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4-(4-Methylpiperazino)Benzoic Acid

    • Product Name 4-(4-Methylpiperazino)Benzoic Acid
    • Alias 4-MPBA
    • Einecs 621-297-6
    • 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

    300300

    Chemical Name 4-(4-Methylpiperazino)benzoic acid
    Cas Number 53559-95-4
    Molecular Formula C12H16N2O2
    Molecular Weight 220.27
    Appearance White to off-white solid
    Melting Point 168-172°C
    Solubility Soluble in water and organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, away from moisture and light
    Smiles CN1CCN(CC1)C2=CC=C(C=C2)C(=O)O
    Inchi InChI=1S/C12H16N2O2/c1-14-7-9-13(10-8-14)11-3-5-12(6-4-11)15(16)17/h3-6H,7-10H2,1-2H3,(H,16,17)
    Synonyms 4-[4-Methylpiperazin-1-yl]benzoic acid
    Logp Estimated 1.3

    As an accredited 4-(4-Methylpiperazino)Benzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10g package features a sealed amber glass bottle with a tamper-evident cap, labeled "4-(4-Methylpiperazino)Benzoic Acid."
    Shipping 4-(4-Methylpiperazino)benzoic acid is shipped in tightly sealed containers to protect against moisture and contamination. It is packaged according to standard chemical safety regulations, ensuring compliance with local and international transport guidelines. Proper labeling, documentation, and appropriate hazard precautions are included to guarantee safe and efficient delivery.
    Storage 4-(4-Methylpiperazino)benzoic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect it from moisture, direct sunlight, and heat. Ensure proper labeling and store at room temperature, unless otherwise specified by the manufacturer or safety data sheet for optimal stability and safety.
    Application of 4-(4-Methylpiperazino)Benzoic Acid

    Applications of 4-(4-Methylpiperazino)Benzoic Acid in Industrial Manufacturing

    As the direct manufacturer of 4-(4-Methylpiperazino)benzoic acid, we support specialty industrial and life sciences sectors with consistent, high-purity supply for critical intermediates. Here, we detail precise downstream scenarios based on actual market integration, formulation practices, qualification standards, and customer QC requirements.

    1. Pharmaceutical Intermediate for Piperazine-Based Antineoplastic Agents

    This compound serves as a core intermediate in the synthesis of select piperazine-containing antineoplastic drugs, notably certain advanced generics for oncology treatment. API manufacturers introduce it at the piperazine ring construction or benzoic acid substitution steps, ensuring controlled purity throughout process scale-up. Our close monitoring aligns with customer QC for batch uniformity in active pharmaceutical ingredient production.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredient (API) manufacture
    • 21 CFR Part 210/211 (FDA cGMP regulations)
    • Ph. Eur. Monograph compliance (upon end-stage API)
    • USP General Chapter <1025> and relevant substance characterization standards

    Typical usage ratio

    • 0.8–1.05 molar equivalents relative to primary coupling agent; precise ratio determined by synthetic route validation and impurity control targets

    Downstream process integration

    • Charged during stagewise condensation or amidation, typically after initial halogenation, then used as coupling intermediate prior to final heterocycle formation and purification

    Final product types

    • Active pharmaceutical ingredients (e.g., new-generation alkylating agents for cancer therapy)
    • API intermediates for branded and off-patent cytotoxic drugs

    2. Dye and Pigment Intermediate in High-Performance Organic Synthesis

    Certain advanced functional dyes utilize this benzoic acid derivative within their chromophore backbone to control electronic properties and shade intensity. Large-scale pigment manufacturers apply it at the ring substitution step, leveraging the stability and electron-donating profile conferred by its methylpiperazine group. Stringent controls on input quality ensure batch-to-batch color consistency in subsequent dye processing and blending applications for plastics and textiles.

