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HS Code |
741511 |
| Chemical Name | 1-Acetylindoline |
| Cas Number | 703-80-0 |
| Molecular Formula | C10H11NO |
| Molecular Weight | 161.20 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 62-65 °C |
| Boiling Point | 352.2 °C at 760 mmHg |
| Density | 1.183 g/cm³ |
| Solubility | Soluble in organic solvents like ethanol and chloroform |
| Synonyms | 1-Acetyl-2,3-dihydroindole |
| Smiles | CC(=O)N1CCc2ccccc21 |
| Inchikey | COWOOLGYYZXUEV-UHFFFAOYSA-N |
As an accredited 1-Acetylindoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with a screw cap. Labeled with chemical name, hazard warnings, CAS number, and supplier details. |
| Shipping | 1-Acetylindoline is typically shipped in secure, sealed containers to prevent contamination and degradation. It should be stored and transported under cool, dry conditions, away from direct sunlight and incompatible materials. Appropriate hazard labeling and documentation are included, and shipping complies with relevant international and local chemical transport regulations. |
| Storage | 1-Acetylindoline should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep away from incompatible substances such as strong oxidizing agents. Store at room temperature and protect from moisture. Ensure proper labeling and limit access to trained personnel to maintain safety and chemical stability. |
Applications of 1-Acetylindoline in Industrial Manufacturing1-Acetylindoline is a specialty intermediate that supports core synthesis and modification in pharmaceutical, pigment, and agrochemical production. Below, we detail the main industry segments where this compound integrates into downstream manufacturing, with regulatory, formulation, process, and final goods specifics for each use. 1. Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers use 1-Acetylindoline as a key building block in the synthetic routes for select indole-based therapeutic molecules. Its acetyl-protected nitrogen facilitates controlled functional group transformations and ring-closure steps during the development of alkaloid analogues and investigational central nervous system drugs. Production environments strictly require traceable batch records and validated impurity profiles throughout the process. Industry compliance standards
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2. Agrochemical SynthesisCrop chemistry manufacturers rely on 1-Acetylindoline to construct indole-derived backbones in selective fungicides and insecticides. The acetyl group stabilizes the molecule during oxidative coupling and halogenation frequently encountered in active ingredient formulations. Technical quality and residue levels must comply with international agrochemical safety and purity directives. Industry compliance standards
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3. Organic Pigment and Dye ManufactureOrganic pigment producers use 1-Acetylindoline to synthesize specialty indole-based azo and anthraquinone dyes for plastics, coatings, and ink applications. The acetyl group serves as a selective blocking agent, allowing for controlled diazotization and coupling to specific chromogen precursors. Procedures mandate strict monitoring of heavy metal and aniline impurities for regulatory compliance in consumer and textile applications. Industry compliance standards
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4. Fine Chemical and Research IntermediateContract research organizations and specialty chemical companies employ 1-Acetylindoline in medicinal chemistry and materials development projects. Its pre-functionalized structure allows for rapid analogue synthesis and structural-activity relationship exploration. Labs and pilot plants subject all processes and documentation to chemical management systems and global transport controls for hazardous intermediates. Industry compliance standards
Typical usage ratio
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Working in the lab, the pursuit always comes back to consistency and reliable results. Over the past decade, our team has made hundreds of batches of 1-Acetylindoline, faced different synthesis demands, and fielded questions from customers who apply it in fields as varied as medicinal chemistry, agricultural research, and specialty material development. Through trial, error, and repeated process improvement, we have learned what clients really need—steady quality, reproducibility in results, and confidence that their starting material won’t let them down at a critical stage in their work.
At its core, 1-Acetylindoline is an intermediate with a reputation for getting noticed in complex syntheses. The structure—an acetyl group attached to the nitrogen atom of the indoline ring—lends itself to a suite of transformations, acylations, reductions, and cross-couplings. This small change in functionality from plain indoline makes a big impact in downstream reactivity. Most clients who reach out, whether from universities or commercial labs, want to know—not just what the molecule does, but how our specific model stands up under bench conditions and how it stands apart from ordinary indoline or other substituted indolines.
We produce 1-Acetylindoline with a focus on chemical purity and controlled batch size. Each production run is tracked from raw material to finished solid. Ask around the chemistry community and you’ll hear: a polar impurity, a byproduct that creeps in during acetylation, can disrupt downstream isolations and throw off yield calculations for new molecule discovery. We have invested years refining crystallization and solvent purification steps. The current process consistently hits 99% HPLC purity, with typical single-digit ppm for common residual solvents and low UV-active byproducts. Every lot comes with a full spectrum, not just a tidy COA; we’ve found this transparency keeps R&D teams productive and helps projects clear scale-up hurdles.
