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N-Boc-Piperidine-4-Carboxylic Acid

    • Product Name N-Boc-Piperidine-4-Carboxylic Acid
    • Alias 1-Boc-4-piperidinecarboxylic acid
    • 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

    961967

    Chemical Name N-Boc-Piperidine-4-Carboxylic Acid
    Cas Number 118108-02-2
    Molecular Formula C11H19NO4
    Molecular Weight 229.27
    Appearance White to off-white solid
    Melting Point 102-106°C
    Solubility Slightly soluble in water, soluble in organic solvents (e.g., DMSO, methanol)
    Purity Typically >98%
    Storage Conditions Store at 2-8°C, keep container tightly closed in a cool, dry place
    Synonyms tert-Butyl 4-carboxypiperidine-1-carboxylate
    Inchi Key WQOIXTVQZMPBHJ-UHFFFAOYSA-N

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

    Packing & Storage
    Packing White crystalline powder, securely sealed in an amber glass bottle, labeled 25g N-Boc-Piperidine-4-Carboxylic Acid, with safety warnings.
    Shipping N-Boc-Piperidine-4-Carboxylic Acid is shipped in sealed, chemical-resistant containers to ensure stability and prevent contamination. It should be transported at ambient temperature, away from strong acids, bases, and oxidizing agents. Proper labeling and documentation are provided, adhering to all relevant chemical shipping regulations. Safety data sheets are included with every shipment.
    Storage N-Boc-Piperidine-4-Carboxylic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as strong oxidizers. Keep the container protected from light. Store at room temperature or as specified by the manufacturer, typically between 2-8°C, and always follow standard chemical storage safety guidelines.
    Application of N-Boc-Piperidine-4-Carboxylic Acid

    Applications of N-Boc-Piperidine-4-Carboxylic Acid in Industrial Manufacturing

    N-Boc-Piperidine-4-Carboxylic Acid serves as a critical intermediate in several high-value synthesis pathways for the pharmaceutical, peptide, and biomedical industries. Our manufacturing process ensures traceability and compliance throughout the supply chain, supporting strict quality and regulatory requirements for each downstream segment.

    1. Small Molecule Pharmaceutical API Synthesis

    Pharmaceutical manufacturers use this compound extensively as a protected building block in the synthesis of active pharmaceutical ingredients, particularly in central nervous system (CNS) and oncology product pipelines. Its Boc-protected piperidine ring enables selective functionalization and minimizes unwanted side reactions during multistep syntheses. Process chemists remove the Boc group under mild acidic conditions at the final deprotection stage, allowing precise control over the API’s molecular structure and purity. Integration into GMP-compliant facilities requires robust traceability and impurity profiling, especially for regulated markets such as the US and EU.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopeia (Ph. Eur.) suitability for raw intermediates
    • REACH Registration for EU market

    Typical usage ratio

    • Batch reactions typically use 0.5-1.2 molar equivalents relative to the next protected amino acid or aryl halide, depending on target API structure and protection scheme

    Downstream process integration

    • Compound enters during protected intermediate formation, usually in the first or second coupling step in multi-step synthetic routes
    • Purification via crystallization and column chromatography before final deprotection
    • API isolation and validation follow deprotection and final purification

    Final product types

    • Piperidine-derived CNS drug APIs (e.g., antipsychotics, antidepressants)
    • Oncology agent active intermediates
    • Specialty chemical intermediates for contract manufacturing

    2. Peptide Synthesis Platforms

    N-Boc-Piperidine-4-Carboxylic Acid functions as a cornerstone protected amino acid analog in the assembly of complex peptides, especially those requiring piperidine motifs for bioactivity or stability. Solid-phase peptide synthesis (SPPS) protocols exploit its manageability in resin loading and cleavage cycles. Process engineers select the Boc strategy to control N-terminal deprotection sequence, crucial for chain elongation and yield. Manufacturing qualification includes compatibility with automated platform protocols, minimal racemization, and compliance with peptide GMP requirements.

