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8-Fluoro-4-Hydroxyquinoline

    • Product Name 8-Fluoro-4-Hydroxyquinoline
    • Alias 8-Fluoroquinolin-4-ol
    • Einecs 629-020-6
    • 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

    962433

    Chemical Name 8-Fluoro-4-Hydroxyquinoline
    Cas Number 823-21-6
    Molecular Formula C9H6FNO
    Molecular Weight 163.15 g/mol
    Iupac Name 8-fluoro-1H-quinolin-4-one
    Appearance Off-white to pale yellow solid
    Melting Point 233-235 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC2=C(C(=O)NC=C2F)C=C1
    Pubchem Cid 146354
    Storage Conditions Store at room temperature, protect from light

    As an accredited 8-Fluoro-4-Hydroxyquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 8-Fluoro-4-Hydroxyquinoline, 5g, supplied in a sealed amber glass bottle with tamper-evident cap and clear labeling for safety.
    Shipping 8-Fluoro-4-Hydroxyquinoline is shipped in tightly sealed containers, protected from light and moisture. It is classified as a laboratory chemical and must be handled following standard safety protocols. Shipping complies with regulations for potentially hazardous chemicals, ensuring proper labeling, documentation, and suitable packaging to prevent leaks or contamination during transit.
    Storage 8-Fluoro-4-Hydroxyquinoline should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature or as specified by the supplier. Ensure proper chemical labeling and restrict access to trained personnel. Store away from food and drink.
    Application of 8-Fluoro-4-Hydroxyquinoline

    Applications of 8-Fluoro-4-Hydroxyquinoline in Industrial Manufacturing

    As a dedicated manufacturer of 8-Fluoro-4-Hydroxyquinoline, we focus on supporting established industrial segments where this specialty intermediate delivers specific functionality. Our material is selected for pharmaceutical synthesis, agrochemical intermediate manufacturing, specialty dyes for electronics, and veterinary active preparation, each demanding distinct formulation, processing, regulatory, and end-use characteristics.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers implement 8-fluoro-4-hydroxyquinoline as a core building block in several synthetic routes for quinolone-class antibiotic actives. The compound enters multi-step processes requiring high chemical purity and defined reactivity, with its introduction carefully controlled to meet ICH guidelines for impurity profile management. Dosage level optimization reflects both conversion efficiency and manageable waste streams using validated in-house protocols based on international regulatory expectations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monograph 5.10, Substances for Pharmaceutical Use
    • US FDA 21 CFR Part 210/211—Current Good Manufacturing Practice for Finished Pharmaceuticals
    • Chinese Pharmacopoeia API Sourcing Specifications

    Typical usage ratio

    • 0.5–2.5 molar equivalents per synthetic batch, adjusted by reaction yield optimization and impurity control protocols; typical w/w addition: 5–15% of batch mass, based on downstream conversion rates and specific API manufacturing route.

    Downstream process integration

    • Charged directly to quinolone cyclization and acylation reaction steps as a heterocycle precursor after solvent pre-treatment and in-process QC sampling.

    Final product types

    • Raw quinolone API crystals
    • Salt forms for tablet compression
    • Sterile injectable antibiotic intermediates
    • Bulk pharmaceutical active ingredients for solid and liquid dose forms

    2. Agrochemical Active Ingredient Synthesis

    Agrochemical producers use our material as a starting monomer in the construction of novel quinoline-based crop protection actives. Its reactivity facilitates the introduction of fluorinated moieties crucial for resistance profiles and metabolic stability in field applications. Careful metering at this stage ensures downstream processability as required by Good Laboratory and Manufacturing Practices, direct traceability, and strict environmental emission control in accordance with agro-industry mandates.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for Pesticide Development
    • ISO 9001 Certified Quality Management for Agrochemical Synthesis
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals Regulation (EC No 1907/2006)
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) Guidelines

    Typical usage ratio

    • 3–8% w/w, calculated as a percentage of total active ingredient synthesis mass, adjusted for each specific quinoline-type herbicide or fungicide pathway and active molecular weight.

    Downstream process integration

    • Batch-fed into heterocyclization and halogenation reactors for formation of target crop protection molecules prior to purification and formulation steps.

