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HS Code |
207001 |
| Cas Number | 615-94-1 |
| Molecular Formula | C9H6BrN |
| Molecular Weight | 208.06 g/mol |
| Iupac Name | 7-Bromoquinoline |
| Appearance | Light yellow to beige crystalline powder |
| Melting Point | 49-53°C |
| Boiling Point | 314°C |
| Density | 1.62 g/cm³ |
| Purity | Typically ≥98% |
| Solubility In Water | Slightly soluble |
| Synonyms | Quinoline, 7-bromo- |
| Smiles | C1=CC2=C(C=C1)C(=CC=N2)Br |
| Inchi | InChI=1S/C9H6BrN/c10-8-3-1-2-7-4-5-11-9(7)6-8/h1-6H |
As an accredited 7-Bromoquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle labeled "7-Bromoquinoline, 98%, 25g." Features hazard/batch info, chemical formula, and manufacturer’s logo. Sealed for safety. |
| Shipping | 7-Bromoquinoline is shipped in tightly sealed, chemical-resistant containers to ensure safety and stability during transport. Packaging complies with relevant regulations for hazardous materials. Shipment is handled by certified carriers with appropriate labeling, documentation, and tracking. It is protected from moisture, light, and physical damage throughout transit, ensuring product integrity upon arrival. |
| Storage | 7-Bromoquinoline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Proper labeling is essential, and chemical spill kits should be readily available in the storage area. Store according to local regulations for hazardous chemicals. |
Applications of 7-Bromoquinoline in Industrial Manufacturing7-Bromoquinoline is a critical intermediate supporting specialized chemical syntheses across pharmaceutical, agrochemical, pigment, and materials sectors. As a dedicated manufacturer, we supply 7-Bromoquinoline built to meet the exacting standards of these industries, with strict production traceability, customizable purity levels, and quality documentation for each application environment. 1. Active Pharmaceutical Ingredient (API) SynthesisDownstream pharmaceutical companies use 7-Bromoquinoline in the targeted synthesis of anti-infective and antimalarial drug candidates, serving as a key scaffolding molecule in the manufacturing of quinoline-based actives. The intermediate is introduced at the early cyclization or coupling stage, enabling precise substitution reactions based on advanced medicinal chemistry protocols and regulatory requirements. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingLeading agrochemical formulators utilize 7-Bromoquinoline to construct complex heterocyclic cores required in new-generation insecticides and fungicides. By introducing this intermediate during selective halogenation and cross-coupling steps, manufacturers achieve molecular frameworks otherwise challenging to construct, ensuring consistent agrochemical performance under stringent residue control guidelines. Industry compliance standards
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3. Specialty Pigment and Dye ProductionManufacturers in the pigment and dye industry employ 7-Bromoquinoline as a precursor for quinoline-based chromophores, prized for their lightfastness and tone. The compound enters early-stage condensation or coupling processes for the creation of high-stability yellow and green dyes, supporting applications where photostability and acid resistance are critical, such as in industrial inks or advanced coatings. Industry compliance standards
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4. Advanced Material Development for Electronics7-Bromoquinoline is utilized as an essential intermediate for organic semiconductor synthesis, especially in the preparation of specialized ligands and small molecule building blocks in the optoelectronic sector. Material scientists incorporate the compound at early functionalization stages to engineer electron-transport layers and luminescent materials for device fabrication under rigorous cleanroom standards. Industry compliance standards
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7-Bromoquinoline stands out in our catalog of quinoline derivatives. Over years working on the synthesis and scale-up of high-purity heterocycles, we have come to appreciate the unique challenges and opportunities this molecule offers. Our team crafts every batch starting from reliable aromatics and halide sources. The goal isn’t just good conversion—it’s consistency, clean profiles, and easy handling for the people who depend on this compound to advance both internal R&D and large-scale processes.
We streamline 7-Bromoquinoline production by constantly refining our process. Typical molecular structure for this material: a quinoline core with a single bromo substituent placed at the seventh position. This positional selectivity changes the game compared with other isomers—where bromination can hit the core indiscriminately—and gives better control when building more complex targets downstream.
