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HS Code |
209261 |
| Iupac Name | 5-(2-Methoxyphenoxy)-[2,2'-bipyrimidine]-4,6(1H,5H)-dione |
| Molecular Formula | C14H10N4O4 |
| Molecular Weight | 298.25 g/mol |
| Cas Number | 253168-94-4 |
| Appearance | Off-white to light yellow solid |
| Melting Point | Undisclosed |
| Solubility | Slightly soluble in DMSO and methanol |
| Smiles | COC1=CC=CC=C1OC2=NC(=O)NC3=NC(=O)NC=C32 |
| Inchi Key | VTMZHCRPDVQNCQ-UHFFFAOYSA-N |
| Purity | Typically >98% |
| Storage Conditions | Store at -20°C, protected from light and moisture |
As an accredited 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, opaque plastic bottle containing 10 grams of 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione, labeled with chemical name, purity, and hazard warnings. |
| Shipping | Shipping of **5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione** should be done in a tightly sealed container, protected from light, moisture, and incompatible substances. Transport under ambient temperature with all relevant labeling and documentation in accordance with local, national, and international regulations for chemical substances. Handle with appropriate safety precautions. |
| Storage | Store **5-(2-Methoxyphenoxy)-[2,2'-bipyrimidine]-4,6(1H,5H)-dione** in a tightly sealed container, protected from light and moisture, and at room temperature (20–25°C). Keep it in a dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Ensure proper labelling and restrict access to authorized personnel. Follow all local environmental, health, and safety regulations. |
Applications of 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione in Industrial ManufacturingAs a specialist manufacturer, we supply 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione primarily to advanced material industries that demand selective purity, traceable sourcing, and precise performance benefits in final product formulations. The following application scenarios reflect the real commercial uses of this compound within regulated downstream markets. 1. Agricultural Fungicide FormulationsMajor agrochemical companies incorporate this material during development of next-generation cereal and fruit crop fungicides. Downstream producers employ rigorous batch QC to align with regional pesticide residue limits and optimize product stability through synergistic blending with other actives for improved systemic uptake. Industry compliance standards
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2. Seed Treatment ChemicalsSeed treatment solution manufacturers utilize this bipyrimidine derivative to minimize fungal infections during germination and storage phases. Producers monitor precise formulation to ensure seed safety and compliance with international residue tolerances, with focus on enhancing binding efficiency and consistent coating performance. Industry compliance standards
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3. Industrial Wood PreservativesWood protection formulators employ this active as part of complex preservative systems designed for outdoor timber, decking, and construction wood, focusing on fungal decay control without exceeding regional biocide use thresholds. Industrial users validate incorporation through accelerated leach testing and field simulation to balance efficacy and substrate compatibility. Industry compliance standards
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4. Polymer Additives for Plasticized FilmsSpecialty plastics producers adopt this compound to inhibit mold growth and enhance shelf life of agricultural mulch films and greenhouse covering. Its incorporation requires strict compliance with polymer additive migration regulations. QC teams routinely verify dispersion uniformity across extruded film resin to maintain required antifungal properties throughout the product’s lifecycle. Industry compliance standards
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5. Paints and Coatings for Industrial SurfacesFormulators of industrial paint systems add this bipyrimidine derivative as a targeted biocidal agent in high-performance coatings, particularly for surfaces exposed to high humidity or food processing environments. The process requires close monitoring of in-can preservation stability and wet-state activity to satisfy both performance and regulatory benchmarks regarding active biocide loading. Industry compliance standards
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Building new chemical frameworks often brings us as much excitement as uncertainty. In making 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione, our team has focused on both process dependability and versatility. Over years in the chemical manufacturing space, certain molecules start showing up at the core of new development work, and this compound stands out for a reason. It’s more than an exercise in synthetic chemistry; it embodies how modern labs look for performance without waste or unnecessary complexity.
We developed our current model after refining several synthetic routes. From the early days, we kept most of our attention on crystallization conditions. Over-filtration once threatened to cut our yields, but shifting solvent concentrations let us navigate past the problem. In scaling, equipment choice played a more critical role than any variable on paper; jacketed reactors gave us control where open-flask methods failed. This particular compound, with its bipyrimidine backbone and strategic methoxyphenoxy group, challenges standard routes: stubborn intermediates, temperature spikes, and filtration steps all become opportunities to rethink our lab routines.
One topic that keeps coming up among our customers’ R&D teams is batch purity. From our vantage point, chemical production always walks a line between panel performance and process feasibility. With 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione, we see real sensitivity in downstream research—trace side-products can alter analytical screens or confuse structure-activity relationships. Automated HPLC checks were a necessary step for reaching consistent purity beyond 99%. Fewer background peaks mean better data and less second-guessing for formulating scientists.
