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7-(Trifluoromethyl)-4-Quinolinol

    • Product Name 7-(Trifluoromethyl)-4-Quinolinol
    • Alias 7-(Trifluoromethyl)-4-hydroxyquinoline
    • Einecs 629-023-6
    • 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

    809019

    Productname 7-(Trifluoromethyl)-4-Quinolinol
    Casnumber 393-13-7
    Molecularformula C10H6F3NO
    Molecularweight 213.16
    Appearance Pale yellow to yellow crystalline powder
    Meltingpoint 130-135°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.40 g/cm3 (estimated)
    Purity Typically ≥98%
    Smiles C1=CC2=C(C=CC(=C2)C(F)(F)F)N=CC1=O
    Inchi InChI=1S/C10H6F3NO/c11-10(12,13)7-3-1-2-6-8(7)9(15)4-5-14-6/h1-5,15H
    Storageconditions Store at room temperature, tightly sealed, away from light

    As an accredited 7-(Trifluoromethyl)-4-Quinolinol 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 7-(Trifluoromethyl)-4-Quinolinol, sealed with a screw cap, labeled with chemical details.
    Shipping **Shipping Description:** 7-(Trifluoromethyl)-4-Quinolinol is shipped in tightly sealed containers, protected from light and moisture. It is transported as a laboratory chemical, following standard protocols: in compliant packaging, with clear labeling and safety documentation (SDS). Shipping adheres to local, national, and international regulations for handling and transport of specialty chemicals.
    Storage Store **7-(Trifluoromethyl)-4-Quinolinol** in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizers, acids, and bases. Protect from light and moisture. Ensure the storage area is equipped to contain any accidental spills, and label the container clearly with appropriate hazard warnings.
    Application of 7-(Trifluoromethyl)-4-Quinolinol

    Applications of 7-(Trifluoromethyl)-4-Quinolinol in Industrial Manufacturing

    As a manufacturer dedicated to high-purity fluorinated quinoline derivatives, we deliver 7-(Trifluoromethyl)-4-Quinolinol for advanced industrial processes where strict performance characteristics, compliance, and reliable supply are required. This compound supports the synthesis and performance optimization of key downstream product classes in pharmaceuticals, crop protection, electronic materials, and specialty dyes. Each industrial application leverages its unique physicochemical properties to achieve consistent quality and regulatory benchmarks throughout the value chain.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers incorporate this raw material as a building block in the synthesis of next-generation active pharmaceutical ingredients (APIs), especially where fluorinated quinolinol cores underpin pharmacological activity. Its high chemical stability enables streamlined multi-step transformations, while trace impurity control is validated against global regulatory expectations. Customers rely on this intermediate in both small molecule drug development and in scaling up to commercial API processes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <1078>
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for starting materials
    • China National Medical Products Administration (NMPA) API import standards

    Typical usage ratio

    • Usually 1-3% molar equivalents as a core substrate; dosage adjusted per target molecular scaffold and required reaction yield.

    Downstream process integration

    • Reactant in heterocyclic condensation or nucleophilic substitution during API intermediate stage
    • Introduced after key halogenation, before final functionalization for API assembly
    • Supplied as high-purity crystalline solid, dispensed under GMP-controlled environment

    Final product types

    • Anti-infective and antiviral drug candidates in preclinical and clinical pipelines
    • CNS-active molecule scaffolds possessing fluorinated heterocycle motifs
    • API process intermediates shipped to CMO/CDMO partners for downstream synthesis

    2. Agrochemical Active Ingredient Synthesis

    Leading crop protection manufacturers employ this compound to synthesize selective herbicide and fungicide actives, leveraging the electron-withdrawing trifluoromethyl group to modulate bioactivity and environmental stability. This raw material enables precise integration into multi-step synthetic routes required to obtain market-approved agrochemical molecules featuring quinolinol cores.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specification
    • ISO 9001:2015 Quality Management for Synthesis Operations
    • REACH (EC No 1907/2006) registration for chemical intermediates
    • GLP (Good Laboratory Practice) compliance for technical materials

    Typical usage ratio

    • Generally 2-6% by weight of total batch mass; fine-tuned according to downstream molecule construction and required yield for active substance registration.

