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HS Code |
380437 |
| Product Name | Methyl 2-Oxoindole-6-Carboxylate |
| Cas Number | 114772-55-1 |
| Molecular Formula | C10H7NO4 |
| Molecular Weight | 205.17 g/mol |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 234-238°C |
| Solubility | Soluble in organic solvents like DMSO, methanol |
| Smiles | COC(=O)c1ccc2c(c1)C(=O)NC2 |
| Inchi | InChI=1S/C10H7NO4/c1-15-10(14)6-3-2-4-7-8(6)9(12)11-5-7/h2-5H,1H3,(H,11,12) |
| Purity | Typically ≥98% |
| Synonyms | Methyl oxindole-6-carboxylate |
| Storage Temperature | 2-8°C |
As an accredited Methyl 2-Oxoindole-6-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5g Methyl 2-Oxoindole-6-Carboxylate is packaged in a sealed amber glass vial with a tamper-evident polypropylene screw cap. |
| Shipping | Methyl 2-Oxoindole-6-Carboxylate is shipped in tightly sealed containers, clearly labeled, and protected from moisture and light. Transportation complies with relevant chemical safety regulations, using secondary packaging to prevent leaks or spills. Handling is restricted to trained personnel, and accompanying documentation includes hazard identification and emergency response information. Store upon arrival as instructed. |
| Storage | Store Methyl 2-Oxoindole-6-Carboxylate in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated conditions). Avoid exposure to heat and direct sunlight. Ensure storage area is equipped for chemical safety and labeled appropriately to prevent accidental misuse or contamination. |
Applications of Methyl 2-Oxoindole-6-Carboxylate in Industrial ManufacturingAs the primary manufacturer of Methyl 2-Oxoindole-6-Carboxylate, we focus on supporting innovative, high-value downstream industries that require precise control of raw material quality, compliance, and consistency in their specialty intermediates. Our product has established itself in several distinct production sectors, including pharmaceuticals, agrochemical synthesis, fine chemicals, and advanced research materials. Below, we detail key application areas with verified industrial workflows. 1. Pharmaceutical Synthesis: API Intermediate for Anticancer CompoundsPharmaceutical manufacturers employ our material as a crucial building block in multi-step active pharmaceutical ingredient (API) synthesis, especially in the preparation of indole-derived anticancer agents. The compound offers a well-defined indole skeleton that supports regioselective functionalization during the elaboration of molecular scaffolds for kinase inhibitors and heterocyclic drugs. Integration typically occurs at the stage requiring formation of substituted indolines or spirooxindole cores, with attention to purity profile and trace metallic residues for downstream compliance. Adjustment of input quantifies responds to target molecular weight, yield optimization, and impurity management across batch-to-batch scale-up. Industry compliance standards
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2. Agrochemical Intermediate Production: Synthesis of Indole-Based FungicidesManufacturers in the agrochemical sector incorporate this compound as a key precursor in the multi-step synthesis of indole-linked fungicides, particularly those formulated to disrupt fungal cell wall formation. The structural features support selective chlorination and esterification reactions vital to generating target molecules with improved bioactivity against resistant strains. Quality inspection at this stage prioritizes validation of residual solvents and low-level organic impurities to comply with environmental safety and toxicological requirements imposed by global agricultural markets. Industry compliance standards
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3. Fine Chemical Manufacturing: Indole-Chromophore Synthesis for Specialty DyesProducers of specialty organic dyes and pigments make extensive use of this intermediate due to its ability to facilitate color tuning through selective modification of the indole ring. It is often included as a feedstock in the synthesis of extended conjugated chromophores, where the purity and moisture content critically influence product crystallinity and lightfastness. The compound is dosed based on the stoichiometry required for C–C coupling or condensation with electron-withdrawing groups to achieve specific absorbance peaks in visible or near-infrared spectra, commonly for high-stability dyes in plastics and advanced coatings. Industry compliance standards
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4. Chemical Research and Discovery: Indole Scaffold Library PreparationInstitutes and contract research organizations select this raw material as a core scaffold for the assembly of chemical libraries targeting novel heterocyclic architectures. It serves as an entry point for parallel synthesis protocols, wherein diverse substituents are systematically attached at positions enabled by the carboxylate and oxoindole moieties. The compound's consistent NMR, GC, and HPLC profile supports traceable batch release, facilitating downstream SAR (structure–activity relationship) studies for new molecule identification and patent application drafts. Industry compliance standards
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Every chemist knows some molecules draw a crowd, quietly threading through themes in research and production. Methyl 2-Oxoindole-6-Carboxylate stands among these—not because it shouts for attention, but because, batch after batch, the labs and process halls return to it for consistent results. Having run reactors, double-checked drying ovens, and compared spectra day in and day out, the story of this compound isn't abstract. Its worth gets measured in every bottle shipped and every chromatograph reviewed.
