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Piperazine Adipate

    • Product Name Piperazine Adipate
    • Alias Piperazine Hexahydroazepine Adipate
    • Einecs 218-889-7
    • 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

    904537

    Chemical Name Piperazine Adipate
    Synonyms Hexahydropyrazine adipate
    Cas Number 142-88-1
    Molecular Formula C10H20N2O4
    Molecular Weight 232.28
    Appearance White crystalline powder
    Solubility Slightly soluble in water
    Melting Point 190-195°C
    Storage Conditions Store in a cool, dry place
    Pharmacological Use Anthelmintic (used for treatment of pinworm and roundworm infections)
    Odor Odorless
    Stability Stable under normal temperature and pressure

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

    Packing & Storage
    Packing Piperazine Adipate is packaged in a sealed, high-density polyethylene bottle, labeled, containing 100 grams, with tamper-evident cap.
    Shipping Piperazine Adipate should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Store and transport in a cool, dry, and well-ventilated area. Handle with care to avoid spills and exposure. Comply with relevant local and international chemical transport regulations, including labeling and documentation requirements.
    Storage **Piperazine Adipate** should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from moisture and incompatible substances. Protect from light and excessive heat. Ensure good ventilation to prevent accumulation of dust or vapors. Always follow local regulations and safety data sheet (SDS) recommendations for safe storage of this chemical.
    Application of Piperazine Adipate

    Applications of Piperazine Adipate in Industrial Manufacturing

    Piperazine adipate, synthesized through controlled reaction pathways in our facility, is a vital intermediate for industrial applications that demand high purity and reproducible performance. The following sections outline real-world downstream usage, technical parameters, regulatory considerations, and finished product profiles for this specialty compound.

    1. Pharmaceutical Anthelmintic Formulations

    Major pharmaceutical manufacturers use this material as an active pharmaceutical ingredient for oral anthelmintic medicines. It specifically targets gastrointestinal nematodes and is incorporated into tablets and suspensions after precise blending and granulation. The compound is selected for its efficacy, tolerability profile, and well-characterized pharmacokinetics, supporting both generic and branded product life cycles. Quality control teams use validated analytical methods to monitor content uniformity, impurity levels, and microbiological safety at each batch.

    Industry compliance standards

    • United States Pharmacopeia (USP) Monographs
    • European Pharmacopoeia (Ph. Eur.) requirements
    • China Pharmacopoeia ChP standards
    • Current Good Manufacturing Practice regulations (21 CFR Parts 210 and 211)

    Typical usage ratio

    • Active ingredient in solid dosage: 90–99% w/w per tablet or sachet, adjusted for pediatric or adult dosing
    • Dilution with excipients varies by tablet size and release profile requirements

    Downstream process integration

    • Weighing and blending into core batch during tablet or powder manufacturing
    • Wet or dry granulation followed by tablet compression or encapsulation
    • Content analysis and in-process control at critical manufacturing stages

    Final product types

    • Anthelmintic oral tablets for human and veterinary use
    • Oral suspensions formulated for pediatric or animal health markets
    • Fixed-dose combination treatments for intestinal parasite elimination

    2. Animal Feed Additives (Veterinary Anthelmintic Premixes)

    Feed manufacturers integrate this compound into engineered premixes and feed pellets for cattle, swine, and poultry. It supports livestock parasite management programs, especially in regions where broad-spectrum worm control is mandatory. The raw material is precisely metered and dispersed within mineral or vitamin blends using batch or continuous mixers, with ongoing residue and stability checks during production and storage.

