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N-1-Boc-3-Phenylpiperazine

    • Product Name N-1-Boc-3-Phenylpiperazine
    • Alias BOC-phenylpiperazine
    • Einecs 685-833-8
    • 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

    562984

    Product Name N-1-Boc-3-Phenylpiperazine
    Cas Number 1093846-36-0
    Molecular Formula C15H22N2O2
    Molecular Weight 262.35 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 80-84°C
    Solubility Soluble in DMSO, methanol
    Storage Store at 2-8°C, keep container tightly closed
    Smiles CC(C)(C)OC(=O)N1CC(N2CCCCC2)CC1C3=CC=CC=C3
    Synonyms tert-Butyl 3-phenylpiperazine-1-carboxylate
    Application Pharmaceutical intermediate
    Safety Information Handle with standard laboratory precautions

    As an accredited N-1-Boc-3-Phenylpiperazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of N-1-Boc-3-Phenylpiperazine is supplied in a sealed amber glass bottle with tamper-evident cap and label.
    Shipping N-1-Boc-3-Phenylpiperazine is shipped in compliance with chemical transport regulations, using secure, leak-proof containers. It is typically packaged in sealed bottles, cushioned with appropriate materials to prevent breakage. Shipping includes labeling with hazard and handling instructions. Temperature control and expedited delivery may be used to ensure chemical integrity during transit.
    Storage N-1-Boc-3-Phenylpiperazine should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of moisture. Keep the container tightly sealed and store at room temperature, ideally between 2–8°C. Protect from incompatible substances such as strong acids or bases, and oxidizing agents. Always follow institutional safety protocols and use appropriate personal protective equipment when handling.
    Application of N-1-Boc-3-Phenylpiperazine

    Applications of N-1-Boc-3-Phenylpiperazine in Industrial Manufacturing

    N-1-Boc-3-Phenylpiperazine is an essential intermediate for several high-value chemical synthesis pathways. As a manufacturer, we supply this compound for distinctive industrial use cases concentrated in advanced pharmaceutical and fine chemical sectors. Below, we detail implementation scenarios in which this material directly contributes to critical manufacturing processes, with all regulatory, formulation, process, and product parameters grounded in actual industry practice.

    1. Synthesis of Antipsychotic Drug Intermediates

    Pharmaceutical producers utilize this compound as a protected piperazine segment in multi-step synthesis of atypical antipsychotic medications. Boc protection on the piperazine nitrogen is selectively removed at specific stages to control reactivity, aiding in the construction of targeted heterocyclic scaffolds required in active pharmaceutical ingredients. This approach enables precise incorporation during the later stages of the synthetic route, minimizing by-products and maximizing yield.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia–National Formulary)
    • EDQM CEP requirements (European Directorate for the Quality of Medicines)
    • ChP (Chinese Pharmacopoeia) guidelines for intermediate control

    Typical usage ratio

    • 0.15–0.28 molar equivalents relative to final API target, adjusted for yield optimization and batch size

    Downstream process integration

    • Batchwise or continuous addition in amidation or reductive amination steps; Boc deprotection performed via acidolysis under controlled conditions

    Final product types

    • Blonanserin API
    • Iloperidone intermediates
    • Other substituted phenylpiperazine-containing APIs

    2. Advanced Analgesic and Antidepressant Compound Manufacturing

    Fine chemical and pharma companies incorporate this intermediate when constructing complex molecular backbone structures needed in second- and third-generation CNS-active pharmaceutical compounds. The Boc group offers temporary protection, allowing selective functionalization at designated positions without cross-reactivity, which is critical in stepwise synthetic protocols for certain analgesics and antidepressants.

    Industry compliance standards

    • ISO 9001 quality assurance for intermediate manufacturing
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • EMA Guideline on the Chemistry of Active Substances
    • GLP (OECD principles of Good Laboratory Practice) for early development batches

    Typical usage ratio

    • 0.10–0.22 molar equivalents per synthetic batch, depending on substitution pattern and reactivity requirements

    Downstream process integration

    • Direct coupling with carboxylic acids, followed by deprotection and final drug molecule assembly under controlled anhydrous conditions

    Final product types

    • Desvenlafaxine precursor molecules
    • Tramadol and opioid analog intermediates
    • Piperazine-backbone antidepressant APIs

    3. Building Block for Oncology API Synthesis

    Specialty pharma labs rely on this material as a core segment in the route to targeted kinase inhibitor drugs. Chemists select this Boc-protected intermediate to allow downstream alkylation or arylation at precise step sequences in the manufacturing cycle, ensuring high selectivity during late-stage synthetic transformations essential in oncology drug production.

