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Piperazine Dihydrochloride

    • Product Name Piperazine Dihydrochloride
    • Alias Piperazine dihydrochloride
    • Einecs 218-407-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    348919

    Chemical Name Piperazine Dihydrochloride
    Formula C4H10N2·2HCl
    Molar Mass 161.06 g/mol
    Appearance White crystalline powder
    Melting Point 235-245 °C (decomposes)
    Solubility In Water Freely soluble
    Cas Number 142-64-3
    Storage Conditions Store at room temperature, tightly closed
    Uses Pharmaceutical intermediate, anthelmintic agent

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

    Packing & Storage
    Packing Piperazine Dihydrochloride, 500g, is sealed in a white HDPE bottle with a tightly screwed cap, bearing hazard and product labels.
    Shipping Piperazine Dihydrochloride is shipped in tightly sealed containers, protected from moisture and incompatible materials. It should be stored in a cool, dry, and well-ventilated area. The chemical is typically transported according to local, national, and international regulations, with clear labeling to ensure safe handling and prevent accidental exposure or contamination.
    Storage Piperazine Dihydrochloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep the chemical away from moisture and direct sunlight. Ensure proper labeling and secure shelving to avoid accidental spills. Follow all relevant safety guidelines and local regulations for chemical storage.
    Application of Piperazine Dihydrochloride

    Applications of Piperazine Dihydrochloride in Industrial Manufacturing

    As a direct manufacturer with years of technical experience, we supply Piperazine Dihydrochloride to global industrial users who require consistent quality and regulatory traceability in downstream processes. Below are established application segments, each with detailed guidance on standards, functional dosing, process role, and finished product lines.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Anthelmintic Drugs

    Piperazine Dihydrochloride serves as a critical intermediate in the synthesis of piperazine-based anthelmintics, especially in the production of drugs targeting nematode infestations. Its purity and controlled chloride content meet strict pharmacopoeial criteria required for oral and suspension formulations. Pharmaceutical manufacturers integrate this compound primarily during the intermediate synthesis stage, followed by specific downstream reaction steps that determine the spectrum and stability of the final dosage forms distributed to clinical supply chains.

    Industry compliance standards

    • USP (United States Pharmacopeia) Monographs
    • Ph. Eur. (European Pharmacopoeia)
    • WHO GMP Guidelines
    • ICH Q7 API GMP Framework

    Typical usage ratio

    • Employed at stoichiometric levels of 1–1.5 molar equivalents per targeted active moiety, adjusted according to molecular route and required impurity profile

    Downstream process integration

    • Introduced during the condensation or substitution step of heterocyclic intermediate synthesis; followed by crystallization and API isolation prior to formulation

    Final product types

    • Oral tablets (e.g., antiparasitic full-dose units)
    • Powder-for-suspension pediatric dose packs

    2. Synthesis of Corrosion Inhibitors for Water Treatment Chemicals

    The compound functions in the formulation of corrosion inhibitor blends for circulating water systems utilized in industrial, commercial, and municipal cooling towers and boilers. Its dual-function as a buffering and complexing agent streamlines the synthesis of water-soluble salts, which later combine with polycarboxylates and phosphonates. Downstream producers achieve the required stability and mitigation of metal corrosion through controlled blending and post-reaction pH adjustment.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • ASTM D1384 (Corrosion Test for Engine Coolants in Glassware)
    • EU Biocidal Products Regulation (BPR) (EU) No 528/2012, for water treatment chemical registration

    Typical usage ratio

    • Added at 2–8% by weight of inhibitor concentrate, depending on target corrosion index and site-specific water hardness

    Downstream process integration

    • Charged into post-neutralization blending tanks after primary inhibitor synthesis; followed by chemical stabilization and packaging as liquid concentrates or tablets

    Final product types

    • Chemical dosing agents for industrial water circulation systems
    • Cooling water maintenance tablets for HVAC and heavy industry facilities

    3. Intermediate in the Production of Epoxy Curing Agents

    Manufacturers of liquid and solid curing agents utilize this raw material to construct polyamidoamine adducts and other polyamine derivatives, essential for high-performance epoxy coatings and composite laminates. Process engineers charge the compound during pre-polymerization steps, controlling reaction kinetics and end-group functionality to match targeted reactivity for crosslinking in downstream applications.

