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1-Boc-3-Benzylpiperazine

    • Product Name 1-Boc-3-Benzylpiperazine
    • Alias 1-(tert-Butoxycarbonyl)-3-benzylpiperazine
    • Einecs 697-804-4
    • 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

    816689

    Compound Name 1-Boc-3-Benzylpiperazine
    Cas Number 104324-72-9
    Molecular Formula C16H24N2O2
    Molecular Weight 276.38
    Appearance White to off-white solid
    Melting Point 65-69°C
    Solubility Soluble in organic solvents like dichloromethane, methanol
    Density 1.13 g/cm3 (approximate)
    Storage Conditions Store at 2-8°C, protect from moisture
    Iupac Name tert-Butyl 4-benzylpiperazine-1-carboxylate
    Synonyms N-Boc-3-benzylpiperazine
    Smiles CC(C)(C)OC(=O)N1CCN(CC1)CC2=CC=CC=C2
    Purity Typically ≥97%
    Usage Intermediate in pharmaceutical synthesis

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

    Packing & Storage
    Packing White crystalline powder supplied in a 25-gram sealed amber glass bottle, labeled with chemical name, quantity, handling, and safety information.
    Shipping 1-Boc-3-Benzylpiperazine is carefully packaged in sealed containers to prevent contamination and moisture ingress. It is shipped in compliance with relevant chemical transport regulations, including labeling and documentation. Delivery is typically through specialized couriers, ensuring safe and prompt arrival, with temperature and handling controls as required for chemical stability and safety.
    Storage 1-Boc-3-Benzylpiperazine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. Protect it from moisture and incompatible substances such as strong acids and oxidizers. Store at room temperature and ensure proper chemical labeling. Handle under a fume hood and follow local safety regulations.
    Application of 1-Boc-3-Benzylpiperazine

    Applications of 1-Boc-3-Benzylpiperazine in Industrial Manufacturing

    1-Boc-3-Benzylpiperazine serves as a precise intermediate in advanced chemical synthesis. Our large-scale manufacturing focuses on supplying this material with high purity and strict batch-to-batch consistency. Below, we outline major downstream application arenas, each defined by unique process requirements, compliance standards, and final product endpoints.

    1. Pharmaceutical Intermediate for Piperazine-Derived API Synthesis

    Originating as a core intermediate in the pharmaceutical supply chain, 1-Boc-3-Benzylpiperazine enters multi-step syntheses of central nervous system (CNS) drug candidates, antiemetics, and antihistaminics. It supports structural protection for the piperazine ring during complex transformations, enabling precise N-deprotection in the final synthetic stage. Consistent assay and low impurity profiles reduce purification demand for API manufacturers undertaking commercial-scale production according to cGMP standards.

    Industry compliance standards

    • ICH Q7/Q11, Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (cGMP for finished pharmaceuticals)
    • EU Regulation (EC) No 1907/2006 REACH registration
    • USP, EP, JP pharmacopoeia references for intermediate substances

    Typical usage ratio

    • Feed ratio of 1.0–1.2 molar equivalent per target API intermediate, depending on desired piperazine transformation
    • Adjusted based on number and type of N-alkylation or N-arylation steps downstream

    Downstream process integration

    • Step-in reagent for the initial piperazine protection stage before functional modifications
    • Deprotection proceeds before final coupling steps to afford active pharmaceutical compounds
    • Integrated into continuous flow and batch reactor systems for API building block supply

    Final product types

    • Antipsychotics (e.g. aripiprazole intermediates)
    • Antiemetic agents
    • Antihistamines based on piperazine scaffolds
    • Piperazine-functionalized peptidomimetics

