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(1,4-Dimethyl-2-Piperazinyl)Methanol

    • Product Name (1,4-Dimethyl-2-Piperazinyl)Methanol
    • Alias Bis-MPA
    • Einecs 610-282-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    849849

    Chemical Name (1,4-Dimethyl-2-Piperazinyl)Methanol
    Molecular Formula C7H16N2O
    Molecular Weight 144.22 g/mol
    Cas Number 38212-30-5
    Appearance Colorless to pale yellow liquid or crystalline solid
    Density Approx. 1.03 g/cm3
    Solubility In Water Very soluble
    Smiles CN1CCN(C)CC1CO
    Inchi Key HTBLNWBZLAQLFF-UHFFFAOYSA-N
    Storage Conditions Store at room temperature, tightly closed, in a dry and well-ventilated place

    As an accredited (1,4-Dimethyl-2-Piperazinyl)Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, sealed with a screw cap and tamper-evident seal, labeled with chemical name, formula, and hazard information.
    Shipping Shipping of (1,4-Dimethyl-2-Piperazinyl)Methanol must comply with relevant chemical transport regulations. The substance should be securely packaged in appropriate containers, labeled with hazard information. During transit, ensure measures to prevent leaks, spills, and exposure. Shipping often requires documentation detailing composition, hazards, and specific handling instructions for safe delivery.
    Storage (1,4-Dimethyl-2-piperazinyl)methanol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure the storage area is clearly labeled and equipped for the safe handling of chemicals. Use secondary containment to prevent accidental spills.
    Application of (1,4-Dimethyl-2-Piperazinyl)Methanol

    Applications of (1,4-Dimethyl-2-Piperazinyl)Methanol in Industrial Manufacturing

    As a direct manufacturer with extensive technical experience, we supply (1,4-Dimethyl-2-Piperazinyl)Methanol primarily for advanced intermediate synthesis across high-value chemical industries. Our material meets rigorous downstream requirements for purity, batch reproducibility, and regulatory conformance. Below we present core industrial application scenarios, highlighting typical usage parameters, regulated quality standards, and integrated manufacturing steps, as practiced by key global producers.

    1. Pharmaceutical Intermediate for Antipsychotic APIs

    Leading pharmaceutical companies source this compound as a key intermediate during multi-step synthesis of selective antipsychotic drugs, such as piperazine-based active pharmaceutical ingredients. The material’s purity is critical at the condensation phase, affecting isomeric integrity and downstream yield. Production lines apply advanced analytical validation (HPLC, NMR) for tight batch-to-batch control, ensuring compliance with stringent quality expectations for regulated APIs.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP and Ph. Eur. monographs for final APIs
    • European Medicines Agency (EMA) and US FDA intermediates tracking
    • GMP site audits and traceability protocols

    Typical usage ratio

    • 5–12% molar equivalence in synthesis route, adjusted by desired end-API yield and impurity control; process R&D will specify tighter ranges per step.

    Downstream process integration

    • Introduced after initial cyclization, prior to final piperazine N-alkylation; stagewise addition ensures selectivity and limits residuals, monitored by in-process QC sampling.

    Final product types

    • Generic and patented antipsychotic APIs (e.g., Quetiapine, Olanzapine intermediates)
    • Regulated pharmaceutical substance supply to integrated and CDMO manufacturers

    2. Fine Chemical Intermediate for Crop Protection Agents

    A major application involves synthesis of agrochemical intermediates, where the material serves as a functional group carrier during heterocyclic ring construction. Large-scale agrochemical facilities utilize this intermediate for selective modifications when producing advanced piperazine-based fungicides and herbicide actives. Process development teams specify purity and impurity index for environmental compliance and efficacy in field-use compounds.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Ingredients
    • ISO 9001-certified production management
    • REACH (EC) No. 1907/2006 registration and CLP compliance for transport and handling
    • Technical Dossier requirements for new crop protection substances (EU, China MOA)

    Typical usage ratio

    • 2–6% w/w in pre-final synthesis steps, adjusted by molecular target and final product registration spec; scale-up trials required to optimize isolation yield.

    Downstream process integration

    • Integrated within coupling and substitution reactions at the penultimate stage before formulation; incorporated via in-line feed reactors with process monitoring to limit hazardous byproducts.

    Final product types

    • Piperazine-derived fungicides
    • New-generation herbicide intermediates
    • Custom synthesis products for multinational agrochemical firms

    3. Polymer Additive Manufacturing for Specialty Materials

    Chemical processing plants add this raw material as an intermediate chain modifier during synthesis of advanced epoxy-modified piperazine resins. Its controlled introduction enhances molecular branching, enabling downstream manufacturers to produce performance polymers for demanding coatings and aerospace-grade adhesives. The additive’s reactivity and trace impurity levels are managed to meet mechanical strength and purity benchmarks set by end-user sectors.