    Industry compliance standards

    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EC No 1907/2006)
    • ISO 12944 (Paints and Varnishes – Corrosion Protection of Steel Structures by Protective Paint Systems)
    • UL Certified VOC Level Compliance for specialty coatings

    Typical usage ratio

    • Formulators add at 10–20% amine hydrogen equivalent basis, regulated according to the epoxy resin being cured and intended application thickness

    Downstream process integration

    • Added during initial amine blend preparation, followed by controlled heating and vacuum stripping to remove residual volatiles prior to packaging of curing agent masterbatches

    Final product types

    • Epoxy floor coatings for heavy-duty industrial settings
    • Composite resin matrices for electrical insulators

    4. Starting Material for the Synthesis of Flocculants in Municipal and Industrial Wastewater Treatment

    Piperazine Dihydrochloride is used as a nitrogen source during the polymerization of cationic polyamines—polymers that serve efficiently as primary flocculants to promote colloidal particle aggregation in municipal sludge, industrial effluent, and potable water processing. Downstream production encompasses copolymerization with acrylamide or other vinyl monomers, followed by batch finishing and functional group analysis to ensure high flocculation efficacy at diverse pH conditions.

    Industry compliance standards

    • EN 1407:2018 (Chemicals used for treatment of water intended for human consumption – Polyamine flocculants)
    • NSF/ANSI Standard 60 (USA) Drinking Water Treatment Chemicals – Health Effects
    • OECD Test Guidelines for Biodegradability (for effluent products)

    Typical usage ratio

    • Charged at 0.5–3% monomer molarity equivalent based on targeted polymer chain length and charge density requirements

    Downstream process integration

    • Introduced at the pre-polymerization step as a chain-initiating or bridging agent, with continuous pH monitoring and subsequent clarification of supernatant layers

    Final product types

    • Cationic polyamine flocculant powder or liquid concentrate
    • Pre-dosed municipal sludge conditioners

    5. Precursor for Custom Synthesis of Organic Intermediates in Fine Chemicals

    This raw material provides core nitrogen building blocks for custom synthesis routes in the fine chemical sector, where pipeline derivatives include specialty ligands, pharmaceutical discovery intermediates, and certain agrochemical scaffolds. Synthetic chemists employ the compound during controlled stepwise reactions involving alkylation, heterocycle expansion, or reductive amination, which are tailored for final molecular design and downstream purification requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • GMP guidelines (where pharmaceutical precursors are concerned)
    • Relevant regional chemical substance registrations (EU REACH, China MEE, US TSCA)

    Typical usage ratio

    • Integrated between 1–10% weight-by-weight of target batch, depending on multi-step sequence and purity specification for end intermediate

    Downstream process integration

    • Utilized in step 1 or 2 during short-path batch synthesis, commonly followed by in-line HPLC monitoring and post-reaction solvent recovery

    Final product types

    • High-purity heterocyclic intermediates
    • Ligand precursors for homogeneous catalysis and metal complexation
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    Certification & Compliance
    More Introduction

    Piperazine Dihydrochloride: Experience from a Manufacturer’s Floor

    Understanding Piperazine Dihydrochloride from a Chemist’s Viewpoint

    Piperazine dihydrochloride isn’t a new face in the chemical industry. Our plant has been producing this white crystalline compound for years, and every step has taught us why quality matters. Its simple structure, C4H10N2·2HCl, makes it straightforward in theory, but the manufacturing process demands hands-on expertise. We’ve seen this chemical go from raw precursors in our reactors to a dependable intermediate for many pharmaceutical and industrial customers around the world.

    How Piperazine Dihydrochloride Emerges in Our Facility

    Chemistry textbooks might sum up the process in a few neat steps, but on our production floor, each batch calls for careful attention. Moisture control and temperature play a bigger role than you’d expect. Raw piperazine reacts with hydrochloric acid under controlled conditions to yield the dihydrochloride salt. As the mixture cools, crystallization takes over, but humidity, mixing rates, and filtration time all decide the outcome. Teams check particle size and purity after each stage, sometimes making process tweaks midstream if lab analysis hints at deviation.

    The resulting solid, after drying and screening, must meet strict limits for impurities, especially chloride, sulfates, and related amines. We maintain a typical purity above 99.5%, confirmed batch by batch. Many buyers point to this consistency as the real difference between manufacturer-sourced material and resellers’ offerings.

    Manufacturing: Details that Set the Tone

    Every batch tells a story. Incoming raw piperazine, whether from local or imported suppliers, undergoes verification using near-infrared spectroscopy and titration—too many unknowns slow down the process later. Hydrochloric acid concentration never varies more than half a percent. Under-dosing or overdosing disrupts crystal formation and influences solubility. Our empirical approach, shaped by years of operator intuition and lab data, helps us spot issues before they become large-scale problems.

    Different markets ask for different forms. The pharmaceutical sector demands a finer mesh particle size, usually 80 mesh or smaller, with moisture controlled below 0.2%. Industrial customers, often using it as an intermediate for resins or rubber chemicals, accept a slightly coarser grade, but always with full traceability. The goal remains the same—a product that dissolves cleanly, leaves no particulates, and stays free-flowing across the supply chain.