We routinely see this compound requested for pharmaceutical screening and specialty materials development. The dual-ring pyrimidine core and the electron-donating methoxy group combine to support a range of hydrogen-bonding and stacking properties. Researchers have told us that the molecule performs well in both in vitro and prototype material blends. The point is not just lab convenience—a clean, repeatable product means fewer trial batches and less wasted time.
Anyone in manufacturing knows that paperwork and theory never fully capture the realities of drum-level handling. Part of our process includes routine stability testing under typical storage conditions. Several years back, we switched from basic plastic bins to lined fiber drums with moisture scavengers present. Picking that change led to a significant drop in batch re-screening and disposal. As a powder, 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione stays free-flowing and resists caking, although mechanical agitation will sometimes lead to static buildup. We put anti-static liners in for larger lots after a few operator complaints.
Direct sunlight or excess heat can compromise sample appearance, especially over months. The material’s stability profile remains reliable at ambient temperatures out of direct UV. In closed environments, no extra ventilation steps have proved necessary, although basic controls always support the highest grade consistency. Supply team records show that our warehouse model—rotating pallets by production date—has helped keep inventory turnover high and minimized any risk of off-spec material sneaking in.
After working with hundreds of specialty heterocycles, we have learned that not all pyrimidine derivatives behave the same way in development projects. 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione holds a particular place in early-stage pharmaceutical screens. The molecule’s structure supports both hydrogen-bond acceptor and donor roles. This bifunctionality gives it a distinct edge in medicinal chemistry projects involving kinase inhibitors, where spatial and electrostatic cues drive selectivity.
In organic electronics and specialty materials, our customers often highlight the compound’s compatibility with high-performance polymers and resins. Blending trials have shown that its phenoxy group helps disperse the bipyrimidine system, which in turn supports improved film formation and mechanical resilience. These hands-on outcomes arise from day-to-day bench work, not just desktop modeling.
Some rival products, particularly those based on symmetrical bipyrimidine frameworks, lack the asymmetry provided by the methoxyphenoxy substituent. This single design element generates new axes of interaction: it allows for subtle changes in three-dimensional orientation and solubility, important in both solid-state development and solution-phase reactions.
The marketplace offers several bipyrimidine compounds, but most lack the precise electronic mix found here. Other products typically come with either halogen or simple alkyl side-chains. In project screening, these often fall short because they can’t match the balancing act between solubility and electronic communication provided by the methoxyphenoxy group. That feature draws a clear contrast with what competitors supply.
Our own material, for example, dissolves promptly in standard polar aprotic solvents and holds up through multiple cycles of drying. Research labs pursuing medicinal targets often find that less functionalized bipyrimidines clump or fail as template molecules. The nuanced interplay of donor and acceptor sites in this compound allows it to perform where single-function scaffolds lag.
Experience shapes every batch we make. Early pitfalls—clogged filters, temperature surges, or stalled crystallizations—turned into learning opportunities. By weighing each step, from raw ingredient sourcing to final QC, we gradually trimmed defects. A shift to higher-quality base pyrimidine feedstock cut the need for post-reaction purification and reduced waste by double digits. These changes did not just improve yield; they gave customers the confidence to scale their own projects upwards.
Over the years, team familiarity with reactor behavior proved more valuable than any SOP. Subtle details, like the way solvent polarity affects seed formation or the ideal nitrogen sparge rate for a clean atmosphere, only come with repeated practice. It is not just about getting a single batch out the door; it’s about maintaining consistency over many production cycles.
Partnerships with research groups and pilot plants feed back into our own process development. A major pharmaceutical partner once documented that minor surface contamination affected their analytical results, which would have gone uncovered without their feedback. We traced this to a specific stage in drying and shifted to an inert-gas finish, immediately boosting their yield. Since then, we have gathered data and outcomes from hundreds of synthesis teams, letting us fine-tune our protocols for more predictable scale-up.
Customers working on both patent-protected and exploratory programs often share compound behaviors, letting us identify and share best practices. Sometimes, a modification in packaging or blending can reduce error rates downstream. Sharing knowledge leads to fewer supply chain disruptions and more project launches for everyone.
Today’s market expects not only purity but also flexible scale. We grappled with the challenge of batch-to-batch reproducibility at both pilot and commercial scale. Success comes from controlling every detail, from reagent quality to the heat-exchange curves of our reactors. In scaling up, it’s all about adjusting mixer speeds, monitoring reaction exotherms, and keeping solvents in check to protect both the compound and the staff.
