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1-Boc-(4-Benzyl)Piperazine

    • Product Name 1-Boc-(4-Benzyl)Piperazine
    • Alias 1-Boc-4-Bn-Pip
    • Einecs 642-140-8
    • 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

    613537

    Product Name 1-Boc-(4-Benzyl)Piperazine
    Molecular Formula C16H24N2O2
    Molecular Weight 276.38 g/mol
    Cas Number 119276-01-6
    Appearance White to off-white solid
    Melting Point 80-84°C
    Purity Typically >98%
    Storage Temperature 2-8°C
    Solubility Soluble in organic solvents (e.g., DCM, MeOH)
    Canonical Smiles CC(C)(C)OC(=O)N1CCN(CC1)CC2=CC=CC=C2
    Iupac Name tert-butyl 4-benzylpiperazine-1-carboxylate
    Synonyms Boc-4-benzylpiperazine

    As an accredited 1-Boc-(4-Benzyl)Piperazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass vial containing 5 grams of 1-Boc-(4-Benzyl)Piperazine, labeled with product name, quantity, and safety information.
    Shipping 1-Boc-(4-Benzyl)Piperazine is shipped in tightly sealed containers under ambient conditions, protected from moisture and sunlight. Packaging complies with regulatory standards for chemical safety. Appropriate labeling and documentation are provided to ensure secure and compliant transport, with expedited options available upon request. Handle with care and in accordance with safety guidelines.
    Storage 1-Boc-(4-Benzyl)Piperazine should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon. Keep it in a cool, dry place away from light, moisture, and incompatible substances like strong acids or oxidizers. Recommended storage temperature is 2–8°C (refrigerator). Always ensure proper labeling and follow local regulations for chemical storage.
    Application of 1-Boc-(4-Benzyl)Piperazine

    Applications of 1-Boc-(4-Benzyl)Piperazine in Industrial Manufacturing

    1-Boc-(4-Benzyl)Piperazine serves as a specialized chemical intermediate applied in several industrial sectors. Below are key validated downstream applications, including industry compliance, actual usage ratios, unique integration stages, and final product examples.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers use this compound as a protective group-bearing building block in multi-step synthesis of therapeutic active pharmaceutical ingredients, particularly for small-molecule CNS drugs. The Boc protection improves handling and minimizes side reactions during N-alkylation or amide coupling stages. Dedicated API plants optimize charge-in ratios based on purity controls and specific route yields, often using direct coupling technologies under cGMP conditions. After full synthesis, purification, and deprotection, the material enables access to high-value clinical trial and commercial batch APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • EU GMP Part II for Intermediates
    • USP General Chapter <1078> for Process Validation
    • FDA 21 CFR Part 211 for finished pharmaceutical production

    Typical usage ratio

    • Ranges from 1.0–1.2 molar equivalents, adjusted based on coupling efficiency and residual reagent analysis
    • Charge-in ratio established in route scouting and validated during process scale-up
    • Adjusted to achieve >99.5% conversion and minimize byproduct formation

    Downstream process integration

    • Added during N-protection steps in stepwise or convergent synthetic routes
    • Deprotected after key functionalization for the final API stage
    • QC monitoring through HPLC/GC for intermediate validation before further transformation

    Final product types

    • Neuroactive therapeutic APIs for CNS disorders
    • Piperazine-based small molecule drugs
    • Investigational medicinal product (IMP) APIs for Phase I–III clinical supply
    • Generic pharmaceutical intermediates for regulated markets

    2. Peptide and Peptidomimetic Synthesis

    Peptide technology companies incorporate this protected piperazine derivative in automated and manual solid-phase synthesis workflows where selective N-protection controls chain extension fidelity. The presence of both benzyl and Boc groups allows site-selective deprotection and controlled introduction of secondary amines. Engineers monitor coupling rates and impurity profiles using dedicated analytics to optimize reagent load and minimize sequence truncation. Final peptides undergo further deprotection, cleavage, and purification to meet stringent purity thresholds.

