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N-Boc-4-Piperidinepropionic Acid

    • Product Name N-Boc-4-Piperidinepropionic Acid
    • Alias ZK-829144
    • Einecs 855-514-6
    • 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

    480063

    Productname N-Boc-4-Piperidinepropionic Acid
    Casnumber 136572-09-3
    Molecularformula C13H23NO4
    Molecularweight 257.33
    Appearance White to off-white solid
    Meltingpoint 69-72°C
    Storageconditions Store at 2-8°C
    Solubility Slightly soluble in water; soluble in organic solvents like DMSO, methanol
    Purity Typically ≥98%
    Smiles CC(C)(C)OC(=O)N1CCC(CC1)CCC(=O)O
    Inchikey GLNZBTDOJUJWNB-UHFFFAOYSA-N

    As an accredited N-Boc-4-Piperidinepropionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing N-Boc-4-Piperidinepropionic Acid is supplied in a 25g amber glass bottle with a screw cap, labeled with safety information.
    Shipping N-Boc-4-Piperidinepropionic Acid is shipped in tightly sealed containers compliant with chemical safety regulations. It is packaged to prevent moisture and light exposure, transported under ambient conditions unless otherwise specified. Proper labeling and documentation ensure safe handling. Delivery typically occurs via ground or air freight, adhering to all hazardous material shipping guidelines.
    Storage N-Boc-4-Piperidinepropionic Acid should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep it at room temperature (15–25°C) in a dry, well-ventilated area, away from heat and ignition sources. Properly label the container and ensure it is kept in a designated chemical storage area, following standard safety and handling guidelines.
    Application of N-Boc-4-Piperidinepropionic Acid

    Applications of N-Boc-4-Piperidinepropionic Acid in Industrial Manufacturing

    As a specialized manufacturer, we supply N-Boc-4-Piperidinepropionic Acid to key sectors requiring controlled intermediate compounds for regulated downstream synthesis. Below, we detail major application segments and the practical details demanded by professional industrial integration.

    1. Active Pharmaceutical Ingredient (API) Intermediate for CNS Drugs

    Major pharmaceutical companies incorporate this acid as a building block during small molecule synthesis targeting central nervous system (CNS) indications, such as antipsychotics and antidepressants. Synthesis protocols require Boc-protection for piperidine-based scaffolds to optimize stepwise alkylation and later deprotection. Plant chemists ensure each batch matches project-specific impurity limits and residual solvent specifications set by regulatory filings. Batch scale-up follows route scouting and process validation, aligning with DMF documentation and strict validation protocols.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • U.S. FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur.) monograph relevant to API processes
    • Controlled Substance Synthesis Permits (as required by molecule/therapeutic area)

    Typical usage ratio

    • 0.85–1.20 molar equivalent per target intermediate, adjusted for route optimization

    Downstream process integration

    • Introduced after initial substrate acylation, during the protected piperidine ring formation or alkylation steps
    • Deprotected using mild acid workup in final steps prior to coupling with melanocortin or azepane-based active cores

    Final product types

    • Branded and generic CNS Active Pharmaceutical Ingredients
    • Small-molecule intermediates with protected piperidine moieties
    • Process validation standards for medicinal chemistry R&D
    • Clinical trial API supplies

    2. Peptidomimetic Synthesis for Oncology Research

    Peptide and peptidomimetic manufacturers utilize the compound as a protected amino acid analog to introduce conformational constraints in small cyclic, linear, or hybrid peptide designs. Synthesis development teams leverage Boc-protection to improve N-selectivity and prevent undesired side reactions in solid-phase or solution-phase coupling. The technical team tightly monitors the purity and enantiomeric excess during each synthesis batch, especially when producing cGMP-grade intermediates for IND-enabling studies or preclinical composites.

