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7-Methyl-1H-Indole-2,3-Dione

    • Product Name 7-Methyl-1H-Indole-2,3-Dione
    • Alias 7-Methylisatin
    • Einecs 219-041-4
    • 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
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    Specifications

    HS Code

    687745

    Product Name 7-Methyl-1H-Indole-2,3-Dione
    Iupac Name 7-Methyl-1H-indole-2,3-dione
    Molecular Formula C9H7NO2
    Molecular Weight 161.16 g/mol
    Cas Number 1640-65-1
    Appearance Yellow crystalline powder
    Melting Point 212-215 °C
    Solubility Slightly soluble in water, soluble in ethanol and ether
    Smiles Cc1ccc2c(c1)[nH]c(=O)c(=O)c2
    Pubchem Cid 31537
    Synonyms 7-Methylisatin
    Storage Temperature Store at room temperature, keep tightly closed
    Hazard Statements Irritant

    As an accredited 7-Methyl-1H-Indole-2,3-Dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, sealed with a screw cap. Labeled with chemical name, formula, hazard pictograms, and safety instructions.
    Shipping 7-Methyl-1H-Indole-2,3-Dione is shipped in sealed, chemical-resistant containers to prevent exposure, under ambient temperature conditions, and in compliance with all relevant chemical transportation regulations. Packaging ensures protection from moisture and light. Safety data sheets are included, and handling is restricted to qualified personnel to ensure safety during transit.
    Storage 7-Methyl-1H-Indole-2,3-Dione should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances, such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure proper labeling and avoid prolonged exposure to air. Store at room temperature and follow standard laboratory chemical storage protocols for hazardous materials.
    Application of 7-Methyl-1H-Indole-2,3-Dione

    Applications of 7-Methyl-1H-Indole-2,3-Dione in Industrial Manufacturing

    7-Methyl-1H-Indole-2,3-Dione supports several specialized manufacturing sectors as a critical intermediate. We supply this material directly to downstream producers where stringent process integration and regulatory demands determine its practical use. The following scenarios highlight established industrial uses, with key details for integration, formulation, compliance, and output products.

    1. Synthesis of Pharmaceutical Active Pharmaceutical Ingredients (APIs)

    This material acts as a vital building block in the synthesis of specific API compounds, particularly within the class of indole-derived pharmaceuticals. Downstream pharmaceutical producers utilize it in multi-step synthesis, introducing it after initial aromatic functionalization to construct complex molecular scaffolds targeting CNS, oncology, and anti-inflammatory indications. Integration into later-stage routes allows precise placement of methyl and keto substituents, which directly impact the pharmacological properties of the final APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMP for finished pharmaceuticals)
    • European Pharmacopeia (Ph. Eur.) ingredient specifications
    • Chinese Pharmacopoeia processing requirements

    Typical usage ratio

    • Batchwise 5–15% molar equivalence in targeted API intermediate assembly; adjusted based on desired methylation and substitution patterns of target molecule

    Downstream process integration

    • Introduced during advanced-stage condensation and ring-closure reactions
    • Used in amidation, reduction, or alkylation steps after indole functionalization
    • Ensured traceability and in-process QA for compliance with DMF submissions

    Final product types

    • Oncology drug substance intermediates
    • Anti-inflammatory API building blocks
    • CNS-active agent precursors

    2. Manufacturing of High-Performance Dyes and Pigments

    This diketone forms a core intermediate for downstream manufacturers producing high-purity indigoid and indole-based pigments for specialty textile and printing applications. Tight color specification and high lightfastness demand precise control of synthetic indices, with the material batch-introduced at the pigment coupling and cyclization stage. Custom pigment shades and purity levels depend on managing the raw material input ratios and downstream oxidative cyclization process.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile and leather dye ingredients
    • ISO 9001:2015 Quality Management system for colorant manufacturing
    • REACH Regulation (EC) No 1907/2006 (EU chemicals regulation for pigments)
    • ETAD Code of Ethics for dye intermediates

    Typical usage ratio

    • In pigment synthesis, 2–10% by weight per formulation; varies alongside dye precursor loading and target chroma intensity