    Industry compliance standards

    • ISO 9001 for pigment and colorant manufacturing
    • REACH (EC 1907/2006) registration or exemption for organic intermediates
    • Color Index International listing practices for finished pigment blends

    Typical usage ratio

    • 0.5–1.2 parts by weight per 10 parts total precursor substrates; adjusted based on required chromophore density and color strength specifications

    Downstream process integration

    • Added during pre-condensation of the dye backbone; undergoes nucleophilic substitution with activated aromatic systems prior to azo-coupling or final colorant modification stage

    Final product types

    • High-performance dyes for synthetic fiber textiles
    • Specialty pigments for polymer compounding and laminated films

    3. Synthesis of Specialty Corrosion Inhibitors for Industrial Water Treatment

    Select water treatment chemical producers employ this molecule as a nucleus for bespoke corrosion inhibitors used in high-value closed-loop cooling and boiler systems. Its piperazine functional group enables formation of complex, stable heterocyclic inhibitors with compatibility for iron and copper alloys. Consistent intermediate quality supports downstream QC during formulation blending and commercial drum filling operations.

    Industry compliance standards

    • ANSI/NSF Standard 60 for drinking water treatment additives (as applicable by target geography)
    • ISO 14001 environmental management for chemical production sites
    • OSHA 29 CFR 1910.1200 chemical hazard communication requirements

    Typical usage ratio

    • 3–8% by weight within multi-component concentrate formulas; dosage varies based on target metal substrate and system volume loading

    Downstream process integration

    • Charged during multi-stage blending with phosphates, azoles, and dispersants before pre-neutralization step; integrated into final inhibitor concentrate after in-line QC release

    Final product types

    • Canned corrosion inhibitor concentrates for HVAC and process water systems
    • Boiler and closed system water protectant blends sold to industrial customers

    4. Key Intermediate for CNS-Active Research Chemical Synthesis

    In the contract and custom synthesis of CNS-active small molecules, research-grade chemical producers utilize this raw material for the construction of both standard and modified benzoic acid derivatives bearing piperazine side chains. The compound is introduced at early-stage assembly, allowing for rapid structure-activity relationship (SAR) exploration in medicinal chemistry and drug discovery workflows. Reliable identity and purity documentation are essential for traceable downstream research supply and project audits.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for non-clinical laboratory studies
    • ISO 13485 where chemicals are used for in vitro diagnostic reagent production
    • Controlled substance precursor regulation depending on jurisdiction (S-List, DEA List I/II if applicable to final analogs)

    Typical usage ratio

    • 1.0 equivalent relative to halogenated arene or polyketide scaffold in combinatorial synthesis; adjustment made for target scaffold complexity or yield optimization

    Downstream process integration

    • Added at initial N-alkylation or amido-coupling stage; serves as a core building block for high-throughput analogue library creation followed by purification and analytical QC

    Final product types

    • Medicinal chemistry intermediates for central nervous system (CNS) research
    • Reference standards and tool compounds for pre-clinical evaluation

    5. Functional Monomer Modifier in Specialty Polymer Synthesis

    Producers of advanced specialty polymers use this benzoic acid derivative as a monomer modifier to introduce piperazine and carboxyl functional groups into engineering resin chains. Its application is especially common in high-performance membrane and coating materials for filtration and separation technologies, where tailored solubility and charge selectivity are required. Quality control includes thorough verification of input composition and performance testing of resulting polymer lots.

    Industry compliance standards

    • ISO 9001:2015 for polymer and advanced material manufacturing
    • REACH (EC 1907/2006) notification/exemption for polymer intermediates
    • Regulation (EU) No 10/2011 for food contact polymers (applies to final formulation if used in food-grade filters)

    Typical usage ratio

    • 1–10 mol% based on total monomer input; ratio selected to balance mechanical strength, functional charge, and chemical resistance in target copolymer architecture

    Downstream process integration

    • Incorporated during solution or melt polymerization with other aromatic and aliphatic monomers; followed by film casting or fiber spinning, depending on final application

    Final product types

    • High-selectivity filtration membranes
    • Chemical-resistant industrial coatings
    • Functionalized polymer resins for water treatment or separation
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    Certification & Compliance
    More Introduction

    4-(4-Methylpiperazino)Benzoic Acid: Experience-Driven Commentary from the Chemical Manufacturer’s Perspective

    Our Experience with the Production and Application of 4-(4-Methylpiperazino)Benzoic Acid

    Every day on the plant floor and in the lab, real-world decisions shape the course of our products. Among them, 4-(4-Methylpiperazino)benzoic acid stands out for both stability and versatility during demanding synthetic routes, particularly in pharmaceutical research. Our team produces this compound to strict technical requirements, understanding exactly how each batch impacts downstream synthesis. Instead of handing off theoretical claims, we see the practical results. Scientists and engineers regularly feed back what works and what doesn’t; this drives us to keep refining both process and purity.

