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5-Chloro-8-Hydroxyquinoline

    • Product Name 5-Chloro-8-Hydroxyquinoline
    • Alias 5-Chloro-8-quinolinol
    • Einecs 201-928-0
    • 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

    392159

    Chemical Name 5-Chloro-8-Hydroxyquinoline
    Molecular Formula C9H6ClNO
    Cas Number 130-26-7
    Appearance Pale yellow to yellow powder
    Melting Point 204-206°C
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, dry, protected from light
    Smiles C1=CC2=C(C(=C1)Cl)N=CC=C2O

    As an accredited 5-Chloro-8-Hydroxyquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a secure screw cap, labeled "5-Chloro-8-Hydroxyquinoline," hazard symbols, and product details.
    Shipping 5-Chloro-8-Hydroxyquinoline is shipped in tightly sealed containers, protected from light and moisture. It should be handled according to standard chemical safety protocols. Transport is generally performed via regulated carriers with proper labeling, documentation, and compliance with local and international chemical shipping regulations. Avoid extreme temperatures and direct sunlight during transit.
    Storage 5-Chloro-8-Hydroxyquinoline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep the chemical away from direct sunlight and sources of ignition. Store at room temperature, and ensure proper labeling to prevent accidental misuse. Always follow local regulations and safety guidelines for storage.
    Application of 5-Chloro-8-Hydroxyquinoline

    Applications of 5-Chloro-8-Hydroxyquinoline in Industrial Manufacturing

    As a direct manufacturer, we support industrial customers integrating 5-Chloro-8-Hydroxyquinoline into several complex downstream sectors. The following sections detail its validated applications, compliance standards, industrial formulation requirements, and production workflows, addressing the technical needs of each field.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antimicrobial Agents

    Pharmaceutical manufacturers use 5-Chloro-8-Hydroxyquinoline as an intermediate for developing antimicrobial drugs, especially in formulations targeting intestinal infections and topical preparations. Regulatory filings recognize this substance for its role in the synthesis pathway of several generic and branded medicines. Stringent traceability and purity control govern its pharmacological use, requiring robust analytical verification at each processing stage. End formulations adopt dosage-justified inclusion depending on local pharmacopeial guidance and product-specific toxicological data.

    Industry compliance standards

    • USP-NF (United States Pharmacopeia - National Formulary)
    • Ph. Eur. (European Pharmacopoeia)
    • ICH Q7 Good Manufacturing Practice for APIs
    • Chinese Pharmacopoeia (ChP)

    Typical usage ratio

    • 0.1% – 2.0% w/w as an intermediate; final API content varies by drug monograph and is determined after yield, purity, and pharmacological safety reviews.

    Downstream process integration

    • Enters during core heterocyclic synthesis step; undergoes coupling or substitution before isolation of the API for further formulation and tableting.

    Final product types

    • Antimicrobial tablets and capsules
    • Topical creams and ointments
    • Suppositories for gastrointestinal use
    • API bulk for export or secondary processing

    2. Veterinary Medicine Additive Manufacturing

    Veterinary pharmaceutical plants source this material for use in anti-protozoal and antibacterial preparations intended for livestock and companion animals. Safety and residue controls, along with product-specific therapeutic indices, shape the inclusion compliance and production verification. Its application predominantly supports formulations administered via feed premixes or injectables, requiring differentiated purity and particle size profiles.

    Industry compliance standards

    • VICH GLs (International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products)
    • 21 CFR 558 (FDA regulations for medicated feeds in the U.S.)
    • EMA MRL assessment (European Medicines Agency Maximum Residue Limits)

    Typical usage ratio

    • 0.05% – 1% in feed premix; 0.2% – 1.5% in injectable or direct oral dosage depending on species and withdrawal period guidance.

    Downstream process integration

    • Enters as a micronized additive post-feed blending or dissolved into solution stage for vaccine or injectable preparations.

