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1-N-Boc-2-Benzylpiperazine

    • Product Name 1-N-Boc-2-Benzylpiperazine
    • Alias N-Boc-piperazine-2-yl-benzyl
    • Einecs 609-055-5
    • 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

    995490

    Productname 1-N-Boc-2-Benzylpiperazine
    Casnumber 98597-96-9
    Molecularformula C16H24N2O2
    Molecularweight 276.37
    Appearance White to off-white solid
    Meltingpoint 77-80°C
    Purity Typically >98%
    Solubility Soluble in DMSO, slightly soluble in water
    Storageconditions Store at 2-8°C, keep container tightly closed
    Smiles CC(C)(C)OC(=O)N1CCN(CC1)CC2=CC=CC=C2
    Inchikey QXHAANLJZNSPDR-UHFFFAOYSA-N

    As an accredited 1-N-Boc-2-Benzylpiperazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 1-N-Boc-2-Benzylpiperazine (10g) comes in a sealed, amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping 1-N-Boc-2-Benzylpiperazine is shipped in secure, chemical-resistant containers to prevent exposure and contamination. The packaging complies with relevant safety and regulatory guidelines, including labeling and documentation. Temperature and transit conditions are monitored as required. Expedited delivery options are available to ensure product integrity during transport. Suitable for laboratory or research use only.
    Storage Store 1-N-Boc-2-Benzylpiperazine in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, preferably at 2–8°C (refrigerated) and away from incompatible substances like strong oxidizing agents and acids. Properly label containers and avoid prolonged exposure to air. Follow all applicable safety and regulatory guidelines for chemical storage.
    Application of 1-N-Boc-2-Benzylpiperazine

    Applications of 1-N-Boc-2-Benzylpiperazine in Industrial Manufacturing

    As a specialized manufacturer of 1-N-Boc-2-Benzylpiperazine, we supply this intermediate to clients operating in strictly regulated downstream sectors. Our material is utilized by pharmaceutical and specialty chemical producers with defined technical requirements across advanced synthesis workflows. The application scenarios below are based on direct customer validation in commercial operations.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    API manufacturers employ this compound as a protected piperazine building block during multi-step synthesis. The Boc and benzyl groups enable orthogonal deprotection strategies, allowing for complex side chain modifications and ring substitutions, particularly in CNS and anticancer API pipelines. Our material is integrated at critical stages to ensure selectivity and facilitate efficient yield optimization as required in patent-expired and pipeline NCE development.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (APIs)
    • USP/NF and EP monograph reference for final APIs

    Typical usage ratio

    • 10–25 mol% input relative to core scaffold, adjustable based on specific target molecule and protection group requirements

    Downstream process integration

    • Used in amidation, alkylation, or coupling steps as the key protected amine intermediate; deprotection occurs at a late process stage prior to final compound crystallization

    Final product types

    • Central nervous system (CNS) drug intermediates
    • Antitumor agent intermediates
    • Antiviral compound precursors
    • Other small molecule NCE intermediates

    2. Peptide Synthesis for Research and Preclinical Development

    Peptide chemistry labs and specialty contract manufacturing organizations use our protected piperazine derivative to introduce conformationally constrained or functionalized linkers into peptide chains. It enables selective incorporation at defined sequence positions, with Boc protection allowing orthogonal Fmoc/Boc strategy during solid-phase and solution-phase synthesis. This addresses stability, biological activity, and cell permeability requirements in therapeutic peptide design.

    Industry compliance standards

    • ISO 13485 (medical device peptides)
    • CFR Part 210/211 (if transitioning to cGMP)
    • ICH Q9: Quality Risk Management

    Typical usage ratio

    • 1–10% w/w per individual peptide batch; actual input depends on peptide chain length and number of modified residues

    Downstream process integration

    • Inserted during solution- or solid-phase coupling as a protected amino component; deprotection after chain elongation, followed by further derivatization or direct purification

    Final product types

    • Therapeutic and diagnostic peptide APIs
    • Peptide receptor ligands for research
    • Preclinical peptide candidates
    • Bioactive peptide tool compounds

    3. Advanced Heterocyclic Building Block for Agrochemical R&D

    Agrochemical innovators leverage our compound to build functionalized piperazine motifs in experimental crop protection agents, veterinary drugs, and plant growth regulators. Its dual protection enables rapid modification of molecular scaffolds to evaluate structure-activity relationship (SAR) in lead optimization. Typical integration occurs at the protected amine incorporation stage for synthesis of novel heterocycles.