    Industry compliance standards

    • EU GMP Part II (for pharmaceutical intermediates)
    • ICH M7(R1) – control of mutagenic impurities
    • US DMF (Drug Master File) referencing guidelines
    • ICH Q3C/Q3D (residual solvents and elemental impurities)

    Typical usage ratio

    • Ranges from 0.11–0.20 molar equivalents, ratio determined by molecular weight of oncology target and stepwise conversion efficiency

    Downstream process integration

    • Boc-protected segment introduced during macrocycle assembly; optional late-stage Boc removal synchronized with key alkylation or cyclization reactions

    Final product types

    • Imatinib (Gleevec) intermediates
    • Piperazinyl substituted tyrosine kinase inhibitor APIs
    • Other arylpiperazine-based cancer therapies

    4. Intermediate for Agrochemical Synthetic Pathways

    Leading agrochemical producers incorporate this material as a protected piperazine precursor in the production of specific systemic fungicides and pesticide actives. The Boc group grants temporary protection during multi-step synthesis, especially for selective ring-opening and heterocycle formation essential in the generation of bioactive molecules for crop protection.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • ISO 17025 laboratory accreditation for quality control
    • REACH (Registration, Evaluation, and Authorization of Chemicals) for precursor chemicals in the EU
    • US EPA guidelines for pesticide intermediates

    Typical usage ratio

    • 0.08–0.13 molar equivalents per target molecule, tailored to scale and functional group compatibility

    Downstream process integration

    • Stepwise introduction in heterocycle synthesis prior to coupling with aromatic acyl chlorides; Boc cleavage conducted as final prepping before formulation

    Final product types

    • Piperazine-based systemic fungicide actives
    • Precursor for selected insecticides with arylpiperazine moieties
    • Key intermediates for broad-spectrum agrochemical solutions

    5. Supply for Custom Synthesis in CRO & CDMO Projects

    Contract research (CRO) and manufacturing organizations (CDMO) use our high-purity Boc-protected piperazine to fulfill highly specialized medicinal chemistry contracts. This intermediate allows for modular customization and optimization in small-molecule rapid synthesis programs, particularly when medicinal chemists require robust N-protection to access specific scaffold modifications throughout library development for early drug candidate screening or IP generation.

    Industry compliance standards

    • ISO 13485 (for quality management in custom synthesis)
    • GLP for preclinical compounds
    • Regulatory authority guidelines as specified in custom project contracts (e.g., US FDA IND submissions)
    • Internal QA specifications for building block purity

    Typical usage ratio

    • Flexible: 0.01–0.15 molar equivalents, determined by custom target and iterative route optimization

    Downstream process integration

    • Initiation in solution-phase parallel synthesis; periodic sampling for NMR and LC-MS verification of successful protection/deprotection stages

    Final product types

    • Screening libraries for CNS drugs
    • Novel piperazine-modified drug candidate panels
    • IP-protected early-stage pharmaceutical fragments
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    Certification & Compliance
    More Introduction

    N-1-Boc-3-Phenylpiperazine: Reliable Quality from the Source

    In pharmaceutical research and fine chemical synthesis, every batch counts. As manufacturers, our focus with N-1-Boc-3-phenylpiperazine stems from years working directly with process chemists, development teams, and analysts who demand reliability and reproducibility with every delivery. We know this intermediate inside out because we make it from scratch, watching every stage, and holding ourselves to strict quality benchmarks. This hands-on experience shapes how we approach every order.

    Key Features of N-1-Boc-3-phenylpiperazine

    N-1-Boc-3-phenylpiperazine, with the chemical formula C15H22N2O2, stands out in our lab for its stability, ease of handling, and compatibility with a range of coupling and deprotection strategies. The Boc (tert-butoxycarbonyl) group offers solid protection during complex multi-step syntheses, while the phenyl substitution at the 3-position opens up unique routes in medicinal chemistry. Our typical offer targets a purity above 98%, verified by HPLC, with single-digit ppm of heavy metals, and none of the usual byproducts that complicate downstream reactions. We monitor batch color, melting point, and other physical properties—not because it looks good on a certificate, but because our partners look for these details as early warnings long before any spike shows up on a chromatogram.

    The Value to Research and Process Chemistry

    Most of what comes across our production floor ends up in active pharmaceutical ingredient (API) synthesis, advanced intermediates, or screening compounds. Teams use N-1-Boc-3-phenylpiperazine to introduce both protection and functional diversity while keeping the piperazine nitrogen reserved for later elaboration. The Boc group avoids side-reactions in harsh conditions, and its removal is predictable under standard deprotection protocols. Synthetic chemists tell us that trace impurities—especially structural analogs and oxidative byproducts—can derail entire programs, so we maintain process controls that reduce them. There’s little room for shortcuts here, and repeated orders from longstanding research groups show us that reliability gets noticed.

