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4-Chloro-7-Azaindole

    • Product Name 4-Chloro-7-Azaindole
    • Alias 4-Chloro-1H-pyrrolo[2,3-b]pyridine
    • Einecs 629-607-9
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    465439

    Productname 4-Chloro-7-Azaindole
    Casnumber 183208-35-7
    Molecularformula C7H5ClN2
    Molecularweight 152.58
    Appearance Off-white to pale yellow solid
    Meltingpoint 120-124°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in DMSO and methanol
    Smiles ClC1=CC2=NC=CC=C2N1
    Inchi InChI=1S/C7H5ClN2/c8-6-3-5-1-2-9-7(10)4-5/h1-4,10H
    Synonyms 4-Chloro-1H-pyrrolo[2,3-b]pyridine
    Storageconditions Store at room temperature, away from light and moisture

    As an accredited 4-Chloro-7-Azaindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Chloro-7-Azaindole, sealed with a screw cap and labeled with safety and product details.
    Shipping 4-Chloro-7-Azaindole is shipped in secure, airtight containers to ensure chemical stability and prevent contamination. Packages comply with hazardous substance regulations, including appropriate labeling and documentation. Handling instructions and Material Safety Data Sheets (MSDS) are provided. Shipping is typically via ground or air, with temperature and safety measures strictly maintained during transit.
    Storage 4-Chloro-7-azaindole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and moisture. Protect from direct sunlight and incompatible substances such as strong oxidizers. Store at room temperature. Ensure proper labeling and keep the container away from incompatible chemicals and unauthorized personnel.
    Application of 4-Chloro-7-Azaindole

    Applications of 4-Chloro-7-Azaindole in Industrial Manufacturing

    As the direct manufacturer of 4-Chloro-7-Azaindole, we support global partners in several advanced chemical industries. Our material’s distinct azaindole structural motif enables high-value synthetic transformations, especially where regulated performance and consistent integration in multi-step synthesis are required. Below, we provide detailed application insights based on established downstream sectors, ensuring transparent and practical information for B2B partners focused on compliance, formulation, process integration, and finished product specification.

    1. Pharmaceutical Intermediate for Kinase Inhibitor APIs

    4-Chloro-7-Azaindole is a validated building block in the synthesis of heterocyclic cores for numerous kinase inhibitor pharmaceuticals. Research and commercial-scale production facilities use it as a key intermediate during Suzuki or Buchwald–Hartwig coupling steps to construct pharmacophores targeting oncology, autoimmune, and CNS indications. Our material aids formulators in addressing batch consistency and impurity control essential for clinical and production batches of small-molecule drugs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients (APIs)
    • US FDA 21 CFR Part 211: cGMP for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) Monographs for related synthetic intermediates
    • International Organization for Standardization (ISO) 9001 Quality Management Systems

    Typical usage ratio

    • 5–15% molar equivalents, depending on stepwise coupling reaction and target yield; formulators adjust loading based on process scale and targeted impurity profile

    Downstream process integration

    • Introduced during heterocycle assembly and subsequent functionalization in the API synthesis route, typically after initial protection and before coupling/cyclization stages

    Final product types

    • Approved kinase inhibitor APIs (such as for ALK, BCR-ABL, EGFR inhibitor families)
    • Advanced pharmaceutical intermediates (APIs in clinical development)

    2. Fine Chemical Synthesis for Agrochemical Active Ingredients

    Top-tier agrochemical producers use 4-Chloro-7-Azaindole as a scaffold in the synthesis of pyridine and pyrimidine-based crop protection agents. Its integration supports the construction of molecules with herbicidal and fungicidal activity, especially where azaindole moieties confer bioavailability or target selectivity. Our customers rely on its reactivity profile to streamline process steps and optimize purity for scale-up.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • OECD Principles of Good Laboratory Practice (GLP) for agrochemical research
    • REACH Regulation (EC) No 1907/2006 for chemical safety in Europe
    • ISO 9001 Quality Management Systems

    Typical usage ratio

    • 1–12% in reaction mixtures; the precise ratio follows active ingredient synthesis step design and desired conversion rates during final condensation or cyclization

    Downstream process integration

    • Usually enters the synthesis at a core-building step for heterocycle introduction, before side-chain addition and final purification of the active ingredient

    Final product types

    • Herbicide technical concentrates
    • Fungicide intermediates
    • Formulated crop protection products containing azaindole-derived actives

    3. Advanced Intermediate for OLED and Electronic Material Synthesis

    Manufacturers in the organic electronic and OLED display industries use 4-Chloro-7-Azaindole in the development of N-heterocyclic carbazole analogs and related light-emitting layer compounds. Its precise incorporation impacts conductivity and charge transport efficiency, making it indispensable during the fabrication of next-generation display materials. Our quality consistency supports batch-to-batch reproducibility critical for optoelectronic component finishing.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substances in electronics
    • IPC-4101B: Specification for Base Materials for Printed Boards
    • ISO 9001:2015 Quality Management Systems for electronic material production
    • Internal QC specifications set by major display panel OEMs