    Final product types

    • Animal feed additive premixes
    • Veterinary tablet and oral pastes
    • Injectable veterinary drugs
    • Topical sprays for livestock

    3. Industrial Water Treatment Biocide Formulation

    Specialty chemical manufacturers incorporate 5-Chloro-8-Hydroxyquinoline as a biocidal agent in cooling tower and closed-loop water treatment programs. Documentation requires strict monitoring for discharge levels and residual handling in environmental management systems. It targets both algae and bacterial agents, justifying its controlled dosage and association with integrated water management best practices. Consistent particle size and bulk density are crucial for automated dosing system compatibility.

    Industry compliance standards

    • U.S. EPA FIFRA registration (as applicable for formulated biocidal products)
    • REACH Annex II (EC) No 1907/2006 – European Union chemical registration for professional use
    • ISO 14001 Environmental Management Systems

    Typical usage ratio

    • 2–10 mg/L in closed loop or recirculating systems; final dosage is optimized per system volume and contamination risk profile, monitored by on-site analytical testing.

    Downstream process integration

    • Dosed into the recirculating water loop post-filtration; integrated with automated chemical feeders and adjusted according to monthly bioburden monitoring.

    Final product types

    • Liquid and solid biocide concentrates
    • Chemical dosing cartridges for industrial water systems
    • Cleaning solutions for membrane and cooling tower systems
    • Pre-mixed water treatment chemicals (multi-agent formulas)

    4. Agricultural Fungicide Intermediate Production

    The agrochemical sector uses 5-Chloro-8-Hydroxyquinoline as a synthetic intermediate in the production of crop protection agents, particularly fungicides. Production-scale campaigns demand consistent quality and establish traceable records for downstream environmental and operator safety reviews. Purity, residual solvent, and metal content directly affect subsequent formulation efficacy and crop application restrictions under regional regulatory schemes.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • China GB 2763 (National Food Safety Standard - Maximum Residue Limits for Pesticides in Food)
    • OECD GLP (Good Laboratory Practice) for pesticide testing

    Typical usage ratio

    • 10% – 30% in technical concentrate during coupling/synthetic step; adjusted for specific fungicide chemistry and regulatory MRLs for agricultural produce.

    Downstream process integration

    • Reacted in the main synthetic sequence; isolated by extraction/filtration before formulation into sprayable or seed treatment products.

    Final product types

    • Technical fungicide active ingredient (bulk material)
    • Water-dispersible granules
    • Suspension concentrate pesticides
    • Crop seed treatment agents

    5. Metal Chelation Agent Production for Analytical and Industrial Use

    Producers of laboratory reagents and process chemicals employ 5-Chloro-8-Hydroxyquinoline for synthesizing metal chelators used in analytical chemistry and industrial separation. The raw material must meet stringent purity and low metal impurity demands. Processing steps require dissolution, purification, and precise pH control to yield reliable chelating compounds. Compliance documentation remains essential due to use in regulated measurement and waste treatment applications.

    Industry compliance standards

    • ISO 17034 Reference Material Producers
    • ASTM E2009 for laboratory test methods
    • RoHS Directive (2011/65/EU) for restriction of hazardous substances

    Typical usage ratio

    • 1% – 10% w/w, varying with targeted chelating capacity; adjusted for analytical reagent grades or industrial agents based on complexation kinetics.

    Downstream process integration

    • Undergoes batch dissolution and pH adjustment; proceeds through precipitation or crystallization for chelator production before drying and packaging.

    Final product types

    • Trace metal analysis reagents
    • Industrial water softeners and scale inhibitors
    • Chromatography separation supports
    • Metal recovery agents in hydrometallurgy
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    Certification & Compliance
    More Introduction

    Introducing 5-Chloro-8-Hydroxyquinoline: A Closer Look

    Our Journey with 5-Chloro-8-Hydroxyquinoline

    Every batch of chemicals carries a backstory. Years ago, our chemists noticed growing attention around 8-hydroxyquinoline derivatives, especially those featuring chlorination. 5-Chloro-8-Hydroxyquinoline (CAS Number: 130-26-7, synonyms like CHQ or chloroxine) rose to the forefront because of its valuable properties in the pharmaceutical, agricultural, and materials industries. Through hundreds of pilot runs, consistent fine-tuning, and meticulous process controls, we have tuned our process to generate reliable purity levels, typically well above 99%. Only rigorous recrystallization and state-of-the-art chromatographic testing assure the low levels of residual contaminants important for sensitive downstream uses.

