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HS Code |
170753 |
| Iupac Name | 8-chloro-2-methylquinoline |
| Cas Number | 86-47-5 |
| Molecular Formula | C10H8ClN |
| Molecular Weight | 177.63 g/mol |
| Appearance | Yellowish powder or solid |
| Melting Point | 61-63 °C |
| Boiling Point | 305-306 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.21 g/cm³ |
| Purity | Typically ≥98% |
| Smiles | CC1=NC2=C(C=CC(=C2)Cl)C=C1 |
| Synonyms | 8-chloro-2-methylquinoline, 8-chloroquinaldine |
As an accredited 8-Chloroquinaldine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 8-Chloroquinaldine, 25g: Supplied in a sealed amber glass bottle with a secure screw cap, labeled with product details and hazard warnings. |
| Shipping | 8-Chloroquinaldine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be stored and transported in a cool, dry place, away from incompatible substances. Proper hazard labeling and documentation in accordance with chemical safety regulations must accompany each shipment to ensure safe handling and delivery. |
| Storage | 8-Chloroquinaldine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from moisture and direct sunlight. Store at room temperature and ensure proper labeling. Follow all applicable safety, handling, and storage guidelines as outlined in the chemical’s safety data sheet (SDS). |
Applications of 8-Chloroquinaldine in Industrial ManufacturingAs the original manufacturer of 8-Chloroquinaldine, we supply this fine chemical to several advanced industrial segments, supporting consistent downstream processes, regulatory compliance, and finished product quality across the chemical, pharmaceutical, and agrochemical markets. Below we outline the specific applications, integration methods, compliance standards, usage ratios, and end products typical for each sector. 1. Pharmaceutical Intermediate for Antimalarial Drug SynthesisPharmaceutical manufacturers rely on 8-Chloroquinaldine as a key building block in the synthesis of antimalarial compounds, including chloroquine derivatives. This intermediate undergoes condensation and further functional group transformations under strictly controlled environments. The integration points, impurity content, and batch traceability follow established regulatory practices for APIs. Consistency in the input quality is monitored through real-time analytics and validated process controls to meet global pharmacopoeial standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate for Fungicide Production8-Chloroquinaldine acts as a core intermediate in the formulation of fungicidal active ingredients based on modified quinoline scaffolds. Agrochemical processors incorporate this raw material during chlorination and alkylation reactions under highly controlled conditions. Monitoring of trace impurities and residual solvents is standard throughout these processes, ensuring compliance with stringent global agrochemical regulatory frameworks. Process efficiency depends on solvent recovery and on specification-matched batch lots. Industry compliance standards
Typical usage ratio
Downstream process integration
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3. Dye and Pigment Synthesis for Specialty ColorantsColorant and pigment producers utilize 8-Chloroquinaldine in the structural modification of quinoline-based dye molecules, particularly for high-stability and lightfastness. The material is introduced in condensation or functionalization reactions, influencing tone, stability, and solubility. Producers maintain documented QC protocols for lot-specific input control to meet the colorant industry’s product safety and consistency requirements. Compliance is demonstrated through internal standards and independent testing certifications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Chemical Intermediate for Photographic Chemical SynthesisManufacturers of fine photographic chemicals and imaging agents integrate 8-Chloroquinaldine as a selective intermediate for quinaldine-based developer compounds. The controlled input of the raw material into sequences involving organometallic complexation and ring substitutions is critical for photoactivity. Process environments utilize precisely controlled light and temperature staging to ensure product reproducibility, and every lot meets analytical and purity expectations for downstream specialty chemical applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Producing 8-Chloroquinaldine at scale gives our team a unique perspective on its real-world performance, especially compared to many intermediates sharing structural similarities. The compound, also called 8-chloro-2-methylquinoline, delivers distinct advantages rooted in its molecular arrangement and reactivity profile. Many have worked with a broad spectrum of quinoline derivatives, each carrying subtle differences that reveal themselves in process reliability and downstream compatibility. Sourcing large quantities, maintaining lot-to-lot purity, and responding to application-specific requests has shaped our approach—not only to ensure consistent product, but also to refine our methods and improve throughput.
8-Chloroquinaldine stands out due to its unique configuration—the methyl group at the 2-position and the chlorine at the 8-position create a molecule that responds differently to reagents than other quinolines. The result is a reliable intermediate for several industrial syntheses, including pharmaceutical actives, agrochemical cores, and certain advanced materials. Chemists in our production teams understand that even minor modifications to the quinoline scaffold unlock or block different synthesis pathways. Each batch we produce comes with this appreciation of structure guiding our quality controls. Analytical work—ranging from NMR to melting point tests—lets us target the low isomer and impurity levels critical for demanding organic transformations downstream.
Working with downstream developers has shown us no two clients approach synthesis the same way. Some production lines run at the kilogram scale, others at several tonnes per campaign. Our 8-Chloroquinaldine leaves the plant as a free-flowing powder—most batches display a pale yellow tint, a sign of minimal oxidation and careful process handling. The material must offer at least 99% purity, as tiniest traces of low-level halide byproducts or other quinaldines quickly compromise pharmaceutical and electronic device outputs. Granule size matters for many mixing systems: larger crystals minimize dust and ensure consistent feeding in automated equipment. Moisture content remains tightly managed; too much water interferes with alkylation and coupling reactions, so our drying and storage protocols have evolved based directly on customer feedback. Every time a client flags residue or variability, we reexamine and tighten not only the finished goods release criteria, but also our solvent swaps and distillation runs.