    Industry compliance standards

    • Peptide GMP Manufacturing Guidelines (ICH Q7 for peptides)
    • USP General Chapter <1047>
    • ISO 9001:2015 for process quality management
    • EU GMP Annex 2 for Biological Substances

    Typical usage ratio

    • Usually charged at 1.0-1.2 equivalents per resin-bound peptide step; adjustment based on expected coupling efficiency and resin substitution level

    Downstream process integration

    • Incorporated during side-chain protection and N-terminal capping steps on automated or manual SPPS equipment
    • Post-assembly, process includes acid cleavage and global deprotection under controlled conditions
    • Peptide purification via preparative HPLC or lyophilization

    Final product types

    • Research-grade synthetic peptides
    • Preclinical and clinical trial peptide candidates
    • Piperidine-modified therapeutic peptides

    3. Advanced Medicinal Chemistry Research

    Drug discovery laboratories leverage the unique protective characteristics of N-Boc-Piperidine-4-Carboxylic Acid during hit-to-lead and lead optimization workflows, especially when scaffold hopping or functionalizing the piperidine ring system. The Boc group’s orthogonal cleavage protocol aligns with combinatorial chemistry strategies, allowing parallel library synthesis with fast turnaround. Documentation and tracking for each batch enable reliable audit trails, meeting CRO and pharmaceutical customer requirements in both early- and late-stage projects.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for medicinal chemistry labs
    • OECD Principles of Good Laboratory Practice
    • Company-specific raw material specification sheets
    • Material traceability policies for clinical candidates

    Typical usage ratio

    • Ranges from 0.3-1.5:1 molar ratio, set by the number of parallel scaffold synthesis or degree of substitution required in the piperidine series

    Downstream process integration

    • Input for initial core structure assembly and functional group diversification via nucleophilic substitution or reductive amination
    • Purification for intermediate libraries by automated flash chromatography
    • Subsequent modification or Boc group removal for downstream bioactivity assays

    Final product types

    • Combinatorial chemistry libraries for high-throughput screening
    • Lead compound intermediates for structure-activity relationship (SAR) studies
    • Proprietary piperidine-based inhibitor scaffolds

    4. Precursor for Specialty Polymer Additives

    Polymer and material science companies utilize N-Boc-Piperidine-4-Carboxylic Acid as a reactive precursor to produce functionalized piperidine derivatives, which act as light stabilizers, crosslinking agents, and antistatic modifiers in specialty polymers. The Boc protection ensures manageable incorporation during initial synthesis steps, yielding precise molecular weights and minimal side-product formation. Our production matches batch-specific quality requirements for high-purity additive integration and supports documentation for product stewardship in demanding regulatory regions.

    Industry compliance standards

    • ISO 9001:2015 certification of additive manufacturing processes
    • EU REACH Regulation compliance for polymer additives
    • Safety Data Sheet (SDS) per GHS for handling and downstream safety
    • Technical data conformance to end-user plastic compounding guidelines

    Typical usage ratio

    • Added in 0.5–2.0% w/w relative to base resin weight during additive masterbatch formulation; level fine-tuned based on intended function (e.g., stabilization or antistatic effect)

    Downstream process integration

    • Introduced during masterbatch synthesis before extrusion or compounding
    • Chemical deprotection or post-modification as required for final incorporation into resin matrix
    • Integration with colorants or other functional additives in production granules

    Final product types

    • HALS (Hindered Amine Light Stabilizer) masterbatches
    • Antistatic additive concentrates
    • Specialty films and molded polymer products

    5. Custom Fine Chemical Synthesis Services

    Contract development and manufacturing organizations (CDMOs) depend on N-Boc-Piperidine-4-Carboxylic Acid for client-driven fine chemical programs, particularly in projects demanding unique piperidine-bearing intermediates for advanced organic synthesis. The controlled protection-deprotection profile allows selective transformation and stepwise building of complex targets, whether for advanced intermediates, ligands, or small molecule tags. Our facility tracks COA, batch history, and residual solvent profiles for custom campaigns, supporting client regulatory filings as needed.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for custom synthesis plants
    • Client-specific raw material acceptance criteria
    • Full traceability per ISO/IEC 17025 for analytical support
    • Confidentiality and quality agreements for customer projects

    Typical usage ratio

    • Determined by client route: usually 1.0–1.5 equivalents relative to core scaffold for protected building block insertion or substitution reactions

