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1,4-Diethylpiperazine

    • Product Name 1,4-Diethylpiperazine
    • Alias 1,4-Diethylhexahydropyrazine
    • Einecs 205-806-2
    • 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
    VTB
    Specifications

    HS Code

    575516

    Chemical Name 1,4-Diethylpiperazine
    Molecular Formula C8H18N2
    Molecular Weight 142.24 g/mol
    Cas Number 106-58-1
    Appearance Colorless liquid
    Boiling Point 186-188°C
    Melting Point -30°C
    Density 0.86 g/cm3
    Refractive Index 1.446
    Solubility In Water Miscible
    Flash Point 70°C
    Smiles CCN1CCN(CC)CC1

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

    Packing & Storage
    Packing 1,4-Diethylpiperazine is packaged in a sealed 250 mL amber glass bottle, labeled with hazard symbols, product details, and batch number.
    Shipping **Shipping Description for 1,4-Diethylpiperazine:** 1,4-Diethylpiperazine is shipped in tightly sealed containers, protected from moisture and direct sunlight. Packages are clearly labeled and comply with relevant safety and regulatory guidelines. It is transported under ambient conditions, using appropriate cushioning to prevent leaks or breakage during transit. Handling instructions and hazard information are provided.
    Storage 1,4-Diethylpiperazine 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 the chemical from direct sunlight and sources of ignition. Store it at room temperature and ensure proper labeling to prevent accidental misuse. Use appropriate personal protective equipment when handling the substance.
    Application of 1,4-Diethylpiperazine

    Applications of 1,4-Diethylpiperazine in Industrial Manufacturing

    1,4-Diethylpiperazine serves as a specialized intermediate in several high-value chemical processes. The following application scenarios reflect our direct manufacturing experience and verified downstream customer usage across regulated industrial sectors. Each section details industry standards, formulation guidelines, integration into downstream processes, and typical end products.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Antihistamines

    Leading pharmaceutical manufacturers rely on this intermediate during the multi-stage synthesis of select antihistamine APIs, especially the piperazine derivatives group. Operators introduce it post-initial ring formation during the amidation or alkylation stage. Careful process control maintains strict traceability and impurity profiles in line with regulatory requirements for APIs bound for regulated markets. Changes in dosage ratios directly impact the impurity spectrum and subsequently the bioavailability of the finished drug substance, therefore formulation protocols demand documented adjustment and validation.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for Piperazine Derivatives
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Japanese Pharmacopoeia (JP) relevant sections

    Typical usage ratio

    • 0.8–1.25 molar equivalents per stage, adjusted based on yield monitoring and impurity control during synthesis of target antihistamines

    Downstream process integration

    • Charged after initial core structure formation during secondary alkylation or amidation
    • Reacted in closed, monitored reactors under nitrogen blanket to prevent degradation

    Final product types

    • Bulk antihistamine API (e.g., cyclizine or meclizine derivatives)
    • Finished oral solid dosage forms like tablets and capsules

    2. Corrosion Inhibitor Synthesis for Oil & Gas Pipeline Protection

    This raw material contributes a key nitrogen donor in formulating bespoke corrosion inhibitor blends specifically tailored for upstream and midstream oilfield operations. Chemists dose and react it with fatty acids and organic acids to build quaternary ammonium compounds that adhere to steel pipeline surfaces, slowing down acid gas-induced degradation. Process engineers optimize the ratio based on specific brine parameters, hydrocarbon composition, and pressure-temperature regime of pipelines.

    Industry compliance standards

    • API RP 14E (Recommended Practice for Design and Installation of Offshore Production Platform Piping Systems)
    • NACE MR0175/ISO 15156 (Petroleum and natural gas industries—Materials for use in H2S-containing environments)
    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals (EU)
    • ISO 9001:2015 certified QC for specialty chemical blending

    Typical usage ratio

    • 6–12% w/w in concentrated inhibitor precursor, fine-tuned through lab-scale weight loss coupons vs. field test results

    Downstream process integration

    • Added during the formation of quaternary ammonium base in closed batch reactors
    • Final formulation blended with solvent and surfactants before field dilution

    Final product types

    • Oilfield corrosion inhibitor concentrate
    • Blended field-ready corrosion inhibitor packages for pipeline dosing units

    3. Accelerator for Polyurethane Elastomer Curing

    Specialty polymer manufacturers utilize this compound as a latent curing accelerator in select non-isocyanate polyurethane (NIPU) elastomer formulations. Its tertiary amine structure catalyzes ring-opening polymerization reactions with cyclic carbonates, significantly reducing cure time without promoting unwanted side reactions. Technical staff optimize concentration based on formulation reactivity, molecular weight targets, and the desired mechanical profile in industrial elastomer end products.

