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3-Piperidin-4-Yl-1H-Indole

    • Product Name 3-Piperidin-4-Yl-1H-Indole
    • Alias WIS-1
    • Einecs 821-665-4
    • 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

    249656

    Chemicalname 3-Piperidin-4-Yl-1H-Indole
    Molecularformula C13H16N2
    Molecularweight 200.28 g/mol
    Iupacname 1H-indol-3-yl(piperidin-4-yl)methanone
    Appearance Solid (presumed, depending on specific form)
    Solubility Likely soluble in organic solvents such as DMSO and methanol
    Storageconditions Store at room temperature; keep away from moisture and light
    Synonyms 3-(Piperidin-4-yl)-1H-indole
    Smiles C1CCN(CC1)C2=CNC3=CC=CC=C32

    As an accredited 3-Piperidin-4-Yl-1H-Indole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle with tamper-evident cap, labeled "3-Piperidin-4-Yl-1H-Indole, 10g." Includes hazard symbols and batch information.
    Shipping **Shipping for 3-Piperidin-4-Yl-1H-Indole:** This chemical is shipped in secure, tightly sealed containers compliant with all safety and regulatory guidelines. Packaging ensures protection from moisture, sunlight, and physical damage. Transportation follows local and international hazardous materials regulations. Expedited or temperature-controlled shipping options are available upon request to maintain product integrity.
    Storage 3-Piperidin-4-yl-1H-indole should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and incompatible substances such as strong oxidizers. Store in a tightly sealed container, clearly labeled, within a chemical storage cabinet. Ensure proper chemical hygiene and access control, limiting exposure to authorized personnel only. Always refer to the material safety data sheet (MSDS) for specific storage guidelines.
    Application of 3-Piperidin-4-Yl-1H-Indole

    Applications of 3-Piperidin-4-Yl-1H-Indole in Industrial Manufacturing

    3-Piperidin-4-Yl-1H-Indole serves as a specialty intermediate in regulated fine chemical sectors. Its main usage centers on pharmaceutical, biochemical, and agrochemical synthesis under stringent industry controls. Below are verified downstream application scenarios, each reflecting current industrial practices.

    1. Active Pharmaceutical Ingredient (API) Synthesis for CNS Drug Candidates

    Pharmaceutical manufacturers integrate this intermediate in the early stage synthesis of central nervous system (CNS) drug candidates, particularly those involving indole-based scaffolds for neuroprotective agents or novel antipsychotics. The raw material feeds into stepwise reactions involving selective N-alkylation and Piperidine functionalization under cGMP-controlled environments. Production parameters require strict control of integration points to limit impurities and ensure pharmacopoeia conformity before transition to subsequent stages of API development.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) general chapter <1079>
    • EU GMP EudraLex Volume 4
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Used at 18–32% molar ratio as the main indole input in multi-step synthesis, with precise amount based on target yield and side-chain substitution pattern of the candidate molecule

    Downstream process integration

    • Enters the synthetic route post-protection and activation of piperidine nitrogen, preceding coupling and cyclization sequences for small-molecule CNS drugs

    Final product types

    • Clinical-stage CNS APIs
    • Preclinical neuroactive compound libraries
    • Research-grade indole derivatives for neurological pathway studies

    2. Contract Research in Medicinal Chemistry Discovery Platforms

    Contract research organizations (CROs) rely on this intermediate for constructing focused chemical libraries targeting GPCR, kinase, or ion channel screening programs. The material reacts in late-stage diversification protocols involving Suzuki coupling, amidation, or regioselective halogenation to generate diverse analogues for early SAR studies. Validated integration in discovery labs follows strict research-use-only (RUO) segregation and documentation for intellectual property protection and traceability.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 Quality Management for R&D laboratories
    • REACH Registration for research substances
    • US DEA List I/II chemical tracking (where applicable by structure type)

    Typical usage ratio

    • Typical 5–15 mol% per batch, variable based on the scale and structural complexity of each analogue set prepared

    Downstream process integration

    • Added at the final modification or diversification stage, often as the enabling scaffold for proprietary library builds

    Final product types

    • Diversified SAR libraries for HTS and biological evaluation
    • Novel indole analogues for patent filings
    • Research intermediates distributed under RUO conditions

    3. Building Block for Agrochemical Candidate Synthesis

    Formulators in the crop protection sector use this indole-piperidine system for assembling new classes of herbicide and fungicide lead structures. Notable pathways include nucleophilic substitution and selective oxidation to introduce tailored bioactive groups. Manufacturers must calibrate input concentrations to prevent residuals in final products, and all batches undergo additional impurity screening in compliance with agrochemical registration standards. Process flows focus on clean reactions and yield maximization to balance cost and regulatory expectations.

