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7-Ethylindole

    • Product Name 7-Ethylindole
    • Alias 7-Ethyl-1H-indole
    • Einecs 628-117-9
    • 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
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    Specifications

    HS Code

    338099

    Name 7-Ethylindole
    Cas Number 2704-20-9
    Molecular Formula C10H11N
    Molar Mass 145.20 g/mol
    Appearance Off-white to light brown solid
    Melting Point 54-58°C
    Boiling Point 292°C
    Density 1.07 g/cm³
    Solubility In Water Insoluble
    Synonyms 7-Ethyl-1H-indole
    Smiles CCc1cccc2[nH]ccc12
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, tightly sealed, away from light

    As an accredited 7-Ethylindole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a tight-sealed cap, labeled "7-Ethylindole, 98%," includes hazard warnings and handling instructions.
    Shipping 7-Ethylindole is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Packaging complies with chemical safety regulations, ensuring secure transit. The product is labeled with hazard information and handled as a combustible organic compound, requiring proper documentation and adherence to relevant shipping guidelines for laboratory chemicals.
    Storage 7-Ethylindole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Use only with proper ventilation and avoid prolonged exposure. Follow all relevant safety and regulatory guidelines for storage of laboratory chemicals.
    Application of 7-Ethylindole

    Applications of 7-Ethylindole in Industrial Manufacturing

    As a direct manufacturer of 7-Ethylindole, we support customers in multiple specialized chemical sectors. Our advanced production controls and full batch traceability ensure supply for exacting downstream industries. Explore key industrial applications for this high-purity indole derivative, with detailed information on standards, usage, integration, and final product outputs below.

    1. Pharmaceutical Intermediates: Synthesis of Antineoplastic Agents

    Pharmaceutical companies source 7-Ethylindole as a core intermediate for synthesizing certain indole-based oncology drugs. Production teams convert it via targeted indole functionalization—crucial in manufacturing third-generation tryptamine derivatives used as kinase inhibitors or receptor modulators. Quality assurance protocols demand strict impurity control and validated synthetic yields in cGMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • U.S. Pharmacopeia (USP) General Chapter 1086, relevant API monographs
    • EU GMP Part II: basic requirements for starting materials and APIs
    • FDA 21 CFR Part 211 (for API synthesis facilities in the United States)

    Typical usage ratio

    • Serves as a key scaffold in 1–3 molar equivalents depending on target molecule; adjusted to batch size and substrate reactivity in route design.

    Downstream process integration

    • Introduced during multi-step synthesis as the primary aromatic building block for functionalization.
    • Downstream chemists perform halogenation, alkylation, or acylation reactions after dissolution in polar aprotic solvents.
    • Intermediate storage and transfer occur under nitrogen to guard against trace oxidation.

    Final product types

    • Oral small molecule antineoplastic APIs
    • Investigational targeted cancer drugs (clinical-stage candidates)
    • Licensed kinase inhibitor intermediates
    • Export pharmaceutical raw materials for further formulation

    2. Agrochemical Building Block: Synthesis of Fungicides

    In agrochemical factories, 7-Ethylindole finds use as a pivotal starting material during the manufacture of proprietary indole-based fungicides. Chemists incorporate it to engineer compounds with enhanced plant systemicity and novel bioactivity profiles, helping downstream producers address evolving pest resistance. Precise tolerances and repeatable batch quality underpin its use, especially before nitrosation or sulfonation.

    Industry compliance standards

    • FAO/WHO specifications for agricultural pesticide active ingredients
    • ECHA REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) for European market entry
    • ISO 9001-certified quality management during batch production
    • Regulations on chemical storage and transport: ADR, IMDG, IATA

    Typical usage ratio

    • Commonly charged at 5–15% weight-to-weight against total reaction substrate in technical-grade synthesis; adapted by compound complexity.

    Downstream process integration

    • Blended into reaction vessel during initial condensation or cyclization steps.
    • Catalyst addition proceeds following full 7-Ethylindole dissolution and temperature ramp-up.
    • Pilot plants maintain controlled agitation to prevent dimerization phenomena.

