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2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine

    • Product Name 2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine
    • Alias 5-Benzyloxytryptamine
    • Einecs NA
    • 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

    471764

    Productname 2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine
    Molecularformula C17H18N2O
    Molecularweight 266.34 g/mol
    Appearance White to off-white solid
    Solubility Slightly soluble in water; soluble in organic solvents such as DMSO, ethanol
    Purity Typically >98% (for research grade)
    Chemicalclass Indole derivative
    Boilingpoint Decomposes before boiling

    As an accredited 2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine, 1g," featuring hazard symbols, lot number, and storage instructions.
    Shipping The chemical 2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine is shipped in tightly sealed containers to prevent contamination and degradation. It is packaged according to standard regulations for hazardous materials, with appropriate labeling and documentation. Temperature and humidity controls are maintained if required, and the shipment includes comprehensive safety and handling instructions.
    Storage Store **2-(5-Benzyloxy-1H-indol-3-yl)-ethylamine** in a tightly sealed container, protected from light and moisture, at 2–8 °C (refrigerator). Keep in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Use appropriate personal protective equipment when handling, and ensure that storage is compliant with safety regulations for laboratory chemicals.
    Application of 2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine

    Applications of 2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine in Industrial Manufacturing

    2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine serves as a specialty intermediate primarily for select segments of the pharmaceutical and fine chemical industry. Its defined functional structure allows downstream producers to access advanced compounds, where purity, compliance, and precise formulation integration are required. Below we detail the real-world industrial application areas, production parameters, relevant regulatory standards, and product endpoints associated with this material.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Serotonin Receptor Modulators

    This compound functions as an advanced building block for pharmaceutical manufacturers focused on developing serotonin receptor ligands. During multi-step synthesis, the ethylamine group provides crucial chemical flexibility, enabling efficient coupling and subsequent derivatization to deliver target APIs aimed at central nervous system disorders. Downstream QC laboratories routinely monitor for carry-over and process-related impurities at sub-ppm levels to meet stringent regulatory submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Parts 210/211
    • European Pharmacopoeia (Ph. Eur.) Monographs—where applicable for final APIs
    • Relevant Japanese Pharmacopoeia (JP) process guidelines

    Typical usage ratio

    • Usually 0.2–1.5 molar equivalents based on the downstream target structure and process yield optimization. Fine-tuned per route selection and impurity profile development.

    Downstream process integration

    • Charged as an intermediate in advanced stage amidation, reductive amination, or coupling reactions within a multi-step batch synthesis; batch or flow processing units accept the compound after in-house analytical release.

    Final product types

    • Bulk APIs for serotonin receptor antagonist drugs
    • Research-grade API lots for preclinical CNS therapeutic studies
    • Clinical stage drug substance for IND-enabling studies

    2. Pharmaceutical Reference Standards Preparation

    Certified reference material labs and quality control units use this material to synthesize and validate analytical reference standards. The molecular scaffold supports chemical derivatization for labeled and unlabeled reference substances, enabling quantitation and system suitability testing in regulated API and finished dosage analysis.

    Industry compliance standards

    • ISO 17034:2016 General Requirements for the Competence of Reference Material Producers
    • USP(United States Pharmacopeia) General Chapter <1220> Analytical Procedure Lifecycle
    • Good Laboratory Practice (GLP) for pharma analytical labs
    • OECD Guidance Document 34: Validation and International Acceptance of New or Updated Test Methods

    Typical usage ratio

    • Stoichiometric quantities based on targeted analytical reference compound synthesis, typically 0.1–0.8 molar equivalents depending on reference purity needs.

    Downstream process integration

    • Input as a core precursor in solution phase or solid phase synthesis, followed by selective functionalization and purification; integrated in high-purity preparative HPLC or crystallization steps.

