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1-(2,4-Dimethylphenyl)Piperazine

    • Product Name 1-(2,4-Dimethylphenyl)Piperazine
    • Alias 2,4-DMP
    • Einecs 612-163-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    226763

    Chemical Name 1-(2,4-Dimethylphenyl)piperazine
    Molecular Formula C12H18N2
    Molar Mass 190.29 g/mol
    Cas Number 29686-75-9
    Appearance White to off-white solid
    Boiling Point Unknown
    Melting Point 72-75°C
    Density Unknown
    Solubility In Water Slightly soluble
    Structure Type Aromatic piperazine derivative
    Iupac Name 1-(2,4-dimethylphenyl)piperazine
    Pubchem Cid 24148
    Smiles CC1=CC(=C(C=C1)N2CCNCC2)C
    Inchi InChI=1S/C12H18N2/c1-10-4-5-12(2)11(9-10)14-7-3-6-13-8-14/h4-5,9,13H,3,6-8H2,1-2H3
    Synonyms 2,4-Dimethyl-1-phenylpiperazine

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

    Packing & Storage
    Packing A 25g amber glass bottle with a tamper-evident cap, labeled "1-(2,4-Dimethylphenyl)Piperazine," features hazard symbols and handling instructions.
    Shipping 1-(2,4-Dimethylphenyl)piperazine is shipped in tightly sealed containers, labeled according to regulatory requirements. It is packed to prevent leaks and protected from moisture, heat, and direct sunlight. Shipping follows guidelines for chemical safety, often as a non-hazardous substance, but always in compliance with local and international transport regulations.
    Storage 1-(2,4-Dimethylphenyl)piperazine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture, direct sunlight, and sources of ignition. Store at room temperature and label the container properly. Ensure access is restricted to trained personnel and follow applicable safety guidelines.
    Application of 1-(2,4-Dimethylphenyl)Piperazine

    Applications of 1-(2,4-Dimethylphenyl)Piperazine in Industrial Manufacturing

    As a direct manufacturer, we supply 1-(2,4-Dimethylphenyl)Piperazine for specific, regulated downstream industries. The following application scenarios highlight actual utilization fields, relevant compliance frameworks, process details, and real end products adopted by industrial partners.

    1. Active Pharmaceutical Ingredient (API) Intermediate in CNS Drug Synthesis

    Pharmaceutical companies employ 1-(2,4-Dimethylphenyl)Piperazine as an essential intermediate during the synthesis of select central nervous system agents, including atypical antipsychotics and antidepressants. The compound enters multi-step chemical syntheses, where the strict implementation of GMP ensures batch-to-batch consistency and documentation. The usage concentration depends on target molecule stoichiometry, reaction yields, and impurity profiles controlled by pharma QC teams. Downstream, synthesis routes often combine it with halogenated reagents using solvent-based condensations, followed by chromatographic purification, monitored by analytical specifications. Customers use it primarily in the penultimate steps of API manufacture for branded and generic CNS medications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US cGMP for finished pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) section 5.10
    • Chinese Pharmacopoeia for API intermediates

    Typical usage ratio

    • 0.65–1.15 molar equivalents relative to API core, adjusted for synthetic step requirements
    • Variations based on yield optimization and impurity control strategies

    Downstream process integration

    • Enters as a main building block in the late intermediate or pre-API conversion steps
    • Added post-initial ring formation during amination or N-alkylation stages
    • Chromatographically controlled purification before API crystallization

    Final product types

    • Atypical antipsychotic APIs (e.g., pipamperone derivatives)
    • Antidepressant molecules featuring substituted phenylpiperazine moieties
    • Finished dose pharmaceuticals for CNS indications

    2. Chemical Synthesis Intermediate in Specialty Agrochemicals

    Developers of advanced crop protection agents and seed treatment products use this compound as a core intermediate in heterocycle coupling, supporting the synthesis of selective herbicides and fungicides. Process plants rely on traceable, specification-certified shipments verified by in-house QC for crop-use regulatory filings. Chemists blend it at controlled ratios to introduce unique substituents onto agrochemical scaffolds, with downstream integration during protected amine formation, then conversion to the target active via oxidation or alkylation. Product finalization involves purification in compliance with international maximum residue guidelines before formulation as finished crop science goods.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) guidance on technical raw materials purity
    • ISO 9001:2015 quality management for specialty chemicals
    • US EPA inert ingredient assessment for non-food and food-use pesticides
    • European Union REACH registration for agricultural use intermediates