    Industry compliance standards

    • European Feed Additives Register (Regulation (EC) No 1831/2003)
    • US Food and Drug Administration (21 CFR Part 558: New Animal Drugs for Use in Animal Feeds)
    • Chinese Ministry of Agriculture GB 13078—Feed Hygiene Standards
    • HACCP and GMP+ feed safety guidelines

    Typical usage ratio

    • Premix inclusion rate: 5–15% w/w in concentrated premix blends
    • Final feed: 0.025–0.1% (250–1000 ppm) depending on animal species, age, and regulatory MRLs

    Downstream process integration

    • Premixing into micro or macro ingredient blends pre-pelleting
    • Monitoring through mixer validation and cross-contamination risk assessment
    • Documentation of batch traceability for farm-to-feedlot supply chains

    Final product types

    • Medicated feed premixes for veterinary supply chains
    • Pelleted compound feeds for cattle, pigs, poultry, and sheep
    • Anthelmintic boluses for ruminant dosing systems

    3. Intermediate for Synthesis of Specialty Polymers

    Chemical processors utilize this material as a diamine source for synthesizing polyamides and other specialty polymer classes. Its reactive groups enable co-polymerization with various diacid and diisocyanate monomers to introduce flexibility and reduce crystallinity in end-use plastics. Process engineers monitor reactivity, water content, and amine equivalence at each step to achieve desired thermal and mechanical properties in the final resin batches.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for polymer synthesis
    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) compliance for polymer intermediates
    • ASTM D5336—Standard Test Method for Identification of Polyamide Plastics
    • Food contact polymer requirements (EU Regulation No 10/2011, FDA 21 CFR 177)

    Typical usage ratio

    • Co-monomer: 3–12% molar share in polyamide blends
    • Adjustment basis: target molecular weight, flexibility, impact resistance

    Downstream process integration

    • Charge into solution polymerization kettles under inert atmosphere
    • Careful feed rate control to minimize foaming and side reactions
    • In-process viscosity and amine end-group analysis during polymer chain growth

    Final product types

    • Flexible nylons for automotive and electrical housings
    • Polyurethane elastomers for industrial rollers and gaskets
    • Engineering thermoplastic resins for extrusion or injection molding

    4. Synthesis of Plasticizer Intermediates

    This compound serves as a precursor in producing adipate-based plasticizers used in flexible PVC and other specialty film applications. Notably, its incorporation enhances low-temperature flexibility and migration resistance while meeting safety and performance targets. Production facilities employ stringent esterification processes and downstream purification to assure consistent purity in the resulting plasticizer intermediates. Ongoing verification includes GC and HPLC checks on residual amines and unreacted acids.

    Industry compliance standards

    • REACH Annex XVII restrictions for phthalate alternatives
    • FDA 21 CFR Part 178—Indirect food additives: adjuvants, production aids, and sanitizers
    • EN 71-3: Safety of Toys—Migration of certain elements
    • ISO 22000 certification for food packaging supply chains

    Typical usage ratio

    • Intermediate: 1–10% in plasticizer synthesis reaction feeds, depending on desired ester profile
    • Final plasticizer content: 20–40 phr (parts per hundred resin) in flexible PVC recipes

    Downstream process integration

    • Batch- or continuous-esterification with excess alcohol or glycol sources
    • Vacuum distillation and phase separation post-reaction
    • Quality control includes acid value, color, and volatility assays

    Final product types

    • Adipate plasticizers for food-grade PVC cling films
    • Cable compounds for electrical insulation
    • Medical device tubing and seals

    5. Intermediate for Agrochemical Synthesis

    Agrochemical companies deploy this intermediate as a building block for specific nematicide and fungicide active ingredients. It provides controlled-release characteristics and improved water solubility in certain agrochemical formulations. The molecule enters proprietary synthetic routes for active ingredient assembly, with each batch certified for purity, identity, and residual amine testing prior to use. Manufacturing records align with international pesticide supply chain requirements to permit global distribution.

