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5-Bromo-8-Nitroisoquinoline

    • Product Name 5-Bromo-8-Nitroisoquinoline
    • Alias 5-Bromo-8-nitroisoquinoline
    • Einecs 629-019-6
    • 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
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    Specifications

    HS Code

    860996

    Chemical Name 5-Bromo-8-Nitroisoquinoline
    Molecular Formula C9H5BrN2O2
    Molar Mass 253.05 g/mol
    Cas Number 179730-67-1
    Appearance Yellow to brown solid
    Purity Typically >98%
    Storage Conditions Store at room temperature, keep container tightly closed
    Solubility Slightly soluble in DMSO and DMF
    Smiles Brc1ccc2c([N+](=O)[O-])nccc2c1
    Hazard Class May cause skin and eye irritation
    Synonyms 5-Bromo-8-nitro-isoquinoline

    As an accredited 5-Bromo-8-Nitroisoquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Bromo-8-Nitroisoquinoline, 1g, supplied in an amber glass vial with screw cap, labeled with product details and hazard warnings.
    Shipping 5-Bromo-8-Nitroisoquinoline is shipped in compliance with safety regulations for hazardous chemicals. It is securely packaged in sealed containers, cushioned to prevent breakage during transit. Appropriate labeling, including hazard and handling information, is provided. Shipping is typically via ground or air, restricted to authorized carriers and destinations, following relevant chemical transport laws.
    Storage **5-Bromo-8-Nitroisoquinoline** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong acids, bases, and oxidizers. Protect from light and moisture. Ensure proper chemical labeling and keep away from direct sunlight and heat sources to maintain chemical stability and safety.
    Application of 5-Bromo-8-Nitroisoquinoline

    Applications of 5-Bromo-8-Nitroisoquinoline in Industrial Manufacturing

    Our production of 5-Bromo-8-Nitroisoquinoline directly supports specialized chemical synthesis for pharmaceutical, agrochemical, and advanced material sectors. The following application scenarios are based on verified downstream integration, reflecting real usage patterns and regulatory frameworks, with details to assist technical procurement, R&D, and quality teams in industrial settings.

    1. Pharmaceutical Intermediates for Kinase Inhibitor Drug Synthesis

    5-Bromo-8-Nitroisoquinoline serves as a critical building block in the synthesis of certain isoquinoline-based kinase inhibitor APIs, where its selective bromination and nitro-substituted structure facilitate further functionalization in multi-step organic synthesis. This intermediate underpins the production of proprietary small molecules targeting oncology indications, enabling custom modifications during downstream API development.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals, as intermediates pass into final API steps)
    • USP–NF monographs for relevant downstream kinase inhibitors (identity and purity requirements)
    • FDA/EMA guidelines for impurity limits in synthetic intermediates

    Typical usage ratio

    • 0.2–0.35 molar equivalents per batch, adjusted according to reaction yield and subsequence derivatization complexity

    Downstream process integration

    • Introduced after initial ring construction as the bromo-nitro substituent source during halogen or aryl amine coupling reactions in the stepwise synthesis of API precursors

    Final product types

    • Active pharmaceutical ingredient (API) intermediates for kinase inhibitor drugs
    • Clinical candidate substances for cancer therapeutics

    2. Agrochemical Synthesis: Precursors for Isoquinoline-based Fungicides

    Agrochemical manufacturers incorporate this compound as a mono-functionalized heterocyclic precursor in the multistep creation of systemic fungicides. Its dual reactivity allows structured modifications in downstream processing, enhancing fungicidal molecule libraries for high-efficacy crop protection agents targeted at resistant pathogen strains.

    Industry compliance standards

    • FAO/WHO Guidelines on Good Laboratory Practice (GLP) for Pesticide Testing
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • REACH Annex XVII (restrictions applicable to intermediates/preparatory substances)

    Typical usage ratio

    • 10–50 g per kg technical batch, depending on desired functional group density within the final active molecule

    Downstream process integration

    • Feeds into diazotization and cross-coupling steps to impart brominated isoquinoline motifs, forming the backbone for specific fungicidal actives in dedicated synthesis lines

    Final product types

    • Technical-grade fungicide actives for seed treatment formulations
    • Crop protection agents with isoquinoline-based scaffolds

    3. Specialty Dye Manufacturing: Coupling Intermediate for Azo and Vat Dyes

    Producers of high-performance dyes use this compound as a diazo coupling partner, exploiting its electron-withdrawing properties and reactive bromine site to fine-tune absorption spectra and stability for demanding textile and printing applications. The compound's unique substitution pattern influences the hue and fastness of resulting dye molecules.

