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1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine

    • Product Name 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine
    • Alias BRL-15572
    • Einecs 846-640-5
    • 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

    320378

    Chemicalname 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine
    Molecularformula C17H21N3O
    Molecularweight 283.37 g/mol
    Appearance Solid or powder
    Purity Typically >98%
    Solubility Soluble in DMSO, methanol
    Boilingpoint Decomposition before boiling
    Storagetemperature 2-8°C (refrigerated)
    Synonyms None specified
    Logp Estimated 2.2-2.6
    Smiles CC1CN(CCN1C2=NC=CC(=C2)CO)C3=CC=CC=C3
    Inchi InChI=1S/C17H21N3O/c1-14-11-19(12-15(13-14)20-16-5-3-8-18-17(16)10-21)17-6-4-2-7-17/h3-8,10,13,18,21H,2,9,11-12H2,1H3

    As an accredited 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass vial, labeled with chemical name and 5g quantity, tamper-evident cap, includes hazard information and storage instructions.
    Shipping The chemical **1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine** is shipped in tightly sealed containers, with labeling compliant to regulatory standards. It is packed securely with protective cushioning to prevent breakage, and transported under ambient conditions. Shipping documentation includes safety data, handling instructions, and relevant hazard classifications to ensure safe delivery and compliance.
    Storage Store **1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine** in a tightly closed container, in a cool, dry, well-ventilated area away from direct sunlight and sources of ignition. Keep separate from incompatible substances such as strong oxidizing agents and acids. Ensure storage under stable temperature conditions, preferably at room temperature, and protect from moisture. Follow all safety and regulatory guidelines for chemical storage.
    Application of 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine

    Applications of 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine in Industrial Manufacturing

    1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine acts as a core intermediate in pharmaceutical and specialty chemical sectors. The following sections detail its use in key downstream manufacturing fields, with attention to actual industry compliance, formulation ratios, process incorporation, and final product types.

    1. Active Pharmaceutical Ingredient (API) Synthesis for CNS Agents

    Pharmaceutical manufacturers employ this compound as a critical building block in synthesizing central nervous system (CNS) drug APIs, including serotonin receptor modulators and related molecules. The compound’s hydroxymethylpyridine motif is essential for targeted ligand development, supporting advanced step-wise synthesis under GMP-controlled conditions in automated reactor systems. Process chemists optimize batch or flow chemistry parameters based on purity targets and dosage form specifications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 1, 13th Edition
    • United States Pharmacopeia (USP) general chapters for API intermediates
    • EDQM certification for precursor use

    Typical usage ratio

    • 0.2–0.5 mole equivalent per API batch, adjustable based on desired substitution position and downstream steps

    Downstream process integration

    • Incorporated in early-stage heterocyclic modification, typically after chlorination or alkylation steps
    • Utilized in Grignard, reductive amination, or Suzuki coupling depending on API structure

    Final product types

    • Serotonin receptor antagonists
    • Dopaminergic stimulants
    • Novel antipsychotic agent precursors
    • Experimental neuroprotective drugs

    2. Intermediate for Anticancer Compound Development

    Chemical process developers integrate this molecule into the synthetic schemes of kinase inhibitor scaffolds and pyridine-functionalized cytostatic compounds. The precise incorporation of the 3-hydroxymethylpyridinyl group enables selective reactivity profiles, essential for generating analogues under process chemistry controls. Manufacturers use the material in regulated pilot and commercial processes with full batch documentation and analytical traceability.

    Industry compliance standards

    • Good Laboratory Practice (GLP, OECD Series No. 1)
    • FDA 21 CFR Part 211 (Drugs: CGMP)
    • Japanese Pharmacopoeia standards for intermediate quality
    • ECHA REACH registration for manufacturing/importation above 1 tonne/year

    Typical usage ratio

    • Used at 0.3–0.8 mole per 1 mole of final compound, modulated according to the chain length of target molecule

    Downstream process integration

    • Introduced during the late-stage coupling or condensation steps post-sulfonation or acylation
    • Monitored by LC-MS and NMR for completion and purity verification

    Final product types

    • Pyridinylpiperazine kinase inhibitors
    • Experimental anticancer small molecules
    • Screening libraries for oncology research
    • Reference intermediates for cytostatic agent manufacture

    3. Precursor in Specialty Chemical Synthesis for Analytical Reagents

    Specialty chemical companies use this precursor for tailored ligand design, particularly for coordinating agents and chelators in diagnostic kits and analytical chemistry. The 3-hydroxymethylpyridinyl piperazine structure fosters strong binding characteristics, contributing to reagent stability and specificity. Quality control follows batch traceability and precise stoichiometry to ensure analytical suitability in clinical or industrial assays.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical production
    • EN ISO/IEC 17025 laboratory reagent specifications
    • OECD Good Manufacturing Practices for chemical reagents
    • REACH compliance for exported specialty chemicals