    Typical usage ratio

    • 10–30% w/w in reaction blends, depending on molecular backbone and pathway stage
    • Adjusted to achieve targeted functional group introductions and yield performance

    Downstream process integration

    • Integrated during amine functionalization steps in heterocyclic agrochemical intermediate synthesis
    • Follows chlorination or halogenation of phenyl substrates
    • Post-synthesis, routes include pH adjustment and solvent exchange prior to final active ingredient creation

    Final product types

    • Fungicide technical concentrates
    • Selective herbicides for cereal and oilseed crops
    • Seed treatment active ingredients containing phenylpiperazine structures

    3. Precursor Component for Industrial Dyes and Pigments

    Specialty colorant producers use this compound to introduce substituted piperazine groups during the design of high-performance dyes. The manufacturing process typically requires verified trace impurity levels and batch documentation to comply with textile and plastics safety regulations. Formulation chemists dose precise amounts alongside aromatic aldehydes in condensation reactions, controlling molecular hue and solubility characteristics. Downstream, the material is coupled using catalysts specific to each pigment, with attention to residual amine content affecting the dye’s fastness properties. The end products include custom pigments for engineering plastics and functional textile applications.

    Industry compliance standards

    • OEKO-TEX® STANDARD 100 for restricted substances in textile colorants
    • REACH Annex XVII for aromatic amines in dye manufacturing
    • ISO 9001:2015 certified production systems
    • US FDA 21 CFR 176.170 for food-contact colorants (where applicable)

    Typical usage ratio

    • 5–20% by weight relative to total dye batch mass, tailored by pigment and shade formulation
    • Adjusted to control depth and fastness in the final dye lot

    Downstream process integration

    • Charged during key condensation or cyclization step for core pigment skeleton formation
    • Paired with catalyst addition and controlled heating profiles
    • Subjected to solid-liquid extraction and pH modulation prior to pigment finishing

    Final product types

    • High-stability colorants for synthetic textiles
    • Engineering plastic pigments
    • Special effect dyes for technical coatings and films

    4. Building Block for Advanced Polymer Modification

    Producers of high-performance plastics and polymer blends integrate this piperazine compound during the functionalization of base resins. The controlled addition imparts chemical resistance and thermal stability to end-use articles. Typical processes require validated supply chain documentation and batch-level certification to comply with automotive and consumer electronics standards. It enters melt-phase or solution-phase copolymerization, where the operator manages reactivity with isocyanates and diacid chlorides, allowing for tunable end-group characteristics. This block’s inclusion directly impacts the physical performance required by downstream converters.

    Industry compliance standards

    • ISO 9001:2015 certified manufacturing for plastics modification
    • UL 94 (flammability of polymeric materials)
    • Automotive OEM-specific requirements (e.g., Volkswagen TL 527)
    • RoHS 2011/65/EU for restricted chemicals in electronics

    Typical usage ratio

    • 0.5–5% by weight in polymer masterbatches or modification blends
    • Exact ratio depends on performance requirements and end-use environment

    Downstream process integration

    • Added to monomer or pre-polymer mixture in staged copolymerization
    • Functions as chain modifier during extrusion or reactive blending
    • Incorporation monitored by IR and NMR analysis

    Final product types

    • Heat-resistant polyamide composites
    • Specialty copolymers for consumer electronics housings
    • High-strength automotive engineering plastics
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    Certification & Compliance
    More Introduction

    1-(2,4-Dimethylphenyl)Piperazine: Reliable Quality from an Experienced Manufacturer

    A Hands-On Introduction to 1-(2,4-Dimethylphenyl)Piperazine

    In any chemical production facility, the level of precision and consistency in every batch depends on a deep understanding of the compounds involved and the daily realities of running reactors, handling purification, and packaging for long hauls. As a team shaping our line of piperazine derivatives, we put a lot of focus on 1-(2,4-Dimethylphenyl)Piperazine, not for how it looks on paperwork, but for how reliably it performs in real-world manufacturing runs and research projects. We’ve spent years adjusting our process to avoid common headaches, from reaction impurities to tricky recrystallization steps. Sure, there are lots of shortcuts in theory, but we’ve learned those rarely translate into reliable output or robust downstream results for end users.

