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HS Code |
565358 |
| Product Name | 4-Bromo-5-Methyl-2,3-Indolinedione |
| Cas Number | 87956-77-6 |
| Molecular Formula | C9H6BrNO2 |
| Molecular Weight | 240.056 g/mol |
| Appearance | Yellow to orange solid |
| Melting Point | 164-168°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Storage Temperature | 2-8°C (Refrigerated) |
| Smiles | CC1=C(Br)C2C(=O)NC(=O)C2=C1 |
| Inchikey | KRGYARQCDLRDTC-UHFFFAOYSA-N |
| Hazard Statements | May cause skin and eye irritation |
| Synonyms | 4-Bromo-5-methylisatin |
As an accredited 4-Bromo-5-Methyl-2,3-Indolinedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical `4-Bromo-5-Methyl-2,3-Indolinedione`, 5 grams, is sealed in an amber glass bottle with a tamper-evident cap and labeled. |
| Shipping | 4-Bromo-5-Methyl-2,3-Indolinedione is shipped in sealed, chemical-resistant containers to prevent moisture and contamination. The package is clearly labeled according to hazardous material regulations, including appropriate hazard symbols. It is transported under controlled temperature and handled by certified carriers, compliant with international shipping standards for laboratory and industrial chemicals. |
| Storage | 4-Bromo-5-Methyl-2,3-Indolinedione should be stored in a tightly sealed 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. Use proper labeling, and store at room temperature, preferably in a chemical storage cabinet designed for hazardous materials. |
Applications of 4-Bromo-5-Methyl-2,3-Indolinedione in Industrial ManufacturingAs the direct manufacturer of 4-Bromo-5-Methyl-2,3-Indolinedione, we supply batches that meet the rigorous quality demands of specialized downstream industries. The following sections outline real industrial applications, practical integration stages, and regulatory considerations for this indoline derivative in advanced chemical manufacturing. 1. Pharmaceutical Intermediate for Kinase Inhibitor Synthesis4-Bromo-5-Methyl-2,3-Indolinedione serves as a core building block in the synthesis of small-molecule kinase inhibitors used for targeted oncology pharmaceuticals. In this segment, process chemists utilize the indolinedione backbone to construct complex heterocyclic scaffolds through substitution and coupling reactions. This intermediate integrates at the pre-final stage of multi-step synthesis, with stringent control and documentation throughout to satisfy GMP compliance and impurity limits for regulated API production. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisThis indolinedione derivative acts as an advanced intermediate in the preparation of brominated heterocyclic compounds for new-generation fungicides and insecticides. Agrochemical R&D teams capitalize on the structure to introduce specific brominated sites, enabling tailored biological activity against crop pathogens. The intermediate enters agrochemical synthesis at the dedicated heterocycle construction step, where bromine addition must be tightly controlled in pilot and commercial scale processes. Industry compliance standards
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3. Dye and Pigment Intermediate ProductionChemical manufacturers in the specialty dye sector use 4-Bromo-5-Methyl-2,3-Indolinedione to generate tailored indole-based chromophores for advanced colorants. By reacting it with aromatic amines and metal chelators, producers introduce functional moieties for dyes with increased lightfastness and chemical resistance. Manufacturers control the incoming material closely, with routine HPLC and trace-metal analysis, to guarantee chromatic properties and batch reproducibility. Industry compliance standards
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4. Electronic Chemical Materials (Organic Semiconductors)Advanced materials laboratories utilize 4-Bromo-5-Methyl-2,3-Indolinedione as a precursor in synthesizing functionalized indole-based small molecules for use in organic light-emitting diodes (OLEDs) and organic photovoltaic (OPV) devices. The brominated structure acts as a site for further cross-coupling with electron-donating or electron-accepting moieties. Rigorous purity control (GC, NMR) allows downstream partners to achieve the electrical and stability parameters essential for large-scale device fabrication. Industry compliance standards
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5. Reference Standard Material Supply for Analytical LaboratoriesAccredited testing and toxicology laboratories use this compound as a certified reference standard to validate analytical methods, calibrate chromatography systems, and support regulatory submissions involving halogenated indoles. Laboratories require consistent batch-to-batch purity (normally >99.5% by HPLC/GC), traceable certificates of analysis, and full documentation regarding origin and impurity profile. This application responds to strict documentation controls and chain of custody requirements essential for international compliance and audit trails. Industry compliance standards
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As a chemical manufacturer investing years into the synthesis and application research of 4-Bromo-5-Methyl-2,3-Indolinedione, we've experienced firsthand what sets this compound apart in practice. A chemist unscrewing the lid on this crystalline solid knows right away that they're handling a building block with significant leverage in modern design, where purity and reactivity shape everything from bench-scale curiosity to wide industrial application. Our engineers, operators, and analysts work daily with this molecule, drawing on the knowledge that each lot influences downstream projects and discovery direction. We don’t just ship drums or flasks; we send out stories built on the backbone of synthesis and the patience of consistent manufacturing.
