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HS Code |
840165 |
| Cas Number | 120-95-6 |
| Molecular Formula | C9H7NO |
| Molecular Weight | 145.16 g/mol |
| Iupac Name | quinoline 1-oxide |
| Appearance | white to off-white solid |
| Melting Point | 60-62°C |
| Solubility In Water | slightly soluble |
| Density | 1.25 g/cm³ |
| Chemical Structure | aromatic heterocycle with N-oxide functional group |
As an accredited Quinoline-N-Oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Quinoline-N-Oxide is supplied in a 25g amber glass bottle, labeled with chemical details, hazard symbols, and batch information. |
| Shipping | **Shipping Description for Quinoline-N-Oxide:** Quinoline-N-Oxide should be shipped in tightly sealed containers, protected from moisture, light, and incompatible substances. It is generally transported at ambient temperature, with clear chemical labeling and documentation. Ensure compliance with local and international regulations. Avoid exposure to heat and handle with caution to prevent spills or inhalation. |
| Storage | Quinoline-N-Oxide should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Keep away from direct sunlight and moisture. Proper storage prevents decomposition and preserves chemical stability. Label the container clearly and follow all relevant safety and regulatory guidelines for handling and storage. |
Applications of Quinoline-N-Oxide in Industrial ManufacturingAs a specialized chemical raw material manufacturer, we supply Quinoline-N-Oxide for a range of established industrial processes. Each application scenario below reflects authentic downstream integration, with operational insight into compliance standards, dosage ranges, manufacturing stages, and real finished product types. 1. Pharmaceutical Intermediate for Antimalarial Drug SynthesisLeading pharmaceutical manufacturers incorporate Quinoline-N-Oxide as an oxidation intermediate during the synthesis of critical antimalarial compounds, particularly 8-aminoquinoline derivatives such as Primaquine and Tafenoquine. Process engineers add our material directly into the targeted oxidation reaction, ensuring controlled N-oxide formation before reduction and subsequent derivatization. Strict adherence to pharmacopoeial standards covers all sourcing, batch records, and traceability. Batch adjustment of incorporation rates responds to route-specific molecular requirements to deliver documented API grade outputs. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisProducers of advanced crop protection agents rely on Quinoline-N-Oxide as a building block during the synthesis of select heterocyclic herbicides and fungicides. The substance functions in ring-activation and N-oxidation of quinoline backbones, supporting downstream chlorination, alkylation, or amination steps in regional toll-processing plants. Quality and trace impurity analysis align with agrochemical safety legislation and multinational registrability. Industry compliance standards
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3. Organic Synthesis Catalyst in Laboratory and Pilot Scale ProcessesFine chemical and research-scale manufacturers deploy Quinoline-N-Oxide as a phase transfer catalyst and ligand in selected oxidation and cyclization reactions. The input supports synthesis routes for complex heterocyclic scaffolds and other specialty intermediates, particularly in pilot campaigns for pharmaceutical, dye, and functional material R&D. All usage outcomes comply with responsible laboratory management, operator exposure control, and trace reactant documentation under international guidance. Industry compliance standards
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4. Photoreactive Intermediate for Specialty Dye ManufacturingManufacturers of advanced colorants and specialty dyes leverage Quinoline-N-Oxide in photoreactive modification of quinoline skeletons. It facilitates directed functionalization prior to coupling with chromophoric groups, producing color-fast and UV-resistant dyes for high-performance textile or polymer applications. The use scenario emphasizes batch record compliance, contaminant minimization, and final product regulatory acceptance for export markets. Industry compliance standards
Typical usage ratio
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Most chemists find satisfaction in getting a reaction right the first time. Around here, the learning starts after the first failed batch. Quinoline-N-oxide keeps things interesting. It finds its way onto our order lists because it brings both challenge and precision. The stuff has a habit of surfacing in work where fine-tuned selectivity matters: pharmaceutical intermediates, pesticide synthesis, dye creation, even some quirky requests from research labs that want tailored derivatives.
Our standard model of quinoline-N-oxide runs at a purity no less than 98%. Over the years, that number’s stuck because anything lower leads to headaches down the line—byproducts muddy downstream reactions, and it’s our reputation on the line if customers report inconsistent yields. We know what happens if we cut corners on dryness or settle for incomplete oxidation. From batch consistency to keeping ultra trace impurities in check, our teams test each lot using HPLC and NMR analysis with a level of scrutiny that came from troubleshooting, not from textbooks.
Quinoline-N-oxide appears as a pale yellow crystalline powder. Smells faintly chemical—less harsh than some nitro derivatives, but unmistakable. In practice, chemists choose it for N-oxidation reactions or as a building block where the N-oxide group sparks off new bonds without dragging in unnecessary baggage. The N-oxide functionality lets you tweak electron properties of quinoline cores. These changes ripple into physical behaviors—solubility increases, hydrogen bonding shifts, results in reactivity patterns that diverge noticeably from bare quinoline.
