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6-Fluoro-4-Hydroxyquinoline

    • Product Name 6-Fluoro-4-Hydroxyquinoline
    • Alias 6-Fluoro-4-Quinolinol
    • Einecs 630-835-5
    • 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

    759822

    Chemical Name 6-Fluoro-4-hydroxyquinoline
    Molecular Formula C9H6FNO
    Molecular Weight 163.15 g/mol
    Cas Number 26160-73-2
    Appearance Light yellow to beige powder
    Melting Point 180-182°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CC2=NC=CC(=C2C(=C1)O)F
    Inchi InChI=1S/C9H6FNO/c10-6-3-4-7-8(9(6)12)2-1-5-11-7/h1-5,12H
    Storage Conditions Store in cool, dry place; keep container tightly closed
    Synonyms 4-Hydroxy-6-fluoroquinoline

    As an accredited 6-Fluoro-4-Hydroxyquinoline 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 6-Fluoro-4-Hydroxyquinoline, tightly sealed, labeled with hazard warnings and chemical identification.
    Shipping 6-Fluoro-4-Hydroxyquinoline is shipped in tightly sealed, chemically resistant containers to prevent contamination or moisture exposure. The package is labeled according to safety regulations, including hazard information. It is typically transported via ground or air, compliant with local and international chemical shipping standards, ensuring safe and secure delivery to the recipient.
    Storage Store **6-Fluoro-4-hydroxyquinoline** in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, well-ventilated area away from direct sunlight. Adhere to all safety regulations for handling chemicals, including use of appropriate personal protective equipment and proper labeling for identification and hazard communication.
    Application of 6-Fluoro-4-Hydroxyquinoline

    Applications of 6-Fluoro-4-Hydroxyquinoline in Industrial Manufacturing

    6-Fluoro-4-Hydroxyquinoline supports multiple industrial sectors as a specialized intermediate, particularly in pharmaceuticals, crop protection agents, veterinary drug synthesis, and specialty pigment production. The following sections detail real-world application flows and requirements for this compound in high-value manufacturing environments.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Fluoroquinolone Antibiotics

    Many leading pharmaceutical manufacturers use 6-Fluoro-4-Hydroxyquinoline as a key building block in the synthesis of fluoroquinolone antibiotics such as ciprofloxacin, norfloxacin, and ofloxacin. Our direct manufacturing supply chain ensures batch traceability and document control in support of clinical application demands.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211 (USA)
    • EU Directive 2001/83/EC on medicinal products
    • Chinese Pharmacopoeia (ChP) requirements for intermediates

    Typical usage ratio

    • Requires 0.95–1.20 molar equivalents per target molecule in multi-step condensation reactions. Usage adjusts based on downstream substitution pattern and yield optimization.

    Downstream process integration

    • Charged into the designated condensation or cyclization step following primary quinoline precursor formation. In-situ monitoring for halogen selectivity and impurity control is standard in validated syntheses.

    Final product types

    • Bulk fluoroquinolone APIs (e.g., ciprofloxacin hydrochloride, norfloxacin base, ofloxacin lactate)
    • Injectable antibiotic preparations
    • Oral tablet and capsule formulations
    • Pediatric suspension concentrates

    2. Synthesis of Agrochemical Active Ingredients

    Producers of crop protection chemicals incorporate 6-Fluoro-4-Hydroxyquinoline into intermediate synthesis for fungicides and insecticides in the quinoline family. It facilitates precise halogen placement, supporting efficacy requirements for next-generation molecule development and regulatory registration in major agricultural markets.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) technical grade requirements
    • REACH (EC) No 1907/2006 substance registration and dossier filing (Europe)
    • OECD Good Laboratory Practice (GLP) standards
    • China GB 2763 MRL (maximum residue limits) for technical materials

    Typical usage ratio

    • 0.85–1.10 molar equivalents relative to agrochemical backbone structure; ratio variation supports either mono-substituted or further derivatized products.

    Downstream process integration

    • Introduced during the heterocycle assembly or halogenation stage, prior to side-chain modifications or coupling with other functional moieties in the final crop protection formulation.

    Final product types

    • Technical grade fungicide actives
    • Formulated wettable powders (WP) and suspensions (SC)
    • Seed treatment chemical concentrates
    • Insecticide intermediates for field application

    3. Veterinary Drug Intermediate Manufacturing

    Veterinary pharmaceutical manufacturers utilize this compound as a selective intermediate in the creation of quinolone-based antimicrobials for large animals, companion animals, and aquatic veterinary use. Quality systems demand high traceability and control of fluorine impurities to support approval processes in animal health sectors worldwide.

