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4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester

    • Product Name 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester
    • Alias Lusedra
    • Einecs 629-715-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    251369

    Chemical Name 4-Piperazin-1-ylmethyl-benzoic acid methyl ester
    Molecular Formula C13H18N2O2
    Molecular Weight 234.30 g/mol
    Appearance White to off-white solid
    Purity Typically >98%
    Solubility Soluble in DMSO, methanol
    Smiles COC(=O)C1=CC=C(C=C1)CN2CCNCC2
    Storage Conditions Store at -20°C, protect from light
    Synonyms Methyl 4-(piperazin-1-ylmethyl)benzoate

    As an accredited 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, sealed with a tamper-evident cap; labeled with chemical name, CAS number, and hazard information.
    Shipping The chemical 4-Piperazin-1-ylmethyl-benzoic acid methyl ester is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transport follows relevant regulations for laboratory chemicals, ensuring proper labeling and documentation. Temperature-sensitive handling and prompt delivery help maintain chemical integrity during transit. Safety precautions are observed per MSDS guidelines.
    Storage Store 4-Piperazin-1-ylmethyl-benzoic acid methyl ester in a tightly sealed container, away from light, heat, and moisture. Keep in a cool, dry, and well-ventilated area, ideally at 2-8°C (refrigerated). Avoid sources of ignition and incompatible substances such as strong oxidizers. Ensure proper labeling and safety precautions to prevent accidental exposure or contamination.
    Application of 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester

    Applications of 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester in Industrial Manufacturing

    As a manufacturer specialized in high-purity 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester, we support global industrial partners in advanced downstream sectors. Our raw material consistently meets demanding requirements for purity, batch reproducibility, and process compatibility. Below we outline real-world application scenarios, presenting specific standards, formulation practices, integration points, and finished goods originating from industrial use of this key building block.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers apply 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester as an intermediate during multi-step synthesis of piperazine-containing APIs, including certain anxiolytics and antipsychotics. Precision input at the stagemarked cyclization and amidation steps makes this raw material essential for achieving target molecular frameworks required by regulated drug molecules.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monograph rules (Ph. Eur.) for chemical purity
    • US FDA 21 CFR 210/211 for pharmaceutical manufacturing
    • China National Medical Products Administration (NMPA) GMP for APIs

    Typical usage ratio

    • 0.45–0.95 molar equivalents, calculated relative to the key starting amine in API intermediate synthesis; adjusted depending on side reaction minimization and desired yield optimization

    Downstream process integration

    • Charged during the intermediate coupling or side-chain functionalization stage, prior to final API crystallization and purification; often followed by hydrogenation or acylation

    Final product types

    • CNS drug intermediates (e.g., quetiapine precursors)
    • Atypical antipsychotic bulk drugs after further synthesis
    • Small-molecule psychiatric APIs

    2. Specialty Chemical Synthesis: Heterocyclic Building Block

    In the production of specialty chemicals and research reagents, manufacturers use this raw material as a vital heterocyclic scaffold. The methyl ester group and piperazine core allow for further functionalization in constructing advanced ligands, agrochemical actives, and custom molecules for probe development.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for specialty chemical production
    • REACH (EC 1907/2006) registration for import and use in the European Union
    • GHS labelling compliance for safe handling
    • TSCA Inventory (if marketed in the US)

    Typical usage ratio

    • 10–30% molar percentage in multi-component syntheses; concentration depends on the designed functional group conversion pathway

    Downstream process integration

    • Introduced into the early-phase coupling, alkylation, or condensation reactions; typically forms backbone for subsequent substitution or derivatization

    Final product types

    • Functionalized piperazine ligands
    • Agrochemical intermediates with piperazine motifs
    • Custom synthons for life science research kits

    3. Contract Research and Custom Synthesis Services

    CROs and custom synthesis providers sourcing this chemical rely on its defined structure for scalable batch development. Its functional groups support rapid library synthesis for pharmaceutical discovery and molecular screening campaigns, serving as a consistent module in diversified reaction schemes.

