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Cyclen

    • Product Name Cyclen
    • Alias 1,4,7,10-Tetraazacyclododecane
    • Einecs 218-248-1
    • 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

    804924

    Chemical Name Cyclen
    Iupac Name 1,4,7,10-tetraazacyclododecane
    Cas Number 294-90-6
    Molecular Formula C8H20N4
    Molecular Weight 172.27 g/mol
    Appearance White crystalline solid
    Melting Point 153-158°C
    Solubility In Water Soluble
    Boiling Point Decomposes
    Density 1.13 g/cm³
    Pubchem Cid 91425
    Smiles C1CNCCNCCNCCN1

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

    Packing & Storage
    Packing Cyclen is packaged in a 25-gram amber glass bottle with a secure screw cap, labeled with hazard warnings and product information.
    Shipping Cyclen is shipped in tightly sealed containers, protected from moisture, heat, and light. Appropriate labeling and documentation specify its chemical identity and hazards. Transportation complies with local and international regulations, ensuring secure packaging to prevent leaks or spills. Only authorized personnel trained in chemical handling should manage receipt and storage.
    Storage Cyclen should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizing agents. Protect it from moisture and direct sunlight. Store it at room temperature and label the container clearly. Ensure chemical storage complies with institutional safety guidelines and local regulations to prevent contamination or accidental exposure.
    Application of Cyclen

    Applications of Cyclen in Industrial Manufacturing

    Cyclen, or 1,4,7,10-tetraazacyclododecane, is a macrocyclic tetraamine recognized for its unique chelation behavior and functional group modification capacity in specialty chemical synthesis. As a direct manufacturer, we deliver cyclen to critical sectors where precise purity, traceability, and process consistency are non-negotiable. Below, we detail key application scenarios—each reflecting authentic industrial usage, regulatory frameworks, and factory-stage formulation practices.

    1. MRI Contrast Agent Precursor Synthesis

    Pharmaceutical and medical imaging manufacturers employ cyclen as a foundational building block in the synthesis of macrocyclic gadolinium-based MRI contrast agents. Cyclen forms the central ligand for stable complexation with gadolinium ions, ensuring safety and precise relaxivity profiles in clinical diagnostics. Its purity and batch-to-batch consistency directly affect the safety compliance and imaging performance of the downstream pharmaceutical final products.

    Industry compliance standards

    • U.S. FDA 21 CFR Part 210/211 (cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia Monograph 01/2019:2384 for Gd chelates
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • ISO 13485:2016 for Medical Devices Quality Management Systems

    Typical usage ratio

    • 0.9 – 1.1 molar equivalent relative to gadolinium in chelation step
    • Formulation adjusted according to reactivity and endpoint assay of ligand completeness

    Downstream process integration

    • Introduced at the chelation reactor stage; dissolved in appropriate solvent and neutralized, followed by controlled addition of gadolinium salt under pH- and temperature-regulated conditions
    • Unreacted excess removed by chromatographic purification before formulation into injectable solution

    Final product types

    • Gadolinium-based MRI contrast injectables (e.g., Gadoterate meglumine, Gadobutrol)
    • Finished bulk pharmaceutical ingredient for contrast agents

    2. Homogeneous Catalysis Ligand Manufacturing

    In fine chemical production, cyclen derivatives serve as ligands for transition metal catalysts, particularly in hydroformylation and asymmetric synthesis. Process efficiency and catalyst selectivity depend on the macrocycle’s structural purity and ability to stabilize metal complexes. Our material supports the manufacture of advanced organometallic catalysts adopted in bulk and specialty synthesis.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical production
    • REACH Regulation (EC) No. 1907/2006 for chemical substances
    • Responsible Care Global Charter for chemical stewardship

    Typical usage ratio

    • 0.5 – 2.0 molar equivalents per mole of transition metal precursor
    • Precise ratio set by catalyst optimization trials; excess monitored via spectrometric endpoint analysis