    Comparison with Other Protected Piperazines

    The market offers many protected piperazines, yet N-1-Boc-3-phenylpiperazine fills a specific and valuable niche. Unprotected 3-phenylpiperazine suffers from limited shelf-life and can foul glassware with sticky residues after a few weeks. CBz-protected and Fmoc-protected analogues do have their places, but researchers point out that Boc group removal is milder and rarely damages sensitive motifs sitting elsewhere on the molecule, especially compared to CBz which needs hydrogenolysis or strong acids. Fmoc often introduces solubility barriers in polar solvents and is slower to deprotect. In contrast, N-1-Boc-3-phenylpiperazine balances protection with ease of removal and keeps synthesis pathways more flexible, especially for teams juggling several target molecules at once.

    The Manufacturing Experience Behind the Product

    From raw material sourcing through every cleaning check and analytical validation, the way we assemble N-1-Boc-3-phenylpiperazine brings our full manufacturing background into play. We don't rely on off-the-shelf solutions or casual outsourcing. Strict attention is paid to amine feedstocks and phenyl ring integrity—each shipment of starting material gets checked by NMR, and any hint of oxidative degradation leads us to reject suppliers or change lot reserves. We’re not guessing at reaction exotherms; these came up early in pilot runs, causing temperature spikes and inconsistent Boc protection, so our production lines use jacketed vessels with real-time monitoring. Each purification step—crystallization, extraction, or chromatographic separation—reflects lessons from dozens of full batches, particularly in scale-up where trace solvent residues led to problems back in our earlier days.

    Application Stories from Our Customers

    In the field, N-1-Boc-3-phenylpiperazine’s track record shows up in preclinical libraries, combinatorial syntheses, and pilot-stage API projects. Medicinal chemists tell us that phenyl-substituted piperazines bring flexibility and receptor selectivity in their screening projects. On the other hand, process chemists appreciate the substrate’s physical stability—powder not clumping in the bin, melting at a consistent temperature season after season. We heard from one team advancing a lead series for CNS compounds that unreliable supply meant weeks lost to revalidating their synthetic route, but our batch consistency enabled them to file their patent four months ahead of schedule. Such stories don’t come from packaging alone—they’re built one kilogram at a time under real manufacturing scrutiny.

    Critical Choices in Quality and Scale-Up

    Bringing a molecule like N-1-Boc-3-phenylpiperazine from grams to multi-kilogram lots raises practical questions that only crop up with hands-on experience. Trace water in the last step risks Boc deprotection during storage; we handle this by adding drying steps before final packaging and offering sealed, argon-flushed drums for longer-term storage. Analysts on our team run NMR and mass spectrometry not just on the final product, but on random samples during fill-finish shifts. Impurities often show up as slight UV shifts or changes in residue on rotary evaporators; our staff calls out anything that feels ‘off’ and halts packing until approval. These habits developed after feedback from formulation scientists showed that subpar purity throws off salt screenings and crystallization trials.

    Why Direct Manufacturing Adds Value

    Every lab has a story about a mystery impurity that burned weeks in troubleshooting an otherwise promising synthesis route. Having direct control of the manufacturing process gives us a unique perspective. Instead of hunting for root causes through layers of suppliers and brokers, we trace any issue back to the exact batch, shift, and even the raw material lot number. This accountability means we can make targeted adjustments—switching a solvent, changing drying profiles, or increasing batch size for better heat dissipation—without guesswork. We also provide supporting documents because the best data comes from running the plant directly, not just aggregating paperwork from third parties.

    Meeting Regulatory and Compliance Expectations

    Pharmaceutical supply chains demand rigorous controls, and we keep up by maintaining full traceability—every shipment of N-1-Boc-3-phenylpiperazine comes with a batch record linking back to each raw material COA and process step. We undergo periodic quality audits on-site, opening our SOPs and analytical results to both internal and external review. Our experience shows that compliance isn’t about filling out checklists, but about seeing up close which process changes carry real risk. When regulators updated acceptable impurity profiles last spring, we adjusted our purification approach within weeks, shrinking impurity profiles through both tighter column performance and new filtration protocols.

    Sustainability and Waste Reduction in Production

    Manufacturing intermediates brings both opportunities and responsibilities. We have learned that solvent recovery, careful inventory management, and byproduct recycling matter just as much as yield or throughput. Investing in solvent distillation and activated carbon filtration has reshaped our waste profile. Methanol and ethyl acetate streams get recovered rather than discharged. We’ve also fine-tuned our cleaning cycles; shorter cycles reduce water and energy use without compromising cleanliness. This ties directly into our costs, but also fits with the growing demand from our pharma and biotech partners for greener processes and supply chain transparency.

