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HS Code |
365274 |
| Product Name | 7-Ethyl-1H-Indole-3-Carbaldehyde |
| Cas Number | 162876-08-6 |
| Molecular Formula | C11H11NO |
| Molecular Weight | 173.21 |
| Appearance | White to off-white solid |
| Purity | Typically >97% |
| Solubility | Soluble in organic solvents such as DMSO, methanol, and ethanol |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Smiles | CCc1ccc2[nH]cc(C=O)c2c1 |
| Inchi | InChI=1S/C11H11NO/c1-2-8-3-4-10-9(7-13)6-12-11(10)5-8 |
| Synonyms | 7-Ethylindole-3-carboxaldehyde |
As an accredited 7-Ethyl-1H-Indole-3-Carbaldehyde 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. White label displaying chemical name, CAS number, hazard warnings, and supplier details. |
| Shipping | 7-Ethyl-1H-Indole-3-Carbaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent leakage and degradation. It is handled and transported in accordance with chemical safety regulations, typically via ground or air freight, and accompanied by proper documentation and labeling. Store in a cool, dry environment away from incompatible substances. |
| Storage | 7-Ethyl-1H-Indole-3-Carbaldehyde should be stored in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Avoid exposure to heat, oxidizing agents, and incompatible substances. Properly label the container and ensure compliance with local safety regulations to prevent accidental exposure or degradation. |
Applications of 7-Ethyl-1H-Indole-3-Carbaldehyde in Industrial ManufacturingAs a direct manufacturer of 7-Ethyl-1H-Indole-3-Carbaldehyde, we deliver high-purity specialty intermediates for several precise sectors, focusing exclusively on pharmaceutical synthesis, advanced fluorescent dye production, agricultural active ingredient development, and fine fragrance formulation. These application fields set demanding requirements for process integration, regulatory compliance, and downstream performance. Our material supports scalable industrial processes, enabling our partners to achieve stringent production and quality benchmarks. 1. Pharmaceutical Intermediates for Antineoplastic AgentsMany pharmaceutical customers use 7-Ethyl-1H-Indole-3-Carbaldehyde as a core building block in the synthesis of indole-based antitumor drug candidates and APIs, particularly for compounds targeting protein kinases. Its structure enables formation of functionalized indole derivatives via condensation and further cyclization reactions. Batchwise introduction during the early synthetic stage allows reliable quality control and effective downstream transformation, which is critical for route reproducibility and impurity profile management in regulated manufacturing. Industry compliance standards
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2. Advanced Fluorescent Dye ManufacturingFluorescent dye producers incorporate this indole derivative as a functional aldehyde moiety for constructing extended π-conjugated systems via Knoevenagel or Imine condensation. Its electron-donating ethyl group enhances emission profiles and photostability in custom chromophores, supporting high-sensitivity detection dyes and specialty imaging probes. Usage must meet quality and regulatory purity benchmarks due to downstream analytical and medical device applications. Industry compliance standards
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3. Agrochemical Active Ingredient SynthesisProducers of crop protection actives adopt this indole-based aldehyde as a key intermediate for assembling heterocyclic scaffolds in herbicidal, fungicidal, and regulatory-approved pesticide actives. The specific substitution incorporates into molecular frameworks via cyclization or coupling, feeding downstream chiral or functional group modification routes. Selection of this starting material enables both patentable and registered technical material production with robust scalability and traceability. Industry compliance standards
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4. Fine Fragrance and Aroma Chemical DevelopmentManufacturers of high-value aroma chemicals leverage indole-based aldehydes to construct specialty fragrance ingredients by acylation and Schiff base formation. The unique ethyl substitution at the 7-position provides nuanced odor profiles suitable for creating fine fragrance top and heart notes. Strict control of addition ratio and downstream purification sustains product consistency critical for premium perfume and cosmetic formulation lines. Industry compliance standards
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In our chemical plant, 7-Ethyl-1H-Indole-3-carbaldehyde does not just roll off the tongue, but it does roll from reactor to drum under the kind of watch that comes from years of making indole derivatives. This molecule might not have the fame of aspirin or caffeine, but in the pharmaceutical and chemical research worlds, it opens the door to a range of complex syntheses you can't get with many other starting materials. Our team controls everything from raw materials sourcing to the final packaging because we want each shipment to stand up to the quality control labs of any research or pharmaceutical company.
Some chemicals stand out because of what chemists can build from them. 7-Ethyl-1H-Indole-3-carbaldehyde carries an ethyl group at the seven position, which, as anyone who has used the parent compound knows, means a different route of functionalization compared with the more familiar 1H-indole-3-carbaldehyde. That small change tunes its reactivity and lets medicinal chemists explore new derivatives that can't be approached via the unsubstituted analog. In the world of structure-activity relationships, a single ethyl can reveal novel physiochemical and pharmacological properties.
