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8-Bromoquinoline

    • Product Name 8-Bromoquinoline
    • Alias 8-Bromo-1-azanaphthalene
    • Einecs 207-587-6
    • 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

    379203

    Product Name 8-Bromoquinoline
    Chemical Formula C9H6BrN
    Molecular Weight 208.06 g/mol
    Cas Number 15930-17-7
    Appearance Light yellow to beige crystalline powder
    Melting Point 63-67°C
    Boiling Point 314-316°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, tightly closed
    Synonyms 8-Bromo-quinoline
    Smiles Brc1cccc2ncccc12
    Inchi InChI=1S/C9H6BrN/c10-8-4-2-3-7-5-1-6-11-9(7)8/h1-6H

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

    Packing & Storage
    Packing The 8-Bromoquinoline is supplied in a 25-gram amber glass bottle, labeled with product details, hazard warnings, and storage instructions.
    Shipping 8-Bromoquinoline is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be kept away from heat, flames, and incompatible substances, with clear hazard labeling in accordance with safety regulations. Transport typically occurs via ground or air under standard protocols for hazardous organic chemicals.
    Storage 8-Bromoquinoline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Ensure the storage environment is free from moisture and ignition sources. Label the container clearly, and follow standard laboratory safety protocols when handling and storing this compound.
    Application of 8-Bromoquinoline

    Applications of 8-Bromoquinoline in Industrial Manufacturing

    As a dedicated manufacturer of 8-Bromoquinoline, we serve specialized sectors with controlled quality and process know-how. Below, we detail core industrial applications where this intermediate contributes specific technical value, in line with sector-based compliance demands and actual production routes.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredients (APIs)

    8-Bromoquinoline holds a critical function in synthesizing quinoline-derived APIs, especially within antimalarial and anti-tuberculosis drug development pipelines. It provides a bromo-functional group that enables selective modifications during heterocyclic compound evolution. Production teams use this intermediate for Suzuki coupling, nucleophilic aromatic substitution, and heteroaryl amination steps. Integration occurs upstream of API crystallization and purification. This route requires strict documentation of input purity and residual solvent profiles under regulatory frameworks. End products involve advanced pharmaceutical intermediates for multinational generic and originator drug manufacturers.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/EP Monographs on intermediates and solvent residues
    • REACH registration for intermediate use
    • FDA 21 CFR Part 211 (Where applicable for US-bound APIs)

    Typical usage ratio

    • 0.5–1.2 molar equivalents relative to starting aniline/quinolone fragment, depending on downstream substitution and yield optimization

    Downstream process integration

    • Introduced at initial heterocyclic core functionalization step; downstream coupling, cyclization, and hydrogenation follow before API formation

    Final product types

    • API intermediates for antimalarial therapeutics
    • Building blocks for tuberculosis medications
    • Fluoroquinolone antibiotic precursors
    • Small molecule cancer drug candidates

    2. Agrochemical Active Ingredient Synthesis

    The compound functions as a starting material in the manufacture of advanced agrochemical actives, especially for herbicides and fungicides containing modified quinoline scaffolds. Research and development units use it to introduce targeted functional groups that impact biological efficacy and environmental breakdown. The compound undergoes bromine displacement and oxidative substitutions during the multi-stage synthesis prior to formulation and packaging of active ingredients. Regulatory traceability is required for batch documentation and impurity profiling. Major agrochemical formulators employ this route to scale specific crop protection molecules.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Ingredients
    • European Regulation (EC) No 1107/2009 on Plant Protection Products
    • ISO 9001:2015 for bulk ingredient manufacture
    • China ICAMA National Pesticide Standards

    Typical usage ratio

    • 0.8–1.0 equivalent per target quinoline or pyridine base, adjustable according to conversion rates and downstream derivatization design

    Downstream process integration

    • Dosed during initial heterocycle modification as electrophilic agent; secondary transformations yield the active substance before formulation

    Final product types

    • Selective herbicide actives (e.g., quinoline-based products)
    • Fungicide intermediates with environmental breakdown profiles
    • Insecticide precursors for specialty crop targets
    • Pest-resistant seed treatment synthesis ingredients

    3. Specialty Dye and Pigment Precursor Manufacturing

    Specialty dye manufacturers employ 8-Bromoquinoline for its key role as a precursor in synthesizing high-performance quinoline dyes used in plastics, textiles, and inks. It enables bromine-mediated coupling, oxidative ring closure, and further functional group introduction. Production lines require reliable consistency in reactivity and chromatographic purity to minimize contaminant profile in colorant batches. This application demands careful process control over reaction time and temperature to maximize color strength and fastness. Downstream industries rely on the intermediate for highly stable and lightfast pigment output.

