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5-Acetyloxindole

    • Product Name 5-Acetyloxindole
    • Alias 5-Acetyl-1,3-dihydro-2H-indol-2-one
    • Einecs 211-590-8
    • 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

    972161

    Productname 5-Acetyloxindole
    Casnumber 10204-32-3
    Molecularformula C10H9NO2
    Molecularweight 175.18 g/mol
    Appearance Off-white to beige crystalline powder
    Meltingpoint 170-172 °C
    Solubility Slightly soluble in water, soluble in organic solvents like ethanol and DMSO
    Purity Typically ≥98%
    Smiles CC(=O)C1=CC2=C(C=C1)NC(=O)C2
    Inchi InChI=1S/C10H9NO2/c1-6(12)7-2-3-8-9(4-7)11-10(13)5-8/h2-5H,1H3,(H,11,13)
    Storagetemperature 2-8 °C
    Synonyms 5-Acetyl-2-oxindole
    Hscode 29339980

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

    Packing & Storage
    Packing 5-Acetyloxindole, 25g, supplied in a tightly sealed amber glass bottle with tamper-evident cap, labeled for laboratory use.
    Shipping 5-Acetyloxindole is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is transported according to standard chemical regulations, typically at ambient temperature, and with appropriate hazard labeling. Ensure handling by trained personnel, and store in a cool, dry place upon receipt to maintain compound stability and integrity.
    Storage 5-Acetyloxindole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Store at room temperature unless otherwise specified by the supplier. Ensure appropriate labeling and keep the container away from sources of ignition and heat.
    Application of 5-Acetyloxindole

    Applications of 5-Acetyloxindole in Industrial Manufacturing

    5-Acetyloxindole is widely applied as a functional intermediate in multiple advanced chemical value chains, most notably pharmaceutical synthesis, crop protection, pigment manufacturing, and specialty fine chemicals. As the original manufacturer, we supply material that meets strict quality requirements for integration into demanding downstream processes where traceability and specification compliance are critical.

    1. Pharmaceutical Intermediates for Anticancer API Synthesis

    Key research-driven pharmaceutical manufacturers incorporate 5-Acetyloxindole as a scaffold-building intermediate in the synthesis of indole-based compounds, especially for small molecule anticancer actives such as kinase inhibitors. Consistent material purity, controlled crystallinity, and trace impurity control are crucial during multistep pathway assembly, as this oxindole derivative enables regioselective functionalization, forming critical pharmacophores before nitrogen alkylation or aromatic substitution. Purification and isolation steps depend on tight starting material conformity, as regulated under international pharmacopoeias and API GMP requirements.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for API intermediates
    • USP/NF reference monographs (where monograph exists)
    • 21 CFR Part 211 (FDA cGMP for Drug Products - applicable to process validation stage)

    Typical usage ratio

    • Typically 0.4 – 1.7 molar equivalents relative to target indole core, adjusted depending on target heterocycle complexity and byproduct minimization strategies.

    Downstream process integration

    • Added at initial step of heterocyclic ring assembly in anhydrous conditions; reacts under controlled temperature before further derivatization, reduction, or halogen exchange steps in batch or semi-continuous reactors.

    Final product types

    • Indole-based kinase inhibitor APIs (e.g., Sunitinib, Pazopanib development candidates)
    • Precursor libraries for oncology research compounds
    • Advanced intermediates for CNS and anti-inflammatory therapies

    2. Crop Protection Active Ingredient Synthesis

    5-Acetyloxindole acts as a key precursor in constructing indolinone frameworks used in modern agrochemical libraries, particularly in the development of systemic herbicides and fungicides. Custom synthesis operations value its reactivity and compatibility with multi-component reactions for building highly substituted indoles, maximizing yield and minimizing process impurities in accordance with regulatory data requirements for agrochemicals.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for pesticide R&D
    • FAO/WHO Guidelines on the Quality Control of Pesticides
    • REACH registration for non-pharmaceutical chemicals
    • ISO 9001 for quality management in specialty synthesis

    Typical usage ratio

    • Commonly 0.8 – 1.3 equivalents per indolinone-based active intermediate batch, varied according to chain length and functionalization density of the target substance.

    Downstream process integration

    • Dosed into nucleophilic substitution or condensation steps under inert atmosphere; proceeds through defined protection-deprotection and chlorination or sulfonation pathways prior to formulation as technical concentrates.

