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HS Code |
731830 |
| Chemicalname | 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One |
| Casnumber | 117558-08-6 |
| Molecularformula | C9H8BrNO |
| Molecularweight | 226.07 |
| Appearance | Off-white to pale yellow solid |
| Meltingpoint | 133-136°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents like DMSO and ethanol |
| Smiles | C1CC2=C(C=CC(=CC2=O)Br)N1 |
| Inchi | InChI=1S/C9H8BrNO/c10-7-2-1-3-8-6(7)4-5-11-9(8)12/h1-3,11H,4-5H2 |
| Storagetemperature | Store at 2-8°C |
As an accredited 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with a plastic cap, tamper-evident seal, labeled with chemical name, CAS, and hazard symbols. |
| Shipping | 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One is shipped in securely sealed containers to prevent moisture or air exposure. Packaging adheres to regulations for safe transport of chemical substances. Appropriate labeling and documentation are included. The product is dispatched via accredited couriers, ensuring prompt and safe delivery to the destination. Store in a cool, dry place upon arrival. |
| Storage | **6-Bromo-3,4-Dihydro-1H-Quinolin-2-One** should be stored in a tightly closed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Store at room temperature or as indicated on the safety data sheet. Ensure the container is clearly labeled and access is limited to authorized personnel. |
Applications of 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One in Industrial ManufacturingAs a dedicated upstream manufacturer of specialty quinoline derivatives, we supply 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One to a select range of advanced chemical sectors that demand a high level of batch consistency, traceability, and regulatory compliance. Below, we outline key downstream industrial applications based on actual demand scenarios, covering compliance, formulation concentration, process integration, and finished product markets, verified by long-term client partnerships and verified regulatory guidance. 1. Pharmaceutical Intermediate for Antihypertensive API SynthesisMany major pharmaceutical companies utilize this compound as a strategic intermediate in the multi-step production of selected antihypertensive drugs. It enters the synthetic pathway specifically in the ring construction steps for certain quinoline-based active pharmaceutical ingredients. Large-scale installations implement stringent compliance and validated process controls at each stage of manufacture. Industry compliance standards
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2. Agrochemical Intermediate for Selective Herbicide SynthesisSeveral agrochemical producers employ the compound as a crucial building block in the production of advanced broadleaf herbicides. Process engineers incorporate the raw material early during the heterocycle assembly stage, influencing the herbicide’s selectivity and environmental degradation profile. High batch reproducibility and regulatory screening are prioritized to prevent off-specification deliveries. Industry compliance standards
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3. Advanced Material Additive for Specialty Polymer SynthesisResearch-driven specialty polymer manufacturers use this substrate to introduce specific halogenated moieties into high-performance engineering plastics. The compound’s function relates to tailored property development, such as flame retardancy or UV stability, within medical device housings and automotive electronics. Purity and trace halide residuals receive rigorous in-line monitoring as part of the compounding process. Industry compliance standards
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4. Chemical Intermediate for Dye & Pigment SynthesisProducers of functional dyes use this compound as a starting material to achieve high purity and defined substitution patterns in the final pigment structures. It is commonly introduced in the sequence of condensation and diazotization stages, determining the desired hue and colorfastness profile required by industrial textile and ink applications. Strict environmental controls and effluent management accompany all phases of dye intermediate synthesis. Industry compliance standards
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6-Bromo-3,4-Dihydro-1H-Quinolin-2-One has attracted more attention in recent years, largely due to its steady role in the early stages of pharmaceutical development and advanced organic synthesis. As a chemical manufacturer, our perspective is shaped by decades of hands-on experience—not just with the substance itself, but with the demands and challenges of producing complex quinolone derivatives that consistently deliver specific performance and purity needs.
We produce 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One under controlled conditions that reflect current best practices in synthetic chemistry. This compound, commonly known in the lab as a bromo-substituted dihydroquinolinone, stands out because its molecular backbone offers unique reactivity for further derivatization. Our typical batch comes as a pale, off-white solid, prepared with careful monitoring of reaction times, temperature, and workup methods to ensure the final product meets strict analysis requirements for pharmaceutical use.
The quality of this compound directly influences how well it performs as a starting material for the synthesis of complex molecules. Our technical team utilizes a series of purification steps, from recrystallization to column chromatography, to deliver material with well-defined properties—especially regarding purity and residual solvent content. These simple-sounding steps make a real difference, especially for downstream users running sensitive pharmaceutical syntheses that do not forgive impurities or inconsistency.