    Industry compliance standards

    • USP General Chapter <1047> for Peptide APIs
    • ICH Q11 for Drug Substance Manufacturing
    • U.S. NIH guidance for preclinical drug development
    • ISO 9001:2015 Quality Management System for intermediate handling

    Typical usage ratio

    • 1.0 molar ratio per target peptidomimetic fragment, occasionally with 5–10% excess for solid-phase protocols

    Downstream process integration

    • Employed during primary coupling steps for non-natural amino acid incorporation
    • Boc-group removal carried out post-chain assembly under acidic cleavage conditions for high selectivity

    Final product types

    • Anticancer peptidomimetic drug candidates
    • Lead compounds for enzyme inhibitor screening libraries
    • Bioconjugates for targeted oncology diagnostics
    • Research-use intermediates for peptide synthesis CROs

    3. Chiral Synthesis for Advanced Agrochemical Intermediates

    Manufacturers of advanced crop protection compounds employ N-Boc-4-Piperidinepropionic Acid as a chiral auxiliary or intermediate to achieve required stereoselectivity in heterocyclic ring construction. Downstream processing targets the integration of this intermediate into piperidine-derived fungicidal and insecticidal actives. Careful control of reaction conditions is necessary to avoid racemization, and downstream cleaning follows agrochemical-specific impurity profiles regulated for environmental and toxicological compliance.

    Industry compliance standards

    • EU Regulation EC 1107/2009 on Plant Protection Products
    • OECD GLP for Environmental Chemistry Testing
    • EPA 40 CFR Part 158 for Pesticide Active Ingredients
    • FAO/WHO Codex Alimentarius for residue limits

    Typical usage ratio

    • 0.9–1.1 equivalent per batch synthesis, modified depending on stereochemistry yield

    Downstream process integration

    • Entered at the piperidine ring formation step or as a chiral auxiliary during asymmetric synthesis
    • Deprotection and subsequent functional group modification prior to active loading in formulation plants

    Final product types

    • Agrochemical actives based on modified piperidine frameworks
    • Chiral intermediates for plant protection R&D
    • Reference standards for quality control in agroformulation
    • Batch samples for toxicological screening

    4. Fine Chemical Synthesis for Functional Material Additive Networks

    Producers of high-value specialty materials use this compound to introduce nitrogen heterocycles within customizable polymer or resin networks. The protected carboxylic acid structure enables controlled reactivity when modifying resin backbones, especially for electronics and coatings requiring precise thermal and mechanical parameters. Integration requires efficient downstream purification to maintain additive compatibility across performance standards and environmental regulations fixed for advanced materials.

    Industry compliance standards

    • REACH (EC) No 1907/2006 for registered chemical substances
    • ISO 14001 Environmental Management
    • UL 94 standard for flame retardant polymer additives
    • RoHS Directive 2011/65/EU for electronics-grade materials

    Typical usage ratio

    • 1–5 wt% loading in resin or polymer precursor mix, tailored based on desired crosslink density and functionalization rate

    Downstream process integration

    • Blended at early resin or oligomer synthesis, followed by thermal curing and in situ deprotection
    • Post-synthesis adjustment for targeted surface modifications or electronic applications in coating systems

    Final product types

    • Heterocycle-modified polymer resins for electronics
    • Specialty adhesives featuring nitrogen functional groups
    • Antistatic coatings for data storage equipment
    • Intermediate stocks for advanced composite materials
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    Certification & Compliance
    More Introduction

    N-Boc-4-Piperidinepropionic Acid: A Manufacturer’s Perspective

    Building Real-World Chemistry into Every Batch

    At our facility, N-Boc-4-Piperidinepropionic Acid is not just another catalog entry. We focus on the details that impact real research and downstream synthesis. Making this compound involves more than mixing reagents—precision at every step brings us closer to what demanding pharmaceutical and specialty chemical teams expect. Crystallization and purification steps play a critical role, since impurities at low levels can stall entire projects or complicate regulatory filings. Every batch reflects our understanding of why consistency and traceability matter so much in advanced molecular design.

    Understanding the Structure for Practical Use

    This compound, with its Boc-protected piperidine core and propionic acid side chain, acts as a pivotal building block for several synthesis routes. In our experience, the Boc (tert-butoxycarbonyl) group safeguards the nitrogen position throughout aggressive coupling and derivatization steps. Customers, especially in custom peptide and CNS-active molecule development, often share how removing the Boc group under acidic conditions opens doors for highly selective functionalizations. This specific compound, with both piperidine and propionic functionalities intact, allows researchers to build new scaffolds and analogues that would be troublesome or inefficient using non-protected starting points.

    Why Our N-Boc-4-Piperidinepropionic Acid Stands Out

    A lot of our knowledge comes from working alongside chemists on site—watching them struggle with unreliable input materials or tedious purification protocols. For N-Boc-4-Piperidinepropionic Acid, we’ve invested in handling techniques that minimize racemization and moisture pickup. NMR, HPLC, and chiral columns let us catch off-spec material before it reaches synthesis lines. Our team keeps an eye on trace-level contaminants, since even small deviations show up in downstream coupling reactions. Where some competitors focus on scale or generic output, we dial in production based on the smallest nuances from batch to batch. Such decisions only come from running multiple campaigns, adjusting reaction conditions, and listening to feedback from both lab and kilo-scale users.