4-Bromo-5-Methyl-2,3-Indolinedione features a fused indoline ring, methyl group at the fifth position, and a bromine atom on the fourth carbon. The presence of these electron-withdrawing and -donating groups on the indoline framework makes it exceptionally responsive under a variety of reaction conditions. In our process, the color and texture changes during crystallization signal the fine line between an acceptable intermediate and a finished material. Years spent tuning parameters, running pilot batches, and performing stability trials inform our lot release criteria. It’s not just about HPLC purity or mass spec; the tactile feedback from handling, the odor upon opening, and even the way the crystals settle all add to the decision matrix about what leaves our facility.
Typical figures from our current standards show purity routinely above 98.5% by HPLC, moisture content kept in tight control via Karl Fischer titration, and very low detectable levels of heavy metals. Storage recommendations come from real batch degradation studies, not just book suggestions. Someone storing this at ambient conditions might face shelf-life issues we caught on earlier lots, so we stress cool, dry, and airtight containment based on what repeated pull samples have taught us.
In practice, 4-Bromo-5-Methyl-2,3-Indolinedione operates as a preferred intermediate in medicinal and fine chemical research. Teams synthesizing kinase inhibitors or advanced organic dyes benefit from the reactivity enabled by both the bromo and methyl substitutions. Over the past few years, we’ve supported labs pushing into unique cyclization pathways, noting how this compound offers tight control over regioselectivity in downstream acylation and condensation reactions. We’ve seen graduate students frustrated by isomer formation with similar scaffolds turn to our material for cleaner progress. When our product enables a one-pot step that previously required two or three purifications, we know we’re delivering more than a commodity—it’s efficiency grounded in hard-won reproducibility.
In dye research, the structure delivers color bodies with improved lightfastness and richer chromatic profiles, a change observed first in formulation rooms before it shows up in performance metrics. Our ongoing collaborations with coating specialists and ink formulators have revealed that substituent positioning deeply influences the final hue and stability—a fact that has led us to minor tweaks in recrystallization solvents and post-synthesis handling. Institutions exploring photoactive layers for devices or pigment dispersions come back to us not because of an abstract promise but from a clear difference in their quality control runs using our 4-Bromo-5-Methyl-2,3-Indolinedione versus “standard” market grades.
We often get asked about how this grade differs from neighboring indolinedione derivatives. Direct competitors on the market sometimes advertise an array of halogenated or substituted indolinediones, but we observe significant variation in impurity levels, batch consistency, and downstream performance. A methyl at the fifth carbon, for example, changes solubility and reactivity—our quality control files are full of chromatograms and NMR spectra from trial runs showing how that small difference impacts real chemical routes. One multinational pharmaceutical group highlighted shorter purification times and sharper product peaks in their HPLC studies, reflecting tighter impurity profiles in material from our plant compared to material sourced without such rigorous oversight.
