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Methyl Oxindole-5-Carboxylate

    • Product Name Methyl Oxindole-5-Carboxylate
    • Alias MOC-5C
    • Einecs 629-551-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    909140

    Chemicalname Methyl Oxindole-5-Carboxylate
    Molecularformula C10H9NO4
    Molecularweight 207.18 g/mol
    Casnumber 78071-71-9
    Appearance White to off-white solid
    Meltingpoint 174-178 °C
    Solubility Soluble in organic solvents like DMSO and methanol
    Purity Typically >98%
    Boilingpoint Decomposes before boiling
    Storagetemperature 2-8 °C
    Smiles COC(=O)c1ccc2c(c1)[C@@H](=O)NC2
    Inchikey KEKJCYIVUMTTFZ-UHFFFAOYSA-N

    As an accredited Methyl Oxindole-5-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, white screw cap, tamper-evident seal, hazard labeling, compound name and CAS number clearly printed.
    Shipping Methyl Oxindole-5-Carboxylate is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with chemical safety regulations. The chemical is transported as non-hazardous under normal conditions, but care is taken to prevent spills or leaks during transit. Appropriate documentation and labeling ensure regulatory and safe delivery.
    Storage Methyl Oxindole-5-Carboxylate should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it away from strong oxidizing agents and moisture. Refrigeration is recommended (2–8°C). Handle under inert atmosphere if possible to prevent decomposition. Make sure to label the container clearly and follow all safety protocols.
    Application of Methyl Oxindole-5-Carboxylate

    Applications of Methyl Oxindole-5-Carboxylate in Industrial Manufacturing

    Methyl Oxindole-5-Carboxylate serves as a specialty intermediate trusted by downstream manufacturers in fine chemicals and advanced material synthesis. Its heterocyclic structure and reactive functional groups enable precise incorporation in multiple formulation and process routes. Below, we detail its established industrial relevance within select application scenarios, showing regulatory context, industrial formulation practices, process insertion, and downstream product outcomes.

    1. Advanced Pharmaceutical Intermediate for API Synthesis

    Within pharmaceutical API manufacturing, this intermediate is a key building block for synthesizing complex indole-based drug molecules targeting CNS and oncology fields. Manufacturers favor its controlled purity profile, allowing seamless integration in multi-step reactions requiring stringent quality risk management. Its chemical reactivity supports selective transformations during N-alkylation, condensation, and cyclization reactions, benefiting established GMP workflows for regulated markets across Europe, North America, and Asia-Pacific.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (API)
    • EU GMP Part II (Pharmaceutical Starting Materials)
    • USP-NF/EP/JP Relevant Monographs (for downstream APIs)
    • REACH Annex XVII – Registration for chemical intermediates

    Typical usage ratio

    • Employed at 0.6–1.8 molar equivalents relative to target API intermediate; exact ratio calculated per synthetic pathway scale and yield optimization studies. Excess may be applied in multi-step condensation to drive selectivity if conversion rates present limitation.

    Downstream process integration

    • Introduced during initial or intermediate reaction setup in multi-pot synthesis sequences, preceding or following key condensation or coupling reactions depending on target API structure. Integrated in stirred tank reactors under controlled temperature and inert atmosphere.

    Final product types

    • Chemical intermediates for indole-based antipsychotics
    • Precursor blocks for oncology drug candidates
    • Synthons in small-molecule CNS modulators
    • Advanced material references for contract/CMO API production

    2. Dye and Pigment Precursor for Specialty Applications

    In the colorant manufacturing sector, Methyl Oxindole-5-Carboxylate is integral to the synthesis of high-performance indole chromophores, allowing formulation of stable, high-saturation pigments for specialty coatings and inks. Chemical producers utilize it for direct coupling or as an aldehyde-reactive component in constructing extended conjugated systems, critical for color strength and fastness attributes demanded in industrial pigment preparation.

    Industry compliance standards

    • EN 71-3 (Toy Safety - Migration of Certain Elements)
    • REACH SVHC (Substances of Very High Concern) compliance for pigment precursor supply
    • ASTM D4963 (Pigments: Chemical Composition)
    • ISO 9001:2015 (Quality Management for Industrial Dye Manufacturing)

    Typical usage ratio

    • Ranges from 2–10% by mass of total pigment synthesis charge; precise dosing dependent on target pigment class and shade intensity. Adjusted to balance yield and purity based on final chromatic properties after downstream chemical coupling.

    Downstream process integration

    • Fed into batch reactors during diazo coupling or condensation steps, following amine or aldehyde partner addition. Incorporated ahead of pigment isolation, washing, and drying stages, influencing overall particle morphologies and tone.

