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

5-Methoxyindole-3-Carboxaldehyde

    • Product Name 5-Methoxyindole-3-Carboxaldehyde
    • Alias 5-Methoxy-1H-indole-3-carbaldehyde
    • Einecs 609-412-7
    • 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

    312136

    Cas Number 2538-94-1
    Molecular Formula C10H9NO2
    Molecular Weight 175.18
    Iupac Name 5-Methoxy-1H-indole-3-carbaldehyde
    Appearance Off-white to yellowish solid
    Melting Point 169-172°C
    Solubility Soluble in DMSO, ethanol, methanol
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Smiles COC1=CC2=C(C=C1)NC=C2C=O
    Synonyms 5-Methoxy-3-indolecarboxaldehyde

    As an accredited 5-Methoxyindole-3-Carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 5-Methoxyindole-3-Carboxaldehyde, 10g: Supplied in an amber glass bottle, tamper-evident seal, labeled with safety, batch, and expiry information.
    Shipping 5-Methoxyindole-3-Carboxaldehyde is shipped in a tightly sealed container, protected from light and moisture. The package complies with all relevant safety regulations and includes appropriate labeling for laboratory chemicals. During transit, temperature and handling instructions are followed to ensure stability and integrity of the compound until delivery.
    Storage 5-Methoxyindole-3-carboxaldehyde should be stored in a cool, dry, and well-ventilated area away from direct sunlight and moisture. Keep the container tightly closed when not in use. Store the chemical in a tightly sealed container, away from incompatible substances such as strong oxidizing agents. Ensure appropriate labeling and follow local regulations for chemical storage to ensure safety.
    Application of 5-Methoxyindole-3-Carboxaldehyde

    Applications of 5-Methoxyindole-3-Carboxaldehyde in Industrial Manufacturing

    As a primary manufacturer in the fine chemical industry, we supply 5-Methoxyindole-3-Carboxaldehyde to advanced sectors where this indole derivative directly supports key synthesis routes and product performance requirements. The following sections outline the main industrial applications, each with dedicated compliance standards, formulation guidelines, integration stages, and finished goods delivered by customers operating in regulated and specialized domains.

    1. Pharmaceutical Intermediate for Tryptamine Analog Synthesis

    Pharmaceutical synthesis employs this compound as a crucial building block for manufacturing tryptamine-based active pharmaceutical ingredients, particularly for indole derivative drugs. It enters the process after initial raw material purification and acts as the aldehyde component in condensation, reductive amination, or cyclization steps. This application falls under stringent regulatory frameworks, and adjustment of the dosage level considers route design and reaction yield. Manufacturers obtain finished APIs or advanced intermediates for further conversion into CNS agents, anti-migraine therapies, and serotonin receptor modulators.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF monographs (for downstream API release)
    • EDQM Certification of Suitability (CEP) for relevant APIs
    • 21 CFR Part 211 US cGMP for Finished Pharmaceuticals

    Typical usage ratio

    • 5–28% w/w relative to total indole compound input, adjusted per target molecular synthesis route and batch scale; detailed optimization based on molar balance and impurity threshold requirements

    Downstream process integration

    • Added after indole precursor preparation or ring substitution, entering as a key aldehyde for condensation or reductive alkylation steps; handled in closed reactor trains under controlled atmosphere to maintain purity

    Final product types

    • Tryptamine-based APIs (e.g., antimigraine agents)
    • Advanced pharmaceutical intermediates
    • Serotonergic receptor ligands
    • Specialty research compounds for clinical development

    2. Active Ingredient Sourcing for Research Chemicals & Analytical Reagents

    Synthesis labs and chemical suppliers utilize this material as the backbone for indole-based reference compounds and analytical reagents. Stringent traceability and analytical documentation characterize this market segment, with end users requiring consistent quality and trace impurities controlled to ppm levels. Utilized primarily as a reactive aldehyde, ratio adjustments depend on target molecule structure and downstream derivatization efficiency. Final goods include high-purity reference substances for chromatography, metabolite tracking, and bioresearch method validation.

    Industry compliance standards

    • ISO 17034 Reference Material Producer requirements
    • ISO 9001 Quality Management Systems (applicable for analytical-grade production)
    • REACH Regulation (EC) No 1907/2006 for laboratory/analytical supply within EU
    • GMP Annex 1 for materials used in sterile validation

    Typical usage ratio

    • 0.5–3% w/w as a reagent, typically stoichiometric or slight excess for derivatization; adjusted to maintain analytical tolerance and product purity above 98%

    Downstream process integration

    • Added during the derivatization or coupling phase of reference compound synthesis, typically dissolved in high-grade solvents and reacted to generate target analytes; QC oversight ensures batch consistency