    Industry compliance standards

    • ISO 9001/14001 for environmental and quality management
    • ASTM D256 and D638 for polymer strength and integrity
    • EU REACH and TSCA pre-manufacture notification (PMN)

    Typical usage ratio

    • 1.5–4.5% by resin-formulation mass; adjusted per batch according to required molecular weight and end-use application (higher for high-impact adhesives)

    Downstream process integration

    • Added during pre-polymerization mixing; in-situ monitoring for reaction kinetics using FTIR or Raman; precision dosing controls avoid over-modification, directly influencing cross-link density in finished products.

    Final product types

    • High-durability epoxy adhesive resins
    • Aerospace- and electronic-grade coatings
    • Structural composite fillers

    4. API Intermediate for Advanced CNS Drug Synthesis

    In the central nervous system therapeutics sector, manufacturers use this material to build early-stage intermediates essential for the targeted synthesis of CNS-active piperazine derivatives. High-grade intermediates support process flows demanding minimal genotoxic impurity thresholds and strict cross-contamination controls, especially where route steps interface with regulated actives for clinical candidates and commercial drugs.

    Industry compliance standards

    • ICH M7 mutagenic impurity guidance
    • FDA Guidance for Industry: Process Validation
    • Relevant sections of European Pharmacopoeia 10

    Typical usage ratio

    • 5–10% stoichiometric ratio in N-methylated piperazine-based CNS active ingredient synthesis; process chemists may further optimize based on analytical characterization outcomes.

    Downstream process integration

    • Supplied as pure batch intermediate, initially input after core skeleton formation and prior to final N-alkyl adaptations; QC sampling after intermediate isolation ensures analytical compliance.

    Final product types

    • Psychoactive piperazine-class pharmaceuticals
    • Bulk API intermediates for neurological disorder treatments

    5. Research-Grade Intermediate for Medicinal Chemistry Screening

    Specialty research chemical labs and pharmaceutical discovery units require this compound at high purity for lead optimization, structure-activity relationship (SAR) studies, and early-stage compound library development. Predictable impurity profiles allow medicinal chemists to accurately study pharmacological relevance in new molecular scaffolds, accelerating the preclinical design of drug-like molecules.

    Industry compliance standards

    • IUPAC nomenclature recommendations for research-grade intermediates
    • GLP (Good Laboratory Practice) for compound library work
    • In-house analytical standards (NMR, LC-MS, HPLC)

    Typical usage ratio

    • 0.1–1.5 mmol per experiment depending on scale; scaled up for pilot batch generation as hits progress through the medicinal chemistry pipeline.

    Downstream process integration

    • Weighing and introduction into SAR library synthesis post-ketone or amine scaffolding; integrated at early diversification stage and carried through stepwise semi-automated workflows to furnish lead compound analogs.

    Final product types

    • Small-molecule screening compounds for pharmaceutical R&D
    • Custom catalog intermediates for contract research organizations
    Free Quote

    Competitive (1,4-Dimethyl-2-Piperazinyl)Methanol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing (1,4-Dimethyl-2-Piperazinyl)Methanol: A Practical Perspective from the Manufacturer

    Our Commitment to Reliable Performance

    For decades, our company has stood behind the careful production of specialty intermediates like (1,4-Dimethyl-2-Piperazinyl)Methanol. This compound has become a backbone in several synthetic routes, drawing on its solid functionality and balanced reactivity. Our team knows the ins and outs of what this material requires, not just at a technical level, but through real, hands-on experience in full-scale chemical synthesis. The consistency of our batches stems from years of incremental process improvement, tight raw material controls, and direct feedback from those who depend on this product to get their jobs done well, every time.

    What Sets Our (1,4-Dimethyl-2-Piperazinyl)Methanol Apart?

    Some intermediates come and go, produced in short runs or drifting in quality as the source changes. That is not the route we have chosen for (1,4-Dimethyl-2-Piperazinyl)Methanol. We manufacture to a verified model specification, which we have refined through longstanding relationships with pharmaceutical, agrochemical, and specialty chemical developers. This material has deserved its reputation for purity and batch reproducibility, because we put in the hard work at each step: from reaction optimization to evaporation and final quality assessment. It is not just a line on a COA — our workers handle, test, and confirm these qualities every cycle, and know the difference that makes downstream.

