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5-Iodoisatin

    • Product Name 5-Iodoisatin
    • Alias 5-Iodo-1H-indole-2,3-dione
    • Einecs 220-585-5
    • 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
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    Specifications

    HS Code

    639747

    Product Name 5-Iodoisatin
    Cas Number 15333-21-6
    Molecular Formula C8H4INO2
    Molecular Weight 273.03 g/mol
    Appearance yellow to orange crystalline powder
    Melting Point 250-252°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Synonyms 5-Iodo-1H-indole-2,3-dione
    Smiles C1=CC2=C(C=C1I)C(=O)NC2=O
    Inchi InChI=1S/C8H4INO2/c9-4-1-2-5-6(3-4)8(12)11-7(5)10/h1-3H,(H,11,12)
    Hazard Statements May cause skin and eye irritation

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

    Packing & Storage
    Packing 5-Iodoisatin, 5 grams, is supplied in a sealed amber glass bottle with a chemical label, hazard symbols, and batch information.
    Shipping 5-Iodoisatin is shipped in accordance with relevant chemical safety regulations. The compound is securely packaged in airtight, chemically compatible containers, clearly labeled with hazard and handling information. Shipments are protected against physical damage and temperature extremes, and are accompanied by necessary safety documentation and Material Safety Data Sheets (MSDS).
    Storage 5-Iodoisatin should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizing agents. Keep the container tightly closed when not in use to prevent moisture absorption and contamination. Store in a designated chemical storage cabinet for hazardous substances, and clearly label the container. Handle with appropriate personal protective equipment.
    Application of 5-Iodoisatin

    Applications of 5-Iodoisatin in Industrial Manufacturing

    As the original manufacturer, we support advanced sectors with precise grades of 5-iodoisatin. Below are verified application pathways, with detail on regulatory fit, dosage ranges, integration with production lines, and final output forms, based on industry-proven practice.

    1. Pharmaceutical Intermediate for CNS Active Agents

    5-Iodoisatin is widely used as a building block in the synthesis of central nervous system (CNS) active substances, especially in the early stages of heterocyclic scaffold production. Many downstream processes rely on its electrophilic aromatic substitution and amidation capabilities for generating specific pharmaceutical moieties, particularly in the production of substituted oxindoles and tryptamine derivatives. Manufacturers require high purity for compliance with process validation and subsequent GMP requirements. The intermediate incorporates into the synthesis stream prior to final active pharmaceutical ingredient (API) coupling steps.

    Industry compliance standards

    • ICH Q7 Guidelines for Active Pharmaceutical Ingredients
    • EU GMP Part II (Pharmaceutical Intermediates)
    • 21 CFR Part 210/211 (FDA cGMP for finished pharmaceuticals)
    • EDQM quality protocols for starting materials

    Typical usage ratio

    • 15–30 mol% relative to other starting aromatic amines or indole units, adjusted during scale-up for reaction yield and process efficiency

    Downstream process integration

    • Charged at initial step in multi-step synthesis reactors for sequential ring modification
    • Often purified via crystallization prior to coupling
    • Subject to in-line HPLC QC after reaction completion

    Final product types

    • Bulk pharmaceutical intermediates (e.g., 5-substituted oxindoles)
    • Precursors for anti-psychotic APIs
    • Research-grade CNS active screening compounds

    2. Dye and Pigment Intermediate for Specialty Colorants

    The halogenation pattern on 5-iodoisatin is valued in dye manufacturing, where it acts as a precursor for functionalized vat dyes and reactive pigments. Downstream producers incorporate this intermediate in the generation of high-fastness colorants, particularly for textile and high-performance coating segments where unique chromatic properties and substantivity are required. Process chemists introduce the material at condensation or cyclization steps, impacting tone strength, light fastness, and wash resistance of final dyes.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (limit values for textile chemicals)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals - Manufacturing Restricted Substances List)
    • REACH Annex XVII (Chemical Safety in Europe)
    • ISO 9001:2015 for pigment and dye manufacturing traceability

    Typical usage ratio

    • 10–20% by weight in condensation reactions; level tuned for chromophore density and shade target

