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HS Code |
827788 |
| Chemical Name | 2-Methyl-Quinoline-4-Carboxylic Acid |
| Cas Number | 16925-46-7 |
| Molecular Formula | C11H9NO2 |
| Molecular Weight | 187.20 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 221-224°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Smiles | CC1=NC2=CC=CC=C2C(=C1)C(=O)O |
| Inchi | InChI=1S/C11H9NO2/c1-7-12-9-6-4-3-5-8(9)10(7)11(13)14/h3-6H,1-2H3,(H,13,14) |
As an accredited 2-Methyl-Quinoline-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, opaque plastic bottle containing 25 grams of 2-Methyl-Quinoline-4-Carboxylic Acid, labeled with product details, safety warnings, and batch information. |
| Shipping | 2-Methyl-Quinoline-4-Carboxylic Acid is typically shipped in tightly sealed containers to prevent moisture ingress and contamination. It is transported as a solid under ambient conditions and labeled according to hazardous material regulations. Proper documentation, including safety data sheets, accompanies each shipment to ensure safe and compliant handling during transit. |
| Storage | 2-Methyl-Quinoline-4-Carboxylic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Protect from moisture and extreme temperatures. Ensure appropriate labeling and store at room temperature unless otherwise specified. Use personal protective equipment when handling to avoid contact or inhalation of dust. |
Applications of 2-Methyl-Quinoline-4-Carboxylic Acid in Industrial ManufacturingAs the original chemical manufacturer, we supply 2-Methyl-Quinoline-4-Carboxylic Acid for use in several advanced industrial sectors. This compound supports high-value synthesis routes where strict compliance and controlled process integration are mandatory. Below, we detail verified application tracks with specific standards, dosage practices, technical process points, and resulting product outputs. 1. Pharmaceutical Intermediate for Anti-Tuberculosis APIsOur 2-Methyl-Quinoline-4-Carboxylic Acid plays a key role as a building block in the multi-step synthesis of quinoline-based anti-tuberculosis active pharmaceutical ingredients (APIs). Downstream users employ this compound in the preparation of advanced intermediates for rifamycin formulations, supporting rigorous validation from regulatory authorities. Formulation laboratories and production sites rely on its defined purity profile for consistent drug substance manufacturing. Industry compliance standards
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2. Advanced Dye Intermediate for Azo and Reactive DyesThis specialty acid serves as an advanced intermediate in colorant synthesis, particularly for quinoline-based azo and reactive dyes. Industrial dye manufacturers incorporate this molecule for extended chromophore construction and fine color tuning, ensuring stability and reproducibility in textile and paper applications. Its use requires adherence to dye industry quality systems and worker safety protocols. Industry compliance standards
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3. Agrochemical Intermediate for Fungicidal AgentsIn crop protection manufacturing, the compound supports the synthesis of selective fungicidal agents, especially where quinoline analogues offer targeted bioactivity. Agrochemical formulation plants use it as a core scaffold for further functionalization, providing efficacy in resistance management programs. All operations require strict alignment with environmental and operator safety rules. Industry compliance standards
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4. Fine Chemical Precursor for Specialty Electronic MaterialsElectronics material manufacturers utilize this compound to prepare functionalized quinoline derivatives critical for organic electronic substrates and sensor components. The precise substitution pattern enables controlled electronic properties and improved device performance. Downstream integration requires chemical purity, low ion content, and trace metal control. Industry compliance standards
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5. Precursor in Synthesis of Analytical Reagents and Reference StandardsAnalytical laboratories and reference standard producers incorporate this acid into multi-stage syntheses of calibration and assay reference substances, especially for environmental, pharmaceutical, and forensic applications. The compound’s unique structure ensures specificity in trace-level determinations and stability in certified reference standards, all within strict quality controls. Industry compliance standards
Typical usage ratio
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Our work with 2-Methyl-Quinoline-4-Carboxylic Acid stretches across years of hands-on manufacturing. Having observed the molecule from the earliest synthetic step to final packaging, some things become apparent. Its structural core, built on a quinoline skeleton with precise methyl and carboxylic substitutions, remains crucial for researchers working in pharmaceutical and specialty chemical applications. Standard production targets a high chemical purity—at least 98%—because even a marginal impurity can generate downstream headaches in multi-step synthesis. This quality focus follows directly from the factory floor, where each batch undergoes repeated filtration, pH adjustments, and drying under controlled temperatures. The solid product--crystalline, pale yellow—retains consistency from lot to lot when operators hold to the established conditions.
We control the molecular weight to about 187.19 g/mol as calculated, matching the C11H9NO2 formula. This core structure doesn’t just happen; it takes real work maintaining reagent ratios and constant vigilance for byproduct formation. A sharp eye on cyclization yields a purer molecule, which then passes our internal HPLC and NMR checks. From firsthand experience, keeping solvent traces low during isolation matters just as much as chromatographic purity. Several partners in custom synthesis projects have made clear that even subtle solvent residues can unravel otherwise solid research.