    Downstream process integration

    • Synthesized as precursor or intermediate based on client-supplied route
    • Incorporated during stepwise assembly prior to deprotection and further functionalization
    • Final product isolation via preparative purification and solid-state characterization

    Final product types

    • Advanced intermediates for pharma or agrochemical projects
    • Fine chemical building blocks for R&D
    • Specialty functional molecules for bioorganic chemistry
    Free Quote

    Competitive N-Boc-Piperidine-4-Carboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    N-Boc-Piperidine-4-Carboxylic Acid: Supporting Precision in Complex Chemical Synthesis

    Meeting Demands in Advanced Chemistry with N-Boc-Piperidine-4-Carboxylic Acid

    Stepping into the world of fine chemical manufacturing, it doesn’t take long to notice the importance of specific building blocks in pharmaceutical and specialty chemical production. Among these, N-Boc-Piperidine-4-Carboxylic Acid has become a regular feature on the benches of process development labs and kilo plants alike. Customers come to us for it because certain projects call for high purity and well-defined reactivity, particularly in medicinal and peptide chemistry. Having watched how research and scale-up teams work with piperidine derivatives, it’s clear why the demand for the Boc-protected 4-carboxylic acid outpaces other protected piperidine acids.

    Understanding the Structure and Selection

    Some colleagues in product development regard N-Boc-Piperidine-4-Carboxylic Acid as a core intermediate, especially when creating compounds where both nitrogen protection and carboxyl functionality are valued. The molecule combines a piperidine ring with a tert-butoxycarbonyl (Boc) group at the nitrogen and a carboxylic acid at the 4-position. This design isn’t accidental—it reflects decades of process optimization in small molecule synthesis.

    Chemists need intermediates that hold up under conditions for subsequent coupling and deprotection steps. Direct feedback from our pilot plant highlights the stability of the Boc group: it stands up to base and mild acid, but comes off cleanly under stronger acid. This lets project teams program a clear synthetic route, avoiding surprises down the line. Other amino-protecting groups, such as Fmoc or Cbz, don’t tolerate the same array of conditions, and their deprotection can complicate purification. Having synthesized both types in the same reactor suites, we’ve found the Boc group significantly streamlines downstream steps—granted, you’re working under conditions accessible to most process groups.

    Specifications Rooted in Reliability

    An end-user once told us, “Quality in means quality out.” That’s been our mantra. N-Boc-Piperidine-4-Carboxylic Acid coming off our line consistently meets minimum purity levels exceeding 98%, as measured by HPLC. Some clients request extra-stringent heavy metal or residual solvent controls, which we can monitor using ICP-MS or GC, depending on need. Over time, we’ve also standardized particle size and minimize clumping by refining our final drying process, since some customers prefer free-flowing material for automated dosing and others want a finer powder for solution-phase reactions. Uniformity lowers batch-to-batch variation—process reliability starts from kg one.

    Water content draws special attention: for solid-phase synthesis, high moisture can wreck yields or stall resin couplings. Our teams monitor Karl Fischer titration data on every batch before shipment. Strict controls separate our product from non-manufacturing traders, who don’t wield the same process insight or traceability.

    Application Expertise from Real Customer Challenges

    N-Boc-Piperidine-4-Carboxylic Acid’s reputation in peptide chemistry comes from real in-lab applications, not just catalog listings. We’ve watched it go into thousands of syntheses of constrained peptides, cyclic peptides, and non-natural amino acid derivatives. Since the protective Boc group survives activation conditions, peptide chemists use it to build more ambitious analogs—ones impossible with unprotected piperidine acids, which lead to branching, incomplete couplings, or decomposition.

    Contract manufacturing partners in our network often ask for custom pack sizes so that their teams can charge the right amount directly into reactors—no repacking, no exposure, fewer contamination risks. It’s the day-to-day details—eliminating caking, keeping bottles sealed with inert gas—that reinforce why chemical manufacturing isn’t just filling containers; it’s easing headaches across the synthesis chain.

