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4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride

    • Product Name 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride
    • Alias EDP-CCl
    • Einecs 610-325-2
    • 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

    666579

    Cas Number 143781-82-0
    Molecular Formula C7H7ClN2O3
    Molecular Weight 202.60 g/mol
    Iupac Name 4-ethyl-2,3-dioxopiperazine-1-carbonyl chloride
    Appearance White to off-white solid
    Purity Typically ≥ 95%
    Solubility Soluble in organic solvents (e.g., DCM, THF)
    Melting Point No specific data available; decomposes upon heating
    Boiling Point No specific data available
    Storage Conditions Store at 2-8°C, protect from moisture and light
    Reactivity Reacts with water, alcohols, and amines
    Synonyms N-(Chloroformyl)-4-ethyl-2,3-dioxopiperazine
    Stability Stable under recommended storage conditions
    Hazard Statements Corrosive, causes severe skin burns and eye damage
    Ec Number N/A

    As an accredited 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride, securely sealed in an amber glass bottle, labeled with hazard warnings.
    Shipping 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride should be shipped in tightly sealed containers, under inert atmosphere, and protected from moisture and light. It must comply with hazardous materials regulations, including proper labeling and documentation. Transportation should be carried out by certified carriers, ensuring temperature control and prevention of accidental release or exposure.
    Storage 4-Ethyl-2,3-dioxo-1-piperazine carbonyl chloride should be stored in a tightly sealed container, under an inert atmosphere such as nitrogen or argon, in a cool, dry place. Protect it from moisture, heat, and direct sunlight. Store separately from water, alcohols, amines, and other incompatible materials. Handle in a well-ventilated area, preferably within a chemical fume hood.
    Application of 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride

    Applications of 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride in Industrial Manufacturing

    4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride serves as an advanced synthetic intermediate for multiple high-value industrial segments, notably in regulated fine chemical, pharmaceutical, agrochemical, and specialty polymer production. The following scenarios outline its direct industrial integration, requirements, and technical contribution to each downstream field.

    1. Pharmaceutical API Intermediate Synthesis

    This compound acts as a selective acylating and cyclizing agent in the multi-step synthesis of specific piperazine-based active pharmaceutical ingredients, such as neuroleptics and antitumor drugs. Operators utilize its stable carbonyl chloride functionality for controlled coupling with nucleophilic amines or hydrazines under tightly regulated batch or semi-continuous conditions. Selection of the appropriate reaction parameters ensures precise molecular architecture and yields, while maintaining compliance with international GMP requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • 21 CFR Part 210 & 211 (FDA cGMP)
    • EU EudraLex Volume 4
    • Ph. Eur., USP, JP monographs (depending on downstream API)

    Typical usage ratio

    • 0.4–1.2 molar equivalents per amine/hydrazine reactant, adjusted for impurity control and regulatory limits

    Downstream process integration

    • Charged to high-shear reactors after initial substrate activation, followed by solvent exchange and crystallization steps

    Final product types

    • Targeted small-molecule APIs such as antipsychotics, antitumor agents, and CNS drugs

    2. High-Performance Agrochemical Intermediate Development

    In crop protection and pest management product synthesis, formulators use 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride to introduce cyclic imide motifs with pesticidal properties. The selective reactivity facilitates controlled substitution reactions, producing core structures for fungicides and herbicides. Production lines require stringent process control to prevent carryover of residual chlorides and to meet agrochemical regulatory specifications.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Ingredients
    • ISO 9001:2015 Quality Management Systems in Agrochemical Manufacturing
    • REACH Regulation (EC) No 1907/2006 for substance registration and pre-registration
    • Global GAP for formulation plants supplying edible crop protection inputs

    Typical usage ratio

    • 0.15–0.9 molar ratio relative to the nucleophilic agent, with adjustment based on required purity and process yield

    Downstream process integration

    • Direct addition to agitated batch reactors following initial substrate deprotonation; downstream purification via phase separation and activated carbon filtration

    Final product types

    • Piperazine-based fungicides, selective herbicides, growth regulator active compounds

    3. Specialty Polyimide and Polymer Additive Manufacturing

    Advanced polymer processors employ this compound as a chain modifier and functionalizing agent in synthesis of specialty polyimides and engineering plastics. Its reactivity with diamines or polyol blocks enables integration into polymer backbones, delivering improved dimensional stability and heat resistance. Operators maintain strict ratio control to ensure batch consistency and compliance with international material safety and purity requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Systems for Polymer Manufacturing
    • REACH (EU) Chemical Registration
    • RoHS Directive 2011/65/EU for electronics applications
    • ASTM D3815 (for polyimides and related copolymers)