    Typical usage ratio

    • 0.5–6% by weight, adjusted based on desired emission wavelength, quantum efficiency, and device layer thickness

    Downstream process integration

    • Added at the early stage of small molecule or polymer backbone assembly, followed by downstream functionalization steps such as alkylation, sulfonation, or metal complexation

    Final product types

    • Blue or green emitter molecules for OLEDs
    • Organic semiconducting thin films for display active layers
    • Precursor compounds for OFET (organic field-effect transistor) applications

    4. Chemical R&D Tools in Academic and Industrial Synthesis

    Specialty research units, chemical CROs, and academic sites regularly employ 4-Chloro-7-Azaindole to create novel small-molecule probes, enzyme inhibitors, and structural analogs for target validation work. Its halogenated structure broadens the palette for SAR studies in medicinal and agrochemical discovery projects. End users value its high chemical purity and documented batch traceability in regulatory documentation and patent filings.

    Industry compliance standards

    • OECD GLP Principles for chemical research
    • ISO 9001:2015 Quality Management Systems for research-grade supply
    • Customer-defined specifications for chemical purity (typically ≥98%)
    • Internal documentation standards for IP support and regulatory submissions

    Typical usage ratio

    • Variable, typically 0.5–5 mmol scales per synthetic transformation, adjusted for target compound design and SAR project throughputs

    Downstream process integration

    • Used during late-stage diversification of core scaffolds or as a halogen handle for selective cross-coupling in medicinal chemistry and molecular probe synthesis

    Final product types

    • Synthesized chemical libraries for screening
    • Novel pharmacological tool compounds
    • Proprietary intermediates for patent applications
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    Certification & Compliance
    More Introduction

    4-Chloro-7-Azaindole: Experienced Manufacturing and Practical Value

    Our Perspective from the Factory Floor

    Turning out specialty heterocycles is a demanding business. We work in shifts, monitor temperatures, handle sensitive reactants, and track every batch closely. Few compounds underscore the learning curve in scale-up like 4-Chloro-7-azaindole. Each production run reminds us how small variations in moisture, feed rate, or even stirring speed influence product formation and crystallization. We express knowledge through the tools in our hands, and this shows up in the consistency of every drum or flask leaving our clean rooms.

    Understanding 4-Chloro-7-Azaindole: More Than a Line Item

    4-Chloro-7-azaindole stands out within the azaindole family for its practical reactivity and versatility. Chemists recognize its structure — the chloro group at the 4-position and nitrogen at the 7-aza site. These features open reaction doors inaccessible to standard indoles, making it valuable in medicinal and process chemistry. We know the struggles of yield loss on purification. That’s why, batch after batch, we’ve focused on refining parameters to minimize side reactions, strip away colored byproducts, and obtain clear, nearly white crystals — a tough feat with heterocycles.

    On paper, it’s described by its CAS number and chemical formula, but in daily operations, workers note its melting point, the angle of its PXRD peaks, and subtleties of its HPLC profile. Material with trace byproduct content brings headaches downstream, leading to filter clogging or unexpected lags in research. By pinpointing critical steps in nitration, chlorine introduction, and cyclization, we minimize these risks.

    Product Characteristics That Matter in Practice

    Most conversations about 4-Chloro-7-azaindole in the industry focus on purity. We gravitate to chromatography, but after thousands of syntheses, small things matter more. Each lot comes dry, fine, free-flowing, generally pale. We read the color under good lighting. Any yellowing signals process drift — too high chlorination temperature, incomplete workup, maybe a moisture blip at the endpoint. These tiny changes create tangible differences for enzyme development or downstream coupling reactions.

    In terms of specification, we prepare lots to ≥99% (HPLC) purity, low residual solvents (our drying runs use vacuum and inert purge schedules), and trace metals below key thresholds. Particle size varies based on customer order. Most researchers request a standard grind for immediate dissolution into polar aprotic solvents, with no need for pre-milling or extra filtration. Before shipment, our quality control chemists compare spectral libraries — if any atypical peak appears, the lot stays in-house until we identify the source.

    Usage Across Vital Sectors

    We see 4-Chloro-7-azaindole ordered by teams designing kinase inhibitors and central nervous system (CNS) actives. Medicinal chemists rely on its heterocyclic backbone to build out targeted libraries, exploring new activity against kinases implicated in cancer and immune disorders. In these workflows, reactivity at the 4-chloro position speeds up Suzuki, Buchwald-Hartwig, or other palladium-catalyzed couplings. The 7-aza nitrogen shifts hydrogen bonding patterns, opening up distinct vectors for further modifications.