    Why N-Boc-Piperidine-4-Carboxylic Acid Stands Apart from Other Protected Acids

    Not every protected piperidine acid fits the same bill. For one thing, 4-substituted isomers like N-Boc-Piperidine-4-Carboxylic Acid create molecules with unique three-dimensional shapes. Med chemists prize these as rigid scaffolds that hold pharmacophores in precise 3D arrangements. By contrast, isomers like the 3-carboxylic acid can complicate downstream structure-activity relationships. Over years of manufacturing, we’ve tracked which isomers show up most in literature and scale-up requests—this one wins out nearly every time for its synthetic flexibility.

    Competing materials protected by Fmoc or Cbz often come up in discussion, particularly for peptide work. In our experience, switching to Boc brings easier scale-up and fewer downstream byproducts during subsequent hydrogenation or deprotection. Fmoc requires base treatment, and not every process team wants to manage the byproducts, especially at larger volume. Boc’s acid-labile nature allows for modular process steps: pair it with base-labile groups elsewhere in the molecule, and you gain extra synthetic control.

    Feedback from formulation chemists taught us to keep an eye on residual solvents and process impurities. Piperidine derivatives, especially with protecting groups, tend to co-elute with minor side-products if the manufacturing process isn’t controlled tightly. Our QC checks reflect these realities. For projects aiming for purity beyond 99%, we offer additional purification—but for most, our standard grade performs beyond expectation.

    Shaping Process Decisions with Direct Manufacturing Experience

    We know from firsthand plant experience that choosing the right intermediate improves workflow far down the line. N-Boc-Piperidine-4-Carboxylic Acid holds up under a range of coupling conditions—amide bond formation, esterification, even some conditions outside classical peptide chemistry. The extra stability during storage also means fewer surprises after long shipments or in humid environments, making inventory management more forgiving.

    Customers often ask about shelf life and reactivity. Because the compound’s Boc group stays put unless exposed to strong acid, it travels well and stores for months without noticeable change, provided containers remain sealed and dry. That makes it fit for high-throughput library synthesis, where small differences in starting material quickly compound into larger issues downstream.

    Over the years, our technical support teams have documented countless process troubleshooting cases—low yield stemming from off-purity raw materials, side reactions traced back to trace metal contamination, unexpected caking during automated dispensing. Having manufacturing insight allows us to build in mitigation at the source. For N-Boc-Piperidine-4-Carboxylic Acid, that’s meant refining our work-up protocols, limiting moisture uptake during shipping, and providing robust CoA documentation to satisfy due diligence.

    Where N-Boc-Piperidine-4-Carboxylic Acid Fits in the Synthesis Landscape

    Looking at customer projects over the past decade, demand for complex, conformationally restricted peptides and small molecules keeps climbing. Drug discovery teams keep pressing for new scaffolds—they’re after molecules that offer unique fit and function. The piperidine core, with its six-membered ring and nitrogen functionality, opens up new vectors in SAR (structure–activity relationship) campaigns. Inserting carboxyl at the 4-position can deliver not just new analogs but entirely new classes of compounds.

    Our synthesis teams collaborate with upstream raw material suppliers to manage purity every step of the way. We’ve clocked the importance of minimizing byproduct formation—not just for regulatory compliance, but to help customers sidestep downstream recrystallization or redissolution. With every batch, spectroscopic analysis (NMR, IR, LC-MS) confirms identity, and we’ve integrated rapid testing protocols to flag outliers before release.

    Since regulatory landscapes for pharma-grade intermediates keep shifting, we proactively adapt synthesis protocols whenever new limits for residual solvents or trace elements go into effect. For customers in regulated markets, having a consistent, well-documented supply chain lets them focus on their API synthesis and formulation, not time-consuming raw material investigation.

    Challenges in Handling and Solutions Developed Over Time

    Early on, we fielded complaints about product clumping during transport in humid months. By adjusting the drying phase and packaging with desiccants, we fixed consistency without overdrying—which would only introduce static and dusting issues at dispense. Each process tweak followed an in-house trial, and newer drum seals now keep oxygen and moisture out for extended periods.

    Temperature stability matters, too. We log temperature excursions in real-time data loggers during international shipments. The compound tolerates cycles between refrigeration and room temp, but prolonged high heat invites hydrolysis. For clients with dedicated inventory, we offer custom shipment schedules—this kind of flexibility sets manufacturers apart from logistics middlemen.