    Final product types

    • Certified reference materials (CRMs)
    • Analytical calibration standards
    • High-purity laboratory reagents
    • Stable isotope-labeled indoles for bioanalytical research

    3. Synthesis of Specialty Agrochemical Intermediates

    In the agrochemical sector, formulators rely on this compound to build advanced indole scaffolds for plant growth regulators and innovative crop protection molecules. It enters multi-stage syntheses that demand reliable input quality and trace impurity documentation. Usage levels depend on intermediate conversion rates and scale, with compliance tied to agrochemical precursor regulations and workplace safety protocols. Downstream processing involves stepwise transformations and purification, producing intermediates for later formulation as biostimulants or regulatory molecules.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • EU Regulation (EC) No 1107/2009 – Placing of Plant Protection Products on the Market
    • ISO 9001:2015 Quality Management for Chemical Production
    • OSHA 29 CFR 1910.1200 Hazard Communication

    Typical usage ratio

    • 0.7–12% w/w, calculated according to the degree of substitution required for downstream indole management and efficiency of coupling/oxidation reactions

    Downstream process integration

    • Incorporated as a functionalized aldehyde after initial indole ring assembly, facilitating oxidation or reductive amination steps to yield bioactive precursors; emphasizes controlled conditions to minimize unwanted byproducts

    Final product types

    • Plant growth regulator intermediates (e.g., novel auxin analogues)
    • Building blocks for emerging crop protection actives
    • Indole-derived agrochemical intermediates
    • Bioactive research compounds for plant science development

    4. Manufacturing of Fluorescent Probes and Dyes

    Producers of advanced fluorescent markers and organic dyes deploy this material to synthesize core indole-derived chromophores. The aldehyde functionality supports multiple coupling and condensation routes, providing the structural foundation for high-performance fluorescent compounds. Compliance centers on specialty chemical formulation standards and batch reproducibility for optical properties. The usage ratio reflects color intensity and dye purity needs set by optical instrumentation end users. Processing integrates the aldehyde late in the sequence, usually after precursor ring formation, to preserve emission characteristics. Typical finished goods range from fluorescence standards to specialty detection reagents for scientific and medical imaging markets.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacturing
    • ASTM E2877 Standard Guide for Validating Fluorescence Methods
    • European REACH compliance for dyes in research use
    • RoHS Directive 2011/65/EU for dyes used in analytical/diagnostic equipment

    Typical usage ratio

    • 0.2–2.5% w/w in final dye coupling reactions, tuned based on target fluorophore brightness, emission wavelength, and purity level requirements

    Downstream process integration

    • Introduced following primary ring synthesis or as a terminal aldehyde during dye assembly, supporting further condensation or coupling to form the active chromophore structure; handled at elevated temperatures with inert gas protection to ensure spectral properties

    Final product types

    • Indole-based fluorescent dyes
    • Synthetic chromophores for biomedical imaging
    • Fluorescent probe intermediates
    • Laser dye precursors for optical instruments

    5. Fine Chemical Synthesis of Fragrance & Aroma Precursors

    Specialty aroma and perfume ingredient manufacturers integrate this material as a precursor for synthesizing complex indole-based aroma compounds and modifiers. The strictest purity standards apply, as residual byproducts affect final olfactory profiles. The compound typically enters the synthetic route post-indole ring derivatization, delivering the required aldehyde group for further transformations such as Grignard reactions or reductive amination. End products focus on high-value-per-kg perfumery intermediates and proprietary aroma molecules crafted for niche fragrance development.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • ISO 9235:2013 Aromatic Natural Raw Materials – Vocabulary
    • REACH Regulation (EC) No 1907/2006 for aroma chemicals
    • ISO 9001:2015 for aroma chemical synthesis

    Typical usage ratio

    • 0.05–0.7% w/w, determined by the specific aromatic note sought and conversion efficiency in downstream transformations; generally minimized to retain high odor threshold

    Downstream process integration

    • Added during advanced aroma precursor assembly after preliminary indole modification, supporting controlled transformations to generate tailored aromatic building blocks; refined under vacuum to enhance purity and fragrance definition

    Final product types

    • Indole-based aroma intermediates
    • Specialty fragrance modifiers
    • High-purity aroma chemicals for perfumery bases
    • Custom blend components for luxury fragrances
    Free Quote

    Competitive 5-Methoxyindole-3-Carboxaldehyde 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

    Understanding 5-Methoxyindole-3-Carboxaldehyde: From Manufacturing to Application

    Real Experience with 5-Methoxyindole-3-Carboxaldehyde Production

    As a chemical manufacturer, we have seen interest in indole-based chemicals transform over the years. The compound 5-Methoxyindole-3-Carboxaldehyde, sometimes referred to as 5-MeO-3-ICA, stands out because of its remarkable versatility in both laboratory synthesis and industrial production. Unlike distributors or resellers, we manage the process from raw material sourcing, through each synthesis stage, to final testing and packaging. This lets us see firsthand how minute details during crystallization or solvent selection can create subtle, tangible differences in quality that customers often only notice downstream during their own research work or process runs.

