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HS Code |
722286 |
| Chemical Name | 8-Chloroquinoline |
| Cas Number | 612-25-9 |
| Molecular Formula | C9H6ClN |
| Molecular Weight | 163.61 |
| Appearance | Pale yellow to light brown crystalline powder |
| Melting Point | 55-57°C |
| Boiling Point | 283°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Density | 1.222 g/cm3 |
| Smiles | ClC1=CC=CC2=NC=CC=C12 |
As an accredited 8-Chloroquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 8-Chloroquinoline, 25g, is packaged in a sealed amber glass bottle with a secure screw cap and safety labeling for laboratory use. |
| Shipping | 8-Chloroquinoline is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous chemical, so transportation complies with relevant regulations for dangerous goods. The packaging is clearly labeled, and all safety data sheets (SDS) accompany the shipment to ensure safe handling and storage upon arrival. |
| Storage | 8-Chloroquinoline should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Protect from direct sunlight and sources of ignition. Clearly label the storage container, and ensure only trained personnel handle and access the chemical. |
Applications of 8-Chloroquinoline in Industrial Manufacturing8-Chloroquinoline serves as a strategic intermediate in multiple advanced manufacturing sectors. Below, we detail authentic industrial use cases where 8-Chloroquinoline is integrated into downstream syntheses, guided by recognized industry benchmarks and precise technical requirements. 1. Active Pharmaceutical Ingredient (API) Synthesis for Antimalarial CompoundsPharmaceutical manufacturers rely on 8-Chloroquinoline as an essential building block in the synthesis pathway of quinoline-based antimalarial agents. The compound enters critical condensation and substitution reactions to yield core intermediates for APIs such as chloroquine and amodiaquine. Strict adherence to multi-pharmacopoeia and current Good Manufacturing Practice (cGMP) requirements governs its use, with tightly monitored input ratios to ensure high yield and consistent API purity. The compound’s role directly influences the impurity profile and yields for finished pharmaceutical batch production. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide SynthesisProducers in the crop protection sector incorporate 8-Chloroquinoline as a precursor in the manufacture of selected quinoline-based herbicides and growth regulators. During process development, agrochemical formulators control the ratio and timing of 8-Chloroquinoline addition to modulate the yield and selectivity of downstream active compounds. The process complies with strict national and international agrochemical quality protocols, and the final products typically target market-registered formulations with well-defined impurity specifications. Industry compliance standards
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3. Dye Intermediate in Organic Colorant ManufacturingOrganic dye producers utilize 8-Chloroquinoline in the synthesis of selected azo and anthraquinone dye intermediates, taking advantage of its electronic properties for chromophore construction. Compliance with global dye safety and quality regulations is mandatory, including AOX (adsorbable organic halides) controls to minimize environmental impact. Manufacturers optimize dosing to balance conversion and downstream dye shade control, as subtle deviations in feedstock quality or input levels directly affect batch color consistency and application performance in fiber dyeing. Industry compliance standards
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4. Ligand Precursor in Specialty Catalyst SynthesisChemical process catalyst manufacturers employ 8-Chloroquinoline as a core ligand precursor in forming complex organometallic catalysts. The quinoline moiety facilitates binding to transition metals, enhancing catalyst selectivity and shelf stability. Adherence to specialty catalyst and fine chemical GMP guidelines remains essential, with process chemists adjusting input concentration to optimize ligand-metal ratio and rigorous in-process QC for coordination efficiency. The resulting catalysts are destined for fine chemical and pharmaceutical process customers demanding high reproducibility and minimal trace metal contamination. Industry compliance standards
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5. Intermediate for Specialty Chemical Synthesis in Electronic MaterialsManufacturers of functional specialty chemicals for electronics leverage 8-Chloroquinoline in the synthesis of charge-transport materials and organic semiconductors. Regulatory control focuses on electronic-grade purity and outgassing minimization, as even trace contaminants may affect performance during device fabrication. Process engineers determine the feed ratio according to device application and material structure, integrating the raw material in early-stage condensation or halogenation steps within nitrogen-flushed reactor systems. The quality of resultant intermediates directly influences the downstream performance of OLEDs and organic field-effect transistor materials. Industry compliance standards
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Inside our production facility, 8-Chloroquinoline stirs memories among the team — each new batch starts with familiar scents and that unmistakable pale yellow tint that signals a product ready for the demands of the laboratory and the plant. This compound, with a molecular formula of C9H6ClN, finds its identity through the careful placement of a chlorine atom at the eighth position on the quinoline ring. Its CAS number, 612-62-4, identifies it among chemists, but we've come to know it as a workhorse for intermediate synthesis, specialty coatings, and pharmaceutical research.
