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HS Code |
935698 |
| Chemicalname | 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid |
| Molecularformula | C11H9NO4 |
| Molecularweight | 219.19 g/mol |
| Casnumber | 38761-43-6 |
| Appearance | Solid, often off-white to light yellow powder |
| Meltingpoint | 220-225°C (decomposes) |
| Solubility | Slightly soluble in water; soluble in organic solvents like DMSO and methanol |
| Purity | Typically ≥98% (depending on supplier) |
| Storagetemperature | 2-8°C, protected from light and moisture |
| Synonyms | 3-Carboxy-4-hydroxy-6-methoxyquinoline |
As an accredited 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5g chemical is packaged in a sealed amber glass bottle with a printed label displaying product name, formula, and safety information. |
| Shipping | **Shipping Description:** 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid is shipped in tightly sealed containers, protected from light and moisture. It is typically dispatched as a solid, labeled for chemical use only. The shipment adheres to all relevant safety and regulatory guidelines, including appropriate hazard labeling and documentation for laboratory chemicals. |
| Storage | Store **4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid** in a tightly sealed container, protected from light and moisture, at 2-8°C (refrigerator conditions). Keep it in a dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure proper labeling and avoid prolonged exposure to air. Wear appropriate personal protective equipment when handling the chemical. |
Applications of 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid in Industrial ManufacturingAs a specialized manufacturer of 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid, we support global partners in pharmaceutical, agrochemical, pigment, and chemical intermediate segments. Below we present detailed downstream application scenarios based on actual industry demand and our collaboration with formulation developers and process engineers. 1. Pharmaceutical Intermediate for Antibacterial Drug SynthesisMany pharmaceutical producers utilize this API building block in the advanced synthesis of quinolone-based antibacterial agents, particularly where selective activity against Gram-negative bacteria is required. Incorporating the compound in multi-step reactions allows for precise substitution at key positions, supporting both pilot-scale and cGMP production environments. Our manufacturing experience ensures material traceability and particle control for pharmaceutical synthesis processes, with adherence to stringent international guidelines throughout the entire supply chain. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide Active Ingredient SynthesisIn crop protection ingredient manufacture, downstream companies select this compound for its quinoline backbone, which enables highly selective inhibition in weed control agents. Synthetic routes frequently exploit the acid and methoxy substituents for regioselective transformations, playing a decisive role in proprietary herbicide molecule development. Our production controls minimize batch-to-batch impurity variation, giving process chemists reproducible starting material for scale-up and registration batches. Industry compliance standards
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3. Pigment Precursor for Specialty Dye ManufacturingSpecialty dye and pigment producers utilize this raw material to introduce heteroaromatic moieties into custom pigment molecules, unlocking unique absorption and emission profiles for use in high-value printing, textiles, and electronics. Our controlled crystallization methods result in narrow particle size distributions, directly supporting pigment purity and chromaticity requirements for performance-critical downstream applications. Industry compliance standards
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4. Intermediate for Advanced Materials and Chemical Building BlocksChemical manufacturers engaged in advanced materials, polymer additives, and specialty intermediates often draw on the substitution capability of this quinoline-based acid in designing molecules with required thermal and chemical stability. It is particularly valued in research-to-pilot projects where fine-tuning the electronic and steric properties of a molecule delivers improved downstream performance attributes. Our plant supports such customers with technical documentation and detailed CoAs tailored to performance chemical sectors. Industry compliance standards
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In our chemical manufacturing facility, 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid is more than a string of complex syllables or a new product launch. Our teams encounter this molecule from synthesis to shipment, and over years, we’ve built up a layered understanding of its properties, value, and day-to-day opportunities in real-world chemistry. Chemists on the production floor keep at it every batch, because this compound delivers precise performance that other quinoline derivatives struggle to match.
The model designation within our plant, HM-Q3CA, stands as shorthand for our own internal tracking. Each time a batch finishes, its identity isn’t just as a code: it represents a culmination of temperature checks, solvent purifications, crystallizations, and HPLC purity assessments—essential components of our method. Every kilogram goes through a regime that’s proven to control for batch-to-batch deviation. Purity, as every technician in our shop knows, calls for vigilance: beyond the advertised minimum of 98%, our own standard insists that we regularly test for residual solvents, metal content, and specific optical characteristics.
This acid’s formula folds in a hydroxyl group and a methoxy function onto the quinoline skeleton. These small shifts in bonding bring significant consequences when working through heterocyclic synthesis pathways. Our technical leads saw early on that the methoxy position in particular can make or break downstream success in medicinal chemistry and advanced material synthesis. Requests from pharmaceutical labs and research institutes often zero in on this compound due to its structure’s ability to accommodate diverse chemical elaborations, especially in the synthesis of kinase inhibitors and bioactive intermediates.
