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3-Azaindole

    • Product Name 3-Azaindole
    • Alias 1H-pyrrolo[2,3-b]pyridine
    • Einecs 212-729-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    407768

    Chemical Name 3-Azaindole
    IUPAC Name 1H-pyrrolo[2,3-b]pyridine
    CAS Number 271-63-6
    Molecular Formula C7H6N2
    Molecular Weight 118.14 g/mol
    Appearance White to pale yellow powder
    Melting Point 60-65°C
    Boiling Point 304°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.23 g/cm³
    SMILES c1cc2c([nH]1)cccn2
    PubChem CID 138542
    Synonyms Pyrrolo[2,3-b]pyridine
    pKa 13.1
    Refractive Index 1.671

    As an accredited 3-Azaindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Azaindole is packaged in a 25-gram amber glass bottle, featuring a secure screw cap and clearly labeled hazard information.
    Shipping 3-Azaindole is shipped in secure, chemical-resistant containers to ensure safety and stability during transit. Packaging complies with international regulations for hazardous chemicals. Each shipment includes proper labeling, safety data sheets (SDS), and documentation. Temperature and moisture conditions are monitored to preserve product integrity throughout delivery.
    Storage 3-Azaindole should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents. Store at room temperature, avoiding excessive heat or direct sunlight. Properly label the container and ensure it is accessible only to trained personnel to ensure safety and stability.
    Application of 3-Azaindole

    Applications of 3-Azaindole in Industrial Manufacturing

    As a specialized manufacturer of 3-Azaindole, we supply this advanced heterocyclic intermediate to support the innovation and production standards of multiple key industrial sectors. Below, we detail the main downstream applications where our product delivers tangible value, covering compliance regulations, recommended formulations, integration into manufacturing processes, and the concrete final goods produced by industry leaders.

    1. Pharmaceutical Intermediates for Kinase Inhibitors

    Major pharmaceutical manufacturers utilize this compound as a critical intermediate in the synthesis of clinical drug candidates, especially kinase inhibitors targeting oncology and immunology. It plays an essential role at the advanced building-block stage, enabling highly specific molecular frameworks tailored for precision medicine. The compound enters established supply chains complying with stringent regulations in both investigative and commercial production pipelines.

    Industry compliance standards

    • ICH Q7 cGMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs for Intermediates
    • FDA 21 CFR Part 210/211: Finished Pharmaceuticals cGMPs
    • Good Manufacturing Practice (GMP) Certification

    Typical usage ratio

    • Formulation input ranges from 0.5%–2% w/w, with adjustments based on targeted drug scaffold and overall molecular design. Dose may be modulated according to the number of indole-incorporating steps in multi-stage API synthesis.

    Downstream process integration

    • Enters during key coupling, acylation, or N-arylation steps in custom synthesis; may undergo further transformation such as selective halogenation or substitution depending on structure-activity requirements in small-molecule API pathways.

    Final product types

    • Small-molecule pharmaceuticals in clinical and commercial trials (e.g. kinase inhibitors, targeted cancer therapies)
    • Advanced research compounds for structure-activity relationship studies
    • Active pharmaceutical ingredient (API) intermediates for licensed drug manufacturing networks

    2. Agrochemical Development for Plant Growth Regulators

    Agrochemical firms use our product for the development of innovative plant growth regulators and bioactive compounds. Researchers favor its ring structure for introducing bioisosteric modifications in molecules that influence plant metabolic pathways, contributing to crop enhancement and yield optimization programs. Market launches rely on robust safety evaluations and compliance with international agrochemical standards.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals
    • ISO 9001:2015 for Agrochemical Production
    • FAO/WHO Codex Alimentarius: Pesticide Residue Standards
    • REACH Regulation (EC) No. 1907/2006

    Typical usage ratio

    • Typical inclusion rate is 1%–5% w/w in plant growth regulator formulations, with variations depending on specific crop application trials and the desired metabolic effect on target plant species.

    Downstream process integration

    • Enters early in the synthetic route for the assembly of lead compounds during agrochemical R&D; used in the key step for analog development or directly as a heterocyclic core for further functionalization in production-scale synthesis of PGR actives.