    Where Piperazine Dihydrochloride Finds Its Voice

    This chemical found its first major calling in pharmaceuticals. Anyone working on an anthelmintic project will recognize pipera-zine-based formulations—kidney-shaped tablets and powdered blends rely on the dihydrochloride form for easy dosing and patient compliance. Veterinary products still count on it, but the human sector prefers it, given the low toxicity and stable shelf life in tablet form.

    Large-scale textile plants source the dihydrochloride as a crosslinking agent for textile treatments, often to improve wrinkle resistance or dye-fixation. It’s not as glamorous as pharmaceutical use, but these applications keep demand steady. In specialty polymer manufacturing, a few grams per batch make the difference between average performance and consistent crosslinking. After spending months listening to feedback from R&D clients, we've seen the impact of trace byproducts in low-grade material—any deviation from the norm stands out in the end product.

    Piperazine Dihydrochloride vs. Its Relatives: Practical Experiences

    Customers sometimes ask why one would choose dihydrochloride over monohydrate, citrate, or even technical-grade piperazine. For chemists who deal with mixing and solubility daily, the answer lies in performance. The dihydrochloride dissolves quickly in water and stays stable under a range of pH conditions. Monohydrate has its place, but rapid absorption and consistent dosing steer most formulators toward the dihydrochloride.

    Technical-grade piperazine, less refined, introduces unknowns—may work in a pinch for non-critical applications, but years of troubleshooting client complaints have shown us the cost of impurity-related batch failures. Resins cloud, pharmaceutical blends fail uniformity testing, and even dye baths precipitate unexpected solids. Choosing the dihydrochloride at our purity levels streamlines production elsewhere.

    Other salts, such as the citrate or phosphate, have specific uses, but bulk industries keep turning to the dihydrochloride for dependable solubility and fast reactivity. Experience tells us switchovers between grades often slow down a production line, mixing teams resetting equipment between batches to prevent cross-contamination. The simplicity of one reliable grade, with batch-to-batch consistency, has proved an advantage time and again.

    Meeting the Tighter Demands of Today’s End Users

    Pharmaceutical makers are some of our toughest customers. Auditors care about more than just the purity—heavy metal content, bioburden levels, and residual solvents show up in every batch certificate. Our plant moved to continuous monitoring several years ago, meaning process data flows straight into a real-time dashboard. If an impurity spikes, production pauses and trouble-shooting begins, whether it’s caused by a raw material delivery or equipment cleaning. This level of transparency builds trust between our plant and the research labs or production facilities that depend on us.

    For export clients, documentation goes further. We track each drum from synthesis through packaging, logging spectrograms and batch data for later audits. Supporting global registrations means meeting not just our country’s standards, but international rules—European Pharmacopoeia, U.S. Pharmacopeia, Japanese standards. Each batch shipped abroad carries a file of test reports, reliability data, and, where needed, compliance with allergen declarations and Good Manufacturing Practices. It’s not just bureaucracy: a rejected shipment means more than lost revenue. It can disrupt medicine production schedules or specialty coatings plants running on tight timelines.

    Packing Practicality into Every Bag

    Bulk chemistry has a reputation for being rough around the edges, but anyone handling fine chemicals sees that packaging plays a frontline role. Piperazine dihydrochloride, though durable, clumps when exposed to air for long. Our engineering team redesigned packaging years ago, switching to double-layer polyethylene liners in heavy-duty fiber drums, reducing moisture ingress and eliminating caking. Even small details—antistatic inner bags, easy-grip closures—came out of late-night troubleshooting after a series of winter complaints from customers who found solid blocks instead of powder.

    Changes weren’t just operational. Shipping containers faced heat and humidity swings crossing continents. What leaves our facility with 0.12% moisture can arrive at 0.2% or higher after a summer at sea. We worked with logistics partners to climate-proof shipments, added humidity indicators to outer labels, and started batch-coding every container for traceability. Clients now check color, particle flow, and SDS sheets against their own internal standards before unloading. These changes reduced complaint rates and kept downstream production lines running without interruption.

    Clean Production: Why Process Matters

    Piperazine dihydrochloride may seem basic, but behind its manufacture sit environmentally responsible protocols. Our plant moved toward a closed-loop hydrochloric acid recovery system, minimizing emissions and cutting sourcing costs. Operators monitor effluent discharge, ensuring chloride ion content meets legal thresholds. No shortcut replaces the peace of mind that comes from knowing regulators won’t halt plant operations over compliance lapses. Employee safety gets constant attention—respirators, dust-proof extraction, and spill procedures get drilled and rechecked routinely.