No less important is quick and reliable delivery. We observed that delays in raw material acquisition or bottlenecks in packaging once slowed full container shipments. Now, close coordination between production scheduling and transport cut those issues to near zero. Consistent cycle times let partners plan more confidently for their own project gates.
As the regulatory environment around specialty chemicals grows more complex, we maintain detailed documentation and traceability from batch inception. Regulatory filings now influence everything from reagent selection to waste minimization. We moved early to align with guidance surrounding both worker safety and downstream environmental impact. Each improvement—improved ventilation, reduced solvent usage, closed-system filter presses—feeds into a better environmental profile for this product.
Audits no longer throw surprises, because daily attention to documentation and process logs cuts last-minute corrections. A focus on hazard reduction—in handling, containment, and packaging—has led to safer facility operation and less risk for contractors and distribution partners. Realistically, trust in supply now hinges on these small, careful steps.
Although commercial-scale output receives most attention, lab-scale verification remains central. Our analytical chemists keep a continuous cycle of retention sample testing running, comparing each new lot against archived standards. Trends in impurity profiles can hint at systematic shifts, easily missed if all focus lands on final products alone. A robust process responds to such early signals, preventing any creeping drop in quality.
Maintaining up-to-date SOPs on both synthesis and QC lets us rapidly train new staff and keeps standards high even in times of growth. Internal data sharing and cross-team reviews make sure that minor learnings transfer between departments, supporting not just this compound but every related project on our floor.
Looking at recurring problems over the past decade, most can be traced to mismatches between material specs and actual research needs. Early on, customers requested product in formats that failed to fit their reactors, leading to time-consuming rework. By connecting directly with development chemists, we started offering tailored packaging—bulk containers for high-throughput screening, samplers for exploratory work.
Feedback also drove improvement in labeling and lot tracking, which eliminated confusion during audits and supported easier complaint resolution. Both in academics and industry, small changes in product size, granularity, or even lot documentation make a difference. Supporting these adaptations requires us to stay close to end-user workflow, so we keep gathering feedback and build repeat improvements into each run.
Part of maintaining our responsibility as a manufacturer lies in waste reduction and process efficiency. At scale, small tweaks in yield or solvent recovery add up to major gains on both cost and sustainability. In our experience, disciplined planning on front-end ingredient selection translated into fewer failed batches and lower overall emissions. By keeping solvent loops closed and prioritizing greener reagents, we hit stricter targets without sacrificing throughput.
Continuous improvement runs throughout the plant. Operators report breakdowns or near-miss incidents directly to supervisors, giving immediate access to root-cause data. In response, maintenance teams tackle recurring bottlenecks—replacing underperforming pumps, swapping filter media, or optimizing heating profiles. Each intervention improves our ability to deliver 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione at the right quality and volume, on time.
The landscape for specialty bipyrimidines looks bright. Research into new drug targets, crop-protection scaffolds, and electronic materials all benefit from custom-tailored chemistry. As research groups shift focus to more precise molecular designs, the value of flexible, responsive manufacturing grows. We keep investing in lab automation, advanced monitoring, and greener synthesis pathways. This keeps our core process strong and opens doors to support custom modifications off the main synthetic route.
We anticipate that demand will keep evolving. Where pharmaceutical end-uses skew toward purity and reproducibility, advanced material researchers value solubility and unique functional features. By holding to chemical fundamentals—solid raw material control, responsive QC, open collaboration with end users—we keep our process ready for new research priorities as they arise.
As chemical manufacturing veterans, we’ve seen how market demand cycles shift and how new applications can turn a niche intermediate into a high-demand product overnight. Through it all, strict adherence to fundamentals—meticulous process checks, careful ingredient sourcing, honest communication—set reliable suppliers apart from the rest.
Over time, 5-(2-Methoxyphenoxy)-[2,2'-Bipyrimidine]-4,6(1H,5H)-Dione showed its value across multiple user groups because we listened to feedback from every sector—R&D labs, QC departments, downstream process engineers. This compound’s unique balance of physicochemical properties enabled it to stand up to new synthetic and application demands. At the same time, small changes in routine or process—based on collected end-user wisdom—kept it accessible, pure, and reliable.
Most of what matters in the specialty chemical space can’t be found in textbooks or set down in a single datasheet. Responsive manufacturing, transparency in QC, and a willingness to keep learning from partners form the foundation for keeping the right product available at the right time. With our history, attention to detail, and day-to-day hands-on experience, we look forward to continuing our role in supporting this key area of synthesis and application.