    Final product types

    • Pharmaceutical primary and secondary reference standards
    • Certified analytical standards (CAS, isotopic labeled derivatives)
    • Calibration solutions for HPLC, LC–MS, GC–MS analytical procedures

    3. Agrochemical Lead Compound Research

    In agrochemical R&D, this indole-ethylamine backbone is incorporated as a strategic subunit during design and synthesis of biological screening candidates, specifically targeting plant growth modulators and selective herbicide discovery. The electronic, steric, and solubility properties offer valuable diversity for medicinal chemists optimizing structure–activity relationships. Compliance and process documentation support patent filing and regulatory review dossier assembly.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • EPA 40 CFR Part 160 (for US agrochemical studies)
    • REACH (EC No 1907/2006) Pre-registration guidance for R&D chemicals
    • FAO/WHO Guidelines for the Development and Use of Crop Protection Products

    Typical usage ratio

    • Between 0.05% and 0.5% w/w based on total candidate synthesis batch weight, adjusted for desired substitution pattern and screening target.

    Downstream process integration

    • Initiates as a key building block in combinatorial or parallel synthesis campaigns; purification via silica gel chromatography or automated flash systems prior to biological evaluation.

    Final product types

    • Pre-commercial screening substances for herbicide and plant growth regulator pipelines
    • Structurally characterized agrochemical research leads
    • Patent-submission intermediates

    4. Fine Chemical Synthesis for Custom Functional Materials

    Chemical manufacturers utilize this molecule as a monomer or functional fragment for assembling specialty organic materials, where the indole structure confers unique electronic or fluorescent properties. Downstream producers value its performance in constructing organic electronics or advanced fluorescent probes, with process integration designed to preserve sensitive functional groups throughout multistep scale-up and allow rigorous identity confirmation via NMR, HRMS, and HPLC.

    Industry compliance standards

    • ISO 9001:2015 for chemical manufacturing and process control
    • Restricted Substances compliance (REACH Annex XVII, as relevant)
    • Product-specific purity standards defined by customer contract specifications
    • GHS Classification and Labelling for workplace safety

    Typical usage ratio

    • Ranges from 0.1–2.5 molar equivalents, determined by targeted degree of polymerization or material property engineering. Adjustments depend on fluorescence yield or electronic performance requirements.

    Downstream process integration

    • Incorporated at controlled addition rates into condensation, cyclization, or cross-coupling processes; handled under inert atmosphere to preserve indole core functionality during critical synthesis stages.

    Final product types

    • Advanced fluorescent dyes for biochemical detection
    • Organic semiconducting materials for electronics
    • Novel functional polymers with application-specific optical or electronic properties
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    Certification & Compliance
    More Introduction

    2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine: A Closer Look from the Manufacturer’s Bench

    A Chemical Built for Changing Demands

    Producing 2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine in our own plant, we listen constantly to chemists in research and industry. The material asks for care at every stage. It stands out for its unique molecular backbone—a union of indole’s flexibility and a custom-tuned benzyloxy group at the 5-position. In our daily work, controlling the purity and yield keeps us alert to every minor change in raw materials and process conditions. With its ethylamine side chain, this molecule opens the door for med-chem teams and fine chemical developers working on small-molecule targets where specificity means everything.

    Bringing In-House Insights to Every Batch

    Every lot reflects choices we make during the reaction, purification, and drying. We opt for boron-doped catalysts rather than less selective metals. Using HPLC and NMR, we take pride in consistently seeing sharp, clean spectra—an unmistakable indicator of diligent processing. Our synthesis routes keep unwanted isomers to negligible levels; that is a key concern for any downstream synthesis or bioassay. One frequent question we face from partners: “How have you controlled side reactions at the indole nitrogen?” The answer comes directly from years spent running and tweaking the reductive amination and protection steps. We adapt with each scale-up or when switching to new analytical standards.

    Understanding Specifications from the Lab Up

    From our side of the table, customers usually seek clarity on specification details. We typically supply this compound as a free-flowing, off-white powder. Moisture sensitivity plays a role in how material travels from our facilities, so we use tightly sealed, argon-flushed containers for shipping. Melting point sits above typical room temperatures. Purity, proven by HPLC, NMR, and mass spectrometry, rarely slips below 98%. We have an internal agreement—if our analysis ever wavers, we halt delivery until we resolve it. These standards come from long-term work with discovery teams and pilot-plant scale-up chemists who push back on lot-to-lot variability.