    Industry compliance standards

    • OEKO-TEX Standard 100 (restricted substance lists for textiles)
    • EN 71-3 for toy safety (colorant ingredient limits)
    • ISO 14001 for pigment production environmental controls
    • EU REACH SVHC compliance

    Typical usage ratio

    • 5–20% by weight in condensation/coupling reactions, adjusted for target chromophore yield and final shade depth

    Downstream process integration

    • Charged into reaction vessels in the pigment color base synthesis stage; post-coupling and purification delivers finished dye powder

    Final product types

    • Quinoline-based fluorescent dyes for textiles
    • High thermal stability pigments for engineering plastics
    • UV-resistant inks for specialty printing
    • Colorfast additives for synthetic fiber manufacturing

    4. Organic Electronic Material Synthesis

    Producers of advanced organic semiconductor materials incorporate 8-Bromoquinoline for synthesizing electron-transporting and light-emitting heterocycles. Its role includes catalytic cross-coupling and functionalization via C–Br bond activation, mainly in OLED and photovoltaic material development. Precision in batch homogeneity and trace impurities is crucial to ensure electronic performance and yield optimization in deposition and film processes. The material is used in micro to pilot scale for novel device fabrication, driven by strict purging of side-products at each process stage. End-users convert it into next-generation display and energy conversion component precursors.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (hazardous substances in electronics)
    • IEC 61249-2-21 for organic material limits in PCB manufacture
    • IATF 16949:2016 for electronic component supply chains
    • Internal QC protocols for semiconductor materials (e.g., <1ppm metal contaminants)

    Typical usage ratio

    • 10–30 mol% relative to core aromatic/heterocycle in cross-coupling reactions, with close adjustment to device-specific performance criteria

    Downstream process integration

    • Added in functional group introduction and conjugated chain extension steps prior to thin film casting and purification

    Final product types

    • Electron-transport materials for OLED displays
    • Precursor blocks for organic photovoltaics
    • Charge-transport layer components for flexible electronics
    • Intermediate materials for next-generation sensor substrates

    5. Catalyst and Ligand Synthesis for Industrial Catalysis

    In the chemical process industry, 8-Bromoquinoline acts as a building block for chelating ligands and coordination complexes that serve as homogeneous catalysts in fine chemical and petrochemical synthesis. The compound is utilized for ligand assembly where bromine substitution enables tailored metal complexation (e.g., with ruthenium, palladium). This application centers on laboratory and scale-up processes demanding tight control of moisture, temperature, and reaction stoichiometry for reproducible catalyst efficiency. Manufacturers support this use via custom packaging, detailed batch testing, and supply-chain traceability for regulated process audits.

    Industry compliance standards

    • ISO 17025 for laboratory reagent quality control
    • Good Laboratory Practice (GLP) for chemical catalyst screening
    • REACH Annex VII–X for intermediate handling and transport
    • Responsible Care Global Charter for chemical management

    Typical usage ratio

    • 5–15 mol% relative to target ligand or metal input, modifiable as per catalyst activity and desired binding characteristics

    Downstream process integration

    • Introduced in synthetic organic laboratories and pilot-scale reactors at early ligand-forming stages; purified ligand is then complexed with transition metals for final catalyst preparation

    Final product types

    • Chelating ligands for metal-catalyzed cross-coupling
    • Pharmaceutical process catalysts
    • Specialty polymerization initiators
    • Fine chemical homogeneous catalytic systems
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    Certification & Compliance
    More Introduction

    8-Bromoquinoline: A Manufacturer’s Perspective on Quality, Application, and Distinction

    A Closer Look at 8-Bromoquinoline

    Years of chemical manufacturing have shown us that fine differences in raw materials create significant changes in end-use value. 8-Bromoquinoline, with CAS number 86-80-6 and a structure featuring a bromine atom at the 8-position of the quinoline ring, stands as a distinct building block in the synthesis world. Finished batches carry a signature pale yellow to light tan crystalline appearance, offered by us at high purity grades to meet laboratory and industrial demand.

    Our facility maintains tight process control, using direct bromination of quinoline under carefully moderated conditions. The result: product lots with minimal impurities—typically less than 0.5%—supported by HPLC, NMR, and mass spectrometry. Batch records and COA copies for every shipment tie back directly to our lot traceability system. We don’t outsource crucial process steps; bromination, product workup, and purification all run under our roof. This investment translates to traceable, consistent product every time.