    Downstream process integration

    • Added in pigment synthesis reactors during ring closure or halogen exchange
    • Undergoes milling and post-treatment with dispersing agents
    • Color strength validated by UV-Vis spectroscopic analysis in QA

    Final product types

    • High-fastness vat blue dyes
    • Functional pigments for inkjet and offset printing
    • Specialty textile dyes for technical fabrics

    3. Agrochemical Intermediate for Fungicide Synthesis

    The isatin core with the iodo substituent enables agrochemical producers to synthesize fungicidal active substances, leveraging the compound’s compatibility with downstream chlorination and condensation. The material serves in structural elaboration steps for certain broad-spectrum fungicides where heterocycle substitution is essential. Integration into pilot and commercial campaigns demands strict controls for residual halides and unreacted starting material, which influences product registration and use authorization in diverse agricultural regions.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD GLP (Good Laboratory Practice) for pesticide intermediates
    • Regulation (EC) No 1107/2009 (EU Authorization of Plant Protection Products)
    • China ICAMA guidelines for agrochemical registration

    Typical usage ratio

    • 5–12 mol% for precursor steps; quantity refined based on batch yield, target purity, and final formulation type

    Downstream process integration

    • Fed as key reagent in ring-forming synthetic steps
    • Follows direct halogenation or Grignard reagent generation for additional functionalization
    • Intermediate undergoes chromatographic purification prior to downstream formulation

    Final product types

    • Triazole-based fungicidal actives
    • Broad-spectrum crop protection intermediates
    • Pre-formulated technical concentrates

    4. Analytical Reagent Production

    Producers of specialty analytical reagents use 5-iodoisatin as a core compound for fluorescent and colorimetric reaction substrates, particularly in derivatization kits for high-sensitivity laboratory analysis. Its electron-withdrawing group introduces reactivity in assays for aldehyde and ketone determination. The reagent enters at the derivatization step, with final QA focusing on purity, stability, and absence of secondary halides in compliance with analytical reference standards.

    Industry compliance standards

    • ISO 17034:2016 for Reference Material Producers
    • USP Reagent Standards
    • Analytical reagent grade requirements (ACS)
    • Certificate of Analysis (CoA) batch specifications

    Typical usage ratio

    • 1–5% by weight in reagent kits; precise level based on analytical detection sensitivity and matrix effect

    Downstream process integration

    • Dissolved in organic solvent blends for kit compounding
    • Aliquoted into ampoules under nitrogen for long-term stability
    • Subject to batch-to-batch verification by HPLC and NMR

    Final product types

    • Fluorescent derivatization kits for HPLC and GC analysis
    • Spectrophotometric detection reagents
    • Diagnostic reference standards

    5. Research Chemical for Medicinal Chemistry Synthesis

    In R&D pharma and biotech labs, 5-iodoisatin forms part of custom compound libraries targeting kinase inhibitors, anti-cancer scaffolds, and structure-activity relationship (SAR) studies. Internal medicinal chemistry teams use it for rapid SAR exploration via Suzuki or Sonogashira cross-coupling, leveraging the iodo position for modular substitution with a wide array of aryl and alkynyl fragments. Strict supply and documentation practices support compliance with institutional chemical management protocols.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 for quality management during R&D
    • Material Safety Data Sheet (MSDS) referencing GHS labeling
    • GLP laboratory notebook traceability

    Typical usage ratio

    • 10–25 mol% relative to fragment coupling partner; adjusted in each synthetic route according to desired product portfolio

    Downstream process integration

    • Used in parallel solution-phase synthesis for library generation
    • Integrated at palladium-catalyzed coupling steps before purification and bioassay screening
    • Typically analyzed by LC-MS for structural confirmation post-reaction

    Final product types

    • SAR library molecules
    • Kinase inhibitor probes
    • Academic and contract research synthesis samples
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    More Introduction

    5-Iodoisatin: Detailed Insight from the Manufacturer’s Bench

    Experience with 5-Iodoisatin Production

    Working with 5-Iodoisatin for years, our production lines have seen the molecule develop from a targeted specialty compound into a consistent, reliable intermediate. Chemists who visit our facility always mention its deep purple crystal; it stands out among related compounds. 5-Iodoisatin, as we produce it, maintains a stable melting point and a purity no less than 98 percent, driven by our multi-stage, controlled iodination protocol. Every batch undergoes HPLC and GC validation because in real usage—especially as a building block for complex heterocyclic synthesis—trace impurities change outcomes, not just in yield but in downstream behavior. We emphasize controlled moisture to stabilize the product and ensure reactivity matches order expectations.