    Industry compliance standards

    • OECD GLP (Good Laboratory Practice) for agrochemical research
    • ISO 17025 for analytical verification
    • Relevant EPA or EFSA guidance in later development phases

    Typical usage ratio

    • Usually 3–15 mol% based on the desired substitution level in the agrochemical molecule; varies with crop protection class and regulatory data package

    Downstream process integration

    • Introduced during heterocycle core assembly, often via nucleophilic aromatic substitution or amidation, followed by demasking for final product derivatization

    Final product types

    • Experimental fungicide lead compounds
    • Herbicide SAR derivatives
    • Insecticide research intermediates
    • Veterinary anthelmintic or antiparasitic precursors

    4. Functional Intermediate in Specialty Polymer Modifier Synthesis

    Specialty polymer producers incorporate our protected piperazine unit as a monomer or crosslinking precursor to engineer advanced polymeric materials, especially for biomedical coatings, drug delivery systems, and select functional membranes. The protected structure prevents unwanted reactivity during polymerization, permitting targeted deprotection or post-functionalization to introduce controlled amine sites for crosslinking, immobilization, or drug conjugation.

    Industry compliance standards

    • USP Class VI materials certification (for medical devices and coatings)
    • ISO 10993 biocompatibility requirements
    • REACH registration (in EU)

    Typical usage ratio

    • Ranges from 0.5–5 mol% of total monomer input, determined according to desired surface functionality or crosslink density in the final polymer

    Downstream process integration

    • Employed as a comonomer or chain extender during prepolymer mixing; deprotection and further reaction or immobilization performed as post-polymerization modification step

    Final product types

    • Biocompatible hydrogel coatings
    • Controlled-release drug delivery matrix
    • Functionalized medical device films
    • Selective biosensor membrane substrates
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 1-N-Boc-2-Benzylpiperazine: Reliable Quality from Direct Synthesis

    Our Commitment to Precision Manufacturing

    Long hours in the lab shape quality chemicals. At our facilities, we do not just bottle intermediates; we monitor every step, from raw materials to the final dry product. For 1-N-Boc-2-Benzylpiperazine, control means accuracy with assay, impurity profiling, and traceability. We synthesize this compound directly, holding ourselves accountable at every reactor stage. That’s how our chemists keep consistency from batch to batch.

    Every lot we release meets a narrow range for color, solubility, particle form, and content. We tune our process and document these controls. We catch subtle changes in crystal habit and yield adjustments and fine-tune to avoid excess by-products. Our equipment has seen plenty of similar piperazine derivatives, and the adjustments needed for this molecule are second nature to our process engineers.

    Key Characteristics and Why They Matter

    1-N-Boc-2-Benzylpiperazine stands out structurally for its balance of protection and reactivity. The N-Boc group shields the piperazine nitrogen, keeping reactions selective at other functional points. This design helps with downstream transformations in API labs or advanced intermediate projects. The benzyl group, attached at the 2-position, opens synthetic pathways unachievable by simple piperazines or unprotected analogs.

    Our expertise comes from years of refining tert-butyloxycarbonyl (Boc) protection protocols. Boc protection improves storage stability, making this compound robust under ambient warehouse conditions. Benzylation brings another layer, so this compound targets a distinct set of end-uses. For example, in pharmaceutical routes aiming at CNS-active targets, the combination enables stepwise deprotection and specific coupling reactions. A lab using this compound can rely on its clean separation in silica-based purification and predictable performance in multi-step synthesis.

    Specification Meets Purpose: What Laboratories Expect

    Model and batch details matter to synthetic chemists. Each batch receives full HPLC and NMR data, not mere summary certificates. Verification reports highlight absence of common side-products (for example, dibenzyl or deprotected residues). Purity runs above 98%, measured by multiple detectors. The crystalline product arrives as a stable white to off-white powder, clump-free for easy handling. Our solvent choices during workup and crystallization avoid undesirable residues—acetonitrile, dichloromethane, and ethyl acetate protocols bring out the cleanest finish.

