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8-Acetoxyquinoline

    • Product Name 8-Acetoxyquinoline
    • Alias 8-Quinolinyl acetate
    • Einecs 242-551-9
    • 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
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    Specifications

    HS Code

    423825

    Name 8-Acetoxyquinoline
    Chemical Formula C11H9NO2
    Molecular Weight 187.20 g/mol
    Cas Number 3034-41-1
    Appearance White to pale yellow crystalline powder
    Melting Point 87-89 °C
    Boiling Point Unknown
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >98%
    Storage Temperature Store at 2-8 °C

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

    Packing & Storage
    Packing 8-Acetoxyquinoline is supplied in a 25g amber glass bottle with a tamper-evident cap and clear hazard labeling.
    Shipping 8-Acetoxyquinoline is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be handled in accordance with all regulatory and safety requirements, including appropriate labeling. Transport is typically via ground or air, as per chemical shipping standards and relevant local and international regulations.
    Storage 8-Acetoxyquinoline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizing agents. Protect from moisture and heat. Store in a designated chemical storage cabinet, clearly labeled and in accordance with local regulations for hazardous chemicals. Ensure appropriate safety procedures are followed when handling and storing.
    Application of 8-Acetoxyquinoline

    Applications of 8-Acetoxyquinoline in Industrial Manufacturing

    8-Acetoxyquinoline plays a key role as an intermediate and functional additive in a variety of industrial manufacturing sectors. As a direct manufacturer, we ensure each application batch meets stringent requirements for process control, purity, and regulatory alignment specific to diverse downstream markets. The sections below offer detailed insights into how industrial customers deploy this material in high-value formulation systems and specialty end-products.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers incorporate this compound as an essential building block in the synthesis of certain active pharmaceutical ingredients, particularly where the quinoline core scaffolding is required for later-stage functionalization or ring transformation. The purity and acetylation degree influence reaction yields and impurity control, making close alignment to GMP and pharmacopoeial standards mandatory throughout production. Batch integration typically occurs via early-stage condensation or cyclization protocols before further derivatization and salt formation, culminating in APIs used for anti-infective and anti-malarial medications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidelines
    • USP and Ph. Eur. monograph requirements for specified APIs
    • 21 CFR Part 210 and 211 (FDA cGMP regulations)
    • EDQM CEP (where required by European clients)

    Typical usage ratio

    • Applied at 0.9–1.2 molar equivalents based on desired API core; adjusted per synthetic pathway for yield and impurity minimization

    Downstream process integration

    • Introduced in initial condensation or ring closure steps within multi-stage chemical synthesis
    • Subsequent deacetylation, alkylation, or substitution as dictated by the final API structure
    • Strict control of reaction environment to meet impurity profile targets

    Final product types

    • Generic and branded anti-malarial APIs
    • Intermediate blocks for antibacterial drugs
    • Custom pharmaceutical intermediates for contract development

    2. Organic Luminescent Material Production

    Chemicals and materials companies utilize this raw material in the preparation of organic luminophores and fluorescent dyes. The acetoxy group increases precursor solubility and facilitates targeted functionalization, particularly for sensor compounds, photoinitiators, and optoelectronic dye precursors. Synthesis protocols frequently call for high batch reproducibility and trace impurity management. Regulatory supervision is focused on REACH and environmental handling specifications given the downstream application in advanced imaging, security printing, and electronic displays.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006) compliance for substance registration and evaluation
    • RoHS Directive (for electronic dye end-uses)
    • GHS/CLP labeling and documentation practices
    • ISO 14001 Environmental Management where required by downstream OEMs

    Typical usage ratio

    • 0.5%–2% by weight as a precursor in dye synthesis; ratio adjusted for chromophore loading and target emission characteristics

    Downstream process integration

    • Condensed with aryl/alkyl reactants in the first stage dye precursor synthesis
    • Deprotection or further acetylation during later modification steps
    • Integrated into polymer carriers or liquid crystal matrices for final device applications

    Final product types

    • Organic light-emitting diode (OLED) materials
    • Fluorescent sensor dyes
    • Security and anti-counterfeiting ink formulations

    3. Metal Ion Chelation Agent for Analytical Reagents

    Manufacturers of analytical reagents leverage this compound as a high-selectivity chelation agent for metal cation detection and extraction systems, especially in spectrophotometric analysis kits and industrial monitoring solutions. Its acetoxy functionality promotes controlled reactivity, allowing downstream producers to fine-tune sensitivity and reduce cross-reactivity with background ions. Adoption within this segment centers on batch reproducibility, verified chelation parameters, and environmental safety standards, with a focus on minimizing interference in multi-ion analytical platforms.

