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(R)-3-Aminopiperidine

    • Product Name (R)-3-Aminopiperidine
    • Alias (R)-Piperidin-3-ylamine
    • Einecs 642-184-3
    • 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

    920400

    Chemical Name (R)-3-Aminopiperidine
    Cas Number 119431-64-4
    Molecular Formula C5H12N2
    Molecular Weight 100.16
    Appearance Colorless to pale yellow liquid
    Boiling Point 175-178°C
    Melting Point -
    Density 0.954 g/mL at 25°C
    Optical Purity Typically >98% ee
    Chirality R-configuration
    Smiles N[C@@H]1CCCN(C1)
    Refractive Index n20/D 1.47 (approximate)
    Storage Conditions Store at 2-8°C in a tightly sealed container
    Solubility Soluble in water and organic solvents
    Synonyms (R)-Piperidin-3-amine

    As an accredited (R)-3-Aminopiperidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing (R)-3-Aminopiperidine, 25g, is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping (R)-3-Aminopiperidine is shipped in secure, sealed containers compliant with regulatory standards for hazardous chemicals. Packaging ensures protection from moisture and contamination. All shipments include proper labeling, Safety Data Sheets (SDS), and documentation per international and local transport regulations to ensure safe and legal delivery to the recipient’s location.
    Storage (R)-3-Aminopiperidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat, sparks, open flames, and incompatible substances like strong oxidizers and acids. Protect from moisture and direct sunlight. Store at room temperature, and ensure the workspace is equipped with appropriate spill containment and ventilation measures.
    Application of (R)-3-Aminopiperidine

    Applications of (R)-3-Aminopiperidine in Industrial Manufacturing

    As a dedicated manufacturer of (R)-3-Aminopiperidine, we deliver this key intermediate to advanced industrial sectors where stereospecific amines provide functional and regulatory value. Below, we outline distinct downstream applications, covering technical formulation, compliance obligations, process integration, and real finished goods built on this material's properties.

    1. Chiral Pharmaceutical Intermediates for CNS Active Compounds

    The pharmaceutical sector sources (R)-3-Aminopiperidine for the enantioselective synthesis of central nervous system (CNS) drug APIs, including monoamine reuptake inhibitors and antipsychotics. This compound forms a core structural motif for multiple NCEs, ensuring required chirality for bioactivity and metabolic profiles. Drug substance teams directly couple (R)-3-Aminopiperidine into multi-step syntheses, with analytical development guided by defined pharmacopeial methods and regulatory filing demands.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA cGMP (21 CFR 210/211)
    • European Pharmacopoeia 2.2.46 (chiral substances)
    • USP General Chapter <1121> Stereochemical Identity

    Typical usage ratio

    • Stoichiometric input (1:1) in key condensation or reduction steps; can range 1.05–1.1 equivalence depending on substrate excess strategy and required final API yield

    Downstream process integration

    • Activated amidation or reductive amination route at the early-to-mid API synthesis stage; introduction before critical resolution or chiral HPLC purification steps

    Final product types

    • Chiral CNS drug substances (e.g., selective serotonin reuptake inhibitors, new antipsychotic scaffolds)
    • Research-scale and commercial drug intermediates (preclinical toxicology and clinical use)

    2. Advanced Agrochemical Synthesis

    Leading agrochemical producers use (R)-3-Aminopiperidine to build chiral centers in novel insecticide and fungicide active ingredients. These fine chemicals demand strong supply chain traceability and high enantiopurity, since specific stereochemistry impacts bioselective action and off-target plant safety. Chemical engineers deploy this intermediate during late-stage construction of heterocyclic frameworks featured in patent-protected crop protection molecules.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Agrochemical Manufacturing
    • European Union Regulation (EC) No. 1107/2009 (Plant Protection Products)
    • OECD Principles of Good Laboratory Practice for development batches

    Typical usage ratio

    • 0.8–1.2 mole equivalents, adjusted for overall process yield and byproduct minimization during alkylation, cyclization, or amide bond formation steps

    Downstream process integration

    • Incorporated at the penultimate synthesis stage before coupling with side-chain groups or protective group removal; strict monitoring of optical purity throughout scale-up

    Final product types

    • Chiral herbicides
    • Stereodefined insecticides and fungicides
    • Technical grade actives for final crop protection formulations

    3. Small Molecule Synthesis in Medicinal Chemistry R&D

    Global contract research organizations adopt (R)-3-Aminopiperidine for SAR investigation, building chiral fragment libraries and probe molecules. Access to this chirally pure amine accelerates analog design by allowing rapid amide, urea, and sulfonamide synthesis with high regioselectivity. In discovery laboratories, scientists substitute multiple amine partners but prefer (R)-3-aminopiperidine for scaffolds requiring conformational rigidity and distinct enantiomeric excess.