    Downstream process integration

    • Charged as a feedstock in cyclization or alkylation steps for herbicide base synthesis
    • Metered dosing using closed-system reactors for worker safety and batch reproducibility
    • Integrated with catalyst or oxidant addition before final formulation of technical concentrate

    Final product types

    • Technical grade active ingredients for post-emergent herbicide formulations
    • Fungicidal quinoline-derivative actives for seed treatment blends
    • Active base shipped to pesticide formulation plants for bulk dilution and packaging

    3. OLED and Display Material Synthesis

    Specialized electronic material producers apply this quinolinol derivative in the fabrication of organic semiconductors for OLED and advanced display technologies. Its electronic characteristics, conferred by the trifluoromethyl substitution, facilitate rigorous tuning of photoluminescence and charge transport in both blue-emitting and electron-transport layer precursors. High purity and trace metal control directly support device consistency and screen performance yield.

    Industry compliance standards

    • JEDEC Standard JESD78D for material reliability in device fabrication
    • RoHS (Restriction of Hazardous Substances Directive, 2011/65/EU)
    • ISO 14001 Environmental Management for Electronic Chemical Production
    • IEC 61249-2-21 Halogen-Free Material Guidelines (when applicable)

    Typical usage ratio

    • 0.5-2% by weight in dopant or host matrix for emission and charge transport layers; ratio based on desired device parameters and emission color tuning.

    Downstream process integration

    • Dissolved into high-purity solvents for thin-film deposition or vacuum evaporation
    • Incorporated during spin-coating or inkjet printing onto ITO substrates
    • Quality control ensures lot-to-lot spectral consistency and contamination below 25 ppb

    Final product types

    • Small-molecule host materials for OLED display and lighting panels
    • Electron transporting intermediates used in flat panel displays and mobile screens
    • Prototype semiconductors for flexible displays and organic electronics R&D

    4. Specialty Dye and Pigment Manufacture

    Dye and colorant companies adopt this fluorinated quinolinol as a precursor for high-performance specialty dyes, where strong fluorescence or photostability is required. Its unique aromatic structure enables synthesis of both high-contrast fluorescent markers and industrial pigments used in security printing, imaging, and laser applications, while ensuring safety compliance for non-food, non-cosmetic sectors.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toys (Heavy Metals Migration for Industrial Markers)
    • REACH Annex XVII (Restrictions on Manufacturing and Use)
    • ISO 9001:2015 for Dye and Pigment Process Control
    • AATCC Colorfastness Standard for Industrial Dye Products

    Typical usage ratio

    • Ranges from 3-10% by weight in pigment or dye precursor syntheses; ratio determined by required optical density and application substrate.

    Downstream process integration

    • Introduced during the heterocyclic coupling for dye intermediate assembly
    • Added prior to quaternization or sulfonation steps in dye molecule functionalization
    • Batch blending under inert atmosphere for photostability and purity

    Final product types

    • Fluorescent dyes for laser marking and security inks
    • Pigments for anti-counterfeit labels and specialty industrial coatings
    • Marking chemicals for imaging, microscopy, and quality inspection systems

    5. Medicinal Chemistry Screening Libraries

    Discovery chemistry groups synthesize fluorinated quinolinol frameworks for entry into medicinal chemistry screening libraries. This material enables the preparation of structurally diverse compounds for high-throughput screening, with strict raw material provenance and batch uniformity supporting reproducible SAR studies and patent application support.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) Principles
    • USP <1058> Analytical Instrument Qualification
    • ISO/IEC 17025: Testing and Calibration Laboratories
    • Record-keeping and traceability under FDA 21 CFR Part 11

    Typical usage ratio

    • 0.2-2% relative to overall compound library synthesis mass; adjusted to meet required virtual library size and diversity index.

    Downstream process integration

    • Engaged in amination and alkylation stages for compound diversification
    • Supports combinatorial synthesis and automated split-and-mix protocols
    • Dispensed to microreactors or automated synthesis robots for parallel processing

    Final product types

    • Purified screening compounds including fluorinated heterocycles for lead identification
    • Stock molecules for SAR and in vitro profiling
    • SAR intermediates supplied to contract research organizations (CROs)

    6. Fine Chemical Reference Standard Preparation

    Producers of high-purity analytical standards use this compound to create reference materials for method validation and instrument calibration across pharmaceutical, agrochemical, and forensic laboratories. Its traceable quality, precise lot documentation, and stable fluorinated aromatic moiety underpin robust reference standard performance in regulated environments.