Instead of racing to hit generic purity numbers, we focus on eliminating specific byproducts known to plague similar compounds. For example, trace brominated side products or less-reactive isomers may look similar during spectroscopy, but can halt medicinal chemistry progress if left unchecked. Our lab invests extra effort in analytical updates and new detection methods, adding tools such as LC-MS alongside standard NMR and HPLC to help pharmaceutical partners avoid surprises on scale-up.
6-Bromo-3,4-Dihydro-1H-Quinolin-2-One earns its keep in medicinal chemistry programs that seek to build up more complex, often bioactive molecules. Researchers rely on its bromo-substituted ring when assembling molecular fragments by palladium-catalyzed cross-coupling or through nucleophilic aromatic substitution. This allows them to quickly attach a range of functional groups, such as aryl or alkyl chains, which unlock new avenues for drug discovery or lead optimization.
Outside pharmaceutical innovation, specialty polymer designers and agrochemical researchers also value this compound. In our experience, one of the key advantages comes from its stability and reactivity balance. It resists air, moisture, and storage degradation better than many halogenated aromatics, yet does not resist further synthetic manipulation in the hands of an experienced chemist. Several clients have shared stories where a shift to 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One saved significant time by eliminating recurring purification cycles or failed couplings in their pilot-scale projects.
We typically supply this compound in solid form, ranging from 100 g laboratory packs up to kilogram-scale shipments. The melting point stability runs within a tight range—a point of pride given the variables inherent in bromoarene chemistry. Residual solvent control draws on our own solvent recovery protocols, limiting contaminants down to single-digit ppm for substances like dichloromethane, ethyl acetate, or hexanes. Our team finds these details make or break client research timelines, especially when analytical purity and batch-to-batch consistency cut down on wasted effort and material in screening or scale-up runs.
Analytical tests rely on HPLC area percent for purity, supported by NMR for confirming structural integrity. Each batch undergoes rigorous visual and instrumental inspection—not only for purity, but for physical characteristics that signal trouble at larger scales, like unexpected crystal morphologies or clump formation, which can clue us into subtle changes in synthesis or drying conditions. Our real-world experience shows it’s never just about numbers on a certificate: actual performance in the client workflow tells the story.
Within the world of quinolinones, subtle shifts in ring substitution dramatically change both synthetic utility and downstream properties. We produce several close analogs—unsubstituted, methyl-substituted, chloro—but the bromo version enables rare flexibility. The bromo group opens the door to milder functionalization by Suzuki, Buchwald-Hartwig, and other key transformations where iodine analogs might degrade or show less selectivity. Compared to the more common 6-chloro or 6-fluoro derivatives, our bromo compound delivers a unique reactivity profile that’s particularly valued by medicinal chemists requiring late-stage functional group introduction without harsh reaction conditions.
As the actual manufacturer, we build deep process knowledge into every lot. We have learned through practice that bromo compounds, unlike their iodo or chloro relatives, require extra vigilance during synthesis scaling to suppress trace formation of polybrominated impurities. Our synthetic strategies emphasize selectivity at the halogenation step, minimizing the need for post-reaction scrubbing that can otherwise decrease yield and increase operational hazards. Our plant operators track environmental and process data continually to keep product specification lock-tight as we move from gram to multikilogram output.
Thousands of syntheses and countless pilot runs have taught us that access to well-behaved 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One saves chemists both time and aggravation. Frequent feedback from our customers highlights two sources of pain that we work every cycle to prevent: unexpected reaction failures due to hidden impurities, and shipment delays caused by poor inventory planning. Our inventory specialists keep real-time records and communication lines open, so project managers aren’t left guessing about available stock or turnaround times. This communication proves critical, as client timelines shift with discovery breakthroughs or setbacks, and projects swing from grams to kilos almost overnight.
Beyond the lab and warehouse, safety matters drive decision-making every step of the way. Bromo compounds bring potential hazards—skin and respiratory irritation, persistent residues, even regulatory concerns in certain applications. We engineer physical containment and quality systems into our facilities to keep occupational risk low and batch reproducibility high. Over the last decade, routine investments in scrubbers, advanced monitoring, and tailored PPE have kept our teams healthy and our output reliable. These investments also help us manage and minimize waste, which reduces downstream costs for everybody.
Medicinal chemists turn to 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One during hit-to-lead campaigns. We see our material pop up in key patent filings or as the backbone for new high-throughput screening analogs. The unique position of the bromo group enables rapid “vector hopping”—the strategic placement of new rings or sidechains that drive biological activity in exploratory programs. Without high-quality starting material, teams face unwanted side reactions or unreliable yields, which slow down pathway exploration and candidate evaluation.