    Understanding Usage in Practice

    8-Bromoquinoline attracts attention not only for its molecular structure, but for its rare flexibility as an intermediate. Medicinal chemists often leverage the electron-withdrawing bromine to introduce functional groups at the 8-position, feeding into pipeline compounds targeting anti-malarials, kinase inhibitors, and antifungals. Our product regularly ships out for combinatorial libraries and fragment-based drug discovery.

    Research teams involved with dye chemistry, polymer modification, and electronic materials have also found reliable performance. Direct arylation, Suzuki-Miyaura cross-coupling, or Buchwald-Hartwig reactions—all can hinge on the accessible bromine. The crystalline nature of our material avoids dustiness, helping automated dosing and reducing cleanup headaches. Our team’s formulation chemists run routine compatibility checks with popular solvents like DCM, THF, and acetonitrile, keeping water below 0.2% to ensure predictability in scale-up.

    Experience has taught us that quality 8-Bromoquinoline pays off: yields increase, purifications become faster, and unwanted side-products fall. Many of the world’s leading pharma and materials R&D groups standardize on our material batch after batch, and their feedback has directly shaped our in-house spec refinement.

    Specifications and Model Philosophy

    We only offer 8-Bromoquinoline produced on our full-scale lines, never resorting to small lot or custom batches that vary in impurity profile. Consistency from drum to drum matters most to downstream users who cannot afford unexpected chromatography curveballs or variable melting points.

    Our typical assays show purities above 99%. Melting range for our batches falls between 74-77°C, conforming to published data and verified by in-house and third-party laboratories. Particle sizing targets sub-millimeter range, allowing fast dissolution even in colder solvents. Moisture is tightly controlled, backed up by regular Karl Fischer titration. Every drum leaves our warehouse with full batch records and clear shelf-life guidance—two years minimum under dry, dark storage.

    We do not compromise on the excipient profile: our product contains no anti-caking agents, extenders, or wetting aids. This means your solvent blends and downstream reactions deliver what the chemistry predicts—without guesswork introduced by “invisible” secondary agents. Point of origin matters as well; our compliance teams monitor halogenated waste and minimize emissions step-by-step, in line with global best practices.

    Key Differences From Other Quinoline Derivatives

    Many ask us about the merits and limits of 8-Bromoquinoline relative to similar molecules. Here, direct experience trumps abstract comparisons. The bromine at the 8-position sets it apart, creating new reactivity that a 2-bromo or 4-bromo derivative just cannot deliver. Electrophilic substitution and palladium-catalyzed coupling show higher efficiency and selectivity, enabling access to complicated, densely substituted heterocyclics.

    Bromine differs from other halogens in both weight and electronic effects. Compared to 8-chloroquinoline, we observe higher cross-coupling success at the laboratory and 200-liter levels. The heavier bromine enables faster and more complete transformation, a fact that scores of pilot plant customers have confirmed. That means less time spent optimizing catalysts and less material lost in incomplete reactions.

    Some competing products on the market show variable color, odor, or oil content. We maintain a single manufacturing process across our output—no random substitutions or low-grade reprocessing. Purity and batch homogeneity make a difference not only in final yield, but also in R&D reproducibility. Unwanted byproducts or residual organic solvents can wreak havoc on sensitive medicinal chemistry, skewing biological test results and introducing unnecessary troubleshooting. Years of field reports from our partners confirm that avoiding these pitfalls improves both cost and confidence.

    Addressing User Concerns and Ongoing Challenges

    Direct conversations with synthetic chemists have given us perspective on the genuine worries surrounding specialty halogenated products. Palladium and nickel contamination, high moisture, or trace organics create persistent setbacks. We adopted investments in closed filtration, vacuum drying, and clean-in-place systems to limit these risks. It is not uncommon for us to perform release testing down to sub-ppm levels for metal contaminants—especially for batches intended for API development or electronic applications.

    Supply chain security remains a top concern. By controlling the entire production—from bromination to packing—we can buffer fluctuations in bromine sourcing and guarantee consistent availability. During regulatory shifts or material shortages, customers have relied on longstanding batch-to-batch consistency. Production currently allows for flexible batch sizing, enabling strategic reserve builds against seasonal or project-specific demand spikes without rushing order fulfillment.

    We also support R&D with non-standard requests, such as alternative packaging for glove box work, or documentation for regulatory submission. This meets growing needs for traceability in the pharmaceutical, agricultural, and battery sectors, where an overlooked impurity or mischaracterized specification quickly translates into loss of project time and resources.