The differences between this molecule and other quinoline carboxylic acids begin with the downstream chemistry. If a process requires site-directed modifications—where substitution patterns change the reactivity profile—you need more than broad-spectrum quinoline products. The 4-hydroxy and 6-methoxy pattern creates a unique electron distribution. Research groups working on novel antibiotics and anti-cancer molecules rely on these subtle changes for scaffold stability and improved target affinity.
In previous years, requests to scale up batches of 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid nearly always originated from advanced pharmaceutical research divisions and top-tier contract development projects. Our process engineers learned the importance of traceability—every flask, every reactor, every scrutiny of process water quality counts. The output can’t be “just another quinoline,” because batches go straight into high-impact projects. Our repeat clients in the pharmaceutical and fine chemicals industries bring questions backed by high stakes: Was the precursor sourced responsibly? Does the batch history meet trace impurities standards for synthetic intermediates, not just analytical reference?
Day in and day out, our workers contend with the differences in lot moisture, filtration times, and purity readings. Our facility does not treat 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid as an interchangeable commodity, and for good reason. Different processes in the literature call for slightly differing crystalline habits, particle grades, and packaging conditions. Some customers want glass ampoule storage, others require inert atmosphere packaging inside anti-static drums. We’ve adapted our protocols over the years, fine-tuning filter-aid selections and introducing slow-cool crystallizations to yield a higher bulk density—sometimes this means adding hours to what might seem like “standard” process times. Our lab team follows up each lot with a suite of tests, focusing on melting point ranges, water content (using Karl Fischer titration), and persistence of key spectral peaks. The small changes are visible not just in paperwork but right under IR spectrometers and the noses of experienced chemists.
Shipping also requires more than a label. For chemistries with this level of purity and reactivity, even trace contamination from packaging materials or environmental exposure means lost work for the next chemist. From the start, we worked directly with logistics partners to reduce vibration and temperature swings. We learned quickly that, depending on the order size, specialized tertiary containers cut back on product degradation during long-haul trips. Years of feedback loops gave us the chance to focus carefully on details that, though invisible to the final user, change how the molecule behaves on the bench.
In practical use, 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid stands out for how it fits into complex organic synthesis. Research and corporate labs want to move fast but can’t compromise on the reliability of reagents. This compound enables coupling reactions and functional group interconversions central to the creation of advanced pharmaceutical candidates: kinase blockers, allosteric modulators, and more. As a manufacturer, we’ve seen requests for custom syntheses where slight modifications to this structure produce physiologically active molecules that could treat infections or interrupt tumor growth. Even small changes on this skeleton shift solubility, pharmacokinetics, and metabolic pathways—so every batch stands at the frontlines of complex science, with every percent of purity impacting outcomes.
Researchers have documented countless transformations of this acid in developing new molecular libraries. Many have shared successes using our batches in fusion reactions with nitrogen heterocycles—a low yield elsewhere but performing better with fresher and better-specified input. In contract synthesis programs requiring strict analytical reporting, having a full LC-MS and NMR record of the material helps align supplier quality with regulatory and customer expectations. Every so often, we field technical support questions about compatibility with oxidants or base-sensitive coupling partners, and our own labs have run those checks, sharing real-world data with academic and industrial collaborators.
Countless products carry the label “quinoline carboxylic acid,” but the specifics change everything. We have synthesized and compared 4-hydroxyquinoline-3-carboxylic acid, 6-methoxyquinoline-3-carboxylic acid, and many more—each one tells a different story in the reaction flask. Our observations support that the dual presence of hydroxy and methoxy functionalities brings more pronounced electronic and steric effects. In the lab, that translates into higher selectivity for substitution, better compatibility in palladium-catalyzed cross-coupling, and enhanced downstream derivatization opportunities. These features led us to refine crystallization and purification protocols so that researchers do not spend unnecessary time filtering out unpredictable byproducts.
Whereas other quinoline-based acids play a broader role in fields like dye chemistry and pesticides, this molecule’s impact resonates strongest in medicine, molecular diagnostics, and high-value specialty chemicals. Its clean, reproducible performance in heterocycle construction reshapes timelines for project completion and regulatory submissions. Over years, feedback from development teams and lead chemists in contract research organizations pressed us toward even tighter controls. We track not only assay values, but also check screening for persistent organic pollutants and process-derived trace metals that could impact high-sensitivity assays.
Our line workers and technical teams face a familiar set of hurdles with each production cycle. Scaling up from bench chemistry requires constant vigilance over solvent recovery, equipment maintenance, and the handling of energetic intermediates. Some competitors cut steps to save time, but our policy does not tolerate trade-offs when purity might suffer. Clean transition between stages, extended drying, and close reading of reactivity profiles let us offer peace of mind to customers. We regularly subject our intermediates and finished lots to impurity profiling—not only to detect the expected residuals, but to expose process-derived tautomers or isomers that standard analyses might miss.
