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5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline

    • Product Name 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline
    • Alias TCC
    • Einecs 694-077-6
    • 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
    VTB
    Specifications

    HS Code

    768552

    Chemicalname 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline
    Casnumber 959366-94-4
    Molecularformula C10H4Cl2F3NO
    Molecularweight 282.05 g/mol
    Appearance Off-white to pale yellow solid
    Meltingpoint 172-175°C
    Solubility Slightly soluble in DMSO, insoluble in water
    Purity Typically >98%
    Smiles C1=CC2=C(C(=C(N=C2C(=C1Cl)Cl)C(F)(F)F)O)
    Inchi InChI=1S/C10H4Cl2F3NO/c11-5-1-2-6-7(3-5)15-9(10(13,14)15)8(16)4-12-6/h1-4,16H
    Storagetemperature 2-8°C
    Synonyms 5,7-Dichloro-4-hydroxy-2-(trifluoromethyl)quinoline

    As an accredited 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline, tightly sealed, with tamper-evident cap and labeled for laboratory use.
    Shipping 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline is shipped in tightly sealed containers, protected from light and moisture. The chemical is handled according to standard hazardous materials protocols, with appropriate labeling for safe transport. Ensure compliance with all local, national, and international shipping regulations for chemicals, including UN classification and MSDS documentation.
    Storage Store 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, sources of ignition, and incompatible substances such as strong acids or bases. Keep at ambient temperature, protected from moisture. Use appropriate personal protective equipment when handling, and ensure proper labeling to prevent accidental exposure or misuse.
    Application of 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline

    Applications of 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline in Industrial Manufacturing

    As a specialty chemical producer, we supply 5,7-dichloro-4-hydroxy-2-(trifluoromethyl)quinoline to integrated manufacturers in sectors that demand advanced performance from pharmaceutical syntheses and specialty agricultural intermediates. The compound functions as a critical intermediate in targeted chemical pathways, supporting product quality, regulatory compliance, and cost-efficiency across multiple regulated industries.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antimalarial Drugs

    Major pharmaceutical companies introduce this advanced quinoline derivative into the multi-step process of synthesizing antimalarial APIs, specifically in the manufacturing of next-generation chloroquine analogues and related agents. The material forms a core scaffold in the construction of proprietary APIs, meeting the precise purity, traceability, and impurity profiles mandated for regulated drug substances. Facilities employ advanced purification and structural confirmation via in-process HPLC, NMR, and mass spectrometry to confirm batch-to-batch reproducibility.

    Industry compliance standards

    • USP (United States Pharmacopeia) monographs for related antimalarial APIs
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Good Manufacturing Practice (GMP) Directive 2003/94/EC
    • FDA 21 CFR Part 210/211 for finished pharmaceuticals

    Typical usage ratio

    • 10–18% of total reactant mass in key cyclization or substitution steps; percentage varies by API pathway and is optimized for yield versus byproduct control using pilot batch data

    Downstream process integration

    • Introduced in the early-intermediate or late-intermediate stage depending on the final API structure, commonly fed into condensation reactions followed by purification and salt formation

    Final product types

    • Antimalarial active pharmaceutical ingredients (APIs), such as derivatives of hydroxychloroquine and related quinoline drugs for regulated tablet or injectable formulations

    2. Herbicide Intermediate Manufacturing

    Leading agrochemical manufacturers rely on this compound as a nitrogen-containing core structure in selective herbicide synthesis, specifically for the design of fluorinated quinoline-based selective post-emergence applications. Formulators benefit from its electronic characteristics and allow for precise regioselective chlorination and coupling in the creation of active herbicide intermediates, further processed into market-ready actives for crop protection.

    Industry compliance standards

    • ISO 9001:2015 for chemical manufacturing quality management
    • REACH registration and compliance under EC No 1907/2006 for designated uses
    • FAO/WHO specification for technical grade pesticide active ingredients
    • CropLife International stewardship guidelines

    Typical usage ratio

    • 3–7% w/w as a structural intermediate in one-pot or multi-step synthesis routes, calculated as molar fraction based on the desired aryl chlorination profile

    Downstream process integration

    • Charged during aromatic substitution or halogenation, followed by coupling and final formulation into technical concentrates or wettable powders

    Final product types

    • Fluorinated quinoline herbicide active ingredients, post-emergence selective herbicide technical concentrates, bulk intermediates for further formulation

    3. Synthesis of Specialty Pigments

    Producers of high-performance pigments, particularly in the electronics and printing ink industries, deploy this advanced quinoline in the synthesis of specialty pigments where halogenated aromatic rings and trifluoromethyl substituents are critical for chromatic stability and light fastness. The compound introduces chlorine and fluorine functionalities required for complex pigment molecules, strengthening color intensity and long-term resistance to environmental degradation.

