Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

7-Ethyl-1H-Indole-3-Carbaldehyde

    • Product Name 7-Ethyl-1H-Indole-3-Carbaldehyde
    • Alias 7-Ethyl-1H-indole-3-carboxaldehyde
    • Einecs 681-409-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 7-Ethyl-1H-Indole-3-Carbaldehyde

    Applications of 7-Ethyl-1H-Indole-3-Carbaldehyde in Industrial Manufacturing

    As 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 Agents

    Many 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

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF and EP monograph compliance as applicable for final drug substances
    • FDA 21 CFR 211 for cGMP manufacturing
    • Global pharmacopoeia-driven impurity and residual solvent controls

    Typical usage ratio

    • 5–15% molar basis in multi-step synthesis, adjusted per target API; process scientists vary charge based on desired yield and impurity threshold

    Downstream process integration

    • Condensation step following raw indole derivative activation
    • Integrated in continuous or semi-batch reactors; in-process analytics employed on site

    Final product types

    • Pharmaceutical bulk active ingredients (API) for oncology pipeline
    • Process intermediates for regulated clinical trial material (CTM) and commercial drug substance manufacturers

    2. Advanced Fluorescent Dye Manufacturing

    Fluorescent 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

    • ISO 9001:2015 quality system for specialty chemical synthesis
    • EN ISO 13485 for dyes used in IVD (in vitro diagnostics) device components
    • RoHS Directive 2011/65/EU for device component approval
    • REACH SVHC communication for EEA market access

    Typical usage ratio

    • 1–7% weight/weight in charge mix—chemists adjust based on target absorption and quantum yield for the intended fluorophore

    Downstream process integration

    • Initial condensation with electron-withdrawing partners during dye backbone construction
    • Fed-batch processing allows purity control prior to dye functionalization

    Final product types

    • Custom fluorescence probes for immunoassays and PCR kits
    • Spectral imaging dyes for cellular labeling kits
    • Dyes integrated in medical device polymers

    3. Agrochemical Active Ingredient Synthesis

    Producers 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

    • FAO/WHO Technical Guidelines for Manufacture of Pesticide Technical Materials
    • ISO 9001 and ISO 14001 for environmental and quality management during chemical synthesis
    • REACH registration for EEA supply if volume thresholds exceeded
    • China GB/T 1603 for technical active substance QC

    Typical usage ratio

    • 2–10% mass fraction in batch input, modulated for specific product routes and impurity allowance per end-use registration dossier

    Downstream process integration

    • Introduced in the early or mid-stage synthetic transformations, enabling late-stage functionalization of indole framework
    • Used in both continuous and discrete kilogram-to-multiton scale setups

    Final product types

    • Technical grade herbicides
    • Fungicide active ingredients for formulation
    • Registered pesticide intermediates for local and export market registrations

    4. Fine Fragrance and Aroma Chemical Development

    Manufacturers 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

    • IFRA Code of Practice (latest amendment) for ingredient safe use
    • ISO 9001:2015 for aroma chemical manufacturing
    • REACH registration for EU fragrance market integration
    • RIFM safety evaluation criteria for new ingredient introduction

    Typical usage ratio

    • 0.1–1% by formulation weight; precise loading set by perfumer based on headspace evaluation and stability requirements

    Downstream process integration

    • Integrated during aromatic compound derivatization or as a precursor for custom indole-based molecules
    • Vacuum distillation and fractional crystallization refine the intermediate into fragrance-grade ingredient

    Final product types

    • Fine fragrance specialties for designer perfumes
    • Cosmetic aroma ingredients for skin and hair care lines
    • High-impact top note chemicals for personal care applications
    Free Quote

    Competitive 7-Ethyl-1H-Indole-3-Carbaldehyde prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    7-Ethyl-1H-Indole-3-Carbaldehyde: A Closer Look at Practical Chemistry

    Real Production, Real Results

    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. 

    Why 7-Ethyl-1H-Indole-3-Carbaldehyde Matters

    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.

    From Bench to Bulk: Specs Informed by Experience

    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.

    What Sets It Apart

    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.

    Application in Industry and Research

    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.

    Handling In-House: Best Practices for Chemists

    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.

    Comparisons to Other Indole Carbaldehydes

    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.

    Pushing for Continual Improvement

    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.

    Supporting Scale-Up and Discovery

    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.

    Learning From Every Batch

    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.

    What the Future Holds

    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.

    Towards Reliable Partnerships

    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.