    Final product types

    • Indolinone-derived herbicidal concentrates
    • Azole fungicide technicals
    • Early-stage insecticide building blocks

    3. Colorant and Pigment Intermediate Manufacturing

    Specialty pigment producers utilize 5-Acetyloxindole as a raw component for synthesizing high-performance arylindole-based dyes and industrial pigments. Its acetyl function facilitates directed acylation and Friedel-Crafts transformations, ensuring chromophore uniformity and brilliant color consistency in both solution and solid state applications.

    Industry compliance standards

    • ISO 9001 and 14001 for pigment manufacturing facilities
    • RoHS Directive (2011/65/EU) for pigment use in electronics and plastics
    • REACH Annex XVII for restricted aromatic amines
    • FDA 21 CFR Part 178 for colorant applications in food-contact plastics (dependent on finished pigment classification)

    Typical usage ratio

    • Standard incorporation levels range 1.5 – 6.2 wt.% per pigment reaction mass, modified for desired shade intensity and dispersibility in end-formulation.

    Downstream process integration

    • Fed during Friedel-Crafts acylation and subsequent oxidative coupling stage, followed by purification and milling to achieve target particle size and gloss.

    Final product types

    • Indole-based pigment dispersions for plastics
    • Organic colorants for coatings
    • High-purity dyes for textile and inkjet formulations

    4. Specialty Fine Chemicals: Synthesis of Aromatic Building Blocks

    Producers of advanced aromatic building blocks leverage 5-Acetyloxindole’s core structure to introduce acetyl and indolic motifs into high-value fine chemicals for use in research and material science. Consistent lot analysis and documentation support batch-to-batch reproducibility and custom modification, serving applications ranging from ligand synthesis to high-purity research reagents in analytical and electronics sectors.

    Industry compliance standards

    • ISO 9001 certification for laboratory reagent production
    • REACH compliance for specialty chemicals
    • Material data requirements as per ASTM standards (e.g., ASTM E2937 for organic analytical reagents)
    • Good Documentation Practice (GDP) for traceability in fine chemical supply

    Typical usage ratio

    • Addition levels typically 0.3 – 1.8 molar equivalents, customized per downstream target’s reactivity and purity grade required by analytical or R&D sector.

    Downstream process integration

    • Introduced during aromatic acylation or amidation steps; reaction monitored by HPLC before isolation and purification for customer-specified applications in instrument calibration or electronic material development.

    Final product types

    • Custom indole-ligand derivatives for homogeneous catalysis
    • Reference standards for pharmaceutical analysis
    • Specialty monomers for advanced material synthesis
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    Certification & Compliance
    More Introduction

    5-Acetyloxindole: Purposeful Chemistry, Proven in Manufacturing

    With years of on-the-ground experience, our team develops chemicals not just by formula, but by putting them to use in real reactions, checking their behavior at scale, and answering practical demands from industry partners every day. 5-Acetyloxindole stands as a fine example of a product shaped by this real-world process. We manufacture this compound through carefully optimized synthesis, always making sure each batch reaches the level of consistency expected by researchers and production specialists alike.

    What Is 5-Acetyloxindole?

    5-Acetyloxindole, also labeled by its CAS number 4, is a highly useful building block in synthetic chemistry. The compound starts with an oxindole backbone and features an acetyl group on the 5-position of the aromatic ring. A glance at its molecular structure reveals why it becomes so interesting for organic chemists: the interplay of the indole core with the acetyl functionality opens up options for downstream modification that few other small molecules enable quite as smoothly.

    Over years of collaboration, we have supplied 5-Acetyloxindole to pharmaceutical developers, agrochemical labs, and academic research groups. Its value goes beyond a single field because the structure encourages innovation in drug discovery, new materials, and development of functionalized intermediates. Not every oxindole behaves with the same balance of stability and reactivity — this compound stands out in how it combines shelf-life with broad chemical usability.

    Product Model, Consistency, and Production Control

    We offer 5-Acetyloxindole as a crystalline powder. Our most requested model typically falls in the purity range of 98 to 99.5% (by HPLC, with documentation), because we see that’s what R&D departments and pilot-scale synthesis teams require to keep side reactions to a minimum. In the lab, no one likes chasing down mysterious byproducts traced back to off-spec material. We test for residual solvents and open-ring analogs, since those usually cause the biggest headaches in downstream chemistry.