    Industry compliance standards

    • ISO 18451-1:2019 for pigments and extenders
    • EN 71-3:2019 for safety of pigment additives in toy applications
    • RoHS Directive 2011/65/EU for pigment applications in electronics
    • REACH Annex XVII for pigment toxicity and environmental restrictions

    Typical usage ratio

    • 0.5–5% by mass input, refined according to the molar stoichiometry needed to achieve complete transformation during the targeted cyclization or post-modification step

    Downstream process integration

    • Engaged during colorant core construction, typically in the stepwise formation of polyaromatic frameworks prior to sulfonation, metallization, or further stabilization stages

    Final product types

    • High-performance quinoline-based pigments, specialty inks for inkjet and flexographic systems, display-grade printing pigment dispersions

    4. Advanced Material Science Research – Electronic and Photonic Applications

    Institutes and innovation-driven electronics manufacturers incorporate this quinoline scaffold as a building block for fabricating model compounds in the development of electron-transport materials and organic photonic structures. The material’s halogen and trifluoromethyl substitutions support studies in tuning molecular orbital energies and electron affinity, facilitating the synthesis of organic thin-film and OLED prototype components under controlled laboratory and pre-commercial conditions.

    Industry compliance standards

    • ISO 17025 for research laboratory chemical analysis
    • Cleanroom processing standards per ISO 14644 for device development
    • RoHS/REACH compliance for prototyping new electronic materials
    • Internal company-specific electronic grade material criteria

    Typical usage ratio

    • Variable: typically 2–12 mol% in mechanistic studies or pilot syntheses, adjusted by molecular design and desired device prototype properties

    Downstream process integration

    • Deployed in molecular assembly or cross-coupling steps, leading to thin-film deposition, device layering, or organic material encapsulation development lines

    Final product types

    • Sample-scale electron-transport materials, organic light-emitting diode (OLED) model components, advanced photonic test structures, reference materials for R&D commercialization programs
    Free Quote

    Competitive 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline: Perspective from the Factory Floor

    Rethinking Specialty Quinoline Production

    For years now, the chemical market has been louder than ever about complex quinoline derivatives, and time on the production line has shown us where the real challenges emerge. 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline stands out among quinolines for more than its tongue-twister name and dense formula, and those who work with the substance know its behavior far better than any outsider copy can tell. From raw material selection to QA testing, a manufactured batch has more stories than simple purity numbers, and that's exactly where significance takes root.

    From the Reactor: How This Compound Forms

    A controlled synthesis of dichloro and trifluoromethyl groups onto a quinoline backbone demands a steady hand—both in terms of process time and temperature, and the diligence applied at every stage of workup. Fluorinated intermediates involve not just higher costs, but stricter containment of emissions, and our team trains regularly to stay ahead on both fronts. Chlorinating agents, if handled without care or knowledge, leave behind trace contamination that doesn’t wash out in final purification steps. That’s why the lab and plant communicate constantly. We don’t simply watch for melting point or crystallinity; our focus is on inter-batch consistency, reduction of by-product formation, and minimizing worker exposure.

    Over the past decade, steady investment in line filtration, vacuum drying, and solvent recycling has paid off through repeatable product performance. By focusing on the details—like the rate of addition of reagents and solvent purity levels—we see fewer process deviations and less stress on our people. Our analytics department focuses increasingly on LC-MS and NMR optimization rather than basic titrations. This helps us verify trifluoromethyl substitution patterns down to individual protons, a detail suppliers without their own production can only hope for their partners to achieve.

    Product Form: What to Expect From an In-House Batch

    Each drum or bulk bag leaving our warehouse carries its own batch sheet, and inside, crystalline 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline offers a distinctly off-white hue—neither yellowed by excess chlorination nor clouded by residual fluorinated starting materials. Moisture levels sit well under industry norms due to extended drying cycles, something we found critical when early batches suffered from premature caking in long-term testing. It’s a challenge to describe this material as simply a reagent; those using it for pharmaceutical and crop-protection research demand material that will hold up under synthetic scrutiny, not just pass a generic, low-resolution QC.