    Industry compliance standards

    • VICH GL3 GMP for Veterinary Drug Intermediates
    • US FDA CFR Title 21, Part 514 (animal drug applications)
    • Japanese Veterinary Pharmacopoeia (JVP) residue limits
    • OECD Principles of Good Manufacturing Practices

    Typical usage ratio

    • 0.90–1.05 molar equivalents in condensation with side-chain amines; precise ratio controlled for target veterinary spectrum and residue minimization.

    Downstream process integration

    • Reacts as core quinoline source in the key coupling step, followed by purification and post-synthetic derivatization into veterinary-dedicated molecules.

    Final product types

    • Veterinary injectable antimicrobials (bulk and formulated)
    • Oral premix powders and suspensions
    • Aquaculture therapeutic agents
    • Livestock feed additive premixes

    4. Precursors for Specialty Pigment Manufacturing

    Manufacturers specializing in high-performance colorants and specialty pigments deploy 6-Fluoro-4-Hydroxyquinoline in the early synthesis steps of quinoline-based pigments. The compound’s defined halogenation pattern allows for pigment molecules with advanced tinting strength, lightfastness, and compatibility required in demanding plastic, ink, and coating applications.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments) safety guidelines
    • EN 71-3:2019 (Safety of Toys, migration of certain elements)
    • GB/T 21869-2008 (China national standards for organic pigments)
    • ISO 9001:2015 certified quality management in pigment production

    Typical usage ratio

    • Varies from 1.02–1.20 molar equivalents to control shade and performance characteristics; adjusted according to synthetic route for copper-complex or monoazo pigments.

    Downstream process integration

    • Charged in the initial condensation or nitration stage, followed by coupling with primary chromophores or transition metal complexation for final pigment molecule development.

    Final product types

    • Solvent-stable pigment powders for plastics and masterbatch production
    • High-tint inkjet and industrial printing inks
    • Lightfast pigment concentrates for automotive and architectural coatings
    • Special effect pigments for polymer films
    Free Quote

    Competitive 6-Fluoro-4-Hydroxyquinoline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    6-Fluoro-4-Hydroxyquinoline: Direct from the Source

    Introduction to Our Product

    Every batch of 6-Fluoro-4-Hydroxyquinoline that leaves our plant stands as a testament to the care and depth of knowledge developed over decades of hands-on chemical production. This compound, also known as 6-fluoroquinolin-4-ol, remains valuable across research and pharmaceutical circles for its versatile profile and distinctive chemical structure. Our customers rely on us to deliver not just the bare compound but the kind of reliability that can only come from a manufacturer who undertakes every step from raw material to finished product under one roof.

    Model and Specifications Based on Practical Considerations

    We produce 6-Fluoro-4-Hydroxyquinoline with the CAS number 1068-57-1, adhering closely to best practices set by years of real-world synthesis and rigorous batch-to-batch analysis. Purity sits at the center of every order: we guarantee a minimum of 98%, routinely achieving even higher with HPLC verification. Moisture content, residual solvents, and trace metals are scrutinized before release—long before you receive a certificate, every flask, valve, and pipe has faced the same high standard that our technical team enforces floor-side daily.

    Consistency emerges in the form of a pale to light brown solid, crystalline by inspection, with melting points and solubility profiles checked not by assumption or third-party reports, but by the skilled hands and eyes of our own analytical chemists. This attention to small details demonstrates our commitment; customers have sent compounds back to traders and resellers when minor deviations appear, but that sort of issue just does not arise with our product.

    Behind the Scenes: Why Experience Matters

    It takes more than a well-stocked lab to deliver a steady stream of specialty quinolines. We have faced the setbacks that only reveal themselves after scaling up from flask to reactor. Some methods described in literature falter outside small-scale glassware—trace color impurities, incomplete reactions, or tricky by-products persist. Expanding production without changing reaction parameters, adjusting solvent systems to coax out the purest crystals, or finding the right temperature gradient for drying—these tweaks separate experienced production chemists from those who only strive for perfunctory compliance.

    What we sell comes shaped by years of research, but more often, it is the result of repair: identifying a yield problem, investigating every solvent, and making iterative improvements until reliability emerges at any scale. Stability and reproducibility set our 6-Fluoro-4-Hydroxyquinoline apart in practical use, not just in claim.