    Every batch follows strict in-process control, confirmed by GC and NMR, and we review trends across years of syntheses. It’s not enough just to hit a specification once; we check that batches maintain the same melting point, appearance, and spectroscopic fingerprint over hundreds of kilos. Any time we see a drift or outlier, we halt shipping to re-examine the process and fix the cause. We also listen to feedback from customers who run long-term animal studies or scale up to pilot reactors — they identify the subtle shifts in behavior before analytics pick up the problem. That feedback loop drives us to keep improving, batch after batch.

    Packing, Handling, Shelf Life

    Feedback from chemists and logistical partners told us early on that moisture and trace amines can alter the color and purity of 5-Acetyloxindole during transit or storage. For that reason, we designed our packaging based on what material scientists and bench chemists reported out of actual storage room tests. We use heat-sealed aluminum-lined pouches, then a rigid outer drum or jar. In our region’s rather humid climate, desiccants make a difference, so we include a humidity indicator card in every pack. Shipping documents reflect lot-specific testing within a week of dispatch, not just the initial certificate date.

    The compound doesn’t show an aggressive tendency for decomposition. Storage at room temperature, in a dry environment, keeps it stable for over two years in our experience. Some pharmaceutical partners run their own five-year shelf studies, and while we always defer to their longer-term results for clinical work, our own testing and returned samples (tested by both HPLC and thin-layer chromatography) show very little degradation after extended storage so long as direct sunlight and excess moisture are avoided.

    Where 5-Acetyloxindole Fits in Synthesis

    Chemists reach for 5-Acetyloxindole when building more complex indole-based molecules, especially those targeting kinase inhibitors, anti-inflammatory drugs, or specialty pigments. The acetyl group opens new cross-coupling and substitution routes; you can go down the path of Friedel–Crafts acylation, or use the acetyl site as a strategic anchor before further elaboration.

    Some labs find it useful in asymmetric synthesis. After protecting the indole nitrogen, the 5-acetyl group gives regioselectivity for subsequent transformations around the aromatic ring. The flexibility of the oxindole isn’t just theoretical; it gets demonstrated each week in real product development cycles. Medicinal chemistry groups have published research on how derivatives of 5-Acetyloxindole influence activity in several biological screens, often showing promising leads for kinase inhibition and anti-tumoral properties. We don’t just supply the starting point; we’ve supported projects from feasibility blends through kilo campaigns when the molecule moves past the exploratory phase.

    Differences from Other Oxindole Derivatives

    Over the years, customers have brought up confusion caused by compounds with very similar names or related structures. An unsubstituted oxindole — which lacks the acetyl group on the aromatic ring — shows vastly different behavior both in reactivity and in physical properties. The 5-acetyl position drives unique downstream chemistry. Products where the acetyl sits on the nitrogen, or at another ring position, will not deliver the same ease in selective functionalization.

    Quite a few requests come from researchers seeking 3-substituted or 7-substituted oxindoles. Our team keeps clear labeling on all documentation, backed up by analytical spectra, to avoid the mix-ups that slow down research or production. Accurate assignment of substitution pattern — not just on MS or HPLC, but by 1H and 13C NMR — distinguishes our batches. Even experienced chemists sometimes misread commercial oxindole spectra, especially if they rely solely on mass spectrometry or IR. Rigorous structure confirmation matters, because a misidentified precursor can set an entire synthesis campaign back by weeks.

    In use, our form of 5-Acetyloxindole stands out for its purity, minimal side impurities, and batch repeatability. With some vendors, you may encounter residual acid or other ring-substituted isomers stemming from incomplete protection/deprotection steps during manufacturing. We monitor for these common contaminants and maintain rejection limits based on actual feedback from pilot trials and chromatography teams.

    Issues and Solutions in Large-Scale Use

    Scaling up from gram to multi-kilogram synthesis brings its own challenges. On that scale, small deviations in process conditions show up as increased levels of byproducts — a fact we know first-hand after handling tons of material. Minor temperature swings and poorly controlled solvent removal can boost the level of hydrolyzed or oxidized byproduct (often giving an unwanted red tint to the raw material). To address these issues, we’ve refined each stage: real-time temperature logging, in-line vacuum distillation, and close monitoring during crystallization.

    Shipping also plays a role in how the product performs at the destination. Time in a hot shipping container can alter the subtle balance of hydration and oxidation that R&D chemists rely on to reproduce results. To prevent this, we work with logistics partners on time-to-ship and shortest route planning — not just to reduce paperwork, but to keep the material fresh and at spec. If delays occur, our replacements come with complete re-analysis before dispatch, not just a reference to the old batch certificate.