    Over years of adjusting solvent exchanges and crystallization rates, the particle morphology has developed into a habit that works well for dissolving in common organics like DMSO, DMF, and dichloromethane. The subtle trick we’ve learned: take time during each cooling stage and skip unnecessary mechanical agitation. This produces solid that pours easily, doesn't dust up and cause safety concerns at point-of-use, while leaving enough surface area for researchers to get the reactions proceeding at a healthy clip.

    Key Uses Understood from the Shop Floor

    People ask about the ‘model’ or ‘standard’ for this compound. We have always said that the real measure is not the litany of numbers printed on the drum, but the results in the final customer application. Most 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline leaves here headed into development projects, many targeting agrochemical product lines and some targeting early-stage pharma research. The fluorine content and double-chlorinated motif mean it can serve as a versatile intermediate in synthesis, resisting premature breakdown in both acidic and basic conditions—a quality not every quinoline or chlorinated heterocycle delivers.

    Some chemists use it as a pivotal building block for introducing further substitutions. Its pattern of functional groups allows for efficient downstream transformations, including Suzuki, Heck, and related cross-coupling reactions. Unlike more basic quinoline derivatives, this structure holds up to tough reaction environments and doesn’t foster formation of unmanageable side impurities. In our testing, even after prolonged heat during step-growth, it stays put until the scientist forces it to react, lowering the odds of rework or failed synthesis.

    How In-Plant Adjustments Affect Real-World Results

    Large-scale chemistries rarely read like textbook syntheses. On-site, we’ve reduced the use of strong mineral acids in the wash stages to dodge corrosion and reduce salt waste. The compound’s stability profile, built by our chemists with decades in heterocycle production, translates to longer shelf life and fewer phone calls about complaints. One factory-floor change—switching to an oxygen-free environment during the final crystallization—meant no more ambient oxidation discoloring product, which kept the research groups and regulatory staff happy.

    Each year brings new requests. “Can you offer higher purity?” “Will a smaller batch reduce exposure risk?” These questions drive us to try every angle on process improvement. Rather than scaling up indiscriminately, we build pilot reactors big enough to replicate commercial-scale stress, so customers aren’t surprised by variability between gram and multi-ton orders. Some years back, we dialed in a new recirculation pump that managed to cut both batch time and temperature fluctuations, making every kilogram more predictable—and ultimately, more valuable to every customer.

    Differences from Other Quinoline, Chlorine, or Fluorine-Derived Products

    Compared with single-chlorine or non-fluorinated quinolines, this molecule occupies a hard-won middle ground. Mono-chlorinated compounds fade faster in long-term light and air tests, while non-fluorinated analogues degrade rapidly in handling and storage, especially under high humidity—perfect recipe for unpredictable performance. Chemical manufacturers often make do with what’s available, but we’ve seen too many batch failures traced to minor differences in starting material grade or moisture levels. Offering this specific multi-substituted quinoline means we no longer gamble with customer timelines or claims disputes.

    Some products pitched as “alternatives” lack the rugged core this compound provides. Customers often come in after their own small-scale trials fail, frustrated at materials more sensitive to light or trace metals. With this compound’s stability and functional group arrangement, cross-couplings proceed more smoothly, downstream purification headaches decrease, and teams see fewer rerun chromatographies. Colleagues working in scale-up have told us numerous times that once they swapped generic quinolines for ours, yields improved and off-spec isolations dropped off sharply.

    The trifluoromethyl group, in particular, sets this compound apart. It reduces electron density on the quinoline ring, makes for easier subsequent halogenations, and pushes up the resistance to hydrolysis or oxidation. Workers handling large drums appreciate not finding sticky, partly decomposed product months after storage. The dual-chlorine arrangement, meanwhile, means even under stress from light or challenging pH, decomposition by-products stay low. Every year, quality teams review stability test data, and so far, few new quinolines (especially those from generic sources) match our profile on shelf life and storage tolerance.

    Reflections: What Drives Improvement Year After Year

    Manufacturing specialty chemicals always teaches lessons in humility and precision. Early on, we underestimated how even a fractional variance in washing solvents showed up as mysterious peaks on customer analyses. Over time, we put more energy into continuous monitoring, streamlining the filtration, and swapping out legacy glassware for modern recirculating systems. These details, rarely visible to anyone outside the plant walls, spell the difference between one-off, “good enough” shipments and a reliable, recognizable profile customers return for year after year.