    Industry compliance standards

    • ISO 9001-certified quality control for polyurethane raw materials
    • REACH Annex V Technical Dossier for Non-Isocyanate Polyurethane systems
    • Standard test methods per ASTM D3574 (Flexible Cellular Materials—Slab, Bonded, and Molded Urethane Foams)
    • RoHS Directive (2011/65/EU) for electronics grade elastomers

    Typical usage ratio

    • 0.3–0.9 phr (parts per hundred resin) in NIPU formulations, with precise tuning based on differential scanning calorimetry (DSC) cure profile analysis

    Downstream process integration

    • Premixed with resin blend before catalyst addition, ensuring even dispersion prior to polymerization
    • Integrated into closed, continuous-feed polymer reactors maintained at controlled temperature and humidity

    Final product types

    • Industrial-grade NIPU elastomer sheets
    • Custom-molded polyurethane machine parts and anti-abrasive coatings

    4. Intermediate for Flotation Collector Formulations in Mining

    Mineral processing reagent producers incorporate this material during the synthesis of selective flotation collectors, targeting sphalerite and other base metal sulfides. Under well-defined process conditions, technical teams react it with fatty acid derivatives to form cationic surfactants tailored for mineral separation in high throughput beneficiation plants. Compliance with site-specific environmental discharge permits and collector performance parameters governs exact dosage levels and process steps.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management System
    • Mine site environmental monitoring per host country Ministry of Environment regulations
    • Quality certification per ISO 9001 for mineral processing aids
    • International Cyanide Management Code (when applicable)

    Typical usage ratio

    • 7–10% w/w in collector base pre-emulsion; adjusted based on ore feed variability and froth recovery analytics

    Downstream process integration

    • Chemical incorporated into sulfide collector synthesis prior to final neutralization and dilution steps
    • Performance validated via pilot plant flotation cell tests before commercial blending

    Final product types

    • Base metal flotation collector emulsions (for Zn, Pb, Cu ores)
    • Blended specialty mining reagents for in-situ flotation dosing
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    Certification & Compliance
    More Introduction

    1,4-Diethylpiperazine: Reliable Performance Built from Manufacturing Experience

    Direct from the Source: Authenticity Matters

    Every batch of 1,4-Diethylpiperazine coming off our reactors reflects decades of hard lessons and earned trust. We handle each stage, from raw starting materials to final purification, watching for those subtle process drifts that only show up after years with this molecule. 1,4-Diethylpiperazine is rarely somebody’s first choice in a piperazine ring series. Chemists who use it are looking for more than just a cyclic amine—they’re after the unique combination of size, hydrophobicity, and reactivity that n-ethyl substitution at both 1 and 4 positions brings. They need predictable outcomes in their end applications, without the headaches that come from off-the-shelf “equivalents.” Field experience has proved one subtle impurity or moisture problem can cause weeks of troubleshooting. The materials we make meet the repeatability standards that real chemists rely on, because we’re not loading a warehouse on speculation—we’re delivering to labs and plants with serious goals.

    Practical Functionality Sets 1,4-Diethylpiperazine Apart

    The draw of 1,4-Diethylpiperazine shows up when you move past the textbook reactions and start solving real-world challenges. Compared to un-substituted piperazine, the diethyl variant resists over-alkylation and N-oxidation. Its steric bulk prevents common side reactions, a trait especially popular in custom synthesis for specialty pharmaceuticals and crop science. The poorly defined “commodities” from the open market often lack this focus, mixing regioisomers or running dry via distillation—our process integrates controlled pressure, inert gas sparge, and staged temperature ramps, yielding a pale liquid with sharp boiling point and high purity by both GC and NMR.

    The ethyl groups at each nitrogen tilt the molecule toward lipophilicity, which in turn alters solubility profiles in mixed organic/aquatic systems. While standard piperazine dissolves easily in water and signals basicity with gassing hydrochloric acid, 1,4-Diethylpiperazine does not foist itself on water—dosing must use a co-solvent or heat. This is a chemical reality in scaling up reaction workups and purification. As a manufacturer, we’ve watched more than one contract synthesis group try to treat it like its close relatives, only to see phase-separation issues grind a project to a halt. Drawing from these kinds of failures pushed us to develop a technical note addressing pH management and extraction for our customers. Working closely with the chemists who order from us helps both sides—feedback from real reactors gets fed right back into process improvements.