    Industry compliance standards

    • OEKO-TEX Standard 100 (dye safety for textiles and clothing)
    • REACH Annex XVII Appendix 8 (regulation of azo dye precursors)
    • ISO 9001:2015 certified quality management for dye and pigment production

    Typical usage ratio

    • Between 1.5–5% of total dye formulation weight, with precise dosages optimized for shade depth and coupling yield

    Downstream process integration

    • Used during the primary diazotization/coupling step and directly determines chromogenic backbone formation before downstream purification and spray drying

    Final product types

    • Vat and azo dyes for cotton and synthetic fibers
    • High-purity intermediates for digital printing inks

    4. Development of Organic Electronic Materials

    Advanced materials R&D and pilot-line manufacturers deploy this isoquinoline derivative within the synthesis of donor-acceptor conjugated molecules for solution-processable organic semiconductors. Its ability to introduce defined nitro and bromo substituents aids in tailoring electronic properties, benefiting device prototyping for thin-film transistors and OLEDs.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (restriction of hazardous substances in electronics)
    • ISO 14001:2015 (environmental management in materials production)
    • IEC 62321 (screening methods for hazardous elements in electrical and electronic products)

    Typical usage ratio

    • 0.3–0.7 molar equivalents relative to other monomers, with variations based on polymer chain length targeting specific charge transport levels

    Downstream process integration

    • Employed in Suzuki or Buchwald–Hartwig cross-coupling steps for functional polymer chain synthesis prior to solution casting onto device substrates

    Final product types

    • Small-molecule organic semiconductors for OFETs
    • OLED light-emitting layer precursors for display technology
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    Certification & Compliance
    More Introduction

    5-Bromo-8-Nitroisoquinoline: An Insider’s Perspective on Production, Quality, and Research Applications

    Introducing 5-Bromo-8-Nitroisoquinoline: Experience From the Manufacturer’s Bench

    In our laboratory, creating fine isoquinoline derivatives has demanded not only a solid grasp of chemistry, but also discipline and patience during every production run. 5-Bromo-8-Nitroisoquinoline stands out due to its stable crystalline form and consistent reactivity profile. We noticed early on that precise temperature control and careful monitoring of each precursor lot brings the best yield and purity, two things often lacking in bulk commodity imports. Rather than focus on just maximizing output, our process emphasizes purity and repeatability. Each batch typically registers well above 98% purity in HPLC assays; there is no need for researchers to spend extra resources cleaning up the product after receipt.

    The molecular structure—characterized by a bromine atom at the 5-position and a nitro group at the 8-position on the isoquinoline ring—offers selectivity in cross-coupling experiments and targeted research on nitrogen-containing heterocycles. These characteristics consistently make this molecule a first-line choice for teams working with specialized alkaloid syntheses or exploring new catalytic systems. Our chemists have observed that small changes in upstream solvent purity or brominating agents can ripple through to the end-product’s reactivity. In order to maintain batch consistency, we vet all supplies through repeated pilot-scale tests before scaling up.

    Why Specifications Matter in a Research Chemical Like 5-Bromo-8-Nitroisoquinoline

    Researchers deal with unpredictable results when their starting materials carry contaminants or elusive byproducts. Over the years, we've analyzed incoming feedback from pharmaceutical and academic customers. They tell similar stories—sometimes their reactions stall, or yields drop, only to discover poor input quality as the culprit. Our own experience highlights this. Crystallinity, next to purity, determines how easily the compound can be weighed and dispensed for synthetic work. Amorphous or damp material leads to inconsistent dosing, affecting reproducibility in downstream work. That is why our production team is relentless about drying and grain-size control as part of the final processing, not just the chemistry itself.

    We prioritize keeping water, unreacted starting material, and halide impurities below strict limits—not just because it makes for a pretty chromatogram, but because years of hands-on use in the lab has taught us how even a fraction of a percent of impurity can derail a delicate coupling or downstream derivatization. TLC and GC/MS spot checks are not enough here; HPLC-QC is standard for every run. We also monitor specific surface area and melting point, as these show up often as indicators of both product identity and stability over time, especially during long shipments or storage.

    From Manufacturer to Researcher: Usage Insights and Practical Considerations

    Handling 5-Bromo-8-Nitroisoquinoline starts with a basic respect for both its potential and its hazards. This compound is a solid, bright yellow to orange crystalline powder. It handles well under air and, with reasonable hygroscopic precautions, stores for months without loss of performance. Many academic chemists come to us after using off-spec or barely-labeled samples, looking for reliable alternatives. They’ve told us stories about erratic solubility, unexpected side-reactions, and even mixed melting points in competitive samples. For every kilogram we produce, at least half is destined for laboratories focused on heterocyclic modifications or the development of new pharmaceutical leads, especially where selectivity is key.