Lab benches can be tough environments. Our solid 1-Acetylindoline holds up thanks to careful control over physical properties and packaging. Every bottle, whether 25 grams or kilogram scale, contains the off-white crystalline solid—not a sticky mass that risks hydrolysis or clumping. Melting range runs narrow for each batch, holding steady between 90–92°C, which reflects a low level of side products or decomposition prone species. Typical particle size lands in the easy-to-handle range, since excessively fine powders dust and hinder transfers and sticky chunks resist dissolution in common organic solvents.
Shelf stability comes built in. Stored in closed containers away from direct light and moisture, our product keeps its integrity for years; customers who order annually have come to trust this. The molecule stands up to normal handling without breaking down or picking up colored tints. With years of shipment history, even global clients with extended transport schedules report that the product arrives as solid as the day it left our plant.
In pharmaceutical research, chemists use 1-Acetylindoline for its ability to undergo selective substitution at the ring or acyl function in multi-step routes toward active pharmaceutical ingredients. Many well-cited syntheses—especially those targeting complex heterocyclic frameworks—lean on acetylindoline as a precursor or building block. The balance between electron donation and withdrawal in the indoline ring delivers reactivity that simple indoline seldom matches.
Custom polymer projects have featured our product, as acetylindoline’s functional group compatibility eases integration into polymers needing robust heterocyclic content. In crop protection chemistry, certain companies have explored using acetylindoline for lead generation in new pesticide candidates, banking on the indoline ring’s already-demonstrated bioactivity.
We have worked with academic teams seeking to develop fluorescent probes, where 1-Acetylindoline serves as a starting point for ring-fused dyes and photoactive materials. They’ve highlighted not just the convenience of the acetyl-protected nitrogen, but the product’s stability during storage and workup—a feature that shortens project timelines when every failed batch means lost weeks.
Small differences in origin mean a lot for downstream results. For example, the way we control reaction temperature during acetyl group addition sharply reduces racemization in certain chiral routes. As a result, our material works for clients running asymmetric syntheses where trace impurities would otherwise threaten enantiopurity. Medicinal chemists, often operating on small scales and tight deadlines, comment on how easy it is to purify products after using our acetylindoline as a reagent. They aren’t forced to chase down obscure impurity removal steps or run excess chromatography just to get publishable results.
Plenty of companies sell acetylindolines, but as manufacturers who run every reaction and monitor every batch, we see the details that separate good product from problematic material. There’s always a temptation to tolerate broader impurity levels or push the boundaries of batch size in favor of yield, but these shortcuts cut into the reliability downstream users expect.
Clients have shared stories of buying generic 1-Acetylindoline—often marked by incomplete data, missing spectroscopic details, or vague guarantees on shelf life. Results include darkening of the sample after only a week on the bench, or unexplained polarity shifts in TLC that derail purification of more sensitive intermediates. Our customers instead benefit from clear IR, NMR, and HPLC data at the time of receipt, and product that keeps its noted appearance and purity through the cycle of application and analysis. Reproducibility of performance matters more in discovery than ever; we have seen more researchers insist on transparent supplier partnerships as a result.
A handful of customers have tested side-by-side comparisons with off-the-shelf grades from trading companies that don’t maintain synthesis or have oversight of packaging. In those cases, the outcome is usually clear within a week—our carefully controlled solid literally stands up longer, resists yellowing, and allows a higher conversion rate when applied in model transformations like Friedel-Crafts acylations or Pd-catalyzed cross couplings.
Many in the chemical community wrestle with variable sample quality, especially with specialty intermediates like acetylindoline. Academic projects ebb and flow with funding cycles, and industrial users tie progress on new candidates to tight development milestones. A missed reaction, triggered by hidden impurities, leads to lost time and eroded confidence on all sides.
We learned some of these lessons the hard way. In one early phase, a change in raw material suppliers, subtle as it seemed, resulted in differences in trace elemental content, which did not appear on routine tests but mattered in later metal-catalyzed reactions. Losses included unusable product, delays, and increased analytical workload for everyone involved. Since then, we have tightened both supplier selection and analytical monitoring. Every gram of 1-Acetylindoline now ties directly back to authenticated, stable precursor lots. Recordkeeping isn’t just a formality—it forms the backbone of a trustworthy audit trail that researchers prize, especially as regulatory guidance tightens across the globe.