    On the safety front, plant experience dealing with piperidine derivatives taught us the value of targeted training and appropriate PPE. Strong odors or irritancy can crop up in confined spaces, prompting custom ventilation during micronization or filling. Those are frontline realities for producers that don’t get discussed on generic vendor datasheets.

    Direct Impact on Downstream Chemistry and Why Purity Matters

    Pharmaceutical chemists remind us daily: inconsistent starting materials ripple forward to cost time, money, and reputation. Feedback loops from multiple development partners made clear that even minor impurities in N-Boc-Piperidine-4-Carboxylic Acid can introduce unexpected chromatographic ghosts, lower overall yield, or trigger cascade problems in solid-phase protocols.

    By investing in in-line analytics and rapid batch release, we keep lead times tight, so clients can stick to aggressive project timelines. For heavily regulated projects, we store reserve samples and provide expanded impurity profiling on request, supporting customer audits as needed. We don’t just hand over a CoA and walk away—we’ve supported tech transfers, provided scaled-up sample lots, and solved process hiccups mid-campaign.

    Supporting the Broader Research Community

    As the push for new drugs and advanced materials accelerates, responsiveness counts. Our knowledge that a small change in a protected piperidine acid can unlock a successful lead candidate, rather than a failed one, underpins our commitment to in-house manufacturing rather than out-sourcing or stock-and-resell models. We meet with researchers, listen to roadblocks, and report back to plant supervisors to adjust process where practical.

    Knowing what happens if particle size shifts a few microns, or how small upticks in residual base can carry forward into product lines, keeps us embedded in the process. This granular approach means each lot’s release involves a review of data, not just checks against a generic spec. That’s a promise field chemists recognize—they know we’ve literally watched product move from reactor to drum.

    Looking Forward: Innovations and Ongoing Process Development

    Building on our manufacturing strength, we invest in new crystallization protocols and solvent systems designed to reduce cycle time and minimize environmental burden. We work to replace older chlorinated solvents with more sustainable alternatives. Less waste cuts environmental impact and keeps the compound’s final profile cleaner—a win for both production and end-users managing complex compliance requirements.

    Scale-up never stops evolving in our industry. We’ve run continuous improvement campaigns to refine yields, manage byproduct streams, and boost throughput without risking purity. Each adjustment comes from batch records, operator suggestions, and customer feedback—no process change occurs in a vacuum.

    For novel applications, we regularly host calls with chemists exploring new ligation chemistry or combinatorial libraries. Some request micronized versions, others high bulk density for specific handling systems. By controlling our process from raw material sourcing through finished packaging, we tailor output to genuine needs—never just to meet a list of generic specs.

    Customers Drive Our Focus on Repeatable Excellence

    Over years in business, customers taught us to focus not just on price-per-batch, but total value: predictability, consistency, and honest technical support. N-Boc-Piperidine-4-Carboxylic Acid is more than a catalog item; it’s a backbone for advanced synthesis strategies ranging from rational drug design to new material discovery. By being present in the details—from particle size uniformity to regulatory traceability—we help chemists skip trouble at the earliest stage.

    The meticulousness we apply to N-Boc-Piperidine-4-Carboxylic Acid reflects our manufacturing DNA. This isn’t about chasing commodity market shares; it’s about upholding the standards set by the most demanding researchers. That means investing in in-process controls, continuous monitoring, and relentless pursuit of feedback-driven improvements.

    Partnering for the Next Wave of Chemical Innovation

    N-Boc-Piperidine-4-Carboxylic Acid has found its way into flagship projects and early-stage explorations alike. We’ve stood with teams racing to new applications, sharing not just product, but technical insight gained from thousands of batches and hard-won lessons in the plant. The compound’s particular combination of stability, flexibility, and reactivity continues to open doors for those solving some of the most complex challenges in synthesis and discovery.

    Our experience has taught us that genuine manufacturing leads to real solutions, not just shipments. Through attention to customer-specific needs, willingness to iterate process steps, and a deep respect for both hands-on chemists and development teams, we strive to make N-Boc-Piperidine-4-Carboxylic Acid a solid foundation for tomorrow’s breakthroughs. By staying true to disciplined, expert craftsmanship at every production stage, we aim to keep earning the trust of those at the forefront of chemical innovation.