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HS Code |
440157 |
| Chemical Name | N-Acetic Acid-Indole-3-Carboxaldehyde |
| Molecular Formula | C11H9NO3 |
| Molecular Weight | 203.20 g/mol |
| Cas Number | 81654-01-1 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 173-175°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place, away from light |
| Smiles | O=Cc1c[nH]c2cccc(C(=O)O)c12 |
| Iupac Name | 2-(1H-indole-3-carboxaldehyde)acetic acid |
As an accredited N-Acetic Acid-Indole-3-Carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle, labeled “N-Acetic Acid-Indole-3-Carboxaldehyde, 10g,” with hazard warnings and batch information, stored in a protective box. |
| Shipping | N-Acetic Acid-Indole-3-Carboxaldehyde is shipped in tightly sealed containers under cool, dry conditions with proper labeling to ensure safety and compliance with chemical transport regulations. Packaging is designed to prevent leaks and contamination. Accompanying documentation includes safety data sheets and handling instructions for secure and compliant delivery. |
| Storage | N-Acetic Acid-Indole-3-Carboxaldehyde should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from light and moisture. Store at 2-8°C or as specified by the manufacturer. Ensure proper labeling to prevent accidental misuse or contamination. |
Applications of N-Acetic Acid-Indole-3-Carboxaldehyde in Industrial ManufacturingAs a specialized manufacturer, we supply N-Acetic Acid-Indole-3-Carboxaldehyde to global industrial clients engaged in advanced biochemical synthesis and fine chemical production. Below, we provide a comprehensive overview of its established downstream applications, covering compliance regulations, dosage practices, integration processes, and the most common end-use products, based strictly on real-world industry usage. 1. Pharmaceutical Intermediates for Anticancer Agent SynthesisMany pharmaceutical manufacturers implement N-Acetic Acid-Indole-3-Carboxaldehyde as a core intermediate during small-molecule drug synthesis, especially in multistep processes for indole-based anticancer agents. Throughout the process, chemists use the high affinity of its indole ring and aldehyde group for key condensation reactions, often in Step 3-5 of the route, precisely controlling parameters to avoid impurities impacting API yield and purity. This application remains tightly governed by pharma cGMPs and regulatory guidelines due to its role in oncology therapeutics. Industry compliance standards
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2. Agrochemical Research and Plant Growth Regulator SynthesisR&D and pilot-scale manufacturers in the agrochemical sector use this indole-aldehyde compound to generate precursor molecules for auxin-like biostimulants and synthetic plant growth regulators. Its chemical structure closely matches motifs needed for controlled substitution and halogenation steps, facilitating high selectivity and improving yield consistency in multi-hectare crop yield trials and production ramp-ups. All downstream operations adhere to strict environmental and safety regulations due to agricultural application end-use. Industry compliance standards
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3. Fine Chemical Synthesis for Aromatic Derivative ManufacturingProducers specializing in fine chemical and specialty aromatic molecules use N-Acetic Acid-Indole-3-Carboxaldehyde as a selective reactant for forming functionalized indole carboxylate esters. The compound’s electron-rich structure permits targeted nucleophilic addition, leading to high-value intermediates with applications in advanced coatings, luminescent materials, and electronic device precursors. Such synthesis occurs under carefully monitored conditions to maintain purity and reproducibility, meeting the rigorous standards of specialty chemical clients. Industry compliance standards
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4. Peptide and Oligonucleotide Modification in Chemical BiologyLaboratories and contract manufacturing organizations (CMOs) focused on peptide conjugates and modified oligonucleotides utilize N-Acetic Acid-Indole-3-Carboxaldehyde for site-specific incorporation into synthetic biomolecule libraries. Its highly reactive aldehyde group ensures stable linkage formation with lysine side chains or nucleic acid backbones under mild aqueous conditions, providing scaffolds for bioactive library generation, diagnostics, and research tools. These applications demand strict analytical validation and impurity profiling throughout the process, consistent with bioanalytical industry codes. Industry compliance standards
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The story of N-Acetic Acid-Indole-3-Carboxaldehyde always starts in the laboratory. Raw materials arrive fresh from trusted sources, no deviations. Careful hands and a sharp eye at each process step have earned our team a reputation for reliability. In our experience, the challenge with this compound lies in its sensitive synthesis—just a little humidity can affect purity, and slight temperature drifts risk side product formation. The workers recognize its pearly crystals, but they don’t just look for appearance. They run repeated checks—thin layer chromatography tracks the reaction, gas chromatography-mass spectrometry confirms identity, and NMR guarantees structure. Every batch stands as a direct reflection of our standards, not somebody else's.