    Downstream process integration

    • Reacted with metal salts under inert atmosphere at ligand complexation stage; subsequent purification by solvent extraction or recrystallization
    • Material purity (≥99%) required to avoid catalyst poisoning in downstream batch or continuous reactors

    Final product types

    • Homogeneous transition metal catalysts for olefin hydroformylation
    • Chiral catalyst systems for pharmaceutical intermediate synthesis
    • Process aids for specialty polymer production

    3. Radiopharmaceutical Chelator Synthesis

    Cyclen forms the core structure for macrocyclic chelators used in radiopharmaceuticals, facilitating stable binding of radionuclides like Yttrium-90 or Lutetium-177 in targeted cancer therapies. Chelator design heavily relies on cyclen’s tetraamine framework to achieve in vivo stability and precise targeting during radiolabeling and subsequent patient administration.

    Industry compliance standards

    • USP Chapter <825> Radiopharmaceuticals—Preparation, Compounding, Dispensing, and Repackaging
    • European Pharmacopoeia Monograph 07/2021:2692 for Radiopharmaceutical preparations
    • GMP for Active Pharmaceutical Ingredients (APIC/CEFIC Guidance)

    Typical usage ratio

    • 1.0 – 1.25 molar equivalent per mole radionuclide precursor
    • Formulation adjusted based on chelation yield and specific activity; minimization of excess to meet radiochemical purity requirements

    Downstream process integration

    • Charged as the main ligand in radionuclide labeling step under sterile, shielded conditions
    • Post-chelation purification through solid-phase extraction to remove free chelator and uncontrolled species

    Final product types

    • Radiolabeled chelator intermediates (e.g., DOTA-conjugates for antibody labeling)
    • Final injectable radiopharmaceuticals for PET and SPECT imaging, targeted radionuclide therapy

    4. Water Treatment Heavy Metal Scavenger Component

    Cyclen-based compounds contribute to industrial effluent water treatment where specific targeting and sequestration of heavy metals such as mercury and lead are required. In high-value water recycling and remediation systems, cyclen derivatives enable selective binding and removal downstream of conventional precipitation or filtration steps, supporting factories’ environmental discharge compliance.

    Industry compliance standards

    • U.S. EPA 40 CFR Part 433 (Metal Finishing Effluent Guidelines)
    • ISO 14001:2015 Environmental Management Systems
    • Local regulatory standards for industrial wastewater contaminants (e.g., EU Water Framework Directive 2000/60/EC)

    Typical usage ratio

    • 5 – 50 ppm in industrial wastewater, optimized by target metal content and flow rate
    • Dosage determined via pilot plant treatability studies and real-time monitoring

    Downstream process integration

    • Dosed directly into effluent collection tanks before selective ion exchange or membrane separation unit
    • Post-treatment filtration removes cyclen-metal complexes before water discharge or recycling

    Final product types

    • Decontaminated industrial process or cooling water for safe discharge or reuse
    • Concentrated heavy metal waste for regulated disposal

    5. Macrocyclic Ligand Intermediate for Specialty Polymers

    In high-performance polymer manufacturing—such as engineering plastics with tailored electronic or barrier properties—cyclen functions as a critical intermediate for specialty ligand incorporation. Polymer properties can be adjusted by crosslinking or functional modification of the macrocyclic backbone, significantly influencing the polymer’s ion selectivity and stability in harsh service environments.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Polymer Intermediates
    • REACH Substances of Very High Concern (SVHC) Notification
    • ISO 1872-1:2019 for General Purpose Plastics—Methods of Test

    Typical usage ratio

    • 0.5 – 3 wt% in base polymer blend; adjusted based on desired ligand density or crosslinking degree
    • Range set by compatibility with polymer matrix and targeted end-use performance

    Downstream process integration

    • Incorporated during initial polymerization or via melt blending at reactive extrusion stage
    • Subsequent crosslinking or post-polymerization modification as per end-use recipe