    Health, Safety, and Environmental Commitment

    Handling 8-Bromoquinoline demands respect for its reactivity. Our plant follows rigorous personal protective measures throughout production and packing. Dust control measures, point-source venting, and effluent management are not back-office details—they are front-line practices that protect workers and simplify downstream logistics.

    Environmental responsibility continues to shape investment in halogen management and waste minimization. We capture and neutralize all process bromine emissions, recycling or disposing of them according to stringent regional and international standards. Our philosophy goes beyond mere compliance; it reflects the real-world lessons learned from working alongside operations teams for decades. Customers relying on our chemical streams in their greener synthesis initiatives can trust in a product modeled on transparency and process control.

    With every market transition or tightening of regulatory guidelines, we adapt by maintaining higher internal targets than any imposed minimum. This enables us to offer a supply chain that supports both leading-edge innovation and growing expectations for safety and sustainability.

    Why Purity and Source Truly Matter

    Modifying a quinoline ring calls for reagents that behave consistently throughout scale-up. Small shifts in impurity profile or water content multiply into larger problems once chemistries move from beaker to pilot vessel. Feedback shows that switching from a lower-purity source to our 99%+ material streamlines workflows, cuts time spent on development, and reduces the need for repeat purification.

    We never blend batches to meet a basic assay threshold; every drum leaves the floor with a full analytical record. Control over particle size and moisture content helps partners tailor dissolution for automated reactors, robotics platforms, or continuous processes. Dealings with international partners in pharmaceuticals, materials science, and chemical research confirm that this reliability trumps aggressive pricing or one-off bulk discounts sometimes offered by brokers or traders.

    Intellectual property protection and confidentiality in chemical sourcing remain top priorities for our customers, especially in exploratory or pre-patent phases. Procurement through a proven manufacturer avoids complications down the road—from uncertain characterization to IP entanglements arising from unclear provenance. Each lot is supported by documentation tracing production history, batch performance, and handling—all maintained in house.

    Global Trends and the Evolution of Specialty Organics

    Growth in specialty halogenated intermediates continues to accelerate, and 8-Bromoquinoline is no exception. Pharmaceutical pipelines, print technology, OLED displays, and agricultural research depend on well-characterized, consistent starting materials. Shifting supply chains have increased the importance of secure, traceable, and high-purity chemicals made at scale rather than sourced through intermediaries.

    Many users work under regulatory frameworks demanding full disclosure and batch traceability. As a manufacturer operating under ISO-certified systems, we supply the information and transparency needed to satisfy even the most demanding QA departments. The move toward greener and more responsible chemistry also places stricter requirements on byproduct management and resource efficiency.

    Competition has led to greater scrutiny of performance data. Published literature and internal evaluations continue to validate that reactions using 8-Bromoquinoline with known and minimized impurity content avoid post-reaction bottlenecks. In an era where research timelines shrink and resource allocation intensifies, a trusted supply partner serves as an extension of your own R&D bench.

    Looking Forward: Commitment to Continuous Improvement

    Decades spent in the manufacturing sector have demonstrated that “good enough” doesn’t carry a project from bench to market. We update our own specification sheets regularly not just to comply, but to anticipate new needs in downstream industries. From updating packaging methods to supporting analytical verification with additional chromatographic data, every enhancement is driven by conversations and case studies shared with our partners.

    Chemistry as a science and a business benefits from sharing lessons learned. Practical improvements—like controlling for volatile impurities, improving drum seals for shipment, or offering technical support for unexpected reactivity—help the entire field progress. By placing each order in the context of years of operational history, we give R&D and sourcing teams headroom to focus on discovery rather than troubleshooting.

    Our message to formulators, process chemists, and researchers is clear: insist on products made from scratch by proven manufacturers, not pieced together from multiple unknown origins. This approach minimizes risk, maximizes chemical utility, and puts end users a step ahead in optimizing cost, time, and data reliability.

    Final Thoughts From the Manufacturing Floor

    8-Bromoquinoline represents more than an entry on a product list; it’s a solution born out of real-world demands in chemistry. By producing it in-house with rigorous batch control and transparency, we aim to contribute to faster, cleaner, and more predictable science around the globe. This commitment to purity, integrity, and partnership sets the difference between tradition and true progress.

    Product quality and source integrity translate to fewer headaches, better outcomes, and smoother progression from the drawing board to large-scale deployment. As technology, regulation, and end-use demands evolve, our approach to 8-Bromoquinoline—and every other product we make—will keep meeting the needs of those who depend on certainty, not just supply.