    2. Fine Chemical Synthesis in Agrochemical R&D

    Manufacturers engaged in crop protection chemistry use 1-Boc-3-Benzylpiperazine as a protective group intermediate for developing new-generation fungicides and insecticidal leads. Its structural features support N-protection and controlled de-benzylation pathways, facilitating scaffold exploration and analog library synthesis. Large-scale production ensures consistent supply for both pilot scale and industrial validation batches.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 Quality Management Systems in chemical synthesis
    • EU CLP (EC No. 1272/2008), Globally Harmonised System (GHS) for labelling and transport
    • National pesticide residue regulations (e.g. EPA, EU MRLs for synthesis inputs)

    Typical usage ratio

    • 0.8–1.1 molar equivalent per piperazine-based agrochemical intermediate
    • Adjusted by substitution pattern and extent of scaffold diversification in R&D pipelines

    Downstream process integration

    • Starting material for Boc-protection step in multi-step heterocyclic assembly
    • Intermediate N-debenzylation and cross-coupling reactions to generate bioactive screening compounds
    • Incorporated in combinatorial library assembly for lead optimization

    Final product types

    • Piperazine-derived experimental fungicides
    • Insecticidal scaffold libraries for field efficacy trials
    • Lead molecules in seed treatment and crop enhancement segments
    • Agrochemical R&D reference standards for analytical method development

    3. Peptide and Peptidomimetic Synthesis for Bioconjugates

    Research-scale and industrial peptide assembly facilities incorporate 1-Boc-3-Benzylpiperazine as a selective nitrogen protecting group when introducing non-canonical amino moieties into bioactive conjugates. Its stable Boc functionality ensures seamless protection during solid-phase and solution-phase peptide syntheses, followed by controlled N-Boc removal for downstream peptide elongation or side-chain modification. Our quality control ensures specification on residual solvents and heavy metals tailored for sensitive bioconjugate applications.

    Industry compliance standards

    • ICH Q3A/B guidances for impurities in drug substances
    • USP <1047> Good Peptide Manufacturing Practices
    • ISO 13485 for medical device bioconjugates
    • REACH pre-registration and SDS compliance for peptide raw materials

    Typical usage ratio

    • Varies from 0.9–1.0 molar equivalent per protected piperazine residue introduced
    • Frequently single-use per elongation cycle in peptide synthesis protocols

    Downstream process integration

    • Immediate loading onto resin as protected nitrogen group in SPPS instrument runs
    • Boc deprotection performed with TFA at predefined elongation cycle post-assembly
    • Controlled amidation or coupling to extend peptide backbone or side-chain structures

    Final product types

    • Bioconjugate-linker systems for ADCs (Antibody Drug Conjugates)
    • Peptide therapeutics bearing piperazine motifs
    • Diagnostic peptides for immunochemistry kits
    • Custom peptidomimetics and cyclic peptides for preclinical screening

    4. Intermediate for Novel Polymer Additives and Performance Materials

    Polymer and specialty materials firms leverage 1-Boc-3-Benzylpiperazine for introducing bulky nitrogen functional groups into polymer additive backbones and advanced cross-linkers. This intermediate supports targeted functionalization of high-performance resins, especially in applications demanding thermal stability or tailored ionic properties. Direct feedstock quality, supplied in large batches, assures uninterrupted production for downstream functional polymer synthesis processes.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems in polymer production
    • REACH Regulation (EC) No. 1907/2006 for advanced material substances
    • US EPA TSCA Inventory listing where applicable for polymer additives
    • Material safety data requirements for specialty chemicals (ANSI Z400.1/Z129.1)

    Typical usage ratio

    • 0.5–2.0 wt% as a monofunctional additive or intermediate, adjusted per polymer matrix and targeted property profile
    • Regularly optimized through pilot-scale formulation trials for balance of mechanical and ionic features

    Downstream process integration

    • Direct incorporation into monomer reactor or compounding blend for additive functionalization
    • Debenzylation or deprotection steps scheduled prior to final polymerization, depending on additive modification route
    • Used in both batch and continuous flow synthesis lines for resin upgrades

    Final product types

    • Polyamide cross-linkers for performance coatings
    • Ion-conductive additives for battery separators
    • Specialty thermoplastics for electronic encapsulation
    • Adhesive and sealant systems with elevated nitrogen content
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    Certification & Compliance
    More Introduction