    Final product types

    • Ion-selective membranes for fuel cells
    • Functional coatings for electronics and packaging
    • Engineered plastics requiring chemical resistance and coordination sites
    Free Quote

    Competitive Cyclen prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Understanding Cyclen: From Our Factory Floor to Your Application

    Sharing Experience With Cyclen Production

    At our facility, Cyclen isn’t just another product code. Over the years, seeing each batch move from raw starting materials to a clear, crystalline solid has shaped our understanding of what quality truly involves. Cyclen, or 1,4,7,10-tetraazacyclododecane, has stuck with us not just because of its solid chemistry but because every single batch brings its own personality depending on small tweaks in the process. Magnesium oxide purity, solvent history, resin type—all of those variables affect the purity and, by extension, the usefulness of the resulting Cyclen.

    We produce Cyclen with a focus on consistency, but our experience reminds us that attention has to go beyond the end product’s purity percentage. Each production cycle has taught us how important trace metal content is, especially for clients working in coordination chemistry or diagnostics. There’s a big difference between a standard chemical-grade Cyclen and the high-purity material required by researchers building macrocyclic ligands or imaging agents. Our controlled heating process, vacuum handling, and purification steps are all grounded in trial, error, and feedback from colleagues who need accuracy in their results.

    Cyclen in the Real World: Not Just Lab-Scale Distinction

    Cyclen’s tetraazamacrocyclic structure gives it a unique place among chelators. The rigid 12-membered ring frame and four precisely spaced amine groups let it form tight, stable complexes with a range of metal ions—something smaller rings like trien or bulkier cousins like cyclam don’t do quite as seamlessly. Watching customers use Cyclen as a blueprint for advanced DOTA-type ligands, as a host for lanthanides in MRI contrast development, or as a platform for functional group diversification, reminds us daily of the value in keeping our quality tight, batch after batch.

    Some clients might only look at the minimum assay figure. We’ve seen how those numbers alone never tell the full story. Spectroscopic purity and low levels of residual starting materials translate directly to cleaner reaction profiles. For example, in peptide synthesis, small amounts of impurities in the Cyclen can mean hours lost in HPLC purification or inconsistent yields. On the other hand, our partners in academic research, especially across the bioinorganic chemistry field, push for ever-lower heavy metal contamination: iron, nickel, and copper levels below 10 ppm. It isn’t just about getting the right structure in a bottle; for real-world results, everything unnecessary must go.

    Specifications Rooted In Practice

    Decades in chemical manufacturing have taught us what matters. Cyclen’s melting point, for example, from our experience, lands around 112–115°C. Too low, and it signals traces of moisture, solvent, or even small-molecule byproducts hanging on from synthesis. Too high, and there might be less-volatile contaminants or incorrect ring formation. Our on-site quality team runs NMR, HPLC, and FTIR checks religiously—not because of a regulatory checkbox, but because a clean spectrum gives us and our partners confidence that the next step in their synthesis won’t get derailed. Solid, white, and free-flowing crystals come off the line when every parameter is in tune.

    Packaging always deserves more discussion than it gets. Cyclen pulls in water from humid air fairly quickly. We learned early that even short exposure leads to clumping and lower shelf stability, especially for researchers who return to the bottle repeatedly. Now, we seal Cyclen under dry nitrogen in airtight HDPE containers, then store it in a temperature-controlled room. Downtime from a sticky, unusable chelator doesn’t just mean frustration at the bench—it ripples through tight project schedules.

    Watching the Industry—Seeing What Matters

    Cyclen rarely works alone. In our experience, it travels with research teams pursuing new diagnostic agents, MRI tracers, radiolabeling, and even catalysis. Feedback tells us that structure alone isn’t enough—impurity profiles must stay predictable across dozens of orders, and specifications have to be clear and reliable. The competitive pressure from large-volume suppliers sometimes pushes the market toward commoditization, but we’ve resisted the urge to cut corners. The difference becomes obvious once we watch how sophisticated applications, like radiopharmaceutical chelation or surface attachment for MRI contrast agents, respond to high-purity Cyclen. By collaborating with leading academic groups and industry innovators, we’ve seen that critical signal-to-noise ratios in imaging, or robust, reproducible chelation, always start with the right macrocycle.

