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5-Bromo-6-Nitroinazole

    • Product Name 5-Bromo-6-Nitroinazole
    • Alias 5-Bromo-6-nitro-1H-imidazole
    • Einecs 836-504-1
    • 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

    127965

    Chemical Name 5-Bromo-6-nitroindazole
    Cas Number 220451-50-7
    Molecular Formula C7H4BrN3O2
    Molecular Weight 258.03 g/mol
    Appearance Yellow to orange solid
    Melting Point 235-239 °C
    Solubility Slightly soluble in DMSO, DMF, ethanol
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Synonyms 5-Bromo-6-nitro-1H-indazole
    Structure Type Aromatic heterocycle, indazole derivative

    As an accredited 5-Bromo-6-Nitroinazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 5-Bromo-6-Nitroinazole

    Applications of 5-Bromo-6-Nitroindazole in Industrial Manufacturing

    5-Bromo-6-nitroindazole serves as a specialized intermediate in high-value downstream industries. As a manufacturer, we support clients in regulated markets that require precise compliance and consistent specification. Below, we outline key industrial applications and integration points for this compound, including relevant standards and process guidelines for each segment.

    1. Pharmaceutical API Synthesis (Indazole-Based Drugs)

    Pharmaceutical manufacturers source this material as a building block for the synthesis of indazole-based active pharmaceutical ingredients—particularly in anticancer, CNS, and anti-inflammatory drug development pipelines. Downstream, chemists incorporate it in multi-step synthetic routes to produce targeted molecules, where its functional groups confer selectivity for specific reaction schemes. This application requires rigorous traceability, full impurity profiling, and alignment with regulatory filings. Use rates vary according to route design, with careful control over reagent excess and residuals during scale-up batches for GMP manufacturing.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, EP, JP pharmacopoeia monographs for relevant APIs
    • FDA and EMA regulatory filings (DMF/CEP reference in submissions)
    • REACH registration for supply into Europe

    Typical usage ratio

    • Reaction input: 0.8–1.2 molar equivalents per step; adjusted per stoichiometric demand and process yield optimization
    • Pilot and commercial scale reactions may modulate input to control impurity profiles and residual reagent content, especially for injectable products

    Downstream process integration

    • Initial introduction during heterocycle construction or late-stage functionalization in route design for indazole APIs
    • Followed by catalytic hydrogenation or nucleophilic substitutions to achieve target drug precursors
    • Intermediate purification through solvent extraction or crystallization prior to further derivatization
    • Final conversion prior to API salt formation or direct formulation

    Final product types

    • Small molecule APIs (oncology, neuroscience, anti-inflammatory agents)
    • Clinical trial materials (Phase I–III study supplies)
    • Reference standards for regulatory submission
    • Commercialized finished dosage forms (tablets, capsules, injectable solutions)

    2. Agrochemical Intermediate Manufacture

    Companies operating in the crop protection sector integrate this compound as a core intermediate for synthesizing indazole-structured fungicides and herbicides. Its bromine and nitro functionalities support downstream coupling operations, enabling tailored activity profiles against plant pathogens and resistant weed species. Compliance extends from environmental permits to product-specific agrochemical registrations, with ongoing updates to accommodate production scale and batch release protocols. Typical usage ratios depend on final active ingredient synthesis route and regulatory maximum impurity tolerances.

    Industry compliance standards

    • FAO/WHO specification for agrochemical technicals
    • ISO 16140 for testing and specification of crop protection agents
    • National pesticide registration guidelines (EPA in US, China ICAMA, EU PPP)
    • REACH registration requirements for EU countries

    Typical usage ratio

    • Employed at 1.0–1.3 molar equivalents for each synthesis batch; ratio tuned for conversion yield and allowable impurity ceilings as set by agrochemical regulations
    • Adjustment may be made to efficiency in multi-ton production, based on process development data

    Downstream process integration

    • Step-wise reaction entry for coupling or cyclization with alkylation/amination agents
    • Used in the main backbone assembly or as a selective functional group donor for structure–activity relationship enhancements
    • Post-reaction phase employs phase separations, extractive work-up, and product crystallization for purity assurance
    • Final integration into formulated agrochemicals post-technical validation

    Final product types

    • Technical grade fungicide concentrates
    • Herbicide actives for post-emergent weed control
    • Seed treatment formulations
    • Pilot and registration batches for field trials

    3. Specialty Dye and Pigment Raw Material

    Dye and pigment manufacturers introduce this indazole derivative in the synthesis of complex organic pigments. The building block supports fine-tuning of chromophore structures to enhance weather resistance, color fastness, and substrate adhesion for automotive, textile, and plastic applications. Production lines typically follow proprietary processes under documented quality policies, with suppliers required to meet batch COA and analytical testing regimes.