    Final product types

    • Technical-grade synthetic fungicides
    • Active ingredients for herbicidal formulations
    • Seed treatment concentrates
    • Bulk crop protection intermediates

    3. Specialty Electronic Dye and Pigment Manufacturing

    Manufacturers of high-performance electronic dyes integrate 8-fluoro-4-hydroxyquinoline for its ability to introduce stable fluorinated moieties that enhance color fastness and charge mobility. It participates in fine-tuned cyclization and substitution reactions, producing advanced intermediates for use in optoelectronic application dyes. The compound’s purity and trace element profile are controlled to meet electronic material standards, safeguarding device performance against batch-to-batch variability.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) restricting hazardous substances in electrical and electronic equipment
    • IEC 62474 Declarable Substances Standard for the Electronics Industry
    • ISO 9001 Quality Assurance for Specialty Chemical Dyes
    • IPC-1752 Material Declaration for the Electronics Industry

    Typical usage ratio

    • 1–4% by weight in precursor dye synthesis reaction volumes, modulated depending on target pigment molecular structure and shade intensity requirements for each end application (e.g., light-emitting diode panel dyes).

    Downstream process integration

    • Dosed directly to coupling and condensation reactions following solvent exchange, forming the key nuclei before final electrophilic fluorination.

    Final product types

    • Photoresist materials for printed circuit boards
    • OLED and LCD color filter dyes
    • Conductive pigment suspensions for display manufacturing
    • Security printing dyes used in electronics

    4. Veterinary Pharmaceutical Ingredient Production

    Producers of veterinary actives utilize this raw material to develop animal health intermediates where fluorinated quinolines are specified for their broad antimicrobial spectrum and chemical stability. Integration occurs in GMP-compliant synthetic suites to guarantee batch traceability, and the level of inclusion responds to veterinary monograph guidance and final application specifications, ensuring species-specific safety and residue compliance.

    Industry compliance standards

    • VICH GL33 Good Manufacturing Practice for Active Substances used as Starting Materials in Veterinary Medicinal Products
    • EU Regulation (EC) No 470/2009 on Residue Limits of Veterinary Medicinal Products
    • USP Compendial Requirements for Veterinary Drug Substances
    • China Veterinary Pharmacopoeia (2020 Edition)

    Typical usage ratio

    • 0.3–1.5 molar equivalents per target molecule in animal-use antibiotic synthesis, proportionate to final batch theoretical yield and veterinary product class (oral, topical, or injectable formulations).

    Downstream process integration

    • Added to primary heterocyclic formation stages, followed by filtration and controlled crystallization steps to isolate veterinary-use actives for secondary formulation.

    Final product types

    • Veterinary API powders for oral administration
    • Solutions for animal injectable use
    • Premix actives for medicated feeds
    • Veterinary topical antimicrobials
    Free Quote

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    Certification & Compliance
    More Introduction

    8-Fluoro-4-Hydroxyquinoline: Field Notes from the Manufacturer

    Why 8-Fluoro-4-Hydroxyquinoline Earns its Place in the Lab

    8-Fluoro-4-hydroxyquinoline isn’t just another specialty chemical that sits on the shelf waiting to fill a narrow need. Anyone who steps into a production line or research bench can tell by its reputation—this compound cuts a unique figure in the world of heterocyclic building blocks, making a mark where precision and consistent quality matter most. Many ask us, as producers, what sets this molecule apart from the dozens of other quinoline derivatives. We don’t have to look far for answers; every batch we make tells a story about stability, adaptability, and how the small substitutions on a ring system can open up big opportunities in medicinal and agrochemical research.

    Specification Built from the Ground Up

    Our 8-fluoro-4-hydroxyquinoline is offered as a pure, high-grade powder, specifically crystallized and filtered for the cleanest downstream reactions. From continuous reactor temperature control to verified solvent removal, we eliminate every possible contaminant that could throw off sensitive syntheses. The final product shines as a free-flowing, off-white crystalline solid. We stand behind a typical purity that regularly exceeds 98% by HPLC, and moisture is kept to trace levels. Because we run full-lot analytical on each batch with techniques ranging from NMR to LC-MS, our customers count on the structural fidelity batch after batch.

    This molecule weighs in at 163.14 g/mol, and as a practical matter, it remains stable at ambient conditions, sealed tightly against air and light. We work daily to ensure that packaging runs as cleanly as everything else we do, because the best synthetic work in the world means little if someone handles the product as an afterthought. There’s no room or patience in a scale-up operation for poorly dried solids, or for chemical dust clouds that lose grams where every fraction points toward cost or waste.