    Industry compliance standards

    • ISO 9001:2015 for peptide production process management
    • ICH Q11 guideline on drug substance development
    • American Peptide Society quality production requirements
    • Manual of Good Peptide Manufacturing Practices

    Typical usage ratio

    • 0.8–1.1 equivalents per targeted peptide coupling, determined by protected amine content
    • Adjusted based on resin loading and in-process coupling efficiency
    • Titrated to avoid excessive Boc presence in downstream deprotection

    Downstream process integration

    • Introduced during amine-protection stages prior to chain elongation
    • Retained on-resin for multidimensional solid-phase synthesis
    • Removed chemically following chain assembly before final desalting or lyophilization

    Final product types

    • Peptidomimetic research tools
    • Therapeutic peptide candidates for metabolic or oncology applications
    • Peptide reference standards for bioanalytical validation
    • Diagnostic peptides for immunoassay kits

    3. Custom Fine Chemical Manufacture for Agrochemical R&D

    Leading agrochemical research labs require this material as a route-specific key intermediate in custom synthesis of novel piperazine-based pesticide candidates. Chemists exploit its specific protective groups to access distinct structural analogs while controlling for side reactions typical in heterocyclic modifications. Raw material dosing and reaction temperature are tightly set to optimize yield to pilot-plant scale, ensuring consistent quality for subsequent structure-activity relationship assessments.

    Industry compliance standards

    • Good Laboratory Practice (GLP) for chemical synthesis
    • ISO 17025:2017 certification for analytical test methods
    • OECD Guidelines on Testing of Chemicals (for precursor safety)
    • REACH Regulation (EC) No 1907/2006 for registration of test substances

    Typical usage ratio

    • 1.05–1.15 molar equivalents, determined via lab-scale optimization and scale-up batch records
    • Adjusted to accommodate differing analog functionalizations
    • Scaled incrementally toward pilot or kilo-lab production

    Downstream process integration

    • Inserted as a precursor in route planning for heterocyclic scaffold formation
    • Applied in parallel syntheses for combinatorial analog generation
    • Handled under inert atmosphere to prevent Boc cleavage during scaling

    Final product types

    • Novel herbicide or insecticide lead candidates
    • Research-use-only screening libraries
    • Intermediate scaffolds for process development
    • Reference substances for regulatory toxicology studies

    4. Development of Functionalized Polymers for Specialty Materials

    Specialty materials producers utilize this functional piperazine derivative for synthesizing chain-modified polymers and crosslinked resins where controlled secondary amine introduction is critical. The Boc group enables programmed deprotection, permitting spatially selective functionalization along the polymer backbone. Process engineers precisely adjust monomer integration and post-polymerization modification to tune finished material characteristics such as film flexibility, surface energy, and chemical resistance for high-value technical applications.

    Industry compliance standards

    • ISO 9001 for specialty materials manufacturing
    • ASTM D638 testing for polymer mechanical properties
    • REACH Annex XVII compliance for polymer additives
    • Material Safety Data Sheet (MSDS) regulatory adherence

    Typical usage ratio

    • 2–8 wt% relative to total monomer weight, depending on desired amine density
    • Direct correlation established during formulation pilot trials
    • Final ratio balanced against mechanical property and crosslink density targets

    Downstream process integration

    • Pre-mixed into polymer feedstocks prior to polymerization
    • Deprotected post-polymerization for site-specific reaction and crosslinking
    • Quality checked for uniformity in amine group distribution

    Final product types

    • Crosslinked thermoplastic elastomers
    • Functional coatings for electronics or medical devices
    • Amine-reactive adhesives
    • Engineered membranes for separation technologies
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    Certification & Compliance
    More Introduction

    Introducing 1-Boc-(4-Benzyl)Piperazine: Insights From the Manufacturer’s Lab

    A Closer Look at Modern Piperazine Derivatives

    For quite a few years, the family of substituted piperazines has shaped both the pharmaceutical and chemical synthesis worlds. Our team has built up a solid foundation in producing these compounds by working directly with clients in pharmaceuticals, agrochemicals, and advanced materials, focusing depth on quality and reliability. Among all the analogs we handle, 1-Boc-(4-Benzyl)Piperazine stands out for its combination of dependable performance and adaptable protection chemistry. Over countless batches, direct hands-on laboratory work has pointed to tangible differences between this molecule and more common piperazine derivatives.

    What Makes 1-Boc-(4-Benzyl)Piperazine Unique?

    This compound falls into a class of N-protected piperazines. The presence of the tert-butoxycarbonyl (Boc) protecting group at the first nitrogen, paired with benzyl substitution at the fourth position, offers practical value during complex synthetic routes. As chemical manufacturers, we care about more than just its chemical structure. Day-to-day production experience shows the Boc group provides a robust buffer against harsh conditions. It allows modern medicinal chemistry groups to approach difficult transformations with a sturdier intermediate, lowering risk during scale-up or process transfer.