Over many production cycles, we’ve gotten to know what causes differences batch to batch. We source cores from trusted partners and run oxidation through well-aged routes based on peracid systems, dialing in the stoichiometry and temperature controls to keep the end-product from harboring unreacted parent quinoline. By monitoring for byproducts and fine-tuning the workup process, our team achieves a crystalline material that releases little moisture to the atmosphere. Fastidious drying protocols ensure long shelf life and straightforward handling for customers weighing milligrams for analytical purposes or kilos for commercial runs.
Many newcomers expect all N-oxide compounds to behave similarly. We’ve seen sharp differences in practice. Quinoline-N-oxide serves as a reliable ligand in metal-catalyzed transformations, outlasting more fragile isomeric forms. Pyridine N-oxide, for example, sometimes decomposes under the temperatures our clients push for in scale-up reactions. Quinoline-N-oxide’s larger aromatic system provides stability—it resists rearrangement, giving you predictable outcomes batch after batch. Some users try to substitute isoquinoline N-oxides for convenience, but the electron distributions aren’t the same. When we hear about side reactions during attempted substitutions, it’s usually because of overlooked differences in molecular structure—quinoline brings 1,2 ring fusion, isoquinoline moves it to 2,3.
Our take, as the factory actually making these molecules, is that not all N-oxides are substitutes in multistep syntheses. In earlier years, some customers reported trouble using third-party material with higher levels of residual reactants. Our process engineers trace those problems to rapid oxidation steps—skipping the careful temperature staging common to small academic labs. We prefer slower peracid addition and staged cooling. This simple choice sidesteps impurity formation and gives users material that matches their spectral needs without tweaking their own reaction setups.
Lab users tend to request quinoline-N-oxide for niche reaction setups. Catalysis teams have told us they value its role as a ligand: it stays put, coordinates how they expect, and supports unusual oxidation states in some palladium or ruthenium complexes. Synthetic chemists tap it for activating quinoline rings at specific positions—especially for C–H activation and arylation tasks that weren’t possible ten years ago. In dye chemistry, research teams blend the compound into routes where the N-oxide directly affects hue and shade permanence for specialty textiles and imaging applications.
One common thread in feedback from researchers is that high-purity material saves them expensive troubleshooting. Impurities can mimic target signals in NMR or mass spec work, slowing down both R&D and QA processes. Our batches frequently show single, sharp peaks, which is what analysts expect in reference samples. We strip out colored byproducts until the product runs bright and consistent. Pharmaceutical customers extend this feedback to cleaner conversions into quinoline derivatives with API relevance, where impurities can quickly trigger regulatory headaches.
Process chemists using our quinoline-N-oxide for scale-up comment on its solubility profile. The N-oxide shifts polarity enough to favor certain solvent systems such as methanol, acetonitrile, and moderate aqueous mixtures. More lipophilic derivatives of quinoline don’t always dissolve as readily, causing filtration and transfer bottlenecks—issues our product avoids by remaining manageable through common transfer and mixing steps. We receive few calls about caking or bridging in drums, because moisture content is monitored up to dispatch.
Some downstream users need to convert the N-oxide group into other functionalities—carbonyl, amino, or even radical traps. Our experience shows quinoline-N-oxide stands up to these demands: the batch-to-batch consistency lets chemists skip repeat purifications. We manage the oxidation’s selectivity to keep side products like quinone imine to negligible levels. Routine QC testing at each lot’s release supports client requests for spectra and impurity profiles—a level of transparency becoming increasingly sought after in modern fine chemical procurement.
People outside chemical plants rarely see what separates a good batch from a great one. Years of hands-on production revealed that consistent reactor loads and agitation protocols make the difference between a product that helps research run smoothly and one that sparks complaints. Peracid addition rate, quenching methods, and post-reactor workup have each prompted reengineering over the decades here. Some trial-and-error moments led us down the wrong path—until failure pushed us to redesign with input from the operators actually running the lines.
Each reaction step logs time, temperature, and pH every minute. Shortcuts that look fine on paper tend to show their faults during real-world scale-up: formation of tarry side products, color drift in the crystalline powder, or poor filtration times. Attention to raw material traceability and legacy supplier relationships serves as an insurance policy for quality. Our purchase teams liaise directly with upstream partners, drawing on years of reliability and mutual accountability. We’ve learned the real costs hidden in inconsistency. From time to time, we’ve even dialed back supply rather than send out batches we couldn’t stand behind.
I’ve watched our QC analysts reject drums that nearly passed specification. They work with a sense of pride that only comes from remembering long nights spent debottlenecking filter press lines or retesting failed samples to find those hidden impurities. Our staff grow into their roles because each product’s quirks rely on human memory and shared troubleshooting as much as on automation or standard operating procedures.
