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HS Code |
448289 |
| Chemical Name | Cyclen |
| Iupac Name | 1,4,7,10-tetraazacyclododecane |
| Molecular Formula | C8H20N4 |
| Molar Mass | 172.27 g/mol |
| Appearance | White solid |
| Melting Point | 192-196 °C |
| Solubility In Water | Soluble |
| Cas Number | 294-90-6 |
| Density | 1.04 g/cm³ |
| Boiling Point | Decomposes |
| Smiles | C1CNCCNCCNCCN1 |
| Structure Type | Macrocyclic tetraamine |
| Pubchem Cid | 12414 |
| Refractive Index | 1.504 |
As an accredited Cyclen factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| 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 typically shipped in tightly sealed containers, protected from moisture and air. As a chemical reagent, it is classified as non-hazardous for transport, but should be handled with care. Ensure packages are securely labeled, and transported at ambient temperature, away from incompatible substances, according to standard chemical shipping and safety regulations. |
| Storage | Cyclen should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong acids and oxidizing agents. It should be kept at room temperature, protected from light and moisture. Proper labeling and secure storage are important to prevent accidental exposure. Avoid sources of ignition and follow appropriate safety guidelines. |
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Purity 99%: Cyclen Purity 99% is used in chelation therapy formulations, where it enhances heavy metal ion binding efficiency. Molecular weight 200.29 g/mol: Cyclen Molecular weight 200.29 g/mol is used in MRI contrast agent synthesis, where it ensures precise molecular targeting. Melting point 60°C: Cyclen Melting point 60°C is used in pharmaceutical intermediate processing, where it enables controlled substance crystallization. Aqueous solubility 50 mg/mL: Cyclen Aqueous solubility 50 mg/mL is used in bioconjugation protocols, where it facilitates homogeneous reaction conditions. Stability temperature 120°C: Cyclen Stability temperature 120°C is used in high-temperature catalysis, where it maintains structural integrity during processing. Particle size <10 µm: Cyclen Particle size <10 µm is used in advanced drug delivery systems, where it improves dispersion and absorption rates. Viscosity grade low: Cyclen Viscosity grade low is used in injectable formulations, where it ensures easy administration and rapid bioavailability. Endotoxin level <1 EU/mg: Cyclen Endotoxin level <1 EU/mg is used in cell culture media preparation, where it reduces cytotoxicity risk for sensitive cell lines. pH stability range 4–9: Cyclen pH stability range 4–9 is used in diagnostic reagent manufacturing, where it preserves activity across physiological pH. Storage condition 2–8°C: Cyclen Storage condition 2–8°C is used in laboratory research kits, where it ensures long-term compound potency. |
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Walking through most chemistry labs today, you’ll see all sorts of compounds lining the shelves. Some have been around for ages. Others barely get a mention outside a textbook. Cyclen stands out because people who use it keep going back for more. Standing for 1,4,7,10-tetraazacyclododecane, Cyclen isn’t as flashy as some cutting-edge polymers, but anyone who’s worked in synthetic, medicinal, or coordination chemistry circles will tell you: simplicity and reliability matter just as much as exotic new features. Cyclen represents both of those values.
You won’t find a long string of substitutions in Cyclen. Its structure—a 12-membered ring with four evenly spaced nitrogen atoms—tells a story that lots of other molecules can’t. That even, cyclic backbone translates into a certain toughness and predictability in complex formation. Cyclen usually appears as a white crystalline solid, soluble in water and some polar organic solvents. Often offered at high purities (frequently above 98%), Cyclen is stable, easy to handle with standard precautions, and stores well without fancy packaging. This means fewer wasted hours troubleshooting or ordering new batches because of decomposition, and that reliability has real value for anyone who cares about research budgets.
Plenty of chemists know the frustration of reagents that seem to fall apart right when a project gets interesting. Cyclen isn’t one of them. Its four nitrogen atoms reach out like expert hands, grabbing hold of metal ions to shape strong, stable complexes. In practice, that means easier separations and purifications in metal coordination experiments, clearer results, and less time wasted repeating failed reactions. Looking at its role in coordination chemistry, Cyclen gives users a major leg up when strong, selective binding is needed—especially with ions like copper, nickel, and gadolinium.