    Our production route for 4-(4-Methylpiperazino)benzoic acid reflects what the molecule gets used for: a key building block in drug discovery, especially for API intermediates and specialty chemical formulations. We developed our process with years of hands-on experience in amination chemistry and aromatic substitution. Anyone working in a scaled research lab or manufacturing environment faces the same pressure points: batch consistency, impurity profiles, and yield. Since clients often require precise reproducibility from gram quantities to multi-kilo lots, we focus on keeping tight control over reaction conditions and workup steps. That means pure powders every time, with low ash content and minimal residual solvent.

    In the lab, 4-(4-Methylpiperazino)benzoic acid appears as a white to off-white crystalline solid, with a molecular formula of C12H16N2O2. Its pKa and solubility profiles allow for predictable functionality, whether you’re forming amides or driving further substitution reactions. We developed our drying and milling procedures around practical downstream requirements. Chemists want reliable material that dissolves easily in DMF, DMSO, or methanol; they emphasize a need for manageable particle size to simplify filtration and measurement. These specifications came not from a textbook, but direct requests from those doing the hands-on synthesis.

    What We’ve Learned from Real Users—and Why Specifications Matter

    Over the years, we’ve seen how a single variable in 4-(4-Methylpiperazino)benzoic acid production affects everything downstream. For example, even minor impurities like N-oxide, unreacted starting aniline, or trace water can ruin a peptide coupling reaction. Years ago, we fielded a flurry of calls from a customer frustrated by inconsistent yields. By walking through their process, running side-by-side reactions with their material and ours, and performing a full impurity profile, we discovered a low-level hydrolysis byproduct as the culprit. This direct troubleshooting led us to redesign our purification step.

    Another point that comes up repeatedly is scalability. Researchers start with 10 g and move up to 1 kg, expecting the same purity and reactivity every time. Here, we found that controlling residual solvent and maintaining uniform particle morphology really begins to matter. Too much moisture from the last filtration step, for example, doesn’t just irritate the next chemist: it risks actual product loss or side reactions. Our plant operators routinely verify moisture levels using Karl Fischer titration, and we’ve instituted batch-to-batch checks based on real-world user needs, not arbitrary standards.

    We also took feedback on packaging and shelf-life. This acid draws moisture from the air, leading to caking or discoloration in humid climates. Years ago, an exported lot arrived half-clumped due to subpar packaging. We switched to better-sealed drums and added silica packets, a simple change that saved our clients hours of extra work. A little direct feedback from those handling the material goes a long way, so we encourage open lines of communication about the performance or packaging in end-use.

    Technical Specification—But with Application in Mind

    We don’t just quote assay numbers to tick a box for pharmaceutical audits; we monitor specification parameters like HPLC and GC purity, water content, and melting point because they have daily consequences for users. Our in-process QC finds problems fast, allowing us to correct trajectories before a batch ships out. We also balance those technical numbers with actual feedback from the field: does the acid dissolve quickly, does it pack well, does it show up clean in NMR?

    Through hands-on experience in handling, storing, and shipping, we see challenges others may miss. For example, repeated cycles of melting and re-solidifying during transit can shift particle size or promote mild decomposition. Chemists might not spot these subtle changes during routine checks, but we built a habit of batch retention and periodic retesting to confirm nothing slipped through. We’re not saints; mistakes happen. But we confront them with transparent sharing of both analytical results and direct troubleshooting, acknowledging what went wrong and how to prevent it in the future.

