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HS Code |
968121 |
| Product Name | 5-Amino-8-Quinolinol Dihydrochloride |
| Cas Number | 37517-12-1 |
| Molecular Formula | C9H8Cl2N2O |
| Molecular Weight | 247.08 g/mol |
| Appearance | Light yellow to beige solid |
| Solubility | Soluble in water |
| Melting Point | 252-256°C (decomposes) |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C, protected from light |
| Synonyms | 5-Amino-8-hydroxyquinoline dihydrochloride |
| Ph 1 Solution | 4.0 - 6.0 |
| Ec Number | 253-588-5 |
As an accredited 5-Amino-8-Quinolinol Dihydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5-Amino-8-Quinolinol Dihydrochloride, 10g, is supplied in a tightly-sealed amber glass bottle with clear hazard labeling. |
| Shipping | 5-Amino-8-Quinolinol Dihydrochloride is shipped in tightly sealed containers, protected from moisture and light. It is classified as a chemical reagent and must be handled according to applicable regulations. Transport typically requires labeling for laboratory chemicals and may involve temperature control to ensure product stability during transit. |
| Storage | 5-Amino-8-Quinolinol Dihydrochloride should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and strong acids. Store at room temperature and always ensure containers are correctly labeled. Follow standard safety and chemical hygiene protocols when handling or storing. |
Applications of 5-Amino-8-Quinolinol Dihydrochloride in Industrial ManufacturingWe specialize in the synthesis and global supply of 5-Amino-8-Quinolinol Dihydrochloride, delivering this specialty raw material into defined industrial verticals where its chemical profile meets rigorous technical and regulatory demands. Our manufacturing, QC, and applications teams collaborate directly with end-use producers to target downstream integration for advanced intermediates and specialty product lines. The following applications detail the major real-world scenarios where our 5-Amino-8-Quinolinol Dihydrochloride serves as a critical process component. 1. Active Pharmaceutical Ingredient (API) Intermediate for Antimalarial Drug SynthesisProducers of antimalarial agents utilize 5-Amino-8-Quinolinol Dihydrochloride in multi-step synthesis pathways to build core structures for pharmaceutical APIs. Incorporation most often occurs at condensation or amination stages, where controlled purity and traceability under validated processes is essential for downstream GMP compliance and drug registration filings. This intermediate is necessary in the manufacture of specific quinoline-based medicinal compounds, requiring careful handling and analytical confirmation at each step. Industry compliance standards
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2. Chelating Agent Precursor for Metal Surface Treatment SolutionsSpecialty surface treatment and cleaning solution developers employ 5-Amino-8-Quinolinol Dihydrochloride as a precursor in the synthesis of quinoline-based chelators. Its ability to coordinate transition metals under precise pH conditions makes it essential for the formulation of cleaning agents used in precision metal finishing, electronic component preparation, and high-purity industrial washing. Compliance with specialty chemical stewardship and traceability is vital due to possible presence of residuals in downstream high-value products. Industry compliance standards
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3. Analytical Reagent for Laboratory Diagnostic Kits ManufacturingProducers of analytical and diagnostic solutions incorporate 5-Amino-8-Quinolinol Dihydrochloride in colorimetric and fluorometric reagent formulations. Its chelation capacity and specific binding to metal ions is used for selective detection of trace metals in water, biological samples, and food matrices. Stringent trace contaminant control and documentation for laboratory reagent grade material are mandatory to support downstream batch release and quality certifications. Industry compliance standards
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4. Synthesis of Biochemical Research Probes and Fluorescent LigandsBiotechnology R&D suppliers and contract research institutions integrate 5-Amino-8-Quinolinol Dihydrochloride as a building block in the custom synthesis of fluorescent ligands and metal ion indicators for biochemical assays. Its amine functional group and aromatic core enable downstream functionalization for luminescence and specific binding affinity, enabling researchers to produce sensitive molecular probes for cell imaging and molecular diagnostics. Accurate quality control, documentation, and batch traceability are prerequisites to support high-impact research projects and downstream life science partners. Industry compliance standards
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5. Intermediate for Agrochemical Active Ingredient SynthesisAgrochemical manufacturers implement 5-Amino-8-Quinolinol Dihydrochloride as an intermediate during the synthesis of specific crop protection compounds such as quinoline-based fungicides or seed treatment agents. It is integrated in selective synthetic routes demanding precise control of functional group placement and purity to achieve designated biological activity and comply with agrochemical registration requirements worldwide. Production batches require documentation and representative sample analysis for regulatory submissions. Industry compliance standards
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Deep familiarity with 5-Amino-8-Quinolinol Dihydrochloride starts from its synthesis, monitoring every flask, temperature curve, and pH swing inside our facility. Our chemists see this material emerge from raw inputs—aromatic quinoline transformed by selective amination, followed by controlled hydrochloride salt formation. Years of scale-up trials have pulled subtle details into our daily routine, producing this compound with consistent quality and minimal byproducts.