    Specifications Informed by Experience, Not Speculation

    The final product leaves our plant at a consistent composition, always exceeding 99% via HPLC, with water content routinely below 0.1%. This means little until a chemist watches their yield rates stabilize event after event, running larger kilos without recalibration. No batch-to-batch “surprises” show up—full traceability and in-process control during hydrogenation, distillation, and filtration assure reproducibility over time. Color control matters, especially for catalysts, Q.A. screening, or formulation, and our lots never drift beyond water-white to pale yellow, as monitored by APHA standards. Heavy metal content, a detail overlooked by some, stays far below pharmacopeial limits because we monitor reactor wear and maintain passivation schedules.

    Packing and transport often defeat fine chemicals before they even reach their destination. We learned after a string of customer complaints about off-odors and contamination: it made no sense to skirt on container selection or filling protocols just to save cents. 1,4-Diethylpiperazine gets filled under inert, in compatible fluoropolymer-lined drums or aluminum bottles, purged and sealed right after sampling. The difference shows in the shelf life and ease of handling at our customers' sites.

    Technical Advantages Over Standard Piperazine Derivatives

    In research and industrial settings, the chemical behavior differences set 1,4-Diethylpiperazine apart from the offerings of traders who barely glance at a spec sheet. Technically, its symmetrical substitution pattern minimizes risk of chiral by-products. For customers calibrating downstream coupling reactions—amide bond formation, diazotization, or heterocycle assembly—the confidence comes from unambiguous NMR and MS results. Unwanted protonation sites are absent, removing one of the biggest sources of batch problems in scale-up or pilot runs. Try running a carbamate protection step or alkylation with generic piperazine; you get a mess of side-products and a slow path to cleanup. Working with our process-verified 1,4-Diethylpiperazine means fewer chromatographic cycles, less risk of downstream impurities, and cleaner isolation.

    This product finds active use in the synthesis of specialty pharmaceutical intermediates, such as those requiring improved pharmacokinetic properties, bioavailability, or reduced central nervous system penetration. These subtle chemical tweaks often hinge on the steric and electronic characteristics that only the diethylated structure provides; our process stands up to these demanding requirements, ensuring the final outcomes are possible in both pilot and production scale.

    Lessons from Real-World Usage: Where Standard Grades Fall Short

    Looking through case histories, customers who switch to our direct-manufactured 1,4-Diethylpiperazine rarely go back to unspecified alternatives. After testing competitor lots—sometimes from generic “piperazine derivatives” or mislabelled intermediates—they hit issues with unknown solvent residues or secondary amines from side reactions. These contaminants may hide at trace levels, but become apparent in downstream performance: LC or GC spikes, poor crystallization, unexplained color development, or off-grade physical characteristics. We document every such client concern, then use failure analysis in our plant to identify the real source. Often, trace solvent occlusion during vacuum distillation or improper inerting allowed unseen reactions—this feedback informed changes in our reflux, gas sparge, and vacuum-leak protocols.

    The issue of false equivalence remains common: buyers assume all diethylated piperazines come out the same, until they experience recrystallization that fails or yields that drop off by double digits. Product coming from a trading house rarely offers records on reactor charge lots, temperature-time profiles, or operator sign-off logs. We show our customers detailed batch records, including which lots of starting amines and which technical staff handled each stage. This transparency proves critical late in a project, when questions emerge and quick answers from the top of the supply chain can mean the difference between project success and rerun.

    Applications Backed by Technical Support

    Our customer base covers more than just R&D chemists. Production sites focused on agricultural actives, photo-initiators, polymer stabilizers, and niche surfactants have all come to us for predictable 1,4-Diethylpiperazine. They value one thing above all—technical help that understands the molecule’s behavior hands-on. We don’t just send out a generic list of reaction conditions. Instead, we find ourselves on video calls, poring over batch records, or walking through IR and GC/MS data with a group of process chemists troubleshooting a new synthesis. This level of support grows from spending years troubleshooting our own reactors and analytical results. We see first-hand how issues with ring-opening, hydrolysis, or phase transfer depend on details of temperature, solvent, and even glassware residue.

    Some customers care less about technical minutiae—they order large volumes for resin manufacturing or functionalized epoxies. For these teams, price and delivery take precedence, but complaints about delayed shipments or off-grade batches make clear that reliability matters as much as cost. Our logistics department tailors promise dates, and resolving the hard details up-front—licensing, customs codes, or compliance certificates—prevents unexpected surprises in transit. Years spent troubleshooting those last-kilometer headaches taught us the value of precise Certificates of Analysis, authenticated packaging tapes, and advance notifications if anything in the order process changes.

    Competitor Parity versus Manufacturer’s Edge

    It’s tempting to assume a piperazine derivative is just a commodity, interchangeable between sources. Our own internal blind trials—handing fresh process chemists a series of unlabeled samples—revealed their clear preference for our material, even before learning origins. In hands-on coupling or acylation, differences in product quality showed up in reaction times and yields. One batch containing excess residual amine slowed progress by days because of unexpected formation of by-product salts, fouling work-up operations. Scrupulous attention to moisture, maintained through proprietary drying and venting cycles before final fill, set our product apart from shipment-aged alternatives. Such differences may not show on a simple COA but translate directly into time and cost at the plant floor.