    Typical usage ratio

    • Present at 1–5% w/w in analytical-grade reagent mixes, adjusted based on chelation strength or kit formulation

    Downstream process integration

    • Added at pre-final formulation stage before lyophilization or solvent exchange
    • Homogeneity checked by UV/Vis and HPLC analysis prior to packing

    Final product types

    • Metal ion-selective analytical reagents
    • Diagnostic test kit chelators
    • Pyridine-based stabilization additives for reagent systems
    • Reference standards for laboratory calibration

    4. Advanced Material Modifier for Polymeric Additives

    Polymer manufacturers employ this compound to introduce functionalized pyridinyl groups into specialty resin backbones, improving hydrophilicity, binding efficiency, or processability. Controlled addition during pre-polymerization or copolymerization stages creates high-performance materials suited for coatings and filtration membranes. Rigorous process validation ensures batch consistency, and analyses confirm integration without residual impurity carryover.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management for manufacturing)
    • FDA 21 CFR 177 (Indirect Food Additives: Polymers, for relevant end uses)
    • EU REACH (Annex VII) for monomer and additive safety
    • ASTM D2578 for polymer surface treatments

    Typical usage ratio

    • 0.25–1.2% w/w of total polymer mass in advanced membrane or coating systems, optimized through lab-scale trials

    Downstream process integration

    • Dosed during main reactor charging for melt or solution polymerization
    • Blending and mixing verified by gel permeation chromatography (GPC) and FTIR

    Final product types

    • Hydrophilic filtration membranes
    • Specialty coatings for electronics
    • Polymeric adsorbents for chemical processing
    • Modified engineering resins for automotive or medical parts
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    Certification & Compliance
    More Introduction

    Introducing 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine: An Advanced Building Block for Specialized Chemistry

    Building on Experience: How We Approach Chemical Synthesis

    To bring a new intermediate or fine chemical to life, every process step draws on both proven protocols and hard-won lessons from the lab. Real chemical manufacturing never follows a script. Every batch tests raw material consistency, process control, and the small details that make for safe, reproducible production. Our team has spent years refining how we handle specific heterocyclic and piperazine derivatives, adapting existing flows and sometimes rethinking how to tackle an unexpected impurity or a tricky crystallization. All that work peaks in products like 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine, which stands out for more than just its long name.

    What Sets 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine Apart?

    This compound serves as a tough-to-manufacture intermediate: one that brings together a piperazine core, a pyridinyl moiety, and both hydroxymethyl and phenyl substituents. Each of these groups means extra considerations for chemoselectivity, sensitivity, and purification. Where many piperazine derivatives can fall short in either selectivity or yield during synthesis, we have settled on reliable multi-step pathways that provide high-purity material on scale. By keeping a close eye on the reactivity of the hydroxymethyl group and the steric effects of the phenyl and methyl substituents, we consistently achieve low residual solvent content and minimal side-product formation—a challenge that can derail less robust manufacturing attempts.

    Consistent Specifications: What We Deliver

    Our experience tells us that end-users, whether in research or in an industrial R&D setting, prize reliability. Every batch comes with a tightly controlled melting point range, HPLC and NMR verification, and near-quantitative purity by GC. Typical product specification includes:

    Nothing replaces the value of receiving the same quality material, shipment after shipment. We have learned that attention to process validation, rigorous cleaning protocols, and batch record traceability are what keep results consistent. Re-testing retention samples years later, we see that well-prepared lot remains within original specifications. That kind of stability speaks to the refinements we've built into production.

    Pragmatic Handling and Storage

    Practical use starts with practical handling. Real-world factory floors have variable humidity, temperature changes, and timing challenges. To counter those, our product packaging guards against moisture ingress and light exposure. The crystalline powder stores for years at room temperature and does not clump. We do not cut corners on container choice, either—each unit is sealed in high-barrier liners and packed with desiccant to avoid any absorption that can impact reactivity. These are practices we adopted from seeing, firsthand, the problems that can arise from sub-par storage.

    How Labs and Manufacturers Use This Compound

    Synthetic chemists turn to 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine mostly as a versatile intermediate in advanced pharmaceutical synthesis. Its unique combination of functional groups offers multiple entry points for downstream reactions: the hydroxymethyl group as a handle for further derivatization, the pyridinyl nitrogen for nucleophilic chemistry, and the piperazine for forming larger, more complex molecules. This configuration stands out when building prototype drug candidates that require a fine balance between steric hindrance and electronic properties.