    Industry compliance standards

    • ISO 9001 quality management for pigment synthesis operations
    • REACH Annex XVII substance restrictions for downstream pigment constituents in Europe
    • Oeko-Tex Standard 100 for textile safety
    • Specific end-market restrictions, e.g., lead-free, azo-free compliance for pigments

    Typical usage ratio

    • Process input typically at 5–10% by weight relative to final organic pigment mass; levels depend on pigment structure and target optical density
    • Adjustment based on panel testing for shade development and lightfastness

    Downstream process integration

    • Initial charge to diazotization or condensation reactors as indazole nuclei precursor
    • Downstream functionalization through aromatic substitutions, followed by filtration and drying
    • Quality checks for shade, particle property, heavy metal content
    • Dispersion, milling, and conversion to pigment concentrates for end-user blending

    Final product types

    • Automotive paints and plastic pigments
    • Textile printing dyes meeting fastness standards
    • High-stability coating pigments for outdoor use
    • Masterbatch color concentrates for polymers

    4. Analytical Reference Material Production

    Analytical and reference standard laboratories employ this compound as a structurally defined entity for developing HPLC, GC, and LC-MS calibration standards. Its purity profile and definitive structure support bioanalytical, forensic, and QC method validation—central to regulatory submissions and routine laboratory accreditation. Strict documentation and batch validation cover traceability, composite impure mapping, and cross-reference to established analytical protocols.

    Industry compliance standards

    • ISO/IEC 17025 laboratory testing and calibration standards
    • USP and EP analytical reference standards guidelines
    • GLP (Good Laboratory Practice) for method validation
    • ICH Q2(R1) for analytical procedure validation

    Typical usage ratio

    • Supplied in quantities from 1–10 mg per individual reference vial for calibration
    • Dilution and preparation conducted based on validated method, typically within 0.01–1% w/v in solvent media

    Downstream process integration

    • Purification via preparative HPLC or recrystallization for >99% purity requirement
    • Aliquoting into certified vials under cleanroom standards
    • Stability and certification testing for shelf life and assay performance
    • Integration into QC systems as calibration or verification standards

    Final product types

    • Certified reference standards for pharmaceutical impurity analysis
    • Analytical calibration kits for regulatory bioanalytical testing
    • Master batch QC standards for synthetic laboratories
    • Internal standards for method development in academic and industrial labs
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    More Introduction

    5-Bromo-6-Nitroindazole: Delivering Precision for Advanced Research

    The Evolution of Complex Chemical Tools

    Advancements in industrial and pharmaceutical chemistry often depend on just a few grams of the right compound. Over the last decade, indazole derivatives have made big waves, showing up in pharmaceutical research labs, academic institutions, and even the design of next-generation agrochemicals. 5-Bromo-6-Nitroindazole has taken on a role in that growth thanks to its structure, which brings targeted performance and predictable reactivity to tasks that demand reliability.

    Model and Specifications Matter in the Real Lab

    Some researchers ask why one should choose 5-Bromo-6-Nitroindazole over other indazole variants. The answer comes down to the practical work in the lab. This compound features a bromine atom at the 5-position and a nitro group at the 6-position: specific placement. That isn’t just a theoretical point. Swap those groups around on the indazole ring and you end up with a different molecule and different activity.

    What sets this variant apart is the way these functional groups impact both solubility and reactivity in reactions like Suzuki-Miyaura couplings, or during selective reductions and substitutions. It’s stable as a solid, easy to handle, and often available as a beige or yellow powder. Its melting point and purity specifications are controlled tightly, supporting effective storage and measured dosing in synthesis or experimentation.

    If you’ve ever run reactions where sterics and electronic effects play out in unpredictable ways, you know you can’t just swap one halogenated indazole for another. The bromine not only makes nucleophilic aromatic substitution possible, it acts as the handle for more sophisticated cross-coupling, while the nitro group pushes the electron density around the molecule, making ring openings and oxidations far easier to control. Every bench chemist has at least once learned the lesson that reaction outcome shifts significantly with subtle changes to molecular footprint. 5-Bromo-6-Nitroindazole’s layout saves time: fewer failed reactions, less frustration.