    Solubility hits a middle ground. In our own test runs, it dissolves easily in DMSO, modestly in methanol, and at lower levels in water. This pattern usually satisfies med-chem researchers aiming to design stock solutions for testing in high-throughput screens or chemical biology libraries. We watch trends in solvent use—over the years, newer green solvents push us to revisit solubility studies with each process improvement.

    Comparing 2-(5-Benzyloxy-1H-Indol-3-Yl)-Ethylamine to Other Indoles

    Over time, we've built libraries containing dozens of substituted indole derivatives. We see consistent demand for 5-benzyloxy substitution because it enhances both lipophilicity and electronic effects in bioactive analogs. Simple 5-hydroxy or 5-methoxy indoles don’t match the metabolic stability or structural heft provided by a benzyloxy group, particularly in animal studies or lead-optimization programs. The ethylamine moiety at the 3-position presents more reactive handle versus methyl or longer alkyl side chains. Our partners often switch between 2-(5-benzyloxy-1H-indol-3-yl)-ethylamine and the corresponding methylamine or propylamine analogs, depending on their need for steric profile or synthetic convenience.

    We run regular comparison assays to check side-product formation, especially in cross-coupling and protection reactions. From direct experience, we spot fewer decomposition products with our benzyloxy-protected indoles than methoxy-protected analogs under thermal or acidic conditions—a detail appreciated by scale-up chemists. Whereas some substituents encourage oxidation or instability during storage, the benzyloxy function delivers shelf stability and clean handling. That translates directly to lower loss rates and less rework at the plant.

    Where We See This Compound at Work

    This indole analog attracts rising interest in discovery-stage pharmaceutical research. Medicinal chemists select it for synthetic routes aimed at serotonin or melatonin receptor analogs and for the design of modified tryptamines. The indole ring plays an important role in neuroscience and oncology drug leads; tacking on a benzyloxy group changes potency, brain permeability, or metabolic fate. The ethylamine side chain gives medicinal chemists a way to mimic or diverge from tryptamine-style scaffolds. Our work with academic collaborators shows its value as a functional group donor in probing protein-ligand binding, and our customers’ feedback reinforces that it adapts well to Suzuki and Buchwald couplings for modular assembly of more elaborate tool compounds.

    Out in the field, not every synthesis project follows the same logic. One team uses our material to construct a series of allosteric GPCR modulators. Another looks at receptor binding in plant biology. The product’s adaptability wins over bench chemists who favor fast diversification of their chemical series. We review these stories and fold feedback into our process, from adjusting crystallization solvents to revising impurity thresholds.

    Differences Arising from Real Plant Experience

    Compared to compounds from resellers or third parties, our batches direct more attention to downstream usability. We keep analyte levels for heavy metals and residual solvents below internationally recognized targets, guided by ICH and regional requirements. Years ago, we handled client complaints about poor solubility or dark coloration from imported samples—problems that vanished after we narrowed our recrystallization parameters and switched to higher-grade solvents for final wash steps.

    Packaging choices matter too. We’ve learned not every customer wants kilogram quantities, so we portion from research scale upwards with the same rigor, preventing cross-contamination and caking. Each new order brings contact with teams who ask about storage, carrier handling, and batch reanalysis—so we keep data and fresh samples ready for scrutiny.

    Traceability starts at the reagent shelf. Our records cover from starting material batches right through to final product QC, tracking any deviation, even if it’s a midday temperature swing in the dryer or a raw material lot flagged for incoming quality review. These measures grew out of real lessons: lost time, unexpected purification failures, and the pressure to deliver on tight project timelines. The wisdom comes directly from troubleshooting at the bench, not from abstract quality guidelines alone.

    Supporting Innovation by Staying Close to the Chemists

    Our involvement does not end at the shipping dock. Researchers come back with challenges, from unexpected NMR peaks to unsuccessful derivatizations. Sometimes the answer lies in a slight adjustment to drying times, other times it means improving batch documentation or sharing best practices for storage and handling. A typical story: a customer in polymer research encountered batch-to-batch variation in color and melting point. We examined sample archives and manufacturing notes to identify a subtle raw material impurity, then refined our sourcing and cleaned up the process for everyone.