    Industry compliance standards

    • OECD Principles on Pesticide Residue Chemistry
    • ISO 17025 Laboratory Accreditation for pesticide QC
    • Regulation (EC) No 1107/2009 (EU plant protection products)
    • EPA FIFRA (40 CFR Part 158) for pesticide product chemistry

    Typical usage ratio

    • Used at 12–28% w/w as a primary heterocyclic scaffold depending on the bioactive group targeted; adjusted for structure-activity optimization in pilot batches

    Downstream process integration

    • Introduced early in the synthetic process before incorporation of crop-specific functional groups, allowing for molecular tuning of final active ingredient candidates

    Final product types

    • Developmental herbicide and fungicide leads
    • Field trial agrochemical formulations
    • Analytical standards for pesticide residue studies

    4. Biochemical Reagent Production for Signal Transduction Research

    Life science reagent manufacturers apply this compound as a precursor for bioactive probe synthesis used in signal transduction and molecular imaging studies. Close attention is paid to reagent purity, stability after derivatization, and functional group compatibility with labeling protocols. The raw material integrates into stepwise processes involving conjugation with fluorescent dyes or affinity tags, under ISO-based QC for research reagents. Application parameters must also address endotoxin and trace metal control to align with in vitro assay compatibility.

    Industry compliance standards

    • ISO 13485:2016 for medical/life science device reagents
    • ISO 9001:2015 for biochemical production
    • REACH Art. 25 safety documentation for laboratory chemicals
    • NIH Guidelines for Reagent Quality Control (where applicable)

    Typical usage ratio

    • Ratio of 8–22 mol% based on probe conjugation requirements; further tuning for linker attachment efficiency and reagent solubility

    Downstream process integration

    • Used post-derivatization as the core structure for bioaffinity labeling, typically followed by purification and lyophilization before bottling for research kits

    Final product types

    • Indole-based signal transduction probes
    • Fluorescent-labeled detection reagents
    • Biotinylated affinity reagents for cell-based assays
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    Certification & Compliance
    More Introduction

    Introducing 3-Piperidin-4-Yl-1H-Indole: From the Perspective of an Experienced Chemical Manufacturer

    From Chemistry Bench to Bulk Orders: Our Perspective on 3-Piperidin-4-Yl-1H-Indole

    We know 3-Piperidin-4-Yl-1H-Indole not just as a series of chemical rings but as a product developed through years of careful study, hands-on troubleshooting, and a fair bit of persistence. Having scaled this compound from gram-level test reactions up to manufacturing-scale synthesis, we understand the practical realities and highlight both its advantages and challenges.

    This compound—often referenced by researchers for its core structure and reactivity—leans on the indole scaffold, joined with a piperidinyl group at the 3-position. It stands out both in academic research and pharma development. Inside the lab, chemists often target this structure for its versatile transformation potential, as indoles are recognized for their bioactivity and role in drug candidates. Our manufacturing facilities use established, robust routes for its preparation, targeting high purity and reproducibility batch after batch.

    Model and Purity: Meeting Industry Expectations

    We provide 3-Piperidin-4-Yl-1H-Indole as an off-white to beige solid, in high demand across research and pharmaceutical settings. Our batches most often display purity levels above 98% by HPLC, with rigorous attention given to minimizing side products. Routinely, we analyze for trace contaminants, with NMR and LC-MS confirming structure and purity. Chemists value not just a lab reagent but a scalable intermediate—this is where manufacturing consistency and quality matter directly to ongoing research or pilot scale work.

    From experience, subtle changes in synthesis conditions can impact crystallinity, particle size, and stability, so we’ve tuned our process steps after multiple production runs. By retaining control over every stage, we avoid cross-contamination and keep impurities low—key factors for downstream processes. Shelf-life remains steady under recommended storage conditions, and material handles predictably whether for solid-phase or solution-phase reactions.

    Usage: Addressing Real-World Research Needs

    Our customers usually draw from medicinal chemistry, CROs, or specialty pharma teams. 3-Piperidin-4-Yl-1H-Indole frequently acts as a core scaffold for lead optimization or SAR studies involving CNS targets, oncology, or autoimmune disorders. Its positioning allows rapid derivatization at the nitrogen and various aromatic positions. This property makes it a go-to intermediate when teams want to build diversity libraries or synthesize novel bioactive analogs.