    Demand for Cyclen ebbs and flows with broader trends—medical imaging spikes can drain inventories quickly, and new synthetic methods published in the literature create sudden requests for specialized derivatives. Over time, we learned to build flexibility into our batch sizes and hold a range of packaging options. Academic groups exploring new Cyclen derivatives value smaller units with detailed batch histories, while production-scale partners need predictability in every drum. This balance between customization and reliability shapes our daily work.

    Comparing Cyclen to Other Macrocycles—From Theory to Factory Line

    Seeing Cyclen across the production floor beside cyclam, DOTA, or even smaller ring amines, the differences jump out in real time. Cyclen’s 12-membered ring hits the sweet spot between flexibility and rigidity when coordinating most divalent and trivalent metal ions. Cyclam, its 14-membered cousin, sits flat in the NMR, but stretches and twists for metals with larger ionic radii, which changes selectivity and strength of binding. In our own experiments, Cyclen stands out for tight, square-planar or octahedral complexes, especially with copper(II) and lanthanides. The smaller ring, like 1,4,7-triazacyclononane (TACN), lacks the coordinating power and sheer binding affinity we observe with Cyclen. Even within a single metal system, the difference surfaces in yield, off-target binding, and even in the longevity of the complex during application.

    We’ve worked with research partners attempting to generalize results between Cyclen and DOTA. The addition of carboxyl arms on DOTA broadens water solubility and kinetic inertness for medical work, but those modifications start from pure Cyclen as a building block. Not all macrocycles cross over smoothly between applications. Cyclen’s size and flexibility mean it will accommodate many functionalizations before steric hindrance becomes a problem, a trait that sets it apart. Customers using it for ligand synthesis in radiotherapeutics or stable isotope chelation will see improved performance, provided the starting Cyclen is consistently pure and well-characterized. No ambiguous impurity profiles—no inconsistent downstream chemistry.

    Process Improvements—Listening and Learning

    Decades on the floor reinforced that real chemistry thrives on iterative feedback. Our early Cyclen production, heavy on old glassware and small-batch thinking, gave way to semi-automated reactors and online monitoring after seeing the limitations in reproducibility. Customers would catch faint yellow tints, indicating oxidation or side products, which never turn up in the dry technical literature. Scaling up forced us to refine not just stoichiometry but material transfers, solvent distillation, and filtration techniques to bring each variable under control. Today, we run additional tests on trace amines and solvent carryover. Our cyclen regularly passes microanalysis checks because of that feedback.

    Powder handling improved once we changed from open scoops to sealed hoppers under nitrogen blanket. One incident—where a batch left exposed to late-summer humidity caked utterly solid—taught us the risks firsthand. We keep a close relationship between production, QC, and even the warehouse crew. A technician’s note about an off-smell or visual deviation carries weight, and we adjust protocols when needed. Sustained improvement becomes a habit, not an aspiration.

    Supporting Research and Production—Beyond the Bottle

    We see firsthand how our Cyclen travels far beyond our gates. Research teams report that our high-purity batches have enabled breakthroughs in ligand frameworks for next-generation PET tracers. Industrial customers developing epoxy curing agents cite its performance in rigorous, moisture-sensitive syntheses. Bioconjugation specialists value the clean NMR profile for downstream modification, allowing for sensitive detection and quantification.

    Sometimes, setbacks from earlier years resurface in user reports. A single shipment sent with poorly-sealed drums led to hydration and delays for an overseas research group—a lesson that’s led to continuous investment in packaging upgrades. We now follow up with both academic and industrial clients to ensure every delivery fits the project timeline and integrity needs. Mistakes shouldn’t repeat themselves.