    We take these inquiries seriously. Cross-industry regulations continue to tighten, especially for building blocks destined for clinical or regulatory review. We have responded with deeper third-party analysis, offering not just in-house data but certificates verified by external labs. These steps slow us down in some cases, but in the long run, fewer project setbacks help teams keep their focus on research progress instead of technical uncertainties.

    The Path Forward: Continuous Improvement on the Factory Floor

    Challenges change every year. From time to time, solvent restrictions demand new crystallization routes. Sometimes new analytical methods expose trace side-products that nobody saw before. Our small team meets weekly to walk through process data. We discuss whether a blip in melting point means a change in the upstream indole supplier or a subtle shift in reaction temperature. We revisit our control strategies for each piece of equipment that handles indoles—many of which require frequent overhauls due to stubborn residue from the benzyloxy group’s stickiness. We swap stories about failed experiments and keep a log of every batch rework. This cycle keeps quality improving, never static.

    Production teams who work closely with chemical buyers notice wider changes in demand, especially as research pivots to ever more targeted applications. We adjust batch sizes—sometimes running several small lots to support startups, sometimes scaling up for launch molecules or pilot plant work. Adapting to customer needs in real time keeps our attention sharp, and pushes us to revisit handling or formulation details that matter at the bench.

    Safety, Environmental Care, and Responsibility in Practice

    Every new molecule means new challenges for handling and safety. We train operators on safe handling under local and federal requirements, using glove boxes, efficient fume hoods, and rigorous waste tracking. We design our processes to reduce hazardous byproducts and to simplify waste stream separation. By fine-tuning reaction conditions, we’ve cut down on the need for harsh reagents, used alternatives for protection-deprotection steps, and aim for solvent recovery whenever possible. Each batch run brings a new set of environmental calculations, not just financial ones.

    We value open lines of communication with researchers, regulatory experts, and our own plant staff. Everyone benefits from clear protocols—a lesson learned the hard way after near-misses and costly plant downtimes from unexpected exotherms. Continuous safety reviews and risk assessments keep our standards from getting stale. We have come to recognize that process improvement and environmental care are not afterthoughts, but core to reliable supply.

    Customer Stories: Real-World Adaptations

    Through years of shipment logs and technical calls, we learn what matters to researchers and process chemists. We’ve seen this product bridge programs from small biotech to established pharmaceutical players, each adapting the base compound for unique targets. One team’s work on indole-based kinase inhibitors required consistent melting points batch after batch—achieved only after we retrofitted temperature controls and changed drying times. Another group, prepping radiolabeled tools, worried about trace metals—a problem solved by upgrading metal-catalyst filtration for every batch. These stories show the persistent, hands-on care behind each drum and bottle leaving the warehouse.

    Feedback cycles drive product improvements that go beyond lab specs. We know from direct discussion that shipment schedules and real-time support often matter as much as spectral purity. When researchers face tight grant or patent deadlines, reliability on our side wins us long-term partners. Each problem solved for a project team feeds back as a lesson, whether changing vial sizes, upgrading packaging, or sharing new data sheets as regulatory expectations evolve.

    Why Internal Expertise Matters More Than Ever

    In the present landscape, the gap between generic, brokered supply and manufacturer expertise has only widened. Every lot that leaves our hands comes with explicit, transparent documentation, attention to impurity trends, and full traceability. These steps take time but mean fewer surprises for downstream researchers—reducing the risk of false positives or wasteful troubleshooting. Skill at the bench translates into trust at the project planning stage.

    Sitting as the manufacturer, each new challenge becomes a learning opportunity. The 2-(5-benzyloxy-1H-indol-3-yl)-ethylamine story, like so many others, is less about “selling” a chemical and more about tailoring process and quality for people who work at research or pilot-plant scale. With every batch, we deliver more than just a compound—we deliver the accumulation of trials, test runs, and the refining touch of decades of factory and R&D experience.

    Ongoing Commitment to Quality and Progress

    For every partnership built around this compound, we keep strengthening trust by sharing updates, process improvements, and reliability born from the factory floor. We stand ready to adapt, clarify, and respond as the research landscape evolves, keeping open doors for discussion and collaboration with every new inquiry.