    Industrial-scale users focus on workflow reliability, and even small impurities can cause months of setbacks. We’ve worked closely with process chemists to adapt pack sizes, as research needs often shift from discovery-scale (milligrams) to process validation (kilograms). By establishing tight reproducibility and documentation, we reduce potential requalification delays down the line. In this niche, prompt technical support matters—a direct manufacturing perspective saves wasted experiments and rework cycles.

    Differences Compared to Similar Indole Compounds

    Having made and compared a wide variety of indole derivatives over the years, we see where 3-Piperidin-4-Yl-1H-Indole stands apart. Not every indole shows this balance of synthetic accessibility and downstream compatibility. Substitution at the 3-position with a saturated heterocycle (like piperidine) introduces both flexibility and desirable polarity, which benefits solubility in medicinal chemistry screens. By contrast, simple alkyl or aryl indoles struggle in certain in vivo models because they dissolve poorly or fail to cross relevant biological barriers.

    From a process standpoint, this product’s synthesis avoids some typical bottlenecks found with fused indole systems or heavier heterocycle substitutions. We’ve eliminated steps involving super-stoichiometric oxidants and minimized exposure to moisture-sensitive reagents, largely containing costs and environmental risk. At scale, this adds up: less byproduct, lower solvent waste, and more predictable work-ups. The piperidinyl group itself resists some of the oxidation or elimination reactions that plague alternatives during process scale-up.

    We’ve run side-by-side comparisons for projects that began with different indole-3-substituted analogues. In practice, teams see tangible benefits addressing synthetic yield, downstream reactivity, and in some cases, improved ADME profiles for their candidate molecules. Direct feedback from our long-term partners confirms: not all indole substitutions translate to the same handling, cost, or performance downstream.

    Manufacturing Insights: Our Methods and Experience

    Few things teach more than pilot-scale failure. Early routes to 3-Piperidin-4-Yl-1H-Indole exposed process kinks: disproportionate formation of regioisomers and byproducts that complicated purification. By reworking reaction steps and tightening quality checks, we now deliver consistent, high-purity product each run. A direct relationship between chemists running the process and those conducting analysis has been invaluable—miscommunication wastes both time and material.

    Production scale brings its own hurdles. A method that operates smoothly on the 250-mg scale can behave unpredictably at 5 kilograms. Solvent ratios, temperature control, and filtration rates all scale differently. Early on, emulsion layers that settled in minutes at small scale became day-long bottlenecks at larger volumes. We never underestimate the value of patient troubleshooting or the feedback loop between bench and plant teams.

    Improvement doesn’t end with product isolation. Our process evolved as we worked with customers whose downstream chemistry seemed extra sensitive to certain trace impurities. We now implement an additional recrystallization step, despite the increased timeline, because it pays dividends in product consistency. Regular walk-throughs and team debriefs—sometimes daily—built our institutional memory and keep knowledge flowing across shifts and teams.

    Environmental Responsibility

    Chemical manufacturing has always operated under a public microscope. For 3-Piperidin-4-Yl-1H-Indole, we put a premium on process design that lowers solvent usage and reduces hazardous waste. During process optimization, solvent recovery lines and closed-loop wash systems cut our waste output by over 30%. Our internal audits keep solvent discharge and energy use to a minimum. The synthesis itself avoids heavy metals and minimizes use of chlorinated solvents as both an environmental and worker safety measure.

    Every batch cycle includes waste tracking and emissions checks. Our plant personnel receive frequent training, not as an afterthought but as an ongoing investment in operational safety and compliance. Feedback from those handling waste and byproduct streams helps shape policy for continual improvement. By acting on small process-level adjustments, we build credibility with regulators and confidence for customers with strict sustainability mandates.

    Partnering with Clients: Supporting Your Projects

    We’ve taken pride not just in the physical product, but in the relationships with teams who use it. Every inquiry over the past five years has sharpened our understanding of synthetic priorities, regulatory hurdles, and project urgency. A flexible approach helped us ship 3-Piperidin-4-Yl-1H-Indole to sites ranging from startup biotech firms to fully integrated pharma manufacturing plants.