    Use Cases Shaped by End-User Reality

    Research teams worldwide use 4-(4-Methylpiperazino)benzoic acid primarily for its lineup of applications in medicinal chemistry and small molecule libraries. In our direct experience supplying contract research organizations and pharma plants, this acid often helps anchor a functionalized benzoic core and enables the introduction of piperazine moieties with basic methyl groups, commonly seen in antipsychotic APIs or kinase inhibitors. Every request for alternate salt forms or derivatives that comes through our technical liaison offers a glimpse into the rapidly evolving medicinal pipeline.

    Some of our customers combine it with activated esters for peptide conjugation, prioritizing high purity and low moisture to prevent unwanted side-products. Others value its basicity and robust structure during multi-step organic transformations with aggressive reagents. Here’s where small compositional changes—such as the level of methylated piperazine—isomer matter. Our close work with formulation chemists keeps us attuned to real-world hurdles: isomer shift, substitution position, or even trace impurities that mask or exaggerate expected spectra.

    Often, developmental chemists run into material problems at pilot or scale-up batches. One client, recently, highlighted a difference in color and melting point even within a nominally batch-to-batch consistent supply. Running extra TLC checks and spectra, we drilled down to storage temperature swings during an unseasonably damp month. This sort of hands-on investigation underlines a manufacturer’s unique position: we’re not just passive suppliers, we’re trouble-shooters with lab-bench experience who care about each gram shipped.

    What Sets This Product Apart—Direct Comparisons with Other Benzoic Acid Derivatives

    For chemists used to working with benzoic acid derivatives, the differences between 4-(4-Methylpiperazino)benzoic acid and related products stand out during synthesis and formulation. The presence of the 4-methylpiperazino group fundamentally changes the basicity and steric influence compared to a plain piperazino or morpholino derivative. We’ve seen this translate directly to better resistance against acid/base hydrolysis or increased selectivity in coupling reactions. Our hands-on experience confirms that during scale-up, the methyl substituent on the piperazine ring offers better solubility profiles and easier isolation in some solvent systems, especially at higher concentrations.

    Working side by side with teams using unsubstituted benzoic acid derivatives, we observe empirically that this product avoids some hurdles—gel formation, unwanted salt precipitation, or difficult chromatography. The piperazine ring, especially methylated at the nitrogen, resists byproduct formation that can appear during ring-opening steps. Several clients have told us it plugs neatly into their synthesis route, expediting process validation, a factor we never underestimate when planning plant capacity.

    Also, in more specialized applications, such as antibody-drug conjugates or linker building blocks in targeted small molecules, 4-(4-Methylpiperazino)benzoic acid offers a unique combination of aqueous solubility and backbone rigidity. Based on hands-on trials in our pilot plants, we see that these features improve shelf storage and downstream chemical modification, benefitting users looking for robust and reliable building blocks for experimental drugs.

    There is a growing trend of medicinal branches exploring the increased metabolic stability the methyl group imparts. Our technical partnerships result in early-stage data sharing, which helps optimize our purification and packaging based on the latest synthetic approaches. It is clear from years of field observation that even small differences in synthetic handle or N-methylation status can tip the balance toward a successful development campaign. This is not generic, out-of-context bench science—it comes from daily interaction with people solving real problems in their labs.

    Quality Through Continual Improvement—No Room for Complacency

    No matter how stable or popular a product line becomes, chemistry does not tolerate complacency. The standards clients set keep moving, especially as regulators raise the bar for documentation, traceability, and process safety. Over the years, we found that simple transparency and rapid communication with users—sharing up-to-date COAs, impurity profiles, and storage advice—saves everyone both money and frustration over time. These aren’t just promises; they represent practical steps we take based on years spent correcting our own missteps.

    Recently, we collaborated with one of our biggest clients, sitting in on their R&D trouble sessions to get live feedback from analytical chemists and process developers. We adjusted assay reporting, shifted primary packaging, and upgraded the drying cycle—all changes based closely on firsthand user input, not theoretical standards. The result: higher long-term satisfaction rates and a sharper reduction in repeat material complaints. There is an undeniable sense of pride and responsibility that comes with taking practical feedback and direct observation into actual plant-floor changes.

