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HS Code |
981751 |
| Iupac Name | 1-Allyl-1H-indole-2,3-dione |
| Molecular Formula | C11H9NO2 |
| Molecular Weight | 187.20 g/mol |
| Cas Number | 2444-31-3 |
| Appearance | Yellow to orange crystalline powder |
| Melting Point | 157-159°C |
| Solubility | Slightly soluble in water, soluble in organic solvents such as ethanol and chloroform |
| Structure Type | Indole derivative with allyl group at N1 and dione at 2,3 positions |
| Smiles | C=CCN1C(=O)C2=CC=CC=C2C1=O |
| Inchi | InChI=1S/C11H9NO2/c1-2-6-12-9-7-4-3-5-8(9)10(13)11(12)14/h2-5,7H,1,6H2 |
| Synonyms | 1-Allyl-2,3-indolinedione, 1-Allyl-isatin |
| Pubchem Cid | 222192 |
As an accredited 1-Allyl-1H-Indole-2,3-Dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle labeled "1-Allyl-1H-Indole-2,3-Dione, 25g, For laboratory use only," tightly sealed with safety cap and hazard symbols. |
| Shipping | 1-Allyl-1H-Indole-2,3-Dione is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. The package adheres to chemical safety regulations, with appropriate hazard labeling and documentation. Shipping is restricted to authorized carriers and destinations, ensuring compliance with local and international chemical transport guidelines. |
| Storage | **1-Allyl-1H-Indole-2,3-Dione** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from direct sunlight and moisture. Use appropriate chemical storage containers and ensure proper labeling. Handle under a fume hood if possible to avoid inhalation of dust or vapors. |
Applications of 1-Allyl-1H-Indole-2,3-Dione in Industrial ManufacturingAs a committed producer of 1-Allyl-1H-Indole-2,3-Dione, we directly serve industrial clients seeking high-precision intermediates for synthetic applications. Below we outline key downstream industrial sectors that source this material for regulated, process-integrated use. Details are provided for standards, usage loads, procedural integration, and the final manufactured outputs in each specialty segment. 1. Pharmaceutical Active Pharmaceutical Ingredient SynthesisMajor pharmaceutical manufacturers use this raw material as a core intermediate for the targeted synthesis of indole-based APIs, including neuroactive agents and anticancer compounds. Its defined reactivity at the indole core enables specific coupling reactions and late-stage functionalization under cGMP, supporting strict process control and traceability from batch introduction through to release testing of finished medicines. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide ProductionR&D and scale manufacturing of new-generation herbicidal actives in the crop protection sector incorporate this compound as a skeleton-forming intermediate. It contributes to the assembly of indole-derived structures with selectivity against broadleaf weeds, with processing carried out under REACH controls and product stewardship requirements for environmental safety. Industry compliance standards
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3. Dye and Pigment Manufacturing for Technical TextilesTechnical dye producers use this specialty indole derivative in the synthesis of high-performance pigments and reactive dyes for polyester, nylon, and acrylic textiles. The chemical's core structure provides strong chromophore anchoring and stability for light-fastness and wash resistance, essential for industrial textile specifications under global standards. Industry compliance standards
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4. Organic Electronic Materials: OLED Intermediate SynthesisProducers of advanced organic semiconductors utilize this indole derivative for molecular engineering of small-molecule layers in OLED (organic light-emitting diode) devices. The compound's unique electron-rich skeleton enables precise tuning of emissive and charge-transport properties, as required by multilayer display and lighting technologies. Industry compliance standards
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5. Specialty Polymer Crosslinking and ModificationManufacturers of custom specialty polymers and advanced resins incorporate this compound as a reactive indole moiety for chain extension and functional group modification. The allyl group facilitates free-radical crosslinking in controlled environments, allowing for precise adjustment of polymer mechanical properties, UV resistance, and processability. Industry compliance standards
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Working with compounds like 1-Allyl-1H-Indole-2,3-Dione, we often hear questions about what sets it apart and where it shines. Every batch leaving our reactors tells a story—one about careful synthesis, distinct molecular structure, and direct value in downstream applications. This indole derivative sits at the intersection of thoughtful molecular design and practical chemical utility. We manufacture it with an emphasis on strict raw material selection, rigorous process control, and consistent output so our partners can focus on innovation, whether in pharmaceuticals, advanced materials, or fine chemical synthesis.
Chemists know this compound by several identifiers—its CAS number, structural formula, or shorthand as an allyl-substituted isatin. In our refinery, you can spot its signature by its crystalline form and stable color profile. Quality control here never relies just on purity percentages. We evaluate crystalline habit, melting range, moisture levels, liquid chromatography profiles, and residual solvent content. A clean NMR spectrum signals more than just purity; it tells us the synthetic route went as planned. Matching a reference mass spectrum or IR pattern is never just a box to check; it’s confirmation that no shortcuts worked their way into the process.