Several attributes of 8-Chloroquinaldine put it ahead in the eyes of experienced synthetic chemists. The chlorine atom at the 8-position resists hydrolysis, providing residue-free performance in multi-step reactions. When manufacturers explore alternative chlorinated quinolines, they often encounter increased byproduct formation or unpredictable side reactions—our 8-Chloroquinaldine neatly sidesteps those pitfalls. Thermally, it tolerates a broad range of reaction settings without decomposing, giving formulators flexibility when temperature ramps are needed. In contrast, close analogs such as 5-chloro- or 6-chloroquinaldine show reduced chemical selectivity; colleagues from both inside and outside the plant floor confirm that yields and purities suffer without the 8-chloro configuration.
Our operations team regularly receives feedback about reduced purification steps when clients switch their routes to our product. Many appreciate that 8-Chloroquinaldine acts as both a leaving group and an activating agent, making it popular for Suzuki or Heck couplings and for further derivatization at the 8-position. The methyl group also plays a strategic role—its electron-donating effect makes certain transformations more accessible, particularly in heteroaromatic ring modifications. Unlike un-substituted quinolines, the presence of methyl influences reactivity patterns, so combination reactions run cleaner and faster.
Chemical manufacturers constantly aim to balance reactivity, safety, and environmental impact. In our hands, 8-Chloroquinaldine has become a keystone intermediate for a range of synthetic sequences demanded by pharmaceutical and agricultural industries. Several active pharmaceutical ingredient (API) pipelines rely on the unique substitution pattern of this compound—an arrangement not easily mimicked by other halogenated quinolines. We’ve observed formulators wrestling with longer routes when forced to use alternatives, often confronting bottlenecks or hazardous reagents that 8-Chloroquinaldine circumvents with ease.
Process chemists recognize that the selectivity of this molecule not only improves isolated yields, but also helps minimize the generation of regulated byproducts. Our close tracking of waste profiles, solvent usage, and side reactions confirms that this compound simplifies waste management compared to less well-matched substitution patterns. As the pressures from environmental agencies become stricter, customers working with 8-Chloroquinaldine see fewer regulatory hurdles and smoother product registrations. This is not theory—it shows up in shorter documentation cycles and less rework along the regulatory path.
Our plant leverages robust process protocols to deliver 8-Chloroquinaldine that meets the expectations of modern industries. Years of production experience have taught us the importance of tight process controls, thorough cleaning schedules, and well-trained staff. We source raw materials not just for price, but for reproducibility. Early runs using lower-cost sources resulted in variability that rippled through the final product: color shifts, higher impurity loads, and problems with recrystallization. Past mistakes guided our supplier choices, and we now work closely with partners for reagent traceability, chemical identity, and sustainable practices.
Production staff run both in-process and final-batch analytics to quickly capture deviations. On the rare occasion that an off-spec batch occurs, tracing root cause and isolating the problem—be it a filtration fouling or a subtle variation in temperature—avoids recurrence. Over time, our commitment to root-cause analysis and production best practices allowed us to reduce lot failures, creating real value not only for ourselves, but most importantly, for the operators waiting for consistent material to feed their own high-value syntheses. We’ve seen that true quality starts from the ground up, with every process engineer’s input valued and every technician responsible for the integrity of their work.
Working alongside many other substituted quinolines has shown our teams what distinguishes 8-Chloroquinaldine in real operations. For instance, 2-methylquinoline, without the chlorine, displays a completely different behavior under electrophilic substitution or in cross-coupling routes. Other halogenated quinaldines—such as 6-chloro or 7-chloro—isomers—fail to deliver the same reaction advantage. Many times, application failures and lower yields point back to substitution at the wrong ring position. Only the 8-position, in our experience, minimizes steric hindrance while retaining enough electron withdrawal to ensure coupling proceeds smoothly. Processing differences can be dramatic: solvent choices, heating profiles, and even catalyst loadings fluctuate when moving from 8-chloro to other positions, inevitably adding time and complexity.
Customers who migrated away from broad, generalized intermediates toward our 8-Chloroquinaldine frequently share improved batch-to-batch reliability and narrower impurity profiles. The intricacies of scale-up—modifying agitator speeds, changing reactor geometries, switching filtration equipment—highlight these advantages. Our staff often supports client process engineers in evaluating differences, drawing from both lab-bench and pilot-plant experience.
The demand for 8-Chloroquinaldine remains strong in several industry sectors, but its reputation has been cemented most firmly within custom synthesis houses and specialty pharmaceutical plants. Over the years, we’ve partnered with formulators who push this intermediate to high throughput routes, relying on both its chemical performance and predictable impurity signatures. The compound’s ruggedness under a range of pH, pressure, and thermal profiles makes it adaptable to protocols that run hot, cold, acidic, or basic. Its solubility profile—extracted through years of solvent compatibility trials—matches well with the most commonly used process solvents, keeping reaction cycles smooth and minimizing waste.
