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Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester

    • Product Name Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester
    • Alias Piperazine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
    • Einecs EINECS 221-542-2
    • 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

    562018

    Chemical Name Piperazine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester
    Molecular Formula C15H18N2O4
    Molecular Weight 290.32 g/mol
    Cas Number 14047-31-1
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in most organic solvents
    Storage Temperature Store at 2-8°C
    Smiles COC(=O)N1CCN(Cc2ccccc2)C1C(=O)O

    As an accredited Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle containing 10 grams, sealed with a blue screw cap, labeled with product name, quantity, and safety information.
    Shipping **Shipping Description:** Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester is shipped in tightly sealed containers, protected from light, moisture, and excessive heat. Ensure compliance with all local, national, and international regulations. Handle as a laboratory chemical; not regulated as hazardous for transport unless specified by the manufacturer’s SDS.
    Storage Store **Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester** in a tightly sealed container in a cool, dry, and well-ventilated area. Protect from light and moisture. Keep away from incompatible substances, such as strong oxidizers and acids. Ensure proper labeling, and avoid exposure to heat or open flames. Recommended storage temperature: 2–8°C (refrigerated conditions).
    Application of Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester

    Applications of Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester in Industrial Manufacturing

    As a committed manufacturer of advanced piperazine derivatives, we focus on direct industrial applications driven by current market adoption and formulation practice. Our material supports selective synthesis, functional polymer production, and high-value intermediate creation where its specific molecular structure advances downstream product performance and compliance. Below, we outline key integration fields with practical technical guidance.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Piperazine-based Medicines

    Pharmaceutical manufacturers employ this compound as a core intermediate when building piperazine moieties into complex antihistamines and CNS pharmaceutical agents. Its esterified carboxylic acid backbone facilitates stepwise N-functionalization and precise molecular modifications in multi-stage organic synthesis. Strict quality and impurity controls apply, given the downstream regulatory landscape and final medical use.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7 guidelines)
    • USP, EP, or JP monograph requirements for finished pharmaceuticals
    • FDA and EMA impurity specifications for process intermediates
    • ISO 9001:2015 certified effective quality control

    Typical usage ratio

    • Introduced at 0.5–2.5 molar equivalents per target API batch, depending on the final drug structure and protection group route.

    Downstream process integration

    • Added after initial piperazine ring assembly and during key esterification or amidation steps for complex API synthesis, often followed by catalytic hydrogenation or functional group exchanges.

    Final product types

    • Second-generation antihistamines
    • CNS (central nervous system) agents with piperazine scaffolds
    • Advanced pharmaceutical intermediates (APIs with functional ester groups)

    2. Monomer or Modifier for Polyamide Engineering Plastics

    Polymer manufacturers incorporate this compound as a nucleating monomer or side chain modifier in specialty polyamide and co-polyamide resins. The presence of methyl and benzyl ester functionality enables fine tuning of crystallinity, mechanical behavior, and melt properties, supporting engineered plastics for demanding applications where standard monomers lack required flexibility or chemical resistance.

    Industry compliance standards

    • REACH Registration, Evaluation, and Authorization of Chemicals (EU Chemicals Policy)
    • RoHS Directive for hazardous substance restriction
    • ISO 9001:2015 production traceability and QC documentation
    • UL 94 and ASTM D638 physical property testing for plastics

    Typical usage ratio

    • Loaded at 1–6% by weight as a co-monomer or chain terminator, adjusted according to desired polymer end use (lower ratios for impact modifiers, higher for flexible sections).

    Downstream process integration

    • Blended with base diamine/diacid monomers in melt polycondensation stages; reacts during thermal polymerization or via catalytic ester exchange mechanisms.

    Final product types

    • High-performance polyamide fibers and films
    • Blended engineering resins for automotive and electronics
    • Co-polyamide adhesives and barrier materials

    3. Building Block for Agrochemical Synthesis (Fungicides and Growth Regulators)

    Agrochemical formulators utilize this compound as a functionalized intermediate in the synthesis of piperazine-derived fungicides and selective growth control agents. The ester side chains provide solubility and reactivity advantages during downstream chlorination, alkylation, or arylation reactions, enabling precise API structure assembly compliant with registration requirements.