In our experience, even slight differences in impurity profiles can throw off a downstream reaction or compromise assay reproducibility. So, we focus on purity targets of 99% or above, measured batch after batch by in-house HPLC and supported by rigorous NMR data. Crystalline solids speak for quality here. Each container, whether drum or small bottle, gets a unique batch label for traceability — a nod to the demands of actual industrial trace-backs, not just paperwork formalities. Visual inspection isn’t just for appearances; we check for color consistency and absence of foreign particulates each time. If a batch falls short, it never leaves the plant.
Supply disruptions and raw material quality shifts can create headaches, especially in the world of aromatics and halogenated organics. Over the past five years, we’ve established multiple supplier relationships for key precursors, and we keep strict records of every kilo of starting material. Our staff regularly samples incoming shipments for off-spec characteristics, especially given the sensitivity of the chlorination process to even low-level contaminant amines or oxidized solvent residues.
The actual chlorination uses controlled temperatures and a carefully timed addition of chlorine-based reagents, with immediate quenching and work-up to avoid formation of unwanted isomers. Finished 8-Chloroquinoline passes through dedicated drying procedures before grading and packing. Our people perform all handling in closed systems to minimize exposure, keeping both our staff and the environment out of unnecessary harm’s way.
The pharmaceutical sector looks to 8-Chloroquinoline as a backbone for API intermediate synthesis. In our experience, researchers don't just want a chemical; they want predictability by the gram and by the drum. Lower grade material can stall reactions, create regulatory headaches, or even prompt costly re-validation runs. Each consignment undergoes repeated purity checks and is held at the warehouse only after it meets our release criteria.
The same drive for reliability matters just as much in the pigment and dye industries. Impurities in the quinoline backbone can translate to faded colors or inconsistent shades. Consistent shelf life and color tone trace back to the chemical integrity ensured at the factory. We keep samples for every batch going back years, which gives our customers clear proof that one lot matches the next and their process isn’t left to chance.
We’ve learned more from our customers than from any catalog or trade show. Sometimes a production chemist from a plant calls, wondering why the flow characteristics feel different compared to their last drum. We investigate — sometimes it traces to a subtle tweak in the drying step, sometimes to a lot of input material with a slightly different melting profile.
These conversations feed back into our batch records and operational playbooks. We keep analytical data on hand and don’t brush off atypical reports. It doesn’t pay to cut corners, and our files tell the unvarnished story of the progress we make from every challenge.
From a synthetic chemist’s point of view, each positional isomer of chloroquinoline leads to subtle variations in reactivity and end-use profile. Compared to 5-chloroquinoline or 6-chloroquinoline, the eighth-position variant consistently shows a preferred balance between nucleophilicity and stability for API intermediate work. Substitution on other positions changes reaction rates, and we’ve seen firsthand that catalyst systems often behave differently, requiring factory trial after trial until the results stick.
When compared with unchlorinated quinoline, the addition of a chlorine atom at position eight brings unique selectivity that opens up reaction space not accessible otherwise. We’ve had projects where switching from a generic quinoline to 8-chloroquinoline cut down by-products by half, saving waste disposal costs and raising overall process yield. Each modification creates new routes for acylation, alkylation, or cross-coupling that pure quinoline and its other chlorinated cousins just can’t match in selectivity or outcome.
The backbone of medicinal chemistry often sits quietly behind the scenes — a halogen here, an amine there, and the profile of a drug compound changes. Our product provides a foundation for some anti-malarial and anti-tuberculosis agents, but more applications come up each year as researchers discover new bioactive scaffolds. Real-world results matter. Our consistent product quality lets process engineers focus on scaling up synthesis instead of chasing down unexpected reactivity or overlooked contaminants.
Material science ventures in OLED production and complex polymer additives sometimes call for highly pure 8-chloroquinoline. A decade ago, requests from this sector came once in a blue moon; now, they make up a measurable slice of our annual volume. End-use applications demand high analytical support, so we partner with clients and supply spectra and stability data with every shipment.