    We package the compound to minimize atmospheric moisture or acid ingress. One of our process chemists found early on that Boc groups break down if humidity sneaks in, so all fill and seal operations happen in controlled atmospheres. Each unit carries batch labels matched to our production history, allowing quick tracking for any issue, no matter how rare.

    Using 1-N-Boc-2-Benzylpiperazine in Synthesis

    This piperazine variant enters the scene where complexity and selectivity meet. Research teams use it as a key protected amine intermediate, especially when multiple downstream steps depend on orthogonal protection. The Boc group can be removed under mild acidic conditions, letting chemists access free amine at will. The benzyl group, stable during most hydrogenation or oxidative steps, serves both as a synthetic handle and a masking group through several transformations.

    We watched (and guided) teams as they used our product for peptide coupling, heterocyclic construction, as well as assembling active pharmaceutical ingredient (API) side chains. Repeat feedback from partner labs says the product’s dryness, reactivity, and handling save hours over bulk intermediates from less consistent sources. Side reactions leading to Boc hydrolysis or benzyl migration have remained below detectable levels in our monitored uses.

    Those building advanced intermediates for CNS-targeted drugs or chemistries reliant on protected secondary amines reach for this compound. It fits cleanly into most solid and solution-phase workflows. Our batch notes show standard cleavage with TFA systems, and coupling partners such as acid chlorides or NHS esters react without fouling.

    Differences from Other Piperazine Derivatives

    Chemists familiar with the quirks of piperazine chemistry appreciate subtle differences. Unprotected 2-benzylpiperazine often suffers from poor selectivity and susceptibility to over-alkylation. With only a Boc group, 1-N-Boc-piperazine retains flexibility but lacks the reactivity shield and synthetic anchor that the benzyl group offers.

    1-N-Boc-2-Benzylpiperazine fills a middle ground. The Boc group protects the primary amine for later unveiling, while the benzyl group adds both steric and electronic influences. This dual modification changes reactivity patterns: electrophilic substitutions now run cleaner, fewer ring alkylations derail the sequence, and purification lines up for easy chromatography. Product loss from side-reactions drops when the right protecting groups stand in the right places.

    In peptide and drug intermediate chemistry, these two protections cut out the guesswork. Synthesis requires control, and the right intermediate leads to fewer impure fractions, easier scale-up, and consistent downstream performance. Even small shifts in protecting group stability can derail a multi-step API campaign—something we learned after much trial with analogs featuring weaker carbamate groups or more labile benzylic substitutions.

    Our Experience and the Value of Operator Insight

    Making and refining 1-N-Boc-2-Benzylpiperazine isn’t just about following recipes. Over years, our shift leaders caught patterns in filtration speed, temperature sensitivity, moisture management, and product aging. Early batches aged prematurely—now, every filling line worker checks for micro-clumping and packages each unit with desiccant. These details seem small until you see rejected material or an irate customer with unduly hygroscopic powder.

    Technical feedback doesn’t vanish into a black hole. Each time a partner reported an unexpected impurity or sluggish reactivity, our process supervisors traced the batch, ran spot checks, and sometimes adjusted wash cycles or phase-separation steps. The aim: a uniform, reliable intermediate for both bench-scale methods and large-scale runs. Every tweak, from the order in which solvents contact the oil to the centrifugal filter settings, echoes through the process and final product quality.

    Labs using this compound run critical reactions, some under hurry or regulatory clock. That sense of urgency matches how we keep our schedules, raw material check-ins, and supply commits. Synthesis never happens in a vacuum; downstream consequences ripple from oversights upstream. We’ve found that avoiding short-cuts, keeping process notes open, and cross-checking all TLC and spectral data gives the confidence that no surprises hit our customers.

    Sourcing Directly from the Manufacturer: Why it Matters

    Direct supply brings the opportunity for feedback loops—a distributor rarely tracks back to the person at the reactor, but we do. Unusual requests, like custom purity checks or alternate packing, find us ready to explore and deliver. If a lab discovers an anomaly, they bypass customer service channels and interact with our chemists who know precisely how each lot was made.