    Final product types

    • Indole-based azo pigments for specialty inks
    • Organic shades for automotive and industrial coatings
    • Textile dyes with improved washfastness
    • Color masterbatches for plastics processing

    3. Fine Chemical Intermediate in Agrochemical Synthesis

    This raw material acts as a reactive intermediate in the construction of indole-derived agrochemical actives, supporting crop protection formulations through robust chemical transformations. Agrochemical manufacturers pursue targeted substitutions and ring-closure reactions, leveraging the substrate for selectivity in producing active herbicides or growth regulators under controlled synthetic and regulatory requirements for technical-grade outputs.

    Industry compliance standards

    • FAO/WHO Guidelines on Specification of Plant Protection Products
    • OECD Guidelines for Testing of Chemicals (Synthesis and Impurities)
    • ISO 17025 (Analytical validation for technical materials)
    • National pesticide registration requirements (EPA, EU, China MARA)

    Typical usage ratio

    • Incorporated at 0.95–1.5 molar equivalents depending on conversion rate, dictated by downstream condensation or cyclization yield targets. Flexibly adjusted for pilot or commercial-scale synthesis in response to impurity profile and technical product standards.

    Downstream process integration

    • Introduced after initial base-catalyzed activation; reacts in controlled charge with aldehydes or halides to form agrochemical actives before formulation. Integration executed in closed reactors to comply with environmental and occupational safety protocols.

    Final product types

    • Indole-derived herbicide technical concentrates
    • Plant growth regulator active ingredients
    • Pre-emergent selective pesticide synthesis
    • Intermediate bulk chemicals for agro-formulators

    4. Monomeric Building Block for Functional Materials R&D

    R&D divisions in specialty polymers and advanced materials valorize this compound for synthesizing customized monomers and oligomers, targeting film-forming, UV-responsive, or electronic substrate applications. Precision placement within molecular frameworks provides downstream flexibility, enabling custom polymer backbone engineering and leading to prototypes for optoelectronic materials or specialty coatings requiring fine-tuned heterocyclic incorporation.

    Industry compliance standards

    • ISO 9001:2015 (Quality Assurance for R&D and Pilot Production)
    • RoHS 2 Directive 2011/65/EU (Electronic application materials)
    • WEEE Directive (Material Recovery and Traceability for electronics)
    • Analytical test compliance: HPLC/GC-MS for purity and residual solvent threshold

    Typical usage ratio

    • Typically introduced at 1–5% by solid weight in resin formulations or adjusted by mole percent (up to 7%) in custom monomer synthesis. Usage depends on required functional group density and targeted end-use characteristics in polymer structure.

    Downstream process integration

    • Added during initial monomer synthesis step or copolymerization reactions in lab reactors or pilot lines. Processes may include solution polymerization under inert atmosphere or stepwise oligomer chain assembly using controlled temperature profiles.

    Final product types

    • Research-grade indole-functional monomers
    • UV-curable resin prototypes
    • Specialty pre-polymers for electronic substrates
    • Experimental thin films for advanced coatings
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    Certification & Compliance
    More Introduction

    Methyl Oxindole-5-Carboxylate: Insights from the Manufacturer’s Floor

    A Chemist’s Introduction to a Versatile Building Block

    Every day in our production facility, work starts hours before sunrise. Batches line up, equipment hums, and the scent of chemical change laces the air. Among our dozens of molecules, Methyl Oxindole-5-Carboxylate steps forward as a compound whose impact spreads far from its modest appearance. Our years handling this molecule have revealed nuances that no data sheet can tell you. On the surface, it’s a pale powder. In skilled hands, it unlocks new routes in pharmaceutical and fine chemical synthesis—just as precise and reliable as the chemists who insist on it.

    From Raw Material to Refined Compound

    Our process does not rely on shortcuts or untested steps. We select our isatin source with strict attention to purity. Years back, supply chain inconsistencies forced us to trial new purification methods—nothing brings out flaws like a faulty starting batch. Each lot undergoes controlled esterification under conditions mapped out over dozens of pilot-scale runs. The heart of our methodology is rigorous attention to temperature control and solvent quality. While it sounds routine, anyone who has battled a runaway exotherm knows that “routine” means constant vigilance, instrumentation, and knowledge of catalytic quirks that textbooks rarely cover.

    After the reaction, we isolate the crude product and launch into a labor-intensive purification. Cold crystallization from ethanol ensures the methyl ester form locks in, minimizing the residual acid. Each run is checked by HPLC, which has helped us identify even low-level by-products from rogue hydrolase activities or incomplete conversions. We pay close attention to the physical form. End-users tell us that crystal habit and particle size impact downstream reactivity; we take that seriously and make production changes when feedback points to clumping, dusting, or segregation in blending steps.