    Final product types

    • Commercial-grade plant growth regulators for cereals, vegetables, and horticultural crops
    • Precursor molecules in the launch of new agrochemical actives
    • Technical concentrates for custom formulation by agrochemical blenders

    3. Dye and Specialty Pigment Synthesis

    Manufacturers of high-performance dyes and specialty pigments employ our material as a core building block for synthesizing colorants used in demanding applications. The heterocycle delivers targeted electronic properties and enhances chromophore stability, particularly for dyes intended for electronics, security printing, and advanced textile markets. Compliance focuses on purity, heavy metal content, and application-specific safety profiles.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toys—Migration of Certain Elements (for pigments in toys and textiles)
    • OEKO-TEX® Standard 100 (for textile applications)
    • ISO 9001 & ISO 14001 (Quality and Environmental Management Systems)
    • REACH Regulation Annex XVII—Restricted Substances

    Typical usage ratio

    • Integrated at concentrations of 0.5%–2.5% w/w in specialty pigment synthesis, titrated by targeted absorption wavelength and substrate compatibility requirements.

    Downstream process integration

    • Employed at the chromophore assembly stage, often via electrophilic substitution, ring-closure, or as a nucleophile in the installation of color-imparting groups; follows strict impurity monitoring before isolation and application blending.

    Final product types

    • Organic electronic pigments for security inks and anti-counterfeiting applications
    • Textile dyes with enhanced wash- and light-fastness
    • Special-effect dyes for optical device coatings

    4. Advanced Material Synthesis for Organic Electronics

    Producers engaged in organic electronics, such as OLED and OFET technologies, source this specialty intermediate for constructing electronic and hole-transport layers where indole derivatives support charge mobility and device longevity. High purity and thorough impurities control are essential to fulfill end-industry acceptance for display and sensor technology supply chains worldwide.

    Industry compliance standards

    • IEC 62341: Display Devices - OLED Requirements
    • RoHS Directive 2011/65/EU: Restriction of Hazardous Substances in Electrical and Electronic Equipment
    • ISO 9001:2015 for Electronic Materials Manufacturing
    • REACH Regulation—SVHC Candidate List

    Typical usage ratio

    • Employed at loading levels between 0.2%–1.2% w/w in functional organic layer formulations, fine-tuned based on target device performance and substrate characteristics.

    Downstream process integration

    • Introduced as a core monomer or dopant during synthesis of small-molecule or polymeric electronic layers; incorporated via coupling or polymerization reactions under tightly controlled conditions to prevent defect formation.

    Final product types

    • OLED emissive and charge-transport materials
    • Thin-film organic semiconductors for flexible electronics
    • High-mobility OFET component materials

    5. Chemical Probe and Diagnostic Reagent Manufacture

    Research tools and diagnostic reagent suppliers introduce this heterocyclic compound into the design of fluorescent probes and biochemical markers, exploiting its electron-rich structure to modify fluorescence intensity and specificity for biomolecular detection and imaging. Strict traceability and QC alignment to international research-grade benchmarks remain central throughout development and scale-up.

    Industry compliance standards

    • ISO 13485:2016 for Medical Devices—Quality Management (applicable to diagnostics)
    • GLP (Good Laboratory Practice) Principles
    • OECD Series on Principles of Good Laboratory Practice
    • USP General Chapter <1040> Analytical Quality by Design

    Typical usage ratio

    • Used at 0.1%–0.8% w/w in most fluorescent probe formulations; concentration calibrated per fluorophore intensity and matrix compatibility in the diagnostic assay.

    Downstream process integration

    • Incorporated during late-stage probe synthesis via coupling reactions with reporter groups; often serves as a scaffold for direct functionalization by click chemistry or amide/bioorthogonal linkages.

    Final product types

    • Fluorescent chemical probes for cell imaging and detection
    • Diagnostic test reagents for molecular biology assays
    • Analytical marker compounds used in drug screening kits
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    Certification & Compliance
    More Introduction

    3-Azaindole: A Reliable Choice from an Experienced Manufacturer

    Our Experience with 3-Azaindole Production and Quality

    For decades, the demand for heterocyclic building blocks in medicinal chemistry has remained steady, and 3-azaindole continues to play a vital part. In the manufacturing plant, we have worked hands-on with the molecule, learning its quirks and strengths during every batch. Working from the raw materials up, with close attention to reaction conditions, our team sees how small variances in temperature or purification steps can have a surprising impact on crystal form and color. Because many customers use 3-azaindole as a precursor for pharmaceuticals or biologically active compounds, we maintain a sharp focus on controlling residual solvents and minimizing impurities—factors that directly shape the outcome for anyone synthesizing downstream products.