    Industry compliance standards

    • GLP-compliant synthesis traceability (OECD GLP for analytical/biological evaluation)
    • ISO 17025 testing for chiral purity and structure confirmation

    Typical usage ratio

    • 0.95–1.5 molar equivalents according to screen design and target binding pocket

    Downstream process integration

    • Inserted in solid-phase synthesis or batchwise parallel solution-phase syntheses; often as the unique chiral building block for principal SAR rounds

    Final product types

    • Medicinal chemistry fragment libraries
    • Chiral tool compounds for biological assay validation
    • Discovery-stage preclinical leads

    4. Specialty Polymers and Functional Materials

    Formulators in specialty polymer and advanced material sectors introduce (R)-3-Aminopiperidine during the production of high-value monomers for optoelectronic and membrane materials. The ring structure and chiral amine functionality confer structural control, influencing polymer tacticity and ionic transport properties in tailor-made film and coating systems. QC departments monitor batch-to-batch chirality and purity to guarantee stable downstream polymerization results and mechanical performance.

    Industry compliance standards

    • ISO 14001 Environmental Management
    • REACH Registration (EC No 1907/2006) for new monomers
    • ASTM D7647-10 for Polymeric Materials Characterization

    Typical usage ratio

    • Typically 2–10% by weight as a functional amine comonomer, or introduced stoichiometrically in specialty step-growth polymerizations; dosage tuned for target molecular weight and physical property endpoints

    Downstream process integration

    • Introduced via controlled addition during monomer feed step in batch or continuous reactors; used as a linking monomer in step-growth or as a crosslinker in post-polymerization functionalization

    Final product types

    • High-performance membranes for gas separation
    • Ion-exchange resins
    • Specialty coatings and electronic film materials
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    Certification & Compliance
    More Introduction

    Introducing (R)-3-Aminopiperidine: Precision in Chiral Synthesis

    Why (R)-3-Aminopiperidine Matters in Pharmaceutical Chemistry

    (R)-3-Aminopiperidine stands out in our workshop because it helps chemists solve tough problems in chiral synthesis. From decades of hands-on manufacturing, I have watched this compound become a backbone in research and production. Designed for precision, (R)-3-Aminopiperidine carries a single chiral center and comes with the kind of close purity control strict pharmaceutical applications call for. With today’s growing push for efficiency and safety in drug development, the demand for well-defined building blocks has never been more obvious. Not all amines deliver the right enantiopurity, and the impact of impurities often ripples much farther than the QA lab.

    On our production line, we handle (R)-3-Aminopiperidine under clean environments with batch records that track everything from raw material source to final lot yield. Here, consistency is not an afterthought—it reflects years of process refinement. Raw intermediates never skip steps. Analytical checks for optical rotation go hand-in-hand with multi-stage purification. I have seen small differences in enantiomeric excess cause huge changes in downstream activity and side reaction profiles. More than once, R&D teams have come to us after troubleshooting failed reactions with off-the-shelf, racemic, or poorly characterized materials from third parties. They needed tighter control, and that meant direct sourcing from a team with full understanding of the reactions inside and outside the flask.

    Understanding the Structure and Role of (R)-3-Aminopiperidine

    At the core, (R)-3-Aminopiperidine features a six-membered piperidine ring with an amino group at the 3-position. Its configuration matches the "R" enantiomer, controlling not just stereochemistry but how the molecule behaves in downstream synthesis. In our reactors, chiral purity doesn't just translate to lab data—it affects yield, isolation, and the pharmacological outcome of the active pharmaceutical ingredient you’re aiming for.

