|
HS Code |
411234 |
| Name | Xanthine |
| Chemical Formula | C5H4N4O2 |
| Molar Mass | 152.11 g/mol |
| Appearance | White crystalline powder |
| Melting Point | 350°C (decomposes) |
| Solubility In Water | Slightly soluble |
| Cas Number | 69-89-6 |
| Iupac Name | 2,6-dioxypurine |
| Density | 2.14 g/cm3 |
| Boiling Point | Decomposes before boiling |
| Pka | 7.7 |
| Odor | Odorless |
As an accredited Xanthine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Xanthine, 25g, is packaged in a sealed, amber glass bottle with a secure screw cap and clear hazard labeling. |
| Shipping | Xanthine is shipped in well-sealed containers, typically in compliance with standard chemical handling regulations. Packaging ensures protection from moisture and physical damage. The chemical should be clearly labeled and accompanied by appropriate documentation. Handling precautions are advised to avoid inhalation or ingestion, and transport must follow relevant local and international regulations. |
| Storage | Xanthine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep it protected from moisture and direct sunlight. Proper chemical labeling and adherence to safety guidelines are important to prevent contamination, degradation, or accidental exposure during storage. |
Competitive Xanthine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to sales3@ascent-chem.com.
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Tel: +8615365186327
Email: sales3@ascent-chem.com
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Working with xanthine nearly every day on the production line, in the laboratory, and out on delivery runs, I get to see firsthand what it brings to the table for our customers across industries. People might glance at the name and just think of another chemical powder, but for us, each batch we produce represents months of real work—mining for the right raw material, refining the extraction, then purifying and testing it over and over until it meets known physical and chemical standards. The xanthine molecule, C7H8N4O2, stands at the root of many well-known derivatives like caffeine and theobromine, but in its pure form, it brings unique capabilities to manufacturing, research, and medicine that are hard to replace.
Physical characteristics can vary based on process. For our xanthine, we maintain a standard white to off-white crystalline powder, with particle sizes controlled through micronization and sieving. Melting points land around 225°C, in line with reference data, and solubility follows predictable patterns: sparingly soluble in cold water but more generous after heating, and moderately soluble in alcohol. We monitor for specific impurities common in xanthine production—such as closely related purines—and batch-to-batch consistency depends on how rigorous the purification is at every stage.
In pharmaceutical research, xanthine shows up as much more than a byproduct. Its enzyme inhibition properties, and its close chemistry with adenosine pathways, makes it indispensable for both direct use and as a starting scaffold for producing medicines. Our regular customers include labs working on bronchodilators, diuretics, and compounds acting on the central nervous system. Because we can fine-tune impurity levels and offer lot-specific documentation, research institutes trust the reliability of our xanthine in sensitive experiments where competing products sometimes fall short due to overlooked contaminants.
Outside pharma, xanthine finds roles in diagnostic kits, biotechnological applications, and in some specialty analytical reagents. The same molecular stability that keeps it reliable in a synthesis reaction also helps it survive extended transport under non-ideal conditions, so we field requests from partners in remote labs or regions with less established logistics. Over the past decade, we have adjusted our drying and packaging processes to minimize moisture uptake—a frequent complaint from formulation chemists who said even trace water made their downstream steps unpredictable. Based on customer feedback, we now double-seal every drum and run Karl Fischer titrations to spot minimal water content: minor improvements, but with major downstream impact.
We start by looking at raw materials. Decades back, xanthine production often leaned on guano or other natural extractions. These sources bring unnecessary variability, so today we use synthetic processes starting from purified uric acid. Even this base ingredient demands precise sourcing and pre-treatment to work well in later stages. Chemical synthesis of xanthine—through oxidation, then cyclization and careful acid or base washes—lets us keep final purity well above 99%. Each production run takes a week from first mix-through to filtration and crystallization, with no compromises on handling or equipment cleanliness.
