- goes far beyond formulae or technical datasheets. It’s about learning, adapting, and prioritizing every input and process step, shaped by what real users experience on their side of the fence. Each drum or flask represents countless process variables managed, improved, and retested—never settling for “good enough." We keep a direct line from the plant floor to the customer bench, closing feedback cycles quickly, and retooling where needed to support evolving demands in discovery chemistry, drug development, and cutting-edge materials assembly. Working hand-in-hand, not simply selling a product, but providing solutions whose reliability and usability reflect old-school craftsmanship filtered through modern innovation. Years of direct experience taught us that every detail counts—the right raw material, the right reaction time, and the right communication channel with those who rely on our product to unlock the next round of scientific progress.