    Using (R)-3-Aminopiperidine, chemists can build a broad range of nitrogen-containing compounds and chiral intermediates. This product finds heavy use in drug pipelines from antiviral candidates to kinase inhibitors, where the spatial arrangement of the amine and ring frame lock in specific molecular recognition. Our plant engineers and QC chemists recognize how even a trace of the opposite isomer can set off costly purification headaches, or worse, clinical trial inconsistencies later on.

    Specifications That Reflect Experience, Not Guesswork

    We supply (R)-3-Aminopiperidine at commercial and research scales. Quality sticks to what pharma and regulatory bodies demand, with enantiomeric excess above 98 percent by chiral HPLC and assay greater than 99 percent by GC. Moisture and volatile content get checked in every batch. By focusing on practical measurements that tie directly to synthetic results, the spec sheet you see matches the product actually coming off the dryer—not just theoretical data from a lab pilot.

    Years of production have taught us the difference between analytical neatness and real-world deliverables. A single missed impurity can derail a synthesis route. Our customers often bring us samples from less rigorous suppliers, and the comparison speaks for itself—sharp NMR baseline, no secondary peaks, optical rotation right at target, and robust performance under typical coupling or reductive amination conditions.

    Available concentration runs from grams in early-stage discovery up to kilogram lots for scale-up. Stability studies show that (R)-3-Aminopiperidine maintains integrity through long-term storage under nitrogen, as well as short-term ambient shipping. Each container leaves our floor with individually labeled trace numbers, tying every shipment back to its original in-process controls.

    Practical Uses and Downstream Applications

    (R)-3-Aminopiperidine opens up new directions in medicinal chemistry when you want to introduce a chiral nitrogen into a molecule. A lot of our large-scale customers use it not only in final API assembly, but also in the development of analog libraries where tiny differences in chirality produce very different biological effects. Successful scale-up often comes down to the reliability of each intermediate, especially because any shortcuts can show up as off-target activities later.

    One of the most common uses involves building azaspirodecanes, substituted piperidines, or heterocyclic scaffolds. Because piperidine rings feature heavily in marketed drugs—think of central nervous system agents and antihistamines—the chemoselectivity that our (R)-3-Aminopiperidine offers becomes a competitive advantage. Our production engineers work alongside process chemists to troubleshoot not just one, but entire cascades of reactions, making sure that each step from amine formation to downstream functionalization runs at optimum efficiency. This hands-on workflow saves months of wasted time and cuts back on development risk.

    Process optimization in modern pharmaceutical manufacturing often hinges on the reproducibility of every component. The cost of revalidating a step or debugging chiral columns due to starting material issues can outweigh the purchase price of pristine amines. This is why our facility invests in continual process validation and in-depth analytical development, far beyond minimum regulatory requirements. Each new lot of (R)-3-Aminopiperidine runs through advanced impurity profiling, with backup reference standards reserved for every critical impurity seen over years of scale-up.

    Comparison With Other Piperidine Derivatives and Racemates

    Many chemists starting a synthetic route pause between using a racemic mixture or a single enantiomer. Experience shows the difference is more than academic. Racemic 3-aminopiperidine will always give you a 50:50 mix of "R" and "S" forms, leading to complicated purification for any application where chiral purity matters. Time lost separating them after synthesis adds a layer of cost and headache, especially in late-phase drug development or regulated markets.

    Some suppliers offer bulk piperidines without rigorous chiral control. Over years of direct feedback from process engineers, we have learned that relying on such material brings surprises in both reactivity and analytical consistency. Products labeled as “chiral” sometimes show only modest enantiopurity once you check by chiral chromatography. In contrast, our synthesis and isolation of (R)-3-Aminopiperidine start from carefully selected chiral catalysts and reagents, with regular checks at every stage, running through validated HPLC and NMR methods until the product meets every threshold for purity, physical properties, and stability.

    Even within the niche of chiral piperidine derivatives, a variety of side impurities come up depending on process. We control for these through slow crystallization and multiple back-extractions, all of which keep the final amine free from polymeric byproducts or side-chain contamination. Over the course of many audits from large multinational customers, these measures have helped us establish a reputation for reliability—and it translates directly into easier scale-up and better clinical outcomes.