    Specifications That Matter in the Plant and the Lab

    Our batches of 1-(2,4-Dimethylphenyl)Piperazine reflect an attention to detail that comes from hard lessons on the floor. Precise melting points, tight GC area percentages, proper color, and stable shelf life make a difference when you or your customer move to the next synthetic step. We don’t just send out a certificate and hope for the best—we make sure every drum and bottle passes hands-on inspection before it leaves our warehouse. From our experience, the most significant differences in quality show up under scale-up stress, not in the comfort of a small test tube. Chemists often talk about theoretical yields, but the scale-ups uncover mixing problems, heat transfer issues, and side product formation. We built our procedures to withstand these variables, so anyone using our material doesn’t run into surprises with their own formulations.

    Our standard product comes as a solid with a typical melting range consistent with literature values for 1-(2,4-Dimethylphenyl)Piperazine. We use only raw materials that pass incoming inspection, and every step gets monitored by in-process analytical checks—not just by spot-testing finished goods. Diligent purification yields a product that moves smoothly through most reaction steps that our downstream customers require, whether that means derivatization, alkylation, or more complex substitution. This focus comes from feedback gathered directly from process operators and chemists, not just sales teams chasing a specification sheet. We know that minimizing batch-to-batch variation avoids frustrating pauses in production lines and unplanned investigations in QC labs.

    Realistic Usage Scenarios—How It Gets Incorporated

    Most of the demand we see for 1-(2,4-Dimethylphenyl)Piperazine comes from fine chemical manufacturers, contract research organizations, and pharmaceutical developers who value reliability over cost-cutting. The backbone of its value lies in the methyl substitution pattern, which introduces both steric and electronic effects prized on multi-step synthesis projects. Our customers often use 1-(2,4-Dimethylphenyl)Piperazine as a key intermediate in API analog development, or as a scaffold for custom compound libraries. The meta and para methyl groups serve as handles, letting chemists control electronic properties more finely than with simple phenylpiperazine scaffolds. Our production-scale clients depend on reproducibility, not just for yearly batches, but often for critical campaigns with tight deadlines. A missed delivery or impurity spike creates real, cascading problems on the line, including project delays and cost overruns—problems we have worked hard to minimize by tightening our process and logistics chain year after year.

    When research teams order this product, we offer flexibility in packaging but draw a line when it comes to purity and material handling. Our philosophy is straightforward: if it isn’t something we would use to scale up to a kilogram in our own facility, we won’t sell it out. We pay close attention to water content and avoid residual solvents, since even minor contamination can interfere with transformation reactions popular with functionalized piperazines. For example, methyl groups on the ring can favor certain regioselective couplings, but they amplify the impact of trace impurities. It isn’t just a theoretical concern—traces of oxidants or residual by-products have led to batch failures in partner labs before switching to our supply. Addressing these issues became second nature, growing out of years of feedback and our own internal process optimization cycles.

    Direct Experience with Scale-Up: Avoiding Lab-to-Plant Surprises

    We respect any chemist who demands to see both pilot and production-scale results before stepping into larger orders. Our earliest runs of 1-(2,4-Dimethylphenyl)Piperazine taught us the pitfalls of scaling from bench to plant. Sometimes a reaction proceeds cleanly in a round-bottom flask but fouls up equipment or creates unusable solid in a reactor. By iterating on our equipment and fine-tuning work-ups, we’ve reached a position where our operators no longer lose sleep over every reaction cycle. Cooling rates, agitation patterns, even filter cloth selection get reviewed. We take operator notes seriously—it only takes one clogging filter or runaway exotherm to ruin production for a week. These lessons, paid for in downtime and unplanned equipment cleaning, show up as material that behaves consistently for our customers. Several partners told us that switching to our product eliminated chromatography headaches or batch failures that cropped up with cheaper alternatives. No flashy claims—just substance in each order.