    Specifications: Real-World Insights

    What matters most for our partners is repeatability. Each customer application highlights a different pain point: a pharmaceutical client might reject a lot for trace benzene, an intermediate manufacturer notices yield drop-offs if moisture rises above 0.2%. Our specs for Methyl Oxindole-5-Carboxylate focus on three measurable areas—purity, trace contaminants, and residual solvents. Routine lots clear 99% by HPLC, with water content at or below 0.1%. GC-MS checks ensure solvents stay below compliance levels, meeting even the stringent European pharmacopeial requirements.

    Over time, user requests have shaped our quality protocols. Early on, one laboratory flagged an infrequent byproduct—a methylated oxindole variant appearing above 0.3% on their NMR. We overhauled filtration and introduced extra cold washing to suppress formation, sacrificing a little yield for a cleaner molecule. With feedback, we've brought the byproduct below 0.05%. This might seem finicky to some, but reproducibility matters far more when the compound walks into medical research or high-value organic synthesis.

    Why Methyl Oxindole-5-Carboxylate Stands Apart

    On paper, many molecules look similar. The real differences emerge in how they perform from one reaction to the next, and which side products they drag along for the ride. Methyl Oxindole-5-Carboxylate combines a robust oxindole framework with a carboxylic methyl ester at the 5-position. The position of that ester has proven crucial—neighboring substitutions affect reactivity, stability, and the ease of further derivatization. Oxindole chemistry is a crowded space. Many chemists reach for 7-carboxylate or 4-carboxylate analogues, but these structural isomers behave differently under acylation or metal-catalyzed coupling. Our years on the bench show that the 5-carboxylate methyl ester unlocks broader reactivity windows, especially for Suzuki-type cross-couplings and nucleophilic aromatic substitution pathways.

    In pharmaceutical research, the 5-carboxylate’s mild electron-withdrawing effects allow for more controlled introduction of new functional groups, without triggering decomposition in sensitive structures. Our partners in agrochemical development highlight its role as a springboard for bioactive modifications—a step away from widely-commoditized indole intermediates. Compared to standard N-methylated oxindoles, the 5-carboxylate builds more complexity with fewer steps and less need for rework, directly impacting cost and lead time.

    End-User Experience: Where Precision Matters

    Production-scale chemistry rewards consistency above all. A customer’s synthesis will rise or fall on the consistency of incoming materials. In our five years supplying Methyl Oxindole-5-Carboxylate, the same buyers have returned with new projects—not out of habit, but because they see fewer failed runs and unplanned maintenance. Scale-up work always comes with surprises, but clarity on impurity profiles and the way our product handles under varying storage conditions lets users plan around real, not theoretical, risks. When one biotech partner started running 100-liter reactions, they noticed subtle batch-to-batch differences from alternate suppliers—differences that became headaches at scale. Problems like off-color batches or crystallization mismatches do not announce themselves in a catalog, but chemists in the lab spot them straight away. We keep close documentation on lot release profiles for just this reason.

    Being customer-oriented does not just mean meeting a spec. End-users have reached out with stories of how our oxindole responds to storage over months, or how a single batch outlasted competitive grades when left exposed to ambient humidity. Picking up the phone and listening to a lab technician’s trouble shooting call carries lessons rarely found in a batch log. That ongoing dialogue has steered us toward smaller packaging sizes for moisture-sensitive clients, and driven us to improve our anti-static measures in bulk shipments.

    Purity and Stability: More Than Numbers

    Purity for this molecule must go deeper than a single-point measurement. What really matters is how the product behaves under different conditions. An HPLC reading provides a snapshot, but storage, transportation, and even grinding for formulation impose their own demands. Moisture pick-up, trace acidic impurities, and interactions with common excipients all impact how the product performs at the bench. We run accelerated aging studies—not just for regulatory purposes, but because we have seen firsthand the consequences of a slight change in stability.

    Our approach takes stability seriously. All packaging is lined to reduce oxygen ingress, and silica desiccant is always included. We verify performance through periodic re-testing, with a log stretching back years, so our long-term partners see the historical trends and can anticipate run-ins with specific impurity classes. Having this level of historical data—and being willing to share it—gives users confidence that each batch will carry through in their applications, rather than introducing surprises several months down the line.

