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6-Bromoquinoline

    • Product Name 6-Bromoquinoline
    • Alias 6-Bromo-quinoline
    • Einecs 210-514-5
    • 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

    943812

    Chemical Name 6-Bromoquinoline
    Molecular Formula C9H6BrN
    Molecular Weight 208.06 g/mol
    Cas Number 612-68-6
    Appearance Pale yellow to brown crystalline powder
    Boiling Point 312 °C
    Melting Point 58-61 °C
    Density 1.57 g/cm³
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Inchi InChI=1S/C9H6BrN/c10-8-3-1-2-7-5-6-11-9(7)4-8/h1-6H
    Smiles C1=CC2=NC=CC=C2C=C1Br

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

    Packing & Storage
    Packing A 25g amber glass bottle with a tightly sealed cap, labeled "6-Bromoquinoline, 98%," featuring hazard and safety information.
    Shipping 6-Bromoquinoline is shipped in tightly sealed containers, protected from light and moisture, to prevent contamination or degradation. It is classified as a hazardous material and must be transported according to relevant regulations. Proper labeling, documentation, and use of protective packaging ensure safe delivery. Temperature control is not typically required unless specified.
    Storage 6-Bromoquinoline 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 oxidizers. Protect it from light and moisture. Ensure that the storage area complies with local safety regulations and is clearly labeled. Personal protective equipment should be used when handling the chemical.
    Application of 6-Bromoquinoline

    Applications of 6-Bromoquinoline in Industrial Manufacturing

    As a direct manufacturer of 6-Bromoquinoline, we supply a critical intermediate utilized across several targeted industrial sectors. Our production is strictly governed by industry-specific compliance, controlled batch traceability, and technical support tailored for process chemists and formulation teams. Below are key downstream applications with precise integration data for industrial partners.

    1. Pharmaceutical Intermediate for Third-Generation Quinolone Synthesis

    6-Bromoquinoline acts as a pivotal N-heterocyclic building block in the synthesis of various fluoroquinolone antibiotics, including the active pharmaceutical ingredient (API) cores for advanced antibacterial formulations. Process development teams rely on its high purity due to strict impurity profiles mandated in regulated drug manufacturing. The raw material enters the multistep route as a halogenated aromatic precursor, contributing essential molecular scaffolding required for the final API structure and influencing downstream yield, impurity management, and crystallization parameters.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monographs (relevant for synthetic intermediates)
    • US FDA cGMP 21 CFR 210/211 (where integrated into regulated API manufacturing)
    • ICH Q3A/B for impurity controls on downstream synthesis

    Typical usage ratio

    • Batch formulations typically use 6-Bromoquinoline at 0.98–1.03 molar equivalents to the cyclization or substitution partner, adjusted based on scale and intermediate conversion rates.

    Downstream process integration

    • Charged directly into the first or second step of quinolone API synthesis via nucleophilic aromatic substitution, Suzuki coupling, or Buchwald–Hartwig amination, followed by directed halogen displacement and subsequent ring closure operations.

    Final product types

    • Pharmaceutical bulk actives: levofloxacin, moxifloxacin, and other fluoroquinolones
    • Finished dosage forms: tablets, injectables, and sterile powders containing fluoroquinolone antibiotics

    2. Intermediate for Agrochemical Active Ingredients

    Many modern crop protection products depend on quinoline analogs for targeted pest and disease control. Our material finds essential use among agrochemical formulators engaged in the development of systemic fungicides and insecticides, where the 6-bromo functionality enables selective derivatization with other bioactive groups. By inputting this compound during the early phases of synthetic routes, customers can control substitution patterns critical to regulatory approval and field performance.

    Industry compliance standards

    • FAO/WHO Guidelines for the Registration and Control of Pesticides
    • REACH: EC No. 1907/2006 Substance Registration for Intermediate Use
    • ISO 9001 Quality Management Systems (applicable to chemical manufacturing chains)
    • OECD Good Laboratory Practice (GLP) for test material synthesis

    Typical usage ratio

    • Used in the range of 0.8–1.2 molar ratio against target ring-coupling agents. Adjustment is based on the specific agrochemical design route and desired substitution profile.