Testing runs through every batch. Our in-house quality control team doesn’t sign off on a drum until it passes HPLC, melting point, moisture, and impurity screens. Side-by-side comparisons often show our batches with lower trace impurities than the industry average, and we keep internal standards higher than what’s widely published. Going beyond minimum compliance gives downstream users peace of mind, especially when sending the product into clinical development or regulatory review.
Many suppliers trade on price. As direct manufacturers, we build value into how things are made and not just what the certificate says at the end. Regularly, researchers tell us that small differences in xanthine purity, residual solvent, or crystal habit have unexpected knock-on effects in their projects. A run of slightly yellowish powder or odd-shaped crystals raises questions in precise analytical work or cell culture. We designed our process to control optical properties and particle morphology with more consistency than casual suppliers.
We also make sure technical teams are available to field real questions—about analytical methods, storage life, and compatibility with intended applications. Sometimes, a customer wants to optimize a reaction or troubleshoot a suppressive signal in chromatography, and generic resellers simply cannot provide insight on that level. Because we work directly with both our production team and our technical support, we can suggest workarounds, run small recalibration batches, and even tweak our final packaging when needed. Having full internal knowledge—from chemical engineering to last-mile logistics—lets us offer help that actually makes a difference.
Regulatory compliance grows more complex every year. When xanthine goes into regulated sectors like pharmaceuticals or diagnostics, customers need more than a product—they count on documentation, traceability, and stability data that meet not just basic certificates but also international audit standards. Our facility maintains GMP, ISO, and local health authority registration, and we keep validation records for all equipment and processes involved in xanthine batches. If your quality team needs to look beyond the COA, we provide stability data so that downstream releases go smoothly. Unlike repackagers, we handle all documentation in house and can answer technical compliance questions without delay.
Teams in R&D work hard enough trying to untangle biological complexity without worrying about reagent consistency. A decade ago, several labs reported activity loss in their kinase assays traced back to low-grade xanthine from inconsistent sources. These failures cost reputable groups both time and grant money, which drove renewed demand for transparency. As a result, our customers now expect these standards. We monitor not only for total organic impurities, but also for tough-to-spot contaminants that may not be visible in standard UV-based purity checks.
In scale-up manufacturing, everything comes down to reproducibility and safety. Formulators in pharma production or diagnostics cannot afford variability—they report back anytime downstream processes yield off-spec batches. Our attention to raw material, process controls, and batch-by-batch analytical data helps production managers sleep easier at night. It also drives more repeat business, because trusted consistency beats chasing the lowest price on the spot-market every time. In tough years, reliability keeps operations running smoothly when supply chains get tight.
We don’t just stick to yesterday’s way of making and moving xanthine from one warehouse to another. We work to minimize environmental impact through solvent recovery systems and optimized batch sizes, cutting both waste and emissions compared to traditional large-scale chemical plants that often treat effluent as secondary. Our technical team routinely audits processes for efficiency. By switching from harsh acids to more controlled reagents and by recycling solvents in closed loops, we send less to disposal and reduce the resources needed per kilogram of finished xanthine.
Customers sometimes ask about sustainable sourcing and traceability, which proves challenging for small-batch specialty chemicals. Yet every year, we increase the share of raw materials sourced from certified partners with environmental and social compliance documentation. Detailed batch records allow us to track from each drum of uric acid to final xanthine lots rolling out the door. This not only answers supply chain questions but builds trust with environmentally conscious customers.
On the technical support side, our scientists spend real time with academic and industrial partners, offering answers on reaction optimization, storage concerns, and analytical surprises. Sometimes a researcher in the field runs into unexpected degradation or solubility changes. Rather than leaving them to guess at causes, we can retrace steps and, if necessary, run further analytics on retained sample splits to help diagnose the cause. This personal attention remains crucial, especially in high-stakes R&D portfolios where years of work ride on a handful of critical materials.
We’ve seen the challenges caused by supply interruptions and last-minute sourcing changes. By maintaining rolling stock and offering batch reservation programs, we reduce headaches tied to variable global shipping timelines—an investment in customer outcomes as much as in our own bottom line. In recent years of uncertainty, being able to promise stable supply on schedule carried real weight with our production partners. In the end, supply chain control directly influences research milestones on the customer’s end.