What stands out about 2-Methyl-Quinoline-4-Carboxylic Acid is its knack for serving as an intermediate in the synthesis of more complex materials. Many colleagues, whether in pilot plants or research teams, count on it as a landmark building block for active pharmaceutical ingredients (APIs) and specialty dyes. Its profile allows selective derivatization: that methyl group at the 2-position can resist unwanted side reactions, and the carboxylic acid group at the 4-position proves valuable for further activation—think acylation, amidation, or esterification. The workflow from starting materials through to this compound isn’t always easy, but our experience shows that a consistent, high-quality product makes those downstream steps more efficient.
Researchers using our product tend to emphasize two points. Reliable melting point allows for streamlined protocol development, removing variables during crystallization. This reduction of ambiguity gives chemists more room to focus on molecule construction and less time troubleshooting failed steps. In multi-kilo projects, regular color checks and impurity profiles disclose lot-to-lot variation, so we deliver product documentation each time, derived from actual lab records, not marketing copy.
A lot of newcomers confuse 2-Methyl-Quinoline-4-Carboxylic Acid with other quinoline carboxylic acids, not realizing how even small structural changes rewrite chemical behavior in practice. Remove the methyl group, and you end up with a parent acid that responds differently to functional group transformations—its reactivity profile starts to change, especially during hydrogenations or oxidations. Shift the carboxyl group to a different ring position and solubility in organic solvents can increase or decrease, changing purification parameters and final product application scope.
Among quinoline-4-carboxylic acid derivatives, that methyl group at the 2-position isn’t just a trivial substituent. Many aromatic carboxylic acids, lacking substituents, run the risk of excessive conjugation and unanticipated reactivity with common acylating or coupling reagents. We see fewer side reactions during standard amide bond formation, as that methyl group provides a modest steric bulwark. These subtle but consistent advantages reveal themselves in the hands of synthetic chemists, not in warehouse stockrooms.
Our approach puts stability at the forefront. 2-Methyl-Quinoline-4-Carboxylic Acid holds up well over extended storage periods, provided operators maintain dryness and avoid prolonged sunlight. Thermal behavior also comes into play: when ramped at five degrees per minute, decomposition is delayed compared to related acids. This small difference has concrete implications in scale-up manufacturing; less material loss under mild heating means lower risk for thermal runaways, cleaner vessels, and lower cleaning costs after the batch run.
Every batch receives GC-MS screening for residual solvents and side products. We learned this the hard way, after observing mid-stream failures in coupling reactions triggered by traces of non-volatile contaminants. Target limit for solvent residue is below 0.1%. At this level, API projects run without unanticipated ghost peaks, and pilot purification teams spend less time chasing contaminants. All handling takes place in dedicated glass-lined systems for acid products, keeping cross-contamination risk below common industry averages. The upshot: technical managers sleep better, and operators see less rework.
We’ve watched companies and institutions use 2-Methyl-Quinoline-4-Carboxylic Acid to create a range of products. Its main career takes place as a precursor to quinoline-based small molecules—these end up in a variety of life science and electronics applications. Some customers modify the acid group, building linkers for peptide conjugation or for ligands in metal complex catalysis. As a coupling partner, the compound's purity and position-selectivity pay real dividends in step complexity reduction. Achieving three or four clean reaction steps without starting material intervention can save weeks of chemist time.
In specialty pigment synthesis, the base quinoline ring system serves as a core scaffold for new chromophores. By functionalizing the carboxyl and methyl groups, researchers unlock access to colors beyond typical industrial palettes—especially useful in applications demanding thermal stability and extended lifetime, such as OLED displays or photostable inks. In agricultural chemistry, similar scaffolds factor into lead optimization for new crop protection molecules. We’ve tracked several patent applications where this compound, through a few simple transformations, delivered higher target binding affinities.
Every quality parameter we set finds its way into application results. Sometimes customers discover that a higher water content correlates with unexpected solubility issues or crystallization failures. We routinely keep water content under 0.5%, using Karl Fischer titration as final confirmation. At this threshold, researchers finish their reactions without unpredictable phase separation or hard-to-remove hydrates.
Early on, we used glass fiber filtration, only to find fiber contamination in downstream filtrates. Swapping to PTFE filtration improved product consistency and reduced customer complaints about particulate debris. Color is another indicator: a product that varies from pale yellow to dark orange means too much process drift. Maintaining tight control over oxidation conditions provides a visual assurance, which users tell us speeds their in-process quality checks.
During custom projects, synthetic teams sometimes need a specific particle size or a coarse-granular form for slurry handling. We accommodate requests because we’ve handled scale-ups ourselves. Achieving the right form without sacrificing purity requires small tweaks at recrystallization or drying phases. These small adjustments matter: teams handling large reactors or continuous flow systems know that incorrect particle characteristics can choke filters or cause uneven dissolution. We review each customization request with our technical team, weighing risks and time requirements, then make the batch to order.