    Our plant runs batches with consistent specifications: 3-azaindole with a molecular formula of C7H6N2, and reliable melting points that fall within the established range. Most partners request the product with a purity above 99%, an achievable target in our routine process. We pack material in containers that protect against moisture and light, reducing chances for degradation or discoloration during long deliveries. We handle numerous inquiries regarding batch-to-batch consistency; the answer always comes from years of monitoring, adjusting, and logging the smallest details in conversion and yield. If our chemists notice an unexpected variation—sometimes a subtle smell or a shift in crystallinity—we dig in to identify and remedy the cause. Over time, we have found that owning the full chain of production gives us tighter control compared to traders or resellers who never see the material itself.

    Why 3-Azaindole Remains Essential in R&D and Industry

    For anyone designing novel kinase inhibitors or preparing new chemical libraries, 3-azaindole often ends up at the top of the reagent list. It serves as a privileged scaffold—meaning it forms the backbone of many successful drug candidates and diagnostic molecules. Over the years, researchers visiting our facilities share how regioselectivity and reactivity patterns of 3-azaindole give them access to unique substitution patterns not easily achieved with other aza-heterocycles. Take, for instance, the difference between 3- and 7-azaindole: chemists working in medicinal development tell us that 3-azaindole’s specific nitrogen positioning unlocks binding properties that lead compounds based on indole or pyrrole can’t imitate.

    Some customers rely on 3-azaindole to supply a constant flow into high-throughput synthesis platforms. Others use quantities small enough to fit in a single flask, often for exploratory routes where a synthetic campaign might fizzle out or explode into a major discovery. Over the years, feedback from these innovators translates into real changes at our site. Input from a team exploring antitumor agents led us to develop a refined version with tighter impurity specs; a request from a team targeting CNS agents prompted upgrades to remove certain elemental traces that affect downstream metal-catalyzed reactions. All these adjustments stem from actual product users, with experience echoing back into the manufacturing hall.

    Unpacking Specifications: What Matters in Production

    Think about what sets high-purity 3-azaindole apart. In a busy lab, even a fraction of a percent of unknown impurities can fundamentally derail scale-up or biological evaluation. The procedures at our plant don’t rely on generic templates, but on lived experience—heating and mixing in carefully controlled vessels, adjusting pH at just the right time, filtering, and drying under watchful eyes. If a customer wants HPLC-grade material, we don’t send them a catalog number; we invite them to review batch chromatograms and recent analysis reports, showing where our product meets or exceeds their criteria.

    Differences from substitutes like 2-azaindole or unsubstituted indole show up quickly during catalysis experiments or ring-forming steps. Process chemists remind us that each ring system has “moods”—stability in strong acid, ability to undergo specific cross-coupling, or tolerance to oxidation. We run in-house tests, subjecting 3-azaindole to conditions that mirror those in real industrial or academic routes. If it discolors, polymerizes, or forms byproducts, our own downstream group feeds that report back to the main production team. Customers with a long history of working with us often ask which specifications will matter most for their approach—a conversation we welcome.

    Handling, Storage, and Long-Term Stability

    3-Azaindole is not the flashiest molecule, but long experience has taught us that the details in handling matter a great deal. On a humid summer day, if the storage vault slips by a few degrees, you get shifts in color and sometimes faint odors. Our facilities keep the atmosphere dry and the temperature steady. For larger shipments, the packaging seals away oxygen and moisture, blocking off any entry to agents that could cause breakdown or slow degradation. Over the years, we have seen the frustration when improperly stored material leads to entire runs ruined by trace oxidation. Feedback and collaboration with end users prompted us to double-layer packaging, place clear lot numbers on labels, and send stability data so customers never have to guess at shelf life or performance.

