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

(R)-3-Amino-1-Cbz-Pyrrolidine

    • Product Name (R)-3-Amino-1-Cbz-Pyrrolidine
    • Alias (R)-1-CBZ-3-aminopyrrolidine
    • Einecs 688-498-7
    • 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

    159545

    Product Name (R)-3-Amino-1-Cbz-Pyrrolidine
    Cas Number 946669-21-6
    Molecular Formula C12H16N2O2
    Molecular Weight 220.27 g/mol
    Appearance White to off-white solid
    Optical Rotation [α]D20 = +28° (c=1, MeOH)
    Purity ≥98%
    Melting Point 75-78°C
    Solubility Soluble in DMSO, methanol
    Smiles NC1CCN(Cc2ccccc2CO)C1
    Chirality R-configuration
    Protecting Group Cbz (carbobenzyloxy) group at N1

    As an accredited (R)-3-Amino-1-Cbz-Pyrrolidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-gram (R)-3-Amino-1-Cbz-Pyrrolidine is sealed in a clear glass vial, labeled with product details, batch number, and hazard information.
    Shipping (R)-3-Amino-1-Cbz-Pyrrolidine is shipped in specialized, sealed containers under ambient or controlled temperature conditions to ensure chemical stability and prevent contamination. The packaging complies with safety and regulatory guidelines for chemical transport. Documentation, including safety data sheets, accompanies the shipment for secure handling and regulatory compliance during transit.
    Storage Store (R)-3-Amino-1-Cbz-Pyrrolidine in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. Keep the container tightly closed and properly labeled. Store at 2–8°C (refrigerated) to maintain stability. Avoid contact with incompatible substances such as acids and strong oxidizers. Use only in a chemical fume hood with appropriate personal protective equipment.
    Application of (R)-3-Amino-1-Cbz-Pyrrolidine

    Applications of (R)-3-Amino-1-Cbz-Pyrrolidine in Industrial Manufacturing

    (R)-3-Amino-1-Cbz-Pyrrolidine supports advanced synthesis in pharmaceutical, fine chemistry, and specialty materials production. As direct manufacturer, we serve downstream sectors requiring strict quality assurance, process reproducibility, and regulatory adherence. Below, we detail main industrial application scenarios, process integration points, and compliance expectations.

    1. Chiral Pharmaceutical Intermediates for CNS Drug APIs

    (R)-3-Amino-1-Cbz-Pyrrolidine functions as a critical chiral backbone in the synthesis of several central nervous system (CNS) active pharmaceutical ingredients, particularly selective D2/D3 dopamine antagonists. Multistep synthesis routes leverage its enantiomeric purity to ensure stereochemical integrity in the final API structure. Upstream with proper validation, it enters amidation and reductive amination stages, aligning with GMP and ICH quality management. Only pharmaceutical companies with advanced NCE (new chemical entity) development pipelines generally require this segment of chiral intermediates at gram to multi-kilogram scale, under full traceability and documentation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • European Pharmacopoeia (quality monograph for intermediates in medicinal products)
    • Chinese Pharmacopoeia (where applicable in API intermediate registration)

    Typical usage ratio

    • 10–40 mol% relative to first key synthetic intermediate; adjusted based on process yield and targeted API batch size
    • Higher excess may be applied to ensure complete chiral transfer in asymmetric catalysis

    Downstream process integration

    • Direct addition into batch reactor during initial amidation or reductive amination sequence
    • Isolation and purification prior to further structural modifications and final salt formation
    • Extensive analytical QC following each synthetic step for enantiomeric excess and impurity profiling

    Final product types

    • Selective antipsychotics (D2/D3 antagonists)
    • CNS modulating drugs (investigational new molecules)
    • Chiral building blocks for further pharmaceutical R&D batch syntheses

    2. Peptidomimetic Synthesis for Oncology Small Molecule Drugs

    In oncology research, our product serves as a non-proteinogenic amino acid building block during scale-up production of peptidomimetic actives. The protected (Cbz) amino function ensures chemical compatibility with solid- and solution-phase synthesis, reducing racemization and side reactions during chain elongation. API manufacturers employ it to enable target binding specificity and metabolic stability in leading-edge cancer inhibitors, following strict chain-of-custody and GMP guidance from early synthesis through to IND-enabling batches.

