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4-Chloro-7-(Trifluoromethyl)Quinoline

    • Product Name 4-Chloro-7-(Trifluoromethyl)Quinoline
    • Alias 4-Chloro-7-(trifluoromethyl)quinoline; 7-(Trifluoromethyl)-4-chloroquinoline
    • Einecs 629-355-8
    • 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

    900438

    Chemicalname 4-Chloro-7-(Trifluoromethyl)Quinoline
    Molecularformula C10H5ClF3N
    Molecularweight 231.60 g/mol
    Casnumber 827-27-6
    Appearance White to pale yellow solid
    Meltingpoint 55-59°C
    Purity Typically >98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.46 g/cm³ (approximate)
    Smiles FC(F)(F)c1ccc2ccnc(Cl)c2c1
    Inchi InChI=1S/C10H5ClF3N/c11-9-6-15-5-7(10(12,13)14)3-1-2-4-8(6)9/h1-5H
    Storagetemperature Store at room temperature

    As an accredited 4-Chloro-7-(Trifluoromethyl)Quinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g of 4-Chloro-7-(Trifluoromethyl)Quinoline is supplied in an amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 4-Chloro-7-(Trifluoromethyl)quinoline is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is typically transported as a solid or crystalline powder, classified as a hazardous material. Proper labeling and handling in accordance with regulatory guidelines ensure safe transit, minimizing exposure to personnel and the environment.
    Storage Store 4-Chloro-7-(trifluoromethyl)quinoline in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Avoid exposure to moisture and direct sunlight. Label the container clearly and ensure proper secondary containment to prevent spills. Follow all appropriate safety and regulatory guidelines for storage and handling.
    Application of 4-Chloro-7-(Trifluoromethyl)Quinoline

    Applications of 4-Chloro-7-(Trifluoromethyl)Quinoline in Industrial Manufacturing

    As an experienced chemical raw material manufacturer, we support diverse sectors by supplying 4-Chloro-7-(Trifluoromethyl)Quinoline for precise downstream synthesis. This advanced intermediate supports controlled transformations in regulated industries. See below for specialized industrial applications across several manufacturing domains.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers use this compound as a specialized intermediate for researching and developing advanced heterocyclic APIs, particularly within antimalarial and anti-infective candidate pipelines. Direct functionalization of the quinoline ring system during late-stage synthesis ensures the integrity of trifluoromethylation, which is critical for bioactivity and metabolic stability optimization. Operators control charge-in ratios based on synthetic pathway and final target requirements using validated batch or flow protocols.

    Industry compliance standards

    • cGMP (Current Good Manufacturing Practice) per ICH Q7
    • FDA 21 CFR Part 211 (USA)
    • EU GMP EudraLex, Volume 4, Part II
    • USP <797>, <823> as applicable to intermediates

    Typical usage ratio

    • Employed at 0.05–0.15 molar ratio relative to the core structure of lead drug candidates; exact ratio adjusted for process yield, impurity control, and physiochemical profile targeting during lead optimization phases.

    Downstream process integration

    • Introduced after initial backbone assembly during ring functionalization or halogen exchange stages via Suzuki, Buchwald, or nucleophilic aromatic substitution reactions.

    Final product types

    • Lead pharmaceutical intermediates
    • Registered APIs (antimalarials, anti-infectives)
    • Analytical reference standards for method validation
    • Proprietary compound libraries for screening

    2. Agrochemical Active Material Production

    Agrochemical formulators rely on controlled integration of this quinoline derivative as a building block for active substances used in fungicides and insecticides. Structural stability, conferred by the trifluoromethyl group, supports environmental persistence and targeted activity against resistant pest populations. Ratio selection is based on pilot crop efficacy studies and environmental residue compliance.

    Industry compliance standards

    • REACH Registration (EU Regulation EC No 1907/2006)
    • EPA Pesticide Registration (40 CFR 152 in the USA)
    • FAO-WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 0.03–0.08 molar equivalents in active ingredient synergist synthesis; adjusted upon results from field trials and LC/MS residue analytics.

    Downstream process integration

    • Reactive incorporation during the heteroaromatic stage of crop protection active ingredient synthesis; process step follows chlorination or methylation, typically via controlled catalyst batch operations.

    Final product types

    • Fungicidal actives (technical grade)
    • Insecticide intermediates
    • Micro-encapsulated granular pesticides
    • Seed treatment agents

    3. Electronic Material Manufacturing

    Advanced electronics manufacturers include this raw material within oligomer and thin-film precursor workflows, where its quinoline scaffold and functional groups support improved photostability and electron transport in organic semiconductors and optoelectronic devices. Precise usage levels are determined by target film morphology and device voltage characteristics.