Over years in the field, demand for N-Acetic Acid-Indole-3-Carboxaldehyde rarely comes from basic research alone. Its place in the indole family is marked by a unique acetic acid moiety at the N-position and an aldehyde at the 3-position, providing extra functional flexibility. Chemists saw early on that these features open doors for designing new therapeutic agents—think anti-inflammatory leads or plant growth regulators. Some colleagues in academic and industrial labs use it as a key intermediate for constructing more elaborate indole-based scaffolds. It reacts cleanly in Knoevenagel condensations, amide bond-forming reactions, and reductive aminations. This versatility, in our experience, accounts for the steady stream of repeat customers.
Our runs settle on a model optimized through years of incremental tweaks. Standard output offers N-Acetic Acid-Indole-3-Carboxaldehyde with purity typically above 98% as determined by HPLC and proton NMR. Water content is kept consistently below 0.5%—our Karl Fischer titrator leaves no guesswork. This material’s light tan appearance speaks to minimal side reactions during synthesis; any batch drifting toward a darker hue gets flagged and reviewed. Granular particle size helps it dissolve more easily in most polar solvents, and our team stores it in amber glass under inert gas until shipment. No product leaves the warehouse without final packaging in air-tight bags, ensuring performance remains intact from our door to yours.
Making and using indole derivatives is rarely boring, yet not all sources deliver consistent results. Stories circulate of batches with impurities affecting biological assays or synthetic yields. Over fifteen years on the production floor, our processes evolved through direct feedback: reactions scaled up or down for tight temperature control; distillation improved to sharpen purification; and Real-Time Release Testing eliminated delays. In crowded chemical catalogs, what distinguishes us is not mere paperwork: every lot comes with full analytical records. We back every certificate with a willingness to repeat QC for any partner who requests it. Pharmacological developers and agrochemical innovators tell us they see fewer false positives using our material compared to others, a claim supported by analytical runs and real-world application tests.
Chemists sometimes ask how this product differs from plain Indole-3-Carboxaldehyde or its methyl and ethyl homologues. Straightforward: N-Acetic Acid-Indole-3-Carboxaldehyde’s acetic acid group on the nitrogen changes both reactivity and solubility. This makes nucleophilic substitutions more predictable and improves water compatibility—useful for medicinal chemists aiming for selective functionalization or biological screens. Researchers still using unsubstituted indole aldehydes come back after meeting toxicity or solubility challenges; they notice the new acetic moiety lets them dial in more desirable targets, or, just as important, improves screening accuracy in plant science.
Handling indole chemistry teaches respect for storage. This compound’s aldehyde group works as advertised only if it stays protected from air and moisture. Over time, we developed a habit of double-bagging with desiccant inside cold storage rooms—reducing trace oxidation and dimerization that plague lesser-managed supplies. Every partner gets these same protections in shipping, not just a bare minimum. Where others rely on surface checks or a single melting point, we make retention samples of every lot, so complaints never fall on deaf ears. Regular feedback from partners guides batch sizes and packaging, adjusting practicality—one lab’s hundred grams may be another facility’s requirement for a kilo.
Lab teams working on peptide-indole conjugates stick to N-Acetic Acid-Indole-3-Carboxaldehyde because its functional handles make site-directed modifications feasible. Peptide coupling becomes simpler, and extra protection steps go out the window, reducing waste. University researchers have cited our material as delivering better reproducibility in enzymatic inhibition assays. In plant physiology, this compound outperforms unsubstituted analogs in trials measuring drought resistance or hormone mimicry. When scale-ups happen, pharmaceutical groups appreciate the lower impurity footprint in their API intermediates—fewer chromatographic purifications, less risk of unknowns compromising downstream steps.
Producing this compound is no smooth assembly line. Early efforts produced more tars and colored byproducts than clean crystals. With years of tuning, every reaction now runs in a vacuum system, minimizing air exposure and keeping temperature spikes contained. Careful monitoring every few hours avoids charring. Column purification parameters, including gradient ratios, reflect real-world adjustments, not theoretical models. Waste is cut down at every step, both for environmental and economic reasons. Recycling mother liquors became standard after solvent costs spiked, and every waste stream is logged and traced—site inspectors regard our logs as a blueprint for responsible chemical management.
Researchers often share stories of frustration over unreliable supply chains. Over the past decade, recurring shortages hit many core indole derivatives. To tackle this, production lines at our facility run small and mid-scale lots on overlapping schedules, giving us the flexibility to respond to sudden surges in demand. Scientists focus on results rather than logistics when back orders disappear from their workflows. We stick to scheduled maintenance, instrument calibrations, and raw materials quality audits to anticipate issues before they disrupt customers. Some new clients who switched after delays elsewhere often tell us our reliability lets them accelerate research and avoid gaps in grant-funded work.