    Industry compliance standards

    • EU GMP Volume 4 (Active Substances)
    • US FDA ICH M7 (Assessment of Mutagenic Impurities)
    • ICH Q3A/B (Impurities in New Drug Substances and Drug Products)
    • Certificate of Suitability (CEP) from EDQM, when required for European market

    Typical usage ratio

    • 9–22 mol% per peptidomimetic core scaffold; acute adjustment per target molecule sequence and yield efficiencies
    • Proportional excess in stepwise or parallel synthesis as buffer against side-product formation

    Downstream process integration

    • Introduction into solid-phase peptide synthesis via Fmoc-SPPS techniques
    • Chemical deprotection and subsequent coupling to extend peptide chain
    • In-line analytical verification (UPLC, LC-MS) after each coupling step

    Final product types

    • Orally available peptide-based oncology drugs
    • Targeted protein-protein interaction inhibitors
    • Small molecule drug conjugates (e.g., proteolysis targeting chimeras, PROTACs)

    3. Fine Chemical Synthesis: Chiral Auxiliary in Agrochemical Actives

    Leading crop protection R&D groups apply our material as a chiral auxiliary in the synthesis of high-selectivity agrochemical actives, such as pyrrolidine-derived herbicide and insecticide intermediates. The Cbz-protected amino functionality enables predictable reactivity during asymmetric transformations, particularly hydrogenations and nucleophilic substitutions. Companies focus on proprietary process efficiency and robust chirality transfer for regulatory submissions such as US EPA and EU REACH.

    Industry compliance standards

    • US EPA Pesticide Registration Requirements (FIFRA, 40 CFR Parts 150–180)
    • EU REACH Regulation (EC) No 1907/2006 for intermediates
    • ISO 9001:2015 (Quality Management Systems for chemical manufacturing)
    • OECD Guidelines for the Testing of Chemicals (applicable screening)

    Typical usage ratio

    • 5–18 mol% relative to primary agrochemical precursor; selection based on desired degree of chiral selectivity and process plant scale
    • Variable depending on whether auxiliary is recovered and recycled following target manufacturing step

    Downstream process integration

    • Incorporation during key stereoselective transformation (e.g., asymmetric hydrogenation)
    • Subsequent removal or derivatization to yield enantiopure active intermediate
    • Inline purity analysis using GC or chiral HPLC techniques before product formulation

    Final product types

    • Enantiopure herbicide or insecticide active intermediates
    • Pyrrolidine-based crop protection active substances
    • Key chemical standards for residue testing and environmental risk assessment

    4. Advanced Material Science: Monomer Unit in Functional Polymers

    Various specialty polymer manufacturers deploy (R)-3-Amino-1-Cbz-Pyrrolidine as a monomeric unit building block to impart specific chirality and functional sites within high-performance polymers. Applications include molecular recognition materials for chiral separation membranes and optical films. Incorporation requires precise control of reaction ratios and protection group chemistry, managed by technical teams using in-process FTIR and NMR monitoring. Material suppliers focus on tailorable polymer backbone characteristics in alignment with end-use certification and environmental safety.