    Industry compliance standards

    • ISO 9001 Quality Management System for analytical reagent production
    • ISO/IEC 17025 tests for batch consistency and analytical accuracy
    • OECD chemical safety assessment guidelines
    • GHS-compliant hazard labeling and transport documentation

    Typical usage ratio

    • Formulated at 0.01–0.1% w/v as a chelating agent within complexometric reagents; proportion modified for target cation and detection sensitivity

    Downstream process integration

    • Added during functionalization stage of analytical reagent concentrate preparation
    • Blended with buffer and indicator dyes before packaging into diagnostic kits
    • Batch tested for chelation index and blank interference prior to distribution

    Final product types

    • Photometric water and soil testing kits
    • Spectroscopic calibration reagents
    • Industrial metal ion detection test strips

    4. Agricultural Fungicide Intermediate Manufacturing

    Primary agrochemical formulators leverage this key intermediate when designing and producing specific classes of fungicide active substances, especially those based on quinoline or quinoxaline derivatives. The acetoxyquinoline motif enables strategic pathway entry for further ring functionalization or halogenation, essential in the development of crop protection agents with targeted bioactivity. Compliance focuses on pesticide residue tolerance, by-product control, and regulatory traceability as required by global crop protection regulations. Integration occurs at the advanced synthesis stage before active moiety derivatization and formulation into market-ready products.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) guidelines
    • European Regulation (EC) No 1107/2009 for plant protection products
    • EPA FIFRA pesticide registration requirements (USA)
    • ISO 17034 Reference Material Producer Certification for batch traceability

    Typical usage ratio

    • Used at 1–1.1 mole equivalents in synthesis route as dictated by target active structure; ratio refined by target conversion and by-product management needs

    Downstream process integration

    • Entered as a core intermediate in ring elaboration or halogenation steps
    • Subsequently processed by oxidation, reduction or etherification to reach active fungicide
    • Subjected to impurity clearance and formulation screening for regulatory submission

    Final product types

    • Fungicide active ingredients (e.g., quinoline-derived fungicides)
    • Custom agrochemical intermediates for multinationals
    • Technical concentrate supply for downstream formulation

    5. Specialty Polymer Additive for Coating Resins

    Polymer and coating manufacturers integrate the compound as a specialty additive to impart enhanced UV resistance, color stability, or surface functionality in high-performance resins and films. The unique acetoxyquinoline structure enables controlled interaction between the polymer matrix and protective or decorative additives, improving final material consistency and durability. Regulatory landscape centers on environmental emissions, worker safety, and downstream product certifications. Addition timing and concentration require precise control to balance target performance with processability and cost.

    Industry compliance standards

    • EU Regulation No 10/2011 on plastic materials and articles in contact with food (where relevant)
    • ISO 16000 for VOC emissions during production
    • US EPA TSCA chemical notification for industrial additives
    • DIN EN 71-3 (migration of certain elements for toy coatings)

    Typical usage ratio

    • 0.05–0.2% by weight in polymer or resin blends; actual ratio determined by durability and migration study results

    Downstream process integration

    • Dispersion into liquid resin or pre-polymer mixture before curing/polymerization
    • Co-extruded with base polymer for film production
    • Post-blending for specialty coatings or masterbatch production

    Final product types

    • UV-resistant coatings and varnishes
    • Functionalized polymer films for electronics and packaging
    • Specialty masterbatches for coloring and stability
    Free Quote

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    Certification & Compliance
    More Introduction

    8-Acetoxyquinoline: More Than Just a Chemical

    Chemistry has a habit of surprising even the most experienced manufacturers, and 8-Acetoxyquinoline is a fine case. Our team first worked with this molecule over a decade ago, just as the demand for acetoxy-substituted quinolines began to pick up. We have always believed that product value grows with deep process understanding and hands-on production work, not just textbook chemistry. Our batch lines push this chemical to tight purities with a genuine focus on what the end-user faces in the lab and on the factory floor.

