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HS Code |
779314 |
| Chemical Name | 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline |
| Molecular Formula | C11H6BrClF3N |
| Molecular Weight | 324.53 g/mol |
| Cas Number | 1133057-98-9 |
| Appearance | Off-white to pale yellow solid |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like DMSO and DMF |
| Smiles | C1=CC2=C(C=CN=C2C(=C1)CBr)C(F)(F)F |
| Inchi | InChI=1S/C11H6BrClF3N/c12-6-7-2-1-3-8-9(7)5-17-10(11(8,14,15)16)4-13/h1-5H,6H2 |
| Storage Temperature | Store at 2-8°C |
As an accredited 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 g of 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline is supplied in a sealed, amber glass bottle with tamper-evident cap. |
| Shipping | 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline is shipped in compliance with all relevant chemical safety regulations. It is packaged in secure, airtight containers to prevent leaks and exposure. Shipping is conducted via certified carriers, with clear hazard labeling and accompanying documentation, ensuring safe and traceable delivery to the customer. |
| Storage | 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from incompatible materials such as strong oxidizers and bases, and ensure proper chemical labeling. Use secondary containment to prevent accidental spills. |
Applications of 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline in Industrial ManufacturingAs the original manufacturer, we supply 6-(Bromomethyl)-4-chloro-2-(trifluoromethyl)-quinoline to a focused set of downstream industrial producers. This advanced heterocyclic intermediate plays a direct and specific role in several well-established chemical manufacturing sectors, supporting the synthesis of complex molecules with strict processing, quality, and regulatory demands. 1. Pharmaceutical Intermediate for Fluoroquinolone SynthesisMajor pharmaceutical manufacturers use this quinoline derivative as a core building block in the synthesis of third- and fourth-generation fluoroquinolone antibiotics. Its halogenated and trifluoromethyl-substituted structure provides a highly functionalized starting point for selective N-alkylation and cyclopropylation steps, essential for scaffold elaboration under stringent cGMP environments. Batch formulation typically adjusts the input ratio based on desired yield, impurity profile, and downstream protection/deprotection strategies to comply with ICH Q7 requirements. Final pharmaceutical actives require full traceability from intermediate to API, with detailed process validation. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisProducers of high-performance agrochemicals utilize this compound for engineering advanced insecticide and fungicide actives, where the polyhalogenated quinoline ring delivers potent bioactivity and metabolic stability. Process engineers tighten raw material input to minimize crop residue and meet FAO data requirements. Each batch undergoes stringent titration and analytical verification in line with global agricultural regulatory programs and stewardship frameworks. Reactant ratios often shift to accommodate the level of substitution or coupling partner within multi-stage syntheses. Industry compliance standards
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3. Fine Chemical Intermediate for OLED Material ManufacturingAdvanced materials manufacturers engaged in OLED display and lighting technology production deploy this quinoline derivative to introduce electron-withdrawing groups at defined sites within light-emitting molecular frameworks. Its reliable halide functionality allows for selective cross-coupling reactions in the late stages of organic semiconductors assembly, directly impacting color purity and device efficiency. Materials engineers set quantitative limits on precursor input to control end-product performance and purity thresholds. Industry compliance standards
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4. Specialty Intermediate for High-Performance Polymer ModificationProducers of specialty engineering plastics incorporate this compound into the synthesis of fluorinated or halogenated functional polymers, particularly where enhanced chemical resistance and thermal stability are critical. Quality managers calibrate formulation ratios to achieve targeted properties in the final polymer matrix, and the addition point typically precedes polymerization to ensure even incorporation. Compliance with advanced materials directives remains essential for downstream sales into electronics, automotive, or aerospace sectors. Industry compliance standards
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Crafting specialty chemicals within our factory often means long hours leaning over reactors, monitoring columns, triple-checking purity, and handling unique molecules that leave a real mark on research, health, and innovation. Few compounds present such an intersection of complexity and utility as 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline. Our team knows this molecule as more than just a formula; to us it’s hundreds of hours of synthesis experience, technical refinement, and relentless focus on what end-users truly need in advanced organic building blocks.
