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4-Cbz-Piperazine-2-Carboxylate Methyl Ester

    • Product Name 4-Cbz-Piperazine-2-Carboxylate Methyl Ester
    • Alias MCULE-3421568565
    • Einecs 666-141-1
    • 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

    994246

    Chemical Name 4-Cbz-Piperazine-2-Carboxylate Methyl Ester
    Cas Number 1416457-08-9
    Molecular Formula C16H20N2O4
    Molecular Weight 304.34
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Storage Temperature 2-8°C
    Synonyms Methyl 4-(benzyloxycarbonyl)piperazine-2-carboxylate
    Smiles COC(=O)N1CCN(CC1)C(=O)OCc2ccccc2
    Inchi Key SSZTXRQHHMKCIC-UHFFFAOYSA-N

    As an accredited 4-Cbz-Piperazine-2-Carboxylate Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 4-Cbz-Piperazine-2-Carboxylate Methyl Ester; labeled with product details and safety information.
    Shipping 4-Cbz-Piperazine-2-Carboxylate Methyl Ester is shipped in tightly sealed, chemical-resistant containers under ambient conditions. It is classified as a non-hazardous substance for transport. The package is labeled according to regulatory guidelines and accompanied by a Safety Data Sheet (SDS). Appropriate cushioning is used to protect against physical damage during transit.
    Storage 4-Cbz-Piperazine-2-Carboxylate Methyl Ester should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area. Keep away from incompatible materials such as strong oxidizers. Store at room temperature, ideally between 2–8°C. Ensure proper labeling and access is restricted to authorized personnel to prevent accidental exposure or contamination.
    Application of 4-Cbz-Piperazine-2-Carboxylate Methyl Ester

    Applications of 4-Cbz-Piperazine-2-Carboxylate Methyl Ester in Industrial Manufacturing

    As a direct manufacturer of 4-Cbz-Piperazine-2-Carboxylate Methyl Ester, we supply this advanced chemical intermediate for precise industrial uses, supported by strict quality control and technical data transparency. The following sections detail principal downstream applications with specific compliance, formulation, integration points, and finished product types based on actual market practices.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Piperazine-Containing Drugs

    Pharmaceutical companies require this intermediate for the targeted synthesis of piperazine derivatives, frequently found in antihistamines, anxiolytics, and antipsychotic agents. Production lines typically use this material as a key nucleophilic building block to construct drug cores with enhanced metabolic stability. QC labs monitor residual unreacted ester and Cbz protection removal efficiency to meet batch release specifications.

    Industry compliance standards

    • International Conference on Harmonisation (ICH Q7) for API manufacturing
    • Current Good Manufacturing Practice (cGMP) regulations (21 CFR Part 210/211, US FDA)
    • European Pharmacopoeia and United States Pharmacopoeia monographs for related substances and impurities (Ph. Eur., USP)
    • ICH Q3A/Q3C for impurity profile and solvent residuals

    Typical usage ratio

    • Employed at 1.0 to 2.5 molar equivalents relative to primary amine reactants
    • Adjusted according to downstream alkylation or acylation steps and impurity formation risk

    Downstream process integration

    • Added after initial nucleophilic ring opening to facilitate core structure assembly
    • Debenzylation and ester hydrolysis performed in late-stage API assembly
    • Purification through repeated crystallization or preparative HPLC post-reaction

    Final product types

    • Quetiapine, aripiprazole, and related piperazine-based antipsychotic agents
    • Hydroxyzine-class antihistamines and derivatives containing substituted piperazines
    • Clinical-stage CNS and oncology API candidates with piperazine motifs

    2. Peptide Synthesis Intermediates

    Peptide, peptidomimetic, and oligopeptide manufacturers use this protected piperazine intermediate to introduce custom N-terminal modifications in solid-phase peptide synthesis (SPPS). Its Cbz-protecting group ensures selectivity during chain elongation, preventing unwanted cross-reactions and ensuring high purity in synthetic peptides intended for therapeutics and diagnostics.