    Purpose Drives Choice: How Labs Use 5-Bromo-6-Nitroindazole

    Functionalized indazoles found their way into drug research, dye chemistry, and material science because the indazole core can offer both biological and material stability. With its unique substitution, 5-Bromo-6-Nitroindazole often serves as a valuable intermediate for building more complicated molecules—acting sometimes as the skeleton for kinase inhibitors, and other times as a precursor for heterocyclic ring systems. In research teams where deadlines are tight, having access to this compound means you start closer to your synthetic target.

    Synthesis aside, the molecule’s bromine offers a clean entry point for new aryl, alkynyl, or heteroaryl substituents through palladium-catalyzed cross-coupling. Medicinal chemists rely on this kind of flexibility. You see, the bromine can be swapped for a range of complex side chains while the nitro group remains as a potential site for further reduction or modification. This dual-functionality simplifies route design, streamlining the pipeline from bench work to pilot scale. For a team working with analogues, being able to shift strategy mid-project without ordering a fresh batch of starting material makes a difference.

    Every Detail Counts: Why Purity and Stability Make the Difference

    Researchers—especially those working with tight yields or precision bioassays—often talk about lot-to-lot consistency. From my own days managing mid-scale drug discovery projects, the unreliability of inconsistent raw materials piled up costs fast, both in time and in wasted effort. 5-Bromo-6-Nitroindazole stands out because quality standards are now far higher than they once were; narrow melting point ranges, careful control against water contamination, and exacting spectroscopic characterization (NMR, IR, MS) are a given. In large projects, where regulatory filings eventually matter, that traceability saves everyone headaches.

    Longer shelf life and a consistent appearance help avoid surprises. Everyone who has reached for a reagent jar expecting a yellow powder and instead found brown agglomerates will recognize why stability makes such a difference. With a shelf-stable indazole, you spend less time troubleshooting side reactions and decomposition, and more time actually progressing in your work.

    Addressing User Needs: Scaling from Milligrams to Kilograms

    Small-scale academic researchers and large-scale process chemists want different things from their chemical inventory, but both care about scale-up. Making an obscure intermediate for a unique study might only require a few hundred milligrams, but a process lab can’t waste precious days and dollars on reagents that vary between suppliers. Contacting chemists from major research teams, I often learned that even when a company advertised near-identical products, reproducibility after scale-up often flagged.

    With 5-Bromo-6-Nitroindazole, improvements to manufacturing and purification have closed the gap between bench and pilot-plant quantities. Labs can now order enough to run several iterations of optimization without shifting purity or encountering troublesome byproducts. Time and again, reliable sourcing meant the difference between getting a clinical candidate to the next phase or getting bogged down in rework.

    No Substitute for the Right Tool

    Other indazole derivatives crowd the catalogue listings, including various mono- or di-halogenated types, nitro-only forms, or ring-fused analogues. Some have similar reactivity in theory, but practice tells another story. If your synthetic plan calls for parallel functionalization or tight regioselectivity, grabbing the cheapest isomer frustrates everyone in the long run. For the medicinal chemist pushing hundreds of variants through SAR, or the material scientist seeking a new high-affinity ligand, the alternative compounds often break down, yield unexpected side-products, or create extra purification challenges.

    From an economic and workflow perspective, using precisely functionalized intermediates like 5-Bromo-6-Nitroindazole boosts efficiency. It let my laboratory group jump straight to parallel synthesis, especially when tackling analog libraries. The same approach kept our failure rates low and cut down purification and rework, freeing up staff for innovation instead of repetitive troubleshooting.

    Environmental Considerations and Safer Handling

    Safe work with powerful intermediates fuels progress but never at the cost of health or sustainability. Most labs maintain strict procedures for hazardous reagents, and stability in storage reduces exposure and lowers the likelihood of accidental release. Unlike highly volatile or water-reactive compounds, 5-Bromo-6-Nitroindazole doesn’t release noxious vapors and remains manageable with ordinary lab skills. It does, of course, still demand respect and basic protective gear, with waste handled per environmental best practice.