    Industry compliance standards

    • ISO 17025:2017 for laboratory test/analysis
    • GLP (Good Laboratory Practice) guidelines
    • Material Traceability (full lot tracking as per customer contracts)
    • REACH/TSCA compliance for hazardous chemical management

    Typical usage ratio

    • Variable: from 0.1 mmol scale (for discovery) up to 500 g scale, based on library size and target diversity; custom calculation as per customer order

    Downstream process integration

    • Dosed into custom combinatorial synthesis reactors; involved in solid-phase or solution-phase parallel reactions for rapid analogue generation

    Final product types

    • Chemical libraries for high-throughput screening
    • Reference standards for pharmaceutical and agrochemical R&D
    • Lead compound analogues for SAR (Structure-Activity Relationship) studies

    4. Fine Chemical Manufacturing for Diagnostic and Imaging Reagents

    Producers of medical imaging reagents and diagnostic kit substrates incorporate this compound as a functionalizing agent during the synthesis of small molecule probes, particularly when designing moleculetags with specific piperazine motifs to improve targeting characteristics and signal properties.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices—Quality Management Systems for IVD reagents
    • EU In Vitro Diagnostic Regulation (IVDR 2017/746)
    • US FDA 21 CFR Part 820 for diagnostic device components
    • Relevant national chemical control regulations (e.g., Chinese Measures for Administration of Precursor Chemicals)

    Typical usage ratio

    • 1–5% w/w relative to the backbone structure in labeling reactions; carefully titrated to optimize probe sensitivity and minimize background signal

    Downstream process integration

    • Reacted at the molecular labeling or modification stage, just before final purification and lyophilization of probe molecules or tags

    Final product types

    • Functionalized molecular imaging probes (e.g., fluorescent piperazine derivatives)
    • Tagged standards for diagnostic assay development
    • Substrate reagents for biochemical diagnostics
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    Certification & Compliance
    More Introduction

    4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester: Meeting Modern Development Needs

    Understanding 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester from the Manufacturer’s Workshop

    As a chemical manufacturer with years of experience, turning raw materials into reliable building blocks for life science projects, I’ve seen countless cycles of innovation and demand in the synthesis sector. One specialty I handle is 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester. Scientists and advanced R&D operations often seek this compound to help push new frontiers in pharmaceutical intermediates and research chemicals. What distinguishes this product is not just its structure but the reliability we build into every batch, an absolute necessity for anyone who has run large-scale syntheses or scaled up from beaker to reactor.

    The Scaffold: Model, Specifications, and How We Approach Purity

    Creating this methyl ester involves strict process control. Customers count on consistent color, melting point, and purity—qualities that sound routine until a minor slip derails dozens of hours of labor. Our on-site analytics focus on key identifiers: nuclear magnetic resonance (NMR) for structural confirmation, high-performance liquid chromatography (HPLC) for purity, water determination, and content testing. Only once every batch passes our in-house criteria do we release it. No data gets left to chance—every shift in spectra prompts a shutdown and investigation.

    While specs like melting point and purity percentage may seem like numbers on a paper, we treat them as signals of deeper quality. In our experience, overlooked minor impurities have spoiled key reactions downstream, costing both money and valuable project time. Our typical batches of 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester show purity above 98%. This is not marketing speak; I have seen how impurities at even 1% take on catalytic, unexpected reactivity, often manifesting only during scale-up or advanced transformations. We test each lot not only for known potential byproducts but also for traces from raw material streams or catalysts, using multiple detection methods to catch subtle deviations.

    Applications: Inside the Lab and Beyond

    Talking about 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester means diving into daily research routines where reliable building blocks make or break a workflow. Organic chemists, especially those in drug discovery, choose this structure as a pivot in their synthesis chains. The methyl ester group allows flexible modification, whether in classic amidation, hydrolysis, or reductive steps. That flexibility becomes critical when optimizing analog libraries or preparing lead structures under aggressive timelines. In some early-stage medicinal chemistry work, speed matters—weeks instead of months. Having a dependable supply of this component means avoiding last-minute substitutions that complicate downstream processing.