Manufacturing halogenated aromatics isn’t for the careless. Each batch generates by-products and waste streams that, if mishandled, pose risks for our workers and neighbors. Over the years, we’ve upgraded solvent recovery units, added multi-stage scrubbers for off-gases, and shifted to reusable shipping containers wherever possible. Our team logs every disposal and recycles whatever fits local regulations, minimizing landfill reliance. Regulatory compliance isn’t just another hurdle here; it’s the backbone of trust with the community and our downstream partners.
Periodic audits by in-house safety teams have identified spots to strengthen containment. For example, we've rebuilt drains and secondary containment around process tanks after a close call with a gasket failure. These investments cost real money, but the alternative — accidents, fines, or production disruptions — would hit our business even harder. Years of experience reinforce that quality and safety go hand-in-hand. There isn’t a shortcut for diligence in the chemical industry.
As world demand for specialty pharmaceuticals and advanced materials grows, the market for chloroquinoline derivatives ebbs and flows. There is nothing static about production; sometimes, scheduled runs must adapt on short notice to fill a demand from overseas API developers. We keep an eye on global logistics, with recent shipping bottlenecks highlighting the importance of robust supply chain management. Buffer stocks at strategic locations ensure continuity, even if import regulations or port congestion creates delays.
Price volatility in upstream feedstocks, such as chlorinating agents, means we constantly reassess our procurement approaches and maintain open communication with our clients about anticipated changes. This openness builds trust, allowing customers to plan their own operations with fewer surprises.
Our technical team doesn’t just review literature or depend on outside research. They run direct trials with different catalyst loading, alternate solvents, and improved crystallization conditions to drive down impurity levels and boost yields. Several years ago, a shift to a custom-designed chlorination reactor brought visible improvements, reducing batch cycle times and limiting off-spec runoff. Investment in better analytical tools, such as automated melting point devices and mass spectrometry, has allowed us to catch subtle profile shifts before they affect downstream clients.
We value collaboration with customers who share feedback from their own process optimizations. This two-way knowledge flow brings new insight into what specific impurity or morphology issue matters for a given reaction. Whether it's a pilot campaign or kilogram-scale run, our plant adapts based on real data and not just industry trends.
Unforeseen disruptions — raw material shortages, freight delays, surging demand from a single market — all leave their mark. We learned hard lessons from spikes in shipping costs and periodic shutdowns of upstream suppliers. To guard against interruptions, we store extra volumes of high-risk inputs. Our logistics staff pre-arranges multi-modal shipment plans to minimize single-point failure risks. This focus bears out every time a major port experiences a backlog, keeping our delivery schedules intact for customers counting on predictable arrivals.
Customs and regulatory needs differ by country. To speed up clearance, we pre-prepare documentation and keep up with changing compliance standards. We maintain a single-person point of contact throughout the supply process, so our buyers can trace every shipment if needed — right down to the ton and container number.
No two users bring the same requirements. Pharmaceutical customers might want ultra-high purity and analytical certificates on request. Industrial users sometimes prefer bulk packaging for process integration. Our filling and labeling lines adjust on demand — flexibility matters if your operation runs batch processes one week and continuous the next.
Sometimes we get requests for specific particle sizes, even though 8-chloroquinoline is usually supplied as a crystalline solid. Our plant scales sieving and controls dust generation. Tight controls on storage environments ensure stability from factory floor to end-use. Experience shows strict attention to the storage protocol shields against spoilage, which otherwise costs not just product, but trust and reputation.
Each day, our team meets the challenge of producing a compound that bridges discovery to commercialization. It isn’t glamorous, but every ton of 8-chloroquinoline plays its part in a process, a tablet, or a new material. We watch the balance between cost, safety, quality, and speed. All our years in the field show that success lies as much in transparency and teamwork as it does in technical details. Customers ask us for more detail, more service, and more partnership than ever before, and we keep adapting to meet those calls.
Looking forward, we stay ready for more complicated requests, greater levels of documentation, and ever-stricter standards. Our purpose doesn’t shift: make each batch right, keep people safe, and put an honest product into the hands of users. The chemical world keeps turning, but our commitment endures.