The process chews through countless control points. At the amination stage, the correct molar excess of ammonia and solvent selection dictates formation of 5-Amino-8-Quinolinol instead of regrettable regioisomers. Workers have tuned reaction times, heat gradients, and purification steps far beyond what textbooks outline. After the base product forms, hydrochloric acid addition in a moisture-controlled reactor ensures salt conversion, and the product precipitates in neat granules. Each lot receives full-phase identity tests by HPLC, NMR, and titration, measured against our in-house reference batch. This practice grew out of real-world need—customers want batches that match, month in and month out. Anything drifted from target specs leads to internal review, not reinterpretation of the test.
On the floor, specifications have been set not only to meet international benchmarks, but also to meet the needs of industrial buyers and research partners. Our current standard for 5-Amino-8-Quinolinol Dihydrochloride (CAS 10563-52-9) reflects what pays off in the lab and in scale-up runs. This batch routinely displays a purity well above 99% by HPLC, verified against multiple methods—because some customers spot degradation peaks that even ordinary HPLC QC would miss. Moisture levels rarely exceed 0.1% due to dedicated drying and packaging in controlled atmospheres, minimizing clumping or hydrolysis during shipment and long-term storage.
Appearance gives an early view of quality. The product offers a pale to light yellow crystalline powder, free of visible contaminants and easy to handle, in contrast to more brittle or sticky batches often supplied by intermediaries. We examine material flow and compaction strength as part of the QC routine—purchasing managers want powder that fills drums evenly and does not dust out, and lab audiences care about easy weighing and dissolution.
For trace impurities, our QC track record is informed by customer feedback and in-house stress testing. Few suppliers test for polyaromatic byproducts or heavy metals as stringently, but our own experience convinced us to lower tolerance thresholds over time. The trend among users in diagnostics or analytical reagent supply has been tighter. We now blend each lot before final packing, confirmed by spot-sampled analyses and retained samples for every shipment.
Chemically, 5-Amino-8-Quinolinol Dihydrochloride stands out due to the specific arrangement of the amino and hydroxyl groups on the quinoline core. This unique scaffold creates a strong chelating ability, making it significant in applications such as metal ion detection, complexometric titrations, and synthetic transformations. Lab professionals value its selectivity for certain transition metals—its affinity varies with subtle changes in cation size and charge, a trait that lets researchers adjust conditions for precise analytical results.
Metal complex formation is not just an academic point. Clients who formulate test kits or reagents for metals like iron, copper, or zinc return to this compound because it yields sharper, more stable complexes than alternative chelators. The amino substituent adds distinctive reactivity, especially in forming colored metal complexes that prove useful for visual assays and photometric quantification. Subtle differences in the molecule’s electronic structure, refined by hydrochloride salt formation, underlie color change and solubility. Chemists designing new sensors or colorimetric assay kits discuss “response profiles” and need material that dissolves consistently at low concentrations—a feat that hinges on the fine texture and genuine purity of the product.