Methyl 2-Oxoindole-6-Carboxylate carries the indole backbone, a structural motif that’s hard to beat for stability in synthetic routes. That extra carboxylate group at the 6-position, along with the 2-oxo function, unlocks a whole branch of reactivity. Many researchers dig for that: the ability to modify, attach, or transform into intermediates for pharmaceuticals or dyes. Our team starts from well-characterized raw materials. Reproducibility doesn’t come from hope—it comes from controlling every step, ensuring reagents haven’t degraded, and keeping a short timeline from synthesis to finished product.
Industry specifications mean little without real verification. We lean on analytics: HPLC for purity, NMR for confirmation, MS for molecular weight. Purity typically exceeds 98%, and anyone who’s ground a sample knows what that translates to in practice: reliable melting points, sharp spectra, a clean slate for downstream chemistry. Moisture matters, especially for esters prone to slow hydrolysis, so we keep each batch in airtight amber glass or robust drums, with desiccants added for every package leaving our warehouse. That isn’t just protocol—it’s a lesson learned after running into trace hydrolysis and unwanted product breakdown years ago.
Our customers range from graduate student benches to multinational project teams. They come for the same reason: this compound’s unique reactivity profile. The 2-oxoindole nucleus, functionalized at the 6-carboxylate, creates a launching pad for ring construction and selective derivatization. In preparing 6-substituted indole derivatives, researchers often use our methyl ester directly, taking advantage of its solubility in common organic solvents and smooth reactivity in transesterification or amidation.
We know how tough it is to source reference-grade intermediates. The methyl ester group handles both protection and activation—it holds firm during elaborate syntheses but can be cleaved cleanly when needed. That translates into fewer purification headaches later on. Process chemists working on scale-up especially notice this; by minimizing side reactions, less time gets lost to column runs and solvent switches.
Choosing the right indole derivative is a balancing act between reactivity, cost, and process control. From hands-on experience, differences show up immediately. The position of the ester group plays more than a cosmetic role. Substituents on other parts of the indole ring—whether methyl, nitro, halogen, or something bulkier—can dramatically shift solubility, melting points, or reaction preferences. We stick with a well-defined 6-carboxylate, knowing precisely how it will react under both acidic and basic conditions commonly used in organic synthesis labs.
Alternative esters or isomers sometimes show up on the market, but their chemistry rarely brings the same reliability. For example, 5- or 7-carboxylate indoles, seemingly close in structure, can differ in aromaticity and steric hindrance, shifting selectivity in key steps like cyclizations or coupling reactions. Some synthetic chemistries favor an ethyl or benzyl ester, often aiming for altered solubility or slower hydrolysis. We’ve trialed these alternatives for customers evaluating scale-up outcomes. Most revert to the methyl ester—it strikes a workable compromise between lability and stability.
No matter how many times we run the reaction, new challenges keep cropping up. Methyl 2-Oxoindole-6-Carboxylate doesn't forgive sloppy technique. Its route typically starts with an indole precursor, which must be perfectly pure. Impurity carryover causes irreproducible yields and unexpected coloring. We rely on local suppliers where possible, running spot checks for isomeric purity before any batch begins. On a larger scale, temperature control becomes a science of its own—one extra degree during cyclization can tip the balance from a clean product to a stubborn mixture.
Once the main reaction wraps, purification starts. Some esters can ride along with the desired molecule—another reason for precise column packing and solvent selection. A few years ago, a customer flagged low performance in their downstream chemistry. Turns out, a small side product from incomplete cyclization snuck past initial checks. We doubled down, extending TLC monitoring and introducing routine gradient HPLC runs. Current practice never lets a batch slip through unchecked.
Methyl 2-Oxoindole-6-Carboxylate’s nature as a privileged indole core means it threads through medicinal chemistry regularly. Drug discovery teams use it to access novel heterocyclic scaffolds, feeding exploratory SAR (structure-activity relationship) campaigns. Some of the most promising kinase inhibitors or CNS candidates emerge from libraries seeded with indole derivatives. Our customers want to trim variables at every stage, so they look for consistent material that handles the same whether used in ten-gram trials or kilogram pilots.
Fragment-based drug design rides on intermediates like this. Rapid access to building blocks that tolerate a wide range of conditions opens synthetic avenues previously closed off due to stability issues. Our batches get selected for fragment libraries, with feedback cycling straight from the field—what worked, what gummed up, where impurities raised flags. Iteration has driven down unwanted byproducts and tightened up our specs over the years.
While pharmaceuticals get most of the spotlight, not every shipment of this compound lands in a drug project. Dye and pigment manufacturers, especially those seeking eco-friendlier routes, have adopted indole-based intermediates for selective color modulation. The 2-oxo group absorbs strongly in the UV-Vis range, imparting unique chromatic characteristics to finished dyes. Before shifting to this raw material, many faced issues balancing reactivity and lightfastness—a matter of small molecular tweaks that never shows up on spec sheets.
Specialty material developers are finding the indole framework useful in electronic materials. Researchers have looked at new polymers and functional coatings by taking advantage of indole’s baked-in pi-stacking and electron-rich character. Methyl 2-Oxoindole-6-Carboxylate shows up in these applications because it stands up to moderate process heat and resists yellowing during extended runs. Without that stability, much more would be lost to reprocessing.