Real manufacturing experience counts for more than just purity numbers. The way a company manages logistics, tracks lot histories, and supports client troubleshooting all help cement long-term relationships. For nearly two decades, we have fielded requests from both budget-limited academic groups and high-volume industrial accounts. The goal stays the same: supply enough material, on time, with the documentation and technical backup to keep research pushing forward.
Shipping our product worldwide, we see how environmental conditions in different regions affect shelf life and usability. Some of our customers in tropical climates, for example, reported that other suppliers’ acetylindoline forms clumps or changes texture after even a short time at high humidity. Our in-house packaging team responded by trialing different seals, moisture-absorbing inserts, and outer containers until stability improved for all climate zones. These small changes, tested batch by batch, show up in the consistency our users report in their own work.
We also invest in direct communications with clients. Questions about non-standard reactivity or novel synthetic targets often come from users piloting new projects with no clear precedent in the literature. Our technical team, including the chemists who build each batch, routinely helps interpret NMR details, troubleshoot unexpected side reactions, or advise on storage and re-use. This ongoing support fosters a research ecosystem where synthesis can progress without being bottlenecked by unpredictable raw materials.
As green chemistry principles take a stronger hold, manufacturers have a responsibility to examine not only raw material sourcing but also process efficiency and waste generation. In the last few years, we shifted key stages in 1-Acetylindoline production toward safer solvents, reusable catalysts, and lower temperatures when possible. These changes reduce our downstream environmental burden, which increasingly matters as large end-users demand Life Cycle Analysis (LCA) support for their procurement reports.
A real-world example: by switching the acetylation stage from hazardous acyl chlorides in chlorinated solvents to milder reagents and greener conditions, our team cut chlorinated waste to less than one-twentieth of former levels. This not only means easier waste handling, but also gentler conditions that preserve the batch’s physical and chemical integrity. The end-user gets a product that behaves predictably without the risk of embedded byproduct from aggressive reagents, which in turn supports cleaner downstream chemistry.
Securing long-term availability and support for emerging applications remains a persistent challenge. As innovation in pharma and materials research grows, synthetic intermediates like 1-Acetylindoline appear in routes that require highly tailored performance, not just basic purity. For us, responsiveness becomes key. Frequent dialogue with research teams flags emerging needs—whether it’s demand for trace metal-free batches for oncology drug synthesis, or lot-specific NMR datasets for material science projects reaching publication.
We address these concerns by investing in in-house analytics, retaining chemists with broad synthetic backgrounds, and building redundancy into our supply chains. Automated monitoring in production, frequent revalidation of synthetic steps, and batch records that tie directly to timeline and component source are all part of our commitment. This rigorous approach rewards our users with confidence—and, occasionally, collaboration, as researchers share feedback that pushes our process boundaries further.
Volume flexibility also plays a growing role. Traditional manufacturers sometimes force minimum order quantities that don’t fit the early-phase needs of modern science. Our plant runs parallel production lines, supporting small academic runs alongside kilogram-scale industrial batches. From experience, this close attention to client needs means less waste, lower cost of entry, and a much higher chance that the best projects won’t be hamstrung by sourcing struggles.
Working from the fundamentals up, our team brings more than just synthetic chemistry expertise. We know that the real metric of success lies in how research teams use and trust the product. That trust must be earned in the lab, not claimed in marketing copy. Every customer experience—each successful synthesis, each unanswered troubleshooting call—is reflected in operational improvements. Maintaining a direct relationship with clients supports both sides; chemists benefit from steady supply and reliable product, while we gain insight into emerging chemical needs.
Innovation cycles shift quickly. New reaction types, from photoredox to organocatalysis, are hitting the journals and industry bulletins every month. As demand for specialized intermediates like 1-Acetylindoline grows, manufacturing must pivot to keep pace with new applications and increasingly stringent purity standards. Staying nimble—updating in-process analytics, working with flexible logistic schedules, and maintaining open scientific exchange—turns industry evolution into opportunity.
Ultimately, our commitment to manufacturing 1-Acetylindoline reflects something bigger: a belief in scientific progress grounded in trust. Sincere transparency in method, unwavering quality in product, and real support in application—these are the pillars on which we’ve built both our reputation and our long-term client relationships. Whether your research investigates new therapeutic classes, targets advanced materials, or pushes for cleaner chemical processes, having a manufacturer that shares these values is not a luxury; it is an essential foundation for success in the chemical sciences.