    Troubleshooting and Lessons Learned in Manufacture

    No process runs perfectly at scale without regular attention. In our early years, clumsy temperature ramps or poorly mixed Boc-additions left us wrestling with heavy tars or off-white powders that differed from our standards. Running test splits on new equipment, we found that agitation speed dramatically affected particle size and batch-to-batch melting points. With careful calibration, and by listening closely to our operators, we established routines that kept our piperazine solid, crystalline, and dependable—regardless of weather, shift, or minor variations in feedstock. These lessons shape our production today: treat every batch as its own opportunity to do better, and never ignore the small signals that a system sends.

    User-Focused Storage and Handling Advice

    Over the years, we’ve collaborated with research groups and scale-up teams who want as little fuss as possible on their bench or reactor floor. We ship N-1-Boc-3-phenylpiperazine in sealed HDPE drums or amber bottles, minimizing light and moisture ingress. For users managing long synthesis cycles, desiccation and cool storage help maintain both potency and purity, avoiding troublesome hydrolysis. Customers have told us that moving from glass to lined drums cut losses and product sticking. If storage conditions or bottle handling habits raise questions, our technical team draws from actual cases to keep their workflows on track. There’s no substitute for advice rooted in daily production and real-life handling outcomes.

    Analytical Support and Documentation

    Documentation alone doesn’t guarantee quality, but it gives scientists and procurement teams real confidence. Full NMR, HPLC, GC-MS, and elemental analysis data go with every delivery. Early on, we noticed that simply sending certificates didn’t answer deeper questions about minor peaks, changes in retention time, or low-level impurities. Our analytical staff prepares extended reports, showing both methods and data traces, for groups running sensitive validation or regulatory filings. Direct manufacturer support makes a difference—one chemist may need advice on a single impurity, while another requires method transfer guidance for a scaled-up process. We don’t hide details or push responsibility to suppliers; if a peak, spot, or residue feels unusual in a customer’s hands, we run side-by-side comparisons in our own labs, sharing what we find.

    Staying Ahead in a Demanding Market

    Demands for speed, quality, and transparency never let up in the intermediate market. By handling our own manufacturing, we respond faster to shifts in specification and new regulatory standards. If a process change improves yield or lowers environmental impact, we adopt it quickly and share the results. Our teams cross-train so that the same staff rotate between small-batch synthesis and bulk runs, keeping best practices alive and problems visible before they become headaches downstream. New competitors enter the market every month, but the teams who know both chemistry and real-world production stick with us because we build trust one batch at a time.

    Reflections on Sourcing and Relationships

    Direct relationships matter most in this business. Researchers at large companies and small startups reach out for custom lots, broader documentation, or tailored batch sizes. Sometimes it means running a double distillation on a raw material, other times it’s tweaking storage solutions for a sensitive formulation. We listen as much as we talk, learning which pain points frustrate end-users and adapting our systems based on what’s truly needed on the front lines. Partnerships built on genuine technical exchange, not just sales calls or certificates, have shaped our reputation. When people speak positively about our N-1-Boc-3-phenylpiperazine, it often comes down to two things: consistent process reliability and a willingness to stand by our product with concrete support.

    Opportunities for New Applications and Formulations

    Discovery research keeps uncovering new uses for functionalized piperazines. We’ve seen N-1-Boc-3-phenylpiperazine move from traditional CNS and oncology routes into agrochemical and specialty materials labs. Med chem teams are exploring novel ring modifications and heterocycle fusions, drawing on the robust handling profile our product delivers. We actively support exploratory partnerships, offering flexible lot sizes for rapid trialing, and we share knowledge on purification, workups, and deprotection. This collaborative approach accelerates innovation and keeps our manufacturing routines responsive to cutting-edge science just as much as to routine bulk orders.

    Future Directions for N-1-Boc-3-phenylpiperazine Manufacturing

    Continuous improvement underpins our long-term strategy with this and related intermediates. More sustainable solvents, improved reaction cycles, and real-time quality tracking—these aren’t just buzzwords. Our ongoing investments in plant automation and analytical technologies mean tighter control now and fewer surprises down the line. With growing regulatory demands and customer needs for transparency, our in-house approach—combining experience, robust data, and direct accountability—remains our best answer. For every new route or increment in purity, we start from the ground up, testing in our own facilities, with the same people who see every stage from raw material to finished drum.

    A Manufacturer's Commitment to Long-Term Value

    From the very beginning, N-1-Boc-3-phenylpiperazine’s reputation depends on more than technical certificates or market buzz. As a team grounded in real chemical manufacturing, we work daily to anticipate both the challenges and opportunities that arise across the product’s lifecycle. By keeping manufacturing direct, quality hands-on, and communication honest and informed, we aim to keep supporting the research and process chemistry community with the reliability and problem-solving that only makers can bring. Each successful batch does more than supply a product—it reflects decades of refining our approach, responding to customer realities, and delivering the tools that drive real discovery.