    What Sets Our 5-Iodoisatin Apart

    Cheaper isatins and isatin-derivatives are sometimes available but present noticeable drawbacks when deployed in demanding research or industrial pilot lines. Over-iodinated, poorly washed, or improperly recrystallized lots lead to color inconsistency, increased batch failures, or in some cases, crop out misaligned analytical spectra. We’ve invested heavily in column set-ups and vacuum filtration which hold up even for scale-ups to multi-kilo runs. Comparing our material to lower-grade alternatives, direct customer feedback points to smoother NMRs, absence of oxidized side-products, and more manageable reaction profiles in Suzuki couplings and related cyclizations.

    Reliable Specifications and Real-World Handling

    Our 5-Iodoisatin (CAS 15333-19-0), molecular formula C8H4INO2, contains a single iodine atom fixed at the 5-position on the isatin ring. Molecular weight equals 273.03 g/mol. Each client receives a lot-specific analysis report, with moisture levels under strict control and no significant presence of mono- or di-iodinated isatin impurities. Our purity assessments utilize chromatographic and spectroscopic cross-verification—no batch leaves our plant without both HPLC and NMR sign-off. This constant attention produces a product well-suited for academic, pharmaceutical, and crop science research.

    5-Iodoisatin features an indole core, and people often compare it to related molecules: 5-Bromoisatin, isatin itself, or less substituted indole-fused derivatives. The presence of the iodine atom makes it uniquely apt for further halide displacement or cross-coupling reactions. Those working on bioactive molecule synthesis select it because it survives high-temperature and basic conditions where regular isatin and chloro-versions degrade or react unpredictably.

    Application Scope Informed by First-Hand Observations

    Chemists pursuing alkaloid synthesis or bioisostere replacement value 5-Iodoisatin for its robust handling in oxidative cyclizations, Grignard additions, and organostannane couplings. More than one research group has published on using our material in the formation of hybrid indole scaffolds or pharmacologically active benzopyrrolones. During scale-up, we find it consistently forms well-organized crystals, which simplify both production and downstream processing. Teams working on heterocyclic libraries often compliment the rapid purification possible with our material, citing minimal need for repeated chromatography.

    Research programs focused on kinase inhibition or protein modification also use 5-Iodoisatin in targeted library expansion. SAS (structure-activity studies) on kinase targets benefit from the molecular weight increment and polarizability delivered by the iodine atom. In the field, a molecule that reliably couples in a few hours, with good conversion and little side-reaction, leads to more efficient screening and less solvent-heavy processing. Our engineering team frequently tweaks crystallization rates and residual solvent parameters for clients requesting specific solvate-free variants—this service arose from direct customer feedback on downstream catalyst poisoning in routine Pd-catalyzed coupling work.

    Scale-Up Challenges and Lessons from the Production Floor

    Scaling halogenated isatins presents unique difficulties. Iodination exotherms require precise control or poor selectivity, and rough workup can trap heavy metal or iodine residues. We learned some hard lessons on batch stability in our early attempts. Temperature deviations during the reaction led to pockets of polychlorinated byproduct and volatility in final melting point. Getting it right demanded custom reactor upgrades and a focus on staged iodine addition instead of dumping reagents. Our staff documents each deviation—our batch records go back more than a decade on this single product, making trend analysis possible when rare out-of-spec measurements occur.