This isn’t a commodity isatin. Attaching an allyl group at the nitrogen atom changes its physical and chemical profile. The slightly enhanced hydrophobicity, along with that reactive double bond, opens up pathways in organic synthesis you won’t find with a plain isatin. Downstream, this means it becomes more than just a core scaffold. It acts as a gateway for Suzuki, Heck, or cross-coupling reactions in a way plain starting materials do not enable. The difference between 1-Allyl-1H-Indole-2,3-Dione and its unmodified cousins is tangible on the bench.
Every chemist has stories about inconsistent building blocks causing headaches in scale-up. Years ago, we heard from a customer who wasted entire weeks because a batch of indole intermediate from a reseller failed to meet consistent specifications. That experience influenced our systems. We never gamble with purity. Our product usually exceeds 99% purity by area (HPLC). Sourcing allyl halides and acetic anhydride, we run multi-stage purification to strip away trace byproducts. Each batch earns its batch number after an odor evaluation and a micro-assay to catch those sub-ppm contaminants which can derail a sensitive catalytic step.
NIST-traceable reference standards and calibration sets ensure comparison, not just internal comfort. Storage matters too. Oxidation or hydrolysis ruins performance, so product heads out in sealed, inert-atmosphere bottles with tamper-evident seals. We keep archived retention samples; we want traceability stretching back years, not months. If a customer ever has a question, we can pull up exact certificate details and even archived spectra for a specific delivery lot. True reliability isn’t just a slogan. It frees research teams to focus on breakthrough steps, not detective work after supply hiccups.
We see this compound crossing paths with diverse research objectives. In medicinal chemistry, structural refinements breathe new life into indole cores. Researchers use 1-Allyl-1H-Indole-2,3-Dione as a substrate in cyclization, substitution, or annulation strategies. Tweaking the allyl group makes it feasible to build libraries of imines, hydrazones, or oximes with predictable yields.
Synthetic organic labs rely on its ability to react cleanly with nucleophiles—even at moderate temperatures—because the carbonyl groups remain accessible and the N-allyl group provides a convenient handle. In more advanced contexts, cross-coupling with boronic acids or organometallic reagents proceeds efficiently, often offering better selectivity or yield than competing nitrogenous scaffolds.
Polymer and material science teams appreciate its stability. In controlled radical polymerizations, introducing allyl functionalities into a backbone brings about unique thermal and electronic properties. The compound resists rapid degradation under moderate heating and has shown favorable shelf-life in controlled-environment studies, making it attractive for trial runs in new resin chemistries or advanced dye synthesis. This kind of cross-discipline adoption results largely from its carefully dialed-in physical attributes.
As manufacturers, we see firsthand how the smallest process tweak alters outcomes. Isatin derivatives from commoditized sources often show minor byproduct peaks or residual metallic impurity signatures. A purity difference of half a percent can push a catalyst poisoning or a color shift in sensitive dye work. In some cases, even operator smell or visual inspection uncovers batch-to-batch inconsistency in the base starting material. We’ve invested years fine-tuning process parameters: reaction temperature windows, solvent selection, washing sequence, and drying environment. The result shows up in sharper melting points, higher recovery yields, and downstream compatibility.
Our process uses high-purity allylating agents and fresh isatin feedstock, and we avoid the ammonia-based pathways that sometimes introduce unwanted amide or amine byproducts. Equipment cleaning protocols block cross-contamination from other indoles run on our lines. These steps add labor, but they protect downstream processing and support regulatory compliance for research clients following GMP guidelines.
We’ve even run analytics on long-term storage. Oxygen-permeable packaging or small moisture ingress creates trace decomposition in some supplier’s bottles. After six months in a humidity-controlled chamber, our retained samples maintain both NMR profile and HPLC purity, matched against the original COA. This stability empowers our partners to plan for both short, just-in-time projects and long-term inventory programs.
We know regulatory requirements continue to tighten. Each lot of our 1-Allyl-1H-Indole-2,3-Dione comes with detailed traceability, impurity profile, and documentation to support hazard assessment and risk analyses. Our safety data sheets lean on real batch data, not borrowed summaries. Storage stability, exact melting and boiling points, and incompatibility warnings stem from actual performance under real conditions—not armchair theorizing. For teams transitioning new molecules into regulatory submissions or internal quality audits, this kind of trace-backed reliability takes worry off their minds.
Scientists often ask how this molecule stacks up to plain isatin, N-methyl isatin, or simple indole-2,3-dione. Each variant serves a purpose, but those subtleties in structure produce real-world effects. Isatin itself, though versatile, cannot participate in the same suite of C-H activation or cross-coupling chemistries. N-methyl isatin resists some nucleophilic attacks, narrowing its downstream opportunities. Our allyl derivative, though more challenging to produce at scale, opens the door to new synthetic routes without introducing steric or solubility barriers.
We’ve watched research teams switch from generic indole-2,3-dione to our product, reporting both higher yields in coupling reactions and cleaner product isolation. In material science, tuning the N-substituent can shift bandgaps or emission wavelengths; this often translates to significantly different optical or electronic properties in the finished polymer or device. Our in-house tests, confirmed by partner labs, show that 1-Allyl-1H-Indole-2,3-Dione increases process flexibility, especially in cases where the N-alkyl functionality doubles as a synthetic intermediate.