    Downstream process integration

    • Added during oxidative cyclization and diazotization/coupling for indigoid dyes
    • Mixed in controlled environments with coupling agents and solvents
    • In-process monitoring for residual diketone and color purity

    Final product types

    • High-grade specialty textile pigments
    • Industrial inkjet printing dyes
    • Colorants for resistant plastics and fibers

    3. Agrochemical Intermediate Production

    Downstream agrochemical producers use this compound in the synthesis of specialty indole-based active ingredients for crop protection. Producers integrate the raw material at a mid-synthesis stage to achieve methylated indole skeletons critical for bioactivity. Reliable compliance with residue and toxicological requirements demands traceable batchwise input and strict adherence to downstream process controls. The methylation pattern enables fine-tuning of biological activity towards specific target pests.

    Industry compliance standards

    • FAO/WHO JMPR Pesticide Specifications and Evaluations
    • ISO 16140 (Method validation for residue analysis)
    • China GB 2763-2021 Maximum Residue Limits for Pesticides
    • Good Laboratory Practice (GLP) for substance characterization

    Typical usage ratio

    • Utilized at 3–9% mol equivalent per total indole reactant mass; ratio set according to target molecule yield and regulatory residue limits

    Downstream process integration

    • Reacted in methylation or halogenation stages of active ingredient synthesis
    • Formulated into pre-concentrates or technical-grade active substances
    • Incorporated with phase purification and toxicity screening

    Final product types

    • Crop protection actives (e.g., fungicides with indole core)
    • Pest repellents for specialty agricultural uses
    • Seed treatment chemical precursors

    4. Fine Chemical Synthesis for Advanced Material Research

    This specialized diketone supports R&D functions in materials science and organic electronics, serving as a controlled input for synthesizing heterocyclic building blocks. Laboratory and pilot-scale users in electronics and advanced polymers integrate the raw material for its enabling role in constructing conjugated backbones. Formulation groups modulate input ratios precisely depending on the intended electronic or optical properties of the resulting substances, using it early in the synthetic route for targeted molecular patterning.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory testing and quality verification
    • SOCMA ChemStewards® minimum stewardship for specialty materials
    • RoHS Directive (EU) compliance for materials assessed for electronics

    Typical usage ratio

    • Formulation input at 1–5% by mole for new material synthesis; ratio optimized based on conjugation length and research scale batch size

    Downstream process integration

    • Added as a key precursor during heterocycle formation or Suzuki/Miyaura coupling steps
    • Integrated with in-situ monitoring and post-synthesis structure confirmation
    • Utilized in custom pilot and research-scale reactors

    Final product types

    • OLED material precursors
    • Heterocyclic monomers for high-performance polymers
    • Test compounds for charge transport layers
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    Certification & Compliance
    More Introduction

    7-Methyl-1H-Indole-2,3-Dione: Real Insights from the Manufacturer Floor

    Working With the Molecule Every Day

    Anyone spending their days up close with chemical synthesis quickly learns that subtle differences in molecular structure shape the outcome for both process and product. 7-Methyl-1H-Indole-2,3-Dione isn’t another generic intermediate; its methylation pattern sets it apart, and over time, we have come to respect both its quirks and its value. With the formula C9H7NO2 and CAS number 31871-12-4, this compound plays a distinctive role in research and industry scenarios where targeted reactivity and molecular scaffolding matter.

    How Specifications Impact Day-to-Day Operations

    Each batch matters. So do the numbers behind the name: purity, melting point, and physical appearance influence everything from handling to conversion rates. Our usual product exhibits a consistently crystalline appearance with a purity above 98 percent, keeping impurities below 2 percent. This standard obviously doesn’t happen by accident; we’ve designed QA checkpoints into each step. A slight drift in moisture or trace byproducts affects downstream yields in synthetic chemistry, so we test each lot with HPLC and NMR before delivering to customer labs. In real production, small deviations grow into big headaches fast.