Process optimization calls for hard work and open lines between R&D, quality assurance, and the shop floor. Our experience has shown that listening to customer feedback—whether it concerns melting point shifts, filtration rates, or stability on storage—feeds directly into process upgrades. Recently, we invested in additional HPLC columns and onboard spectroscopy equipment, based on insight gathered from repeated issues with trace contamination seen in labs undertaking high-resolution pharmaceutical crystallography. The bulk of our customers operate in stages where a few milligrams can mean days of work lost or gained, so our workflow focuses on batch reliability over fancy cost-saving measures that do not survive close scrutiny.
Not every problem finds an immediate fix. Occasionally, our team encounters clogging in reactor lines or overlapping spots in TLC analysis that slow the entire production cycle. Drawing on collective troubleshooting experience, our chemists adjust solvent ratios, change drying parameters, or alter crystallization rates to restore purity and yield. For recurring supply chain hurdles, we develop fallback sourcing protocols, so customers experience fewer shut-downs in research and manufacturing.
Several products line our shelves, but 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid earns a steady reputation based on customer experience. Pharmaceutical companies bring high-stakes projects where reliable input can shorten preclinical development by weeks. Academic research groups tend to share feedback unsolicited, discussing reaction outcomes and how specific impurities influence synthesis steps or bioassay signals. Data comes back to us as chromatograms, melting point reports, and sometimes even final patent disclosures—a validation for the attention paid to reproducibility.
We’ve witnessed firsthand the value of open dialogue with end users. Collaborative troubleshooting between our chemists and researchers on the customer side uncovers underlying process nuances that can often be missed by an eye glued to paperwork alone. Our chemists have flown out to consult on pilot installations, helped reroute batches to prevent exposure to incompatible reagents, and shared solvent handling tips—all in the spirit of solving hurdles before they grow. After-market support grows the cycle of incremental improvement. Lab managers tell us nothing frustrates a research team like discovering their building block doesn’t behave as promised due to trace contamination or excessive storage time. Backward tracing lots and reviewing our own process logs closes the loop, letting us share honest findings and, where necessary, correct issues by replacing or reworking shipments.
Regulations piece together a puzzle that grows more complex each season. Raw material traceability, in-process testing, and final product integrity all stand under scrutiny by regulatory bodies and client audits. Manufacturing 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid means working in the shadow of cGMP expectations, even when the immediate end-use is for research or as an intermediate. We keep extensive batch logs and ensure all reprocessing falls within agreed parameters—not just for our own documentation’s sake, but to guarantee researchers and regulatory affairs teams can trust what they receive on delivery.
Sustainability has become central to our decisions about solvent use, waste disposal, and energy consumption. Early in our experience, we saw less concern among clients about these issues, but industry conditions have shifted. Our solvent recycling system cuts environmental impact and operating costs. The lessons from integrating more efficient distillation and wastewater treatments provided data we now share in compliance disclosures. Direct emissions monitoring and iterative process changes reinforce a transparent relationship with both regulators and clients.
Everything we know about 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid’s role in synthesis stems from ongoing work with the broader community—people solving real chemistry problems. New projects come in demanding custom functionalization or crystalline grade, and we respond not with stock answers but with process tweaks grounded in what works at the bench. If a combination of purity, particle size, or moisture content gets a better yield or faster reaction rate, our plant adapts.
Academic researchers often ask for analytical data sets and side-by-side comparisons, so we’ve assembled supporting documentation with NMR, HPLC, and mass spectrometry readings, including detection of impurity signatures. Researchers have shared pre-publication data with us, which sharpens our own outlook on process effects well before industry standards catch up. Results find their way back into revised operating procedures: subtle shifts in crystallization temperature, experiment with alternate drying cycles, and new stock management timelines.
As synthetic needs evolve, so do customer expectations for documentation and support. We extend technical collaboration through regular updates, providing empirical evidence of the improvements. Our history demonstrates that partnerships with customers, not just transactions, deliver steady gains in quality and scientific progress.
Innovation in chemical synthesis ties back to the reliability of key inputs. As more industries look for advanced scaffolds in medicine, diagnostics, and materials, our commitment to rigorous process control and practical problem solving with 4-Hydroxy-6-Methoxyquinoline-3-Carboxylic Acid only deepens. Our plant continues to refine production, blending technical accuracy with the wisdom gained from real-world problem solving. As fresh requests and process challenges arise, our teams stand ready—because every scientist counting on these building blocks deserves confidence in every gram, every shipment, every result.