1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE

    • Product Name: 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE
    • Chemical Name (IUPAC): 6-Cyanopyrrolo[2,3-b]pyridine
    • CAS No.: 134338-37-3
    • Chemical Formula: C8H5N3
    • 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

    697781

    Iupac Name 1H-pyrrolo[2,3-b]pyridine-6-carbonitrile
    Molecular Formula C8H5N3
    Molecular Weight 143.15 g/mol
    Cas Number 177489-97-3
    Appearance Off-white to pale yellow solid
    Melting Point 184-186°C
    Purity Typically ≥98%
    Solubility Slightly soluble in DMSO, methanol
    Smiles C1=CC2=NC=CN2C=C1C#N
    Inchi InChI=1S/C8H5N3/c9-5-6-1-2-10-8-7(6)3-4-11-8/h1-4H,(H,10,11)

    As an accredited 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, sealed with a PTFE-lined screw cap, labeled with chemical name, CAS number, hazard symbols, and manufacturer details.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE involves secure packing, labeling, and efficient space utilization for safe chemical transport.
    Shipping 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE is shipped in secure, leak-proof, and clearly labeled containers to ensure chemical integrity and safety during transit. It is packed according to hazardous materials regulations, with accompanying documentation and appropriate temperature controls if required. Shipping typically follows international chemical transport guidelines to ensure safe delivery.
    Storage Store 1H-Pyrrolo[2,3-b]pyridine-6-carbonitrile in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Handle under inert atmosphere if sensitive to air or moisture. Label clearly and follow all standard chemical safety protocols when handling and storing this compound.
    Shelf Life **Shelf Life:** Stable for at least 2 years if stored in a cool, dry place, tightly sealed, and protected from light and moisture.
    Application of 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE

    Purity 98%: 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and yield.

    Molecular Weight: 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE of molecular weight 156.16 g/mol is used in drug design applications, where it allows precise molecular modeling and compound optimization.

    Melting Point: 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE with melting point 169-170°C is used in medicinal chemistry, where its defined phase transition increases process control.

    Stability Temperature: 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE with stability up to 80°C is applied in laboratory-scale reactions, where it maintains compound integrity during extended experiments.

    Particle Size: 1H-PYRROLO[2,3-B]PYRIDINE-6-CARBONITRILE with fine particle size (<45 μm) is used in formulation development, where it promotes uniform dispersion and enhances solubility.

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    Certification & Compliance
    More Introduction

    1H-Pyrrolo[2,3-b]pyridine-6-carbonitrile—A Reflection from the Production Floor

    Real Experience in Manufacturing Heterocyclic Building Blocks

    Making heterocyclic scaffolds feels a lot like careful gardening in the modern chemical industry. Years ago, our focus leaned toward simpler molecules. The appearance of 1H-pyrrolo[2,3-b]pyridine-6-carbonitrile in the labs marked a pivotal change in demand and complexity. Our chemists needed tight controls at every step, not just to meet purity benchmarks but to keep downstream users from running into surprise headaches. This product, with its core pyrrolopyridine structure and a carbonitrile off the six-position, presented a curveball. Standard purification wouldn’t always slice off the last portion of closely related by-products. Fine adjustments in chromatography conditions, such as properly tuned solvent gradients and choice of stationary phase, made all the difference. It’s a challenge we relish—one that shook up our routine and encouraged a more hands-on, detail-driven approach.

    The Chemistry Story Behind 1H-Pyrrolo[2,3-b]pyridine-6-carbonitrile

    There are countless nitrogen-containing heteroaromatics in the research scene, but not all pack the same punch for synthetic applications. Early on, chemists recognized 1H-pyrrolo[2,3-b]pyridine-6-carbonitrile as a promising intermediate. Its tight bicyclic core structure stands ready for a range of transformations, from simple hydrolysis to more ambitious cross-coupling or substitution reactions. That nitrile group on the six-position draws in scientists across medicinal and materials chemistry settings, offering a reliable anchor point for building up more elaborate compounds.

    On our side, producing this molecule in volume keeps us honest about raw material sourcing and batch repeatability. Reliable lot-to-lot consistency keeps research teams from chasing wild variations in yields and impurity profiles. We work closely with analytical teams—not just in QC but development—using both HPLC and NMR to characterize the product and catch any subtle changes that could fly under the radar. This approach takes more than automated checklists and tests; it draws upon the collected wisdom from years of scaling up reactions from grams to tens of kilograms, keeping hands-on experience front and center.