    The benzyl group adds another level of selectivity, helping researchers target transformations that would otherwise be messy or challenging. Through years of pilot runs and custom syntheses, it’s become clear that this specific arrangement of Boc and benzyl substituents creates a chemical “handle” for selective deprotection, functionalization, and downstream modifications. Outside industry settings, these subtleties can get lost in product catalogues but stand out when scaling up in real-world manufacturing.

    Practical Experience From Scaled Production

    Manufacturing 1-Boc-(4-Benzyl)Piperazine at scale offers specific insights. We refine every batch and control purification steps using in-house protocols designed for tight specifications. Through hundreds of kilograms of routine and custom orders, we’ve seen first-hand that the stability of this molecule surpasses many comparable building blocks. It tolerates changes in temperature, agitation, and solvent composition better than most N-protected piperazine derivatives we’ve handled, reducing loss and speeding up batch transitions.

    The practical implications are hard to overstate. Waste minimization, cost control, and batch-to-batch consistency stem from chemical robustness. Each campaign teaches us more about the limits and resilience of this compound—a feedback loop that allows us to improve production design and troubleshoot quickly.

    Model and Physical Specifications

    Our routine output of 1-Boc-(4-Benzyl)Piperazine centers on a crystalline white powder, featuring strong handling characteristics and low tendency to absorb atmospheric moisture. Melting point observations remain tight and predictable between 84-87°C, depending on solvent regime during final crystallization. The most common purities approach or reach 99% by HPLC, with minor trace byproducts systematically eliminated by in-lab recrystallization and solvent washing steps. Packing in double-lined, moisture-resistant containers avoids caking and preserves the powder’s free-flowing nature.

    Every shipment includes full certificate of analysis reflecting not only basic purity but also NMR/IR spectra and trace metal content data, evidence of residual solvent titers, and, if requested, GC-MS quantitation. The consistency of the physical characteristics—bright, fine crystal, low lumping—stems from hands-on experience rather than just adherence to written procedures. Our process operators have learned to spot subtle signs of process drift and can adjust real-time for better outcomes.

    Applications in Drug Discovery and Beyond

    Across the world’s R&D pipelines, pharmaceutical scientists and chemists rely on smart intermediate choices. The structural features of 1-Boc-(4-Benzyl)Piperazine invite creative use in custom libraries and lead optimization—its dual protection allows selective construction of complex heterocyclic scaffolds. Anyone grinding through multi-step syntheses knows the pain of incomplete deprotection or cross-reactivity; this is often where our product finds value.

    Process chemists building bulk APIs lean on its stability when moving between protection/deprotection cycles. With Boc and benzyl both removable under well-documented, orthogonal conditions, the molecule slots naturally into modular synthesis plans. The Boc group comes off under acidic conditions without disrupting benzyl—meanwhile, benzyl cleavage under hydrogenolysis proceeds cleanly, leaving Boc intact. These patterns shorten purification steps and sidestep undesired byproducts.

    Analogs without this dual protection sometimes demand more sideline purification, costlier reagents, or introduce longer timelines. By getting both selectivity and stability in one intermediate, downstream timelines shrink and more experiments move forward at once. It is this blend of one-pot utility and compatibility with high-throughput chemistries that anchors much of the demand.

    Outside pharmaceuticals, custom materials companies have come to us for the controlled reactivity this compound enables. Advanced materials sometimes call for multiple functional groups added one by one— the dual-protected piperazine backbone lets researchers tease apart highly specific modifications within a planned sequence, while keeping the rest of the molecule untouched.

    Differences From Other Piperazine Derivatives

    Having manufactured both standard piperazine and its myriad analogs — mono-protected, di-protected, N-alkylated, and variously substituted—allows us to spot where 1-Boc-(4-Benzyl)Piperazine outshines or falls short compared with its siblings. Boc alone on piperazines yields good protection, but reactivity at the fourth nitrogen position can still drag in impurities or oxidize under process conditions. With the benzyl in place, the path to high-purity, mono-removable products gets much smoother.

    Manufacturing standard N-Boc-piperazine, we find more instability during shipment and more traps during crystallization. Similarly, benzyl-only protection creates a product with certain vulnerabilities: rapid oxidative discoloration, challenging work-up, or shortened shelf life. With 1-Boc-(4-Benzyl)Piperazine, we've seen fewer off-odors and a resistance to both ambient oxygen and light after packing.

    There are trade-offs. Some downstream chemistries require unprotected nitrogens; for these cases, our customers opt for basic (unsubstituted) piperazine or N-monoalkyl derivatives. Dual protection, as found here, is not an automatic upgrade for every synthetic plan—only for those stages demanding maximal selectivity and minimum reactivity elsewhere on the core.