    Overcoming Limitations in Chiral Building Block Supply

    In our factory, raw material pipelines face the same global pressures as everyone else—unexpected customs delays, volatility in chemical feedstocks, shifting environmental and safety regulations. Yet the experience gained from long-term contracts and repeat audits has shaped our response to market constraints. For (R)-3-Aminopiperidine, we use several redundant sourcing routes for starting materials, backed by onsite storage and just-in-time manufacturing for urgent projects. Our team monitors not just supplier certifications, but key property data on each incoming drum of intermediate.

    On days when competitors scramble with shortages or off-spec batches, we rely on in-house process data to adjust reactor parameters or solvent ratios, to keep product coming off the line at the right specification. Downstream partners in pharmaceutical development tell us that this sort of reliability is what allows them to hit regulatory submission timelines and keep clinical trials moving.

    Delivering Peace of Mind: Traceability, Technology, and Workforce

    Our commitment to traceability goes beyond the norm. Every batch of (R)-3-Aminopiperidine carries a digital trail—granular enough to document every operator, analytical method, and lot cross-reference clear back to inbound inventory. Over time, our digital systems have been a resource for troubleshooting reaction anomalies or regulatory queries in customer plants. There is satisfaction in knowing that every reportable value from optical rotation to Karl Fischer water content stands on data that can be pulled up within minutes.

    Success in producing (R)-3-Aminopiperidine consistently also depends on operator training. Our workforce spends as much time on lean chemical engineering as on classical bench skills. Cross-trained production teams know the quirks of every plant reactor and recognize the signature signs of batch deviations before they affect product quality. As technology evolves, we keep up—adopting inline reactors or distributed control systems without losing the watchful eyes and hands that flag issues before they can emerge downstream.

    Tailoring Our Process to Meet Current and Future Needs

    Over years of manufacturing, we've scaled (R)-3-Aminopiperidine processes through several generations. Lessons learned from glassware to stainless production have paid off in formidable product stability and reproducibility. Today, we adjust our plant for both custom specifications—such as low moisture or tailored counterions—and standard production runs for large-volume pharmaceutical production.

    We welcome projects pushing into novel chemistry, as research partnerships allow us to iterate and improve isolation, purification, and packaging of chiral amines. Methods used in our plant today do not rest on static SOPs; they grow with new regulatory expectations and with open feedback from clients facing emerging demands.

    Whenever a drug development partner asks about the limits of (R)-3-Aminopiperidine availability or character, we bring operational transparency to the table—explaining the practical details of lead times, analytical support, and documentation instead of hiding behind dense paperwork or pass-through risk from trading houses.

    Our Perspective: Evolving Alongside the Industry

    The field of chiral chemistry evolves rapidly. Drug targets once rare or hypothetical now require high-purity, well-documented building blocks in volume. As a manufacturer, we have seen the bar for chiral amine quality rise ever higher—and we respond not with shortcuts, but with knowledge gained from the shop floor and from years of back-and-forth with chemists tackling synthesis at every scale. (R)-3-Aminopiperidine stands as a case in point: it provides essential structure and reactivity for cutting-edge pharmaceuticals, and its journey from raw material to finished amine runs through generations of hard-earned experience.

    Supply chain hiccups, global regulations, and shifting therapeutic priorities force all of us to stay on our toes. By investing in process transparency, employee training, and continuous technological upgrades, we keep our edge and deliver peace of mind along with every bottle of (R)-3-Aminopiperidine. If your lab or plant values reliability, data integrity, and responsiveness in every kilogram, we aim to be that rare partner you can talk to, learn from, and rely on.

    Final Thoughts: Why Source (R)-3-Aminopiperidine from Dedicated Manufacturers?

    Over decades, the difference between production-oriented thinking and transactional trading sets itself apart. As a dedicated chemical manufacturer, we live with our products, facing the daily reality of regulatory audits, raw material scrutiny, and the troubleshooting that comes with running a live plant. It pushes us to know our chemistry inside and out—not just as a list of specs, but as a story of process, people, and constant improvement.

    If you need consistent, high-quality (R)-3-Aminopiperidine, tested under real-world conditions by a team who stakes their reputation on every batch, our operation offers not just a product, but direct access to decades of practical know-how. We welcome every new challenge that chiral synthesis brings—and we stand ready to support projects new and old as the landscape of chemical manufacturing continues to evolve.