    Final product types

    • Active fungicide ingredients for cereals, vegetables, and fruits
    • Pre-mix technical concentrates for formulated crop protection
    • Seed treatment additive intermediates
    • Custom-synthesized indole derivatives for R&D screening

    3. Dye and Pigment Manufacturing: Indole-Based Colorants

    Dye-molecule specialists employ 7-Ethylindole as a precursor in synthesizing high-performance colorants for specialty inks and textile dyeing. The ethyl substitution promotes intensification of chromophore characteristics. This enables downstream producers to engineer lightfast and shade-stable anthraquinone or azo dyes for demanding end-use applications, including technical textiles and documentation inks.

    Industry compliance standards

    • OEKO-TEX Standard 100 and ZDHC MRSL for colorant safety
    • REACH registered dye compound lists for EU export
    • ISO 105-B02 lightfastness testing standards
    • GHS/CLP chemical labeling and handling compliance

    Typical usage ratio

    • Typically integrated at 3–10% of the main dye feed, subject to target CI (Color Index) structure and shade optimization.

    Downstream process integration

    • Dosed into early diazotization or coupling phases during pigment or dye molecule synthesis.
    • Process engineers adjust solvent polarity to maximize indole incorporation rate.
    • Inline QA assesses conversion via TLC or HPLC prior to downstream blending.

    Final product types

    • Disperse and reactive textile dyes (especially for nylon, polyester fibers)
    • Applications in high-definition inkjet printing inks
    • Specialty colorants for industrial coatings
    • Visible and near-IR security mark pigments

    4. Flavor & Fragrance: Production of Aroma Compounds

    Our partners in the fragrance industry employ 7-Ethylindole to build foundation notes in musk and floral accord compositions. Its pronounced indolic backbone allows perfumers to create complex animalic or jasmine-type aroma compounds. Manufacturing control is crucial due to stringent impurity and residual solvent thresholds set by fragrance safety bodies. Usage extends to advanced esterification and acylation steps for both bulk fine fragrances and tailored aroma intermediates.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • EU Regulation (EC) No 1223/2009 for cosmetic ingredients
    • Food Chemicals Codex (FCC) if applied in food-grade applications
    • ISO 9235 for natural raw materials (synthetic conformity protocols)

    Typical usage ratio

    • Blended at 0.05–0.5% of total concentrate mass for fragrance compounds; exact level customized per olfactory strength and regulatory allowances.

    Downstream process integration

    • Introduced in the initial synthesis of indole core aroma compounds under tightly controlled anhydrous conditions.
    • Following derivatization, QC samples tested for purity and stability pre-formulation.
    • Material then proceeds to secondary reaction or blending lines for integration with alcohols, esters, or aldehydes.

    Final product types

    • Fine fragrance bases (musk, jasmine accord)
    • Industrial perfumery intermediates
    • Cosmetic grade aroma chemicals
    • Flavor enhancement precursors (with separate food-grade validation)

    5. Specialty Chemical Synthesis: Research and Development

    R&D laboratories and contract development organizations utilize 7-Ethylindole for exploratory synthesis of advanced functional molecules. Its ethyl group expands structure-activity relationship (SAR) studies, supporting the creation of new molecular scaffolds for pharmacological evaluation or material science testing. Stringent quality documentation and batch consistency are necessary for valid experimental results in project-based and pilot scale workstreams.

    Industry compliance standards

    • ISO/IEC 17025 laboratory competence
    • GMP R&D pilot plant requirements for pharmaceutical discovery
    • Responsible handling in line with local hazardous chemical regulations (e.g. US EPA, EU CLP)
    • Proper chemical tracking as per OSHA standards

    Typical usage ratio

    • Applied at 10 mg to 10 g scale per reaction depending on syntheses; ratio determined by target molecule complexity and SAR breadth.

    Downstream process integration

    • Weighing and transfer under controlled atmosphere as a foundational reagent for lead optimization studies.
    • Entry into multi-step synthetic campaigns involving alkylation, cross-coupling, or cyclization.
    • Purity checks via GC-MS or NMR confirm suitability for further research use.