    Understanding This Molecule’s Profile

    Unlike its close relative 8-hydroxyquinoline, the 5-chloro substitution adds more than just a chlorine atom to the structure—it pushes the compound’s whole chemical behavior in a different direction. The content of the molecule, C9H6ClNO, offers an apparent yellow to amber crystalline powder, faintly aromatic, with decent solubility in ethanol and organic solvents, but limited movement in water. Researchers, formulators, and industrial users prize this selectivity as it helps to control unwanted leaching or interaction in finished products. Side-by-side with standard hydroxyquinoline, 5-Chloro-8-Hydroxyquinoline demonstrates enhanced antimicrobial activity and a broader band of antifungal and antiseptic capabilities. Over decades of documented use, especially in medicines and personal care applications, this precision has made it a more reliable replacement in many situations where resistance or unwanted side effects from less-selective antimicrobials caused setbacks.

    Compare and Contrast: Why Not Any Hydroxyquinoline?

    Stepping into a lab or factory that expects sensitive, consistent results, you count on more than a chemical name on a container. 5-Chloro-8-Hydroxyquinoline doesn’t just shoehorn into roles meant for ordinary 8-hydroxyquinoline or 5,7-dichloro analogs. That single chlorine substitution at the 5-position delivers a tight spectrum of biological activity, offering targeted antimicrobial and antifungal results. Classic 8-hydroxyquinoline—sometimes called oxine—covers a different ground, commonly used for metal ion complexation or as a forest of broad-spectrum applications, but often falls short on selectivity or can present more environmental concerns. Double-chlorinated options (like 5,7-dichloro-8-hydroxyquinoline) swing even farther, pushing issues around toxicity or unwanted side-reactions.

    With a single halogenation, this product stands apart. It lends a measured touch, supporting precision where safety, regulated residue, or selective inhibition matter most. Users in the over-the-counter drug space have leaned on this attribute for years; it anchors topical treatments, antifungal creams, and specialty disinfectants. In crop protection, formulators appreciate the reduced environmental burden when residues are tracked stringently. We have witnessed formulators troubleshooting legacy materials displaced by regulations, who then turn to 5-Chloro-8-Hydroxyquinoline to achieve compliance without losing control over microbial stability.

    Industrial Manufacturing: Lessons Learned

    Running a chemical plant, expectations sit high. Our team learned early that straightforward chlorination reactions often spiral into unpredictable yields, unless handled with painstaking attention. Direct chlorination of 8-hydroxyquinoline with molecular chlorine can produce a mess of over-chlorinated byproducts if the temperature or reaction times slip. So we built process controls around phased addition and careful cooling cycles. Instead of chasing yield at the cost of purity, we focus on consistent crystal formation and slow, gentle purification steps. Real-world lessons highlighted hidden impurities that could sneak in if any step cut corners—from pH swings to solvent choice, every detail impacts the outcome. Over years, iterative process improvements pushed batch failure rates to just a fraction of what we saw in the early days.

    Our QC department plays referee through every run. Spectrophotometric analysis, HPLC, and loss-on-drying tests remove any guesswork. The sort of oversight that picks up a one-degree deviation or a shifted melting point (real-world: usually 242 to 244°C) gives our product a reputation among technical buyers. Downstream processors in the pharma or crop protection world don’t accept less, because even minor contaminants lead to batch failures or regulatory hold-ups.

    Where 5-Chloro-8-Hydroxyquinoline Finds a Home

    Medicinal chemistry and health care drift toward 5-Chloro-8-Hydroxyquinoline for good reason. We work with partners who produce antiseptics, topical antifungals, and preservative systems. They select this compound for its activity spectrum, but just as importantly, for its track record of predictable skin compatibility. Compare the regulatory dossiers on general hydroxyquinoline to 5-chloro: serious review consistently shows a lower tendency for dermal sensitization or toxicity. That does not invite reckless use, but formulators building OTC drugs or medicated shampoos look for this kind of data-backed assurance.