    Typical usage ratio

    • 0.02–0.1 wt% relative to total monomer content; fine-tuned based on polymer architecture and end-use specification

    Downstream process integration

    • Introduced during polycondensation or post-polymerization modification steps; followed by extrusion or molding into engineering components

    Final product types

    • High-temperature polyimide films, engineering plastics, composite resins for automotive and electronics

    4. Fine Chemical Intermediate for Dye and Pigment Synthesis

    Manufacturers of advanced organic colorants exploit the compound’s carbonyl chloride function to enable ring closure and functional group integration needed for high-purity pigment intermediates. Chemical engineers precisely meter the raw material into the condensation step to tailor pigment color, intensity, and stability, while controlling chlorinated byproduct formation to comply with workplace and product stewardship standards.

    Industry compliance standards

    • ISO 9001:2015 Quality Management (Dye and Pigment Sector)
    • OECD SIDS for chemical intermediates
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) code of practice
    • GHS/CLP labelling and manufacture provisions

    Typical usage ratio

    • 0.3–0.8 molar equivalents per aromatic amine reactant, adapted by process color yield and impurity profile

    Downstream process integration

    • Pumped into jacketed reaction vessels under inert atmosphere before azo coupling or phthalocyanine complexation

    Final product types

    • Specialty dyes for textiles, high-stability organic pigments for coatings and plastics

    5. Advanced Chemical Research and Custom Synthesis Services

    Organizations specializing in contract synthesis and research rely on this compound to construct complex heterocyclic frameworks for pharmaceutical screening, target validation compounds, and proprietary process development. It supports scalable, reproducible synthesis for pilot and commercial proof-of-concept under fully documented process conditions.

    Industry compliance standards

    • ISO 17025 Accredited Laboratories (analytical verification)
    • GLP (Good Laboratory Practice)
    • Material Transfer Agreement (MTA) terms for client-specific projects
    • Export Compliant Documentation according to ITAR/EAR as required

    Typical usage ratio

    • 0.1–1.0 molar equivalents, as determined by experimental design, target molecule structure, and project purity requirements

    Downstream process integration

    • Metered into custom multi-step synthesis flows; integrated with analytical QC checkpoints for intermediate recovery and validation

    Final product types

    • Reference standards, impurity markers, advanced building blocks for pharmaceutical and material science applications
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    Competitive 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride: Production Insights and Real-World Impact

    Introduction

    As the manufacturer behind 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride, our story with this compound goes beyond formulas and batch numbers. Every lot leaves our site shaped by hands, tested by seasoned chemists, and built on years of adjusting real-world processes. We know it by feel, not just by certificate, and we don’t take shortcuts with quality or transparency—especially for a product as specialized as this. The market keeps growing for heterocyclic intermediates that drive pharmaceutical and advanced material progress, and we have seen firsthand how the details matter with this molecule more than most.

    Getting to Know the Molecule

    In structure, 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride takes shape as a chlorinated derivative of a six-membered nitrogen ring, bearing both dioxo and ethyl substitution. The carbonyl chloride group, highly reactive under controlled conditions, transforms the molecule into a sought-after intermediate in medicinal and fine chemical synthesis. The difference from basic piperazine ring compounds starts with the extra functional group activity: with a carbonyl chloride, labs unlock routes to amides, ureas, or hydrazide chains—key links in complex drug and agrochemical discovery.

    Production Experience: What We’ve Learned

    Manufacturing 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride consistently pushes us to blend technical expertise with sharp safety awareness. Chlorinating a dioxopiperazine base under tightly managed systems, then purifying to a high grade, demands equipment free from chlorinated byproduct corrosion and strictly controlled water content at every stage. As any plant manager will notice early on, the reactivity of the carbonyl chloride function brings extra hazards during quenching and transfer. We have learned to build extra containment and air scrubbing into our layout, based on things you don’t see in standard lab scale instructions. This makes splitting a lab synthesis recipe from a true industrial approach essential: raw skill in handling, not just pure theory, has shaped our SOPs and batch controls.

    The market expects not just high assay but also precise documentation, and we put our fingerprints on every test run. With this molecule, thorough HPLC and GC-MS profiles are not negotiable—any trace of hydrolysis or mixed chlorides shows up in yield drops and application failures downstream. Solvents, seal grades, and inert gas purity all end up visible in the final result. Monitoring these tightly makes the difference between a research grade and a true manufacturing-grade product, and we have seen customer syntheses saved from failure when using genuinely pure 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride.