    Each request for higher-purity product or customized particle size brings a new set of hurdles. Not every batch can scale evenly from glassware to a ten-thousand-liter reactor, but sweating these details clears up recurring inconsistencies found in material procured from anonymous sources. Our site team keeps an eye on subtle process weirdnesses: pH drift, unexpected color changes, or temperature spikes in the middle of a crystallization. Even after so many batches, a seasoned operator can usually spot trouble sooner than any sensor, and catching those blips means fewer release holds and higher confidence.

    The journey from raw chemical to drum-ready product involves a lot of sweat and plenty of discovery. Our work isn’t just about assembling a formula, but making good on the promise that every kilogram performs—whether in somebody’s pilot plant or lab, in long-term shelf storage, or during downstream processing. That reputation doesn’t build on advertising; it builds on the trust our partners place in the result, backed by our own willingness to improve line by line and year by year.

    Regulatory and Safety Knowledge Earned on the Floor

    Handling halogenated and trifluoromethyl-containing molecules costs more than a safety data sheet. Tight controls on air and wastewater mean a slip-up affects every neighbor inside and beyond the factory fence. Regulatory compliance starts in how tanks and reactors get cleaned, and moves through every drum’s shipment. Every operator handling the product trains on spill procedures and the specifics of local and international transport requirements. What we ship today will meet scrutiny months or years from now, so we approach every documentation and lot release meeting as critical—not just rote paperwork.

    Management does not simply hand down protocols; many of our best safety routines have emerged from the very operators moving drums or washing down tanks. Anything toxic, persistent, or mobile in the environment deserves that depth of respect—especially where fluorinated by-products are concerned. As a team, we see environmental rules as ongoing commitments, never a box-checking exercise. Emissions, water concentrations, and air samples get tracked throughout the year. If a new challenge pops up, we invest in secondary containment or revise workflows. That culture, built from real risk and real experience, sets apart material sourced from a responsible manufacturer versus short-lived traders with little local impact.

    Working With Customers: Transparency and Performance

    Questions always come in from researchers and process engineers about solubility, drying, or downstream conversion. We welcome those. Years in production have shown that sharing our real-world results, not just “guarantee” numbers, leads to fewer surprises. People working at the bench level want to know how product morphology changes under different storage conditions, what to expect under uncommon reaction scenarios, and what’s likely to fail if they push the limits.

    The customer-supplier relationship stays healthy because we prefer problems surfaced early over last-minute panics. Not every order is a perfect fit: sometimes a user needs micronized material, sometimes full crystal size for filtration, other times a reformulation. We discuss any limitations, unusual findings, or process notes right up front. With today’s focus on robust traceability, every shipment carries records back to first batch, and if doubts ever creep in, our data and experience make all the difference in resolving technical questions.

    Collaboration goes both ways. Feedback from formulation labs helped us devise tighter controls around moisture pickup, while pharmaceutical group input led us to develop blended lots for consistent downstream reaction rates. These improvements—born from open exchange, not isolated development—pay off on both sides, saving waste, time, and headaches.

    Looking Ahead in Quinoline Chemistry

    Complex quinolines like this don’t often trend in headlines, but they quietly carry programs forward in both public health and food supply. New demands arrive almost every season: stricter storage rules, requests for trace impurity reduction, solutions for better environmental handling. By running a chemical factory with long-term commitment, the cycle of incremental improvement stays alive.

    Work does not end after shipping material out the door. Every lot we make is another chance to revisit old process hiccups, refine the stop points, and keep learning what the research community values most. The years have taught us that specialty quinolines, especially those with challenging group combinations like dichloro and trifluoromethyl, deserve manufacturers who live by their process and pride—not just their paperwork.

    Conclusion: Why Factory-Direct Experience Matters

    Anyone working deep in specialty chemicals learns quickly that product data sheets tell only a sliver of the story. Having a team that takes responsibility for every step—from raw materials to careful drying, to controlled storage—matters when results are on the line. 5,7-Dichloro-4-Hydroxy-2-(Trifluoromethyl)Quinoline stands as an example where in-house, hands-on work transforms a tough synthesis into a dependable product. For those depending on quality, stability, and performance—not just a name on a label—partnerships built with manufacturers who own the process often pay back the most, batch by batch and project by project.