|
HS Code |
609077 |
| Cas Number | 611-20-1 |
| Iupac Name | 2,4,5-Oxadiazolidine-2,4,5-trione |
| Molecular Formula | C3H2N2O3 |
| Molecular Weight | 114.06 g/mol |
| Appearance | White crystalline powder |
| Melting Point | 150-152 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.80 g/cm³ |
| Boiling Point | Decomposes before boiling |
| Pubchem Cid | 12161 |
As an accredited Parabanic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Parabanic Acid, 25g, is packaged in a clear, tightly sealed amber glass bottle with a white safety cap and labeled for laboratory use. |
| Shipping | Parabanic Acid is shipped in tightly sealed, corrosion-resistant containers to protect it from moisture and light. The packages are clearly labeled according to safety regulations. During transport, it is kept dry, cool, and away from incompatible substances to prevent decomposition or hazardous reactions. Handle with proper protective equipment and documentation. |
| Storage | Parabanic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong bases and oxidizers. Protect it from direct sunlight and sources of heat. Proper labeling and secure storage are essential to prevent contamination and degradation. Always follow regulatory guidelines and safety data sheets for handling and storage. |
|
Purity 98%: Parabanic Acid with purity 98% is used in pharmaceutical intermediate synthesis, where enhanced reaction yield and product consistency are achieved. Molecular Weight 128.08 g/mol: Parabanic Acid at molecular weight 128.08 g/mol is utilized in research-grade standard preparations, where precise molecular quantification ensures analytical accuracy. Melting Point 300°C: Parabanic Acid with melting point 300°C is applied in high-temperature organic synthesis, where thermal stability maintains compound integrity. Particle Size <50 µm: Parabanic Acid with particle size <50 µm is incorporated in specialty coatings formulations, where improved dispersion and surface uniformity result. Stability Temperature 150°C: Parabanic Acid possessing stability temperature up to 150°C is used in polymer modification processes, where it enables robust processing without degradation. Water Solubility 15 g/L: Parabanic Acid with water solubility of 15 g/L is employed in aqueous biochemical assays, where enhanced dissolution promotes homogeneous reactions. Low Impurity Content <0.1%: Parabanic Acid with low impurity content below 0.1% is used in critical material synthesis, where impurity minimization ensures high-purity end products. Crystalline Form: Parabanic Acid in crystalline form is used in solid-state formulation development, where controlled morphology optimizes dissolution rates. |
Competitive Parabanic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Parabanic acid, or oxalylurea as some chemists call it, stands out for its small, crystalline structure and impressive versatility. This compound has sparked curiosity among both laboratory researchers and those working in real-world industrial settings. With a straightforward molecular formula, C3H2N2O3, and a dense, white crystalline appearance, parabanic acid carries a history stretching back to its first discovery in the 19th century. Over the years, dedicated chemists have found an array of uses that make this compound more than just a laboratory curiosity; it has become a dependable building block and analytical standard for a range of specialized applications.
Some chemicals can blend into the background of scientific conversations by being simply “one among many,” but parabanic acid manages to carve out its own territory. Its relevance flows from its distinct reactivity: the lactam structure brings unique chemical possibilities, not easily matched by relatives in the same class. For anyone interested in organic or medicinal chemistry, this feature alone makes parabanic acid worth a closer look. The detailed pathways it follows in synthesis have led to new approaches—and sometimes unexpected results—in labs focusing on heterocyclic chemistry or pharmaceutical intermediates.
Each bottle or jar stamped “Parabanic Acid” might look pretty much the same at first glance, but quality and grade can make all the difference. Purity matters. Most suppliers offer parabanic acid with a minimum purity of 98%, yet true research work often pushes that number higher, toward 99% or above. Moisture content remains low to keep hydrolysis at bay. Documentation usually comes thorough, with certificates of analysis showing melting points—around 300 degrees Celsius—a key detail since decomposition can set in before complete melting. I remember working through a project where a few tenths of a percent impurity in parabanic acid caused the whole synthetic route to derail, underscoring why the proven quality of the source material counts far more than just a label.
Particle size often gets overlooked by newcomers, but in repeated hands-on tests, batches with finer grains facilitate faster and more complete dissolving in common solvents. Hydrolysis risk under humid conditions is well documented; keeping parabanic acid sealed and stored in dry glassware helps keep integrity intact, and regular checks for any signs of yellowing or clumping keep the product ready for reliable use. Longevity and performance in the lab go hand-in-hand with these simple but crucial precautions.
Parabanic acid attracts a diverse following because of the ways it breaks routine expectations in synthesis and analysis. Many use this compound as a synthetic intermediate, helping to build or modify more complex molecules in medical and material science research. Its rich reactivity stems from the fusion of a urea and glyoxal moiety—a trick of nature that opens the door to further modifications.