    Industry compliance standards

    • FDA 21 CFR §210-211 for peptide drug manufacturing
    • GMP standards for peptide synthesis (PIC/S PE009-16)
    • ICH Q6B for biochemical purity and analytical characterization
    • Peptide-specific quality expectations in Japanese Pharmacopoeia

    Typical usage ratio

    • Typically used at 1.0 equivalent per elongation cycle
    • May be increased to 1.2 equivalents to offset steric hindrance in difficult coupling steps

    Downstream process integration

    • Introduced during automated SPPS cycles after amine deprotection
    • CBz group retained through main chain elongation and removed in final global deprotection step
    • Rapid monitoring of coupling efficiency with HPLC and MALDI-TOF

    Final product types

    • Therapeutic peptides (e.g., piperazine-modified GnRH analogs)
    • Diagnostic peptides labeled with bioactive moieties
    • Research peptides used in target validation studies

    3. Agrochemical Intermediate Synthesis

    Crop protection manufacturers apply this material as a masked piperazine core when constructing fungicide and insecticide active ingredients. The ester and Cbz protections stabilize the piperazine ring through aggressive conditions, then are removed or transformed at designated stages to yield structurally unique pesticide molecules with improved soil stability or selective action.

    Industry compliance standards

    • ISO 9001:2015 for chemical process management
    • European Union Regulation (EC) No 1107/2009 and REACH for active substance registration
    • OECD Good Laboratory Practices (GLP) for impurity monitoring

    Typical usage ratio

    • 1.0–1.3 molar equivalents based on final fungicidal or insecticidal target structure optimization
    • Adjustments according to methyl ester reactivity and desired yield in multi-step sequences

    Downstream process integration

    • Integrates during scaffold assembly, often pre-halogenation or arylation
    • Subsequent hydrolysis and further derivatization, depending on the lead compound route
    • Final step formulation into technical-grade concentrates for field trials

    Final product types

    • Piperazine-derived triazole fungicides
    • Novel insecticidal active ingredients with enhanced environmental profiles
    • Lead compounds for next-generation crop protection agents

    4. Biopharmaceutical Building Block for Cytotoxic Conjugates

    Biologic drug manufacturers utilize this compound for constructing cytotoxic payload-linker systems in Antibody-Drug Conjugates (ADCs) and drug delivery conjugates. Its Cbz-protected piperazine scaffold offers a controlled release profile, and supports stable linkage to antibodies or polymers via amide or ester functionalization strategies.

    Industry compliance standards

    • ICH Q7 for pharmaceutical contract manufacturing of cytotoxic intermediates
    • USP <1079> and <85> for sterility and bacterial endotoxin tests
    • cGMP Annex 2 for biological API production (EU Guidelines)
    • OECD Principles of GLP for batch documentation and traceability

    Typical usage ratio

    • 0.8–1.5 molar equivalents, dependent on conjugation efficiency and target drug-antibody ratio
    • Optimized for minimal unreacted payload to maximize batch homogeneity in ADCs

    Downstream process integration

    • Coupled to cytotoxic small molecules using carbodiimide or HATU coupling reagents
    • Linker-payload system conjugated to monoclonal antibody or polymer backbone post-purification
    • Extensive in-process analytics for release kinetics and stability evaluation

    Final product types

    • Antibody-Drug Conjugates (ADC) with cleavable/non-cleavable linkers
    • Peptide-drug conjugates
    • Nanoparticle-based chemotherapeutic delivery systems

    5. Specialty Polymer Modifiers

    Specialty polymer manufacturers adopt this compound for controlled piperazine ring introduction into functional materials, such as cross-linked hydrogels, responsive membranes, or adhesive resins. The Cbz and ester groups serve as orthogonal protection during multi-step modification, facilitating post-polymerization functionalization with precise spatial orientation.