    Specifications and What They Mean in Practice

    Our typical output lands well above 98% purity by HPLC, and we’ve found the real test lies in the absence of persistent trace impurities like unreacted piperazine or minor chlorinated side-products. Moisture content barely crosses a fraction of a percent, avoiding premature hydrolysis—a common culprit behind unstable carbonyl chloride shipped long distances. Particle size control matters in handling bulk powder (keeping it free-flowing and jam-free through transfer hoppers), while attention to packaging with solid liners and sealed drums stops unintended environmental contact.

    Testing specifications reflect zones learned from batch records, not just industry wants on paper. Early customer feedback pointed us to keep a close eye on color: off-white to pale yellow signals good control, while any brown hints at decomposition or excess byproduct, a plot we’ve traced when reusing solvents or pushing reaction rates beyond plant comfort. Each element grew out of end-use demands in API (Active Pharmaceutical Ingredient) synthesis, where even a slight contaminant can jeopardize downstream catalytic steps or cause regulatory headaches.

    Applications: Where Real Users See Impact

    Across sectors—from pharmaceuticals to fine materials—4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride acts as a true gateway molecule. Our partners in pharma innovation often target its versatile carbonyl chloride for introducing new acyl groups onto piperazine rings, producing next-generation kinase inhibitors or CNS-active molecules. In polymer and specialty coating fields, it allows tailored monomers with both cyclic rigidity and reactive sites. Unlike simpler acid chlorides, the backbone of this molecule resists uncontrolled hydrolysis, allowing for selective downstream manipulation that saves both time and money.

    Teams in research, scale-up, and regulatory validation see the difference from classic piperazine or mono-chlorinated analogs: they need a linker that can perform exact amide formation, with the ring structure delivering stability and the ethyl group tuning the electronic signature. Some large molecule developers tell us they’ve tried cheaper ring chlorides, only to see erratic yields from instability, requiring extra purification or, worse, scrapping whole phases of candidate build-out. Over the last few years, streamlined syntheses using this particular intermediate have helped users cut out extra protection-deprotection steps, saving significant time and raw material, as confirmed by customer feedback and their own published case studies.

    Differences from Other Piperazine-Based Carbonyl Chlorides

    From the perspective of someone who has synthesized, tested, and cleaned up after many piperazine derivatives, the unique chemistry of 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride isn’t just semantics. A familiar acid chloride group placed directly onto a dioxopiperazine ring with an ethyl tail doesn’t just offer another flavor of reactivity—it presents application advantages and process practicalities absent in its cousins.

    Classic piperazine carbonyl chlorides like 2,3-dioxo-1-piperazine carbonyl chloride, lacking an ethyl substituent, can show higher reactivity and lower selectivity towards certain nucleophiles. That translates, for real users, to more frequent problems in achieving high-purity amide targets without overreaction or unwanted polymerization. By contrast, the ethyl group on the four position (placed by us with consistent precision) modulates electrophilicity, resulting in a smoother, more controlled profile during coupling reactions. Some customers in drug discovery point directly to this feature when adapting new SAR (structure-activity relationship) lines—what they can do with the ethylated intermediate simply isn’t possible with other variants.

    We have run parallel syntheses ourselves to see this play out: the ethylated version, under the same reaction temperature and catalyst, produces cleaner end-products, minimizing side-chain scrambling or decomposition. Residue analysis shows fewer unidentified peaks, translating into easier scale-up for those who struggle with multi-kilo runs. The dioxo (double-keto) substitution built on the piperazine ring brings a higher rigidity and planarity, which shows up in increased structural predictability downstream, critical for those controlling conformation in drugs or advanced materials. Familiar mono- or tri-chloro piperazine derivatives, in contrast, often struggle with solubility and inconsistent reactivity profiles.

    Why Purity and Integrity Matter in Sourcing

    Real-world customers often walk a risk line with specialty reagents sourced from secondary brokers or discount vendors—what comes with their price tag can haunt a whole project with ghost peaks or mysterious byproducts. We’ve heard stories from clients who traced an entire month of screening failures back to a small batch of off-spec 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride: one drifted moisture level, a trace impurity, and the domino effect sets in. After these hard lessons, our team invests deeply in repeated batch stability screening, random spot-checks, and authentic samples available for verification.

    Each drum rolls out under our laboratory’s direct supervision, with tamper-evident seals and individually certified COAs tied to the batch. We track every step, from raw materials (our piperazine source checked not just for assay but for exact impurities that can carry through) to the final stock’s free acid content. We also ship with a focus on container quality—end users report fewer caking or degradation issues when drums are lined with appropriate non-reactive films, so we refuse to compromise on this even at higher packaging costs.