    Waste minimization takes many shapes. Mother liquors from the crystallization stage get recycled in-house or sent for chemical treatment. Solid cake from filtration, previously a costly waste stream, now undergoes secondary extraction, pulling additional product and reducing landfill waste more than twenty percent year over year. Beyond the environmental benefits, these tweaks created new line manager roles and fostered a culture of “what can we recover next?”

    Listening to End Users: Beyond the Datasheet

    Actually talking with formulation chemists, mill managers, and buyers changes a manufacturer’s priorities. Datasheets look the same on paper, but the real test happens under the customer’s roof. A sudden switch in downstream product color, a clogged feed line, or a batch failure in tablets triggers a call to the production team. Over the years, our technical support staff shifted from reading lab values off screens to running parallel lab tests with customer samples. Each inquiry improved our process—sometimes tuning our drying protocol, sometimes revamping the milling stage for a less dusty powder.

    Sometimes, application feedback reshaped entire practices. Life sciences researchers, developing new drug delivery formats, tipped us off to how trace organic impurities in the dihydrochloride hampered their encapsulation yields. Next lot, we introduced a secondary carbon filtration stage between synthesis and crystallization. Ongoing feedback ties the manufacturing floor to the researcher’s bench.

    Challenges in Scaling Up and Staying Consistent

    Few chemicals highlight the challenges of scale like piperazine dihydrochloride. On a bench scale, almost any chemist can control purity and color, but once demand crosses several metric tons a month, small variables balloon. Water quality, agitation rates in reactors, filtration cloths, and even staff rotation schedules create subtle shifts in output. A product that was “good enough” for a local detergent formulator may cause trouble in a pharmaceutical API plant.

    Our team built a living library of process tweaks and fixes. Most days, plant engineers walk the line with operators, using smell, color, and viscosity as real-world checks alongside automated sensors. The best results come from a tight link between batch records and action. Each finished lot earns a report card: appearance, pH, loss on drying, assay result, and particle profile. Fail a margin? That batch gets a targeted rework protocol, and we don’t hesitate to rerun filtration or milling to bring standards back in line.

    Supply chain logistics also come under stress as demand grows. Sourcing consistent piperazine precursors requires reliable partners, often in regions facing regulatory or seasonal hurdles. We learned to keep safety stocks, and, in more volatile years, diversify raw input sources. Without these buffers, even a temporary shortfall ripples through to finished lot reliability. Customers who faced delays shifted to us because we carry that extra inventory commitment.

    Piperazine Dihydrochloride in Future Applications

    Emerging tech always brings fresh uses. Over the last few years, our R&D team supported a group working to optimize CO2 capture, using amine solutions based on piperazine salts. Early findings suggest the dihydrochloride form outperforms generic amines in absorption rates and stability during cycling. Interest from this field keeps us experimenting with new grades, pushed by research partnerships that demand tighter controls on trace metals and organic contaminants.

    Diagnostics teams also use small batches to build buffer solutions and calibration standards, where consistency down to the microgram matters. While these customers represent a tiny fraction of our annual output, they hand us valuable lessons on achieving the next level of refinement in process and documentation.

    As applications diversify, so do end-user precautions. Years ago, most customers only asked for basic chemical analysis and a safety sheet. Now, they request background data on process water sources, cleaning validation, and allergen declarations. Staying ahead means updating protocols not through committee but through the lived experience of each QA batch review.

    Why Source Direct from the Manufacturer?

    Buying direct brings down uncertainty. As a plant-based manufacturer, we back each batch with process data and a record of every hand that touched the product. When an issue arises, our team digs into the lot history, cross-checks with shipment conditions, and—if needed—immediately produces reference samples stored on site. Decades of dealing with unexpected requests have built a robust support system: from technical data tweaks for a regulatory submission to same-day document turnaround for delayed shipments.

    These practical benefits explain why research organizations, pharmaceutical companies, and materials engineers return to direct manufacturers. A decade ago, resellers might have sufficed, but today’s pace means nobody wants to risk a critical ingredient running short, or, worse, ending up with a warehouse full of product that falls short in use.

    Etching Trust with Every Shipment

    Doing the basic things well matters in chemical manufacturing. Piperazine dihydrochloride seems like a simple product to produce, yet every client conversation reminds us the details build or break trust. With every order, our job runs deeper than fulfilling a specification. We protect downstream processes, troubleshoot alongside R&D professionals, and build relationships based on consistent performance, not just certificates.

    Our ongoing improvements—smarter packaging, cleaner synthesis, better supply chain resilience—reflect conversations with the people who actually open the drums and run the experiments. New requests for tighter specifications or environmental credentials only push us to get better. Every kilogram we ship tells the story of these shared efforts, from the chemists and operators in our plant to the engineers turning that drum into solutions for healthcare, manufacturing, or emerging technology. Our commitment has always been to deliver not just product, but dependable experience—something every user of piperazine dihydrochloride can sense from the first use.