    Industry compliance standards

    • FAO/WHO specification 351/2009 for pesticide manufacturing processes
    • ISO 17025 QC for laboratory procedures
    • EU Regulation (EC) No 1107/2009 for active substances in plant protection products
    • GLP (Good Laboratory Practice, OECD Principles) for traceability and reporting

    Typical usage ratio

    • Employed at 0.8–2.0 equivalents per target molecule during active ingredient synthesis, with process optimization depending on specific agrochemical API complexity and intermediate conversion rate.

    Downstream process integration

    • Incorporated after piperazine activation and during early-stage ring substitution, preceding deprotection or further oxidation steps in the multi-step route to the final active compound.

    Final product types

    • Piperazine-derived triazole fungicides
    • Plant growth retardants for cereals and horticulture
    • Specialty agrochemical intermediates with enhanced water solubility

    4. Intermediate for Specialty Chemical Synthesis (Chelating Agents and Catalysts)

    Producers of fine chemicals apply this material as a customizable precursor in the formation of ligand-based chelating agents and organic metal complex catalysts. Its dicarboxylate scaffold, combined with benzyl and methyl ester groups, supports functionalization for selective metal binding or organometallic activation, with stringent purity and consistency expectations for catalyst and chelate performance in critical reactions.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacturing
    • Responsible Care (International Council of Chemical Associations)
    • REACH compliance for specialty chemicals
    • QC method validation (HPLC, GC-MS) for purity and traceability

    Typical usage ratio

    • Integrated at 1–10 mol% relative to target chelate or catalyst loading, selected in accordance with performance testing and target complexation stoichiometry.

    Downstream process integration

    • Functionalized in early synthetic steps, then converted through controlled hydrolysis, amide/ester exchange, or direct metalation pathways, depending on the ligand/catalyst design.

    Final product types

    • Polycarboxylate chelating agents for industrial water treatment
    • Ligand precursors for homogeneous and heterogeneous catalysts
    • Selective extraction agents for metallurgy and analytical separations
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    Certification & Compliance
    More Introduction

    Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester: Performance, Experience, Application

    Introduction to a Distinctive Molecule

    Working with fine chemicals over the past two decades, none stand out in quite the same way as Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester. The structure alone already points to a versatile intermediate with selective reactivity, offering pathways to many complex pharmaceutical and specialty material syntheses. Our development team spent years refining the production process, focusing on purity and consistency. This focus is crucial; minor contaminants, even below 0.1%, can derail whole projects in the lab and at scale. We manufacture this ester in our facilities, operating under strict protocols from feedstock selection through final filtration and drying. We test for isomeric purity, along with residual solvents and unwanted byproducts.

    Practical Attributes from Experience

    A batch might look clear once it leaves synthesis, but subtle impurities show up in how reactions behave later. Consistency makes the difference between a day wasted on troubleshooting and a smooth, predictable process. As manufacturers, we’ve watched colleagues in partner companies experience headaches after cutting costs with off-brand sources. That rarely ends well. Streaks, off-odors, even sticky residues can point to corners cut upstream. Our own process builds in regular checkpoints—HPLC, NMR, and specialized residue testing—so repeats don’t bring surprises to bench chemists or plant engineers.

    The methyl and benzyl esters built onto the piperazine-1,2-dicarboxylic acid core offer selective sites for downstream functionalization. Methyl groups block reactive sites, steering the molecule into desired reactions and protecting it from side reactivity during multi-step syntheses. The benzyl ester can be removed by hydrogenolysis, a standard approach in API development and advanced intermediates. There’s a reason the pharmaceutical sector relies on esters like this: each functional group brings both protection and reactivity, letting customers build precisely shaped molecules for a new drug candidate, advanced material, or catalytic intermediate.

    Reliable Specifications Through Direct Production

    Following years of incremental improvements, we now offer Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester as a crystalline solid with a defined melting range and robust batch records. You’ll find NMR spectra (proton and carbon) showing clean separation with minimal baseline noise and absence of obscure low-concentration impurities. Color rarely drifts from pure white, with the occasional slight cream hue that never exceeds published limits.

    Moisture content is more than a checkbox for us. Too much, and you risk hydrolysis. Too little, and static charge interferes with flow and weighing. Through careful solvent exchange and vacuum drying, we hit the middle ground that supports steady handling in both bench and plant settings. Particle size comes controlled to minimize dust and packing issues, ensuring ease of use without unpredictable clumping or segregation. Each lot comes with a batch-specific analytical report, never a recycled template. Stability has been proven under both ambient and refrigerated conditions, with accelerated studies guiding our ongoing review of shelf life assumptions. Packaging materials are selected by those who actually see the dust and flakes during transfer—not just by the purchasing department.