    Anyone serious about medicinal chemistry or advanced polymer synthesis recognizes how quickly a single impurity can wreck a campaign or force costly retesting with regulators. Our open communication with customers, publishing full impurity profiles and analytical chromatograms, wasn’t always the standard, but years of joint troubleshooting have proven that complete transparency wins trust and helps everyone reach their goals faster.

    Supporting Users Through Change and Innovation

    Many leading research organizations push the boundaries of chemistry with novel intermediates every year. In our site, that means rapid adjustments to synthesis routes, downstream coupling techniques, and even storage conditions based on real feedback. Take the example of teams developing new anti-tumor libraries: requests for micro-scale sealed ampoules, focused on protecting the carbonyl chloride functionality for combinatorial chemistry, led us to upgrade not just container selection but also guide sheets and design custom desiccants.

    The demands aren’t just technical. Shifts in regulatory scrutiny have ramped up needs for traceability, batch record retention, and a clear chain of custody—especially on exported products entering the US, EU, or Japanese pharmaceutical supply. To keep pace, our quality team tracks every COA and re-analysis, offering full access to customers during audits or routine reviews. These steps came out of necessity: failing to meet traceability standards on a minor shipment could lead to shipment rejection, surprise audits, or worse.

    Partners who run high-throughput screening depend on consistent delivery times and straightforward customs declarations, factors at the intersection of production expertise and real-world logistics. We have tuned our scheduling and logistics systems to meet critical project timelines, handling emergency shipments when customer launch dates slip or scale-up plans jump. We don’t just supply a molecule—we carry part of your timeline, and we take pride in it.

    Troubleshooting and Continuous Improvement

    Producing chloroformates and carbonyl chlorides isn’t a “one-and-done” scenario. From our very first campaign, we’ve seen surprises—process shifts when temperature surveillance falters, or when minor feedstock deviation echoes all the way through to the final product. Our engineers frequently dissect failed runs, examining chromatograms and residue samples, swapping notes between R&D and production teams.

    Clients sometimes catch things we missed: fractionally higher baseline signals on NMR, or a persistent color shift after storage. By running split batches and new pilot scales, we refine our drying, purification, or isolation phases, often taking a feedback loop directly from user reports. Not every improvement comes from the inside—many customer-driven tweaks have reshaped our protocols and raised overall batch-to-batch stability.

    Given the sensitivity to moisture and temperature, clients constantly face packaging and storage challenges onsite. We began working with partners on remote condition monitoring and redesigned secondary seals after a large user reported decomposition when storing the product for longer than two months. Our dialogue led to fresh recommendations: dry, cool storage backed by continuous monitoring, and reminders to check package integrity before each transfer.

    Solutions for Common User Issues

    Over the years, end users have flagged a few recurring hurdles with 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride. These range from physical handling (clumping from humidity) to synthetic scale-up (unexpected byproduct in amide formation). We have developed sample troubleshooting protocols with our QC group, offering direct support for issues like:

    Beyond chemistry, our after-delivery support centers on real communication: rapid response to issues, ongoing improvements, and a willingness to acknowledge and fix problems when they arise.

    Looking Ahead: The Future of This Intermediate

    As synthesis sophistication grows and new drug leads emerge, so do the requirements for advanced intermediates. 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride fits into a future focused on targeted synthesis, green chemistry, and data-driven scale-up. Over the past decade, our customers' move toward automated or continuous flow processes revealed new needs for flow-compatible intermediates, and we have started tailoring product forms and packaging for push-button, automated use.

    Regulatory trends point to even tighter controls and full-lifecycle tracking. We constantly review environmental, health, and safety (EHS) data from our runs and collaborate with large downstream processors on reducing hazardous waste. Redesigning our systems to process and recover side-products creates value and shrinks our environmental footprint, and we regularly share both best practices and lessons learned with industry partners.

    We have trained and built teams who see every batch as the start—not the end—of our responsibility, carrying each lot from raw ingredient selection to safe delivery in your lab. As demand for complex, high-stakes intermediates rises, our experience and insistence on transparency remain our most valuable contribution to the industry.

    Conclusion

    Few products emphasize the connection between production rigor, user needs, and real-world performance like 4-Ethyl-2,3-Dioxo-1-Piperazine Carbonyl Chloride. As manufacturers, we have lived the full journey, and what keeps our operation running isn’t just technical knowhow—it’s our ongoing relationship with users, our honesty about challenges, and our relentless pursuit of quality. Every order carries the weight of someone else’s breakthrough, process efficiency, or regulatory peace of mind, and we take that seriously. Through continual adaptation, rigorous control, and direct engagement with the field, we aim to keep this and every future batch ready and right for the next step in science.