    What stands out with this compound is its role as a versatile link in multi-step syntheses. Sometimes it forms the backbone for further piperazine-ring derivatizations. Sometimes it acts as a connector for benzoic acid-based pharmacophores. I have watched it go directly into candidates for anti-inflammatory, CNS-active, and anti-cancer agents. Its stable methyl ester function tolerates moderate bases, many nucleophiles, and a range of coupling agents, allowing researchers to experiment quickly without worrying about side-reactions from a fragile ester. Customers who run pilot syntheses at scale appreciate the thermal stability and straightforward work-up procedures possible because of the methyl ester’s consistent behavior.

    Why Purity and Lot Consistency Dictate Success on the Bench

    Working at the bench or in a kilo lab, results hinge on repeatability. The variability that occurs batch-to-batch from inadequately controlled manufacturing can cost a whole experimental run. I’ve worked through periods when market shortages forced reliance on lesser offerings: frequent failures in downstream coupling or precipitation issues that never occurred with in-house product. Off-spec intermediates have cost us weeks as we traced an unexpected deprotection yield back to tiny, hard-to-detect contaminants.

    We keep a tight rein on documentation and sample retention for every lot of 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester. Whenever customers report unexpected test results, we track back by re-analyzing both archived samples and process logs. This vigilance has led to process improvements, waste reduction, and, above all, trust from R&D chemists navigating competitive, deadline-driven environments. We also maintain QA records that comply with ISO guidelines, making our product traceable and dependable for regulated workflows.

    Distinctions from Other Piperazine & Benzoic Acid Derivatives

    Piperazine chemistry covers a broad territory. Many piperazine-linked esters differ in small but crucial ways from 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester. We keep a reference library of related intermediates, so we’ve seen firsthand how small structural changes shape both reactivity and handling. Other benzoic acid methyl esters might carry substituents that increase steric hindrance or change polarity; ours strikes a balance between reactivity and manageable physical properties.

    In downstream chemistry, the methyl ester on our compound offers more hydrolytic stability compared to ethyl or tert-butyl esters. Some researchers prefer tert-butyl esters for fast, acid-triggered deprotection, but they often risk premature cleavage or incompatibility with basic conditions. We’ve noted our methyl ester consistently survives standard amide-coupling protocols, allowing multiple divergent modifications before the need for selective removal. Our routine purification steps, such as crystallization and chromatography, are tailored for this core scaffold, making isolation practical and efficient for further processing.

    Why Sourcing from the Manufacturer Fuels Results—Not Just Supply Chains

    Over years spent in chemical production, we’ve responded directly to customer questions about origin, impurity profiles, and process changes. Many chemists working at universities or pharmaceutical companies have faced setbacks from resellers—batches supplied with incomplete documents, uncertain storage conditions, or undetectable byproduct carry-over. Our direct knowledge of every synthesis step lets us deliver both product and critical details to support compliance, route design, and safety.

    A manufacturer’s role extends beyond pushing material out the door. We test shelf-life and long-term stability under real-world storage, not just in controlled chambers. For those working on extended, months-long projects, knowing how a methyl ester like 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester tolerates ambient humidity or repeated opening makes a difference. Our technical team fields questions on solvent selection for dissolving, filtration tips, and solid state handling—all based on day-to-day experience, not only data sheets.

    Challenges and Solutions: From Scaling up to Sustainable Practices

    Bulk synthesis brings another layer of challenge—condensation, filtration, and purification steps get trickier by the kilo. Waste minimization, solvent recovery, and safe operation aren’t checkboxes; they represent the fine line between successful production and unforeseen shutdowns. Through years of process optimization, we’ve developed in-line monitoring and quick shutdown protocols that let us act before small shifts mushroom into big setbacks. Steam tracing, continuous-flow upgrades, and closed cycle filtration have all played roles in keeping waste low and consistency high.