    Specifications That Connect to Practical Results

    We make N-Boc-4-Piperidinepropionic Acid in several purity grades, typically ranging from standard laboratory grade above 98% to higher grades for regulated applications. This range exists because synthesis doesn’t happen in a vacuum—sometimes, early-stage projects accept more flexibility, and sometimes, late-stage work for clinical candidates calls for substantial analytical support. Water content analysis, checked by Karl Fischer, and low heavy-metal levels confirmed by ICP-OES, form part of standard QA. Often, clients request microanalytical details or batch-specific COAs that show exact impurity profiles. We commit to these requests, because each synthesis story is a little different. Someone scaling for pilot production may focus on gram-to-kilogram reproducibility, while a medicinal chemistry team might want smaller lots that allow fast iterations on SAR cycles.

    Key Applications Shaped by Real Demand

    Over the past decade, our N-Boc-4-Piperidinepropionic Acid has supported projects in CNS therapeutics, peptide analogues, and linker technology for targeted delivery systems. In the CNS space, the piperidine motif remains a go-to core for modulating receptor affinity and improving BBB penetration. The Boc-protection enables stepwise syntheses and late-stage diversification that let scientists try a range of modifications before deprotection. Peptide researchers use this compound for introducing turn-inducing elements or unusual residues, since its protected amine resists side reactions during chain elongation. The propionic acid tail opens up versatile ways to connect to larger fragments or introduce new functional groups via amide or ester formation. Advanced linker work—think antibody-drug conjugates—relies on the integrity and purity of such building blocks, since downstream stability or release kinetics depend heavily on trace-level impurities.

    Lessons Learned from Scale-Up and QC

    Sourcing feedback from kilo-lab and pilot-plant chemists taught us that static conditions rarely suit multiple users. We track not only spectral purity but also physical properties like melting point and particle size, as these can affect solubility and dispensing in automated platforms. Some customers have optimized batch splits and reaction temperatures based on how our N-Boc-4-Piperidinepropionic Acid performs, so we document lot histories and any process tweaks. Advanced purification (often recrystallization or preparative chromatography) helps us hit target purity without unnecessary solvent or energy use. Years back, we encountered a run with slightly elevated residual solvents, and that single deviation led us to implement more robust solvent-removal protocols, even at the cost of cycle time. Such continuous learning directly benefits research speed and troubleshooting downstream.

    Practical Differences Compared to Related Products

    Many science teams ask about the differences between this acid and similar piperidine derivatives, including unprotected forms, N-methylated analogues, or different chain lengths. Out in the lab, the Boc-protected acid offers far more versatility during selective functionalization—the Boc group easily removes under mild acidic conditions after more challenging transformations are finished. Unprotected 4-piperidinepropionic acid tends to run into side reactions or lower selectivity during peptide couplings, since the amine group remains open. The N-methyl version, which we also make, has reduced reactivity in certain alkylations and sometimes fails to deliver comparable biological activity in screening assays. By dialling in how and when the nitrogen protection falls off, chemists hold more cards in sequential synthesis strategies.

    Chain-length variants also serve some programs, but our customers tell us three-carbon spacing balances rigidity with synthetic flexibility—longer linkers, like those based on 5-carbon side chains, can lead to conformational challenges in peptides or complicate cyclic structure formation. In our experience, the 4-piperidine core decorated with Boc and a propionic acid remains a solid fit for both small-molecule and bioconjugation workflows. Because certain regulatory filings hinge on molecule consistency and documentation history, the batch-to-batch stability we deliver with our process brings peace of mind to both R&D and regulatory units.

    Operational Reliability and Direct Support

    Among the most valued aspects for end users is our approach to technical support and root-cause troubleshooting. As manufacturers, we respond to questions not by quoting specs, but by digging into the synthetic and analytical details. When a major pharmaceutical company flagged minor discoloration in a recent delivery, we traced the oxidation back to minute exposure during drying—a seemingly innocuous step, but critical to process reproducibility. By making in-house adjustments and reviewing every post-synthesis log, we corrected this at the source and refined our protocols. This hands-on feedback cycle shapes both day-to-day production and long-term improvement.