    Downstream process integration

    • Undergoes bromo–substitution, coupling reactions, or nucleophilic attachment steps during the formation of complex quinoline-based actives prior to formulation into bulk pesticide or fungicide concentrates.

    Final product types

    • Fungicidal actives (e.g., quinoline-based systemic fungicides)
    • Insecticidal intermediates used for final product blending
    • Granules, microcapsules, and suspension concentrates commercially supplied to the agriculture sector

    3. Dye and Pigment Intermediate for Specialty Colorants

    In the synthesis of select azo and heterocyclic dyes for high-value textile, plastics, and electronic display markets, 6-Bromoquinoline serves as a halogenated precursor. Technical teams in pigment manufacturing use it during the base coupling reaction, introducing defined quinoline structures that confer color stability, light fastness, and unique shade characteristics. Its chemical compatibility with diazotization and condensation systems reduces side-reaction pigment impurities, which is critical for compliance in high-end applications.

    Industry compliance standards

    • GHS/CLP Classification, Labelling and Packaging of Substances (EC No. 1272/2008)
    • ISO 9001 for quality assurance in dye manufacturing
    • Oeko-Tex Standard 100 (for pigment use in textiles)
    • EU REACH Registration requirements for specialty colorant intermediates

    Typical usage ratio

    • Introduced at 5%–15% weight basis in pigment preblends, depending on target quinoline chromophore loading and desired color yield in the final pigment synthesis.

    Downstream process integration

    • Participates in coupling or cyclization stages following diazotization, where the halogenated aromatic ring is incorporated into the pigment backbone or linked during the formation of azo dye complexes.

    Final product types

    • High-stability textile dyes (reactive, direct, and disperse types)
    • Specialty pigments used in plastics, coatings, and display applications
    • Color pastes for high-specification printing inks

    4. Intermediate for Electronic and OLED Material Synthesis

    The electronics sector uses 6-Bromoquinoline as an advanced heterocyclic building block for the production of organic light-emitting diodes (OLEDs) and functional organic semiconductor materials. Specialist materials teams harness its halogenated structure during the design of electron-transport and host matrix molecules, where routine quality control is crucial due to the high purity demands for devices. Material is introduced at the initial coupling stage, shaping the electronic energy levels of final thin-film functional components.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (lead, mercury, cadmium and brominated flame retardant content)
    • ISO/TS 80004 Nanotechnology – Quality Management for Nano-enabled Materials
    • IPC-1752 Material Declaration for Electronic Products
    • Japanese Chemical Substances Control Law (CSCL) for import/export of relevant intermediates

    Typical usage ratio

    • Applied in 3–10% by mass in custom syntheses depending upon electronic layer configuration and device design, with precise feed adjustment based on targeted molecular functionality.

    Downstream process integration

    • Feeds into Suzuki–Miyaura or Buchwald–Hartwig cross-coupling reactions at the precursor assembly step, producing electron-transport materials that become part of OLED emitter or host layers.

    Final product types

    • OLED emitters and charge transport materials for display and lighting panels
    • Organic semiconductor compounds for thin-film transistor (TFT) arrays
    • Functional intermediates for advanced electronic inks

    5. Fine Chemical Synthesis in Specialized Research and Development

    Leading laboratories and pilot-scale manufacturers integrate 6-Bromoquinoline as a custom building block for the exploration and scale-up of heterocyclic compounds, especially in the context of pharmacological research and specialty reagents. It enters complex synthetic routes demanding controlled halogen placement for subsequent functional group modification. Quality teams strictly monitor analytical purity, as trace by-products can influence experimental reproducibility or downstream catalyst activity.