    Sustainability and Future Challenges—Industry Experience in Perspective

    Running a chemical manufacturing facility today demands not just technical skill but also environmental mindfulness. Sourcing raw materials for 4-(4-Methylpiperazino)benzoic acid, narrowing down waste streams, and choosing greener solvents whenever possible means we shoulder our share of sustainability. The practicalities aren’t always simple or cheap. But clients now ask pointed questions about carbon impact, solvent recycling, and manufacturing waste. That feedback echoes our own aims—keeping effluent below legal minimums and minimizing single-use plastics in both packaging and handling.

    We’re currently trialing a closed-loop solvent recovery system, targeting a drop in non-recovered DMF emissions. Our engineering team learned the hard way that small plant modifications—baffling, chillers, new in-line monitoring—deliver real emissions savings only after many cycles of fine-tuning. Every operator on our floor knows why a leak in the distillation column—even intermittent—can wipe out months of compliance effort. Building this culture of responsibility, not treating environmental standards as an afterthought, pays off in both community goodwill and long-term viability. We don’t hit every target on the first round, but ongoing effort and transparency keep us aiming higher each year.

    The Value of Direct Dialogue—Manufacturing as an Ongoing Collaboration

    Nothing beats a direct call from a client who spotted a problem or made a discovery in their workflow. As a manufacturer, we see each conversation—good or bad—as a chance to deepen our understanding of both the product and its applications. It’s not uncommon for researchers to share reaction conditions, analytical challenges, or even raw spectra, trusting us as more than suppliers. We respond by re-evaluating our methods, running extra checks, and sharing proposed solutions as equals, not just vendors.

    Years of direct exchange shaped how we respond to both common and rare production issues. If a batch hits an unexpected color change, or if an end-user identifies a new trace impurity during scale-up, we follow through by reviewing logs, pulling reserve samples, and bringing our process experts together with the user. This approach does not always guarantee instant fixes, but it does build trust and leads to real progress. Over time, this collaboration generates collective expertise that a manufacturer working in isolation could never match.

    Continuous Feedback Drives Everyday Excellence

    Our approach to 4-(4-Methylpiperazino)benzoic acid reflects a simple principle: regular, honest feedback leads to better products. This applies as much to classic technical parameters—purity, particle size, solubility—as it does to “soft” factors like packaging durability or customer support response times. We routinely share product updates, challenges, and new findings with long-term clients, encouraging frank dialogue about areas needing improvement.

    We hold onto a habit developed early in our growth: logging not just analytical data, but every user question, return, or complaint. Over time, these real-world snapshots drive shifts in how we formulate, package, and distribute. Staff learn to see each sample issue as both an immediate problem and an opportunity to fix underlying process gaps. This sense of shared ownership and direct accountability sets us apart from traders or resellers, where lines between responsibility and results often blur.

    Real Results—Not Just Numbers on a Page

    Ultimately, our perspective as a manufacturer means caring about more than purity percentages or warehouse throughput. Every batch of 4-(4-Methylpiperazino)benzoic acid reflects the work of dedicated people—lab techs, operators, field reps—working with real materials, responding to real-world demands. Our reputation stands or falls with every container shipped. Years spent confronting industry challenges, solving user issues, and refining our methods keep us grounded, always ready to adapt our approach.

    We keep investing in both people and equipment. Recent expansions added new purification columns and in-line QC checkpoints, not because of technical curiosity but because users demonstrated a need for tighter impurity profiles. The lesson is simple: let facts from the field guide investment and innovation. By listening, testing, and improving persistently, we earn the trust of not just clients, but every partner along the supply chain.

    In making and supplying 4-(4-Methylpiperazino)benzoic acid, we built our sense of quality and responsibility from experiences at the bench, on the floor, and in the field. Long-term commitment to transparency, problem-solving, and open communication defines how we improve every product cycle. Here, decisions track real usage, not hypothetical data. This focus, shaped by years of learning and adaptation, carries through at every step, driving not only the quality of the acid, but also our role as a partner in discovery and development.