    Industry compliance standards

    • RoHS Directive 2011/65/EU
    • IEC 61249-2-21 flame retardancy limits
    • UL 94 flammability for plastic materials
    • ISO 14001 for Environmental Management

    Typical usage ratio

    • Used at 2–6% by weight in conjugated monomer blends; optimization based on absorption/emission requirements in OLED or OFET device builds.

    Downstream process integration

    • Directly incorporated into spin-coating or solution-casting steps during precursor polymer production, following pre-dispersion in high-purity solvents under nitrogen.

    Final product types

    • OLED display layer precursors
    • Organic photovoltaic films
    • Photoactive transistors
    • Advanced photoresist systems

    4. Specialty Dye and Pigment Intermediates

    Manufacturers in the specialty dye sector utilize this molecule for the production of organic pigments and high-performance dyes. It supports improved color fastness, light stability, and chemical resistance, critical for technical textiles and pigment masterbatches. The usage ratio, set during R&D color matching, reflects the required spectral profile and stability specification.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile chemicals)
    • REACH Annex XVII–restricted substances
    • ISO 105-B02 color fastness testing
    • Global Organic Textile Standard (GOTS) dye requirements

    Typical usage ratio

    • Implemented at 0.5–2.5% in pigment intermediate blends; adjusted by shade depth, bath chemistry, and substrate compatibility.

    Downstream process integration

    • Added post-coupling during azo or anthraquinone precursor synthesis in closed reactor systems, followed by filtration and isolation.

    Final product types

    • Technical textile dyes
    • Plastic color masterbatches
    • Specialty inks for ID document printing
    • High-stability automotive pigments

    5. Fine Chemical Synthesis for Analytical Reference Materials

    Producers of analytical standards incorporate this compound in multi-step synthesis of certified reference materials used for impurity profiling and analytical method validation. Ensuring traceability and ultra-high purity levels, formulators designate charge levels according to target analyte structure and comparability to regulatory standards.

    Industry compliance standards

    • ISO 17034 Reference Material Producers
    • ISO/IEC 17025 Laboratory Accreditation
    • Pharmacopoeia: USP, EP, JP as applicable
    • OECD Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.01–0.06 equivalents per target reference structure; final calibration adjusted for required analytical signal and purity correction factors.

    Downstream process integration

    • Deployed during high-purity microscale synthesis protocols post-initial ring construction, preceding final purification and lot-specific certification.

    Final product types

    • Certified impurity standards
    • Analytical method calibration mixes
    • Stability testing controls
    • Proficiency testing materials
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    Certification & Compliance
    More Introduction

    4-Chloro-7-(Trifluoromethyl)Quinoline: Manufacturer’s Commentary on Value, Quality, and End-Use Potential

    Purposeful Synthesis and Our Commitment to Quality

    At our facilities, we produce 4-Chloro-7-(trifluoromethyl)quinoline with a focus on controlled, reproducible processes. Our chemists do not view this molecule as just another entry in the labs; it represents countless hours spent on process optimization and purity improvements. We put our experience to use by choosing modern reagents for Friedländer quinoline syntheses. Years ago, finding a reliable route with consistent yields was a challenge. Our production now centers on cleaner halogenation and tailored fluorination, building confidence in each batch.

    Before releasing any material, our team checks every lot for both chemical and physical consistency. We do not compromise on using premium starting materials like 2-chloroaniline and trifluoroacetaldehyde derivatives, nor do we settle for minimal purification. Our process routinely produces sharp-melting, bright yellow crystalline material with clear NMR and LC-MS profiles. From HPLC to Karl Fischer water content, we pay attention to the finest details, so every customer repeats success using our product, not trial and error.

    The Real Function in Modern Synthesis

    Those of us producing 4-Chloro-7-(trifluoromethyl)quinoline see that demand keeps growing as the molecule carves out valuable space in pharmaceutical, agrochemical, and advanced material industries. No longer is quinoline chemistry a specialty for boutique labs alone. Medicinal chemists want new heterocycles that bring both strong electron-withdrawing character and rigid planarity. The trifluoromethyl group at position seven transforms molecular recognition profiles. In real-world terms, this means new leads in kinase inhibition, biofilm disruption, and anti-inflammatory compounds.

    Our partners in crop protection apply the same logic. We work alongside teams looking for tough, weather-stable chemical scaffolds. The 4-chloro atom discourages metabolic degradation, while the trifluoromethyl group blocks microbial transformation. Research pipelines feature dozens of derivatives stemming from our core quinoline. By choosing a manufacturing approach that avoids heavy metals and harsh acids, we grant downstream chemists more flexibility. Their catalysts and biocatalysts do not get fouled with trace contaminants, and waste treatment stays more manageable.