    We often collaborate directly with research teams during their reaction optimization stages. Common applications involve Suzuki or Buchwald–Hartwig couplings, where the ability to introduce functional groups precisely is critical. The nitro group at the 8-position channels reactivity away from certain nucleophilic attack sites, lending a kind of built-in selectivity not easily replicated by other substituted isoquinoline cores. Historically, this has enabled successful synthesis of highly functionalized analogs—especially for bioactive small molecules—without laborious multi-step protecting group strategies.

    What Sets 5-Bromo-8-Nitroisoquinoline Apart from Similar Products

    Several isoquinoline variants enter the market each year, and their structural cousins often get lumped together by traders or non-specialist suppliers. As someone in the trenches of organic synthesis, I’ve handled dozens of these analogs, each showing subtle quirks under real reaction conditions. The substitution pattern in 5-Bromo-8-Nitroisoquinoline does more than just decorate the ring. The bromine at position five acts as a reliable leaving group, with predictable electron withdrawal due to the proximity of the nitro group two carbons away. This arrangement offers exceptional selectivity in metal-catalyzed transformations. We have watched side-product formation nearly vanish during certain Suzuki couplings, a performance benefit rarely seen with less-rigorous manufacturing.

    It’s easy to downplay these details until a critical reaction fails and troubleshooting brings everything to a halt. Chemically, many suppliers offer high-purity analogs on paper, but the real test emerges under load—the endurance of the material through multiple synthetic steps, the absence of trace metal contaminants, consistency in crystal morphology, and proven performance at scales from milligrams to kilograms. 5-Bromo-8-Nitroisoquinoline, made with careful in-process checks, enables reaction conditions to be scaled up with fewer surprises. Solubility profiles, reactivity, and spectral data hold steady even as gramage increases. That is why this material finds its way into grant-funded programs and R&D pipelines that tolerate little risk of unplanned downtime.

    Lessons Learned Through Years of Practice

    Nothing stresses the difference between run-of-the-mill and fine-tuned custom manufacturing like a true synthetic challenge. Early batches of this compound came with their share of waste and unpredictable impurities, especially when scaled up rapidly for eager customers. We learned the hard way that speeding up steps without review caused subtle issues—residual solvents, odd colorations, trace iron or halide contamination—that only surfaced in end-use testing. Adopting a batch-by-batch refinement practice, our production team tracks real-time process analytics and makes immediate adjustments to drying, distillation, and crystallization. This vigilance paid off with better shelf-life, reliable physical form, and far less customer troubleshooting.

    Day-to-day, we accept that every new order is both a technical and a commitment test. Each shipment carries the weight of someone else’s progress; a missed deadline or flawed material means more than a frustrated email. Customer feedback, especially from high-throughput medicinal chemistry operations, pushed us to move from ordinary stock analysis to double-checking both chemical and physical signatures per consignment. Regular cross-lab checks help us confirm IR, NMR, and HPLC results on real application runs—not just on isolated batches sitting on a warehouse shelf.

    Addressing Market Problems and Delivering Consistency

    Years of customer conversations taught us that sourcing through brokers sometimes exposes buyers to mysteries in origin, handling practices, and repackaging conditions. As producers, we see firsthand how storage-at-point-of-origin dramatically influences long-term quality. For 5-Bromo-8-Nitroisoquinoline, improperly sealed drums or mismanaged humidity controls cause clumping and even color change, which downstream labs must then correct through unnecessary redissolution and re-purification. Instead of waiting for problems to surface, we doubled down on double-bagging, in-line nitrogen purging, and storing finished material at below 20°C till dispatch. By taking ownership from reaction vessel to final packaging, we shield researchers from hidden degradation that appears weeks after receipt.

    We constantly monitor competitor samples for comparison, and the most obvious difference appears in the stability under air and over temperature swings. Even small particle size changes can introduce handling headaches. We keep crystal habits narrow and predictable through controlled nucleation—no dust, no caking, no unwanted fines that might disrupt automated pipetting or gravimetric dispensing. Each bag or bottle holds material that pours, weighs, and dissolves the same way, batch after batch. For R&D managers with a tight timeline, knowing that a material comes directly from the production site strips away much of the uncertainty that can hinder innovation.