    Every so often, process chemists push scale. Five grams turns to fifty, then kilos, then pilot-scale runs. Here, subtle changes in impurity levels affect product crystallization and filter cake integrity. Researchers ask for details: How consistent are batch peaks? How quickly can powder disperse in DMF or DMSO? Does a given lot handle high-throughput screening conditions? We know because we run these stress tests before bottling every kilogram. We see who’s planning a scale-up by the size and pattern of their repeat orders, and we support them with technical diagrams and hands-on advice gained from our own upscaling.

    Beyond pharmaceuticals, 4-Chloro-7-azaindole turns up in crop protection research, dyes, and functional polymers. Our customers in these fields come back to us for lots that avoid common cross-contamination—those trace boron or chloride contaminants that kill yields in sensitive polymerizations. We understand because similar issues blow up in our own trial runs, prompting us to upgrade checklists and swap out pieces of the workup.

    Comparisons: 4-Chloro-7-Azaindole and Sibling Compounds

    Chemistry doesn’t reward stubbornness. Changing the substitution on the azaindole skeleton, like swapping the chlorine for a bromo or replacing the 7-aza with an adjacent nitrogen, alters the entire reactivity landscape. Early on, we realized 4-Chloro-7-azaindole stands out for its balance: the 4-chloro group offers good leaving ability, yet proves stable in standard storage, unlike iodo analogues that darken or decompose over time.

    In our hands, 4-Chloro-7-azaindole purifies more easily than 7-azaindole itself, which tends to smear on chromatography columns and picks up hydrolytic degradation. Regular 4-chloroindole lacks the nitrogen you need for specific hydrogen bonding networks, while most other positions on the indole ring don’t have the same cocktail of reactivity and practical handling. We’ve made analogues with fluoro, bromo, methyl, and methoxy groups, and watched customers switch back to 4-Chloro-7-azaindole for speed and predictability in common N-arylation protocols.

    Making Quality Mean Something Day-to-Day

    Quality stems not from slogans but from everyday routines. Every operator on our team knows what to look for — not just the numbers posted on COAs, but subtler signs. We calibrate reactors, double-check pressure ratings, and document cleaning cycles between similar heterocycles to prevent cross-contamination. A batch of 4-Chloro-7-azaindole with a tell-tale off-smell or extra haze means lost time, rework, or in the worst case, disposal. These are real costs that show up nowhere on a spreadsheet, but every person in manufacturing feels them.

    Communicating with customers helps us understand what quality actually means in laboratories. We’ve stopped using certain filter aids that leech trace tin into some products — a learning process that came from honest feedback and repeat analytic hits. Knowing that an odd residual impurity can halt progress in a medicinal chemistry campaign, we continuously review analytical data and internal process logs. Our approach is practical: fix issues at their root, keep records accessible, adapt to process improvements pushed by both our own R&D and those solving problems with our material.

    Supply Responsibility: Planning for Stability and Predictability

    Over the years, we’ve seen global supply chains tested by surges in demand, raw material price jumps, and shipping bottlenecks. We did not always have enough buffer. Now, we keep extra stock of precursor substrates, lock in agreements with vetted reagent suppliers, and operate parallel purification lines. This lets us supply 4-Chloro-7-azaindole reliably, supporting programs that cannot afford delays.

    We track every incoming reagent, document its COA, and challenge-test them in real reactions to catch hidden variables. After being burned by a contaminated lot of phosphorus oxychloride years ago, we set stricter incoming goods policies and multiple supplier approvals. When a researcher asks about our chain of custody, or the specific handling of raw materials, we give direct answers. Sharing insights and records helps build trust — there’s no shortcut for this, only years of consistent follow-through. We’ve also invested in modular warehousing, allowing us to offer emergency stock draws or split shipments to align with pharmaceutical project schedules.

    Supporting Innovation, One Batch at a Time

    We see requests from startups, large research organizations, and global pharmaceutical firms. Each has unique requirements — some search for lots suitable for clinical intermediates, others for screening small libraries. Our technical team consults regularly with process chemists, passing along practical details such as dissolution rates in water-miscible solvents, compatibility in ammonolysis steps, or tolerance to freeze-thaw cycles.

    We answer technical questions honestly, drawing from field experience. If something doesn't work — say a filtration breaks down on scale — we communicate setbacks and propose workarounds. If we learn a batch of 4-Chloro-7-azaindole outperforms competing compounds in a new coupling strategy, we update standard handling protocols and share findings, so the next customer benefits. Documentation extends beyond paperwork; it’s a commitment to reproducibility.