    Experience in Application and Downstream Chemistry

    Most requests for this ester come from medicinal chemistry groups and process development teams deeply involved in scale-up campaigns. Because of its structure, they use it as a central building block for the synthesis of active pharmaceutical ingredients needing controlled reactivity in late-stage functionalization. Working closely with those teams, we’ve helped adapt particle size and solubility profiles for different kinds of reactors: glass, stainless steel, or jacketed pilot-scale vessels.

    Chemists can selectively remove the benzyl group through hydrogenolysis using standard palladium catalysts, revealing a carboxylic acid site for further coupling or salt formation. The methyl ester’s stability gives predictable behavior in both ester hydrolysis and amide coupling reactions—a must for process reproducibility and efficient route scouting in drug manufacturing. Careful design, including lessons from failed syntheses, stands behind the choice of ester groups in this molecule. An inexperienced hand might favor universal unprotected carboxyls, but side reactions and cleaning validation issues quickly teach otherwise. Protection grants selectivity, saving valuable resources and time through fewer process steps and higher yields.

    Over the years, we have often seen downstream teams run pilot batches with samples from different manufacturers. The results reveal everything: color changes, variable purity, off-odors, and yield swings, even at published “identical” purities. Reports often come back noting ours as easier to work up and purify, resulting in fewer isolation steps and lower solvent consumption. It looks small on paper, but any chemical engineer knows two extra distillations cost real money and downtime. Reputations grow quietly, through hundreds of calls and emails from returning chemists who now default to our batches.

    Beyond APIs, some clients leverage this building block for selective cross-coupling studies—for example, creating libraries of lead candidates or probing enzyme selectivity in chemical biology. The balance of protecting groups supports custom route development—no two programs treat this intermediate in quite the same way. Customization requests have led us to devise alternative purification sequences, offer micronized versions, and develop alternate packaging for humidity-sensitive geographies.

    Key Distinctions From Related Compounds

    Plenty of esters crowd this chemistry space. We’ve made them all, from monoesters and parent acids to the full spectrum of alkyl and aryl derivatives. Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester stands out for its balance of reactivity and protection. Monoesters bring limited flexibility; too reactive or too labile, they often trigger downstream lability, leading to low recovery rates or off-target side products. Fully deprotected diacid variants jump at nucleophiles and bases, fouling up reaction sequences that depend on staged group removal.

    With methyl and benzyl esters in place, this compound demonstrates resilience under a variety of acidic and mild basic conditions. Each functional group defends part of the backbone, granting the chemist selectivity—choosing where, when, and how the molecule opens up to further reaction. We never rely solely on literature; our methods are tuned by literally thousands of pilot and full-scale batches, revealing the true behavior hidden behind a simple reaction scheme. Batch traceability ensures customers receive products made under the same quality regime, batch after batch, without unexplained variability creeping in.

    Compared to bulk commodity versions with less stringent quality controls, ours avoids issues such as dark spots, inconsistent grain size, or batch smells that betray process shortcuts. We never add anti-caking agents or unnecessary stabilizers, because we know how those interferents can shut down a sensitive late-stage reaction.

    The market sees copycat intermediates sold by trading houses, re-bottled for a quick margin. The end result: missed project deadlines and wasted material as off-brand batches fail under real-world process conditions. This compound simply costs too much in downstream value—whether you’re producing a high-value API or inventing new molecular scaffolds—to introduce avoidable risk for the sake of a few percentage points in upfront costs.

    Troubleshooting and Process Solutions Based on Practical Lessons

    No plant or lab process stays perfect without constant vigilance. Even with a thoroughly characterized material, challenges can arise. A slight uptick in water content can throw off crystallization. A subtle solvent shift in a client’s lab exposes poor solubility data or unwanted cloudiness. Our technical teams work directly with process chemists to address these hurdles—not as a ticketing service, but through real troubleshooting and method adjustment.

    Recently, a customer scaling up from pilot to full commercial scale faced issues with filtration times. Standard advice was to swap solvents; instead, we dug into the lot’s granularity and isolated a particle-size deviation missed in routine inspection. After adjusting micronization parameters, filtration time dropped by thirty percent, saving hours per batch.

    Another example involved removal of residual palladium after deprotection. Rather than treating this as a downstream burden, our development staff collaborated with the customer to tune reaction conditions, cutting residual metal levels by half. By tuning methods and working back through possible sources of metallic contamination, the scale-up process became robust, reliable, predictable.