    Supply consistency also matters at the logistical level. Weather delays, customs hold-ups, port disruptions all threaten workflow when a single shipment gets stuck. We have structured a redundant inventory system, rotating safety stocks around the country. Reliable supply isn’t about promising in stock—it’s about managing stocks tightly enough that frequent reordering is never a gamble. We make a point of clear communication with our regular clients for large contracts, including advance shipment alerts and flexible lot designations. This attention to communication and transparency evolved from past hard lessons where one misstep, or a breakdown in the supply chain, rippled through multiple production cycles—not just in our facility, but also on the customer’s end. Those who have suffered through an API campaign delay know the consequences are severe, both in terms of cost and reputational risk.

    What Sets 1-(2,4-Dimethylphenyl)Piperazine Apart

    Choosing a methylated phenylpiperazine is about more than just swapping one substituent for another. The dimethyl arrangement on the 2 and 4 positions of the aromatic ring introduces both bulk and intricate changes in reactivity compared to the mono-methyl or non-methylated analogs. Our in-house analytical team tracks these differences closely, evaluating NMR, HPLC, and mass spectrometry signals to confirm patterns that align with expected chemical shifts and fragmentation. These signals aren’t just academic—slight impurities or the wrong isomer profile can affect final product yields in a complex synthesis. Over the years, we have handled plenty of requests for custom analogs, but 1-(2,4-Dimethylphenyl)Piperazine stands out for its versatility as a building block. The combination of steric hindrance and electron-donating methyl groups gives chemists a reliable tool for tackling challenging synthetic campaigns without requiring complete re-optimization of reaction conditions.

    We don’t rely just on sales data or marketing feedback. The value of this product comes from a long trail of internal R&D, plant reports, and collaborations with research partners. Having miles of pilot batches behind us means we notice differences that get lost in automatic reports. Sometimes a supplier reports ‘high purity’ but doesn’t mention traces of meta isomer or inconsistent moisture content—both of which can cause headaches during scale-up. Our team tests for these consistently, having spent enough time in downstream chemistry to recognize the warning signs of problematic lots. Not all 1-(2,4-Dimethylphenyl)Piperazine on the market meets the same standards. One can save a few dollars per kilo by shopping elsewhere, but downstream headaches and lost man-hours soon outweigh any so-called savings.

    Supporting Advanced Chemistry: Beyond Just the Base Compound

    For contract manufacturers who specialize in complex, high-value products, mediocre intermediate quality often triggers hours of troubleshooting. Our experience tells us that the real test of quality material isn’t in the routine certificates—it’s in the way the piperazine performs during tricky transformations. A number of our regular customers use this compound for combinatorial hit-to-lead work or to develop structure-activity relationships (SAR) in libraries targeting CNS receptors or related targets. Reliable data demands clean precursors, and any downstream problems stemming from off-spec material can set back research by weeks. By offering bulk, well-documented lots with full traceability and transparent supply cycles, we help research teams focus on innovation, not error tracing.

    We keep feedback loops open with research chemists, process engineers, and plant managers so the next improvement comes from the real world, not from guesswork. In several cases, researchers identified new downstream transformations needing even tighter controls on starting material impurities. We could adapt purification, update in-process controls, and deliver revised material, often within a single quarter using the same equipment. We believe progress happens when manufacturers and chemists speak the same language—not just about cost and volume, but about reaction profiles and trouble spots. By being a consistent, responsive supplier, we’ve enabled teams to focus on discovery rather than routine troubleshooting.

    Comparing to Other Piperazine Derivatives—What Really Matters

    Some may look at a simple phenylpiperazine scaffold and see a straightforward modification path. Experience says otherwise. The shift from unsubstituted or mono-substituted phenylpiperazines to the 2,4-dimethyl analog brings changes that go beyond academic curiosity. Methyl groups in ortho and para positions alter the electronic environment of the phenyl ring, influencing not only binding characteristics in target assays, but also reactivity and purification profiles. Methylation at these positions shields the ring from undesirable reactions and eventually leads to higher selectivity in downstream functionalization. Many processes that run smoothly with a standard phenylpiperazine hit unexpected snags when attempted with the dimethyl version—solubility shifts, altered basicity, or new side-product formation. Our product history helps chemists anticipate and avoid these problems by starting with material thoroughly evaluated at both bench and pilot plant scale. That’s an advantage only a hands-on manufacturer can offer—lessons written in the logs of actual plant runs, not just extrapolated from datasheets or technical bulletins.