    Industry compliance standards

    • FAO/WHO pesticide specification guidelines
    • ISO 9001 and ISO 14001 systems for sustainable chemical manufacturing
    • Chinese ICAMA registration for pesticide active substances
    • EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act) compliance for US market

    Typical usage ratio

    • 1–6% of batch feed as key building block, depending on active ingredient backbone design
    • Adjustment determined by desired DL50 and environmental fate properties

    Downstream process integration

    • Introduction at initial stage of multi-step synthetic process
    • Monitoring for conversion yield, impurity profiling, and phase separation
    • Isolation and purification under closed-system containment for operator safety

    Final product types

    • Water-dispersible granules for soil treatment
    • Suspension concentrate nematicides
    • Fungicidal seed treatment agents
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    Certification & Compliance
    More Introduction

    Piperazine Adipate: Introducing a Reliable Solution from Experienced Chemists

    Our Journey with Piperazine Adipate

    On our production line, we live with every detail of Piperazine Adipate from the moment raw material deliveries hit the dock. Over the years, we've seen demand grow in pharmaceutical and intermediate synthesis, where trust in raw material reliability means everything. Out here, not every piperazine salt acts the same. Adipate offers unique performance compared to other counter-ions, and that has direct effects on downstream product quality—not just in analytic data, but in how final formulations behave on the line or when scaling up a new process.

    After countless batches through our reactors, we can speak to why piperazine salts sometimes attract special interest from process chemists and quality managers. Piperazine Adipate supplies a stable, relatively neutral profile that fits both as an API intermediate and as a building block. In comparison to hydrochloride or citrate variants, the adipate structure brings different solubility, reactivity, and handling traits. These might sound like small tweaks on paper, but our customers have fixed crystallization or purity headaches by switching to our adipate model. Not just one case: this keeps repeating itself every year.

    Our Production Standards and Model Insight

    Many years ago, our first successful model met rigorous pharmaceutical adoption guidelines, which shape everything we do—from reactor cleanliness to analytical monitoring and batch traceability. Consistently hitting high assay values (often above 99%) remains critical for us. Moisture control, typically under 0.5%, requires disciplined drying protocols, and we run regular loss-on-drying checks between every loadout. Experienced workers notice that the adipate salt handles with less dusting than others, and that, for a chemist or analyst, means a neater, more reproducible weighing process.

    In any large-scale operation, small deviations cost both time and downstream troubleshooting. So we keep particle size and free-flowing condition as tight as possible—no assumptions, just real daily monitoring. Some customers have strict granulometry preferences for oral solid dosing, while others prefer a finer fraction for intermediate synthesis. Our team makes direct adjustments—not by guesswork, but from feedback and our own historic batch dialogs.

    Why Chemists Request Piperazine Adipate

    Pharmaceutical development projects often run into bottlenecks rooted in raw material selection. Some drugs or intermediates decompose, show out-of-spec stability, or fail to cooperate in downstream granulation steps. The adipate version of piperazine brings a distinct advantage: its organic acid counter-ion gives a more “neutral” touch, both chemically and in terms of taste when used as an intermediate. Piperazine Hydrochloride, for instance, may solve an API solubility hiccup but at the cost of exposure to chloride ions, potentially risky for sensitive chemistry or formulations. Citrate and succinate salts offer their own unique profiles, but with adipate, everyone in development gets a more predictable manufacturing process—less variability, fewer weird polymorph surprises.

    We have conducted batch-by-batch stability tests and found that Piperazine Adipate holds up well under standard storage conditions. This translates to less batch variability for those formulating solid dose preparations. Animal nutrition and feed additive vendors also report fewer issues with caking or sorption compared to citrate variants, possibly owing to its lower hygroscopicity.

    Practical Details: From Process to Packout

    Each kilogram of Piperazine Adipate passing through our facility represents an entire chain of careful decisions. We source our adipic acid and piperazine stocks only from trusted suppliers after qualifying analytical audits. Both components undergo in-house identity checks for each new lot—if a lot does not pass NMR or melting point, we send it back. Our reactors combine the two in water under monitored pH and temperature. Here, anybody can make a batch, but few achieve the required reproducibility. We've refined the isolation and drying sequence to produce material that resists agglomeration and holds minimum water content.