    Sustainability remains a topic of constant discussion in our facility. We review solvent choices, catalyst recyclability, and energy demands for heat-intensive steps. Whenever possible, we swap out hazardous reagents for safer alternates, leaning on green chemistry guidelines if they fit our scale and product requirements. Some partners ask for customized solvent exchanges or dried substance to simplify their downstream use and reduce their own energy footprint. Instead of resisting these demands, we’ve built flexible packaging and drying options into our system—delivering either damp-proof, nitrogen-packed drums or single-use lab bottles.

    Direct Feedback from Chemists: What Drives Real Improvement

    Open channels with end-users drive meaningful quality improvement. One example involved a customer working with a close analog of 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester whose project ran into solubility issues during upscaling. After cross-checking our production method with their feedback, we tweaked our solvent swap in the final stage to yield a more crystalline, manageable final product. Direct experience and two-way communication bore more fruit than any blind adherence to legacy processes.

    We’ve also changed our analytical protocols based on persistent requests: standardizing on both proton and carbon NMR spectra, running additional LCMS on every lot, and retaining reference spectra for comparison years later. The lesson from years of manufacturing is that honest mistakes and gaps in information happen, but openness in sharing results and troubleshooting leads to iterative improvement, not finger-pointing.

    Global Supply Demands, Local Solutions

    In recent years, global events and supply chain disruptions have highlighted the risks of relying on long-distance, multi-node sourcing for complex chemicals. Direct manufacturing, as we see it, boils down to local problem solving. We keep enough raw material stock for buffer production, meaning that when an order spikes or an urgent sample request arrives, we don’t scramble for outside supply. On one occasion, an academic group’s research hinged on just a few extra grams of 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester; prompt delivery from our retained stock made the difference between missed and met deadlines.

    Shipping this compound presents its own hurdles—some territories require special paperwork, restricted transportation, or exact certificates of analysis. Maintaining compliance means more than ticking regulatory boxes. We monitor updates in customs practices, liaise with logistic handlers, and walk new colleagues through handling the red tape. All shipments go out with precise labeling and traceability, based on both years of routine and adapting quickly to new border requirements. For products destined for regulated labs, we can supply extended documentation, impurity profiles, and stability data on request.

    Looking Forward: Where Methyl Ester Chemistry Is Headed

    As R&D shifts toward more advanced synthesis, the importance of robust chemical building blocks grows. Features like selective reactivity, modular design, and scalable process fit drive choices in every pharma innovation center. Our hands-on development and feedback loop mean we adapt 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester production to meet both tried-and-true methods and emerging trends. Higher-throughput screens, automated chemistry, and green process goals are all influencing requests from our partners. We field regular calls for documentation supporting environmental fate studies, downstream process compatibility, and non-target impurity minimization.

    Pharmaceutical and scientific progress increasingly depends on reliable access to well-characterized chemical intermediates. We see rising interest in both scale-flexible supply and greater transparency in manufacturing. There is no single pathway to success—instead, we focus on supporting creative researchers eager to push forward their discoveries. Responding to precise questions, running custom specifications, and maintaining meticulous records make up our daily routine. Backing that up, the physical reality of every gram we produce speaks beyond technical claims; feedback from everyday lab heroes continues to shape our priorities.

    Our Ongoing Commitment

    Producing 4-Piperazin-1-Ylmethyl-Benzoic Acid Methyl Ester is not a static task. It involves daily attention to minor details, close interaction with users, and adaptability as projects evolve. We treat every batch as part of a larger process to support drug discovery, academic research, and industrial applications. Challenges are solved with practical know-how and hands-on philosophy, from scaling to sustainability to transparency.

    Direct engagement and technical experience make our offering more than just a commodity—it underpins the hard work of chemists aiming to improve health, science, and technology. As manufacturer, the best feedback comes not from our records but from shared success with our users in real projects, where every molecule matters and every improvement shapes what comes next.