    Collectors from educational institutions purchase smaller packs for teaching and demonstration. To them, a stable product means students don’t encounter confusion from unexpected decomposition, which could send a lesson off track. In the pharmaceutical pipeline, larger research groups demand not just stability, but detailed documentation. Our reports stretch back to the original raw materials, proving identity, packing conditions, and integrity over time. It’s not simply about completing a transaction but supporting everything from student labs to major innovation projects with verified, reliable supply.

    Leveraging 3-Azaindole’s Unique Reactivity and Advantages

    Those who have tried replacing 3-azaindole with other indole family molecules often return to the original for solid chemical reasons. The placement of the nitrogen atom offers a distinctive electronic environment, which brings out new behaviors in coupling reactions, directed lithiation, and functionalizations. In conversations with process teams at contract research organizations, we often hear how the reactivity profile of our 3-azaindole translates into higher yields, fewer steps, or greater selectivity in late-stage functionalization, compared to alternate scaffolds. Stepwise optimization during many different syntheses confirmed for us that pushing for a cleaner starting material pays dividends down the line.

    Researchers working on kinase inhibitor libraries, for example, have shown us structure-activity plots where small changes in the core translate into dramatic biological effects. Having a trustworthy, contamination-free source for 3-azaindole helps them avoid failed synthetic routes or false activity signals caused by byproducts. Several times, input from these projects prompted us to fine-tune crystallization and purification, supporting very low levels of heavy metals and halide impurities. These interactions improve the product not just for one user but for the entire community.

    Tackling Supply Chain and Scalability Issues

    Chemicals like 3-azaindole don’t lend themselves easily to just-in-time supply chains—especially when used as regulatory starting materials or for Good Manufacturing Practice pipelines. In the early 2000s, disruptions in precursor markets (including key amino-pyridine suppliers) sent shockwaves through the pharma sector. We balanced these disruptions, modifying our sourcing and increasing our own inventory. Today, we maintain close communication with both upstream suppliers and downstream users, buffering against sudden shocks. When surges in demand hit—often prompted by a clinical candidate’s success—our flexible manufacturing lines pivot rapidly to boost capacity. Having direct control over production (and not playing the game of distributor arbitrage) lets us commit to longer-term partnerships, price agreements, and emergency deliveries. We see ourselves as partners with our clients, recognizing that the success of their project depends on the real availability and predictable quality of this vital molecule.

    In more than one case, teams planning for scale-up have visited our site personally, walking through the synthesis, QA, and packaging lines. These exchanges lead to honest discussions about challenges, such as removal of color impurities caused by extended exposure to air, or ways to tighten control over residual solvents below even the most demanding regulatory thresholds. By collaborating directly, we avoid the risk of a supplier misunderstanding a requirement, which can easily occur when resellers handle requests through email and spreadsheets alone.

    Standardization and Continuous Product Development

    3-Azaindole’s demand doesn’t spark headlines in the trade press, but those of us in production see slow and steady shifts in requirements over time. Years back, buyers didn’t often ask about nitrosamine content or ultra-trace metals, but growing regulatory pressure now makes these questions routine. Our laboratory upgraded to more sensitive detection methods, lowering the threshold for reporting and exclusion of contaminants. The difference is most pronounced during toxicology evaluation or GMP submissions for oral drug candidates. Customers return with their results, and together, we integrate these lessons into our validation and documentation. Sometimes this means adjusting an entire unit operation for a single customer, but these adjustments often yield improvements that lift the standard for all our batches. 

    We also see growing interest in alternate forms or tailored properties—micronized powders for rapid dissolution, or larger crystal forms for slow-release formulations. While our standard product fits most uses, we take pride in adapting routes and purification to match novel applications. This flexibility comes directly from our long-standing technical team, many of whom have experience that stretches back to the first laboratory syntheses we attempted decades ago. Working from direct feedback, we introduce real product improvements, avoiding gimmicks or needless complexity.

    Real-World Evidence and Support for 3-Azaindole-Driven Research

    Many scientists know 3-azaindole from published screens and patent filings, but what’s less obvious is the mountain of unpublished data generated by actual users. In our quality team meetings, reports come in from universities in Asia, startup biotech labs in the US, and contract manufacturing partners in Europe. The diversity of these tests gives us a wide view—from organic transformations to bioassays and device development.