Storing quinoline-N-oxide is straightforward for labs used to aromatic amine derivatives. The N-oxide group adds mild hydrophilicity, so we keep drums and bottles tightly sealed to avoid clumping and unnecessary exposure to ambient moisture. Light-sensitive reactions prompt us to use amber glass containers for smaller orders. Customers working at scale often request lined steel drums or HDPE options to reduce contamination risk. We advise safe, dry handling and basic PPE for process teams—gloves, goggles, lab coats—because, while it isn’t the most hazardous material we ship, it can cause irritation if mishandled or inhaled.
Customers come to us for stable packaging. We embrace overkill on moisture control, using desiccant packs and low-humidity environments both during packing and before shipment. Few things frustrate a production chemist like opening a batch to find material agglomerated from moisture ingress. Oversight and attention in our warehouse mean fewer complaints, swifter batch dissolution, and clean resuspension during syntheses. Our experience points to a simple rule: anticipating user needs based on where problems start in the supply chain, not just where they show up.
We do not stand still in improving how we make quinoline-N-oxide. Over years of production, we have pushed to reduce our environmental impact by switching oxidation systems from hazardous chlorinated solvents to greener alternatives wherever the chemistry allows. Early on, we faced setbacks with solvent switches, but gradual process adaptations, solvent recovery investment, and partnering with researchers led to a process yielding less than half the hazardous waste per kilo compared to the older method.
Dealing with stricter regulations for export and local storage forced us to re-evaluate our labeling, tracking, and documentation. Audits inspire tangible upgrades—introduction of real-time monitoring, digital batch tracking, and faster retrieval of analytical data for customer reference. We have opened our lines to regular internal reviews, and every process improvement stems from actual incidents or slowdowns our team encountered. The insights come less from external consulting than from shop-floor inspections and testing batch anomalies early in the production shift.
The need for adaptability presses most on long-standing products like quinoline-N-oxide. We adapt not because it is glamorous, but because we want to maintain the trust in every order we fill. Long-term customers remind us which product features help them deliver science with fewer complications—batch clarity, solid purity, reliable performance in oxidative coupling, and practically zero need for pretreatment or adjustment before use. Each time a client scales up, our technical staff stands ready to consult, share best practices, and adopt customer feedback into future batches.
Those new to quinoline-N-oxide often ask about shelf life. Our batches carry at least two years’ guaranteed stability under dry, sealed conditions. Some users store it at room temperature, others in cool, dark storage—our experience confirms both are adequate as long as the seals remain uncompromised. If clumping or color drift appears after months of storage, it almost always traces back to incorrect closure or humidity exposure, not inherent product instability.
Another recurring question covers compatibility with automated feed and transfer systems during large-scale synthesis. The crystalline powder flows easily with basic auger and vibrating transfer setups. Only when loaded in high-humidity or exposed for extended periods does caking become a potential issue. To address such scenarios, our advice is simple: run product straight from sealed packaging, minimize headspace, and reseal unused stock promptly.
Thirdly, our technical line often fields questions about pre-dissolution, especially for those planning electrochemical or screening assays needing exact concentrations. We recommend stir-and-wait in compatible solvents and gentle warming for fast suspension. Trying to rush the process or force the material into too polar or too nonpolar solvents can result in stubborn clumps. Over the years, the chemists and production teams here have arrived at short, practical guides that spare users unnecessary lab time.
Our dialogue with end-users directly shapes how quinoline-N-oxide leaves the line. Some customers prefer pre-weighed aliquots to avoid exposure or contamination during frequent weighing. Others ask for custom particle sizes or for the product to be delivered in inert gas-flushed bottles. We treat these not as special favors but as part of maintaining relationships built over decades. Each request reflects a genuine challenge faced in synthesizing new molecules or scaling production safely. Our hands-on approach translates to swift adjustments based on real feedback, not on production dogma or marketing.
Long-term academic collaborators cite not only product purity but reliability in documentation and responsiveness to regulatory clarifications as a deciding factor in sticking with our materials. Researchers drop messages about anomalous spectra, inconsistent crystallization, or unexpected side reactions. That feedback travels straight into our review process—often resulting in tweaks to purification stages, tighter in-process testing, or focused stability studies. Our respect for bench-level experience informs how we handle every interaction, from planning the next production campaign to writing up the latest quality report.
We don’t claim perfection with quinoline-N-oxide. Each batch distills lessons learned on the shop floor. Problems—whether from raw material blips, process drift, or new regulatory wrinkles—present themselves without warning. What separates experienced manufacturers from repackers or traders is how we respond: root cause analysis, staff retraining, real investments in analytical capability, and a commitment to owning mistakes. Clients judge us by how our quinoline-N-oxide performs in the real world, how consistently it arrives, and how quickly we adapt based on collective experience.
Those qualities, earned batch by batch and shipment by shipment, are what turn a fine chemical into a trusted foundation for scientific progress. Our story is one of translating complex organic chemistry into tangible, reliable outcomes for those who demand consistency and quality—one drum, one bottle, and one successful synthesis at a time.