    The melting point, often found in the 228-233°C range, shapes drying cycles and storage. At this level, heat exposure during purification has to match both the chemistry and the physical qualities of the material or you lose yield and risk decomposition. We keep solvent residuals below standard PPT levels, not to hit a label specification but to give formulation chemists peace of mind. When formulating indole-2,3-diones for pharmaceutical or pigment research, uncontrollable residue can complicate isolation and contaminate end products.

    How Experience Teaches Product Handling

    On the plant floor, watching operators work with 7-Methyl-1H-Indole-2,3-Dione gives plenty of lessons about material flow, dust control, and weighing accuracy. Unlike lower-melting compounds, it doesn’t clump easily under normal storage, but exposure to excess humidity sometimes causes slow block-formation or mild caking. We learned this the expensive way, so all packaging now uses low-moisture barrier liners. Customers who had issues with earlier generations of packaging now see a difference as soon as they open the container.

    Particles are fine, nearly talc-like in most production runs. Our equipment suppliers see this as fairly standard, but in practice it means more attention at the weighing and dispensing stage. Any operator who’s ever watched a cloud of indole dust drift off a scoop knows dust collection isn’t optional, especially since indole derivatives have a pronounced odor. We invested in better vacuum and enclosure technology for this exact reason—worker comfort and safety come up every day, not just in safety audits or paperwork.

    How 7-Methyl-1H-Indole-2,3-Dione Supports Research and Industry

    From the research bench to pilot scale, this compound steps into projects looking for more than a generic intermediate. Medicinal chemists appreciate the methyl group at the 7-position, which changes electronic distribution across the indole core and opens up routes that are tricky (or impossible) with unsubstituted indole-2,3-dione. We receive regular feedback from small pharma companies and university labs that methylated indoles accelerate SAR studies, support fluorescent probe development, or act as selective inhibitors in focused screening.

    Formulation scientists in pigment and dye industries use it for its colorfastness and stability; the methyl group isn’t a cosmetic change. It improves resistance to oxidative fading and changes the hue profile in ways not reproduced by blends of other indoles. Based on consistent orders from several pigment manufacturers, the demand for tighter purity control in color applications surpasses that in medicinal chemistry—the reasons vary, but the need for uniform reactions and color outcomes is often at the core.

    Another application emerges in agrochemical research, where methylated indole structures play a role in developing new plant regulators and bioactive candidates. Here, a consistent starting point means that the screening data stays meaningful between batches. Removing variables at the synthesis stage prevents expensive troubleshooting later.

    Differences from Similar Products on the Market

    Indole-2,3-dione derivatives come in several forms, and not all are created equal. Unsubstituted indole-2,3-dione might seem similar on a spec sheet, but experienced chemists know subtle changes can make one batch manageable and another stubborn. The methyl group at the 7-position shifts reactivity, changes solubility, and influences both the color and the stability of end products. We see these differences in daily operations, as routine TLC checks run faster with the methylated derivative and scale-up reactions tend to be more forgiving under real-world conditions.

    Price is one thing people ask about. Adding a methyl group increases synthetic steps and cost, but for many of our customers, the benefits in selectivity, speed, and final product yield matter more. It’s tempting to cut corners with cheaper intermediates, yet projects that do so circle back after seeing unexpected side products. Our long-standing customers rarely make this mistake again.

    Storage differences also surface over time. While some indole derivatives degrade with routine temperature fluctuation, our packing and storage protocols keep the 7-methyl compound stable over longer periods, even if supply chain delays extend shelf life. We track product integrity with real samples sent back from customer shelves. Testing residual moisture and decomposition tells us the methods work, not just on paper.

    Challenges with Scale and Consistency

    Manufacturing to scale isn’t a matter of running larger reactors and hoping for the best. We run test cycles whenever raw material suppliers change processes, since the smallest shift in chlorination or reflux time echoes across the finished product. Getting consistent particle size means tuning the cooling profile and grinding stages, not just screening out oversize lumps. Anyone who has switched suppliers on indole derivatives only to find gumming or flow issues in their mills knows just how much the upstream work matters.

    Environmental control in drying areas remains a daily concern. This compound releases trace organic vapors during drying, so exhaust setups and worker exposure limits stay under regular review. Years ago, open-tray drying left faint contamination even in nearby batches of unrelated chemicals. Upgrading to contained drying resolved those issues and cut our cleaning costs, underscoring how interlinked operations depend on thoughtful facility design.