    Industry compliance standards

    • ISO Guide 34 / ISO 17034: Competence of Reference Material Producers
    • USP Reference Standard Certification Requirements
    • OECD Guidelines for the Testing of Chemicals
    • GLP record traceability and material archiving best practices

    Typical usage ratio

    • 95-100% purity reference standard formulation; single-use ampoules or vials prepared at typical concentrations of 1–50 mg per unit, based on analytical method requirements.

    Downstream process integration

    • Recrystallized and purified using chromatography prior to dissolution and aliquoting
    • Dosed into inert-atmosphere filling lines for reference cataloguing and distribution
    • Stability and identity confirmed by NMR, HPLC, and MS before lot release

    Final product types

    • Analytical reference standards for LC-MS, GC-MS, NMR calibration
    • Certified quality control reagents for laboratory proficiency testing
    • Working standards for regulated pharmaceutical and agrochemical QC labs
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    Certification & Compliance
    More Introduction

    Bringing 7-(Trifluoromethyl)-4-Quinolinol to the Market: A Chemist’s Perspective

    Engineering with Precision: Inside the Lab

    Synthesizing 7-(Trifluoromethyl)-4-Quinolinol requires more than a recipe—it takes a close eye on purity, yield, and reliable batch-to-batch performance. Over the years, our factory teams have experimented with different fluorinating agents and reaction temperatures. Fluorine isn’t an easy element to tame, so achieving a clean trifluoromethylation step is as much a matter of practice as theory. Mistiming a step, letting the reaction mix run too long, or skimping on purification saddles downstream users with unpredictable results.

    The model we produce, identified in our logs as TFQ-419Q, displays a high degree of chemical consistency. Each crystal batch gets characterized by NMR and HPLC in-house—no outsourcing or generic certification. Since clients working at the level of pharmaceutical intermediates can’t afford speculation, they frequently run parallel analysis, and we welcome any technical back-and-forth that follows.

    Our routine builds on well-understood reaction chemistry, yet scaling any process from a small flask to a multi-hundred-liter reactor uncovers fresh challenges. Microimpurities that looked irrelevant in the lab sometimes cause precipitation in a bulk vat, so our operators keep close tabs at every checkpoint. We don’t chase the lowest cost, because inconsistencies end up costing more in lost batches and wasted effort. Reliable quinoline-based products emerge from vigilance, not shortcuts.

    What Stands Out: Specifications and Identity

    Chemists who order this compound often ask about its appearance—they usually expect a pale solid, but minor process tweaks can tilt it toward a faint yellow color. Purity by HPLC must exceed 98%, or we won’t release it. We document any detected side products above 0.2%, since these can affect later-stage reactivity, especially when the product goes into sensitive syntheses. Typical melting ranges hover within two degrees from batch to batch. Moisture control matters, as quinolinols react to even traces of water, so sealed pouches and quick transfer reduce risk of hydrolysis.

    Some customers want to see trace metal content below one part per million, especially those pursuing medicinal leads. To meet this expectation, we deployed a dedicated glass-lined reactor for the key steps and analyzed each lot for heavy metal residues before packing. In our experience, a lot of industrial-grade products from other markets can introduce contaminated loads without the client realizing until their own process gums up.

    Packing matters more than many realize. This delicate solid travels in double-layered polyethylene, then into a rigid drum with desiccant canisters locked inside. Any breach invites moisture and kills shelf life, so we keep stockpiles to a minimum and refill based on regular customer forecasts. Those who handle the product carefully report years of stable results, given cool and dry storage.

    Application: More Than a Reagent

    Development teams come to us mostly from the pharmaceutical and agrochemical sectors, seeking a reliable fluorinated scaffold. The strong contribution of the trifluoromethyl group to metabolic stability, and its electron-withdrawing nature, makes this compound central to modern heterocycle design. Medicinal chemists routinely modify the C-4 position, taking advantage of the available phenol for further functionalization. Not all quinolinols offer this versatility, so it finds a place in lead optimization pipelines.

    In one recent collaboration, a biotech firm used our TFQ-419Q as a building block in kinase inhibitor research. Their synthetic scheme required the robust electron-donating patterns that only this fluorinated derivative could deliver. Since their processes demanded consistently low sulfate and chloride ion concentrations, we adapted our washing and recrystallization steps to meet their needs. Today their scale runs into multi-kilogram lots, and we haven’t once received feedback of unexpected contamination—a rarity in our field, where every residue counts.