    For personal care, the shift away from parabens and persistent phenolics has left a gap. 5-Chloro-8-Hydroxyquinoline steps in, covering microbial protection for creams, ointments, and even sprays, where regulators are watching for both performance and residue control. Its application in dental products, antifungal powders, and even certain veterinary lotions comes up precisely because the balance between potency and selectivity fits real demands.

    In crop protection, the compound plays a different tune. We have customers who run greenhouse trials: adding the material to coatings or growth substrates drives down incidence of soil-borne fungi and bacteria. Because environmental authorities clamp down aggressively on persistent breakdown products, the structure of 5-chloro-8-hydroxyquinoline attracts scrutiny, but a robust scientific dossier coupled with cautious application supports continued registration in many major markets.

    Further outside pharmaceuticals and agriculture, a handful of industrial applications lean on this molecule. Complexation of metal ions, specialty polymer stabilization, and use as an intermediate pop up less often but illustrate the versatility. The compound’s balanced reactivity profile and strong shelf-stability lower the risk profile in storage, even under moderate temperature swings.

    Using Our Product: What Customers and End Users Tell Us

    Laboratories and manufacturers who choose our product highlight more than the chemical data sheet. Comments often point out that our material comes in a granular, free-flowing powder that avoids caking—a direct result of our post-synthesis drying protocol. Long-term storage, especially for pharmaceutical manufacturers buying in bulk, hinges on this consistency: a clumpy or partially degraded shipment doesn’t make it through incoming goods inspection. Some clients shared that switching away from alternative suppliers overcame regulatory headaches because our routine batch release includes not just HPLC purity, but heavy metal screening and consistent documentation for audit trails.

    Users working up formulations in semisolids or liquids have found that the measured solubility in ethanol or DMF means fewer surprises during scale-up. Some competitors offer slightly higher bulk density, but our QC-driven control of the particle size distribution gives smoother dispersion and less mechanical wear for their mixing pumps. Smaller-batch customizations, such as low-dust versions for inhalable or sterile incipient uses, stemmed directly from customer feedback, leading us to invest in more precise milling and dust control inside our facility.

    Handling in the workplace deserves a mention. Our internal safety officers, after plenty of trial and error, developed workflow layouts to avoid cross-contamination issues typical in multi-product plants. Some competitors run continuous lines and face higher risk of mixing with other halogenated products. Our batch-segregated process translates into lower risk for allergen or impurity carry-over, reflected in low recall rates across a decade of tracking.

    Quality, Stability, and the Regulatory Landscape

    Quality and regulatory acceptance can make or break a product like 5-Chloro-8-Hydroxyquinoline. National pharmacopeias and regulatory agencies place this compound under careful review. In pharmacopoeial listings where it features, requirements touch on identification, limits for related substances, and maximum residual solvents. Batch records matter—lost paperwork or incomplete COAs have stopped more than one shipment in customs. Our chemists keep a running archive, going back for each lot, tying analytical results to shipping documents. Routine audits by outside third parties help keep us sharp. Internal fail-safes—like double barcoding and sample retention past expiration—have solved more than one downstream investigation.

    For international shipping, customs look closely at this class of antiseptic-related chemicals. Updated safety sheets prevent delays; robust container sealing keeps atmospheric moisture from degrading open shipments. In some regions, authorities demand nearly solvent-free material, driving us toward vacuum drying and solvent-stripping technologies most suppliers skip for cost reasons.

    The Environmental Angle: Challenges and Response

    Every chemical producer faces increasing scrutiny about environmental fate and safety. Chloroquinoline derivatives, including this one, draw special attention because halogenated aromatic compounds feature in environmental control debates. Over the years, we listened to both the regulatory community and independent lab reviewers voice demands for credible biodegradation studies and data on aquatic ecosystem effects. Real-world compliance has meant investing in advanced waste-water treatment for our plant, plus extensive batch monitoring for halogenated process residues.

    During industry workshops, participants from crop protection and personal care highlighted a common point: regulators and end-users now want transparent reporting on degradation products and environmental persistence. For us, the push led to more collaboration with academic partners analyzing real sample breakdown in soil and water. Over time, the emerging picture shows that single-chlorinated quinolines have faster breakdown compared to multi-chlorinated alternatives, with fewer persistent byproducts. This means 5-Chloro-8-Hydroxyquinoline generally stands a better chance of passing environmental risk assessments—if used responsibly and under controlled conditions.