End users often tell us that their most frustrating challenges come from unpredictable reactivity. With indolinedione scaffolds, just a few tenths of a percent impurity swings the yield or causes an unwelcome by-product—affecting budget and timelines. Our in-house feedback loops, process chemist troubleshooting, and routine communication with customers have given us a clear understanding of which process controls matter most. Small differences in atmospheric controls during bromination or solvent choices in crystallization don’t appear in specification sheets but show up in the bottom line for any scale-up operation. That’s experience embodying expertise—using literal trial and error rather than theoretical tables.
Daily work with 4-Bromo-5-Methyl-2,3-Indolinedione has shaped our approach to safety for our operators and the chemists using our material in their own labs. We developed our current handling protocols from many rounds of laboratory and plant observations. Donning appropriate protective gear, working with local exhaust, and minimizing exposure to powdered forms all stem from lessons learned through incident and near-miss reviews. Material safety isn’t a theoretical chart but a collection of practices shaped by real incidents, audits, and efficiency studies. While we don’t push “one-size-fits-all” suggestions onto end users, we openly share issues we encounter: sensitivity to prolonged air exposure, handling recommendations for scale-up, and warning signs of degradation from improper storage. This direct flow of information strengthens both sides, fostering a culture where safety grows from the ground up.
Our manufacturing process for 4-Bromo-5-Methyl-2,3-Indolinedione didn’t appear fully formed; it matured over years of pilot and full-scale production. Early runs showed how small nitrogen leaks during halogenation introduced byproducts that fouled the product. Troubleshooting these faults meant hands-on learning for our process chemists, not just resetting a synthesizer or relying on literature values. Each improvement, from refining wash solvents to tightening final drying steps, carries a direct link to observed product performance in practical applications. No innovation in this space ever stays static, because every new customer application pushes us to revisit our own assumptions and workflows.
We often collaborate with method development teams to troubleshoot application failures. Our willingness to pull archived production logs, review storage trends, and even test experimental purification methods has led to measurable improvements at both ends. These conversations drive us to challenge industry habits, set tighter benchmark standards, and maintain lines open for new scientific insights from partners. Occasionally, we’re the first to notice a trend—such as a subtle color shift before chemical breakdown—that no technical data sheet ever listed, because it stems from day-in, day-out observation and care.
Committing to high-performance indolinedione derivatives like 4-Bromo-5-Methyl-2,3-Indolinedione has involved marrying bench-to-pilot translation to actual plant-scale realities. We engineer each production run for repeatability, controlling pressure, atmosphere, and solvent conditions. By comparing lot-to-lot physical characteristics—length of crystals, density, even flowability when poured—we keep the tightest tolerances possible. Process improvement has also steered us toward greener chemistry: solvent recovery systems, improved aqueous waste management, and targeted catalytic alternatives from our R&D pipeline. These strategic moves foster customer trust while keeping a realistic eye on cost and regulatory trends.
End users need scalable solutions. We routinely transition from multigram research batches to multihundred kilogram lots, fielding requests for pilot lots to full-scale manufacturing quantities. Every scale-up teaches us about heat transfer, impurity load, and the subtle ways plant equipment impacts final product characteristics. We share this information not as a selling point but because it answers practical questions our customers face during tech transfers and validation exercises. Over the years, we’ve watched small biotech labs grow into large-scale operations on our 4-Bromo-5-Methyl-2,3-Indolinedione, adapting our support to keep pace with regulatory, documentation, and analytical needs.
Customers switching from non-brominated indolinedione derivatives to 4-Bromo-5-Methyl-2,3-Indolinedione often report step-changes in reaction selectivity and target functionalization. In our own applications lab, we rerun classic syntheses with both products and chart the differences: cleaner reaction profiles, fewer side-products, and distinctive color behaviors in downstream chemistry. The bromine substitution, rarely included without a specific need, serves to activate or deactivate positions in electrophilic substitution reactions with great specificity—a fact that surfaces only in real-world test runs rather than theoretical prediction alone.