    Community engagement gives us a deeper view into Cyclen’s impact. We sponsor regional chemistry workshops where students and researchers present findings from their Cyclen-based projects—ranging from supramolecular assemblies to targeted drug delivery. These events provide us with critical insight into emerging needs and application pain points. At the same time, they push us to maintain a supply chain flexible enough to respond quickly to custom requests, which sometimes means making small, tailored batches for exploratory work.

    Responding to Safety and Regulatory Trends

    Safety expectations around Cyclen keep evolving. Research teams in Europe demand thorough documentation for registration under REACH and other compliance frameworks. We’ve built up a repository of spectral data, heavy metal tests, and material trace records, recognizing that knowledge builds both trust and efficiency when researchers face regulatory and ethics reviews. We continually refine our health and safety practices to keep exposure risks low for our production team. Dust control, local exhaust, and stricter SOPs come directly from seeing firsthand the results of lax habits. A safer workplace produces better chemistry.

    On the regulatory side, Cyclen finds its way into fields where oversight ranges from light-touch research environments to heavily governed pharmaceutical and diagnostic development. Our technical manager, after months spent assisting an MRI contrast agent startup, reminds us that complete transparency about impurity profiles and batch history can make or break a development program facing regulatory scrutiny. The effort on documentation and QC doesn’t just satisfy an auditor—it forms the backbone of relationships with clients on tight timelines.

    Facing Environmental Responsibility—Refining Extraction and Waste

    Attention to environmental matters isn’t just a talking point. Early feedback about solvent waste and water discharges led us to install on-site recovery and neutralization systems, reducing the resource footprint of each Cyclen kilogram produced. Fine-tuning the extraction steps to minimize chlorinated solvent residues started as a concern for downstream actors but now shapes our in-house choices; tracking solvent consumption per batch and recovering reusable volumes saves real cost and keeps our operation sustainable in the long run.

    A focus on efficient synthetic routes, using renewable energy, and minimizing raw material transport distances, has slowly shifted our plant toward more responsible production. By working directly with suppliers to source high-purity reagents and adopting green chemistry principles, we continue to cut waste and improve the final quality. Sharing these experiences with visiting researchers often prompts new perspectives, and our work on smaller, modular manufacturing units aims to reduce both community impact and logistical strain.

    Looking Ahead—Shaping Cyclen’s Next Chapter

    Our experience with Cyclen draws a clear line between technical possibility and real-world utility. Reliable, well-documented product flows from factory floor to research bench not only support the growth of the chemical industry but open the door to new applications in medicine, imaging, and materials science. Over the years, direct conversations with users have led us to invest in new analytical instruments, automate aspects of production, and continually sharpen quality control criteria. Every batch of Cyclen still carries the legacy of all that we have learned and improved as needs have shifted.

    The work never fully ends. Technological advances in diagnostics, shifts in regulatory frameworks, and pushes toward cleaner production methods continually move the goalposts. From the small, precise demands of academic research to the robust, scalable requirements of industry, Cyclen has proven flexible and reliable—as long as its manufacture stays rooted in honesty, technical rigor, and ongoing conversation with partners. Our journey with Cyclen is one of constant adaptation, and every day offers another chance to do better for our users, the industry, and the environment.

    Staying Connected—Welcoming Collaboration

    Manufacturing Cyclen gives us unique insight not only into the molecule itself but also into the many hands, minds, and programs that rely on its consistency and purity. The heart of our process relies on sharing knowledge between production and end use, confronting failures openly, and celebrating advances when they come together in new projects or published results. We invite open and direct discussion about real-world application challenges, custom batch needs, and opportunities to push Cyclen’s capabilities further.

    Our team’s daily work revolves around keeping feedback channels open with those who know Cyclen best: the scientists, researchers, and engineers who drive innovation forward. By doing so, we aim to be more than a supplier; we strive to be a trusted partner in discovery, development, and application, creating value grounded in authenticity and attention to detail. Cyclen continues to be at the center of important advances—from imaging diagnostics to new materials—and we are proud to contribute to each new chapter written with it.