    Specifications Built for Real Processes

    Our standard production model tightly controls ID and purity. We monitor not just the major analytes but the trace components that would otherwise show themselves in side-reactions or batch inconsistencies in our customer's final products. Reliable purity means less troubleshooting, shorter syntheses, and less rework. The team does not rest at a minimum spec; we sample, test, and track trends, because we know where issues start long before they become a customer complaint.

    Each lot ships with full documentation. If you ask our lab team about typical moieties or potential side products, they won’t offer textbook guesses — only details on what they actually observed, how they chased down outlier samples, and their work on designing new purification steps in response. Customers working on regulated end-products should know our (1,4-Dimethyl-2-Piperazinyl)Methanol comes with traceability built in, right down to solvent lots and utility records.

    Usage: Learnings from Industrial and Laboratory Applications

    We have seen (1,4-Dimethyl-2-Piperazinyl)Methanol serve as a robust intermediate for both small molecule drug research and as a block in the synthesis of functional materials. In real plant conditions, its handling parameters are sensible. Several of our clients mention how its melting and boiling points allow for direct use without exotic process aids. Our team assists researchers scaling from bench to pilot to larger reactors, offering direct guidance on storage and transfer. The viscosity and solubility we maintain allow easier handling both for automated dispensing in labs and for bulk operations.

    One misunderstanding we sometimes encounter is a mistaken belief that this compound can be swapped interchangeably with other piperazine derivatives. Our on-the-ground experience says otherwise. We have seen projects stall or yields plummet when formulators or process chemists substitute less refined analogs or those with differing substitution patterns. The precise methyl group placements and alcohol function in our product are not minor details; these features strongly influence reactivity and selectivity in downstream chemistry. Researchers with synthetic bottlenecks often share that after moving to our version, off-target byproducts drop, and purification costs fall.

    Differences from Other Piperazine Derivatives

    We often field questions about choosing between (1,4-Dimethyl-2-Piperazinyl)Methanol and other related materials, like basic piperazine, N,N-dimethylpiperazine, or N-methylpiperazine. In practice, none match the performance or reactivity profile of our product, especially in the critical syntheses seen in medicinal chemistry or agro-intermediate development. We have compared impurity levels and yields with competing materials. In many cases, our customers reported fewer extractables, improved shelf-life, and easier work-up procedures. If you have worked with less pure materials, the difference is easy to see at the filtration or isolation step — filtrates run clearer, and recoveries increase.

    The alcohol group at methanol’s position on our compound enables targeted functionalization, not just a minor tweak. Customers in complex heterocycle synthesis point to its more predictable contribution in ring closure reactions and salt formations. Our discussions with development chemists show that pathway-specific derivatizations — particularly those needing selective alkylation or oxidation — move more efficiently with this product versus other piperazine bases. Our team’s repeated analysis of final product NMR and LC-MS supports these claims; lower impurity baselines often tie directly to this reagent’s use in the earliest synthesis stages.

    Real Process Benefits: Fewer Surprises and More Predictability

    On the plant floor or in the pilot bay, process predictability saves both time and cost. Our formulation and packaging approaches contribute to steady performance. Whether sending multiple drums via road or handling lab-scale deliveries, protection from contamination, moisture ingress, and mechanical shocks receives consistent attention. Many of those working in hot, humid, or cold environments tell us they value how our packaging choices directly improve shelf life and reduce stress on site operators.

    Every batch reflects knowledge we gained not from isolated data, but from customer outcomes and successive feedback cycles. As process chemistry grew more demanding, we built new filtration lines, dried under more rigorous atmospheric controls, and improved analytical release checks. Customers facing tough regulatory deadlines rely on this level of assurance. We have learned that while many can claim “purity” or “batch control,” only hands-on vigilance from the actual manufacturing team makes these terms matter beyond paperwork.

    Supporting Evolving Industry Needs

    Shifts in pharmaceutical and agricultural regulation have raised the bar for raw materials. Our site receives regular auditor visits and third-party verification, driven by requests from clients needing audit-ready traceability and chain-of-custody on every input. Rather than treat this as a burden, we see it as a valuable driver for both discipline and customer trust. Detailed documentation habits in our plant shop floor give purchasing, R&D, and quality assurance teams what they need in order to pass inspections and progress new filings without hesitation.

    Certain downstream projects require us to refine material further or reduce allowable heavy metals even below the legal minimums. Our in-house team has grown proficient at working with advanced purification media and process modifications, always seeking ways to answer new challenges from evolving customer expectations. On more than one occasion, a newer client has faced failed reactions with another vendor’s product and brought their process back to life just by switching to our (1,4-Dimethyl-2-Piperazinyl)Methanol. They often point out how consistent response between lots — across months or years — gave their project momentum and reliability.