    Compared to sulfonyl-protected or carbamoyl-protected piperazines, Boc-benzyl stands out due to the ease of switching between orthogonal protective strategies. In selective hydrogenolysis or strong acid deprotection scenarios, residues stay low and downstream filtration or extraction steps go faster with this product than with many alternatives. Our plant operators and customers alike have noticed the drop in chromatographic artifact levels across a series of tests.

    Meeting High Standards: Safety and Purity

    Our site adheres closely to environmental and regulatory safeguards, both out of duty and self-interest. Many of our steps use only low-impact solvents, recycling whenever possible, and we monitor each operation for byproduct generation. Regular training keeps everyone up-to-date not only with regulatory shifts but with best practices learned from daily plant operations. As a result, every container of 1-Boc-(4-Benzyl)Piperazine leaving our facility meets tight in-house and third-party requirements for purity, contaminant control, and trace residue levels.

    For specialty research or pilot-scale production, we remain open to custom processing. With clients sometimes requesting tighter specs, smaller or larger lots, or tailored purification regimes, we lean on our lab knowledge rather than defaulting to standard runs. These adaptations draw directly from past campaigns and real-world trial outcomes, building on mistakes and victories from earlier efforts.

    Supply Reliability and Customer-Focused Support

    Consistent quality isn’t an abstract promise to us. Each plant operator, QC chemist, and shipment coordinator bears direct responsibility for checking, double-checking, and logging each run. If a client’s route calls for bulk shipments or unique pack sizes, these are managed in close collaboration, drawing on our warehouse and logistics experience.

    Recurring projects show where shipment cycles can improve—adjusting for seasonal shipping temperatures, moisture challenges mid-transport, or regional regulatory preferences on packing and labeling. Tracking lot-by-lot stability in the hands of researchers around the globe provides insight few resellers capture. Frontline feedback from process chemists and scientists helps us update storage advice and packaging materials, reducing waste and spoilage over time.

    We don’t outsource support on technical issues. If a research scientist encounters a solubility puzzle or step failure using our product, our chemists talk with them directly, pinning down the point in the route where things went sideways. Trust develops when troubleshooting is collaborative, not transactional, and it’s a cycle that returns value not only to the client but also to our future manufacturing strategies.

    Troubleshooting, Continuous Improvement, and Sustainability

    Chemical manufacturing isn’t just about cranking out product—it means a willingness to re-examine standard procedures and adapt them. Over the years, iterative process tweaks—from minor temperature or solvent shifts to overhauling drying equipment—have pushed our output of 1-Boc-(4-Benzyl)Piperazine toward higher yields and lower impurity profiles. Line operators and chemists meet often to review campaign outcomes and address root causes of deviation, leaning on both recorded parameters and firsthand observations.

    On the environmental front, our experience shows solvents matter as much as the core chemistry. We favor recyclable and lower-toxicity solvents, especially as regulatory rules get tighter and customers demand higher environmental transparency. Our waste streams for Boc- and benzyl-related byproducts undergo close scrutiny. Investments in solvent recovery and emissions reduction have forced us to pay closer attention to fine points of process timing and waste segregation, cutting costs and shrinking our environmental impact.

    Continuous improvement does not stop with plant operations. By listening to clients, keeping tabs on global sourcing and price trends for critical reagents, and responding to unexpected shifts—be they regulatory or scientific—we’ve held steady supply lines and predictable costs. This kind of real-time adaptation would not work without a culture of openness and shared problem-solving, both among plant staff and in client interactions.

    Supporting Modern Research and Scale-Up

    In the vast and fast-changing world of chemical research, 1-Boc-(4-Benzyl)Piperazine delivers tangible value where selective protection, operational stability, and downstream adaptability matter. Each lot, shaped by targeted feedback as much as by SOP, provides a reliable foundation for researchers confronting ever-tighter timelines and slimmer margins for error.

    Our journey manufacturing this compound has taught us that descriptions in catalogues or datasets say little about the day-to-day realities of real-world synthesis. Ongoing investment in more robust purification, flexible loadout, and hands-on troubleshooting keeps elevating the utility of what might otherwise seem a simple reagent.

    For every researcher facing a tricky step in a new synthetic route or every plant technologist recalibrating a process, the qualities intrinsic to 1-Boc-(4-Benzyl)Piperazine—backed by years of plant experience—provide peace of mind, chemical resilience, and a little room for creativity. We look forward to learning from each project and continuing to refine our craft, one batch at a time.