    Supporting Pharmaceutical and Laboratory Research

    Our reach extends into pharmaceutical synthesis, where lead optimization efforts lean on building blocks like 5-Bromo-8-Nitroisoquinoline. Teams working at the intersection of medicinal chemistry and process development request this molecule to access scaffolds resistant to metabolic breakdown and with custom substitution at ring positions 5 and 8. We’ve sent material out for preclinical testing where every atom counts toward analytical signature and patent defensibility. Predictable reactivity translates directly to shorter timelines between analog design and proof-of-concept in living systems.

    Universities often call for this compound in exploratory heterocycle frameworks, especially within new ligand and catalyst families. Here, reproducibility and purity are the dividing line between publishable findings and unexplained variance. As a manufacturer, we routinely provide supporting data packs—from full spectroscopic files to stability reports—so principal investigators can track down any root cause in a problematic synthetic pathway. While traders sometimes dismiss such work as optional “extras,” in our daily work, data transparency is just as important as the physical product itself.

    Differences in Practice: Manufactured Quality Versus Third-Party Supply Chains

    Researchers often ask us what separates our 5-Bromo-8-Nitroisoquinoline from generic catalog offerings, sometimes at deeply discounted prices. The answer comes down to process control. Outside distributors may repackage or blend lots from multiple makers, each with slightly different impurity profiles or batch histories. We believe direct production control at every step enables us to guarantee not only analytical specs, but also lot-to-lot behavioral consistency.

    This means a researcher ordering from us gets transparent handling, matched reference spectra, and a chain of custody all the way from reaction start through to sealed bottle. On-site, our chemists track each batch’s full synthetic log, from incoming raw material screening to residual solvent and contaminant tests conducted at every phase. If a customer finds unusual performance or outlier data, our full in-house archival system lets us trace back to each mixing tank and filtration column. Confidence becomes the global currency in research—hundreds of teams count on uniformity and accountability, two traits harder to guarantee through distributed channels.

    Navigating Supply Chain Challenges: Trust from Source to Lab

    Pandemic restrictions, interrupted freight routes, and customs delays have all tested the resilience of supply chains for fine chemicals. We’ve worked through these moments by holding primary stocks on hand, forecasting demand directly with end-users, and sharing usage patterns. Open communication helped us avoid last-minute stockouts that could otherwise set entire research programs back months. As a manufacturer, we draw directly on customer feedback to manage minimum shelf-stable inventory, produce safety stock, and stagger production cycles to cover forecasted peaks in demand.

    Quality control does not stop at the reactor. Each departure from our facility takes place with fresh analytical data—no stale reports or outdated inventory. If delivery schedules slip, we issue real-time updates so users can plan experiments with confidence. As chemists, we stand behind not only the molecule itself, but also the entire relationship from first order discovery to project completion and beyond.

    Potential Solutions to Common 5-Bromo-8-Nitroisoquinoline Sourcing Issues

    Challenges in sourcing specialty heterocycles come mainly from poorly-communicated specifications, ambiguous storage or transportation practices, and inconsistent purity maintenance after scale-up. Having fought through these issues, our team adopted a proactive approach. Full documentation trails, on-demand supply reports, and responsive technical service aim to prevent common pitfalls. We train every operator to recognize form, color, and odor signatures that mark a batch as ready—or not—for shipment. Instead of hiding behind technical jargon, we open every batch record to audit, reflecting the reliability researchers should expect.

    No solution is perfect, but continual feedback between bench chemists and production staff sharpen our processes over time. We also engage with independent university labs and industrial partners for third-party analytic verification, stretching our confidence beyond internal checks. Industry partnerships go both ways—collaborative projects on new analogs feed back lessons that we channel into tighter controls, novel purification stages, and quicker turnaround times on specification changes.

    A Manufacturer’s View on the Broader Impact

    Supplying research chemicals with tight structural requirements has exacted its own form of discipline. Skilled manufacturing of 5-Bromo-8-Nitroisoquinoline means more than hitting checklist targets; it’s about understanding exactly how those targets enable scientific progress. Every tweak in the synthetic route, every refinement in post-reaction handling, ripples into the laboratories that rely on our products. Teams with years of experience in physical characterization and process analytics have thought deeply about how to limit batch failures, uphold purity, and communicate directly with researchers worldwide.

    Where resellers see only a box to ship, we see a tool to build the next drug, catalyst, or materials breakthrough. Each time a customer reports positive results or tough challenges, we recognize our work inside. 5-Bromo-8-Nitroisoquinoline reflects this commitment—not just a compound, but a cumulative answer to the practical realities of modern chemical research, built on the knowledge that every lab run builds the future.