    To stay connected to the realities of bench work, we routinely send our technical team into commercial and academic partner labs. We glean insights directly from failures and unexpected reaction outcomes, since an upstream problem with an intermediate like N-Boc-4-Piperidinepropionic Acid can cause downstream synthesis headaches or even derail whole programs. By owning the manufacturing process, adjustments and documentation can be implemented without third-party negotiation delays. Shipments reflect not only a certificate of analysis but also personal accountability—our results travel with every lot.

    Considerations for Environmental and Safety Footprints

    As regulations evolve and sustainable approaches become core to every synthesis operation, our focus now reaches past purity and QA to include the environmental impact of preparing, handling, and disposing of materials. N-Boc-4-Piperidinepropionic Acid benefits from process modifications that cut back on waste and energy. We’ve moved away from toxic solvents and focused on recyclable auxiliaries wherever possible. Our operators receive regular safety training, and our equipment includes robust controls to contain emissions during acidolysis and recrystallization. Years of process development have also let us eliminate certain hazardous intermediates used in earlier synthesis methods.

    Lab users should avoid direct inhalation or skin contact due to the reactivity of the acid group and possible trace solvents. We provide suggestions on safe storage—dry, well-sealed vials away from light—and disposal practices compatible with current environmental guidelines. We help customers navigate safety data and regulatory filings, especially in larger-scale or GMP-bound programs. These steps cut risk and paperwork while supporting innovation with a responsible mindset.

    Feedback-Driven Continuous Improvement

    Real progress often arrives from end-user feedback—sometimes when a client’s initial application falls through, or synthetic problems pop up midway. Recently, a team aiming for a macrocyclic peptide ran into stubborn coupling issues; together, we traced the failure back to an unexpected trace impurity in a competing supplier’s intermediate. This triggered us to share not just our own product, but also full chromatograms and NMR data, letting their team troubleshoot effectively. Such transparency grew into a new understanding of how minor differences in N-Boc-4-Piperidinepropionic Acid quality drive very different synthetic outcomes. This sort of collaboration informs many of the control points we now use in scale-up—so that even clients working at microgram levels benefit from kilo-scale diligence.

    Our process documentation and retention of analytical results help over time, not just for present needs. Repeat orders don’t mean shipped-and-forgotten. Many long-term partners come back asking for historical batch details when scaling up, preparing for audits, or re-examining failed syntheses, and we back up each story with hard data and clear records, not abstractions.

    Integration Across Research and Commercial Workflows

    Unlike traders and repackers, our relationship to N-Boc-4-Piperidinepropionic Acid runs deeper. From early analytical screening to tired hands rinsing the last bit of cake from the filter, our involvement doesn’t stop at the production floor. We constantly monitor market shifts and shifts in discovery chemistry, adjusting our quality and logistics solutions to speed up synthesis cycles and support changing research priorities. New assay requirements, evolving regulatory expectations, and the trickle-down effects of global supply disruptions promote change. By running production under our own roof, out-of-spec shipments are rare, but more importantly, learnings from every challenge cycle back into better materials and faster response times.

    Custom requests—unusual purities, tailored phase solubilities, special pack sizes—are common, and our process is nimble enough to supply both the smallest vials and full multi-kilogram batches. In a recent bioconjugate development project, scientists needed a tightly controlled particle size for automated dispensers. We retooled packaging and post-milling processes to meet the spec, supported by batch testing and direct technical discussion. These experiences convince us every exchange with practicing chemists builds value beyond written specs or generic catalog descriptions.

    What Sets Real Manufacturing Apart

    Hands-on manufacturing yields advantages that reach far beyond price or shelf life. By staying close to the day-to-day of production and application, we spot process shifts, seasonal variability in key reagents, and practical issues chemists report using our materials. R&D doesn’t always happen linearly—teams pivot between synthesis plans, switch from milligram to kilogram scale, or revise targets after biological readouts surprise initial expectations. Our role involves supporting those pivots, sharing not just pure product but also insight, guidance, and proven troubleshooting.

    By focusing on robust analytical data, timely communication, and willingness to adapt, we keep N-Boc-4-Piperidinepropionic Acid a reliable ally for research teams. Years from now, regulatory standards and synthesis methods will evolve, but the need for dependable building blocks and responsive support remains. Our commitment comes built into every batch and every response. Successful projects begin with materials made to real-world expectations, not generic standards.