    This link goes beyond shipping boxes. Technical support draws on lived process data, not textbook summaries. Sourcing straight from our plant avoids relabeling, storage ambiguities, or unknown cross-contamination risks. Each order ships from one line, with no intermediate stops, keeping shelf-life fresh and handling events transparent.

    Partnership with research or API divisions means tailoring output for actual customer chemistry. If pilot plants need bulk lots—our reactors are sized to flex up within lead time windows. Smaller R&D teams get their allotments packed and dispatched fast, with individual mockups and reserve batches if method development falters. The back-and-forth between plant and customer improves outcomes on both sides.

    Addressing Common Issues and Solutions

    Problems arise in every synthesis operation. Years back, we ran into bottlenecks with Boc group instability on hot, humid days. A series of solvent swaps and air curtain installations handled the problem at the packing line. Another recurrent issue involves trace by-products from side-reactions at the benzyl position. We mitigated those spikes by extending phase separations and fine-tuning crystallization temperature windows.

    Our approach includes real-time process oversight—inline NMR and HPLC checks catch deviations early. Operators keep logs during each batch, not just at lab QC. This vigilance cut down complaints, improved lot reproducibility, and raised on-time shipment ratings. Our aim centers on catch and fix, not defer and explain.

    Occasionally, end users request custom specification tweaks, such as minimal particle sizing or higher thresholds on residual solvents. We tailor process steps at the lot level, avoiding late-stage surprises. Our staff keeps open files with development teams to make sure scaling up doesn’t upend original lab results. If a customer sees insolubility during scale-up, our chemists walk through process variables, sometimes recommending alternate workups. This technical dialog minimizes waste and turns mistakes into improvements.

    Why Reliable Sourcing Supports Better R&D Outcomes

    R&D workflows depend on supply chains that hold up under stress. A missed shipment or batch recall hits productivity hard in any lab, and odd performance from an intermediate eats budgets and deadlines. By managing synthesis and supply end-to-end, we offer more than a chemical; we offer actual process stability.

    Researchers using 1-N-Boc-2-Benzylpiperazine benefit from predictable results, whether running small exploratory reactions or longer campaigns. Reliable performance comes from tight batch control and from people on the floor who understand where errors sneak in. Handling and delivery also impacts success—dust-free filling, tamper-evident packaging, and carefully staged shipments mean the intermediate arrives just as intended, every time.

    Our iterative improvements stem straight from operator and customer feedback. Process adaptation, line upgrades, tighter drying cycles, and packaging tweaks all happened for concrete supply or usage reasons, not arbitrary targets. Trust in the supply source feeds trust in resulting data and commercial outcomes.

    Supporting Environmental and Regulatory Obligations in Manufacturing

    We recognize modern synthesis carries ecological and compliance responsibilities. Over years, solvent choices have shifted away from more hazardous options—our refinement now uses fewer liters of dichloromethane and replaces parts of the workup with ethyl acetate. Recycling protocols pull more solvent from mother liquors and waste, and emissions controls meet both local and international limits. Waste water from the process leaves the plant only after full treatment and testing, not just dilution.

    Shipping hazardous intermediates introduces further compliance requirements. Our outgoing logistics paperwork reflects not just international shipping codes, but also full traceability. Each order includes documentation linking batch results to in-plant QC, and MSDS paperwork offers practical guidance to storage and handling. Inspection logs are open on each order’s request, reinforcing transparency.

    Continuous Process Improvement and Future Directions

    Manufacturing never sits still. Each cycle reveals inefficiencies, unseen loss points, or rare deviations. Process chemists, in-house analysts, and line techs hold weekly reviews to address quality data and flag any chronic drifts. New reactor monitoring, improved drying infrastructure, and better in-line analytics strengthen every new batch of 1-N-Boc-2-Benzylpiperazine.

    Customer input drives much development. Regular dialogue about problems in use, appearance, or reactivity pushes us to test and refine. The goal stands: a high-performing intermediate, delivered quickly, and ready for its next transformation.

    Summary Insights

    Years working as a manufacturer—rather than a trader or middleman—gave us technical depth and pride in delivering reliable 1-N-Boc-2-Benzylpiperazine. Each batch draws on lessons learned, attention to process, and open relationships with partner labs. Our product supports modern research and commercial campaigns, reflecting a real respect for experimental needs, end-use chemistry, and accountable production.