    How Our Manufacturing Experience Sets Us Apart

    We recognize that on paper, many suppliers list 4-Chloro-7-(trifluoromethyl)quinoline with similar CAS numbers and molecular weights. Having stood in reactor bays troubleshooting resin fouling, runaway exotherms, and unexpected gas evolution, our team knows that reliable supply means more than statistics. Customers notice the difference between a compound made in a controlled reactor environment versus hastily batched runs. Each drum shipped holds product that matches the certificate of analysis we've scrutinized against internal reference standards, not general literature figures.

    Manufacturing at industrial scale brings hard lessons in risk management and employee safety. We operate custom jacketed reactors with tight temperature and pressure control, not off-the-shelf glassware. By scaling up chlorination and trifluoromethylation in contained systems, we protect both the product and our operators. Corrosive off-gassing and fine-powder dusting threaten both yield and worker health if left unchecked. We respond with engineered ventilation, smart dosing valves, and regular maintenance that goes beyond regulatory minimums.

    Key Differences: What Sets Our 4-Chloro-7-(Trifluoromethyl)Quinoline Apart

    Many chemists have encountered so-called “off-the-truck” quinoline derivatives. They often come with a lingering odor, strange off-white tint, or unreliable melting range. It is not uncommon to see dropout during crystallization or NMR peaks showing unidentified byproducts. In contrast, our material features precisely-measured purity confirmed across independent techniques. We do not shy away from running full impurity profiles because we know researchers base years of synthesis on the consistency of our inputs.

    Other manufacturers may list products with the same IUPAC or CAS, but our approach to quality means fewer batch-to-batch surprises. Chemists often mention more predictable reactivity and cleaner spectra when switching to our product. One researcher in lead optimization described the difference like “removing fog from a window”—subtle at first, but transformative in intensive, multi-step synthesis. For solid-state applications, the uniformity of our crystallization means easier weighing and less material loss to sticky residues or static-laden fines.

    Our Choice on Model and Specifications: Practical Decisions, Not Just Numbers

    We make the decision to offer 4-Chloro-7-(trifluoromethyl)quinoline within a purity range that consistently exceeds 98%. Analytical teams sometimes push us for even finer cuts, but we have learned from scale-up experience that chasing 99.9% introduces wasteful losses without tangible downstream benefit for most applications. Instead, our methods let us guarantee high chemical integrity, plus tight limits on residual solvents and persistent metals—criteria tuned based on years of feedback from large process chemistry groups.

    We package the finished material in high-barrier, clean containers to avoid environmental swings in temperature or moisture during storage and shipment. Batch records trace back every kilogram, documenting the temperature logs, operator signatures, and equipment used. Many newcomers overlook these tracking steps, but we know missed details can erode customer trust years down the line. Having serviced pilot plants and clinical supply chains, traceability is strict policy for our team.

    Challenges We Have Overcome—and Why They Matter

    Every chemical comes with hurdles, and 4-chloro-7-(trifluoromethyl)quinoline teaches patience. Years ago, we saw issues with side products during chlorination, leading to lingering monochlorinated and over-chlorinated byproducts that complicated purification. Rather than ignore these signals, we adjusted reagent quality and switched to in-situ monitoring that cut these impurities by over 90%. These technical tweaks seem invisible to outsiders, but anyone formulating with our compound benefits by avoiding erratic byproduct reactivity.

    Another reality is workforce training. Chlorinated aromatics and volatile trifluoromethylation reagents present operational hazards. We invest time on the plant floor, reviewing safe handling during both transfer and reaction work-up. Simple practices, such as double gloving or using dust collection, can mean the difference between incident-free shifts and avoidable contamination. Each improvement in handling protocols protects not just our people but keeps environmental releases close to undetectable.

    In-Depth End-Use Scenarios

    We keep close tabs on how researchers actually apply 4-chloro-7-(trifluoromethyl)quinoline. With every inquiry, our technical team meets the customer where they are—whether developing new fluorescent tags, medicinal candidates, or pesticide leads. For most, the appeal is in the molecule’s unique blend of aromatic rigidity and heavy electron withdrawal supplied by the chlorine and CF3 groups. It serves as a core building block for libraries of urea, amide, and fused-ring syntheses. Those properties let chemists guide regioselective cross-coupling and late-stage C-H activation reactions, pushing medicinal chemistry in new directions.

    We also see usage in advanced materials and device fabrication. Scientists need molecules that hold up under elevated temperatures, radiation, or aggressive etching conditions. The quinoline core, strengthened by the chloro and trifluoromethyl substitutions, grants higher thermal and photochemical resistance. Application in OLEDs and specialty coatings calls for such robustness, and customers value that our strict process guarantees fewer contaminants to interfere with device yields.