    The Role of Direct Manufacturer Support

    Our place as a manufacturer, rather than a trader or reseller, gives us unique perspective and responsibility. We answer daily questions from lab heads about specific functional group reactivity, not just logistics. Sometimes customers run into unexplained side reactions. They call our technical team, who checks not only paperwork but actual retained samples, batch records, and recent trends in byproduct formation. Our feedback has shaped customer decision-making — especially with new or modified synthetic routes — and we keep detailed, confidential logs of these interactions, both for regulatory reference and internal process improvement.

    We review feedback and recommendations with urgency. Sometimes clients need to know about inert gas requirements for storage, or best practices for tank flushing, or what test panel to run on their own batch intake. Unlike third-party brokers, we have direct visibility into the real production records and analytical runs. This reduces delays on critical questions. We can adjust production timing, run test syntheses in our application labs, and share first-user know-how, instead of generic product guidance. Our teams stand behind every package shipped — not because it’s required, but because the customer’s results make our company’s reputation.

    Real-World Quality Oversight

    Quality means more than numbers on a sheet. Each lot of (1,4-Dimethyl-2-Piperazinyl)Methanol faces thorough quality oversight because of the demands in high-value synthesis environments. Plant-side team members run repeated cross-checks at each stage, not just at the endpoint. Surprises or process upsets get logged, evaluated, and resolved — not ignored until a pattern forms. Our labs deploy industry-standard, sensitive chromatographic methods but do not rely only on technology; they combine automated screens with the practical intuition that working chemists bring every day. By reviewing historical trends and actual user returns, we manage both current quality and anticipate needs before a run ever leaves our facility.

    We know unexpected contamination or process interruptions do more than ruin a single lot — they disrupt schedules, create downstream purifications headaches, and can set a whole plant team back days or weeks. Our customers remember which suppliers solved problems rather than blamed them, so we act with full transparency. We run controlled pilot trials when a customer’s process uses unique process conditions, ensuring not just technical, but operational compatibility.

    Stewardship and Safety Considerations

    Safety stewardship stands alongside quality and performance. Process team members routinely review hazard profiles and handling experiences. They update safe handling guides and onsite precautions based on firsthand plant observations, not just regulatory minimums. Recent trends toward operator exposure reduction and sustainability push us to explore new containment solutions and minimize waste at every step. Whenever possible, we work with user sites to coordinate safe returns for unused material, develop cleaning protocols specific to the product’s characteristics, and implement rigid containment best practices during packaging.

    While (1,4-Dimethyl-2-Piperazinyl)Methanol is handled safely in a controlled environment, our experience shows that minor process changes can lead to unexpected outcomes. Operators respect its reactivity, especially during scale-up to larger vessels. We encourage regular review of batch records, environmental data and safe limits, and often participate in joint hazard workshops with our partners. Our teams find direct communication with plant engineers leads to safer, more trouble-free handling of each lot shipped.

    Driving Trackable Improvement

    Continued improvement means not only better product quality, but also backward compatibility and consistent customer experience. Experienced chemists on our team know their work never stands still; they audit process data, refine reaction parameters, and draw lessons from peer manufacturers when appropriate. We invest in advanced analytical platforms and staff training, which in turn drive tangible betterment in product quality and reliability. Sometimes incremental improvements lead to new control measures or trigger a switch in raw material suppliers—the result is always reflected in both batch performance and feedback from end users.

    With (1,4-Dimethyl-2-Piperazinyl)Methanol’s increasing use in high-purity chemical synthesis, customers require ever-higher confidence in each delivery. We dedicate part of our production line to continuous testing and trackable output metrics. Plant supervisors own each process, not just quality managers or analysts at the end of the chain. This culture shifts responsibility closer to production, resulting in a product that users trust for its consistency, traceability, and suitability for demanding projects.

    Reflections and Forward Outlook

    Our journey with (1,4-Dimethyl-2-Piperazinyl)Methanol is rooted in listening to those who use it, testing against the toughest specifications, and always insisting on clarity, traceability, and reliability. By keeping process control personal — with individual ownership, mentoring, and knowledge-sharing — we maintain a level of confidence that does not come from documents alone. It is built from hands-on experience, a willingness to learn from setbacks, and a commitment to providing not just a chemical, but a foundation for customer success.

    Looking ahead, we see demand for this versatile intermediate growing along with complexity in the chemical and pharmaceutical industries. Direct dialogs with research, scale-up, and plant teams keep us in tune with evolving needs. As downstream chemistry shifts toward greener, safer, and more efficient paths, we stand ready to adapt, learn, and deliver the kind of quality that removes surprises and helps drive the next successes in synthesis.