    Final product types

    • Pharmaceutical lead compounds
    • Material science intermediates (OLED, specialty polymers)
    • Chemical libraries for high-throughput screening
    • Reference standards for analytical method development
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    Certification & Compliance
    More Introduction

    7-Ethylindole: A Closer Look From the Lab Floor

    Understanding 7-Ethylindole in Practical Terms

    In our daily operations, 7-Ethylindole stands out as a unique platform molecule with value that has steadily grown as research in bioactive heterocycles advances. The molecular structure, defined by its ethyl group attached at the 7-position of the indole ring, does more than provide an adjustment in mass or hydrophobicity—it can fundamentally alter how the molecule participates in synthetic sequences compared to unsubstituted indole or isomeric ethylindoles. Our typical production batch ensures purity above 98%, with trace-specific impurities monitored to support high-performance applications.

    The physical reality of 7-Ethylindole, a pale solid with a characteristic aromatic odor, means handling procedures require close attention to detail. A fine balance between temperature, atmosphere, and solvent choice during crystallization means every batch requires vigilance to secure batch-to-batch consistency. From long experience, slight differences in crystallization patterns or stabilization with specific solvents can shift how the compound behaves in reaction setups. Many colleagues who use generic or cheap resourced indole derivatives encounter problems with off-odors or colored impurities—symptoms that signal side contamination. Controlling for byproducts and secondary isomers during scale-up makes the difference between a reliable synthesis and difficult downstream cleanup.

    The Real-World Importance of Our Product

    Labs working in medicinal chemistry, agricultural research, or pigment development typically seek out 7-Ethylindole because its ethylation pattern cannot be easily substituted elsewhere in the molecule without shifting reactivity. As a direct manufacturer, we see requests for gram through multi-kilogram quantities targeted for use in alkaloid synthesis, fused-ring studies, or intermediate coupling reactions. Over the years, customers have shared stories about how small variances in starting material purity or polymorphic form can severely affect chromatographic resolution, particularly when scaling from milligram to kilogram quantities. Reliable 7-Ethylindole means incorporating a dependable baseline material—if there’s less to worry about at the starting gate, less time is lost troubleshooting further downstream.

    Chemical behavior diverges significantly between elementary indole and its substituted analogs. Attaching an ethyl group at the 7-position restricts possible oxidation, tightens regioselectivity, and grants new options for electrophilic substitutions. A medicinal chemist relying on unsubstituted indole would see unwanted side chains or over-alkylation, while 7-Ethylindole channels specific reactions into more predictable terminal products. Our production teams have refined the dehydrogenation and alkylation sequences so impurities like diethyl or overalkylated byproducts are limited to below 0.2% in the crude, and final purification consistently produces colorless or faintly off-white material.

    Differentiating 7-Ethylindole From Other Indole Derivatives

    Over the past decade, requests for 5-ethylindole and 2-ethylindole have cropped up, but the downstream reactivity is never quite the same as the 7-ethyl arrangement. The location of that single ethyl branch lends a distinct steric effect, steering addition pathways and engagement with aromatic partners in ways lab chemists exploit routinely when constructing targeted molecules for pharmacological or electronics uses. The synthetic routes for 7-Ethylindole also differ: starting materials require careful upstream selection. One popular method involves the Fischer indole synthesis routed through 7-ethyltryptamine intermediates; this sequence demands precise control and an understanding of the feedstock’s isomer distribution. Our in-plant experience is that shortchanging the reaction temperature or solvent drying protocols lets side isomers creep in, which lengthens isolation and hurts overall yields.

    In my experience, smaller laboratories that rely on resellers sometimes encounter inconsistency in their supplied 7-Ethylindole. Traders and distributors usually blend material from multiple sources to adjust quantities. This blending, intentional or not, produces a composite product that seldom matches a single-lot manufacturer’s integrity, particularly noticeable in sensitive pharmaceutical work. Our customers in specialty ink and pigment industries seek tight standards because minor color variations, even at the parts-per-million level, result in costly batch waste. We keep a strict chain of custody and can reproduce the chromatographic fingerprint of each lot, so if issues arise, troubleshooting is faster.