    Industry compliance standards

    • ISO 14001 (Environmental Management Systems for chemical manufacturing)
    • RoHS Directive 2011/65/EU (if polymers target electronic/optical application)
    • ASTM D638 (Test Method for Tensile Properties of Plastics)
    • REACH SVHC notification for monomer substances (when required by downstream application portfolio)

    Typical usage ratio

    • 2–10 mol% as co-monomer; may vary based on desired level of functional group density and membrane selectivity
    • Adjusted according to final product performance requirements (mechanical, optical, or separation properties)

    Downstream process integration

    • Co-polymerization with standard or specialty monomers within a controlled reactor environment
    • In-situ or post-polymerization deprotection to activate amino functions for further functionalization
    • Extensive quality control on polymer chain composition and molecular weight distribution using SEC techniques

    Final product types

    • Chiral separation membranes for enantiomeric purification
    • Optical and electronic specialty films
    • Advanced functional resins for analytical and sensor applications
    Free Quote

    Competitive (R)-3-Amino-1-Cbz-Pyrrolidine 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

    (R)-3-Amino-1-Cbz-Pyrrolidine: A Foundation for Modern Synthesis

    Our Perspective on (R)-3-Amino-1-Cbz-Pyrrolidine

    At our facility, every batch of (R)-3-Amino-1-Cbz-Pyrrolidine starts with choosing raw materials of uncompromising quality. We understand that even a trace impurity at the source can spell issues down the line—especially for building blocks as crucial as this one. Over our years refining this product, the demand from both pharmaceutical and fine chemical sectors has underscored its place as a reliable chiral intermediate, offering the kind of stereocontrol and reactivity that opens doors in synthesis others simply can’t.

    Unlike bulk commodity chemicals, (R)-3-Amino-1-Cbz-Pyrrolidine never gets lost in storage or blending. Every gram carries with it the care of multistep synthesis, cautious handling, and regular analysis for enantiomeric excess. We leave nothing to chance, as our partners in research and industry rely on precise molecule-by-molecule control to build more complex structures—be it for active pharmaceutical ingredients, agrochemical leads, or specialty polymers.

    Choosing (R)-Enantiomer: Why This Matters

    We see frequent confusion over the importance of the (R) configuration. In our experience, that single chiral center defines utility for asymmetric synthesis, especially where downstream stereochemistry must be locked in. Laboratories synthesizing chiral drug scaffolds routinely specify (R)-3-Amino-1-Cbz-Pyrrolidine for work where the wrong enantiomer simply won’t fit the process—and trying to correct it later wastes both resources and capital.

    One distinction lies in how we assure stereopurity batch by batch. We use chiral HPLC and other analytical checks on every run, not because regulations ask us to, but because years of feedback have taught us how minor drifts become major roadblocks at scale. Making sure enantiopurity stays high isn’t just a selling point; it’s the difference between reaction success and a round of troubleshooting that can stall a production schedule for weeks.

    Carbobenzyloxy (Cbz) Protection—A Tool, Not an Afterthought

    We’ve worked with customers who once tried to use unprotected amines instead of a Cbz-protected pyrrolidine. The result? Troublesome side reactions, especially during peptide couplings or reductive amination. The Cbz group acts as a reliable shield, preventing unwanted reactions and surviving a range of conditions. Removal afterwards stays straightforward through hydrogenation—a technique we have scaled up numerous times with good yields and clean product isolation.

    Other protecting groups occasionally show up in the catalogues, but Cbz strikes a unique balance: stable enough for most synthetic routes, yet removable under mild enough conditions to preserve functional groups elsewhere in the molecule. That flexibility has given this product a robust track record among both medicinal chemists and process engineers.

    Understanding Physical and Chemical Properties

    Batch-to-batch consistency matters especially with (R)-3-Amino-1-Cbz-Pyrrolidine because certain downstream reactions require a crystalline solid as starting material, while others need a clear oil. We maintain tight control over residual solvents, moisture content, and melting point throughout production. From our experience, even small deviations can impact yields and reproducibility in downstream transformations like alkylation and cyclization.

    Our team measures optical rotation, melting range, and purity through both chromatographic and spectroscopic means. Over time, the feedback we received from chemists running gram-to-multi-kilo reactions has driven us to set tighter limits than industry averages, especially around visible trace impurities known to interfere with palladium or nickel catalysis.