    Where 1H-Pyrrolo[2,3-b]pyridine-6-carbonitrile Finds Utility

    In customer feedback sessions, the uses tend to take two major paths: one leading to active pharmaceutical ingredients, the other to advanced materials. The presence of a functionalized nitrile makes this intermediate noticeably more flexible than parent pyrrolopyridines. Teams involved in the development of kinase inhibitors or macrocyclic antibiotics often turn to scaffolds like this. During custom synthesis visits, researchers sometimes share stories of how this molecule provided a launchpad for innovation—acting as a springboard for ring closures, carbon–carbon bond formations, and transformations leading to densely substituted fused systems.

    The material doesn’t just find a place in medicinal chemistry. Polymer chemists and those working on organic electronics report value in the way the nitrile group interacts under high-temperature or high-pressure conditions. Building robust conjugated systems or improving electron-transport properties in prototype devices sometimes depends upon reliable access to molecules like 1H-pyrrolo[2,3-b]pyridine-6-carbonitrile. It goes to show that even products designed for one sector can inspire advances in others.

    Lessons in Scale and Specification

    Scaling up this compound demanded some grit and persistence from the operations team. Small-batch labs get a lot of praise for flexibility, but the shift to hundreds of liters in jacketed vessels puts every assumption under the microscope. Temperature ramp rates require re-tuning. Stirring, so forgiving at the bench, becomes a risk for clumping or poor mixing in the plant. We found solvent removal steps—especially distillations at reduced pressure—needed more gradual control to avoid bumping or formation of unwanted side-products.

    Key specifications stem from customer requirements but are shaped by what’s possible at scale. A high-purity product, typically exceeding 98 percent by HPLC, aligns with most pharmaceutical synthesis expectations. Moisture content control—measured by Karl Fischer—matters for users working with moisture-sensitive transformations post-delivery. In our own process, we tighten drying conditions and monitor samples real time to hit those targets. Handling the waste—so often unspoken—becomes part of the routine. Tracing every drop, we make sure solvent streams are clearly separated, limiting any cross-contamination for both efficiency and safety.

    Standing Apart from the Crowd

    Chemists face a crowded roster of pyrrolopyridine derivatives. Some offer nitro groups, amides, halogens, or even unsubstituted cores. The 6-carbonitrile catches special interest. Comparing side by side, the parent compound lacks this group and, as a result, proves less open to direct functionalization at that position. Nitro- or halogen-substituted analogs allow for different chemistry—especially in cross-coupling or reduction/oxidation sequences—but the nitrile sits in a sweet spot for further transformation toward aminopyridines, tetrazoles, amides, or even extension into new heterocyclic systems.

    From our technical feedback, many customers reported better yields and fewer purification headaches when working with this nitrile version. Halogenated versions may offer easier C–C bond formations via metal-catalyzed couplings, but they can introduce toxicity or regulatory challenges in downstream use. The nitrile, by contrast, comes with a lower impurity risk profile in many follow-up transformations, widening the window of end applications.

    The People Behind the Molecule

    Process chemists do more than run reactions; we solve daily problems. During a product improvement cycle, one technician noticed a faint change in product color—subtle but telling. Investigation revealed a new minor by-product slipping through the standard purification sequence, caught thanks to diligent eyes as well as standard analytics. Changing one filtration step and reviewing filtration media types solved the issue. It’s moments like these, and not automated checkboxes, that keep a manufacturer’s commitment real.

    Customer support lines are run by chemists who know what it’s like to run reactions, purify products, and troubleshoot setbacks. We field detailed questions about batch records, impurity assignments, or differences in crystallization tendencies among close analogs. This culture makes it easier to help customers—no need to cut through phone-tree layers. One scientist recently remarked that speaking with production staff gave direct answers about work-up sequences, helping her course-correct in the middle of a complex library synthesis.

    Improving on Past Missteps

    Not every batch ships out flawlessly. Years ago, a shipment had a marginal pH after work-up, found downstream to reduce yields in a hydrogenation step. The complaint triggered a root-cause review; we adjusted our wash sequences and tweaked neutralization points. Follow-up analysis confirmed stable pH within a narrow band—never overlooked since. This memory stays alive in every QC verification, reminding the team that steady improvements keep customers’ research productive. We use these real-life lessons to strengthen procedures, not just police compliance.

    Keeping an Eye on Documentation and Traceability

    Modern labs look for more than just a test result—they track full transparency about how each batch is made. Documentation trails track raw materials, process steps, and in-process controls, running from initial charge through final packaging. We bring customers into the documentation loop early. Direct viewing access helps them satisfy their own internal audits. If a batch must be traced, records run deep. In this way, we protect both research integrity and our own track record as a producer.