    Agrochemical researchers look for potent, environmentally stable backbone molecules. With the inherent hydrophobic and electron-dense nature of the trifluoromethyl group, pesticides built around this core resist metabolic degradation in the field, extending active ingredient lifetimes. This property helps reduce overall application rates, cutting costs and potential environmental runoff. Most off-the-shelf quinolinol derivatives do not match this performance, and years of field data show measurable differences in product outcome when they switch to our material.

    Comparing to Other Quinolinols and Trifluoromethyl Quinoline Products

    Many ask us how our material stacks up against analogous compounds or competitors’ offerings. From what we’ve observed, standard quinolinols without the trifluoromethyl substitution lack the metabolic stability prized in latest-generation pharma targets. Their synthetic flexibility shrinks, and end products tend to display less resistance to oxidative breakdown. Even minor changes on the ring—like swapping the 7- for a 6-position substituent—shift reactivity profiles noticeably, affecting both synthetic ease and the biological activity of the end products.

    We’ve sourced competitive samples for side-by-side tests. While some materials claimed high purity, their chromatograms often displayed hard-to-remove tailing peaks, hinting at incomplete synthesis or over-simplified purification. Several times, samples packed in regular plastic bags picked up moisture during transit, rendering the material partially degraded on arrival. By contrast, we use time-tested packaging, so users receive the compound in pristine condition.

    Low-grade or technical-grade material does not cut it for the fine synthesis sector. We once ran a controlled trial with multiple suppliers in a large-scale pesticide intermediate project. Process yields correlated directly with the source—our batches contributed to a 7% higher overall conversion. That margin translates into bigger profits for the finished product, less rework, and fewer headaches for downstream technical staff.

    Some firms sell similar compounds with broader impurity profiles, suitable for dye or pigment synthesis. Our TFQ-419Q targets specialists who prioritize batch traceability and analytical support. For customers struggling with unexplained batch variability, we've taken the unusual step of offering co-analysis, sending reference spectra along with material lots. Over time, this transparent approach builds trust and minimizes guesswork.

    The Role of Analytical Data and Open Collaboration

    We have always taken pride in supporting customers beyond shipment. Many teams operate under regulatory oversight and need more than an invoice—they want analytical proof and technical dialogue. That's why every lot comes with a detailed certificate, not just a generic quality guarantee. If a customer project stumbles or analytical readings raise concern, our technical staff get in touch directly with their counterpart to troubleshoot.

    A critical part of our process involves retaining split control samples from every batch. When clients question a measurement, we have immediate access to the reference material, allowing fast, fact-driven resolutions. On rare occasions, external contamination or handling errors have surfaced in client labs, and we have demonstrated through matching NMR and mass spectra where the divergence began. This two-way transparency sets a higher standard and lowers frustration for all.

    For development-stage projects, every additional 0.1% impurity can jeopardize toxicology data or patent claims. Our commitment to sharing our analytical pipeline—down to the calibration curves and trace impurity logbooks—reassures regulatory teams working under pressure. By minimizing surprises, our quinolinol product helps innovators keep projects on track without wasted sprints troubleshooting raw input quality.

    Our technical team encourages clients to reach out before scaling up or switching suppliers. We can help adjust work-up protocols or pinpoint analytical artifacts that could otherwise lead to costly false trails. Through ongoing communication with customers, we learn about emerging requirements, such as lowered trace amine content for sensitive pharma projects, and update our own methods accordingly. This collaborative dynamic strengthens the material’s reputation and ensures it fits evolving end-use demands.

    Solving Production and Supply Hurdles

    Manufacturing specialty chemicals resembles fieldwork more than textbook chemistry. Process interruptions, supply chain shocks, or shifts in raw fluorine prices test the resilience of every producer. During global shipping bottlenecks, we streamlined operations by switching to local suppliers for precursors, investing extra time in qualifying each source. While some larger players chase volume at the expense of stability, our customers have voiced appreciation for our consistent delivery, even in tight markets.

    Our experience shows that prepping for the unexpected beats scrambling after the fact. We diversified storage for key intermediates and trained staff on multi-step backup workflows, minimizing single points of failure. Once, when a critical catalyst vendor faced operational hurdles, we ramped up in-house regeneration—a process that takes weeks but paid off by avoiding missed shipments.