Results make or break product trust, and in this line of work, word spreads quickly about reliable suppliers. The journey with this compound began in a cramped pilot lab, two chemists developing a process in borrowed glassware, running GCMS at midnight before an early deadline. Today’s runs echo those lessons—how humidity can sneak in through a loose seal, how grinding the ester too vigorously can degrade the surface, how every analytic readout tells a part of the story. We invested in temperature logging, automated dispensing, and small-scale test batches for each new order. Lessons from every failed run have shaped current procedures.
Feedback often shapes the way we produce and refine this compound. Customers will mention a new reaction condition, and sometimes we get called in to troubleshoot. It's not unusual for a researcher to ask about batch-to-batch variability, or whether switching solvent systems will change outcomes. Having walked through those scenarios ourselves, we supply detailed COAs plus typical impurity profiles. Technical support draws from direct lab experience, not guesswork.
No intermediate survives the shipping process without care at every step. We use amber bottles and steel canisters for larger orders, sealing each with both liner and desiccant. Exposure to moisture, more than heat, has proven the biggest risk for esters like this. Early on, local climate swings taught us to avoid standard cardboard packaging for all but the briefest transports. It takes little to spoil a carefully synthesized batch, so we encourage cool, dry, well-ventilated storage at the end user’s facilities. Customers asked about long-term shelf life; with proper conditions, samples remained in spec for more than two years. The product doesn’t cloud or crystallize unless exposed to open air repeatedly—proof that manufacturing and packaging both pull their weight.
Bridging the gap between small-batch synthesis and reliable supply chain takes a real investment in process control. Many initial requests came from custom syntheses, where a customer would specify gram-scale needs for method development. What began as bespoke runs has grown into regular, semi-automated production. Yet every scale-up step uncovers hidden variables—a hot spot in a mixing tank, variable feed rates, solvent retention during workup. Tweaking those details transformed tolerance thresholds and minimized batch failures. We document every change, running small lots to ensure nothing unexpected comes up. It means growth stays manageable and no customer faces the dreaded mid-project “out of stock.”
Fielding special requests is routine—such as alternate solvents for those aiming to minimize ecological impact, or requests for micro-packed samples for screening campaigns. Working directly with end-users, not traders or distributors, builds mutual trust that shows up in their willingness to share method improvements. Bringing customer data into our process loop pushes us to raise all benchmarks—yield, purity, turnaround time, and waste minimization.
While not every user asks about regulatory status, experienced manufacturers keep an eye on changes in classification and transport rules. For Methyl 2-Oxoindole-6-Carboxylate, we monitor regulatory updates to ensure safe and lawful logistics. Classification under hazardous materials varies by region, affecting everything from labeling to packaging. Our documentation tracks each lot from raw goods to outbound shipment, keeping records accessible for any audit or customs inquiry. Detailed batch histories and clear traceability cut down on delays at borders or during inspections.
Eco-responsibility shapes a lot of internal decisions. By favoring greener solvents and improving energy efficiency in our core process, we reduced overall waste by nearly 18% in the last operating year. Customers increasingly weigh these factors, and clear communication around sustainability efforts bridges manufacturer goals with user values. None of these improvements come from a playbook copied from somewhere else. Every lesson reflects specific, sometimes hard-earned experience.
Mistakes shape manufacturers more than any string of successes. Early in production, oversized reaction vessels led to uneven heating and erratic byproducts. Rather than doubling down or pushing the flawed batches, we stopped, retooled, and added inline thermocouples for continuous monitoring. That reset cost weeks up front, but it saved months later by establishing more stable operations. Communication between production staff and research chemists remains open. Nobody forgets a failed scale-up for a major customer that could have been avoided with closer monitoring—so post-mortems remain standard.
On another occasion, a change in a raw material supplier led to off-spec product, causing headaches for a researcher. Swift recall, transparent reporting, and a replacement shipment restored trust. No manufacturer avoids errors entirely, but long-term customers know us by how we handle these bumps.
Success as a producer of specialized intermediates doesn’t just depend on equipment or facility size. Experience, accumulated batch by batch, makes the real difference. Knowing Methyl 2-Oxoindole-6-Carboxylate inside and out translates directly into more predictable results for users. A routine run still gets full attention. We know the quirks—how slight shifts in pH leave a detectable fingerprint in the NMR, how unfiltered solvents drag in micro-impurities, what temperature ramp avoids unwanted decomposition.
Looking forward, we’re moving towards more flexible production systems that can adapt quickly to volume surges or new purity requirements. Customers exploring automated synthesis or high-throughput applications already ask about micro-lot customization. We welcome these conversations—they sharpen our methods and drive product improvement.
There’s a big divide between moving chemical barrels and building a relationship over time. Our team lives the ups and downs of every batch, treating each customer problem like their own. Methyl 2-Oxoindole-6-Carboxylate reflects this philosophy: more than just a reagent, it’s a tool sharpened by decades in the lab and on the factory floor. Every improvement stems from listening to real feedback and making real-world changes. The story behind every bottle shipped reflects countless careful decisions, a commitment to detail, and the honest hard work of a team that knows chemicals from the inside out.