    Packaging and supply chain adjustments followed. Our logistics team introduced recyclable, low-permeability liners to bulk drums. The aim was to prevent moisture absorption during long ocean or overland shipments. These moves reduce spoilage and waste, but also keep grade stability, avoiding unexpected polymorphic transitions that might change solubility or handling. Periodic review with our partners updates these standards as new research tightens performance benchmarks.

    Troubleshooting: Common Customer Challenges and Practical Answers

    Over the years, customer support requests have spotlighted areas where real-world challenges emerge. Sometimes a formulator will question why a clear topical gel grows hazy overnight; experience suggests incomplete dissolution of 5-Chloro-8-Hydroxyquinoline, often due to choice of cosolvent or mixing speed. We suggest pre-warming both the solvent and compound, steering clear of rapid temperature cycling, and always performing small pilot tests before full-scale mixes. Other users have tried dissolving the compound in hard water, meeting slow uptake or precipitation. Using pretreated, softened water or switching to an appropriate alcohol generally sidesteps the issue.

    In agriculture, challenge arises when users overshoot intended concentrations, chasing fast microbial knockdown. Our long engagement with the field tells us that more does not mean better: optimal results come from adherence to trial-based mixing rates. Excessive dosing only raises cost and unnecessarily increases the regulatory burden of environmental residue tracking.

    Shelf life, always a hot topic, depends on careful closing and storage below 25°C, kept dry. Samples stored on the edge of production areas in humid climates have shown color shifts or caking, reducing performance. We advise storage in sealed containers with desiccant packs, away from direct sunlight. Our retained sample program, where we hold reference material from every lot for regular re-testing, acts as a real-world backup should customers run into shelf-life questions months or years later.

    A Manufacturer’s Perspective: Building Trust Through Transparency

    As a chemical producer, day-to-day trust builds not just on lab numbers but on years of performance, honest reporting, and practical response to customer issues. We have learned that buyers large and small come back not only for chemical consistency but for the reassurance of supply, documentation, and collaborative problem solving when challenges arise. Open access to our technical team, willingness to share validated data, and communication during market uncertainty build confidence audiences have come to rely on.

    Market shifts and regulation mean no static product or process ever survives for long. We keep refining our facility, adjusting our purification and packaging to rising demands. Emerging trends—shifts away from legacy preservatives, stricter environmental controls, push for lower-residual pharmaceuticals—all steer our ongoing product development. We see 5-Chloro-8-Hydroxyquinoline holding relevance across industries because its carefully balanced properties meet real-world needs without overstretching risk profiles or regulatory lines.

    Feedback from technical partners often drives our next round of improvements. New analytical tools, refined particle attributes, and evolving audit standards fold back into our next production run. This loop—field experience linking directly to process upgrades—anchors our ability to offer not just a stable compound, but a trusted solution for those building their own advanced products.

    Looking Ahead: Challenges, Responsibility, and Opportunity

    Bringing a specialty chemical from production to community means walking a balancing act between innovation, cost, and accountability. We have faced and continue to face environmental risk questions, regulatory adjustment, and competitive pressures from lower-cost overseas makers. Our response remains quality-driven: documentation, supply continuity, and technical partnership. For users, the confidence in a well-characterized, robustly controlled source matters as much as the molecule itself.

    As demand grows for safer, less persistent antimicrobial solutions in both regulated and open markets, 5-Chloro-8-Hydroxyquinoline stands as a proven option, provided users respect its correct application and environmental impact. By investing continually in quality, transparency, and process innovation, chemical manufacturers can position this molecule to address the needs of pharmaceutical, personal care, and crop protection fields with confident, responsible supply.

    Our experience shows that working closely with clients and staying ahead of both regulation and practical needs achieves more than simply selling a product—we help support safer, more effective solutions for industries that shape daily life. The story of 5-Chloro-8-Hydroxyquinoline doesn’t end in the factory. It continues in the progress, safety, and reliability it brings to the hands of those who count on it in their own labs, products, and communities.