    Industry compliance standards

    • ISO 14001 for environmental management in specialty polymer production
    • ISO 10993-5 for cytotoxicity in medical device polymer matrices
    • RoHS Directive (2011/65/EU) for electronics-related polymer applications

    Typical usage ratio

    • 0.2–1.0 wt% relative to monomer mix for hydrogel or coating matrices
    • Higher rates up to 5 wt% for adhesives requiring improved crosslink density

    Downstream process integration

    • Dispersion into polymerizable mixtures before thermal or UV-induced curing
    • Deprotection and activation after base polymer structure formation via solvent washing or catalytic hydrogenation
    • Post-integration characterization by FTIR, NMR, or crosslinking density assays

    Final product types

    • Piperazine-crosslinked hydrogels for wound dressings
    • Stimuli-responsive filtration membranes
    • Structural adhesives for electronics and microfluidics
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    More Introduction

    4-Cbz-Piperazine-2-Carboxylate Methyl Ester: Practical Insights from the Source

    From Our Facility to Your Synthesis Bench

    Handling specialty chemicals every day, we take particular interest in products whose structure makes a genuine difference for research and production, not just another name in a catalog. 4-Cbz-Piperazine-2-Carboxylate Methyl Ester stands out in this respect. In our plant, we have tuned this intermediate to fit real-world demands, shaped by our own team’s hands-on work and direct feedback from chemists in both pharma development and academic spheres.

    We know the value of reliable building blocks, especially for rapid exploration in medicinal chemistry. No chemist wants delays because of batch inconsistencies or unregistered impurities. When we talk about 4-Cbz-Piperazine-2-Carboxylate Methyl Ester, we’re not simply repeating what’s in the formula—C14H18N2O4—we pay just as much attention to what our customers experience in the lab and on the production line. Our focus as actual manufacturers means we track every step, from raw material inspection to finished product analysis.

    What Sets 4-Cbz-Piperazine-2-Carboxylate Methyl Ester Apart

    The compound features a methyl ester at the 2-position of a Cbz-protected piperazine ring. This configuration catches the eye of medicinal chemists and process scientists working on piperazine derivatives, a class that recurs across diverse drug discovery projects. The methyl ester brings reactivity tailored for transesterification or hydrolysis steps, while the Cbz group offers stability, easy removal under hydrogenation, and a predictably clean deprotection path.

    In our hands, the final product comes as a white crystalline solid, with purity consistently testing above 98% by HPLC. Detailed NMR and mass spectra go out with every lot, because there’s no substitute for verifiable identity—especially when downstream processing can run into scale-up issues if early intermediates carry over residual solvents or related impurities. Our team has tightened control over solvent removal and crystallisation, to eliminate surprises that could hold up batches at our partners' facilities.

    Usage Where Precision and Consistency Matter

    You can find 4-Cbz-Piperazine-2-Carboxylate Methyl Ester in the heart of peptide synthesis, advanced intermediate libraries, and combinatorial research. Our customers depend on its clean cleavage characteristics for stepwise deprotection or for introducing carboxylate functionalities under controlled conditions. Where a piperazine backbone is required for key central nervous system therapies or as a linker in antibody-drug conjugates, this product offers a direct route.

    Labs specializing in small-molecule lead optimization value the product for making derivatives with defined protection schemes. We've seen our 4-Cbz-Piperazine-2-Carboxylate Methyl Ester picked for SAR studies, where time pressure drives the search for new activity profiles without the risk of unknown side reactions. Contract research and manufacturing organizations rely on it not just for the reactivity, but for reproducible scale-up—the methyl ester resists premature hydrolysis, and Cbz offers an orthogonal protection handle compared to Boc or Fmoc alternatives.

    The Value of Experience Over Mere Availability

    We have dealt with a flood of catalog suppliers, and we've seen the challenges when materials come from a chain of traders and resellers. Too many delays, too much paperwork, and above all, uncertainty about origin. Our plant has responded by taking product qualification beyond a checklist. Every step, from starting piperazine chemistry to purification, falls under a single roof, so we have eyes on every operation. In-process samples never leave our hands. There’s no relabeling, no third-party blending, no risk of commingling with lower-grade batches.