    Many research managers now select intermediates with toxicity, persistence, and downstream disposal in mind. 5-Bromo-6-Nitroindazole, when used thoughtfully, reduces unnecessary environmental impact. Runs that go as expected, without byproducts or spills, keep projects and compliance teams equally satisfied. On-site experiences show that minimizing accidental releases depends as much on reagent quality as user vigilance.

    Real-World Applications: Stories from the Field

    Experienced chemists recount time and again how off-brand or poorly characterized reagents set projects back by weeks. In the start-up years of small biotech labs, margins for error almost don’t exist. I remember an anti-infective project where switching to thoroughly characterized 5-Bromo-6-Nitroindazole resolved puzzling low yields and recurring purification headaches. The compound’s batch consistency made workflows faster and cut down on wasted solvent, and it let chemists focus on the design of promising analogues rather than patching basic supply issues.

    Teams working in fields from enzyme modification to photochemistry report similar stories. Some attribute the move to this intermediate as a turning point—less friction during method validation, easier reproduction of results, and smoother transition between scale-up phases. These may not make the headlines, but they leave their mark in project timelines, patent filings, and peer-reviewed publications.

    Balancing Innovation and Cost

    Many research heads look for creative solutions without bankrupting the lab budget. It’s tempting to cut costs on standard intermediates, but skimping here rarely pays off. With 5-Bromo-6-Nitroindazole, the upfront expense comes back in saved time, fewer troubleshooting cycles, and more meaningful data. Labs investing in this compound find the upfront cost is absorbed quickly as syntheses run cleanly and reliably.

    For academic groups under grant limitations, pooled purchasing or consortia-based orders have sometimes made bulk supply economically feasible. In my own consortium experience, coordinated purchases for several chemistry departments unlocked high-quality supply at a fraction of the solo price—and allowed more research projects to share in scalable, state-of-the-art workflows.

    Technology Drives Better Chemistry

    The past five years brought automation and high-throughput experimentation to the forefront of research. Having a backbone intermediate like 5-Bromo-6-Nitroindazole in the chemical toolbox enables robots and liquid handlers to assemble analog sets faster and without time-consuming validation of new suppliers. Many institutions now bake such compounds into their library design software, making rapid output of chemical candidates—the currency of modern drug and materials research—possible at reasonable cost and with minimum error.

    Automated procedures amplify the downstream impact of upstream quality. When intermediates behave consistently, machines run with fewer errors, chemists spend less time debugging, and the overall pace picks up. More discoveries, and fewer headaches in regulatory reviews—these don’t happen by accident, but by putting the right molecules in the right researchers’ hands.

    Choosing Wisely: The Difference that Expertise Makes

    Chemistry isn’t just about what’s possible—it’s about what works day in and day out. Having worked with a range of indazole derivatives, I’ve seen firsthand how small changes change everything. While screening for novel kinase inhibitors, routine experiments exposed the pitfalls of poorly chosen starting materials: missed deadlines, inconclusive data, and wasted material. Switching to 5-Bromo-6-Nitroindazole, with its robust profile and batch-to-batch uniformity, brought projects back on track.

    Expertise in the lab doesn’t eliminate all challenges, but it steers teams toward smarter choices. Those who recognize the significance of the small molecular details, and who value reproducibility as much as creativity, save time and resources in the end. Trusted intermediates like this one are not just tools—they’re force multipliers.

    Future Needs and Sustainable Progress

    Looking ahead, synthetic chemists and process scientists expect reagents to do more than just function—they must enable greener processes, lower emissions, and align with new regulatory demands. The next wave of research will rely on intermediates whose provenance, impact, and safety profiles can stand up to scrutiny. Compounds like 5-Bromo-6-Nitroindazole are building blocks not only for innovative drugs, dyes, and materials, but also for a lab culture that values integrity and safety.

    Global supply chain disruptions highlight the importance of maintaining relationships with reputable suppliers committed to transparency. Choose sources that publish detailed certificates and respond to concerns, not just push catalog numbers. Informal networks among top chemists often share trusted supply sources—nobody wants to repeat the same mistakes with fly-by-night vendors. In my experience, open dialogue with a supplier about batch consistency or documentation can prevent months of headaches later.

    For research groups and companies working towards more sustainable and effective chemical processes, 5-Bromo-6-Nitroindazole offers a reliable partner. Its established role in synthetic routes, and its consistent performance across reaction conditions, means researchers can build without second-guessing the beginning of their journey. In the end, the right starting point sets the tone for everything that follows, from simple bench experiments to breakthroughs that change the field.