    Take catalysis: multiple partners shared side-by-side yields for heteroarylation reactions, comparing our product to off-brand sources. In one case, a single contaminant in the comparison sample led to nearly total deactivation of a bespoke Pd-catalyst. Over the years, we have responded by adding an LC-MS check for such contaminants, ensuring chemists have confidence in their screens. For chemical biology groups, the fine granularity of the analytical certificate means they understand what’s in the bottle, not just what’s missing. In a field where novel results depend on eliminating false positives, this kind of transparency makes all the difference.

    Differences from Other Indoles and Azaindoles

    Chemists who reach out to us usually have deep experience with related heterocycles. They point out real, practical differences among the indole family: ease of N-functionalization, directing effects during metalation steps, and differences in solubility and handling. From hands-on experience, 3-azaindole offers a more forgiving profile during classical functionalization and protection reactions compared to its isomeric cousins. Its unique nitrogen arrangement changes not just reactivity, but how it interacts with reagents, solvents, and systems under combinatorial screens. Some groups shared direct evidence: yields for a C–H activation diverged sharply for 3- versus 5-azaindole, not due to conditions but the underlying electronics.

    There are times substitutes like 2-azaindole or even unsubstituted indole get mentioned, especially for budget reasons or perceived availability. After repeated trials, most teams revert to 3-azaindole for its reliability. We see that choice reflected in repeat orders and open feedback. The differences in molecular orbitals and hydrogen bond donors/acceptors directly translate into altered biological and material properties, meaning the right starting block saves time and money far more than short-term procurement shortcuts.

    Working Together for Better Outcomes

    Our role as a manufacturer is more than shipping drums or jars. Every kilo of 3-azaindole shipped represents direct conversations, troubleshooting, and a few lessons learned from the last batch. Academic chemists, process developers, scale-up engineers, and purchasing managers all bring new demands and problems. As one customer described it: getting the molecule is just the beginning—the partnership really starts with open communication about challenges, whether that means accommodating sudden increases in demand or supporting complex analytical documentation.

    Our goal is to keep improving the quality, consistency, and usefulness of 3-azaindole. Stories from clients drive daily changes in our plant—whether that means installing new analytical instruments, tightening documentation, or offering new packaging sizes. Through years of experience, what stands out isn’t the marketing pitch, but the track record shown by reliable deliveries, clarified test results, and product improvements shaped by real chemical work.

    Future Directions and Ongoing Challenges

    Synthetic chemistry moves rapidly. Today’s key intermediate can become tomorrow’s restricted substance as regulations tighten or new health concerns are raised. We keep watch for emerging rules on nitrosamines, genotoxic residues, and trace contaminants. Instead of waiting for regulation to catch up, we meet with client safety teams and standard-setting committees to anticipate the next round of improvements. This kind of continuous progress grows out of an ongoing conversation between production and practical users. For 3-azaindole, that means being ready for new grades, forms, and tighter specs as science pushes forward.

    The growing field of sustainable chemistry challenges manufacturers to examine every aspect of process mass intensity, waste minimization, and environmental impact. Our own plant shifted to greener solvents and closed systems where possible, which not only helps with sustainability goals but also improves purity and consistency. Customers from large pharma want concrete evidence—data on solvent recovery, reduced waste, and minimized resource use. By working together, we turn shared challenges into progress that benefits the entire industry, not just one partner or project.

    Final Thoughts from the Manufacturing Floor

    3-Azaindole may not stand in bright lights, but in the hands of a dedicated R&D team or a scale-up engineer, it’s an invaluable asset. Every barrel or bottle we ship carries with it a shared record of trial, error, adjustment, and commitment to quality. Manufacturing isn’t just pushing output or drawing up a specification—it’s a shared responsibility, measured batch by batch in the success of research, process development, or production. What sets us apart as a manufacturer is not just our knowledge of the chemical structure, but the stories, feedback, and results exchanged with every user along the line. Each improvement, whether sparked by the smallest suggestion or the biggest research milestone, reflects the ongoing partnership at the heart of making and delivering 3-azaindole.