The difference between good chemistry and great chemistry lies in details that outsiders rarely notice. Many improvements come from direct partner feedback. When one team flagged a subtle baseline impurity troubling their spectroscopy, we invested in more sensitive detectors and trained teams on calibration. We now run impurity profiling beyond published requirements, translating insights directly into process corrections. Open calls between our QC technicians and customer labs produce a cycle of improvement not found through sales channels or distribution points. This openness builds trust, and many longstanding collaborators see us less as suppliers and more as quiet partners in their innovation journeys.
Even with a streamlined workflow, hiccups happen. Once, after a minor formulation change elsewhere in the plant, carryover issues popped up unexpectedly. We instituted stricter batch sequence control, preventing cross-contamination before it becomes an issue. Every month, crews audit the entire production line for gaps. If new standards arise, adjustments follow—in cleaning protocols, in documentation detail, or even in packaging design. No fix happens in isolation; frontline staff and management weigh in so that cleaning up one issue doesn’t create another. These practices grew organically, not from outside mandate, but through learning what works.
As the field shifts toward open science and full data disclosure, we keep transparency a priority. Every shipping document includes a full analytical dossier—NMR scans, HPLC chromatograms, water content, and spectral libraries. We keep at least two years’ worth of records accessible for partner review by request, not just when there’s a dispute. As more groups request sustainability data, lifecycle tracking, and provenance, we prepare tailored reports that document raw material origins and waste handling. Some researchers ask for expanded trace reporting, particularly in regulated industries, so we scaled up internal reporting tools and broadened staff training to handle these demands confidently.
There’s a persistent view that compounds with functionalized indole rings present safety hazards too severe for small labs. Ongoing risk assessment and routine safety training helped our own teams balance speed and safety with care. Material data sheets speak plain language about storage, handling, and potential side effects. Rather than assuming expertise, our staff routinely consults with end users, walking them through ideal setup for weighing powders, avoiding cross-contamination, or managing waste. Such outreach grew out of our early years, when assumptions about skill levels sometimes led to actionable incidents. Today, incident rates have plummeted, and our partners report higher confidence in handling even sensitive loads.
N-Acetic Acid-Indole-3-Carboxaldehyde stands as a model of specialty chemistry. Global fluctuations in solvents, raw indole derivatives, or energy mean prices shift regularly; we keep lines of communication open about supply pressures, offering alternatives or substitutes if pinch points arise. Scaling up might drive down unit costs, but excessive volume brings storage and spoilage risks, so we carefully match forecast to actuals. Ongoing investments in cleanrooms, waste capture, and staff skill building don’t show up in immediate costs, but partners notice reduced batch-to-batch variability and loss minimization. The overall return comes not from cutting corners but from stable, long-term partnerships.
Tighter rules on specialty chemicals are here to stay. From our seat, this is good news—more care leads to safer workspaces and more reliable products. We track regulatory movement in relevant markets, documenting every required specification without guessing or rushing. Colleagues on the production chain and in logistics hold certifications in chemical safety and food-grade GMPs, reflecting ongoing training. Site audits welcome outside scrutiny, leading to recognition in quality reports from auditors and partner companies alike. Our philosophy—genuine compliance protects both our teams and everyone who uses our product down the line.
Producing N-Acetic Acid-Indole-3-Carboxaldehyde requires solvents, reagents, energy, and water. Local groundwater purity guides decisions on waste treatment; all solvents pass through distillation columns, with recovery rates told plainly in annual reports. By capturing solvent vapors or recycling off-stream materials, production impact remains lower than typical industry averages. We have replaced several hazardous reagents with green alternatives, even when their up-front cost was higher. Ongoing collaboration with community and regional regulators keeps waste emissions within strict bounds, and every discharge is measured and documented. Feedback from environmental audits transforms into ongoing improvements for both facility and wider community.
Every production run writes a new chapter in the story of this compound. As synthetic demands change, chemists require building blocks with more options for robust modifications, greener profiles, and traceable provenance. Leaders in the life sciences and agriculture sectors seek more adaptive production, not just a static catalog. The foundation for tomorrow’s improvements is dialogue—not just between sellers and buyers, but across the discovery and fabrication spectrum. In doing so, breakthroughs in crop management, new pharmaceuticals, and basic research will always have the reliable building blocks they deserve.