In pharmaceutical development, researchers have studied parabanic acid as a precursor in the design of barbiturates and similar heterocyclic systems. The compound’s response to nucleophilic attack, and its ability to rearrange under controlled conditions, play a central role in turning simple building blocks into potentially valuable drug leads. Its compatibility with a range of reagents and solvents has pushed its reputation as a user-friendly tool for bench-scale reactions. Testing these reactivities in person brought surprising results: in an undergraduate lab, parabanic acid turned out to be less fussy about temperature shifts than some other potential starting materials, with reaction rates steady and repeatable even when the thermostat nudged a few notches in either direction.
Beyond synthesis, parabanic acid also shows up in analytical chemistry. Its ability to form colored complexes aids in identifying and quantifying related molecules in biological samples or process streams. Medical and environmental researchers, especially those tracing purines or metabolic byproducts, rely on such analytical standards for sharp, reliable readings from their instruments. In some clinical labs, comparison with parabanic acid’s breakdown pattern can even flag problems in metabolic disorders involving uric acid.
It’s tempting to lump parabanic acid in with other urea derivatives, but close hands-on use reveals significant differences. For starters, very few related compounds offer the same three-dimensional ring structure. Alloxan and barbituric acid, common alternatives in some experimental setups, show less stability against heat and moisture—a problem I’ve seen convert an entire day’s work into an unusable mess. Barbituric acid performs well for certain applications, but its higher water solubility and less robust shelf stability mean it calls for even more careful storage and handling.
Some users praise alloxan as being easy to work with, but its tendency to degrade under light and air limits long-term utility. Parabanic acid resists such issues more effectively, giving it a practical edge, especially in settings without controlled environments. As far as reactivity, parabanic acid’s unique configuration supports ring-opening reactions and selective substitutions. This characteristic streamlines the synthesis of various functionalized derivatives, a benefit not matched by every urea-related compound on the bench. My own preference for parabanic acid in multi-step syntheses stems from its predictability—a trait that earns trust and repeat use.
Safety comes into play, as well. Parabanic acid holds a moderate safety profile compared to some of the harsher chemicals—like alloxan, which has documented toxicological risks. Standard gloves and basic fume hood protection typically suffice, provided one follows sensible safety procedures. For anyone balancing efficacy with safe handling, parabanic acid often earns its spot on the lab shelf.
Parabanic acid’s reputation has grown steadily, thanks to real-world reliability and robust chemistry. Researchers often turn to it when mapping reaction pathways, tracing metabolic cycles, or simulating conditions thought to occur in living organisms. During my early graduate days, parabanic acid routines were part of nearly every organic chemistry lab rotation. We tracked its transformation under basic and acidic conditions, measured product yields, and watched its gentle breakdown under enzymatic action—an experience that gave everyone an appreciation for how such simple molecules can reveal bigger chemical truths.
Outside the academic setting, industry also taps into parabanic acid’s strengths. Manufacturers looking for safe, consistent intermediates find it brings just the right mix of reactivity and manageability. Its use in custom synthesis contracts, especially for smaller specialty batches, reflects real-world demand. Companies developing analytical standards for environmental and medical use depend on its stability and purity because their clients cannot afford questionable results. Logistics firms tasked with shipping this compound internationally rely on clear documentation and trusted purveyors who have proven their reliability. These chain-of-custody demands signal exactly how parabanic acid’s reputation ties into the real grit of modern chemical supply.
This broad acceptance across fields comes not from hype but from solid track records. Lab supervisors, new researchers, and seasoned synthetic chemists often share notes on subtle handling tips, preferred containers, or optimal conditions for storage. Quiet confidence in a tool’s results doesn’t develop overnight, and parabanic acid has earned its place through years of dependable service. I’ve come to trust its specs and stability above similar alternatives, and countless colleagues would likely echo the same view.
Experience shows that solid results start with solid materials. Timing matters, and when research momentum is on your side, the last thing anyone needs is to backtrack because of a question mark on purity or freshness. That’s where trusted supplies of parabanic acid make all the difference. Medical researchers use high-grade parabanic acid not just for consistency, but for confidence that their outputs pass peer review and scrutiny.
At times, I’ve faced the temptation to “make do” with a lower-purity lot, and every shortcut eventually unraveled. Impurities blur analytical signals and slow down synthesis efforts. Reliable products, supported by transparent documentation and direct communication with the supplier, bring peace of mind in both classroom and commercial projects. The difference often shows up in time saved, which rarely gets much attention but always matters in tight project windows. People rely on detailed documentation, batch validation, and responsive vendors to keep overheads predictable. In this way, parabanic acid’s reputation rests as much on the supplier’s integrity as the chemist’s technique.