    The Chemistry and Production Know-How

    8-Acetoxyquinoline, also known as quinolin-8-yl acetate, carries an acetoxy group neatly onto the edge of the quinoline ring. As organic chemists, we see the difference that the acetoxy at the 8-position brings to reactivity and downstream utility. The molecule behaves differently compared to unsubstituted quinoline or those bearing other esters. Our scientists don’t just run the standard acetylation—time and solvent play a real role in yield and impurity profile. In our reactor halls, temperature control and gradual addition make or break an entire kilogram batch, and subtle shifts during crystallization have taught us more about this product than any literature reference.

    We source our starting materials directly and screen them with high-performance liquid chromatography for trace amine and nitro contaminants. In our view, if you don’t control incoming raw materials, you cannot claim to be a manufacturer you, in fact, just repackage. So, each lot leaving our site sees HPLC and NMR scrutiny. Users working in pharmaceutical research especially notice unexpected trace byproducts, so we never cut a corner by substituting grades. Customers have run into ring chlorination traces from lesser sources. In response, we rewrote our reaction quenching steps, eliminating persistent halogenated side products years ago.

    Application Breadth: Beyond the Textbook

    Many standard descriptions list “pharmaceutical intermediate” as a major use, but speaking as someone who spends time walking the line, the molecule finds its way into metal chelation, catalyst precursor formulations, and dye chemistry as well. Pharmaceutical chemists appreciate the way the 8-acetoxy group increases solubility, but the versatility of this compound stretches further. We started getting requests about a decade past from researchers exploring functionalized ligands—turns out, the acetate group comes off easily under mild basic or enzymatic conditions. This handle opens new routes when classic ligation strategies fall short.

    Not all customers want milligram research samples; some need kilogram lots for pilot campaigns. We scale up in air-swept, sealed vessels and avoid plastic process contact, which has paid off when regulatory agencies look at extractables. One client came to us after another batch failed at the chromatography stage—plasticizers leached in during mixing from an overseas supplier’s vats. Once we tracked down and removed these problem steps, our repeat orders spoke for themselves. While some see only the raw material, we see the entire campaign resting on a clean, consistent intermediate.

    Distinctions from Everyday Quinoline Derivatives

    What sets 8-Acetoxyquinoline apart from its chemical cousins starts at the ring position. Where 2-substituted derivatives direct reactivity mainly toward electrophilic sites, the 8-acetoxy variant interacts with transition metals and organic substrates thanks to the unique spatial orientation on the aromatic core. In organometallic catalysis projects, our industrial partners report that chelation patterns change dramatically with the acetoxy group sitting at carbon-8. Such findings usually skip the mainstream product sheets, but those in the trenches designing ligands notice the impact quickly in yields and selectivity.

    The acetate side group also introduces a point of lability uncommon in more rigid quinoline ethers or straight esters. Process chemists value this when stripping protection groups under gentle conditions, limiting degradation of advanced intermediates. Years on the manufacturing floor taught us that easier workups save time, waste, and costly purification overhead. More stable ether analogs may offer shelf life, but the trade-off shows up during late-stage steps—no one wants to fight with a stubborn protecting group under a deadline. Our product lets teams keep greener chemistry in sight and avoid months of method development just to release a single functional group.

    Ensuring Purity: Real-World Testing

    Manufacturing specialty quinolines brings daily reminders of how rigorous protocols must be. We check our own batches at every stage, not just after the final crystallization or drying. Common impurities—unreacted quinoline, acetic acid, and side acetylated isomers—show up on our chromatograms during in-process QC. Each time we adjust a process parameter, it’s not just for batch record compliance; it’s because real customers flagged purity drifts in final applications. One pharmaceutical customer measured a sharp drop in catalyst efficiency linked to a persistent isomer contaminant. Their feedback pushed us to modify solvent phase ratios and bring in a new distillation stage before crystallization.

    On the analytical chemistry front, real-world users need more than a COA with theoretical values. We include side-by-side overlays of NMR and IR spectra for every lot, giving researchers confidence that what they get in the bottle matches what they see in their development work. Our belief is that surprises should not come out of a drum or bottle, and transparency with data has cemented long-term partnerships. Many times a client’s own chemists will share IR traces of questionable intermediates; we provide in-house data support and reproduce suspicious signals to track down issues together.

    Challenges in Manufacturing and Customer Support

    Scale-up does not always go as expected. Once, our pilot reactor began foaming violently during solvent swap, creating a bottleneck that slowed orders for weeks. Rather than shifting blame, we treated the event as a lesson: batch documentation now includes antifoam dosing based on product volume, and no operator skips line-sweeping logs. Another challenge with this molecule is vapor pressure and the reactivity of acetic anhydride—qualified PPE and fume systems are not an option, but a must. We advise users to store the product in airtight glass, away from bases or moisture, based on how the acetate group reacts. Our own long-term stability studies back up each guideline with measurable data rather than assumptions.