    We take pride in owning the process from molecule to shipment. Every update—be it a reactor baffle redesign for better mixing or a modified analytical protocol—gets tested in a full field context. Customers feel the difference not just through high yields or smooth reactions, but by the experience: technical questions answered promptly, documentation that stands up to audits, and variability that shrinks as process sophistication increases. The devil remains in the details, and manufacturing has taught us to search for these hidden contributors to what buyers ultimately value most—no-excuse performance under pressure.

    Staying Ahead of Industry Needs

    We watch industry trends for a reason: research groups and industrial clients increasingly demand higher performance and traceability, especially where products enter regulated sectors like pharmaceuticals and specialty chemicals. Periods of raw material volatility pushed us to establish redundant sourcing, so our customers stay supplied and avoid critical delays. Frequent upgrades in our analytical labs, including LC-MS and GC-MS systems calibrated for trace impurity profiling, allows us to catch problems before they become costly recalls or performance failures on the client end.

    Technologies for green synthesis and waste minimization are also making their mark. Regulatory scrutiny doesn’t wait for laggards, and salt or solvent waste from amination reactions continues to trigger environmental review. We incorporate feedback from both regulatory auditors and our own plant operators—the former demand compliance, the latter live with the chemistry day-to-day. Practical upgrades like closed-loop solvent recovery, continuous nitrogen blanketing, and secondary containment ensured our product lines can withstand audits and reduce our long-game costs. Our plant’s evolving layout reflects years of hard feedback.

    Challenges and Solutions: Process, Safety, and Documentation

    Handling 1,4-Diethylpiperazine is not without risks. Its toxicity to aquatic organisms, inhalation risk, and potential as a skin and eye irritant get constant review. Unlike trading companies detached from the hands-on hazards, our operators and plant managers take the brunt of real safety concerns. Routine training, rigorous PPE protocols, and layered EHS reviews reduce incidents and downtime. Safety isn’t a paper trail here—it’s what keeps our team coming back each day. Documentation reflects this culture: clear Safety Data Sheets, training logs, and hazard label compliance run as part of the routine, audited both internally and by third-party experts with direct access to our manufacturing workflows.

    Automation plays a bigger role each year, reducing the likelihood of human error during reactor charging, phase transfers, or sampling. So do old-school operator walkthroughs—the “smell test,” sound checks, and visual monitoring driven by experience that machines still cannot fully replicate. These steps, though sometimes questioned for efficiency, consistently catch process upsets before they escalate. It’s a company culture rooted in practice, not slogans—one shaped by both regulatory requirement and pride in delivering a catalog product with the dependability of a bespoke intermediate.

    Traceability and Customer Transparency: A Modern Manufacturing Imperative

    Modern customers show little patience for black-box manufacturers. We answer this with full batch-level traceability and openness to audits. Customers frequently request not just certificates, but information about process changes, raw material shifts, or even operator training cycles. This openness has served both sides well. More than once, sharing a minor alteration or test condition has allowed a client to pinpoint a downstream inconsistency or confirm batch consistency in their own regulatory filings.

    The shift toward digitalization—barcode scanning of batches, paperless chain-of-custody systems, analytical instrument data logs—only strengthens this transparency. Our approach to 1,4-Diethylpiperazine isn’t rooted in paperwork for its own sake; it comes from real-world customer demand for honesty about what they are buying. Auditable records stop minor hitches from snowballing, especially when regulatory or end-user requirements ratchet up on short notice. Being forthcoming about blend lots, solvent changes, or even product returns has built confidence and durable partnerships that outlast transient price wars or market disruptions.

    Looking Forward: Continuous Improvement Informed by Day-to-Day Manufacturing

    Chemistry, at its root, is as much about adaptation as it is about the molecules themselves. We carry forward that lesson every day in our approach to 1,4-Diethylpiperazine. Constant review of field feedback, continuous refinement of our reactor processes, hands-on troubleshooting, and a refusal to treat chemicals as anonymous “grades” keeps us relevant to both new and veteran users in this space.

    By focusing on what matters—repeatability, transparency, support, and hands-on knowledge—we’ve not just manufactured 1,4-Diethylpiperazine, we’ve redefined its place in the supply landscape. Our product stands as a reference for specialists who value both the detail and the story that experience brings to chemical manufacturing. Every drum, bottle, and batch leaving our site tells this story—one of lessons learned, improvements made, and performance trusted where it counts most.