Long-term partnerships with academics, diagnostic kit firms, and specialty synthesis groups have taught us which properties matter most in practice. In life sciences and clinical chemistry, fast, consistent response with low noise is everything—for titration, sensitivity to background contaminants makes or breaks a protocol. Our QA team routinely reviews reports from end users who run dozens of parallel samples, often flagging unexpected haze or sluggish dissolution in competing products. Packing stability, flow, and actual solubility can determine whether an industrial process succeeds at scale, making core quality control a matter of pride as much as compliance.
Beyond laboratory analysis, 5-Amino-8-Quinolinol Dihydrochloride finds roles in organic synthesis and as a building block in pharmaceutical R&D. Synthesis-specific feedback tells us much about how structural features impact reactivity. The amino group at the 5-position opens paths for further functionalization, expanding the compound’s portfolio to more advanced intermediates and specialized chelators. The balance of reactivity and stability keeps it attractive to synthetic chemists, who need predictable outcomes across long production batches. Practical experience shows that reproducible purity and moisture control help avoid bottlenecks at the pilot or scale-up stage.
Some colleagues develop fluorescent or colorimetric metal indicators based on 8-quinolinol derivatives. Their feedback on spectral shifts, background absorption, and reactivity under various pH conditions shapes the tweaks in our process. Improvements in recrystallization and post-reaction workup have come out of months of trials with these specific needs in mind.
Deep familiarity with 8-quinolinol and its numerous derivatives spots immediate differences between unsubstituted, methylated, and aminated variants. Many use plain 8-quinolinol in metal chelation studies, but the introduction of an amino group at the 5-position creates altered electron distribution and binding characteristics. Compared to the parent molecule, 5-Amino-8-Quinolinol Dihydrochloride forms stronger, often more selective complexes, making it better for certain analytical and preparative tasks.
Other derivatives, like 5-chloro-8-quinolinol or 2-methyl-8-quinolinol, offer different solubility and reactivity profiles, but none match the balance found here between metal affinity and functional group compatibility. The dihydrochloride salt enhances water solubility and stability, allowing easier formulation into aqueous systems, a distinct improvement over the basic or neutral forms of quinolinol that may precipitate or oxidize under storage.
In practice, substituent effects prove crucial. Chemists working with highly selective assay kits have pointed out increased color intensity and faster reaction times using the aminated, dihydrochloride salt. In synthetic chemistry, the precursor’s unique arrangement sometimes enables pathways inaccessible to methylated variants, opening access to new classes of pharmacophores or ligands. From our shop floor, technicians report the dihydrochloride form packs, weighs, and dissolves more easily than pure base, suiting high-throughput or automated workflows common in industry.
Scalability often distinguishes real chemical manufacturers from the rest. We learned that running a five-liter glass reactor teaches different lessons from managing a 500-liter stainless vessel. Heat distribution, mixing intensity, and impurity release change at scale, sometimes in unpredictable ways. Finding optimal conditions for reproducibility has shaped the evolutionary path of our batch records, as we document every deviation and corrective tweak. Controlling salt formation for the dihydrochloride is particularly sensitive—too rapid or uneven acid addition encourages local supersaturation and erratic crystal morphology.
Our team’s daily challenge rests in translating this knowledge into predictably high-quality product. Many customers rely on multi-kilogram drummed batches, with a guarantee of lot-to-lot consistency, no matter the production date. This means adaptive quality control strategies: monitoring impurity signatures, solvent residues, and moisture profiles at points neglected by casual suppliers. Regularly replaced and calibrated analytical instruments, experienced oversight during every process step, and transparent specification tracking combine to keep the supply steady and predictable.
Feedback cycles with customers often result in incremental improvements. Industrial users share yield figures, reaction times, and unexpected byproducts, letting us adjust purification timing or drying conditions. This feedback loop grounds our operation—what leaves our plant must fit smoothly into customer equipment and processes, or we hear about it. These long feedback chains help improve not just our product, but also users’ workflows, supporting mutual reliability and efficiency.