Typical orders for research scale demand 10 g to 100 g. For process development, 1 kg to 5 kg batches become more common, and here, packaging quality plays a role. We use moisture-barrier bags and secondary containers, followed by full labeling by lot and production date, so traceability remains absolute. With critical intermediates, manufacturing errors snowball fast, so each operator documents every batch change and cleaning cycle in electronic logs. These records save both time and trouble for teams running regulated or patent-driven projects.
We have learned from the manufacturing floor that direct contact with quinoline-carboxylic acids often leads to skin and mucosal irritation. So, personal protective equipment—nitrile gloves, splash goggles, and basic fume hood containment—become standard. Each lot’s MSDS comes from our own experience, not drawn from general literature. Our plant once implemented double filtration to cut manual exposure, cutting accident reports related to this product by two-thirds last year.
Waste handling presents another real challenge. Neutralization steps for spent acid streams take careful balancing: too much base creates a stubborn emulsion, too little leaves corrosive residue in drains. Using automated pH monitoring stations on our effluent lines, we keep acidic runoff below government discharge thresholds consistently, based on real data. This commitment goes well beyond paperwork compliance—it saves us reprocessing costs and neighbor complaints.
Our industry sees constant pressure to minimize solvent and energy consumption, especially through greener synthesis routes. Quinoline derivatives historically came from coal tar distillation, then shifted to more modern synthetic routes. Our facility relies on catalytic cyclization steps, but we work to limit high-boiling and chlorinated solvent use, targeting mid-polar aprotic solvents like DMF or THF within exposure guidelines. Recovering and reusing solvents—through in-house distillation—pays off, and we invest these savings in improved ventilation and worker safety monitoring.
Handling batch-to-batch variance remains another reality. Process drift from inconsistent temperature ramps, imprecise reactant weighing, or over-working during filtration—which sounds small but results from overzealous new technicians—can shift color and purity away from targets. We run regular training talks to share batch errors, and managers encourage staff to log process anomalies as soon as they appear. Holding open Q&A sessions encourages operators to speak up about even minor fluctuations. This feedback loop keeps process quality robust and product rejection rates the lowest on our block.
Customers increasingly ask for full traceability, from raw chemical sourcing to finished product. We keep purchase orders, shipping manifests, and batch production sheets tied together in a single system. Investors or auditors can walk straight from the receiving dock to the shipping bay and see a transparent path. In the rare case of a returned drum, we investigate root cause and publish findings to both staff and the client. Building this culture of transparency has paved the way for longer-term supplier relationships, making life easier for both sides.
The rise of regulatory expectations in pharmaceuticals, electronics, and fine chemical sectors means the days of generic “industrial grade” have faded for specialty building blocks like 2-Methyl-Quinoline-4-Carboxylic Acid. We see more requests for multi-grade offerings: research, process, and GMP-compliant lines. Each extra layer of documentation, analytical backup, and change notification adds work, but we welcome it. At the end, the improved relationship with our partners—built on evidence, not promises—lets us move from short-term commodity business to true collaboration.
Direct client collaboration influences how we upgrade downstream processing equipment and quality protocols. For instance, we updated our crystallization system last year after a customer flagged changes in melting behavior during an intricate scale-up. Adding programmable cooling cycles and inline turbidity monitoring gave us a sharper handle on endpoint determination, cutting waste and improving yield. Those who use the product long-term tell us this single change translated into better packing densities and increased storage life, both relevant for anyone aiming for high-throughput, high-precision synthesis.
Plant teams operate on the principle that each error is a lesson. Keeping open access to process data lets both junior and senior staff see trends and suggest process tweaks. Several years ago, uneven drying left pockets of clumped material in finished goods. By shifting to low-humidity, controlled-circulation ovens, we realized tighter bulk density, easier handling, and customer kudos for better dissolution profiles. These adjustments stem from real user reports, combined with a willingness to swap equipment, try new settings, and scrap ineffective protocols.
We listen to input from users who share details of their synthetic challenges, whether for a new research molecule or a large-scale production run. By welcoming this feedback, we can test changes in real time. Whether that means piloting a solvent-free isolation method or exploring microwave-assisted crystallization, our goal is practical—not just compliance, but improvement. Relationship and process improvement tie together in the daily realities of manufacturing a complex molecule like 2-Methyl-Quinoline-4-Carboxylic Acid.
Our shop avoids generic product descriptions. Drawing on years working side by side with this compound, our perspective puts actual production knowledge first. Whether it’s the right downstream impurity profile or minor tweaks to crystal morphology, we draw on lived experience, not just lab manuals. This attitude shapes how we approach both new orders and established relationships. Instead of hype or jargon, we share what we know from handling, refining, and delivering this material across projects and borders.
We offer 2-Methyl-Quinoline-4-Carboxylic Acid with confidence grown from real-world process challenges and solutions. Clients get not just a drum of material, but the support of colleagues who’ve faced—and solved—the same obstacles. Our goal, each time a batch finishes, is clear and simple: to support users with a product we’d trust on our own benches, in our own scale-ups, for our own research and manufacturing needs.