    Some clients run into challenges scaling their own syntheses after lab success with our material. We offer direct process support, with team members onsite or via remote troubleshooting. In one documented project, the abrupt drop in yield at pilot scale traced to a subtle solvent compatibility issue. Our familiarity with industrial-scale quirks helped flag and resolve the problem. This hands-on partnership takes root because both sides understand chemical manufacturing isn’t just about shipping a drum—it’s about powering innovation from bench to plant.

    Beyond Molecules: A Human-Scale Approach

    Chemical manufacturing at this level doesn’t thrive on automation alone. Skilled people make the difference: technicians who notice a subtle change in crystal texture, plant managers who offset a pH dip before it ruins purity, logistics staff who spot the difference between weather-tight containers and those just “good enough.” Over years of operation, we’ve developed an ecosystem tied together by trust, not just compliance.

    Our team frequently compares stories with other manufacturers, learning both from missteps and clever workarounds. While digital monitoring and process analytics help tighten tolerances, it’s the hands-on time spent troubleshooting quirky batches that sharpen judgment. Colleagues have identified process drifts while adjusting for minor fluctuations in utility supply—sometimes the difference between a perfect batch and rework spirals lies in catching a deviation in time.

    We keep production grounded—no shortcuts, no hasty scale-ups that compromise on analytical scrutiny. When customers push for aggressive cost savings, we demonstrate why holding the line on purity, packaging, and technical support keeps their total overhead lower in the long run. Products like 7-(Trifluoromethyl)-4-Quinolinol justify the additional investment through fewer failed syntheses, higher yields downstream, and less regulatory grief.

    Some clients wonder if “premium” really means anything in commodities like specialty chemicals. Our experience proves it does. Teams who switch from unverified sources report smoother operations and better end-product reliability. Our own record maintains consistent supply, even in market turbulence, a testament to a process grounded in long-term relationships across procurement, QC, and technical divisions.

    What Comes Next for Advanced Quinoline Derivatives

    Preparing for the next wave of field and laboratory demands shapes our continual improvement. New drug candidates and pesticide formulations ask more of starting materials than ever before. Regulatory environments toughen each year, not just for trace impurity limits, but full supply chain transparency. Our team now devotes part of each weekly meeting to update each other on changing customer specs, adjusting process windows as targets shift.

    We anticipate more requests for sustainability data and carbon tracking. Converting sensitive organofluorines with minimal waste, solvent recycling, and tighter emissions reporting set new industry benchmarks. We participate in discussions with major sector consortia to ensure anything we supply is ready for the next layer of scrutiny. There’s no hiding behind vague claims—fully documented chain-of-custody and green chemistry evaluations already show up in the tenders we receive.

    Knowledge about 7-(Trifluoromethyl)-4-Quinolinol, from upstream precursor sourcing to validated destruction of waste streams, circulates in real time. Our technical documents grow thicker, but so does our understanding of the best practices across labs and plants worldwide. Logbooks, not marketing memos, prove our work when regulators or customer QA teams arrive unannounced.

    Feedback from innovative small labs and Fortune 500 companies loops directly into our batch records and SOPs. Incremental upgrades—like better dust filtration or switching a non-critical solvent to a greener alternative—sprout from listening to the people who handle the chemistry daily. No improvement feels too minor if it steadies the supply of a sensitive, high-value intermediate like ours.

    Trust Earned in the Lab, Proven in the Field

    Years of working closely with research, agricultural, and pharma development partners have shown that meticulous attention to the production and quality of 7-(Trifluoromethyl)-4-Quinolinol pays off. Each decision, from reagent selection to packaging, ripples downstream. Sustaining the confidence of demanding customers, who vet every shipment against tight specs, underpins our long-term partnerships.

    Prospective customers examining options for quinolinol derivatives often discover differences reveal themselves only under close analytical review or during pilot-scale workups. What distinguishes our product: no corners cut, a full trace of technical engagement, and readiness to adjust both process and support based on direct experience.

    As research and industry applications demand more robust, stable, and high-purity building blocks, our commitment stands—to produce and deliver 7-(Trifluoromethyl)-4-Quinolinol with the expertise, responsiveness, and reliability that only years of hands-on manufacturing can provide. The future of complex molecule synthesis—from discovery phase to broad commercial launch—rests on these foundations, built molecule by molecule, batch by batch, in partnership with our customers worldwide.