In agrochemical pipelines, process reliability is especially prized; even subtle issues like unwanted polymorph formation or delayed filtration can set schedules back by weeks. 8-Chloroquinaldine delivers reproducibility batch after batch, even under tight production windows. In one recent example, a large-scale process struggled to scale benchtop work into full batch mode due to unanticipated byproduct levels with a different chloroquinoline. Once swapped for our product, total cycle time shortened, and output composition stabilized—feedback that continues to sharpen our own process parameters and raw material pre-screening protocols. We have learned, through long partnerships, how process chemistry and material characteristics are deeply intertwined.
Complex molecules frequently create environmental or regulatory headaches. 8-Chloroquinaldine offers a different experience; downstream transformations produce minimal regulated side products, and the parent compound itself aligns with the needs of commercial registrations in multiple regions. Our own production lines emphasize solvent reuse, closed systems, and waste stream reduction. Customer feedback shows similar patterns in their own settings—from crop protection chemicals subjected to strict environmental limits, to pharma active ingredients requiring detailed impurity tracking.
Traceability and documentation now shape every large-volume chemical, and 8-Chloroquinaldine’s pathway from raw material to finished product is thoroughly documented at every handoff. Any deviation from normal release data is traced, corrected, and fed back into our process controls. Unlike “black box” suppliers, we provide analytical snapshots and batch histories to customers needing them for compliance filings or multi-market submissions. The volume of regulation and the speed at which compliance needs change keep manufacturers on their toes—being ready is a survival skill, not just a marketing point.
Manufacturing 8-Chloroquinaldine efficiently requires a keen understanding of its chemical and physical traits. During scale-up, our process engineers encountered persistent bottlenecks tied to mixing regime and solvent compatibility. Early approaches favored narrower solvent choices, but collaborative problem-solving uncovered options that maintained purity while improving throughput. Each learning cycle—crystallization failures, slow filtration, unexpected color development—fed directly into revised standard operating procedures.
On the technical side, our experience underscores the importance of managing exothermic profiles as the batch moves through halogenation steps. Temperature probes and real-time monitoring during these critical windows reduce hot-spot formation, keeping impurities below specification. Cleaning protocols for reactors and transfer lines emerged after several cross-contamination incidents, further anchoring our team’s belief that consistent product starts with thoughtful plant design. These hard-won insights help not only keep our batches pure, but give us the confidence to respond to unusual customer requirements or new market demands.
Sustaining leadership in manufacturing 8-Chloroquinaldine calls for more than technical know-how. Constant improvement—listening carefully to clients, dissecting the details of production incidents, seeking feedback from users—drives our evolution. No product remains static, and our technicians devote considerable effort to trialing incremental enhancements. One such change, adopted after input from a major pharmaceutical developer, involved optimizing the cooling profile to reduce seed crystal overgrowth. This refinement dropped downstream filtration times by thirty percent and reduced blockages in client transfer pumps.
This type of feedback loop, between manufacturer and customer, creates value on both sides. Technicians responsible for drying, packing, and sampling each lot regularly update our process documentation, capturing not just “what works,” but also “what didn’t.” These institutional memories, committed to writing and discussed at cross-team meetings, make each new production run slightly more robust than the last. At scale, these improvements translate into tighter release specs, fewer rejected batches, and a broader reputation for reliability in the marketplace.
Chemical markets evolve, and new application areas for 8-Chloroquinaldine constantly arise. Materials science teams have started to explore derivatives as fluorescent probes and corrosion inhibitors. Device manufacturers, seeking even higher standards and narrower impurity windows, regularly approach us for in-depth consultation. Often, these projects require tailored specification—tighter particle size, enhanced dryness, or non-standard packaging. Our response draws on the thorough process knowledge acquired over years of practice, not a one-size-fits-all glossary.
In-house analytical labs stand ready to develop custom assay methods for new regulatory filings, while production staff adapt drying or recrystallization protocols as the need arises. Such flexibility—not simply turning a lever, but intelligently assessing which intervention makes sense for each request—comes directly from deep familiarity with the material and trust in the plant team’s capabilities. Our willingness to trial new protocols reflects both customer priority and internal readiness, further strengthening confidence in our offering.
Years of producing 8-Chloroquinaldine have provided clear evidence of its value to specialists across different fields. Its unique combination of chemical performance, process stability, and regulatory compatibility sets it apart from similar quinoline derivatives. Every improvement we implement—whether in feedstock traceability, optimized purification steps, or end-of-line packaging—springs from days spent on plant floors and hours listening to feedback from technicians and end-users alike.
Manufacturing a compound doesn’t stop at hitting a purity figure or producing a powder with a particular hue. It depends on embedding lessons from every batch, navigating the challenges that real-world operations bring, and anticipating how demands and standards will shift in the coming years. Our experience shapes every aspect of our 8-Chloroquinaldine, translating technical expertise into material that meets and exceeds the expectations of a demanding chemical marketplace.