    Shipping remains a critical step that doesn’t get enough attention in chemical supply. Hot weather during transit has, in our early days, caused partial hydrolysis and sticky residue in poorly sealed drums. We overhauled container standards to require foil-sealed liners and vapor-phase desiccants, lowering incident rates in global deliveries. Informal checks from partners in India, Europe, and the US keep us on our toes, as sometimes receiving labs request sealed sublots or special documentation to align with regional tracking protocols. We see these as opportunities to strengthen mutual trust and to learn more about international differences in regulatory controls.

    Feedback Loops: How Experienced Manufacturers Learn

    Bright ideas from customers bring practical changes. A research client in organic electronics shared insights on modified workup for highly pure 8-Acetoxyquinoline, enabling them to extend the shelf life in photoresist applications. We piloted their process improvements in parallel runs and found decreased yellowing at prolonged storage—adding real value for advanced uses outside pharma and catalysis. We also encourage clients who need custom packaging sizes, call-in QC reporting, or joint method validation. This feedback fuels process evolution, pushing our standards higher each year.

    We have also seen the limits of standard approaches. Raw material bottlenecks in times of market volatility force roster diversification for our purchasing department. We built relationships with trusted upstream suppliers rather than navigating through layers of traders. Whenever we see shifted GC retention times on a sample, we track down the specific batch at the source, not just issue retests. Handling setbacks openly with long-term clients has built respect both ways—on rare occasions when customers uncovered off-spec batches, transparent investigation and make-up shipments kept their projects on schedule.

    The Human Touch in Specialty Chemical Production

    No automated system replaces the trained eye of a plant technician who knows when a vessel sounds wrong on a quiet night. Our operators spot changes in reaction hue, phase separation speed, and crystal density that instruments might miss. Over years, their notes have shaped process modifications as much as lab data has. People sometimes overlook the time and skill involved in cleaning glass and steel to prevent cross-contamination—especially when cycling from one quinoline family product to another. We reward thoroughness at each shift and share best-practice tips with new hires. This craftsman approach results in fewer lot deviations and improved operator safety.

    By holding ourselves to the highest standards in specialty organic chemicals, we pass on advantages to every researcher and manufacturer relying on purity and repeatability. We don’t view our product as just a specification to be met but as a key material supporting crucial innovations in healthcare, materials science, and analytical research. Our team does not shy away from hard questions or challenging requests. Over time, we have learned that the best innovation comes from the interplay between frontline operators, analytical chemists, and the users who push each batch to its real limits.

    Environmental and Community Responsibility

    Running a chemical plant brings responsibility for more than product supply. Waste management and emissions control around acetylating agents demand real proof of compliance, not generic statements. Our facility tracks VOC emissions every quarter, posting results for community review and to regulators. We upgraded all on-site solvent recovery lines years before regional mandates. We also divert usable by-products to partner firms for secondary value streams. Instead of landfill, a good portion finds use in industrial cleaning or other non-pharma sectors, a practice born from our drive to see zero waste as more than a slogan.

    Neighbors care about odors, so our odor abatement systems operate year-round. Regular local open days let us explain what happens behind our gates. Young students from the region visit for guided tours to see how real science and careful control turn raw feedstocks into high-value compounds that support critical industries. We have welcomed project input from local universities working on greener process optimization and offer internships so new talent can learn both the science and the ethos that keeps a facility running safely and responsibly.

    Final Thoughts from the Manufacturing Floor

    Unlike bulk industrial products, specialty quinoline derivatives such as 8-Acetoxyquinoline need constant hands-on oversight and real-world technical partnership. Innovation comes both from improvements made in our plant and from honest, sometimes tough, conversations with researchers in the field. Each kilogram produced carries the lessons earned through solving complex purification problems, ensuring safety, and listening to chemists who rely on consistency year after year.

    We remain committed to continuous improvement, not as a marketing strategy but in recognition of the shared responsibility that comes with handling specialty chemicals. Our decade-long journey with 8-Acetoxyquinoline gave us a clear sense: it is not just about molecules, but about the networks of trust, technical understanding, and long-term vision that turn an intermediate into a core part of the world’s scientific progress. The chemistry will always keep us humble and hungry for each new insight from both plant operators and end-users.