Our plant workers and research chemists have handled enough indoles to appreciate the difference in behavior between the basic backbone and one with a tailored side chain. The ethyl substitution changes how the molecule handles in crystallization, alters color and odor, and shifts solubility in both organic solvents and water. This means certain reactions run easier. Cleaner purification, sometimes fewer side products, other times a need to watch for dimerization or sensitivity to oxidants. Decades of batch records and real process troubleshooting back up this assessment.
While some buyers only care about molecular weight or melting point, our teams have spent long shifts learning that real-world performance does not hinge only on these numbers. Purity requirements can vary. Research labs testing biological activity may go for analytical grade, while process development or scale-up projects may handle slightly lower purities if cost and yield are a concern. Our QC team offers chromatography traces and NMR data, but having run hundreds of batches, we also know if a batch is showing unusual color, tendency for haze, or odor, it pays to investigate. Small off-specification details can spell the difference between a straightforward heterocycle coupling and a day of tracking down rogue byproducts.
Spec sheets give the headline numbers, but building a usable stock from 7-Ethyl-1H-Indole-3-carbaldehyde means keeping moisture low, avoiding bottle-to-bottle variability, and using package linings that won’t leach contaminates over months in lab storage. Every order gets a QC sheet, but there’s a reason our partners send feedback, not just on paperwork, but on how the product handled during column chromatography or whether it survived an overnight route without degradation. We take this feedback seriously—improving particle size, tweaking drying times, and retraining staff whenever a process adjustment is needed.
The world already has plenty of chemical catalogs listing dozens of indoles and carbaldehydes. So what changes with our 7-Ethyl-1H-Indole-3-carbaldehyde? Speaking as a manufacturer, not just a packager or distributor, it all comes down to process control and transparency. Our synthesis does not leave residual solvents easily confused with the desired product on a TLC plate. We use in-house developed, reproducible steps to guarantee the ethyl group stops exactly where it should—on position seven, not five, not six, never on the nitrogen.
We have seen too many incoming samples from small-scale providers where indole impurities or migration products turn up even after a single recrystallization. Our team re-runs spectra on random drums and has the machinery to dry, grind, and repack under inert atmosphere. If research demands a unique cut or a special grade, we hear it firsthand, and our plant manager and R&D staff actually sit down to troubleshoot it.
A flask of bright yellow crystals may look impressive, but sending off-grade indole intermediates to a customer means trouble down the line: extra column runs, false positives in bioassays, or—worst of all—delayed development milestones. Unlike traders passing along whatever specification comes with the drum, our factory’s doors open to audits, in-plant visits, and customer-run reaction trials.
The main use for 7-Ethyl-1H-Indole-3-Carbaldehyde lies in the labs working on small-molecule pharmaceuticals, agricultural active ingredients, and new organometallic catalysts. The ethyl group brings diversity for combinatorial libraries, an advantage for anyone rushing through SAR tables and analogue synthesis. This particular indole carbaldehyde sees frequent application in constructing heterocyclic frameworks where direct substitution or further modification at the three-position is a necessity.
Our best feedback tends to come from groups designing kinase inhibitors, CNS-targeting drugs, or even pigment chemistry, who have found that a single synthesis run with the wrong aldehyde version can upset months of screening. By using real chemical manufacturing control, we keep batch-to-batch reproducibility high, so that these research cliffs get flattened out. Researchers handling five, ten, or a hundred grams at a time often let us know if there’s a change in behavior—like an uncharacteristic impurity profile—so we can catch mechanical problems before a large-scale lot gets out the door.
Our sessions with scale-up chemists showed us where small slip-ups cause waste. Close air-tight storage beats just capping a jar, especially on humid days. Open bench transfers raise contamination risks. Glass, not plastic spatulas, avoid transfer static that leaves valuable powder stuck behind. Our warehouse keeps material in opaque, lined containers to slow potential photodegradation. We’ve fiddled with container designs to strike a balance between easy access for R&D and contamination prevention for bulk storage.
Some customers run columns in air, others only under nitrogen. We work with either, but recommend inert handling where possible. Every batch comes with the residual solvent data our chemists look for because certain customers report different reactions to sodium borohydride reduction depending on whether even trace acetone or toluene survived the final drying. Seasonal changes in humidity can call for tighter ambient storage standards, and we adapt packaging runs in real-time as needed.