    Key Features Based on Hands-on Experience

    We manufacture 5-Methoxyindole-3-Carboxaldehyde as a white to pale yellow solid with a defined melting point. Consistency in particle size and purity matters to researchers and process engineers because these subtle physical traits affect reproducibility of reactions. In our experience, even tiny deviations in drying method or solvent removal will change the flow and handling properties of the compound. For those working at scale, proper drying ensures that the aldehyde resists caking and remains easy to weigh or dissolve, which reduces batch-to-batch headaches.

    We produce this compound using synthesis routes that avoid halogenated solvents and prioritize mild conditions, reducing contaminant byproducts that often require extra purification steps down the line. By focusing on solvent control and careful pH regulation, our staff can consistently achieve purity levels above 98 percent (as validated by both HPLC and NMR). A researcher using our material for tryptamine or peptide synthesis rarely reports side-reactions from minor impurities. This level of feedback, collected over hundreds of batches, gives us confidence that each new lot meets practical laboratory needs from medicinal chemistry to flavor and fragrance development.

    Practical Uses and Its Role in Laboratory and Industry

    5-Methoxyindole-3-Carboxaldehyde is a building block rather than a finished product. Labs often use this aldehyde to construct tryptamine derivatives, peptide mimics, and various heterocyclic scaffolds with pharmacological potential. As chemists innovate, we respond to requests for higher purity or larger-scale batches, allowing new reaction types or scale-up feasibility testing without material-related obstacles.

    Pharmaceutical R&D groups value this compound because the methoxy and carboxaldehyde groups enable site-selective transformations. They often report that batch clarity, lower moisture content, and minimized residual solvents can make or break a tricky indole alkylation or reductive amination. On the materials side, specialty chemical companies transform 5-Methoxyindole-3-Carboxaldehyde into optical brighteners and specialty dyes, where even trace iron or oxidizable impurities will affect product color or stability.

    Distinctions from Other Indole Derivatives

    While all indole aldehydes share a core structure, the methoxy substitution at the 5-position gives 5-Methoxyindole-3-Carboxaldehyde unique properties. We watch trends in process chemistry and observe that subtle electronic effects from the methoxy group impact reactivity in condensation or cyclization reactions. This reactivity profile lets users access analogues not easily reachable with unsubstituted or different methoxy-positioned aldehydes.

    For instance, the 5-methoxy function increases electron density at key indole positions, favoring more selective reactions in building complex molecules. Researchers who once used 3-indolecarboxaldehyde without the methoxy often report higher yields and fewer byproducts with our 5-methoxy version, especially in conditions sensitive to electronic effects. Compared to 2-methoxyindole-3-carboxaldehyde, the 5-methoxy regioisomer offers distinct synthetic outcomes, such as improved selectivity in multistep synthesis or reduced risk of isomer formation during ring closures.

    Feedback from Real Users and Common Trends

    Academic labs take more of our small pack sizes, aiming for high purity and reliable spectral data. They report that our compound dissolves quickly, allowing efficient batch preparation in peptide and alkaloid synthesis. Because purity remains high across lots, research teams spend less time troubleshooting contaminant peaks during chromatographic workups or analyzing NMR residues.

    Process chemists in industry usually request multi-kilogram batches with detailed impurity profiles. Our process scale-up has shown that maintaining moisture content below 0.5% by Karl Fischer titration remains critical. Higher water content, even by 0.2%, triggers complaints about clumping or streaking in solid-feed reactors and can limit the efficiency of downstream condensation reactions. Feedback like this has driven our investment in vacuum drying and improved lot-by-lot testing for water and residual solvents.

    Glow and fluorescence specialty companies try a small lot before moving to larger orders, watching for color changes on storage. Through regular process audits, we limit exposure to air and trace metals so the end product retains its pale color and stays free-flowing over time. End-users have confirmed that fresh, well-packed lots avoid yellowing or visible oxidation, outcomes often observed in poorly processed batches from less experienced suppliers.

    Reliability in Sourcing and Traceability

    Because we manage all synthesis steps in-house, raw material traceability stays under full control. Certificates of Analysis reference both batch-specific purity and key residuals, based on GRH and custom customer requirements. Several of our largest clients in pharmaceutical and specialty chemical sectors conduct annual or even more frequent audits, reviewing exact chain-of-custody through our ERP and laboratory systems. This transparent documentation reassures customers that the material quality they specify during successful R&D experiments matches the material delivered to their scale-up or manufacturing operations months or even years later.