    Contract research and pharma lab teams often rely on this molecule for lead optimization campaigns. The hydroxymethyl serves as a convenient anchor for both arylation and alkylation, often in medicinal chemistry programs aimed at CNS-active agents. Unlike generic building blocks, our product’s consistent quality allows seamless scale-up from milligram trials in a discovery phase to multi-gram pilot batches for preclinical supply. Researchers value not just the chemical structure, but the assurance that each gram behaves predictably in synthesis, without unexpected by-products or batch-to-batch variations.

    Our View on Sourcing Raw Materials and Green Chemistry

    Getting the raw materials right makes all the downstream difference. After testing multiple supply routes, we identified sources where both the pyridine and piperazine precursors meet stringent QC. For us, traceability means more than paperwork—it means regular supplier audits and backup verification with non-destructive testing when incoming consignments arrive. Over the past decade, we've also worked to phase out especially hazardous reagents from this process, inspired by industry moves towards greener chemistry. For example, employing catalytic rather than stoichiometric oxidants and maintaining strict solvent recovery systems minimizes waste. For many chemical companies, these could be wish-list items. On our shop floor, they have become daily rules.

    How Does This Compound Stack Up Against Other Piperazine Derivatives?

    Many available piperazine intermediates compromise between functional group diversity and chemical stability. Some variants do not survive the basic or acidic conditions common in scale-up, while others resist further derivatization due to electronic constraints. The presence of the 3-hydroxymethyl group on the pyridinyl ring opens the door to selective transformations that plain piperazine or N-phenyl-piperazines cannot match. At the same time, by keeping the methyl and phenyl groups positioned for optimal synthetic utility, we find this compound avoids the solubility issues or side reactions that can arise with others. In our plant, small changes in substituents or ring positions have huge impacts on ease of crystallization and final product isolation, so we monitor those effects closely.

    By offering a pure, structurally versatile intermediate, we support customers in taking their process in a direction that less specialized derivatives cannot go. Whether they build on the hydroxymethyl for fluorination, couple the pyridinyl ring with custom side chains, or exploit the piperazine for macrocycle formation, they achieve transformations otherwise out of reach with standard toolbox materials.

    Process Reliability: What We Have Learned Over the Years

    Scaling up this product taught us a lot about both the chemistry and the small human factors that make for safe, consistent output. Early pilot batches made in 10-liter glassware showed how time and temperature control at each stage affect both conversion and impurity profiles. After scaling to stainless steel reactors, we fine-tuned agitation rates and worked out the best balance between throughput and reproducibility. Mechanical durability of seals, paddle mixers, and filters means fewer interruptions and less exposure to air, which could risk product oxidation.

    Repeated operator training, routine instrument calibration, and GMP-style documentation make a difference in getting the chemistry right every single time. In our view, a process that only works under ideal laboratory conditions fails the purpose of chemical manufacturing. We have worked to create contingency plans for handling off-spec raw materials and sometimes adjust process parameters in real time, guided by in-process control testing. Reliable chemistry always comes from more than the reactor—it flows from a team that pays attention to every detail, each step of the way.

    Solving Real-World Challenges in Shipping and Compliance

    Shipping fine chemicals worldwide means managing not just time and cost, but temperature fluctuations and evolving customs regulations. This product consistently holds up under both air and sea transit, based on our long experience. Regulatory compliance remains a moving target, as authorities update registration and reporting requirements. We navigate these changes with full disclosure, detailed certificates of analysis, and documentation for all batches.

    We know that our customers often need detailed impurity profiles and certificate data to satisfy internal audits or regulatory submissions. By keeping analytical records, we can provide this information whether an order occurs months after initial production or as part of a multi-year supply contract. Traceability is not just reassurance—it unlocks smooth customs clearance and helps our customers keep their processes running without a hitch.

    Batch Consistency and What It Really Takes

    We have never seen a synthetic process that runs a hundred times exactly the same on paper and in practice. Even with the best-designed chemistry, slight shifts in temperature, raw material lots, or filtration steps show up in the numbers. To guarantee consistency, we run tight process checks at each stage, and cross-check in-process samples with finished lots. No instrument can substitute for an experienced operator’s eye for unexpected color changes or off-gassing. Over decades, we learn to read and react to these signs, catching potential issues before they cascade into downstream problems.