    The Chemistry Behind the Name

    Fluorine atoms bring more than just resistance to metabolic breakdown—they push reactivity in smart, targeted ways, especially in aromatic systems like quinolines. Researchers often hunt for ways to balance bioactivity with stability, and this compound answers that challenge by anchoring a fluorine at the 8-position, right on the quinoline ring. From the production side, the site-selective fluorination isn’t trivial. We reject off-flavors in our synthesis because one misplaced atom can spoil downstream cross-couplings, hydrogenations, or oxidations. With 8-fluoro-4-hydroxyquinoline, every substituted position carries years of cumulative process know-how.

    For synthetic chemists, the hydroxy group at the 4-position opens another door. This functional handle gives direct access to ethers, esters, or coupling reactions without the risk of unwanted rearrangements. Try building the same complexity onto the parent quinoline or onto a methylated analog, and the story changes. 4-hydroxy provides not only synthetic access but also a quick pivot for those chasing patent landscapes or scaffold-hopping in hit-to-lead campaigns.

    Unique Advantages over Other Quinoline Derivatives

    Quinoline scaffolds have seen every kind of substitution, but the specific pairing of fluorine at 8 and hydroxy at 4 has direct effects in how the molecule behaves both in vitro and in process chemistry. Fluorine tweaks the electron density of the ring, warding off some oxidation reactions while potentiating nucleophilic aromatic substitutions elsewhere. From our pilot plant to full-scale reactors, this fine-tuning shows up as increased reliability in coupling yields and cleaner extractive workups.

    We’ve handled dozens of analogs over the years—6-fluoro, 7-fluoro, and multi-ring expanded systems all have their place. Yet, as a single substitution, 8-fluoro strikes a balance where cytotoxicity, metabolic stability, and synthetic tractability align for pharmaceutical investigators looking to develop antibacterials, antimalarials, or enzyme inhibitors. In contrast, our customers who work with simpler quinolines often report higher rates of side reactions or breakdown during scale-up.

    The 4-hydroxy site creates a reactive anchor absent in other fluoroquinolines, especially those substituted at different positions or protected by methyl or alkoxy groups. This group paves a simpler and more reproducible road toward further diversification without recourse to heavy protection-deprotection cycles that add cost and time. Our experience tells us, plain and simple: less handling, fewer surprises, and strong consistency in product performance.

    Applications We’ve Witnessed Across Sectors

    Rarely does a month pass without at least one inquiry from a pharmaceutical group seeking to build out new antibacterial agents based on the quinoline core. The 8-fluoro group in our product serves as a keystone for blocking undesired metabolic processes—often crucial when testing compounds for bioactivity in animal models or cell cultures. Since regulatory agencies can scrutinize metabolic byproducts, having a stable fluoroquinoline backbone saves researchers from unforced errors in early screening.

    Others come to us from the world of agrochemicals, where modifying plant defense pathways demands both structure-activity insight and scalable, clean materials with robust regulatory documentation. Over the years, we’ve watched the 8-fluoro-4-hydroxy scaffold form the core of fungicidal development and plant-protection agent screens because it stands up against photo-degradation and stays active in hostile soil microclimates. Natural product chemists reach for this compound while mapping out new antifungal or antiparasitic leads.

    The reach continues into dye and pigment research, where the electron-rich nature of the hydroxy group and the electron-withdrawing fluorine create interesting color fastness properties. Instead of dealing with rapid fading or chemical inactivity from similar quinolines, these tailored ring modifications open a fresh chapter for those searching out stable chromophores.

    What the Production Line Teaches Us about Reliability

    It’s easy to talk of purity and usefulness, but actual chemical manufacturing teaches respect for process discipline. Every month, we see the pressures of fluctuating raw material markets, changing environmental requirements, evolving customer specs, and the realities of chemistry at scale. 8-Fluoro-4-hydroxyquinoline proved itself adaptable in the face of such challenges: a reliable reaction profile gives predictable yields, easy filtration, and consistent profiles on analytical checks—even when running hundreds of kilograms per campaign.

    This advantage goes beyond technical sheets. For a manufacturer, routine translates directly to less downtime, fewer rejected lots, savings on solvents and energy, and trust among those developing new products or scaling from milligrams to metrics tons. We finished one campaign last year where the cost variance from missed specifications on a less robust analog grew into the low six figures. This experience keeps us committed to discipline, long-term partnerships, and batch-to-batch traceability. Our chemists often hand-check the physical characteristics of every shipment before loading. Not out of routine, but out of pride in product delivered with confidence.