    Quality assurance runs through wet-chemical titration, HPLC purity reports, and finished product release under our in-house documentation. Every pack receives a batch-specific report, not as a paperwork requirement but because it protects both our reputation and the customer’s critical project timelines. Shipments leave only after passing appearance, moisture, and solubility checks. We insist on hard packaging controls (foil-lined drums or well-sealed PE bags) because Piperazine Adipate remains sensitive to ingress of humidity—a problem our first few years taught us to take seriously. Feedback loops have led us to sturdy, stackable packouts that avoid compression or bridging, saving production floor workers from dealing with rock-solid product blocks.

    What Sets Piperazine Adipate Apart in the Chemical Marketplace

    Many companies sell piperazine salts. Those outside production often overlook that seemingly simple changes to the counter-ion shift everything—storage, downstream synthesis, and even regulatory compliance. Piperazine Adipate, unlike the hydrochloride or phosphate options, brings a naturally lower ionic strength and less corrosive impurity profile. These factors not only help when adhering to GMP and cGMP practices but also ease final purification and reduce equipment maintenance cycles at scale.

    In our experience, the pharmaceutical, veterinary, and chemical synthesis sectors each approach us with their own unique reasoning. Some value the more manageable taste in oral veterinary medicine, as hydrochloride versions can render feeds unpalatable. Others point to crystallization purity and less tendency toward forming multiple polymorphs—one less variable in API process development. Energy storage and specialty polymer research groups appreciate the cleaner, lower-ash profile Piperazine Adipate brings into pilot reactors.

    As producers, we rarely see off-spec returns or complaint tickets when our adipate leaves the warehouse. This doesn't happen by chance: it's the product of lessons from repeated process audits and real-world conversations with plant chemists and formulators. We encountered and reduced color formation during drying stages, re-developed filtration strategies to stave off micro-particulates, and keep adapting our process as analytical technology advances. Piperazine Adipate continues offering a smoother, less trouble-prone track record compared to alternatives, sometimes even unlocking a previously blocked formulation path.

    Navigating Challenges: Storage, Shelf Life, and Handling

    No chemical manufacturer ignores headaches surrounding shelf stability and handling convenience. Piperazine Adipate offers a favorable profile on both scores, as long as it’s protected from moisture and crude contamination. Our packs utilize moisture barriers, not from box-ticking but from repeated customer returns after exposure to high summer humidity—those early lessons shape our current high-bar standards.

    From a storage perspective, Piperazine Adipate typically provides 2 to 3 years of stable, compliant shelf life under sealed conditions. Our own batch monitoring tracks assay evolution and moisture uptake, especially in the transition from climate-controlled warehousing to actual customer storage environments. We’ve identified patterns of caking and solved these by reworking particle size and packaging—details driven by continuous improvement, not by regulatory compulsion.

    Supporting Formulators and Researchers

    We interact with R&D chemists who test various salt forms for their candidate molecules. Because Piperazine Adipate dissolves easily in water but doesn’t contribute strong acidity, it slots into processes where other salts interfere, slow down, or produce incompatible by-products. Most valuable, it eliminates the possibility of extraneous chloride or phosphate ions that would later complicate downstream synthesis or provoke stability concerns. Some specialty applications, including research on new reaction mechanisms or solubilizers, require that “clean slate” profile offered only by adipate couplings.

    Lab-scale and pilot-scale users often notice the practical benefits during scale-up. Our Piperazine Adipate model maintains both surface area and bulk density within narrow limits. That predictability helps transition a synthetic route from 500g lab trials to commercial output, with fewer surprises on yield or crystallization. Feed-study researchers and solid-dosage development techs trust its less abrasive, non-caustic nature to minimize wear on handling equipment, layer presses, or blenders. For us, these are not brochure claims—we hear the same stories from end users adapting our product batch-by-batch.

    Where regulators require traceable or impurity-minimized intermediates, our Piperazine Adipate routinely passes with high scores. Our continuous, self-critical auditing means we catch and reduce impurities (both organic and elemental) to levels far beneath industry maximums. Audits and customer validation runs carry meaningful real-world consequences for us; a missed out-of-spec trend affects both partners, so our model is always anchored in analytical transparency.