We supply material in batches cut from consistent crystallization and purification. The bright, off-white powder signals a high degree of purity; HPLC shows values over 98%, and each lot is checked for residual starting materials, typical halogenated byproducts, and moisture. The melting range falls in the brackets expected from literature sources. Solubility behaves predictably in organic solvents and the molecule exhibits stable characteristics for long-term storage under controlled conditions.
Since contamination or impurities impact reactions, our customers (and our own chemists) demand tight specs. We use GC, LC-MS, and elemental analysis to confirm structure and removals of unwanted byproducts—organics and halides—down to the limits that interfere in real-world synthesis, not just on paper.
From year one, we noticed patterns among our users: some push for advanced pharmaceuticals, others chase novel materials or chemical intermediates. Medicinal chemists recognize brominated quinolines as valuable intermediates for anti-infective, antimalarial, and anticancer initiatives. The bromo handle is reactive—our partners in process chemistry build out aryl, alkyl, and amine substitutions using cross-coupling methods like Suzuki or Buchwald–Hartwig couplings. No versatile building block behaves in a vacuum; our customers taught us how a predictable, highly pure 7-Bromoquinoline makes a real difference in route development and regulatory submission.
We see more projects in specialty dye and pigment labs, where the quinoline frame supports performance characteristics that plain aromatics can’t deliver. In electronic materials, this compound supports the synthesis of complex ligands and donor–acceptor compounds used in organic LEDs and sensing arrays.
Academic research counts on reliable supply for the construction of libraries—especially for exploring structure-activity relationships and new functional group combinations. Our experience with university contracts reminds us that even milligram amounts must meet the same tough standards as quantities moving to a plant.
Quinoline chemistry is full of subtle differences. Substitution at the seventh position, rather than more typical second or fourth positions, carries real impact on electronic properties. Chemists tell us 7-Bromoquinoline reacts with better control—lower tendency to undergo unwanted side reactions than its 5- or 8-bromo related compounds.
The regioselectivity we achieve—placing the bromo group exactly at the seventh position—opens more room for further transformation. For cross-coupling and metalation reactions, our feedback shows the seventh position gives better yields, less poly-substitution, and smoother purification compared with otherwise similar quinolines.
Where other brominated, chlorinated, or iodinated quinolines may drag in more background impurities, our process gives fewer residual halides and byproducts. We solved persistent problems others had—especially under upscaled conditions—by implementing in-process monitoring and staged crystallization to purify without excessive filtration or harsh trituration.
Every chemical process brings its own headaches. Bromination at a precise site on an aromatic is no exception. Temperature swings, misfeeds, and variable reagent quality all spell ruined batches and inconsistent quality. From our own learning curve, close attention to temperature control—especially at initiation and quench—and sourcing of high-purity starting quinolines proved most important for reproducibility at kilogram scale.
We made early investments in reaction monitoring equipment, letting us catch runs drifting off spec. Brominated aromatics bring added risk, so our team sharpened safety protocols for reagent handling, exhaust management, and waste disposal. Local rules grow tighter yearly, so our shops emphasize solvent recovery and minimize hazardous effluent. We recover and reuse spent brominating agents wherever possible, which lowers environmental impact and keeps costs in check.
Customers working on scale-up projects benefit directly: material passing internal quality checks has better performance in their own reactors, with less downtime spent screening for process contaminants. We’ve partnered with pilot-plant groups to adapt batch and flow methods, and we share feedback on improved yields, faster batch times, and less solvent loss.
Anyone who has handled research or scale-up projects knows sourcing isn’t just about price or delivery time. Commercial samples can vary wildly in terms of byproduct content, color, residual solvent, and even stability. Several years ago, one of our major pharma collaborators reported recurring off-spec lots from another supplier. Their issue: batches containing 8-bromo and 5-bromo isomers, which interfered with downstream coupling. Switching to our controlled process, they saved weeks on purification and confirmed consistent impurity profiles suitable for regulatory submissions.
Lab-scale producers may offer small amounts but often can’t guarantee batch-to-batch reproducibility once orders reach the multi-kilogram stage. We step in by validating new lots against existing analytical fingerprints. Our chemists keep tabs on changes in reagents and plant layout, revalidating process steps after even minor tweaks.