    Industry compliance standards

    • GLP (OECD Guidelines on Good Laboratory Practice) for molecules destined for preclinical research
    • ISO 17025 Accreditation for analytic validation where used in reference standards
    • Material Safety Data Sheet (MSDS) requirements for lab chemical handling
    • Local chemical substance notification and approval (where applicable)

    Typical usage ratio

    • Dosed between 0.5–3.0 mmol per reaction batch depending on target molecular framework and desired reaction conversion in medicinal or materials chemistry experimentation.

    Downstream process integration

    • Added early in stepwise syntheses as a core scaffold or brominated functional handle for regioselective transformations, protected-group chemistry, or palladium-catalyzed coupling studies.

    Final product types

    • Screening libraries for pharmaceutical R&D
    • Custom chemical probes and bioactive molecule candidates
    • Reference standards for quality control analytics
    Free Quote

    Competitive 6-Bromoquinoline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 6-Bromoquinoline: Built for Precision Applications

    A Direct Look at 6-Bromoquinoline from Our Production Lines

    Every chemical manufacturer knows that not all fine chemicals deliver the same value where it matters: total reliability batch after batch. In our experience, 6-Bromoquinoline (CAS 612-68-4) stands out as more than just another halogenated quinoline. Its bromine position at the 6-spot on the aromatic ring makes it fundamentally different during synthesis, purification, and performance in target applications. We’ve run 6-Bromoquinoline through benches and reactors across many campaigns and there’s no mistaking what sets it apart. From the pungent scent during crystallization to the distinct yellowish sheen of pure product, its physical cues signal a quality we’ve fine-tuned over years of hands-on manufacturing.

    Understanding the Molecular Structure—Not Just a Number

    For researchers and process engineers, the six-position bromination isn’t a cosmetic tweak. Most of our clients come to us looking for a bromoquinoline that delivers consistent reactivity in Suzuki and Buchwald–Hartwig couplings or where bromine selectivity directly affects the outcome. Field work and pilot runs confirm that ortho- or meta-bromination changes everything: yield, byproducts, easy work-up, and product safety. The 6-bromo isomer cuts down side reactions common with the 5- or 8-bromo analogs. Chemists chasing new heterocycles or specialty intermediates see this difference laid out in their HPLC traces and final crystallinity.

    Purity Standards Matter in Downstream Synthesis

    We monitor purity by GC-MS, NMR, and Karl Fischer titration every batch, but numbers only tell half the story. Low traces of unbrominated quinoline, moisture, or isomeric contaminants spell trouble for catalyzed couplings and complex pharmaceutical intermediates. Water content can kill palladium cycles and too much unreacted starting material throws off yields and causes column nightmares downstream. Our teams have learned—sometimes the hard way—that reliable 6-Bromoquinoline output means tweaking synthesis to stay ahead of trace impurity patterns. Our facilities run glass-lined reactors with automated bromine metering and strict temperature controls, not just for regulatory audits but because we've seen what a shortcut does to customer reactions.

    Specifications Shaped by Actual Lab Demands

    We usually prepare 6-Bromoquinoline to a purity of at least 98%, measured directly using proton NMR and HPLC; water content never goes above 0.3%. The product comes out as a pale yellow to tan crystalline solid. In practice, complaints about difficult handling arise when too much bromine remains unreacted or when non-volatile impurities sneak through. People running high-value API syntheses, dye manufacture, or advanced materials need solid, clump-free crystals—no sticky fines that clump during weighing or dosing. Over time, we learned this only comes from real process investment, not a quick distillation or rough filtration.

    Reliable Supply for Projects That Can't Stop

    In our shop, we don’t just fill drums because the lab says so. We scale production only after confirming each lot behaves in the customer's process, whether that means kilograms for a pilot program or multi-ton batches moving toward commercial scale. Across dozens of projects, we’ve adjusted crystallization solvents, optimized drying, and often repacked fresh product only hours before shipment to lock in quality. No one likes uncertainty in a weekly delivery—so we've taken to producing 6-Bromoquinoline with rolling batches, finetuned to match contracting needs, minimizing warehouse time and exposure to ambient air or light. End users can count on a flow that never interrupts their research calendar or manufacturing deadlines.