    Sometimes, new clients ask about our methods for minimizing residual metals such as sodium, iron, and copper. During purification, we apply sequential solvent washes and acid-base extraction steps tested across multiple projects. This hands-on purification work enables us to keep typical trace metals below 10 ppm, verified on ICP-MS. By holding ourselves to these benchmarks, we rarely receive requests to supply additional retest samples or documentation, which demonstrates sustained trust from quality-focused clients.

    Adaptability in Packaging and Shipping

    We learned early that packaging directly changes customer experience. Prioritizing stability, we select airtight, light-blocking containers that prevent the mild oxidation and moisture uptake seen in unprotected aldehyde shipments. Especially for high-purity batches, we provide moisture indicator inserts or argon-purged containers to protect sensitive cargo during long transport, whether travelling to urban research centers or remote industrial plants. We have observed that even short exposure to damp storage can slump powder and create handling problems at the customer site. These problems evaporate with careful packaging, a lesson earned after investigating a few avoidable issues in our early days.

    With larger industrial clients, packaging must support both forklift handling and manual weighing. We developed outer drums that protect against crushing and inner liners that maintain chemical integrity. Close coordination with trusted shippers proves essential, since missed temperature or moisture controls en route once led to avoidable returns. Sharing these shipping stories helps us maintain vigilance and reinforces our commitment to real-world product reliability.

    Meeting Regulatory and Quality Expectations

    Many of our end-users work within tightly regulated environments, especially in pharma and biotech. We develop lot-specific dossiers that align with ICH Q7 and other recognized guidelines, reflecting honest, unfiltered data for every batch. Randomized in-process checks throughout manufacturing and packaging help uncover rare errors before product release, a strategy built from years of tracking outlier events and customer feedback.

    Our labs keep retain samples from every lot, so if a user reports an odd result, we can directly retest material from the same production run, offering an unusual level of accountability. Over time, our real-world batch data demonstrates consistent quality and traceability — a crucial requirement for anyone integrating 5-Methoxyindole-3-Carboxaldehyde into validated synthetic pathways or regulated product lines.

    An academic researcher told us that knowing the aldehyde’s chain of custody provided needed confidence during the review of experimental data for a key publication. This feedback echoes across our industry clients when conducting regulatory audits: traceable purity and manufacturing data supports faster validation and smoother project progression.

    Troubleshooting and Continuous Improvement from the Front Line

    Manufacturers face recurring challenges with sensitive aromatic aldehydes like this. Small solvent impurities or metal ion traces, not obvious by eye, can sabotage multi-step synthesis downstream. When our team switched to lower-six-carbon alcohols for final recrystallization and eliminated open metal mixers, we tracked measurable improvements in both chemical purity and color. This codified process change stemmed from persistent customer feedback and our own root cause investigations after unexpected off-spec results.

    Handling feedback proactively, our production chemists and sales support team track every customer report, whether about long-term storage, solubility quirks, or unexpected impurities on analytic tests. By aggregating user feedback and internal data, we spot improvements that keep shipping, storage, and synthetic reliability at the level discerning groups require.

    Supporting Research, Scale-Up, and Production

    Our direct experience as a manufacturer shapes every facet of how we prepare, pack, and document 5-Methoxyindole-3-Carboxaldehyde. Both research and industrial clients rely on a partner capable of responding rapidly to custom requests: altered grind size for flow chemistry, modified solvent residue levels for downstream regulatory submissions, or specialized packaging for cold chain or export compliance.

    Academic researchers request technical support for reaction optimization or purity troubleshooting. We provide NMR, GC, and HPLC data along with full run protocols upon request. Conversations with these users often reveal new trends in peptide or heterocycle synthesis, informing our own process upgrades. Industrial customers depend more on security of supply, scale-up support, and continuous quality documentation. We commit to maintaining step-by-step batch records and to proactively updating users about any process or specification change.

    Collaboration across these user groups highlights how robust manufacturing processes and real dialog yield the highest-performing chemical building blocks. Our collective experience, spanning thousands of kilograms and hundreds of unique customer projects, underpins reliable delivery of every batch. We see learning, adaptation, and detailed process control not as buzzwords but as the lived reality essential to making top-quality 5-Methoxyindole-3-Carboxaldehyde.

    Commitment to Authenticity and Advancement

    Over years of manufacture, we’ve learned that transparency, traceability, and continuous communication enable customers to move confidently from benchtop work to industrial-scale production. Competing products may offer similar chemical structures, but our careful process, transparent data, and honest feedback channel set the standard for long-term collaboration and mutual success.

    By listening, documenting, and refining with every new project, we create a product that supports research innovation and industrial progress. Through every lot of 5-Methoxyindole-3-Carboxaldehyde we produce, our focus rests on supporting the next wave of scientific discovery and industrial development, grounded by years of hands-on experience and real customer partnership.