    Typical Applications and Industry Feedback

    Many of our clients work in medicinal chemistry. Here the purity of precursors can decide whether a project moves forward. Methyl Oxindole-5-Carboxylate serves as a gateway molecule for new CNS-active drugs, advanced intermediates for protease inhibitors, and as a core building block in peptidomimetic design. Our partners in university research investigate it for entirely new scaffolds—places where even a slight contaminant or isomer can ruin assay data.

    Working closely with contract manufacturers, we have seen the wide embrace of this compound for peptide coupling and complex alkaloid synthesis. Time and again, project delays can be traced to unpredictable purities or overlooked secondary byproducts. We have altered crystallization protocols to meet demand for material compatible with microwave-assisted reactions, and responded to requests from major pharma for tighter control on endotoxin levels—even when these requirements push our analytical capabilities. This dialogue pushes innovation, making future runs safer and more reliable for everyone in the chain.

    Batch Processing vs. Continuous Manufacture

    All good manufacturing balances tradition with progress. For Methyl Oxindole-5-Carboxylate, early efforts followed classic batch sequencing. As demand grew, we experimented with continuous processing. That shift brought improvements and setbacks. At scale, even slight inefficiencies multiply costs, but continuous flow reactors uncovered several new impurity formation routes unique to fluid dynamics and residence time. Instead of ignoring the evidence, we adapted—installing inline analytics and tightening filter changes.

    Every challenge fed back into the process. When off-white batches appeared during a mid-summer run, we traced the cause to a heat exchanger failure that passed unnoticed in batch scale but proved disastrous for product color on continuous. No instrument or analytical technique substitutes for visual and tactile skills developed from years at the bench, so we build those checks into every production line. By iterating on both continuous and classic batch approaches, we offer flexibility in order size and maintain the stringent quality our customers expect.

    Comparisons with Similar Products

    Many alternatives exist on the market, from structurally-similar carboxylate esters to N-protected oxindoles. Buyers often ask about “drop-in replacements.” Experience has taught us to caution against assuming all sources perform equally. Methyl Oxindole-5-Carboxylate, precisely prepared and quality-controlled, enables rapid progression in synthetic work without the drag of repeated troubleshooting. Even small changes—a swap from methyl to ethyl ester, for example—can slow a program by introducing unanticipated hydrolysis, poor solubility in standard reaction solvents, or downstream issues in deprotection.

    Beyond chemical structure, the difference lies in impurity profiles and performance in scaled reactions. Buyers from high-value segments, such as oligonucleotide synthesis or specialty agrochemicals, share that tighter control at the point of manufacture pays dividends during downstream isolation. This differentiator doesn’t make headlines but saves weeks of lost effort on the project timeline. By maintaining close relationships with end-users, we continue to dial in purity and optimize our crystallization regime, offering a product that consistently meets the high bar set by our most exacting partners.

    Logistics and Customer Support From the Manufacturer’s View

    Logistics play a defining role in success. Delivering by standard courier doesn’t cut it; temperature and humidity spikes during transit can deteriorate sensitive lots. Our operations team has learned to anticipate seasonal swings that push warehouse environments outside ideal ranges. Every box dispatched includes batch-specific data, links for prompt analytical support, and a commitment from the same team who oversaw manufacturing. When a client in humid regions ran into trouble with caking and loss of reactivity, we responded with a packaging upgrade—double-walled drums, inert gas backfilling, and inner pouches—all tested in-house before rollout.

    Shipping regulations change yearly. Proactive monitoring helps us prevent delays at customs, especially when new controls arrive on precursor chemicals. We have seen firsthand how unfamiliar paperwork can tie up valuable lots at borders, souring time-sensitive development schedules. Experience has shaped our export protocols and driven us to invest in compliance training for our logistics team. It’s costlier than the “ship-and-forget” model, but our track record with repeat customers shows that direct engagement, not blind outsourcing, pays off.

    Continuous Improvement and Looking Forward

    We do not stand still. Every lot teaches us something new, whether it’s from a downstream complaint or a rare analytic finding in long-term stability. We invest in method development, scale new analytics, and remain open to updating our process flowcharts in ways that strike some as risky but ultimately lower batch costs and tighten impurity windows. Chemists drive these choices, not just business plans.

    A product as specific as Methyl Oxindole-5-Carboxylate finds its edge at the place where science and execution meet. Success demands partnership—not just a signed contract. Our people know the rhythms of production, the attention to detail demanded by years on the floor, and the satisfaction that comes from seeing their work in the hands of researchers and developers worldwide. In our industry, reputation builds batch by batch; progress depends on trust. From the inside, that’s where we see the molecule’s true value, and those are the standards we carry forward, one shipment at a time.