    On the post-reaction side, drying too rapidly introduces amorphous or glassy solids while overdrying embrittles the product, complicating later handling. Long-term storage studies helped us pinpoint optimal containers and dessicant pairings; clients rarely face product caking or clumping now. These lessons came less from published protocols and more from listening to synthetic chemists burdened by failed reactions and lost time. In storage trials at varied humidity, our packaging kept product within specification for above a year. Rigorous post-filtration and wash protocols, originally built for kilo-scale jobs, now benefit research and pilot batches as well.

    Comparative Utility: The Role of Iodine in Downstream Chemistry

    Isatin by itself offers limited functionalization possibilities compared to its halogenated analogs. Adding an iodine atom at the 5-position drastically enhances cross-coupling and leaving group chemistry. It unlocks C–C bond formation, which simplifies assembly of extended heterocycles or drug-like architectures. Our collaborators report superior conversions in Negishi, Sonogashira, and Buchwald–Hartwig couplings, especially when compared to 5-Bromoisatin or commercial 5-Chloroisatin. The greater reactivity of the C–I bond in substitution reactions makes multistep syntheses less susceptible to bottlenecks at arylation or alkylation steps.

    Direct substitution with organometallics works more smoothly, and catalysis reproducibility rates higher versus mixed-halide commercial lots. Comparative tests in library settings illustrate meaningful differences in side-product reduction and isolated yields. Students who visit our plant for training projects see, in practice, fewer purification steps and clearer product bands during TLC monitoring. Behind these outcomes stand years of trial-and-error optimization guided by close client consultation.

    Understanding the Spec Differences: Purity and Impurity Profiles Matter

    The market contains a range of isatin derivatives, sourced from various jurisdictions and manufactured under different quality paradigms. The presence of residual iodine, unreacted isatin, or over-iodinated byproducts can wreck complex synthesis protocols, especially those sensitive to oxidative contaminants or trace metals. Our plant invested in split-harvest methodologies and staged washing routines proven to drop impurity load well below competitive offerings, not just on paper, but as observed in tens of thousands of syntheses performed worldwide using our material.

    Our isatin purity measurement does not treat small molecule residuals or halide byproducts as background noise. We monitor for signals as small as 0.05% by GC-MS and routinely flag mixed halides, organics, and even trace transition metals introduced by unwatched reaction hardware. For customers synthesizing target molecules for clinical-phase research, such attention means reproducibility, less reanalysis, and confidence in scale-up.

    Safety and Handling Perspectives from Factory to End-User Lab

    5-Iodoisatin behaves like most halogenated aromatics, and we label each shipment to support standard laboratory protocols. Our operators train continuously on minimized personal exposure. The dust, if handled incorrectly, irritates mucous membranes and reacts with strong bases or oxidants. For this reason, our dedicated workspaces run low-dust extraction and utilize double-sealed packaging, reducing degradation and loss. Out in the research community, colleagues report consistent shelf-life and no unusual degradation odors, issues which plagued earlier commercial batches from the broader market.

    Because pharmaceutical and biotech clients expect both safety and consistency, we maintain a record of each product lot, tracking its analytical profile, packaging conditions, and delivery journey. This way, if unexpected performance issues arise in customer labs, we track down variables in handling or storage, offering rationales or troubleshooting tips based not on guesswork, but on years of shipments and analytical feedback. Factory staff understand the impact small shortcuts make and engage directly with clients to resolve concerns.

    Building Trust through Transparency—Real Data, Real Results

    Clients routinely request raw analytic spectra, stability results, or detailed impurity profiles before incorporating 5-Iodoisatin into their pilot and production lines. We believe in full data sharing, granting direct access to batch-characteristic NMRs, HPLC traces, and MS profiles, beyond mere certificates of analysis. This means our research partners see precisely how our material matches their method development expectations—no generic statements, only direct evidence from the batch they receive.

    The feedback loop runs both directions. Commonly, our technical team learns new work-up or storage tweaks directly from users performing challenging transformations—then builds those lessons into future batches and standard protocols. For example, a customer’s notification about a particular solvent carryover at trace level led us to introduce new vacuum drying controls now standard worldwide in our 5-Iodoisatin lines.