    1-Boc-3-Benzylpiperazine: Practical Insights from the Manufacturer

    Genuine Performance, Direct from the Source

    Year after year, chemists in our plant work at the front edge of synthetic organic chemistry. From these benches, 1-Boc-3-Benzylpiperazine stands out as a specialty building block. Its distinct structure arises from introducing a benzyl group to the piperazine ring at position three, combined with the Boc-protecting group on the nitrogen atom. Those who understand molecular scaffolds recognize the practical advantage this brings to synthetic pathways, whether aiming for improved functional group compatibility or precise selectivity in downstream transformations. In our experience, handling and process reliability mark the difference between quality and frustration in scale-up projects. Consistency matters more than almost anything else, which is why we focus on strict batch controls and validated methods rather than generic promises.

    The Value of Reliable Specifications

    Working directly with 1-Boc-3-Benzylpiperazine, we maintain a sharp focus on purity and moisture content. Analytical data drive choices in our facility, not just to satisfy paperwork but to ensure reaction results match what process developers expect. Drawing on our years of process optimization, we typically keep purity above 98%—verified with NMR and HPLC—before releasing product. This isn’t just about hitting numbers. Impurities, especially traces of over-alkylated piperazines or excess benzyl chloride, can sabotage catalysts and downstream yields. Process engineers benefit from our efforts since they can avoid the troubleshooting headaches that come from batch inconsistency. Our practical experience shows that water content under 0.5% takes much of the risk out of moisture-sensitive coupling reactions, so that’s the level we target on every run.

    Applications—Built on Real Process Use Cases

    Medicinal chemists tell us 1-Boc-3-Benzylpiperazine brings unique benefits in constructing piperazine-based pharmacophores. The Boc group shields the nitrogen, which makes selective alkylations or acylations on the opposite end straightforward. Benzyl substitution at position three introduces both steric and electronic effects that medicinal chemists exploit to modulate receptor binding profiles in discovery programs. In peptide synthesis labs, we've seen teams use this compound for incorporating rigidified piperazine units, offering backbone conformational control. Several of our clients in pharmaceutical research leverage this intermediate to fine-tune ADMET properties. Through repeated campaigns, production chemists confirm that the protected amine avoids unwanted side reactions—especially during multistep syntheses where functional group discrimination matters. This isn’t about textbook possibilities; it’s what current project demands require in practice.

    Key Differences That Matter on Scale

    Plenty of piperazine derivatives cycle through the specialty chemicals market. Not all are created for reliability. Our 1-Boc-3-Benzylpiperazine differs from other N-protected piperazines—like N-Boc-piperazine or N-Boc-4-benzylpiperazine—because the benzyl group at position three subtly alters solubility, reactivity, and compatibility with common deprotection sequences. We have tested alternative protecting groups such as Fmoc and Cbz in the process lab. Boc brings a predictable cleavage profile under moderately acidic conditions, usually with TFA, and that means downstream steps finish cleaner. Labs using non-standard piperazine isomers often call us seeking troubleshooting advice when side reactions or solubility mismatches stall progress. Over time, our team has mapped out which applications gain most from the position-3 benzyl substitution. For instance, it imparts just enough steric hindrance to slow down undesired over-alkylations without choking off reaction rates. This insight comes from direct synthesis runs, not theoretical speculation.

    Handling, Storage, and Stability in the Real World

    Mcg-scale chemists and process engineers agree—no one enjoys handling powders that clump or degrade on the shelf. From decades of manufacturing batches of Boc-protected piperazines, we've optimized our storage protocols. The solid form of 1-Boc-3-Benzylpiperazine flows freely and resists agglomeration. Properly sealed, it holds up under typical warehouse conditions without yellowing or forming by-products. Once, a shipment returned due to heat exposure in transit reminded us of the compound’s stability window, so now every lot passes short-term heat stability screening before packaging. No one wants to lose time redissolving gunky, degraded intermediate. By minimizing transit degradation, we’ve cut waste and frustration on both ends.