    Everything from pumping rates to the humidity control in the drying room can affect product appearance and shelf life. It takes effort to keep every lot within target specification, year in and year out. Some customers request custom particle sizes, and we adjust milling parameters only after careful stability and lot representative testing. Cutting corners in any part of the process leads to more work and potential recalls down the line: we’ve seen plenty of cases where a minor shortcut early on becomes a much bigger problem after shipment.

    The Value of Product Knowledge and Application Support

    Supporting customers does not end after shipping a drum of material. Our technical team fields questions on reaction protocol adjustments, compatibility with solvents and reagents, and real-time troubleshooting advice. Many applications require adaptation, and our first-hand familiarity with the product helps customers avoid pitfalls. For instance, common pitfalls with this compound include over-heating during alkylation steps, or using incompatible acid scavengers during derivatization. After discussing with dozens of process engineers worldwide, we offer practical tweaks that shorten their development timeline, and in a few cases, dramatically increase downstream yields.

    Direct feedback from users has saved us from complacency—an overlooked minor by-product observed by a customer can drive us to re-examine an upstream reaction and upgrade purification protocols for everyone. This loop between manufacturer and application chemist powers real process improvements. Our investments in technical documentation and product-specific user guides stem from seeing, project after project, the value of hands-on support over boilerplate responses.

    Real-World Impact in Drug Discovery and Analytical Chemistry

    This compound, with its unique substitution pattern, has proven useful for pharmaceutical early-stage discovery, often in research on neuroactive agents. The piperazine core anchors molecular scaffolds for CNS targets. By introducing both electron-donating and electron-withdrawing capacity via the pyridinyl and phenyl rings, chemists balance molecular properties to suit bioactivity profiles. Our work collaborating with research institutes has helped to extend the range of applications for this intermediate, particularly where novel receptor modulators are needed.

    Analytical chemists working on impurity profiling often require authentic standards to validate their HPLC or GC-MS methods. By providing reference standards with detailed spectral data, we help speed up method development and validation. In a few instances, our technical advice helped research teams avoid costly misassignments due to co-eluting side products.

    Safety and Handling Lessons Learned

    We know that even the best building blocks can present handling challenges on the shop floor. Since this piperazine derivative carries both a pyridine and a hydroxymethyl, proper PPE—including gloves and eye protection—matters. Bulk storage in our plant always runs under dry, cool conditions with precisely labelled containers to minimize risk of cross-contamination or exposure. Repeated safety drills keep our teams prepared for equipment failure or minor spills, reducing the risk of occupational injuries. This hands-on experience has also shaped the way we structure user guidance for off-site labs—real, practical dos and don’ts, nothing generic.

    Transportation safety means more than just sealed drums. It includes regular inspection of containers, documentation of shipping conditions, and clear, accurate Safety Data Sheets matched to real-world risk rather than theoretical hazard statements. Over time, we learned to anticipate questions from site safety officers and build those answers into our support materials.

    Adapting to Customer Process Needs

    Process chemists often push synthetic building blocks well outside of the textbook conditions. We have partnered with several customers facing scale-up backlogs or unexpected bottlenecks, tracing the issue back to impurity build-up or inconsistent lot-to-lot performance. By inviting direct pre-shipment sample requests and encouraging joint troubleshooting with our technical team, we have developed a more flexible approach: customized filtration, targeted particle size reduction, or even staged deliveries to keep pace with high-throughput campaigns. This adaptability has earned long-term partnerships with some of the most demanding customers in fine chemical R&D.

    For teams developing new molecules under tight timelines, having a dependable supply of high-purity intermediates becomes one less thing to worry about. Our internal scheduling systems allow for just-in-time production and buffer stock, built around customer project calendars. That kind of reliability can't be automated: it comes from real-time communication and a shared understanding of what customers need at each step.

    Continuous Improvement and Future Directions

    No synthetic pathway or product line remains static forever. Every year, we invest in new process optimizations, safer reagents, and more efficient isolation techniques. As the demand for more complex drug-like molecules rises, so do requests for even more elaborate piperazine scaffolds. Some of these calls for novel protecting group chemistry or selective functionalization strategies; others involve finding greener solvents or moving away from legacy reagents. By working closely with both suppliers and customers, we stay ahead of shifting industry standards and regulatory expectations.

    Our team’s motivation remains rooted in the same principles that built our reputation: consistency, openness, and a willingness to learn from every challenge. We know that each new lot of 1-(3-Hydroxymethylpyridin-2-Yl)-4-Methyl-2-Phenylpiperazine reflects not just the work of the day but the cumulative knowledge of years spent mastering the chemical details. That is the difference between a commodity and a crafted building block—between just manufacturing and making chemistry work, batch after batch, for customers who depend on it.