    We keep our standards strict—trace metals, residual solvents, and water content fall within defined limits from real world feedback. Batch records flag every deviation, and all documentation links directly to our on-site lab data—no outsourcing of quality. Every shipment includes not just a CoA, but full spectral data and stability commentary if you’re planning on storage or shipment through varying climates.

    The Real Differences: Cbz vs Other Protection Strategies

    We’ve worked with the full range of piperazine derivatives, and it’s a fact that choice of protecting group shapes both the synthetic process and the ease of scale-up. Cbz protection, in our experience, holds advantages where you want hydrogenolysis compatibility and minimal basic byproducts. The methyl ester functions as both a handle for future transformations and as a resistance point against aqueous instability. That means you can plan multi-step syntheses without complications from premature reactions or side product formation.

    Compared to Boc or Fmoc protected versions, Cbz-piperazine routes allow for lower temperature deprotection—critical when you’re working with delicate ligands or complex scaffolds. Boc routes tend to require acidolysis, which brings risk for certain acid-labile partners. Fmoc routes demand strong bases or specific non-aqueous conditions. The Cbz group avoids those pitfalls and the methyl ester gives flexibility in the downstream sequence without committing you too early to a final carboxylic acid under harsh conditions.

    Supporting the Full Spectrum: Small Scale to Bulk Production

    Our plant setup is designed not just for kilo-scale, but with modular reactors allowing controlled scale-up. We have invested in crystallisers, inert handling stations, and analytic tools that don’t just validate the batch once—it’s a point-by-point monitoring system with in-line sensors and offline checks. This lets us respond fast if a process deviation shows up, especially on impurity profiles or solvent residues.

    Research scale materials—from a handful of grams to a few hundred—rolling off our lines draw on the same SOPs as multi-kilo lots. That’s not marketing spin; our own process development depends on it. For wider distribution, we keep intermediary stocks stable with monitored temperatures, humidity control, and inert packaging. Chemists ask us about long-term sample storage, and we share our own results from stress tests, including freeze-thaw cycles and light exposure.

    A research chemist working on SAR cycles and a production engineer building up for regulatory submission have different pressure points. The research user may handle only grams at a time; the plant team wants drums that remain free-flowing and easy to sample. Packaging, batch size, and documentation fit those needs. Small glass bottles for trial reactions, moisture-barrier drums for bulk shipping. No matter the format, spectral data, IR profile, and chromatography traces come with every unit.

    Practical Lessons: What Careful Handling Looks Like

    In practice, handling 4-Cbz-Piperazine-2-Carboxylate Methyl Ester means attention to temperature, humidity, and sealed containers. Our own tests have shown that the product holds up well under dry, room-temperature storage for months without measureable degradation. For analytical purposes, we recommend DMSO-d6 or CDCl3 for NMR, and HPLC runs use standard acetonitrile-water gradients.

    The biggest reason our clients choose our version of this compound isn’t just purity figures—it is the real consultation that comes from our development chemists. If a lot shows even a slight deviation in m/z ratio or unusual baseline drift on HPLC, we re-examine both the process and the full batch. Full transparency on process adjustments translates to confidence for project chemists, especially as projects grow from milligram scale library builds to 10-kilogram campaigns.

    Challenges We’ve Addressed in the Manufacturing Process

    Producing 4-Cbz-Piperazine-2-Carboxylate Methyl Ester at high reliability has called for several hard-won improvements. Early on, we encountered issues during the hydrogenation step leaving trace amounts of unremoved catalyst. Control over catalyst loading, hydrogen feed, and specialized filtration has now eliminated that concern. Our analytical team tests each completed batch for palladium or other trace metals, with rejection limits that match or exceed common pharmacopoeia demands.

    Residual solvent has also been a recurring challenge at scale. While many smaller suppliers rely on atmospheric drying, we moved to controlled vacuum drying with jacketed vessels. Our team developed a drying cycle profile using real moisture sensor data. This has proven critical for customers qualifying materials for regulatory filings. We record every batch’s endpoint moisture and include this in release documentation.