    Feedback from Process Chemists—No Middlemen, Direct Experience

    Many process teams skip third-party intermediaries because direct support from the actual producer saves time and removes uncertainty. Our technical staff fields questions on solubility in various organic solvents, optimal deprotection conditions, and common pitfalls in scale-up. Project chemists have reported that, compared to similar derivatives lacking the benzyl group, our material dissolves more smoothly in polar aprotic solvents like DMF and DMSO, facilitating automated synthesis workflows. During collaboration with a mid-sized contract development team, we discovered that swapping other protected piperazines for our 1-Boc-3-Benzylpiperazine improved chromatographic profiles, leading to easier purification of key drug candidates. These observations flow from first-hand feedback—data we record and incorporate into production adjustments.

    Regulatory and Documentation Practices—For R&D and Beyond

    Documentation remains a constant in every regulated supply chain. Our production records, analytical certifications, and traceability documentation meet the reproducibility demands of both internal R&D and clients moving toward regulated markets. We keep full batch records available for audit or tech transfer. In our experience, efficiency in documentation directly translates to faster onboarding in collaborative research projects—nobody benefits from hidden surprises or missing certificates. For instance, recent technology transfer with a major pharma scale-up team moved twice as quickly because our manufacturing and validation record provided exactly the data needed for their Quality team review.

    Reducing the Pain Points of Custom Orders

    Not every synthesis calls for drum-scale lots. Over the years, we’ve seen project scopes shift overnight, so our operations accommodate sample orders as well as scale-up. Handling smaller batches lets us verify rapid analytical turnarounds; scaling up for larger projects, our process engineers maintain process stability to avoid batch-to-batch performance shifts. The demand for precise timelines and documentation pushes us to keep communication tight between synthesis, QC, and customer teams. More than once, a client has returned at scale-up only to request a pilot batch under new impurity thresholds—flexibility that only close coordination between manufacturing and QC can really achieve.

    Common Use Cases—Highlights from End Users

    From conversations with customers, certain trends emerge. Drug discovery groups appreciate how protective Boc chemistry enables divergent synthesis, letting them reactivate the nitrogen only after other steps finish. The benzyl group at position three offers new vectors for scaffold tuning, letting med-chem teams search for structure-activity relationships without scrambling foundational chemistry. In recent academic collaborations, we’ve seen graduate students use this compound as a well-behaved partner in carbon-carbon coupling reactions, illustrating the balance between reactivity and selectivity. Biotech firms advancing peptide-based therapeutics deploy our 1-Boc-3-Benzylpiperazine for rigidifying target molecules—results that translate directly into late-stage preclinical leads. Across these cases, the product’s performance in hands-on chemistry forms the main narrative.

    Longevity and Consistency—Cornerstones of Supplier Trust

    We’ve heard too many stories about one-off lots or “lab bench only” material arriving with surprise impurities or mixed-phase content. Reproducibility cannot hinge on luck. Our raw material sourcing, synthetic route selection, and recrystallization protocols all result from direct, ongoing use. If a batch fails our internal testing, it never leaves the site. Teams in pharmaceutical process development value batches that behave the same way, every time, letting them focus on innovation rather than recovery work. Our investments in process engineering stem from decades of seeing how slight deviations in process geometry, solvent selection, or timing alter final purity and yield. It’s these granular details—handled by actual process chemists and floor supervisors—that let us promise reliability not as an ideal but as an expectation grounded in practice.

    Product Improvements—Driven by User Feedback

    Every feedback message adds to our working library of process tweaks. For example, when a customer working on CNS-active ligands reported sensitivity of their downstream coupling to traces of potassium ions, we refined our post-reaction neutralization and washing steps. These details, combined with pilot run experience in our own optimization, led us to adjust both solvent system and filtration techniques—an improvement that also reduced drying times and increased batch throughput. Rather than chasing one-size-fits-all claims, we enlarge our technical capabilities to meet new requests in real time. Open communication between technical staff on both ends drives progress faster than regulatory push alone ever could.