    Companies often look for easy answers, but real answers demand a partnership between supplier and process developer. Details matter—the right dryer setting, the perfect crystal habit, the subtle hue revealing trace byproducts. Those subtleties accumulate into the confidence that lets innovators scale safely up from milligrams to tons.

    Environmental Stewardship in Manufacturing

    Handling raw materials and protecting the environment go hand in hand in our operations. Any chemical synthesis produces waste—byproducts, heat, and emissions. Over the years, we’ve implemented closed-loop solvent recovery systems, reducing the load on air and water treatment. Every lot of piperazine ester runs through solvent reclamation and distillation to recover acetonitrile, methanol, and other key fluids. Lab technicians track emissions, and environmental engineers regularly audit compliance. Fume capture keeps both line workers and surrounding communities safe, never trusting shortcuts or “good enough” venting.

    We limit energy consumption by optimizing reaction times and calibrating equipment to operate at just the right intensity. Early mistakes taught us the value of oversizing chillers and pumps—but not by so much that resources waste away. The result is a safer, cleaner, and more cost-effective operation—which benefits both our customers and our local community.

    Waste disposal comes after careful neutralization and separation, ensuring nothing leaves the facility untreated. Trace piperazine and ester wastes go through thermal and chemical degradation so they do not persist in local waterways. Periodic internal reviews hold us to evolving standards, ensuring future generations inherit a cleaner industry.

    Direct Engagement With End Users

    Buyers from trading companies rarely call with questions about how a batch crystallized or what the NMR baseline looks like around the aromatic region. We work one-on-one with synthetic chemists, process engineers, and scale-up managers who need answers before they place their next order. That kind of communication keeps us sharp, forcing us to see the molecules as living, changing entities—never as a commodity to be packaged and forgotten.

    Our technical support starts with deep product knowledge and hands-on troubleshooting. Customers describe not just results, but ideas, questions, and sometimes setbacks. We provide direct technical consultation and, if needed, sample analysis or modification of a current lot. Sometimes this involves simple advice—solubility tweaks or pH adjustments. Other times it means shipping a tailored sample within hours, or even modifying our packing process to handle a rush order in harsh weather or remote destinations.

    Follow-up is key; we don’t walk away after a sale. Data from field applications flows back to the production floor to fuel improvements in drying, filtering, and testing. If a client experiences crystal bridging or minor residue in a filtration step, those details get logged, investigated, and inform our next round of process control adjustments.

    The Value of Trusted Manufacturing

    The chemical supply world is crowded with resellers and copyists. They rebrand, mark up, and move on, never sweating the pain of delayed production or failed validation. Here, we see every batch as a reflection of decades’ experience and attention to detail. Quality assurance isn’t paper; it’s a discipline etched into our manufacturing culture. Customers can expect the same behavior and response every time they engage with us. A slight drift in melting point, or a puzzling spot on a TLC plate, triggers action—not excuses.

    Buyers soon learn that cost savings on the unit price quickly evaporate if a batch leads to process failure, higher solvent use, or cGMP recleaning. Those who have switched back from low-cost suppliers often do so quietly, after quiet agony with yield loss and process deviation. For something as central as Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester, quality saves far more than it costs.

    Supporting Innovation and Future Growth

    Major projects depend on the foundational quality of their building blocks. In this space, Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester gives R&D teams the flexibility to explore new synthetic routes and create next-generation pharmaceuticals. We see these projects unfold, molecule by molecule and trial by trial. As manufacturers, we shape our processes to meet emerging needs—from new regulatory demands to custom batch sizes and evolving delivery requirements.

    Supporting the evolving demands of research means investing in people and infrastructure. Our talent pool draws from hands-on operators and scientists who know the subtle cues of well-behaved material. Training, mentorship, and constant exposure to live plant operations keep our teams competent and committed. Customers gain more than a product—they access accumulated experience, directly applied to their current projects.

    In this business, trust accumulates slowly. We’re always ready to stand behind our batches, listen to developing needs, and help customers adjust as new discoveries shift project priorities. True value shows in the smallest details, in the clean recovery of a difficult intermediate, or a pilot campaign that sails through without unplanned shutdowns.

    For anyone acknowledging the true complexity of modern synthesis, Piperazine-1,2-Dicarboxylic Acid 1-Benzyl Ester 2-Methyl Ester is more than a chemical—it represents a partnership in precision, reliability, and the pursuit of scientific progress.