    Supporting Innovation: The Manufacturer’s Viewpoint

    Our team thrives on supporting cutting-edge research. It’s rare that a month passes without a customer requesting a new derivative or larger lot size. We recognize our role as an essential link in the innovation chain. Our site managers remember the uncertainty of landing a first multi-kilogram delivery for a new pilot run. By maintaining back-up inventory, up-to-date technology, and predictable scale-up timelines, we take pride in helping partners hit project deadlines.

    Not all requests go smoothly. Sometimes a researcher’s route calls for alternative crystalline forms, micronized powders, or solvent-wetted batches. Because we run our own lines, not third-party blends, we can verify process conditions match the user’s practical needs. One small biotech needed strict particle size criteria to improve dispersibility in solvent-screening. By collaborating directly with their R&D group, we adapted our milling protocol, saved downstream time, and built trust from the outset.

    Environmental, Health, and Safety Responsibilities

    As direct producers of specialty organics, we understand our footprint. Handling trifluoromethyl reagents brings concerns about persistence and downstream environmental fate. Instead of shortcuts, we commit resources to closed-loop systems for solvent recovery, inert gas handling, and thorough air scrubbing. Our local compliance team reviews wastewater and ambient monitoring more often than regulation requires. Years in the field have taught us that predictive maintenance pays for itself in uptime and sustainability.

    Health and safety reach beyond compliance paperwork. We issue regular training for everyone, not just senior staff, on hazard awareness and emergency response. Sharing near-miss stories—such as an unanticipated dust cloud or a minor reagent spill—creates culture where incident prevention gets real attention. Open communication and visible corrective actions boost both morale and safety numbers. In our experience, customers increasingly value knowing their chemical supplier takes real responsibility from raw input to final packaging.

    Regulatory and Analytical Rigor

    We produce this quinoline derivative with full awareness of global regulations governing specialty chemicals. Our internal quality system aligns with Good Manufacturing Practice standards by default. Libraries of validation data are kept up to date—covering every batch, every analytical run, every deviation. Third-party audits and customer site visits are standard fare, welcomed as evidence that we do not cut corners. Customs agents, importers, and corporate procurement departments look for traceable documentation. We respond with clear batch-by-batch records and open access to our own quality and regulatory team.

    Advanced analytical support runs throughout our workflow. Each lot is tested not just for basic purity, but also for residual metals, halogen balance, particulate contamination, and solvent carryover. Any deviation from expected spectra prompts immediate investigation. After years troubleshooting HPLC shifts and GC ghosting, our lab staff catch problems early, cutting avoided costs and missed opportunities for downstream innovators.

    Continual Improvement and Open Problem-Solving

    The world of specialty organics changes fast: new synthetic routes, fresh regulatory guidelines, and competitor benchmarking keep us sharp. We rely on regular customer feedback to refine not just product, but the way we interact with the market. Small improvements like automating a safety vent or refining our filtration step compound into larger efficiency gains over time. Visiting customer labs and attending international conferences remind us how our work directly fuels new discoveries. Seeing publications and patents mention our core quinolines serves as ongoing motivation.

    We face ongoing challenges, including raw material pricing and more stringent regulatory thresholds for halogenated organics. Rather than push these obstacles off to end users, we invest in secure supplier relationships and test alternative greener reagents. Our technical team reads research from both academic and industry groups, scanning for safer, cleaner, and less energy-intensive routes to the same high-quality product.

    Direct Support for Industry and Research Partners

    Our support extends to technical troubleshooting, not just order fulfillment. Whether a researcher faces unexplained reactivity or a scale-up manager struggles with isolation, we provide practical advice drawn from real plant-floor experience. Common questions surround solvent choice, temperature ramping, and impurity management. We often share guidance gained from our own process development work—what worked, what failed, and why certain changes matter.

    In some cases, researchers discover unexpected behaviors, such as altered solubility in certain polar organic solvents or slight shifts in NMR when packed in different matrices. By comparing analytical fingerprints and running joint lab experiments, we help clarify these puzzles. We believe transparency and shared problem-solving trump over-polished marketing.

    Final Word: Pride in Manufacturing Excellence

    Seeing how far we’ve come as a company—from trial runs and early technical setbacks to meeting high international standards—gives us a sense of accomplishment. Every kilogram of 4-chloro-7-(trifluoromethyl)quinoline we ship out reflects real effort, real expertise, and a real promise to researchers and manufacturers. We measure our success through the progress customers make, the publications their teams write, and the innovations that grow from our foundations.

    Producing this molecule is no longer a niche exercise. It’s a core function in a value chain that reaches across health, agriculture, electronics, and green chemistry. From the shop floor to the analytical bench to your research bench, our goal is continuous improvement and straightforward, responsive support.