    Suitability in High-Purity Applications

    For researchers grooming lead candidates toward the clinic, batch-to-batch consistency trumps everything. Our analytical team validates every lot with full NMR, HPLC, and mass spec data packs. We frequently discuss method validation parameters directly with client QC teams, adjusting techniques when new pharmacopoeial standards or customer SOPs require extra detail. Feedback from API process developers pointed out the need to suppress certain non-UV-active side products, so we implemented deeper LC-MS scans in routine QC. Instead of waiting for customer complaints, we combine direct lab feedback and proactive outreach to ensure our product lines meet next-generation analytical scrutiny.

    Choosing a Partner Over a Vendor

    Buying direct from a manufacturer saves headaches that often go unseen until deadlines loom. Over the years, labs have recounted struggles with resellers who couldn’t address nuanced technical questions, leading to costly delays. We keep formulation and manufacturing teams in close collaboration with customer project leads, so that answers come from colleagues who work with 1-Boc-3-Benzylpiperazine on the bench. This philosophy cuts out the finger-pointing and lets us fast-track solutions if anything seems off. When supply chains faced upheaval, our agility—backed by in-house chemistry, not trading platforms—kept projects on track where generic catalogs fell short. Those relationships, forged in actual process troubleshooting, offer value that paper specifications alone never capture.

    Responsible Manufacturing—Cleaner and Safer Every Year

    All chemical production impacts its surroundings, so over time, we have re-engineered waste reduction into each process stage. By optimizing solvent systems, we have both cut total solvent use and achieved higher yields per batch. Plant engineers now recycle several process wash streams after on-site treatment, minimizing hazardous waste transport. These improvements stem not from external certification drives, but from direct investment in our plant and people. On-site environmental staff monitor air and water regularly, giving real-time data that influence both day-to-day runs and long-term process redevelopments. Emissions cuts aren’t left to distant planning documents—our plant engineers and operators own those numbers because they see the benefits not just in compliance checks, but in smooth-running production systems and improved worker safety.

    Learning from Real-World Challenges

    One cannot predict every issue a customer will face. Our most successful improvements come when communication stays tight between lab, production, and the chemists using our products. Several years back, a customer flagged unexpected by-product formation after a supplier switch. Through discussions, we tracked the issue to a subtle difference in crystal morphology. This led us to revamp not just our crystallization step but also the drying methodology. Since adopting those changes, both our process and our customers’ have seen significant drops in downstream purification headaches. Such stories illustrate why actual manufacturing experience, not just theoretical competence, builds the base of trust between supplier and chemist.

    The Case for 1-Boc-3-Benzylpiperazine in Evolving Chemistry

    Chemical synthesis keeps advancing, but key building blocks like 1-Boc-3-Benzylpiperazine anchor much of the daily work in discovery teams, scale-up engineers, and development labs. Each lot leaving our plant carries not just a certificate, but also the cumulative attention of hands-on chemists whose livelihood depends on doing the job right. This compound distinguishes itself by offering predictable protection strategies, reliable benzyl functionalization, and a proven track record in medicinal and material chemistry advances. We do not oversell its role, but rather trust the documented success in applications ranging from fine-tuned lead optimization to advanced process R&D.

    Collaborative Progress

    Our journey with 1-Boc-3-Benzylpiperazine continues to evolve. Each partnership brings new process feedback and pushes us to refine or sometimes reinvent parts of our workflow. Everybody on the team—from synthesis chemists to packaging operators—draws on decades of collective experience for quality and innovation. We see that close communication with users fosters the most reliable results and the fastest progress toward scientific goals. Choosing a manufacturer with a vested interest in your project’s success shifts the conversation from “just supply” to real collaboration. In our daily work, this commitment shapes every batch, every shipment, and every response to the challenges that modern chemistry projects bring.