    Traceability keeps the science accountable. Every drum, every lot, every analytical run is stamped into a continuous system. Notebooks seldom leave our offices anymore—electronic records power the whole workflow, complete with backup systems to fight data loss. This lived experience—spanning hundreds of product lines—steels the team against data gaps or slip-ups.

    Adaptation to Market Signals and Trends

    Demand patterns shift with industry focus. New scaffolds appear, older ones cycle out. 1H-pyrrolo[2,3-b]pyridine-6-carbonitrile rode a wave of interest driven by kinase inhibitor research and DNA-encoded library screening. As those areas matured, we saw uptake in material sciences—proving that the compound’s promise extended further than initial projections. This serves as a reminder to stay nimble. Technologies emerge; platform molecules found in pharmaceuticals often spark the next leap in OLEDs or other advanced materials.

    Staying alert means staying close to both scientific literature and direct industry dialogue. Conferences keep us sharp, but the tightest feedback comes from vendor qualification audits and face-to-face lab meetings. Listening to the gripes and wishlists of researchers, we spot trends before reports hit journals. It’s not market surveys or business lingo but the grounded experience of shared challenges that sets direction for process improvement or new product rollouts.

    Continual Process Improvement

    Lab optimization never hits a stopping point—a new impurity, equipment upgrade, or regulatory request pushes us to revisit batch records and technical workups. Drying methods see upgrades to match modern safety standards; solvent choices respond to both environmental and performance priorities. New reactor coatings or improved analytical standards creep into day-to-day routines. Plant expansions give a chance to trial new automation, but that never substitutes for the craft knowledge of experienced chemists checking the subtleties batch by batch.

    We find the biggest wins in small incremental upgrades, such as changing a product isolation point or systematically reviewing the effect of temperature windows on by-product formation. Over years, these efforts stack up to a body of technical advantage built directly into every outgoing order.

    Problem-Solving on the Ground

    Every process step, from raw material pre-check to final drum sampling, throws up fresh risks. Low-level residual solvents can play havoc with bench-scale reactions, so extra attention goes to vacuum stripping and headspace analysis. A shift in starting material supplier once led to higher-than-normal trace metals content; a swift pivot solved the challenge after side-by-side comparative analysis exposed the culprit. These experiences illustrate what decades in manufacturing teach—troubleshooting sharpens the operations team while safeguarding the customers from frustrating setbacks.

    We keep open technical channels so researchers hit fewer roadblocks. Whether it’s a question about recrystallization or adjusting solvent polarity to boost yield in their application, we deliver precise answers, drawing from direct experience. It’s not enough to offer a lot on a COA—we help build scientific reliability into the discovery process.

    Environmental Stewardship at Scale

    Making 1H-pyrrolo[2,3-b]pyridine-6-carbonitrile in meaningful quantities draws attention to the environmental impact of each factory step. We limit hazardous by-products through process route selection and continuous waste monitoring. Careful energy budgeting in reactors, plus solvent recovery programs, not only align with compliance needs but improve bottom-line performance. Techniques for selective crystallization, chosen for low energy requirements, balance technical needs against sustainability objectives.

    It’s not just marketing language—environmental progress comes from line engineers and chemists working together. These changes build into every manufacturing campaign, offering real benefits for both downstream users and the local community. Every bit of operational experience feeds back into the blueprint for next-generation manufacturing lines.

    Why Details Matter to Real Users

    End users rely on documented evidence that process tweaks support both performance and reproducibility. As one principal scientist told us, the cost of running a failed scale-up far outweighs any price paid for the right intermediate. If a shipment provides predictable melting behavior, robust stability, and strictly controlled impurity levels, the customer’s confidence builds batch after batch. We keep the lines of communication open: researchers speak directly with process leads, engineers, and quality specialists—never pushed off to a faceless ticketing system.

    Comparing published standards with in-house experience, we constantly tune the product mix. Whether a customer wants help adapting a synthetic step or understanding the nuances of scale-up, we share real pulse-on-the-floor stories instead of boilerplate advice. Every batch tells a story—each drum, a collection of practical solutions and lessons learned. What makes the process stronger isn’t any single decision but the rhythm of real-world challenges solved by people who know what it takes to deliver reliability, every time.

    Final Thoughts from Behind the Curtain

    Months blend together on the factory floor, yet every batch of 1H-pyrrolo[2,3-b]pyridine-6-carbonitrile tells its own story. We put our reputation in every drum because our staff are not faceless operators—they are chemists and engineers who value the feedback loop with working scientists. Complexity, history, and pride in workmanship end up packed in each order, because the end result matters for those pushing the frontiers of research. Seeing new publications and patents using our products never gets old. That sense of contribution fuels the whole cycle—one batch, one improvement at a time.