Chemical manufacturing isn’t just about standard product lines. We’ve seen growing demand for customized specifications. Instead of supplying standard bulk grades, we’ve worked closely with research teams to tailor particle size distribution or moisture specification for specific reactors or synthesis plans. In the pharmaceutical sector, even trace residual solvent can stop a project in its tracks. Our investment in vacuum drying lines delivers lot-to-lot consistency. In dye development, color shifts from micro-impurities have prompted us to build redundancy into our purification and QA steps.
One project demanded a variant suitable for flow chemistry. Traditional batch dried forms didn’t suspend or dissolve well enough in their microreactors. By tweaking particle engineering during crystallization, followed by a controlled granulation process, we produced a form that suspended evenly, avoiding clogging and lumpy dosing. That’s a lesson in collaboration and in listening to those attempting the most demanding work.
Production of nitrogen-containing heterocycles has raised environmental questions for decades. We take solvent recovery, effluent management, and raw material source tracing seriously. Our plant operates closed-loop solvent recycling for most organic phases, and waste streams head to certified disposal partners. Catalyst recovery isn’t just an afterthought; we track heavy metal usage, capture spent media, and submit samples for external analysis. Even small volume users want assurance about responsible production—our goal is to provide verifiable data, audit trails, and transparency from synthesis through packaging.
We also review life-cycle impacts. By sourcing greener starting materials and partnering with logistics teams who use recycled packaging, we help our clients fulfill compliance and reporting obligations under REACH, RoHS, and other international directives. It’s no longer enough to manufacture a clean molecule; the origin and footprint of every precursor matter. Our monthly internal audits and cross-team meetings drill down on these details, reflecting the priority they hold for our largest, most innovative clients.
Most chemists have wrestled with supplier issues: delayed lead times, shifting pricing, or unfortunate geopolitical disruptions. Being a manufacturer, not a broker or third-party handler, keeps us closer to both the chemistry and the calendar. We keep raw inventories deep enough to absorb supply shocks, and our multi-step process has built-in backup pathways. Our supply chain partners must meet our minimum standards for both quality and ethical sourcing. Batches are released only after full internal QA sign-off.
We learned the hard way during global events that flexibility isn’t just about technical prowess—it’s about maintaining strong raw material relationships and a committed operations workforce. Our delivery forecasts, adjusted seasonally, help our clients plan projects around academic cycles, clinical trial launches, or patent windows. This direct integration between operations and customer support ensures problems are addressed rapidly, often before they emerge on the client’s radar.
Inside the manufacturing facility, the standards for weighing, handling, and transferring this compound are high. Exposure reduction, spill containment, and dust minimization all follow written protocols. We see many research partners automate dispensing, especially for scale-up work. The crystalline structure and low volatility reduce airborne risk, but our teams treat the compound with the same care reserved for more exotic heterocycles.
For bench chemists, we recommend closed containers, chemical gloves, and clean-room storage—just as we do inside our own QA labs. Long-term relationships thrive when nobody faces unwelcome surprises over product behavior, whether at gram or kilogram scale. Our on-call technical support team, powered by hands-on process chemists, offers guidance drawn from actual production and lab experience, not theoretical advice.
After a decade of supplying this intermediate, we’ve learned that real-world chemical challenges rarely stand still. As researchers push for more demanding syntheses, higher levels of purity, or new functionalizations, we’ve upgraded our own methodologies. This includes more advanced chromatographic analysis, multi-stage impurity profiling, and in some cases, isotope-labeling for traceability in mechanistic studies. Our technical staff takes pride in collaborating to troubleshoot reaction issues, elucidate pathway bottlenecks, or propose alternate solvent systems stemming from granular in-plant data.
Open dialogue with both end-users and purchasing teams leads to iterative product enhancement. Formal stability studies, regular method audits, and third-party proficiency testing mean our COAs carry real meaning—not just on paper, but in daily research progress. We encourage feedback—from process performance quirks to hard-won troubleshooting victories—so our future batches reflect collective field experience.
Chemical research, whether in early-stage discovery or late-stage validation, depends on solid starting materials. We control sourcing, synthesis pathways, and quality checkpoints from start to finish, informed by years of practical experience. Our long-term employees oversee every batch, run visual as well as analytical checks, and reject any material not meeting our internal standards. For customers, this translates to fewer headaches and more productive hours in the lab.
Supplying 1-Allyl-1H-Indole-2,3-Dione isn’t just about moving molecules. It’s about enabling bold new research directions and supporting teams moving from hypothesis to scaled deliverable. That’s the lens we use to view every production run, every lot release, and every future improvement. By grounding our approach in hands-on manufacturing experience, scientific transparency, and a respect for the diverse landscape of modern research, we deliver a product that stands up in practice—not just on paper.
Our knowledge of 1-Allyl-1H-Indole-2,3-Dione continues to grow, driven by application feedback, new analytical tools, and ongoing process optimization. We keep an active dialogue with both established and emerging partners working across pharma, materials, and chemical synthesis. Our goal remains clear: to offer a reliable foundation on which ambitious scientific endeavors can build. The chemistry is complex, but the value of direct, consistent, and transparent manufacturing never goes out of style.