    Environmental Considerations and Workflow Changes

    Production of halogenated aromatics prompts hard questions about sustainability and waste minimization. Our plant, after years of traditional chemical processing, pivoted to more responsible solvent recycling systems and lower-reactivity iodination agents. All iodination residues now go through recovery channels, and process water recapture runs for every large batch. This lower environmental toll is not always baked into fine chemical pricing—nevertheless, our direct clients understand the value of responsible production, especially academic and multinational teams with strict sustainability targets. Both our staff and our clients prefer this approach, motivated by a shared responsibility for safer, less polluting chemistry.

    We continue to invest in process visibility, offering clearer explanations of iodine sourcing and solvent disposal to any client who asks. These shifts slowly change larger workflows in industry, showing that specialty chemical production can both scale and meet rising environmental standards.

    Collaboration—Why Dialogue With Chemists Shapes Our Product

    The relationship between manufacturer and user matters deeply in specialty chemical production. We track not just how many kilos of 5-Iodoisatin ship per month, but how each lot performs, what purification steps cause headaches, and where process delays occur. From these conversations, we identify unexpected bottlenecks: unusual filtration behavior at larger scale, or minor color instability in long-term storage flagged by an academic collaborator. We address reported issues with concrete changes, not apologies. Technicians have re-optimized multiple parameters at the request of one major pharmaceutical program facing scale-up reactivity collapses during late-stage development.

    This approach springs from respect for the complexity of organic synthesis work—no production batch occurs in a vacuum, so we take the time to actively communicate with research and process chemists from initial order through final product deployment. Sometimes this means splitting batches, customizing washes, or shifting dryness specs. These services grow out of the reality that good chemistry flows from direct knowledge exchange, not commodity thinking.

    The Subtle Differences—Why Choices in Isatin Derivatives Matter

    Chemists know that on paper, one isatin derivative looks much like another. The real differences emerge during synthesis. Minor changes in halogen placement, molecule integrity, and impurity burden have measurable downstream effects. 5-Iodoisatin’s heavy atom presence imparts peptide mimicry potential in medicinal chemistry, and its higher density supports advanced molecular design. The overall crystal habit matches modern FTIR and X-ray workflows, so labs can quickly validate structure without concerns over isomeric impurity or unwanted hydrates.

    In practice, the leap from conventional isatin to its 5-Iodo version delivers new catalytic possibilities, lets researchers explore harder coupling reactions, and underpins unique library diversity. The choice pays off both in run efficiency and in expanding the types of molecules accessible from a single building block.

    From the Factory Floor to Final Application

    Walking through our plant, visitors can observe every step of 5-Iodoisatin’s journey, from iodination reactors monitored by experienced operators, to purification columns running at all hours, to the final hand-packing of lot-tested, endpoint-purified product. Our pride stems from direct engagement in every part of the supply chain—no re-batching, no middlemen adjustments, only chemistry driven by rigorous in-house standards. We see the impact when a research program reports higher yields, fewer false starts, and more reproducible results due directly to the care invested in our production cycles.

    Over time, even small differences in quality surface during method development, screening, or scale-up. Each lot we produce represents not just a chemical entity, but the collective work of dozens of chemists, analysts, and engineers—all motivated by the goal of supporting real-world, impactful research and industry progress.

    Challenges and Ongoing Commitments

    The work does not end at shipment. Industry, regulatory, and scientific expectations evolve, sometimes faster than supply lines. We keep pace by tracking published synthetic routes, regulatory changes, and purity standards across global markets. Clients know they reach direct formulators and quality managers with their needs, not faceless offshore suppliers. Our warranty stands for product as well as for the knowledge, transparency, and adaptability we offer.

    5-Iodoisatin serves as more than a catalogue entry; it acts as an engine for discovery in labs ranging from small university spin-offs to multinational pharmaceutical giants. Our approach—built around trust, data-sharing, and hands-on technical support—empowers that discovery, batch by batch, year after year. The story of our 5-Iodoisatin is written both in production records and in feedback from chemists who depend on its performance. This cycle of manufacturing, analysis, and collaboration drives every improvement, shaping the future landscape of compound building blocks and advanced chemical synthesis applications.