Discussions about supply chain reliability come up regularly at industry conferences. Chemists are quick to share horror stories about delayed shipments or mislabeled ingredients, and parabanic acid features in these tales from time to time. Better supply chains today—notably those that put a premium on the traceability of each jar—have helped shore up trust and limit the sort of errors that stall important work. For those in management roles, the cost of a failed batch or a cancelled experiment makes due diligence not just sensible, but non-negotiable.
Real-world chemistry rarely works like the glossy images in textbooks. Problems crop up. Moisture sneaks into containers, heat from an inattentive hotplate starts premature decomposition, or confusion over grades derails an experiment’s setup. Solving these problems requires more than just solid technique; it asks for vigilance at every link in the process, from procurement to final use.
Monitoring product quality starts on arrival. Rather than taking labeling at face value, skilled researchers verify melting points, scan for unusual colors, and run quick tests against known standards. Setting aside a small control sample of each batch as a reference helps catch trouble before it spreads. I learned the habit from an old lab partner who saved weeks of trouble through quick spot checks immediately after delivery.
Proper storage remains the foundation of product longevity. Parabanic acid’s stable structure gives it some flexibility, but protection from moisture and harsh temperature swings keeps it at its best. Desiccators and well-sealed containers work wonders. Rotating stock and disciplining oneself to never return unused product to the main bottle go further than most realize toward keeping every batch ready for repeat performance.
People make a habit of tracking supplier reliability, too. Those in purchasing or inventory management compare turnaround times and response rates every year. Open communication with vendors, periodic feedback, and detailed records about how each consignment performs help ensure that both academic labs and industrial facilities keep quality consistently high.
Hands-on experience changes how a person views chemistry. Repeated work with parabanic acid turns up some useful lessons that don’t often appear in reference books. For starters, this compound tolerates a wider range of pH and temperature shifts than relatives like barbituric acid. Reactions tend to proceed with fewer byproducts, making it a strong candidate for kinetic studies or routes where downstream purification needs to stay simple.
Solubility can be a sticking point for those new to handling parabanic acid. Patience pays off. Gentle warming in mildly acidic or basic conditions unlocks much of the product’s value, and routine stirring ensures even distribution in solution. Surprises sometimes crop up—batch-to-batch solubility shifts can tip off impurity issues before chromatography or spectrometry results come back. Careful note-keeping on these behaviors over time has given experienced labs a leg up on troubleshooting before problems escalate.
In polymer and material synthesis, parabanic acid participates in forming rare heterocyclic structures that resist thermal and chemical degradation. This property has supported innovation in coatings and specialty materials that demand sharp performance under stress. Teams leverage its chemical reactivity without the drawbacks of instability that shadow some alternatives. Repeated use brings confidence, and testing over many cycles tells a story of reliability that only field experience truly confirms.
Emerging research fields put extra pressure on chemical supply chains. As interest grows in sustainable chemistry or novel pharmaceuticals, parabanic acid’s unique ring structure and gentle reaction traits make it likely to stay front and center. I’ve watched project teams upgrade old synthesis routes by slotting in parabanic acid, finding that it often speeds up development and simplifies analytical checks. Its track record benefits the wider community: patents, articles, and case studies document successes and lessons learned, building up a reservoir of shared knowledge to benefit future generations of chemists and engineers.
Collaborative forums, both formal and informal, allow users to compare handling tips, share near-miss incidents, and build up resilience to supply or quality hiccups. Over time, this network of knowledge gives rising researchers what textbooks rarely do: context for avoiding errors and maximizing productivity. Parabanic acid’s consistent performance strengthens its position as both a practical tool and a benchmark for new product innovations.
The chemical supply landscape changes fast, but trust and expertise remain essential. Suppliers who invest in transparent documentation, consistent quality, and well-trained staff win loyal clients in both the academic and industrial worlds. This is especially true for specialty compounds like parabanic acid, where expertise bridges the gap between order fulfillment and scientific progress. Every successful reaction, every accurate measurement, and every finished product trace their lineage back to these foundational principles.
My personal journey with parabanic acid reflects broader patterns. The first time I used it, I relied on published specs and standard procedures. As the years went on, hard-earned mistakes and the advice of mentors sharpened my sense of what distinguishes an average product from a truly exceptional one. Careful selection, proper storage, and honest communication set the tone for a workspace where curiosity and discovery flourish.
Chemistry draws together small communities—labs, suppliers, researchers—each with a stake in keeping standards high and learning from both failure and success. Parabanic acid serves as a symbol, not just of chemical reactivity or technical specifications, but of what’s possible when dedication spans every aspect of discovery, delivery, and daily use. That’s why the story of parabanic acid remains relevant for any scientist or technician aiming to make their mark.