Many labs use the parent 1H-indole-3-carbaldehyde, or variants with chlorine, methyl, or methoxy substituents. Why go with the ethyl version? After running head-to-head screening experiments for local fine-chemicals suppliers, our chemists saw certain building blocks only form under the slightly bulkier, more lipophilic ethyl group. Its electron-donating profile can nudge reactivity so that difficult C–C bonds form cleaner, and in some reactions, cut down the tars and dark side-products that plague the unsubstituted version.
Customers working in N-alkylation report that downstream transformations stay more predictable with an ethyl group in place, especially during cross-couplings or reductive aminations. We have helped several research teams avoid reaction model surprises by providing detailed literature and our own data regarding side-reactions or unexpected rotamer formation in the presence of common coupling agents.
In pigment chemistry, the ethyl derivative lends subtle but measurable changes to bathochromic shifts, allowing formulations with distinct color properties—yet few outside pigment or dye chemistry report on it. A pharmaceutical group recently shared that their use of ethyl at this position improved blood-brain barrier predictions in computational assays, broadening their options for CNS drug leads. These kinds of technical tricks rarely show up in published reviews, but working in manufacturing means picking up the difference between plausible literature routes and chemistries that actually deliver on yield and purity at scale.
As a manufacturer, we see trends before most catalog houses catch up. Regulatory requirements can change rapidly. New findings on environmental impacts of certain solvents or intermediates push us to improve not just the 7-Ethyl-1H-Indole-3-carbaldehyde itself, but the entire route to making it: We have moved to greener solvents where research and production allow. Our engineers overhaul purification steps, aim to reduce hazardous waste, and search for ways to recover even more solvent each year, not because regulation dictates it, but because it matches our own goals for safer, more sustainable production.
We do not rely on marketing talk. The proof lies in the growing repeat buying from international labs, and the near-zero return or complaint rate. Instead of pushing out as much as possible, we dedicate vessels and staff to fewer, more complex intermediates. That kind of focus develops the in-house expertise needed to catch problems before buyers ever notice them. By testing staff on new analytical methods, carrying out pilot runs on fresh reagents, and keeping lines of communication open with project managers at partner labs, we stay flexible while maintaining high standards.
Pharmaceutical and agrochemical companies scale up fast once a lead candidate hits the right biological marks. Small inconsistencies between test and pilot lots can upend that progress. From our side, we fine-tune both small pilot runs and full-scale manufacturing so partners do not get unwelcome surprises further downstream. We deploy larger clean areas, antistatic filling technology, and rigorous impurity profiling. The focus stays on getting batch reproducibility and regulatory support right on non-GMP as well as late-stage projects.
Collaboration does not stop at the loading dock. We often set up video calls with project scientists to discuss their reaction details, check our analytical protocols against their requirements, and sometimes even suggest process tweaks that save them weeks in the lab. Our openness to sharing not only what works, but what sometimes fails, brings real-world detail to customers who want a partner, not just a supplier.
Every production run offers something to learn. Minor changes in temperature ramp or catalyst charge shift impurity profiles. About a decade ago, a spike in column failures for a single customer prompted us to revisit how tightly we controlled formylation—retracing every step, we found a source of cross-contamination with a methylated analog. That led to stricter line cleaning and downtime scheduling.
We also look for ways to improve convenience—rider lots, flexible packaging sizes, and a willingness to custom-pack for multipurpose research environments save time and reduce repackaging on the customer end. Sometimes our small changes, like using a higher-quality desiccant packet or a new drum liner, save a morning’s trouble and hundreds of dollars in wasted effort in research labs around the world.
Progress in indole-based chemistry is rapid. New methods for oxidative coupling, photoredox catalysis, and direct C–H functionalization continue to emerge, meaning researchers always need intermediate products with reliable, documented handling and traceability. Here, our approach stays hands-on and realistic. We keep pace with advances but never compromise product integrity for trend chasing.
7-Ethyl-1H-Indole-3-carbaldehyde is not an off-the-shelf commodity. It sits on the critical path for scientists building new molecules in pursuit of tomorrow’s drugs, dyes, or specialty chemicals. As manufacturers committed to both the integrity of the chemical and the value it brings to end-users, our approach combines technical mastery with the kind of cooperative outlook that leads to advances across industries.
In our experience, manufacturing fine chemicals like this indole derivative is not just about making a product and moving it out the door. Chemistry, like any real craft, is built on trust, skill, and ongoing learning. By focusing on responsible sourcing, skilled teams, and honest feedback loops, we ensure that our 7-Ethyl-1H-Indole-3-carbaldehyde reaches researchers and process chemists in the exact condition they expect. Whether supporting a single groundbreaking reaction or the rollout of a full product line, our work reflects both the science and the pride of real chemical production.