We’ve encountered research programs where unmodified indolinedione analogs failed to deliver the desired coupling or substitution efficiency, leading to wasted time and resources. By providing a material with a bromo and methyl positional pair, we enable routes previously thought too cumbersome or low-yielding. This isn’t an incremental difference—it’s a transformative effect for certain synthetic strategies. Our technical team doesn’t shy from discussing the variances we see in purity drift, stability under process conditions, and ease of isolation during purification, because real change starts with honest self-assessment and feedback.
We supply 4-Bromo-5-Methyl-2,3-Indolinedione to academic chemists, pharmaceutical process teams, and industrial R&D, fielding questions that span from advanced spectroscopic data to hands-on troubleshooting. Research customers often choose this compound to build new pharmacophores, single-crystal X-ray structures, or novel pigment prototypes. We see how their feedback—crystal growth quirks, unexpected minor impurities, or solvent-specific solubility curves—feeds back into our process control loop. There’s no substitute for the insight gained from regular conversation with those working at the sharpest edge of synthesis.
We also see differences in demand and requirements across the sectors. Some partners need small, ultra-high-purity lots, while others want production-scale reliability. Their notes on reactivity trends at unusual pH, stability in aggressive solvent systems, and long-term shelf performance have guided us to make micro-adjustments in process and packaging. We take every technical query as a learning opportunity, opening new channels for application-specific development and method validation. That approach, grounded in real experience rather than sweeping assertions, propels lasting collaboration and better chemistry for everyone involved.
Stability and impurity formation remain recurring themes in discussions around indolinedione derivatives. Over the past years, we’ve discovered oxidation and slow hydrolysis at storage or transit stages, particularly when exposed to humid or variable climates. Confronting these issues, our facility’s packaging and storage upgrades arose from more than just theory; we observed the outcomes of dozens of stored reference lots and engaged in shelf-life studies that simulated everything from warehouse storage to extended overseas shipping. This vigilance, guided by constant measurement and practical error, assures our customers receive robust material ready for immediate work.
Another challenge often mentioned by research groups involves batch reproducibility, especially when transitioning from microgram to multigram or kilogram quantities. With indolinedione scaffolds prone to temperature and solvent sensitivity, we see how slight shifts in crystallization technique or drying profile can subtly affect reactivity. By integrating advanced monitoring throughout every production stage—reactor feeds, in-process sampling, final packaging—we tighten control on each batch. That approach didn’t come from dictates in an SOP but from the hard lessons of variable batch outputs years ago. Now, those corrections mean our end users see predictable behavior, fewer troubleshooting cycles, and fewer costly delays.
Our technical support for 4-Bromo-5-Methyl-2,3-Indolinedione stems from years of troubleshooting syntheses alongside academic, pharmaceutical, and industrial users. We don’t offer prescriptive answers for every synthetic question; instead, we encourage open discussion of the unique quirks that each user encounters. Some days that means poring over impurity profiles after a failed coupling, sharing solvent history, or coaching through changes in chromatography response as scale increases. Other days we help develop custom stabilization protocols, risk mitigation plans, or QA/QC approaches suited for niche applications. In every exchange, both our team and the end user walk away with deeper understanding and stronger trust.
What separates our approach from a generic supplier is the practical commitment to sharing the lessons embedded in our product’s development. We document peculiarities like the transient color changes in certain reaction media, subtle odor shifts on air exposure, or the variable dissolution profile after long-distance transport. Feedback comes through every channel—phone calls, site visits, batch returns, and honest emails. These data points refine not just our product but also the practices of every end user counting on our material for daily results.
At root, 4-Bromo-5-Methyl-2,3-Indolinedione stands as a measure of our commitment to practical, human-driven chemistry. Every year brings new applications, challenges, and successes. Each lot we ship reflects both controlled precision and lessons learned from direct application. From the plant operator inspecting crystal morphology to the R&D manager troubleshooting application problems, real expertise grows from repeated, careful observation and transparent, ongoing dialogue. Quality assurance for us means not just checking a specification box but forecasting and addressing potential customer challenges before they arise. Years of manufacturing this molecule have proven that outcomes improve most when theory and hands-on experience intertwine—making the difference between a good product and one that drives lasting value in every vial, drum, and process that follows.