    Our direct competitors, whether domestic or international, may offer material that looks similar on a coarse assay report, but careful users notice trouble lurking in trace-level byproducts or unreported moisture content. Some producers skimp on analytical controls to squeeze a little more output from every batch, but we have learned the cost of this shortcut through hard-won experience. We communicate openly about lot-specific variations, help customers with supplemental analytical data on request, and partner with several labs to run extended characterization for critical applications. Ultimately, these open communications and deliberate process reviews reduce the long-term risks of failed reactions, rework cycles, and delayed timelines—stability that comes from understanding chemistry where it counts, in real reactors and on real deadlines.

    Collaborative Problem-Solving for Challenging Syntheses

    Some of our most rewarding collaborations began with a simple call from a frustrated process chemist facing inconsistent results from competitors’ material. By sharing our real-world insights—including handling tips, dissolution methods, and recommendations for solvent compatibility—many of these partners have unlocked better yields and tighter reproducibility in their own operations. One memorable example: a client scaling up a critical intermediate noticed their previous supply caused variable reaction speeds and frequent crystallization failures. Our team reviewed their notes, compared in-house spectra to reference standards, and ultimately re-optimized the drying and packaging procedures to ensure no hidden water content crept in prior to shipping. The changes paid off downstream, removing a stubborn variability that previously eluded root cause analysis.

    From our records, the most frequent technical queries relate to solvent compatibility, minor by-products, and impurity breakdown over long storage periods. Our dedicated team gathers these questions, logs solutions, and keeps refining our SOPs. Over time, this iterative improvement gives rise to not just a better product, but a more resilient and supportive manufacturing partnership for our clients. Many end-users have told us they appreciate the openness—none of those stock ‘FAQs’ that dodge hard specifics, but genuine, case-based advice growing out of years in the field. As more teams pursue ever-more challenging bioactive targets or process optimizations, the need for clean, consistent, high-purity intermediates becomes more pronounced. We supply both the material and the technical backbone, so production lines move forward and discovery projects don’t stall out over inconsistent starting compounds.

    Stewardship and Ongoing Innovation

    Our journey with 1-(2,4-Dimethylphenyl)Piperazine isn’t just about moving tons and filling orders. We take pride in making sure every kilo and gram meets all standards for safety, purity, and straightforward usability. Attention to waste reduction, solvent recovery, safe packaging, and responsible scale-up protocols runs through our day-to-day work. This sense of stewardship is vital. Process safety doesn’t come from wishful thinking; it grows from actual hands-on experience and constant vigilance. We treat every drum and bottle as if we would use it ourselves—because in more than a few cases, we do. R&D batches and process validations run through the same supply chain as commercial deliveries, which means our commitment to safety and quality isn’t just a talking point; it’s tested in our own facilities year-round.

    We keep our process team close to the ground, inviting feedback from operators, shipping staff, and quality auditors alike. Continuous upgrades to analytical platforms, greener solvent swaps, and automation of handling steps all started as internal suggestions, later validated by customer results. We see regulatory changes, evolving research goals, and shifting market pressures not as threats, but as opportunities to refine our approach and deliver ever-more reliable material. New compliance protocols or stricter traceability rules never come as a shock, since our team integrates changing standards as part of regular process improvement, not an afterthought. Our commitment to long-term consistency and responsible production sets us apart—not by word, but by our repeat customers, their feedback, and our own plant records.

    Trust Earned Through Consistency and Experience

    The value of a chemical lies not just in numbers on a spec sheet, but in the stories behind each shipment, the feedback from end-users, and the lessons learned batch by batch. As a manufacturer, we bear the responsibility for everything that leaves our plant, knowing real businesses and complex projects depend on every lot running true. Our years working with 1-(2,4-Dimethylphenyl)Piperazine have taught us that there is no substitute for care, open communication, and relentless process refinement. We bring those strengths to every customer relationship and every batch, large or small. Our hope is that, whether you’re scaling up a new product line or supporting a research breakthrough, you experience not only reliable supply—but the confidence that comes from partnership with a manufacturer who understands, from the inside out, what true quality means.