Some customers new to the purine field ask about substituting xanthine with structurally similar compounds. Caffeine and theobromine both share a similar backbone, but the methyl groups on those molecules change their activity in biological systems and applications. In pharmaceutical or research settings that demand specificity, using off-the-shelf caffeine or theobromine fails to deliver the same enzyme inhibition or reactivity. In simple terms, xanthine serves as a raw building block for new drugs or diagnostic reagents, while caffeine and theobromine act as finished molecules for consumer products.
Furthermore, xanthine’s restricted solubility and defined melting point help process engineers design reliable crystallization or analytical protocols. Switching to derivatives means sacrificing that tight control and opens the door to unexpected byproducts—especially problematic in assay development, where signal clarity counts above all else. Handling and storage requirements also diverge across the purine family; for instance, xanthine’s moisture sensitivity is less pronounced than in some related compounds, lending it more reliability during transportation and long-term storage. These details only emerge through years of hands-on work with the product and are often overlooked by new market entrants.
Challenges keep shifting, demanding constant vigilance. Regulatory expectations tighten with every major review cycle, supply disruption remains a real risk as global logistics creak under distributed demand, and pressure mounts to cut environmental impact without sacrificing throughput. Inside the plant, every new production run brings a chance to hone process controls, update analytical calibration curves, and engage directly with partners to discuss future demands or regulatory forecasts.
Cost pressures affect every chemical sector. Temptations always exist to buy low or cut process corners, but those choices catch up quickly—lost business, expensive recalls, negative audit results, or irreversible damage to reputation. Our approach builds long-term partnerships rooted in transparency, batch-level accountability, and willingness to invest in better analytics, greener processes, and workforce training. That’s not a marketing line; it’s the way we guard against the pitfalls that trip up less experienced or less committed suppliers.
Looking ahead, demand for high-purity xanthine seems steady as new biopharmaceutical and research applications emerge. We anticipate rising requests for higher analytical documentation, including full impurity profiles and real-time stability data. Smaller research groups often operate far from established distribution hubs, so we maintain flexible logistics capabilities—cold-chain packaging for sensitive batches, and tailored labeling for regions with strict import requirements. This adaptability helps us keep our promise of getting customers exactly what they need, right when they need it.
Direct manufacturing brings unmatched benefits. Sourcing straight from us links you to the people who know the strengths and limits of the product, field troubleshooting questions with insider knowledge, and react rapidly if you need formulation or packaging changes. We stay in step with evolving analytical demands; our in-house lab uses state-of-the-art HPLC, thermal analysis, and impurity profiling, so if adverse trends emerge or customers need deeper analysis, we provide it rapidly. All this adds up to greater confidence for formulators, researchers, and downstream manufacturers counting on repeatable results.
We see the full life cycle of our product, from first raw material deliveries to return shipments and customer feedback after months of storage or field use. That experience helps us anticipate problems before they develop. We’ve redesigned processes, retrained staff, and updated data packages in response to issues flagged by engaged customers. These upstream controls only become clear over years of close attention to both process and real-world application—and they’re difficult to match from outside the actual manufacturing chain. For researchers, formulation scientists, and production managers, the peace of mind that comes from knowing exactly where and how a critical input was made can be worth more than the lowest commodity price.
Xanthine rarely makes headlines, but it powers a surprisingly wide set of advances in science and technology. Every kilogram we dispatch comes backed by the history and accountability of a manufacturer’s process—not simply a trading house or anonymous vendor. We measure value not just in price-per-kilo, but in how many research breakthroughs, consistent production runs, and successful applications our material supports for years to come. Chemistry remains a hands-on business, and it’s the day-to-day commitment to customers and product that defines quality. Long-term success depends on real technical backing and openness—qualities we bring to every partnership built around xanthine today, and every upgrade on the horizon.