    Market Dynamics and Our Response as a Producer

    Pricing and availability trends often shift in the specialty chemical world, especially where raw materials ride the wave of global supply shocks. As one of the few producers who maintain their own stock of upstream adipic acid and piperazine, we shield our own customers from the worst swings. Our procurement arm monitors global trends and develops “insurance” contracts to keep material available even through unexpected surges. Several customers have cited us as among the last to allocate, or place rationing, in periods of shortage—a track record born from grit and deliberate supply chain investment.

    Our technical team works with process chemists and project leaders at major manufacturers, aiming to customize our Piperazine Adipate’s flow or purity grading when projects demand it. This responsiveness and openness to customer conversations have won us more than repeat business—it has shaped how we run our facility and which certification pathways we chase. We built our quality standards, shelf-life claims, and routine external batch validation in response to partners who needed more than promises.

    Unique orders or specifications (such as micronized fractions or packaging under inert atmosphere) arise more often every year. Working directly with users, we’ve supported projects that range from scaled-up pharmaceutical campaigns to animal health studies. We bring our field experience, mistakes, and fixes into every batch. This isn’t an abstract service—we believe in a transparent, retraceable workflow from intake through packout, something only a full-vertical producer can guarantee.

    Environmental Considerations and Manufacturing Philosophy

    Stringent manufacturing controls come with the territory, but we pushed beyond minimum compliance years ago. All water streams from Piperazine Adipate synthesis run through closed-loop treatment before return or discharge. By refining yield and optimizing recovery steps, we’ve cut waste and solvent losses year after year. Energy use is another focus: reactor temperatures, drying protocols, and HVAC management blend operational efficiency with environmental care, a balance we revisit every year.

    Waste minimization is not jargon for us—it’s a key advantage in both cost and regulatory scrutiny. Each production run gets logged for water, energy, and consumables. Where customers require, we supply post-production environmental audits. Veterinarians and animal health buyers especially ask for proof of standards that fit into their “green” supply chain story, and we answer this challenge batch-by-batch, not by PR announcement.

    Insights from Years in the Field

    No two formulation or process campaigns look alike. Often, our clients reach out after they face a concrete problem: a drug candidate precipitates unexpectedly, a batch fouls equipment, or a regulatory audit flags undisclosed trace ions. Piperazine Adipate has become the corrective step more than once—the swapout that solved the immediate challenge and simplified their long-term process. Customers remember our rapid reactivity in these moments and stick with us project after project.

    For those starting a new product or troubleshooting a chronic issue, our staff and technical team always suggest contacting us directly. We field real, specific questions and return with historically proven, not theoretical, adjustments. Several breakthroughs in taste masking, synthesis streamlining, and impurity reduction started with a call and ended with a custom Piperazine Adipate batch run. We see ourselves as more than chemical vendors. Our role stretches from production through collaborative improvement, guiding scientists and manufacturers not just to a commodity, but to a better-performing raw material.

    Over the years, we’ve realized that persistence in process control, personnel training, and frank result reporting matter more than any label claim. Piperazine Adipate’s success in our facility stands on old-fashioned stubbornness—batch records, line checks, real correction for every out-of-bounds variation, and a habit of listening to production techs as much as research chemists. This culture has built a lot of goodwill, and it shows in our client retention and repeat orders.

    Pathways Ahead with Piperazine Adipate

    Looking forward, we see continuous process updates as the norm, not a disruption. As analytical tools sharpen, as user demands evolve, and as regulatory bars rise, our team adapts—sometimes ahead of the curve, sometimes by learning from the last tough batch. Piperazine Adipate will stay core in both our product lineup and our development focus. We monitor variation trends, customer feedback, and emerging science to continually push for improvements, not just in theoretical performance but in real-world, practical use.

    Our experience as hands-on chemists and manufacturers tells us that every kilogram counts—every step, from synthesis to storage, shapes the outcome in the customer’s production line or R&D project. Piperazine Adipate is more than a catalog number for us; it’s the output of experience, collaboration, and commitment to long-term partnerships rooted in transparency, reliability, and predictable performance.