Supplying bulk lots to industry and research groups shapes our approach to filling, packing, and shipping. Handling of 5-Amino-8-Quinolinol Dihydrochloride requires airtight, moisture-minimizing packaging, as the compound’s hygroscopic nature means unchecked exposure at any point can introduce clumping or minor decomposition. We select drum liners, tamper-evident closures, and outer containers for maximum seal integrity and easy transfer to lab or process settings. Labels document batch numbers, QC release signatures, and full analysis on request.
Some long-term users order custom particle size fractionation, based on reported downstream requirements. We have developed procedures to sieve or mill product to specific mesh ranges, though the bulk majority of demand prefers the moderate, free-flowing powder format. Demand for smaller or single-use vial packaging from clinical users rises year by year, so we run parallel packing lines to cover both ends of the spectrum—multi-kilogram drums and pre-aliquoted sample kits.
Material handling in our plant follows both regulatory guidelines and practical norms sharpened over thousands of drum fills. Workers wear gloves and respirators not just for compliance, but from direct experience with dust exposure during open-drum transfers. Operators log every container movement, reducing the risk of mix-ups and maintaining chain-of-custody documentation. Years of hard-won improvement in traceability pays dividends if a client ever reports a discrepancy—usually, the answer is there in our records.
Producing and distributing chemical compounds, especially specialty ones like 5-Amino-8-Quinolinol Dihydrochloride, means navigating complex safety and environmental guidelines. Our team manages on-site waste collection and treatment—aminated quinolines demand strict effluent controls, so our internal wastewater system is upgraded beyond baseline permits. This care lowers the risk of off-site environmental issues and helps us keep good standing with regulators and neighbors.
For users, safe handling revolves around chemical hygiene: closed storage, limited airborne exposure, and emergency readiness for spills or accidental skin contact. Packaging includes both regulatory warnings and practical advice picked up from decades of field experience, such as secondary containment for open-drum handling or storing away from strong oxidizers.
Product stewardship extends to post-use: helping industrial or R&D users dispose of surplus or expired lots, and maintaining guidance on how to neutralize and dispose of waste streams safely. Our technical team fields questions not just on regulatory compliance but also on real-world best practices, acting as a knowledge bridge that supports safe and responsible product lifecycle management.
Advancing product quality stands on years of direct feedback and cooperative development with end users. Researchers flag edge-case performance gaps—a slow reaction, unexpected decomposition, shift in assay sensitivity. Industrial partners send back process flowcharts and yield logs, highlighting how even a minor deviation in color or solubility from batch to batch can disrupt multi-stage synthesis. We respond with tailored adjustments, refining everything from drying times to mesh size distribution and trace impurity controls.
Users of advanced diagnostics push for lower trace impurity levels and offer back results from analytical panels that supplement our own QC routine. The dialogue leads us to upgrade testing standards and revise process checkpoints. This partnership culture does not just serve sales—it builds trust and outlasts price wars or short-term market trends. A satisfied customer who sees quality improve based on their input often brings more business and more challenging technical puzzles.
Learning from each shipment, each analysis, and each troubleshooting call, we refine the product bit by bit. No two years look quite the same on the production line or inside the analytical lab: demand, regulations, and customer needs shift. The ability to respond quickly and meet those changes, using direct technical expertise and long-term memory of what works at kilogram and multi-ton quantities, keeps our operation moving forward.
Decades of hands-on synthesis and supply have shaped our approach to making and delivering 5-Amino-8-Quinolinol Dihydrochloride. Each drum holds the results of technical progress—improved process design, stronger quality assurance, and a routine feedback loop that closes the gap between factory floor and user bench. Users rely on this substance for its unique mix of solubility, reactivity, and stability; our unique perspective as producers means we understand both the technical backbone and the practical realities of getting it reliably into the world’s labs, reactors, and diagnostic kits.
Being a genuine manufacturer means living with the consequences of each production step, batch sheet, and final shipment. This experience, built over years of customer dialogue and constant technical refinement, brings confidence to users who depend on consistently high-performing 5-Amino-8-Quinolinol Dihydrochloride for their research, analysis, and industrial scale-up needs.