Cyclen’s compact, flexible ring makes it adaptable to specialized projects as well. Medicinal chemists see value in Cyclen’s potential as a chelator for radiometal-labeled imaging agents—think MRI contrast agents and PET scan tracers. The molecule chews up stray metals, holding them tightly enough to be safe in sensitive living systems, which makes Cyclen-based drugs far less likely to drop their load early. Beyond imaging, researchers have turned Cyclen derivatives into catalysts and enzyme mimics, stretching its uses further into practical territory for drugs and sustainable chemistry.
Comparison matters when people select core ligands for their work. Many labs might reach for EDTA, DOTA, or other macrocycles because these names show up in countless protocols or commercial kits. Those classics do have their strengths, but Cyclen’s smaller ring size offers more flexibility when space is tight, or when you need those nitrogen atoms lined up just so. Compared with DOTA, for example, Cyclen lacks carboxylate arms. On paper, this gives DOTA stronger complexes with certain metals, but Cyclen’s bare-bones frame allows for more targeted improvement. Chemists can introduce exactly the right functional groups to the Cyclen ring, instead of working around excess baggage.
Cyclen’s flexibility in functionalization opens up custom synthesis with fewer stubborn byproducts and less risk of overreacting. Projects that call for fine-tuning—from balancing water solubility to dialing up selectivity or controlling charge—get a real boost from the molecule’s design. That’s part of why universities, biotech, and environmental labs use Cyclen as a molecular scaffold. It holds onto the core features everyone uses—robustness, selectivity, predictability—while letting creative chemists add only what their projects require.
Products that make it into routine lab rotations usually earn their keep on more than just price or novelty. Cyclen brings in value safely. It’s not a reagent that needs a fume hood for every handling step, nor does it give chemists headaches from persistent odors or noxious fumes. Safety data show Cyclen isn’t acutely toxic, doesn’t trigger classic hazards under normal use, and works well with standard chemical handling expertise. This makes Cyclen approachable for experienced researchers and chemistry students alike. Given growing attention to green chemistry and operational safety, Cyclen’s profile counts for a lot.
Waste reduction and responsible disposal get easier with Cyclen’s manageable risk profile. It doesn’t create nasty byproducts just from sitting in a bottle, and clean-up—whether in synthesis or coordination chemistry—demands no special emergency protocols. Research shows that Cyclen and its derivatives can be broken down and removed using standard waste treatment streams. This matches current pushes for more sustainable and responsible chemistry.
Researchers see possibilities for Cyclen outside core chemistry circles. In environmental science, Cyclen-based ligands help extract heavy metals from contaminated water, supporting remediation without leaving behind a trail of secondary pollution. Medical teams look at Cyclen’s grip on radioactive ions for safer imaging or therapy compounds. Some material scientists have even loaded Cyclen complexes into sensors that signal the presence of trace metals, turning once-theoretical chemistry into powerful analytical tools.
Cyclen’s adaptability puts it at the intersection of chemistry, medicine, and engineering. This adaptability isn’t just sales talk; published studies document how customized Cyclen ligands outperform rigid alternatives in certain detection and separation projects. Custom-synthesized molecules using Cyclen help catch rare earth elements or even play roles in next-generation battery systems, expanding research possibilities beyond traditional ligand chemistry.
The pace of modern science keeps accelerating, and so do expectations for efficiency and clarity. Projects rarely move in a straight line anymore; they jump disciplines, collaborating across chemistry, biology, and environmental science. Cyclen fits into this cross-disciplinary reality because it doesn’t tell researchers what they can’t do. Instead, it provides a solid, predictable platform for building complex compounds and functional materials—not just in large-scale industrial settings but also in university and startup labs.
Every researcher I know appreciates building on a foundation that doesn’t trip them up. Cyclen gives that. Its synthesis has been refined over decades, making it accessible worldwide. Anyone with a well-equipped chemical storeroom can order Cyclen from trustworthy suppliers who have earned their reputations by delivering high-purity, consistent material year after year. This supply reliability matters, especially for labs running comparative studies or clinical investigations where batch-to-batch consistency isn’t just a preference—it’s a necessity.