    Collaborating With Customers Brings New Ideas

    Some of our improvements grow directly from customer feedback. Requests for tighter impurity limits or alternate packaging turn into process adjustments after enough hands-on testing. Once, a customer wanted 7-Methyl-1H-Indole-2,3-Dione in pelletized form for an automated feeder. We ran several extruder tests and discovered the compound’s brittle nature led to excess fines. A granular cut held up better and maintained its handling properties through transit. This combination of process feedback and practical demands keeps us sharp—and focused squarely on how the product holds up outside our facility.

    Pharmaceutical partners sometimes ask about heavy metal contamination, even in non-GMP grades. Our QA team worked with upstream suppliers to reduce exposure during synthesis—sticking to high-grade solvents and using dedicated reactor lines for preparative steps. The result has been a measurable drop in trace metal analysis, which now falls well under ICH guideline targets even for the standard research grade. These are invisible differences that show up in biological screens, so we keep them front and center when reviewing batch histories.

    How Real Manufacturing Experience Improves Product Integrity

    Running labs and plant lines teaches plenty about both the theory and the hard reality behind a specification sheet. One season of wide humidity swings taught us lessons about bulk storage—indole compounds pick up water vapor more than most, and desiccant bags only solve part of the problem. We responded with a continuous monitoring system in the bulk warehouse. Fluctuations now trigger real-time alerts, and we haven’t seen a caked drum shipped in over two years. These everyday adjustments never make it onto a product label, but they define whether the compound in a customer’s hands matches what they expect for their project.

    Cross-contamination between indole products is another field lesson. The lithium salts used for another line left micro-residues in shared filtration units, impacting purity. We made the switch to dedicated filter trains for methylated indoles, and brought all cleaning validation in-house. Solvent residues in the finished product dropped noticeably, and we saw far fewer field complaints about line contamination during scale-up.

    Looking to the Future of Specialty Indoles

    As the needs of pharmaceutical, agricultural, and materials scientists shift, the demand for specialized intermediates like 7-Methyl-1H-Indole-2,3-Dione keeps expanding. Custom derivatives with alternate methylation or halogenation patterns receive more inquiries each quarter. For companies pushing the boundaries with new molecular scaffolds, the lessons learned with this compound directly inform which synthetic routes bring both efficiency and consistency.

    New regulatory guidelines—especially on purity and trace contaminants—push us toward ever-tighter process control. It’s clear that meeting both published standards and customer-dictated custom specs will define industry leaders in the coming years. We see ourselves as partners with every formulator, researcher, and process chemist using our 7-methyl derivative, aiming to resolve not just today’s specs, but tomorrow’s challenges as new regulations and applications emerge.

    Sustainability and Responsible Production in Practice

    Balancing production efficiency with environmental impact shapes every upgrade. For indole-2,3-dione derivatives, solvent selection across each synthesis stage remains a key source of risk and cost. We transitioned most of our routes away from chlorinated solvents, not because of regulatory push, but after internal audits showed the waste and emissions costs were outstripping landfilling fees. Water recycling and copper-catalyst recovery from spent reaction mixtures offer direct cost savings and quieter environmental profiles.

    Worker safety took a leap forward after ergonomic reviews of drum handling. Indole dust irritates mucous membranes, and glove choices make a difference—nitrile outperforms latex in long-term comfort and reduces allergic reactions. These practical, plant-level upgrades let operators spend less time worrying about personal safety and more time focusing on accuracy, which reflects through every delivered batch.

    No Substitute for Direct Manufacturing Insight

    Plenty of listings for 7-Methyl-1H-Indole-2,3-Dione appear across catalogs, but direct manufacturer experience shapes how the product performs in a real facility and in your project. Every process improvement, packaging revision, and analytical protocol comes from repeated trial and response—not just copying data sheets. For every lab or plant that depends on reliable methylated indole intermediates, these everyday insights underpin both confidence and successful project outcomes. The best chemistry happens only with an honest account of what a product really is, and how it responds from shelf, to scale-up, to final application.