    How End Users Deploy This Compound

    Our 6-Fluoro-4-Hydroxyquinoline finds a home in laboratories dedicated to synthetic organic chemistry, medicinal research, and candidate drug development. Customers range from startup biotech ventures to multinational giants looking for new leads in antimicrobial efficacy or kinase modulation. The molecule’s biological backbone—and specifically its fluorinated quinolinol motif—renders it valuable for scaffold exploration. Fluorination at the 6-position makes this compound particularly intriguing: it enhances metabolic stability and often modulates the electronic properties of the quinoline core, providing medicinal chemists with a tunable synthon no simple hydroxyquinoline matches.

    Some researchers embark on total syntheses, building complexity atop the quinoline ring. Others use it as a central fragment for further derivatization, tapping into the reactivity of the hydroxyl group at position 4. Process chemists at our client firms often share feedback with us: reliable physical properties make the material easier to handle, and consistent purity reduces the headache of purifying downstream intermediates or encountering unexplained biological results. The feedback loop between manufacturing bench and customer lab flows directly at our company, unfiltered by layers of re-labeling or telephone tag between go-betweens.

    What Sets This Compound Apart from Other Analogs

    Many molecules cross a customer’s bench in a year, but few offer the blend of reactivity and stability seen with 6-Fluoro-4-Hydroxyquinoline. Fluorinated quinolines present unique behavior that hydroxyquinolines or chloroquinolines simply do not match. The 6-fluoro substituent increases lipophilicity and can enhance penetration into biological membranes, which, paired with its 4-hydroxy handle, offers paths toward motifs that probe new chemical space. Our teams have compared a range of quinolines over the years—tracking yield losses, stability during storage, and reactivity patterns in both pilot and full-scale production—and this compound consistently draws more requests from medicinal and agrochemical programs exploring new frontiers.

    There is a stark difference between materials sourced directly from a chemistry manufacturer and those that have passed through multiple trading hands. By producing at origin, we control not only purity and consistency but the logistical footprint as well. Degradation during warehousing or inaccurate relabeling in trading networks never comes into question with our shipments. Our product leaves our site accompanied by traceable batch records, analytical profiles, and a transparent production history. This direct connection builds trust and accelerates research in ways no third-party supplier can replicate.

    Challenges and Solutions in Manufacturing

    Scaling up production encounters reality checks often unseen in the benches of academia or specialty catalog outlets. Exothermic reactions drift dangerously if unattended, leading to hot spots or failed crystallizations. Our operations team encountered these issues early—these lessons embedded themselves in our process controls. Solvent selection proved critical; the "book" solvents produced marginal results at larger volumes. We approached scaling problems from two ends: modifying reactor design and optimizing agitation. Where other producers have fallen back on batch variability as "unavoidable," we persevered until process tweaks brought robustness.

    Material storage conditions also demanded attention after initial production. Trace moisture or ambient atmospheric exposure led to inconsistent appearance and solubility—a problem many only discover downstream in their own facilities, often at considerable cost. Our logistics team responded, adopting inert packaging protocols and desiccation for every shipment. We also record precise humidity and temperature logs, giving our partners confidence that the compound in their flask matches the certificate in every meaningful way. Chemists at client sites have even commented that the uniformity from shipment to shipment saves them days of troubleshooting, highlighting a small but tangible return on the investments made in rigor at every step.

    Listening to Our Customers’ Needs

    Over the years, researchers have approached us with requests for custom packaging, sorted particle sizes, or alternative solvents. We have accommodated almost every need when feasible—bringing production chemists into direct conversation with research leaders. Most academic suppliers cannot accommodate such flexibility or traceability. This service-driven model flows from the freedom and control of being a direct manufacturer. Internally, any suggestion triggers technical evaluation, not endless negotiation with an unseen supplier abroad.

    Some scientists report frustration receiving off-color or partially decomposed material from traders. Our protocol involves a final pre-shipment quality check using the very methods applied during synthesis: if it does not match the original analytical fingerprint, it does not ship. We know lead times matter—having built relationships with custom synthesis teams and procurement managers, our approach centers on honest communication about expected delivery, real-time updates on synthesis progress, and rapid troubleshooting should demand spike or unforeseen interruptions arise.