Our focus starts at the bench, where each batch of 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline, or BCTQ as the staff nicknames it, is rigorously controlled from raw material evaluation to final packaging. The bromomethyl and trifluoromethyl groups, coupled with the quinoline core, make this intermediate valuable for researchers chasing after difficult targets. Medchem groups in pharma R&D cite this compound for its solid track record in C–C and C–N bond formation, especially when selectivity is make-or-break. We developed our process to deliver low-moisture, free-flowing crystals with a distinct pale yellow tint, and we keep strict impurity profiles so synthetic chemists avoid surprises in late-stage reactions.
We hear from customers making kinase inhibitors, imaging agents, and agrochemical scaffolds. Feedback gets back to the plant floor. If filtration clogs, we adjust particle size. If HPLC traces show stubborn side-products above 0.5%, we tune the workup and purification steps. We tune process temperatures and solvents to minimize chloro- or fluoro-substituted quinoline analogs that can shadow the main product. We also conduct batch-to-batch reproducibility studies for tight purity, because wasting time double-purifying off-standard material is expensive no matter the industry.
Brokers often market similar molecules without in-house testing, but direct factory control gives us the chance to solve problems firsthand. In customer projects involving Suzuki and Buchwald-Hartwig couplings, our crystalline BCTQ offered increased reactivity over older, moisture-sensitive batches found in the open market. Researchers noticed reduced formation of homocoupling byproducts, partly attributed to lower heavy-metal traces that we manage through process controls. These real-world differences define our product’s performance in scale-up and research projects.
Every specification, from crystallinity to purity, is designed with insight born of experience. Our 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline provides:
This care pays off. We ship worldwide, from multi-gram samples to multi-kilo lots, packed in high-density polyethylene containers that survive cross-continent transport. Each consignment faces our final in-house test panel; if color drifts or an impurity creeps across thresholds, we reprocess. That’s not an extra—it’s our signature.
Many laboratories buy halogenated quinolines expecting to tweak them for their own project. We spent years listening to how these compounds break new synthetic ground. In medicinal chemistry, the precise substitution pattern edge of BCTQ sets up key functionalizations—especially the trifluoromethyl group at C2, which brings both high lipophilicity and metabolic stability. In cancer drug discovery, we heard how quinolines bearing trifluoromethyl moieties favorably alter kinase selectivity, often pushing experimental series past challenging SAR dead-ends.
In crop science, research teams employ BCTQ for building new herbicide cores, manipulating the bromomethyl handle to introduce more complex aryl or alkyl groups. The chloro and trifluoromethyl substituents give improved resistance to degradation in the field, which means higher biological activity and a longer product shelf life.
Beyond those, we have seen BCTQ used in development of ligand scaffolds for fluorescence labeling and PET imaging, where the electron-withdrawing groups help tune photophysical properties and radiolabeling efficiency. Academics come to us with early requests for multi-step syntheses, and we sometimes consult on purification strategies where the starting material must be extra clean so that downstream spectral assignments aren’t clouded. The molecule, with its smart design, enables fast access to C7 substitutions as well—the methyl bromide’s position allows for efficient nucleophilic substitution, a feature not available to all haloquinoline analogs.
Sitting at the junction of innovation and manufacturability, BCTQ stands out against older, less-specialized quinoline derivatives. The three distinct functional groups—bromomethyl, chloro, and trifluoromethyl—present orthogonal handles for further elaboration, and each batch we produce reflects real operational care. In the earliest days, a lack of control over minor impurities led some researchers to expend inordinate effort reworking material from commodity distributors. Over time, we fine-tuned our protocols to avoid mixed halides and ensure single, well-defined starting points for synthetic work.
Direct comparison with other products in the quinoline series often comes down to reactivity and impurity management. Products such as 6-chloromethyl-4-chloroquinolines or simply 4-chloroquinoline produce unpredictable outcomes for researchers looking for exquisite control in nucleophilic substitution and palladium coupling protocols. The trifluoromethyl group offers an electronic and steric effect not found in similar compounds; researchers needing strong electron-withdrawing character for their SAR studies won’t achieve the same bioactivity patterns using non-fluorinated alternatives. The bromomethyl handle, in particular, provides greater leaving group ability than chloride, which expands compatibility to milder nucleophiles without harsh base or elevated temperatures.
We often run side-by-side tests with competitor materials. In palladium-catalyzed transformations, our product enables shorter reaction times and simplified workups. The reliability allows chemists to push their series further without backtracking due to inconsistent starting material. In contrast, lesser-controlled products from third parties can introduce batch variability, jeopardizing whole project timelines.