    Addressing Synthetic Challenges in Real Life

    As manufacturers, we deal with the fine balance between reactivity and selectivity. The methods behind introducing a single fluorine atom without scrambling the entire quinoline ring are not always forgiving. Early in our production, we noticed that reaction conditions—even tweaks as seemingly minor as solvent polarity or degree of agitation—could throw NMR signatures off by just enough to lose the batch for tight pharmaceutical applications.

    The solution came not from chasing new technology for its own sake, but from carefully walking through each synthesis stage, monitoring reaction progress with frequent spot-checks, and leveraging feedback from colleague partners who run downstream applications. Over time, we solidified a protocol that brought reproducibility and eliminated off-target fluorination.

    We learned, too, that crystal habit makes a difference when it comes to customer outcomes. A dustier, more amorphous solid might still pass a chemical assay, but it clogs reactors during downstream runs or fails to pack evenly in automated dispensing machines. Through hundreds of iterations and paired close-out meetings, we tuned recrystallization and drying methods until our product delivered not just in chemical purity but in physical consistency.

    Supporting Research Needs, Not Just Orders

    We’ve spent many afternoons on the phone with clients walking through not just storage or shipping needs but also tailored tweaks to meet unique research demands. Specialty quinolines carry a reputation for headaches in shipping and handling, yet we’ve reduced worry by improving packaging, shortening delivery timelines, and—where needed—adjusting lot sizes to minimize degradation or waste.

    Supporting E-E-A-T—Experience, Expertise, Authoritativeness, and Trust—isn’t abstract. We back up claims with a track record of supporting published research, regulatory filings, and complex custom syntheses. Our technical team fields requests for additional documentation—certificate of analysis, spectral data, process residuals—and sometimes walks clients through structure confirmation on joint calls, screen sharing full spectral libraries and supply chain transparency documentation.

    We stand by every delivery, making it a point to address challenges before they can disrupt routines in a client’s lab or plant. Any chemist facing a rush timeline or grant deadline knows the value of speaking directly to a manufacturer who remembers their process in detail—not rerouting questions to generic distributors who lack technical background.

    Lessons from Partner Feedback and Industry Trends

    Feedback from those working on scale-up, formulation, and even biological screens often drives our iterative improvements. For instance, researchers developing active pharmaceutical ingredients highlighted that a trace impurity—undetectable via simpler color or melting point checks—has the potential to derail later enzymatic assays. We invested in higher-resolution chromatography validation and extra purification steps. Though this can raise unit cost, the end result supports cleaner, defensible bioactivity claims for those seeking regulatory approval.

    Others in agricultural development noted that previous lots of imported quinolines from traders ran into photoinstability issues in field trials. Responding to this, we ran controlled stability studies under simulated solar exposure, refining our drying and packaging cycles to stave off photo-induced degradation during transit and split-use cycles.

    More broadly, global regulatory bodies raise the bar every year, pushing for full transparency on supply chain, batch traceability, environmental impact, and process safety. We match these expectations, proactively disclosing pathway impurities, residual solvents, and byproduct profiles to our research and regulatory partners. Ongoing investment in greener processes—more efficient reactions, closed-cycle solvent recovery—aligns with demands for both performance and responsibility.

    In Sum: What 8-Fluoro-4-Hydroxyquinoline Brings to the Table

    For us, the story of this quinoline analog isn’t told through standard catalog numbers but through daily conversations, process adjustments, and hands-on engagement with end users. It’s a compound that stands up under scrutiny, supporting not just experiments but commercial-scale production lines and clinical candidate pipelines. Each kilogram shipped reflects the checks, controls, and expertise we stake our reputation on.

    The versatility of 8-fluoro-4-hydroxyquinoline sets it apart from a sea of other building blocks. The pairing of position-specific fluorination and hydroxy substitution enables creative solutions across pharmaceutical, agricultural, and material science fields—delivering cleaner reactions, robust resistance to breakdown, and greater downstream adaptability. The long hours invested into production stability, customer collaboration, and real-world validation pay off every time a new innovation traces its roots back to this molecule.

    Chemists, formulation scientists, and process engineers know the difference between an ingredient pulled off the shelf and one produced with targeted precision, batch integrity, and technical backup. This has been our experience running the line—not taking shortcuts, always listening to partner feedback, and refining the approach continuously. In every respect, 8-fluoro-4-hydroxyquinoline earns its place on the bench by delivering tangible, documented value, backed by years of focused manufacturing knowledge and an ongoing partnership with the people who push the boundaries of science and industry.