    Over time, close communication shapes how we refine our own product. A customer running a combinatorial screen gave feedback on crystal morphology — large, irregular crystals slowed down automated picking robots. In response, we tweaked solvent gradients and altered drying cycles, achieving finer and more reliably sized powder. Practical changes in manufacturing arise from conversations and continuous improvement, not from solitary theorizing.

    Handling, Storage, and Real-World Safety

    Managing 4-Chloro-7-azaindole starts with controlling moisture exposure and light sensitivity. Material goes from reactor to vacuum filter, then to inert-gas-purged storage drums. Warehouse staff monitor humidity and temperature, logging it twice per day. As the compound heads for shipment, double-sealed liners keep trace water out, reducing risk in transit.

    In the lab, experienced users dissolve 4-Chloro-7-azaindole in DMSO, DMF, or acetonitrile, often under mild heating. Chemists conducting scale-up anticipate its potential for hydroscopic pickup, so they prepare suitable atmospheres. Our safety training covers accidental release, waste handling, and first aid for minor exposures. Early on, we sustained a shipment loss when open handling let fine particles escape — since then, we doubled bagging and retrained handlers on transfer protocols. Learning doesn’t stop after a successful shipment; every near-miss pushes us to improve.

    Challenges and Solutions in Daily Production

    4-Chloro-7-azaindole offers unique technical challenges. Achieving high selectivity during cyclization means monitoring gas evolution and using high-grade acids, both to minimize polymeric byproducts that are tough to remove. Operators recognize that an off-standard exotherm signals deeper root causes — an impure chlorinating agent, or over-concentration during workup. Instead of masking defects with extra purification, we revisit synthesis pathways, using feedback to lower temperature swings and dilute any sensitive crudes.

    Reactive impurities don’t just impact specification sheets — they cause downstream issues for chemists who depend on reliable reactivity or clean coupling to complex building blocks. Each time an issue arises, we record the deviation, review it as a team, and share strategies: change a glass-lined reactor, modify a quench step, alter agitation speed for better phase transfer. Hard-won solutions seldom appear in textbooks; they’re borne out of repeated work and error correction.

    Practical Aspects of Scalability and Delivery

    Scaling up 4-Chloro-7-azaindole has pushed our process team to solve crystallization and filtration bottlenecks that only show up at kilogram scale. As demand increases, we invest in larger reactors and upgrade dust collection systems. Bulk lots wind up in double-liner drums with desiccant packets. Smaller quantities for research often go in specialized amber bottles to avoid light-induced decomposition.

    Our logistics crew tracks regulatory documentation and shipping codes, but above all else, they coordinate closely to avoid temperature spikes en route. Delayed or damaged shipments slow down not just us, but all research downstream. Each crate is overpackaged, because a lost lot means extra downtime, reruns, or at worst, forced rerouting of entire synthetic campaigns.

    By moving key purification stages in-house, and keeping extra analytical QA/QC capacity available, we cut down on turnaround times and replace material quickly when a client faces yield impact due to unexpected events. We know the pain of missed targets, so we act swiftly to mitigate supply gaps, never resting on generic promises. We strive for traceability and rapid response, as these are the measures that make a difference across every research program fueled by our 4-Chloro-7-azaindole.

    Continuous Improvement: Listening and Adapting

    Innovation never stops. Recent years have seen more advanced methods for functionalizing heterocycles, and new safety standards. Our R&D staff develop and test greener oxidants and solvents in pilot batches, looking for efficiency boosts and reduction in waste. Customers who try novel coupling methods provide feedback, sometimes catching unexpected reactivity or stability benefits. Insights gained in-house get shared with our clients to help them avoid pitfalls.

    We know that trusted partners shape practical improvements. Keeping channels open has allowed us to refine the workup, cut batch times, and improve sustainability across waste streams. This level of collaboration only works by showing a willingness to change plans, test new ideas, and follow up rapidly. Labs using our 4-Chloro-7-azaindole as a core intermediate drive us to adapt, ensuring we don’t settle for “good enough.”

    The Value We Carry Forward

    Supplying 4-Chloro-7-azaindole means balancing technical know-how, supply stability, and a respect for the hands-on realities of chemistry. Trust only comes through proven results. Every member of our production, QA, and logistics teams contributes to the reliability built into each kilogram. There’s no faceless routine — someone personally inspects each order, ensuring the material matches what researchers require to push science ahead.

    Each day, we see the benefit of years of problem solving, adaptation, and honest conversation. That’s what shapes our approach to 4-Chloro-7-azaindole — a compound whose impact in the laboratory depends as much on experience and teamwork as on reagent quality or process innovation. As demand grows and workflows evolve, we keep improving. Precision, transparency, and responsiveness form the foundation of how we manufacture and deliver this essential heterocycle.