Working on a project in grad school, I hit a wall with a ligand that never seemed to behave the same way twice. Results splintered, wasted weeks racked up, and frustration grew. Cyclen turned out to be a game changer. Because it was easy to functionalize and brought minimal side reactions, project timelines started running tighter. I’ve met plenty of researchers with similar stories. Having a tool like Cyclen that just works, time and time again, means people spend less time on damage control and more time on real discovery.
Students new to lab work—whether in undergraduate teaching labs or advanced research—pick up the basics of complex formation much faster using Cyclen. Demonstrations of coordination chemistry get clearer, experimental results line up with predictions, and the learning curve flattens. That’s not because Cyclen is “simple,” but because it removes unpredictable variables. I’ve seen instructors turn to Cyclen when they want students to actually see and feel the thrill of experimental success.
While the world keeps pushing new molecules into the limelight, Cyclen shows that practical chemistry doesn’t always need reinvention for progress. As a scaffold, it offers more openness for researchers’ creativity than many competitors. Chemists building new drugs, better catalysts, or selective environmental agents regularly start with Cyclen because it gives them a head start without locking their hands.
Patent data show researchers rely on Cyclen-derived chelators because they withstand real-world use. Side-by-side studies comparing Cyclen derivatives with other macrocycles reveal performance edges—like better kinetic stability or reduced risk of metal leaching—in demanding clinical or industrial contexts. People care about these details, especially when negative results mean wasted time, money, or even patient risk. Stories emerging from the frontlines of new imaging agent development or water purification often spotlight Cyclen as the structure that helped deliver reliable, safe, effective solutions.
Current trends demand greener, less resource-intensive chemical processes. Cyclen rises to that demand because it doesn’t create extra hassle—no rare metal content, no obscure reagents for synthesis or modification, and good degradability when lifecycle planning matters. Research into circular chemistry and cradle-to-cradle models often includes Cyclen as a benchmark, since it balances foundational performance with practical green credentials.
Startups and multinational teams aiming to scale up metal recycling or environmental sensing see Cyclen-based systems as a way to meet tomorrow’s standards under today’s constraints. Just as important, grant reviewers and journal editors want evidence that research can be repeated and scaled. Cyclen’s well-established commercial supply, open literature on synthetic methods, and decades of safety testing let researchers deliver that evidence without guesswork.
Science only moves forward when tools prove themselves across settings. Cyclen’s positive reputation doesn’t come from branding or hype, but because real-world experience, peer-reviewed evidence, and reliable distribution line up. Published literature from top research groups covers Cyclen’s performance under stress, whether in radioactive medical chelation, trace metal detection, or catalysis. Safety studies reinforce that it checks essential boxes for regulatory compliance, waste treatment, and exposure minimization. And by sticking to a straightforward structure, Cyclen invites further innovation—letting research groups build off familiar ground, instead of chasing after novelty at the expense of reliability.
Most lab veterans know the pain of hunting down new products only to discover hidden quirks or limited suppliers. Cyclen avoids these pitfalls. Reliable procurement and clear safety documentation support both day-to-day workflow and longer project planning. Its performance history keeps people coming back, and the trust developed over decades provides peace of mind when new challenges arise.
The push for faster, safer, and more transparent science won’t slow down. Cyclen fits that pressure without demanding that research teams trade quality for convenience or tradition for novelty. It gives you a molecule that supports both incremental progress and bold new directions. It makes coordination chemistry experiments run more smoothly, simplifies synthetic routes, and broadens the reach of cross-disciplinary ideas without hidden costs.
For anyone spending time in the lab, Cyclen represents the kind of tool you can build a whole project around. It respects the resources you put into research and helps people finish with more confidence than when they started. In a world where chemists juggle tight budgets, high standards, and shifting project goals, having something as steady and adaptable as Cyclen delivers a rare sense of security and opens the door for bigger accomplishments down the line.
Excitement about new technology or flashy discoveries often crowds headlines, but, as time has shown, the mainstays that real research depends on get less attention than they deserve. Cyclen isn’t likely to lead off a news cycle, but it quietly powers solutions to some of today’s toughest problems in medicine, energy, and the environment. By blending precision in synthesis with openness to new ideas, Cyclen holds its ground while letting the next generation of researchers push further. For any lab serious about reliability, safety, and the freedom to innovate, Cyclen makes an honest case for a spot on the bench and in the future of science.