    Making the Case: Why 6-Bromoquinoline Works Where Others Don't

    Direct substitution at the 6-position influences not only reactivity but also solubility and downstream handling. The molecular weight sits at 208.05 g/mol, but chemists focus more on how it dissolves in DMF, DMSO, and other polar aprotic solvents. We’ve watched biologists, dye chemists, and electronics developers trying alternatives—like 5-, 7-, or 8-bromoquinolines—and run into yield gaps or synthesis bottlenecks. The 6-bromo isomer yields consistent reaction profiles, less polymerization, and fewer side reactions during scale-up. Its melting point (typically around 66–70°C) also helps with precise dosing in continuous flow or solid-phase settings.

    Usage in Discovery and Manufacturing

    We serve customers spanning small biotech labs, university chemistry groups, and large pharma plants. In real research setups, 6-Bromoquinoline most often becomes a core intermediate for introducing amine, thiol, or alkoxy groups on the quinoline scaffold. Its bromo substituent, centered at the 6-position, enables regioselective cross-coupling—key in heterocyclic compound discovery. Material scientists and OLED developers have also approached us, seeking this molecule for its role in exotic electronic materials or light-harvesting layers. The consistent take-home from R&D is that the 6-position doesn’t just improve synthetic access but also enhances downstream material function—whether that means drug solubility, dye stability, or charge distribution in an advanced wafer.

    Every synthetic chemist who’s scaled an N-arylation knows the difference a well-behaved aryl bromide brings to a vessel. In our own quality assurance labs, side-by-side comparisons prove it: runs using tired, recycled solvent or older, oxidized 6-Bromoquinoline consistently show more off-color intermediates and reduced purity post-quench. That’s why our focus remains locked on color, dryness, and fast transfer from reactor to drum.

    Safety Focus From Start to Finish

    Handling 6-Bromoquinoline requires the kind of respect we bring to all aromatic bromides. Our plant operators wear respiratory protection since even small amounts of dust or vapor can irritate the airways, and we run local exhaust to handle off-gassing during loading. We keep it sealed in nitrogen or argon, protected from light and moisture, to stop decomposition and hydrolysis. Over years of logistics, we've seen more than a few customers surprised by odor or minor discoloration—so we work hard to ship orders in tight-seal HDPE drums or glass containers, never thin polybags that can’t handle real transit conditions.

    What Sets Our 6-Bromoquinoline Apart?

    Chemicals are more than data on a spec sheet. We’ve spent years optimizing for batch consistency and minimizing byproduct carryover, and our site is audited regularly for both GMP and ISO compliance. The big value we deliver comes from actual reliability—users tell us our 6-Bromoquinoline behaves predictably whether dissolved at 10-gram scale or charged into a 500-liter vessel. Some competitors offer broad “bromoquinoline” ranges, but we've held firm to fine-tuning the 6-bromo isomer specifically. This niche focus pays off in reproducibility and clean downstream reactions.

    Most feedback centers on ease of purification at subsequent stages. Teams engaged in pharma synthesis, building kinase inhibitors or antimalarial frameworks, see cleaner extraction profiles with our batches. We don’t cut corners when it comes to final washing, drying, or size grading—practices that, over countless runs, reduce downtime and reject rates in customer workflows. Practically, this helps move projects forward without the false economies that come from off-grade or mixed isomer raw materials.

    Differentiating From Similar Compounds

    We work with a full slate of haloquinolines—chloro, iodo, and other bromo isomers—in house. Our process team directly compares their synthesis routes, shelf life, and chemical reactivity. The 6- position bromo quinoline offers a unique set of balance points: it stays more stable in normal storage but reacts cleanly when given the right catalyst or coupling partner. By contrast, 5-Bromoquinoline and 8-Bromoquinoline often require extra column runs or lead to more persistent color during reactions.

    Chloroquinoline derivatives sometimes get proposed as drop-in alternatives, but real-world testing shows their lower reactivity in metal-catalyzed couplings. Iodoquinolines, while more reactive, come with much higher cost and more persistent shelf-life challenges. Based on our own experiences, the sweet spot for a wide range of academic, industrial, and pharmaceutical transformations remains solidly with 6-Bromoquinoline.