    Production Challenges and Quality Control

    Making 7-Ethylindole at scale isn’t simple. Maintaining a consistent ethylation pattern while preserving high indole content requires careful selection of both starting tryptamines and catalytic systems. A few years ago, a run using slightly aged starting amines produced an off-odor batch, which even repeated recrystallizations could not fully remedy—the experience led to even tighter controls on raw material storage and stricter acceptance criteria. Chemists in the pharmaceutical sector sometimes reference our material by fingerprint, comparing NMR, IR, and GC-MS results for each batch, expecting negligible variance. Feedback like this has taught us the importance of supporting both analytical transparency and on-demand technical documentation.

    The cost of analyzing every large batch may seem high to outsiders, but unnoticed isomer content or slight excess of non-volatile residues will create process headaches for anyone attempting high-purity isolations downstream. We always recommend running a rapid TLC or GC check before committing to long, multi-step syntheses. Sharing full chromatographic and spectrometric data with partners helps shorten troubleshooting if they hit a snag. On several occasions, timely alerts about trace polycyclic impurities prompted quick process adjustments, keeping both our teams and customers on schedule.

    Some buyers have reported problems with other suppliers regarding inconsistent flow properties or contamination by halogenated side products. This issue arises when indole is alkylated with cheaper base-promoted methods, which often leave behind traces that complicate purification, particularly for sensitive electronics or biological applications. Our technical staff follow-up to ensure the indole core remains untouched by such artifacts, running halogen and metal screens as part of the release protocol. Customers tell us repeatedly that this diligence makes the difference when producing drug leads, bioassays, or optoelectronic prototypes where uncontaminated starting material is the only acceptable standard.

    Applications We Encounter Most Often

    Most requests for 7-Ethylindole come from teams running heterocycle development programs, custom active pharmaceutical ingredient synthesis, or specialty pigment programs. Many new agrochemical leads are indole-based, and the ethyl substituent at the 7-position sharply alters bioavailability and binding patterns in assay work. Electrochemists also use 7-Ethylindole as a stepping stone toward building more complex fused ring systems for OLEDs, solar cells, or photoactive layers. We’ve supplied material for projects ranging from basic laboratory investigations to full-scale pre-clinical lots. In pigment formulations, our product is valued for how the substitution shields downstream chromophores from over-oxidation and helps modulate solubility in organic carriers.

    Custom syntheses can demand hundreds of grams of nearly colorless, odorless material, especially in pharmaceutical research. A large drug company relied on consistent 7-Ethylindole supply to ensure their process didn’t stall at the pilot plant, with timelines shaved by weeks because revalidation wasn’t necessary every batch. Conversely, several customers working with non-pharmaceutical purity have opted for slightly less refined grades where trace color and odor are acceptable. This spectrum of use cases makes control over impurity profile, polymorphic consistency, and batch tracking concrete concerns on a daily basis.

    Pigment manufacturers stand out for their sensitivity to hue and performance in sunlight. Even a small excess of oxidized byproduct, recognizable as faint yellow or brown tints, sends a batch back for reclaiming. We’ve tuned our storage protocols, light shielding, and packaging to minimize photo-oxidation and moisture uptake—many downstream failures trace back to material improperly handled before it ever reaches final formulation.

    Strategies for Meeting Industry Needs and Avoiding Common Pitfalls

    Over two decades in production, we’ve refined methodologies based on both experience and feedback from hundreds of chemists worldwide. Supporting customer pilots and offering transparent analytical data has helped clients in regulatory filings, technology transfer, and even in securing IP positions where unique starting-material fingerprints support patent claims. In collaborating on process optimization, we’ve learned that spending extra time confirming batch reproducibility pays dividends—especially in scaling from lab to pilot plant.