Inside a chemical plant, achieving a clean, reproducible BCTQ synthesis takes more than just knowing the literature. A textbook method that might work for grams can fall apart on the kilo scale: side-reactions, exotherms, and filtration difficulties crop up unless every parameter, from stirring intensity to workup solvent, is relentlessly optimized. We test for peroxide traces and run headspace analyses for residual halides. Once, one batch nearly failed because a vendor’s starting material supply drifted in purity; we halted production, qualified another source, and only released finished material that passed our most sensitive endpoints. That vigilance sets our material apart from warehouse-stocked, drop-shipped alternatives.
Alongside the chemistry, we dig deep into packaging and transport. Fluorinated and brominated intermediates can degrade in suboptimal containers or under high humidity. Every container seal, every port, every label must be checked. Over the years, international clients have pointed out ways to simplify handling—so we abandoned glass bottles for larger shipments in favor of double-sealed, tamper-evident drums and reinforced cartons. Our approach may seem fussy, but delivering intact, uncompromised BCTQ means fewer operational headaches for the users who rely on our product for critical steps.
Not all chemistry is predictable, and sometimes new application ideas surface from customers outpacing today’s standard protocols. One example came from a biotech group, specializing in covalent inhibitor synthesis. Steric hindrance is a recurring concern in such discovery work. The compact, electron-deficient core of our BCTQ enabled rapid alpha-functionalization and arylation, pushing their workflow faster without additional protecting or activating steps. Later, a group working on solar cell materials discovered that small variations in the trifluoromethyl signal in NMR could hinder accurate quantitation. We altered the batch workup to suppress trace stabilized contaminants, and those researchers reported sharper spectra and easier characterization downstream.
This iterative process—collecting the feedback, running new production trials, and refining the batch—produces better outcomes for everyone. Unlike middlemen or unresponsive inventory holders, we keep our lines open to the real researchers wielding our compounds. Each piece of input shapes the next round of improvements.
Trust in chemical production doesn’t happen overnight. We comply with international chemical regulations, shipping with full traceability and documentation. Our in-house QA and compliance teams audit suppliers regularly, inspect all incoming materials, and maintain internal records that cover each batch for accountability. Each consignment includes a certificate of analysis with relevant analytical data—not just for show, but as a snapshot of what end users actually receive in their labs. Where regulations require, we provide detailed safety and handling information alongside our shipments. If a customer’s workflow involves environmental or occupational safety checks, our transparent documentation removes uncertainty.
Our approach ensures that research and production teams get not just a bottle or drum of reagent, but the reliability needed to keep their projects on track, reduce waste, and remain future-proofed as guidelines or protocols evolve. We’ve dealt with urgent requests and short timelines—we’re often the partner pulled in when “off-the-shelf” alternatives let labs down. Our plant runs in a continuous dialogue with clients, not an isolated silo.
Having produced BCTQ for years, we see firsthand how advanced fluorinated quinolines help drive molecular discovery. Customers report stronger yields, clearer mechanistic insight, and smoother patent filings when their intermediates and starting materials come clean, defined, and ready to use. More than just a product, 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline embodies our ongoing commitment to quality, safety, and innovation. Innovation doesn’t slow down; neither do we. By involving ourselves in customer projects, answering tech queries, and championing process improvements, we help scientific progress move from the bench to pilot scale without costly setbacks due to material issues.
Day in and day out, we fine-tune every aspect—synthetic chemistry, packing, and user support. The chemical world makes no allowances for complacency, and the real difference shows in the results delivered. With every kilogram, we know research teams can trust that every technical promise we make is built and checked inside our plant walls.
For manufacturers, real leadership in specialty chemicals like 6-(Bromomethyl)-4-Chloro-2-(Trifluoromethyl)-Quinoline comes not just from putting something on the shelf, but through careful stewardship of the molecule from raw input to final application. In every project we support and every batch we release, quality and dependability come from knowing both the product and the people who depend on it. Our process, our feedback loop, and our daily commitment mean every unit we ship gives researchers a fighting chance to break new ground in chemistry, medicine, and technology. And we’re ready to answer every new challenge, molecule by molecule, knowing just how much depends on getting BCTQ right.