    The Impact on Real-World Applications

    Customers often share project stories that highlight just why specificity matters. A university research lab synthesizing a rare heterocyclic antibiotic hit a yield wall using non-selective bromoquinolines. Detailed root-cause work, done in close collaboration with our technical team, pointed to low-grade isomer contamination in a product from a bulk trader. Once we supplied our 6-Bromoquinoline—manufactured under controlled, in-house conditions—their yields rose and side reactions dropped by nearly half. This isn’t a rare anecdote; the vast majority of our customer success stories stem from a willingness to invest in reliable starting materials.

    Small differences in impurity profiles lead to major risk during process qualification phases. Biotech firms and CDMOs trust our 6-Bromoquinoline for scale-up into pilot and commercial production, because we always keep documentation, batch retain samples, and open channels for technical feedback. This feedback loop often results in further process optimization—altered drying regimens, faster drum transfer, or adjusted packaging to better match shipping realities in different climates.

    Research, Quality, and a Constant Push for Improvement

    Our approach to chemical manufacturing relies on listening to repeat customers and acting on real use-case learnings. Each unresolved customer complaint—from clumping in extreme humidity to minor shifts in color over time—feeds directly back into our process improvement programs. Quality control doesn’t mean resting on last year’s certificate but running live checks on key indicators, from moisture and heavy metals to spot-check NMR. We test our 6-Bromoquinoline in trial-scale couplings alongside control samples. This is done not just for show but to see the effect of each tiny process change on downstream results.

    Staff development matters as much as instrument calibration. Our technical staff spends time in customer labs, not just reading feedback emails. We’ve learned nuances—from crystal appearance to solution haze—by working shoulder-to-shoulder with folks who actually use the product. By making every batch and QC step transparent, we give researchers grounds to trust the material they’re using for their most sensitive targets.

    Sustainable Practices and Transparent Manufacturing

    We care not only about quality but also about minimizing our environmental impact. Our facility recycles mother liquors, employs solvent recovery at each main distillation and purification stage, and contains all byproducts safely for later treatment. Waste bromine doesn’t get vented or dumped—our environmental managers track every gram to ensure safe handling. Every solvent drum and glass reactor gets thorough tracking in our inventory and documentation systems, so clients know where their chemical comes from.

    What Long-Term Users Say Makes the Difference

    The highest praise comes from customers who return for repeat batches, confident that what arrives will perform exactly like last time. Fine details—whether that’s dryness, lot homogeneity, or color stability—are what separate generic supply from real, outcome-driven specialty products. Those relationships are built not from advertising slogans but through cycles of technical problem-solving: we’ve supported urgent overnight shipments, assisted with impurity troubleshooting, and provided analytical support when downstream hiccups happen.

    In the field, this means fewer late-stage synthesis surprises, more efficient API or advanced material manufacturing, and confidence in scale-up from kilo labs to production lines. Researchers know us because we deliver dependable material, answer technical calls, and—perhaps most importantly—believe in the value of producing specialty chemicals without excuses or shortcuts.

    Looking Forward: Why We Continue Growing with 6-Bromoquinoline

    Years spent manufacturing, packaging, and supporting users of 6-Bromoquinoline have shown us just how central this compound is across drug, material, and chemical innovation. The strict demands we place on our own process control—from bromination step through to rapid post-reaction cool-down and solid isolation—stem from active engagement with those actually driving new discoveries. As the market grows for more complex and functionally tailored quinolines, we’re committed to investing in updated tech, closer end-user support, and expanded capacity.

    Partnerships thrive on consistency, direct technical engagement, and the commitment to keep materials flowing without interruption. Our 6-Bromoquinoline remains a prime example of what deep manufacturing expertise can deliver—a specialty compound trusted by chemists who care about results, not just assurances on a certificate. It’s this handshake across the laboratory and production line that we value most, and what keeps our process always moving forward.