    Working with Regulatory and Quality Standards

    Processes reflect more than internal targets; they answer to international expectations for data integrity and environmental responsibility. We long ago adopted trace contaminant controls far tighter than industry averages, anticipating the direction of regulatory scrutiny rather than lagging behind it. Certifications for analytical methods and material handling protocols faced audits not just from our own staff, but from partner companies conducting on-site visits as soon as supply relationships began.

    Our documentation does not only serve compliance. By maintaining detailed records and cross-batch quality control, we root out anomalies long before they find their way into customer projects, avoiding setbacks that might otherwise trigger project delays. This preventive attitude, paired with the flexibility to introduce additional analytical metrics should a partner’s project require it, leads to long-term relationships with some of the world’s leading discovery teams.

    Commitment to Continual Improvement

    Manufacturing, especially for high-purity intermediates like 6-Fluoro-4-Hydroxyquinoline, demands constant auditing. Industry standards shift, markets demand new grades, and analytical sensitivity improves each year. Our team tracks trends in detection—some ambient impurity that went unnoticed a decade ago may pose challenges under today’s standards. We stay ahead by investing in new analytical tools, recruiting process experts who thrive under shifting goalposts, and fostering an atmosphere of open problem-solving across the company.

    Feedback from customers regularly influences the evolution of our production lines. Calls and emails describing unusual chromatograms or unanticipated yields in follow-up synthesis have led to process adjustments. Rather than viewing these messages as complaints, we treat them as collaborative opportunities. Sometimes our QC team works alongside partner labs, reanalyzing retained samples and running parallel tests to reach root causes, demonstrating both technical competence and real-world concern for the people relying on our compound to drive their own work forward.

    Reducing Environmental Impact at Every Stage

    Preparation of complex intermediates like 6-Fluoro-4-Hydroxyquinoline often brings the risk of hazardous waste generation. Early in our journey, we faced mounting solvent disposal costs and environmental impact concerns. Stepwise, we have shifted to closed-loop solvent recovery and greener alternatives, reducing not just environmental footprint but operating costs as well. Continuous monitoring finds further savings in both resources and compliance margin.

    Our waste treatment protocols receive routine re-evaluation. Feedback from environmental audits and internal reviews ensures we stay ahead of required controls, benefiting both the communities around our plant and the researchers using our products. Being a direct manufacturer places the responsibility to clean up after ourselves—I have witnessed firsthand the difference in community engagement and reputation between companies who take this seriously and those who do not.

    Supporting Innovation and Education

    Some of our earliest collaborators now lead departments and discovery teams in respected institutions. Their trust motivates us to maintain open lines for feedback, sharing characterization methods, and providing technical support beyond what a catalog distributor can offer. We occasionally present case studies and bulletins on synthetic routes and best practices, drawing generous feedback and fresh insight from our own customer base.

    Academic groups working with limited resources often approach us for guidance. We support these projects with not only quality product, but technical notes and troubleshooting support. Each shipment to a new lab or classroom feels like a small investment into the next generation of synthetic chemistry, and we take that role seriously.

    The Value of Provenance

    Traceability matters as much to us as purity. Each gram of 6-Fluoro-4-Hydroxyquinoline passing through our doors carries a story—one recorded in batch logs, chromatograms, and the hands-on experience of chemists and engineers at every process stage. Direct manufacturing offers advantages that scale and multiply over years: faster response to market needs, transparency in every engagement, and a culture built around sustained, knowledgeable improvement rather than short-term gain.

    Researchers buying from direct sources cut weeks off their project timelines, bypassing the uncertainty and delay associated with traders and generic suppliers. Our team delivers not just a high-quality product, but a technical partnership formed through the conviction that what leaves our facility has to match not only regulatory code, but the everyday realities and ambitions of the people relying on it.

    Conclusion: Partnership Rooted in Experience

    Supplying 6-Fluoro-4-Hydroxyquinoline to the world’s research community means embracing the real-world challenges of both chemistry and business. Our process, product, and people serve as proof that manufacturing excellence grows from lived experience, continual adaptation, and honest communication. Every success and every misstep over years of production have found their way into current best practices, giving our customers stability and support they will not find elsewhere.

    The partnership between direct manufacturer and research scientist brings value far beyond a certificate of analysis or shipping manifest. Our doors, inboxes, and phone lines remain open to those who want to understand, shape, and innovate with this trusted compound. From optimizing synthetic steps to supporting first-time users, we build lasting collaborations—one batch, one project, and one conversation at a time.