    Chemists seeking to scale reactions using 5-Acetyloxindole must often adjust parameters for beyond-lab scale vessels: stirring rates, solvent ratios, temperature ramp rates, choice of scavengers, and timing of workup. We’ve collaborated directly with process engineers who bring production bottlenecks to our attention. Our own manufacturing records give practical insight into optimizing these variables. For example, some scale-up campaigns found that slow evaporation minimized polymorph contamination, while a faster workup gave more consistent yields at the kilo-scale. Field feedback, supported by our in-house R&D teams, turned these discoveries into standard operating procedures.

    Regulatory and Environmental Observations

    Any serious chemical manufacturer can’t ignore increasing attention to regulatory documentation, environmental risk, and operational transparency. For 5-Acetyloxindole, the main environmental concern has to do with proper management of manufacturing byproducts, especially solvents and acidic waste. Based on monitoring at our facility, we have optimized solvent recycling lines, cutting down hazardous waste output compared to prior processes. Wastewater from the final purification step gets tested by independent labs, meeting local discharge requirements.

    On documentation, we produce full characterization files with each shipment, including up-to-date analytical data — not simply recycled reports. The documentation covers COAs signed by our QA chemists, spectra, and notes on synthetic origin. Since academic and pharmaceutical partners have strict requirements, we include certificate copies for audits upon request. Our regulatory staff keep up with changing guidelines, recognizing that transparency earns the trust chemists expect from the supplier, especially as projects approach clinical or agrochemical trials.

    Partnership With Chemists and Project Teams

    Supplying 5-Acetyloxindole goes beyond simply shipping a batch and marking an order complete. Chemists and process managers rely on a responsive supply chain and a clear line of communication with manufacturers.

    Whenever customers reported shifts in solubility, color, or unexpected chromatographic peaks, our technical support team worked directly with their chemists to narrow down the cause, reproduce the issue if possible, and put forward adjusted specifications for next runs. In one case, a process development team found trace iron impurity influencing hydrogenation reactions downstream; our QC department introduced new testing steps, excluding that trace metal in future batches. These cycles of feedback and iteration let us deliver a form of 5-Acetyloxindole that continues to meet evolving project needs.

    Collaborative problem-solving isn’t just reserved for crisis situations. We’ve joined technical calls with multinational research teams to answer questions about batch-to-batch comparability, impurity profiling, and process scalability. Such conversations give us insights into upcoming research trends, while clients benefit from our hands-on manufacturing knowledge. Instead of vague assurances, we provide method validation data, cross-referenced with anonymized partner benchmarks.

    Building Toward the Next Generation of Indole Chemistry

    Market demand shapes how products like 5-Acetyloxindole evolve. As medicinal chemists look for more tailored oxindole cores and as regulatory scrutiny increases, we’ve seen requests shift: lower residuals, purer crystalline fractions, and greater adaptability for green chemistry conversions. Rather than sticking to a fixed recipe, our process development group pilots new crystallization techniques, solvent swaps, and purification approaches, backed by routine stability and performance checks.

    Increasing interest in environmentally safer protocols led us to investigate new reaction routes with lower solvent and energy input. Such process adjustments lower overall waste and cost — savings we pass on by keeping our pricing stable for returning partners. We also document new findings, so contract R&D teams receive full transparency about any minor process shift and its impact on product performance.

    As electronic data systems move into chemical manufacturing, we’re adapting our record-keeping, integrating data from reactors, filtration, and analytical checks. This means more accurate, real-time process control, which has directly improved repeatability in 5-Acetyloxindole production. Some might treat these steps as bureaucratic overhead; we know from practical experience that better process data equals fewer surprises for our customers and more efficient delivery cycles.

    Conclusion: Getting the Details Right, Every Time

    Supplying 5-Acetyloxindole isn’t about filling an order; it’s about knowing that each batch shipped supports the next stage of a customer’s innovation pipeline. Manufacturing at scale means keeping an eye on the details: controlling every step of synthesis, packaging with the user’s reality in mind, and working hand-in-hand with the chemists who rely on the product, whether for an early-stage research project or a late-phase scale-up. That’s the reason we pursue direct technical conversations, technical documentation that matches actual need, and a mindset that treats each lot as if the next breakthrough depends on its quality.