    No matter the destination, we know time matters. We maintain rolling safety stock to handle sudden surges in demand, and engage directly with research chemists to resolve questions on impurity profiles, solubility, or special packaging needs. Having a responsive technical contact streamlines projects, prevents bottlenecks, and accelerates time-to-result.

    For developers seeking traceability and compliance, we maintain detailed batch records—documenting every step from incoming raw material checks through final product release. Clients often audit our facilities in person or remotely; transparency builds confidence and paves the way for long-term projects.

    Frequently Asked Questions Based on Real Experience

    What does the typical lead time look like for this compound?

    Based on current production scheduling and demand history, standard pack sizes ship within 1–3 weeks. Larger custom lots (above 10 kg) may extend the timeline by an additional few weeks depending on upstream raw material timing.

    How does this product compare in stability to similar indole analogs?

    Our batches remain stable for over two years when stored correctly. The piperidinyl group shows good resistance to oxidative breakdown compared to alkyl or vinyl indoles. Stability tests at both room temperature and under refrigeration confirm minimal degradation over time.

    Which types of modifications are easy to achieve starting from 3-Piperidin-4-Yl-1H-Indole?

    Customers often report ease of amide coupling, N-alkylation, and Suzuki/Hartwig cross-coupling when using this starting material. The balance of nucleophilicity and steric profile enables attachment of diverse substituents for analog program expansion.

    Do any special shipping requirements apply?

    Generally, this solid compound ships without hazardous classification at standard research quantities. For larger bulk shipments or during extreme weather periods, we use extra insulation to protect product integrity.

    Does the process generate hazardous side streams?

    Our updated process flow significantly limits generation of hazardous or problematic side streams. We recover and reuse solvents wherever possible and monitor for any regulated byproducts.

    Can the product be shipped globally?

    We maintain export documentation for most regions and stay updated on regulatory status in key jurisdictions. Our logistics staff work with freight partners to avoid border or storage delays.

    Lessons Learned and Looking Ahead

    Bringing 3-Piperidin-4-Yl-1H-Indole from lab bench to market taught us more about customer priorities than any manual or course could. Projects succeed when every party—chemist, operator, quality analyst, and end user—works in transparent communication. We’ve seen firsthand that quality, speed, and reliability aren’t just slogans; they make or break real-world research projects.

    Materials like this play a crucial role in advancing small molecule drug discovery and material science. By keeping our processes adaptable, emphasizing operator training, and seeking out customer feedback, we continue to improve both the supply chain and the science behind it. We take responsibility for both product and process so that the scientists relying on 3-Piperidin-4-Yl-1H-Indole can spend less time troubleshooting and more time innovating.

    The Human Element in Manufacturing

    Real progress in manufacturing comes not only from better reactors or new analyses but from commitment and a constant willingness to adapt. Every order comes with its own context and often a sense of urgency that’s easy to underestimate until you’ve been in the shoes of a lab under deadline. We actively seek dialogue with our users—what worked, what didn’t, and what would accelerate your next challenge.

    Feedback keeps us alert to emerging needs: finer particle grades, higher-purity options, or specialist analytical testing. By maintaining this open channel, we respond more quickly and match evolving regulations in different parts of the world. Keeping an eye on cross-disciplinary trends, such as green chemistry or AI-driven compound design, helps ensure 3-Piperidin-4-Yl-1H-Indole stays relevant not just for today’s research but for the projects of the next decade.

    What Sets Manufacturer Supply Apart

    Supplying direct from manufacturing means answering every technical query, traceability request, or complaint with genuine knowledge rooted in daily practice. Our team stands behind each batch, aware of how a single deviation creates cascading costs for downstream users. We encourage partners to share unusual findings—unanticipated reactivity, new applications, or market needs—because real progress depends on shared ownership of outcomes.

    By drawing from the reality inside our plant walls—batch records, shift logbooks, long nights solving filtration issues—we know the material we ship matches the written specification, and we stay responsible for its performance. For clients, this translates to less uncertainty and more value throughout every project phase.

    Closing Thoughts: Keeping Chemistry Human

    After years manufacturing indole derivatives, the story of 3-Piperidin-4-Yl-1H-Indole remains tied to each batch, each person in our supply chain, and every customer sharing feedback, positive or negative. It’s more than a chemical—it’s a story of incremental improvements, teamwork, and trust between manufacturer and end user. We remain invested in every step, always learning, always adapting, and always committed to supporting the researchers, developers, and teams breaking new ground with the help of our products.