    Application and Value in Synthesis

    Day by day, there’s a growing list of intermediates and APIs built from pyrrolidine scaffolds. (R)-3-Amino-1-Cbz-Pyrrolidine finds its way into synthesis sequences for antivirals, antipsychotics, and a raft of bioactive molecules where both the ring and its precise amine configuration matter. It works especially well where the challenge is controlling both ring geometry and side-chain substitution patterns.

    Many of our contacts in custom synthesis count on our material for robust N-substitutions, peptide coupling, and further ring transformations. The ease of deprotection has let process chemists streamline routes and avoid unnecessary purification steps. From project kickoff meetings to pilot plant scale, we often discuss trade-offs between protected versus unprotected amines, and the Cbz-protected variant wins out in both processing and regulatory compliance.

    Our Process—Experience Builds Reliability

    Making (R)-3-Amino-1-Cbz-Pyrrolidine starts with years of know-how. We don’t just follow a set recipe: our operators are trained to recognize subtle shifts in reaction kinetics and color changes that might point to side reactions. Each run starts with precise weighing and ends with comprehensive analysis—including HPLC, NMR, and mass spectrometry—to guarantee the chemistry holds throughout, not just at the start.

    We put extra emphasis on purification, using both crystallization and chromatography where necessary. The result is a product with minimal by-product levels, which may not matter in microgram research work, but becomes crucial in scale-up. We routinely document and track every process step, so if any variable shifts over time, our team can review and implement adjustments before variability can propagate further.

    Comparing to Other Pyrrolidine Derivatives

    We’ve been approached more than a few times with questions about why one wouldn’t just use racemic or unprotected pyrrolidine. Our experience highlights several key differences. Racemates either need laborious separation or end up producing unwanted by-products downstream. Unprotected amino groups invite side reactions that don’t manifest until someone scales up or tries multi-step synthesis. The (R)-Cbz-protected version solves both these issues before they start, saving countless hours spent troubleshooting unpredictable chemistry.

    Market interest in related molecules—such as the (S)-enantiomer, N-Boc-protected pyrrolidines, or simple N-alkylated derivatives—remains strong, and we have experience manufacturing these as well. Still, the combination of (R) configuration and Cbz protection consistently gives superior performance, especially for customers focused on developing new therapies or scaling efficient API routes.

    Reliability in Delivery and Documented Traceability

    We’ve seen projects derail from missing or incomplete CoA documentation, or from batch variation between suppliers. Our customers can trace each lot to specific production runs, starting from the raw materials all the way through finished product. We supply documentation that covers not only purity and identification, but also residual solvent analysis and detailed impurity profiling.

    Our clients value direct communication. When they call us with a technical query or to discuss synthesis plans, they’re speaking with people who actually run the reactors and QC labs. That kind of access often resolves technical obstacles before they appear, as we’re able to suggest minor modifications to reaction conditions based on the observed characteristics of a given batch. In turn, this collaborative approach produces less waste, higher yields, and more successful projects.

    Environmental and Safety Commitments

    We manufacture under a commitment to reduced environmental impact. Over the years, we’ve invested in solvent recovery and waste minimization, both from necessity and conviction. Organic solvents used in Cbz deprotection and subsequent purification can create waste streams that are costly to treat if mismanaged. By tracking each downstream process, and by working with local waste partners, we have achieved steady reductions in solvent consumption per kilo of product, benefiting both our operation and the community around us.

    Safety isn’t a checkbox. From raw material handling to the last stage of hydrogenation, our team follows strict protocols, having trained on both the chemistry and the practical risks that come with high-energy reactions. Our operations team reviews near-misses and process hazards regularly, learning and adapting alongside changing production volumes and new customer needs.