    Those working on tight deadlines often need flexible shipping quantities and rapid documentation. Frequent questions from contract research organizations relate to the long-term chemical stability and shelf-life of 7-Ethylindole under rigorous handling. Early on we encountered issues with sublimation losses under warm, dry storage, so now we advise storage under inert atmosphere, in dark containers below 20°C, at all customer sites. These safeguards have cut down on unexplained purity drifts and enhanced shelf life, allowing our partners to keep reliable stocks on hand without the frustration of untimely degradation.

    We often discuss best practices with users: avoid multiple freeze-thaw cycles, partition off working stocks to prevent cross-contamination, and always reseal after sampling. Subtle differences in handling, particularly in groups not accustomed to reactive aromatic solids, can have outsized impacts on both performance and waste stream management. In regions with high humidity, desiccant packs inside outer drums reduce clumping and decomposition.

    It’s also worth noting that regulatory environments and green chemistry concerns are shifting. Laboratories worldwide now look more closely at the lifecycle of specialty intermediates, including safe disposal of mother liquors and non-volatile residues. As a manufacturer, we adapted our on-site waste treatment and solvent recycling systems to meet stricter guidelines, reducing both environmental footprint and costs in parallel. We’re often asked for confirmation on REACH status, RoHS screening, or traceability to support registrants in regulated markets.

    Supporting Innovation Without Compromising Standards

    Today’s research environment is relentless: tighter project windows and more complicated molecular targets require absolute trust in starting materials. Inconsistent batches can derail grant-funded projects or clinical studies, often at extraordinary cost. By working closely with principal investigators and production leads, our team has learned that transparency and responsiveness build lasting trust. Open lines of communication about batch release, impurity profiles, storage conditions, and even anticipated regulatory shifts matter just as much as the final kilo of product.

    In sharing analytical details without delay, we help customers avoid guesswork—by supplying up-to-date spectra, chromatograms, and certificates, time spent debugging anomalies drops meaningfully. This partnership-based approach encourages two-way feedback. Chemists pursuing new process routes often alert us early about subtle analytical shifts or unpredicted degradation pathways; our response includes not only supplying replacement material but often feeding process improvements right back into production and documentation cycles.

    Across applications, customers report that clean, consistently manufactured 7-Ethylindole shortens development times, reduces purification headaches, and improves overall reliability from gram to multi-kilogram scales. The added investment in deep technical support, rapid batch tracking, and flexible shipping pays off when compared to risks inherent in generic or overseas-sourced analogs. We routinely supply samples for comparison against existing stocks to facilitate smooth transitions and ensure project continuity.

    Looking Forward in 7-Ethylindole Manufacturing and Application

    Industry trends point to an uptick in multi-functional indole core structures, especially as pharmaceutical and electronics innovation pushes deeper into custom heterocycle landscapes. With more complicated scaffolds comes sharper demand for precise, pure, and consistently available core materials like 7-Ethylindole. Many of our clients pursue strong intellectual property positions, and their synthetic success often hinges on highly characterized, traceable intermediates.

    We are already investing in further tightening error margins in both upstream feedstock control and downstream final testing. A new batch release system designed to satellite analytical files within minutes of physical shipment is cutting errors and delays, building more trust between bench chemists and our technical staff. Conversations with researchers who run into scaling challenges often come back to quality of starting material, and we’re always open to customizing purification parameters or packaging options to match each team’s workflow.

    Sustainable manufacturing also features prominently in our future planning. Advances in closed-loop solvent recycling, expanded real-time quality analytics, and more robust occupational safety protocols are all underway. Customers expect conscientious stewardship, not only over the purity and analytical soundness of specialty chemicals, but over the entire procurement and post-use lifecycle. By staying engaged with the laboratories, procurement specialists, and regulatory liaisons who comprise the next generation of innovators, we make it easier for discovery to thrive—without compromise in quality or trust.

    The journey in refining and supplying 7-Ethylindole is ongoing. Every batch, new application, and customer feedback loop sharpens our commitment to technical precision and responsive partnership. Those who rely on 7-Ethylindole for breakthrough research or advanced technology know the difference a manufacturer’s experience, vigilance, and adaptability bring to the table—and as demand grows, we stand ready to meet the challenge, molecule by molecule.