Chemical process engineers working beyond the discovery stage look for scalability and consistency during optimization. Our manufacturing trials show this molecule performs well under a range of standard lab and plant conditions. Its solubility in organic solvents, resistance to early oxidative decomposition, and relatively low volatility make it a favorite for those scaling multistep routes. Users have reported smoother purification and isolation cycles, helping them hit key milestones in route scouting and bulk API production. Knowledgeable customers appreciate realistic timeline and availability conversations; we keep clear lines of communication open to help them balance R&D and production demands.
Delivering consistently high-quality 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One has its share of hurdles. Halogenation chemistry creates byproducts that prove difficult to remove via standard crystallization or washing procedures. Batch-to-batch uniformity depends on both reproducible reaction conditions and frequent intermediate sampling, which places high demands on line chemists and QA staff. Investments in automated sampling, rapid analytics, and sequenced addition protocols came directly from years of practical problem-solving, not from top-down mandates.
As demand for this intermediate rises, lead times and raw material availability grow more pressing each year. Fluctuations in bromine pricing, transportation delays, and changing regulations push us to rethink how we schedule production cycles and purchase feedstocks. We tackle these issues through long-term supplier partnerships and buffer stock planning, which reduces last-minute surprises that would ripple through pilot-scale or full API projects for our clients. Stability in our own supply chain allows R&D teams to proceed with confidence, without endless risk assessments or timeline slip.
Producing bromo compounds carries more than routine chemical precautions. We adopted closed-system transfers, enhanced PPE, and localized air handling protocols after early plant incidents taught us the hidden dangers of brominated intermediates. Continuous review by in-house safety committees and external auditors has forced us to raise our operational standards over time, leading to better air quality, fewer lost-time accidents, and lower worker turnover. Since some application chains route through regulated environments—the pharmaceutical industry, in particular—we maintain thorough records on provenance, transport conditions, and analytical data. Customers regularly audit our practices and documentation, and we keep transparent logs available for repeat clients or regulatory authorities. Our focus isn’t just about regulatory compliance, but about real confidence in the chemical’s performance and safety, built up through a track record of plant-level care and operational scrutiny.
Bromine chemistry creates waste streams with persistent organics and halide salts. We approach this problem with a mix of process redesign, solvent recovery, and in-plant treatment, drawing from both regulatory pressure and a drive for continuous improvement. Our facility’s closed-loop recycling setup and in-house waste treatment help minimize not just regulatory headaches, but overall process costs. It makes a measurable difference for both us and our customers, since streamlined waste handling often allows faster release of compliant batches and reduces the shelf life of hazardous byproducts. The operational knowledge developed over years of improvement directly benefits every kilogram shipped.
6-Bromo-3,4-Dihydro-1H-Quinolin-2-One’s position within quinoline chemistry will only grow as drug discovery targets move into increasingly complex territory. Clients have begun asking for custom-tailored analogs or scale-up support for GMP manufacturing, and we’re expanding our analytical toolkits, automation systems, and safety training in response. Rather than resting on proven procedures, we keep pushing to localize new synthesis trends—like flow chemistry—or consider biocatalytic routes to specialty intermediates if they improve impurity profiles or overall efficiency. Plant chemists often move from producing this compound into adjacent structures, carrying forward process lessons and keeping cross-contamination risks top of mind.
We encourage open feedback from the bench scientists that rely on our work. Over the years, real conversations with process chemists and project managers have highlighted both successes and pain points, shaping our production schedules, inventory planning, and technical support. Close, candid communication matters more than any certificate of analysis or templated MSDS, because failed syntheses or untrustworthy shipments create costly downtime. Our goal—developed through hands-on manufacturing, not just consulting—is to consistently deliver quality, reliability, and support. This approach lets discovery and production teams focus on their own challenges, without second-guessing their incoming raw materials.
The story of 6-Bromo-3,4-Dihydro-1H-Quinolin-2-One runs deeper than its technical description. For teams advancing the frontiers of drug or material design, the behind-the-scenes reliability and real-world experience backing each lot matters as much as the molecular formula. As producers who live and breathe quinoline chemistry, we aim to deliver more than specification sheets—we provide a foundation for scientific progress, forged from safety investments, process rigor, deep technical understanding, and a respect for the end-user’s needs. Our clients drive invention and discovery, but their results depend—every day—on the consistency, communication, and commitment we bring as the direct manufacturer of this essential intermediate.