    Quality Assurance Guided by Experience

    A lot of what defines (R)-3-Amino-1-Cbz-Pyrrolidine’s reliability lies in the experience of people working in every part of the process. We recall early batches years ago, where inconsistent stirring or slight overreaction during protection steps caused off-color products. Turning mistakes into improvements has shaped how we set up reactors, choose purification strategies, and talk with end users about specification needs.

    We place high value on record-keeping. Every deviation gets documented, not as a burden, but as a guide for future adjustments. Our quality department analyzes every trend—not just headline numbers, but patterns in impurity formation, solvent residues, and reaction work-up—to predict where issues might crop up. For customers scaling new syntheses, this experience forms a foundation they rely on; trust often boils down to how a supplier reacts to unexpected changes.

    Regulatory Perspectives

    Many of our customers are developing clinical candidates that can’t afford regulatory setbacks from inconsistent raw material. We maintain compliance with global quality and safety standards, undergo regular audits, and review dossier requirements for both the US and EU. Each batch comes with complete analytical data and traceability. Our regulatory affairs team reviews new requirements as they emerge, bridging the gap between chemistry expertise and regulatory approval.

    Product changes are always communicated clearly, with detailed justifications for any shift in process or specification. Open dialogue with regulatory reviewers has smoothed several customer programs, where fast answers and thorough documentation made the difference between project momentum and unnecessary delay.

    Continuous Improvement and Customer Partnership

    Continuous improvement never stops for us. We draw lessons from every customer audit, every shipment, every feedback call. As the needs of pharmaceutical synthesis or specialty chemistry evolve, so too do our manufacturing standards. Our process chemists interact directly with customers, helping them optimize synthetic sequences or troubleshoot unexpected reactivity.

    Several times a year, our R&D group pilots new process improvements—be it cleaner hydrogenation methods, alternative protecting groups, or scalable crystallization techniques. While not every trial turns into routine practice, the cumulative insights keep our work both relevant and resilient.

    Pioneering New Applications

    Ongoing projects at our facility have opened up novel applications for (R)-3-Amino-1-Cbz-Pyrrolidine. Beyond its classical role as a chiral intermediate in pharmaceutical synthesis, we’re seeing its N-protected structure utilized for generating building blocks in bioactive peptides and as precursors for asymmetric catalysts. Project teams working in early-stage discovery have found that this compound’s versatility often allows them to explore several synthetic routes in parallel—reducing development times and increasing their chances for success.

    We support such explorations through both technical advice and prompt material supply. In collaborative projects, our scientific team works side-by-side with external researchers to adjust reaction protocols or design new derivatives that fit their emerging targets. The hands-on knowledge from our reactors and QC labs turns into a form of “institutional memory”, often surfacing practical suggestions that go beyond any literature precedent.

    Why Direct Sourcing Matters

    Dealings with resellers or brokers tend to introduce unpredictability—be it in lead times, documentation quality, or batch consistency. Direct engagement with a manufacturer connects users with the source, the only place where both technical feedback and practical questions receive informed, timely answers. We encourage our partners to work with us early in project development, so we can recommend the variant or grade best matched to their intended application, rather than leave such choices to late-stage troubleshooting.

    Upholding Trust through Experience and Transparency

    Decisions around sourcing (R)-3-Amino-1-Cbz-Pyrrolidine shouldn’t just focus on price or immediate delivery, but on the reliability of long-term partnership. We’ve worked with teams who have gone from milligram quantities in R&D to metric-ton pilot runs, often adjusting process steps along the way. Success in such scaling depends less on what’s written in a price quote and more on the ongoing problem-solving that a good manufacturer brings to the table—something we strive to provide each day.

    Through each shipment, audit, and technical call, we keep learning. Our team’s years within the plant floor, at bench scale, and engaged directly with process chemists worldwide have shaped our approach. By offering not only (R)-3-Amino-1-Cbz-Pyrrolidine, but also the expertise and accountability behind it, we intend to keep raising the standard—one batch and one customer conversation at a time.