    Clumping, caking, and static charge can trip up even an experienced technician. We have adjusted particle size distribution by tuning crystallization temperature and agitation speed, ensuring the solid flows smoothly and can be measured without excessive static.

    Downstream Innovation: Where We See Real-World Impact

    The route to an active pharmaceutical ingredient or screening compound starts with solid building blocks. 4-Cbz-Piperazine-2-Carboxylate Methyl Ester lets process chemists test new functionalizations at the 2-position, opening routes to either acids or amides as downstream options. By avoiding excess protecting group migration or unwanted ester hydrolysis, project teams save weeks in troubleshooting.

    Our ongoing partnerships with pharma R&D teams give us an early look at what features chemists want—whether that’s lots completely certified for elemental analysis or trace-level impurity data for LC-MS. We now routinely include expanded screening for isobaric impurities. Some projects have called for enantiopure variants, and though this compound is not chiral in its core, we have worked side-by-side with development chemists to confirm stereochemical integrity for more complex routes.

    Academic users have brought feedback about ease of handling during multi-step library construction. The clean deprotection of Cbz by catalytic hydrogenation streamlines workflows, and the methyl ester survives peptide coupling strategies that use mild bases.

    Why Experience in Manufacturing Beats a Simple Price Comparison

    We understand that procurement decisions often hinge on price, purity, and availability. What sets our offer apart is the level of process oversight, history of resolved scale-up problems, and a record of supporting chemists through every batch run. As the original producer, we provide a direct chain of accountability—no ambiguity over supplier sources, no surprise changes in raw material sourcing.

    By remaining focused on this specialty in-house, we react quickly to changing regulatory needs, formulation notes, or user feedback. A customer with an urgent preclinical milestone can count on consistent supply, because our process is not subject to the uncertainties and hidden changes that come with third-party aggregation. This control translates into fewer project delays and a reliable partner for both custom work and routine campaigns.

    Many users tell us they switched to our product after encountering unexplained NMR peaks, batch discoloration, or failing to meet their own stability endpoints with catalogue materials. Our plant and team stand behind every container shipped, with open lines for technical support, requalification, or new process advice. This is what experience means when it’s measured at the bench, not just on a datasheet.

    Continuous Improvement: Listening to Chemists and Innovators

    In our company’s journey, every incremental improvement has followed a challenge raised from the field. Some chemists want a version dried to below 0.1% water. Others have asked for alternative solvents during crystallization to match their own downstream requirements. And sometimes, simply being able to talk to a process chemist—rather than a call center—makes the entire difference.

    We do not chase one-size-fits-all solutions. Instead, our expertise comes from working batch after batch, tracking both lab and plant feedback, and applying what’s learned to every order. Open feedback channels and ongoing process improvement keep us nimble, while regular on-site audits back up every claim with evidence.

    True quality is not abstract; it shows in the absence of delays, the clarity of every spectral trace, and the trust that grows after many successful campaigns. 4-Cbz-Piperazine-2-Carboxylate Methyl Ester is not just a line in our portfolio, but a living example of what disciplined manufacturing and direct communication can accomplish.

    Looking Ahead: Supporting Evolving Needs in Chemistry

    Research and production in both pharmaceutical and academic fields never stand still. Intellectual curiosity and pipeline needs drive ever-diversifying applications of protected piperazine compounds. We see 4-Cbz-Piperazine-2-Carboxylate Methyl Ester as a reliable stepping stone for routes requiring fine-tuned reactivity and clean deprotection sequences, whether for new therapies or fundamental screening tools.

    As users push toward greener processes, safer handling, and tighter impurity control, we continue to adjust practice in-house to meet rising standards. Analytical transparency, batch-to-batch traceability, process documentation, and the willingness to adapt set the tone for everything we produce.

    We stand ready to share our journey, data, and experience on every aspect of 4-Cbz-Piperazine-2-Carboxylate Methyl Ester, confident that this attention to detail provides customers not only with a product off the shelf, but a partner in moving ideas from bench to reality.