In some global markets, regulatory scrutiny now extends to trace-level brominated byproducts and even unknown impurities from raw materials. Neglecting these details invites extra rounds of requalification and extra spend on analysis. We invested in both method validation and instrument upgrades to satisfy evolving needs.
Building and supplying 7-Bromoquinoline isn’t a static process. Each feedback loop is a chance to improve. Every few cycles, our analytical group reviews historical batch data—tracking impurity drift, analytical flags, or even packaging stability. Once, a sharp client flagged trace decomposition during summer shipping. We responded by switching to lined HDPE containers, halting the issue before it damaged sensitive downstream chemistry.
Pressure from advancing end-use industries drives our upgrades. Semiconductor and electronic applications ask for extra analytical data—such as trace metal analysis—requiring new partnerships with contract testers. Pharmaceutical innovators bring higher standards for documentation and trace impurity analysis. Every challenge sparks reformulations and sharper SOPs.
We also see greater customer focus on green chemistry. Working with recycled and lower-impact solvents, optimizing energy use, and minimizing waste at every step has shifted from a side project to a core business practice. It’s become clear that thoughtful chemical production supports not only efficiency but trust with our partners.
Our engagement often begins with a simple sample, but rarely ends there. Many users need advice on solubilization, reactivity, or even disposal of spent quinoline compounds. Fielding these questions, our team has compiled guidance for typical reaction concentrations, acceptable solvent choices, and purification alternatives. This practical support comes straight from our plant-floor experience and from the hundreds of customer syntheses reported back over time.
We also collaborate with academic labs to troubleshoot unusual reactivity—whether a coupling fails for an unknown reason or if a trace impurity gets in the way of a biological screen. Our willingness to replicate or scale up test procedures and share real insights builds relationships, not just transactions.
Looking at broader industry trends, we see a rising demand for customized packaging, shorter lead times, and bulk orders prequalified for regulatory inspections. Instead of supplying “commodity” intermediates, we invest in specialized plant capacity and expanded documentation for shipping, handling, and use across borders.
Growing international focus on chemical tracking and end-use reporting affects almost every actor in the market. Regulatory bodies require impurity data and handling precautions aligned to the latest guidance, especially for pharmaceutical and specialty materials. Using our in-house compliance group, we generate data packages supporting REACH, Chinese, and North American import standards—cutting down the delays partners used to face sourcing elsewhere.
On safety, 7-Bromoquinoline deserves respect like all halogenated aromatics; off-gassing, dust control, and solvent use are treated as priorities. We issue recommendations for safe handling, based not only on literature but on our own incident tracking and near-miss investigations. We carry lessons learned into updated training, shipping, and storage specifications, updating partners as standards move forward.
Demand for reliable intermediates grows as research deepens in both small molecule pharmaceuticals and functional materials. End-users increasingly look beyond functional group content, asking for full-chain traceability, thorough analytical documentation, and proven supplier accountability.
Feedback from early adopters guided much of our product improvement. Chemists using 7-Bromoquinoline in late-stage functionalization regularly report fewer failed reactions and simpler purifications with our material than with other suppliers. Our approach—regular direct engagement, ongoing analytical review, and willingness to adapt packaging and formats—keeps us aligned with evolving customer needs.
Our own R&D group continues to push the boundary, investigating next-generation derivatizations, greener halogenation approaches, and digital tracking for batch records. Smoother workflows, lower environmental footprint, and better chemistry come from the persistent pursuit of quality and improvement.
For years, 7-Bromoquinoline has been more than a line item in our inventory. Each batch reflects the commitment to hands-on control, feedback-driven improvement, and knowledge built through repeated runs—not just textbook chemistry. Against a backdrop of shifting regulatory standards, unpredictable supply chains, and fast-paced scientific advancement, our manufacturing team stands confident in delivering material that supports real discovery and production.
From our perspective, 7-Bromoquinoline is best seen not as a mere intermediate, but as a foundation for enabling results in the hands of talented chemists. By keeping quality, transparency, and long-term partnership front and center, we keep both our customers’ and our own projects moving forward.