|
HS Code |
743247 |
| Iupac Name | 5-(3-methylphenoxy)pyrimidin-2(1H)-one |
| Molecular Formula | C11H10N2O2 |
| Molar Mass | 202.21 g/mol |
| Cas Number | 1228936-87-9 |
| Smiles | Cc1cccc(Oc2cnc(=O)nc2)c1 |
| Pubchem Cid | 52944374 |
| Appearance | Solid (typical for similar compounds) |
| Solubility | Likely soluble in DMSO, DMF, and other polar aprotic solvents |
| Boiling Point | Decomposes before boiling |
As an accredited 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a tightly sealed cap, labeled “2(1H)-Pyrimidinone, 5-(3-methylphenoxy)-” and hazard symbols. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- involves secure, efficient packing of the chemical for bulk sea shipment. |
| Shipping | The chemical 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- is shipped securely in sealed, chemical-resistant containers, clearly labeled per regulatory guidelines. Packages are cushioned and protected from light, moisture, and extreme temperatures. All relevant safety data sheets (SDS) are included. Shipping complies with local, national, and international hazardous materials regulations. |
| Storage | 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect from light and moisture. Ensure proper labeling and secure storage to prevent spills or accidental exposure. Follow all relevant safety guidelines and local regulations when handling and storing this chemical. |
| Shelf Life | The shelf life of 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- is typically 2–3 years when stored in cool, dry conditions. |
Competitive 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- prices that fit your budget—flexible terms and customized quotes for every order.
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Every batch tells a story in the chemical world. Manufacturing a specialty compound like 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- comes with unique challenges and rewards. Over decades in synthesis labs and scale-up workshops, I’ve watched the evolution of pyrimidine-related chemistry—how stringent demands from pharmaceutical innovators pushed manufacturers to refine every detail from reagent quality to purification method. Now, more than ever, companies look for consistency, traceable origins, and advanced properties in new intermediates. This particular pyrimidinone stands out because its structure unlocks distinct reactivity profiles and compatibility for drug research, pesticides, and dyestuff applications.
In the past, procuring such intermediates meant compromising between production volume, purity, and the risk of contamination. As a firsthand producer, I have seen how hands-on adjustments—changing stirring speeds, fine-tuning temperature ramps, or deploying new analytical methods—directly impact the quality of each batch of 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)-. Small manufacturers sometimes ignore the trace-level byproducts that can undermine a research project. Large-scale companies occasionally miss the mark with cGMP compliance, jeopardizing downstream applications. I’ve always put process control above shortcuts. The result is a product line that researchers trust for instrument calibration, polymers, or biological screening.
2(1H)-Pyrimidinone, 5-(3-methylphenoxy)-, generally offered as a white to off-white crystalline powder, distinguishes itself by real, tangible features. The backbone comprises a pyrimidinone ring substituted at the 5-position with a 3-methylphenoxy group. This functionalization imbues new solubility behaviors and opens up selective reaction possibilities compared to unsubstituted relatives. I’ve heard process chemists comment that this subtle tweak—adding the 3-methylphenoxy group—improves stability under moderately basic conditions, a property lacking in other commonly encountered pyrimidinones.
Working on this molecule, our teams run batches at both pilot and metric ton scales. Integrity shows in the melting point consistency and specific purity profiles tracked using NMR and HPLC. We never aim at “industry standard” as a plateau. Instead, feedback from pharmaceutical and agrochemical customers has shown that the unique substitution pattern of this compound streamlines synthesis flows. For instance, certain palladium-catalyzed cross-coupling reactions proceed more efficiently, saving time and resources in medicinal chemistry discovery pipelines.
In analytical testing labs, customers have highlighted the clean chromatographic behavior of our batches. The difference comes from the commitment to controlling moisture levels, minimizing trace impurities from vendors, and conducting extra purification cycles despite added labor. I’ve supervised runs where the impurity profile showed a persistent minor peak—which led us to replace a batch of solvent and solve the problem for future lots. These behind-the-scenes adjustments drive the reliability of our 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- in sensitive applications.
Our product never comes with vague assurances: values are measured, logged, and trended. Typical purity reaches past 98% as confirmed by HPLC—because lower specs result in more waste and corrective work in end-user labs. Residual solvents, checked by gas chromatography, remain below thresholds required by pharmaceutical R&D. Every lot carries an accompanying analytical report, built on spectra and tests run in our own facility.
Molecular weight, melting point, solvation data, and UV characteristics all influence the compound’s practical handling. Product stability gets tested in real temperature and humidity chambers—not just hypothetical figures. A lot of chemical manufacturers quote values found in literature or databases, but in our day-to-day work, we put each claim to the test across actual production runs. We do not ship batches that fall outside agreed benchmarks. If I spot deviations, I halt the process for further purification, putting end-use confidence above short-term output targets.
We store the product in tightly-sealed drums or glass bottles, derived from documented shelf-life data. Our experience with pyrimidinone derivatives revealed problems with peroxide formation and color changes in substandard packaging, so we updated procedures to prevent these issues. The difference has been measurable: customers consistently report better recovery rates and fewer incidents of out-of-spec material compared to less rigorously produced options.
Chemists in the pharmaceutical industry see 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- as a versatile building block for heterocyclic libraries. This compound often participates in Suzuki and Buchwald-Hartwig couplings, taking advantage of its well-positioned phenoxy substitution. Formulators working on antimetabolite drug candidates have commended this intermediate’s reactivity and its low levels of metal contamination—a direct result of stringent purification in the production process. Academic groups interested in enzyme inhibition studies also purchase this molecule to screen for bioactivity. They rely on vendor transparency for consistent results: a test only has meaning if every compound behaves the same way each time.
Beyond pharma, researchers in agrochemical development put this pyrimidinone through stress screens. The methylphenoxy arm shapes the compound’s profile, offering routes to potent pesticide scaffolds. Because field work depends on reproducible synthesis, agricultural customers value explicit analytical data even more highly than catalog prices. From our end, shipments reflect a commitment to traceability and full batch documentation. Each customer knows which lot their sample came from, the date of manufacture, and the purity achieved—gathered from decades of running robust chemical plants.
As for dyestuff and polymer manufacturers, their needs focus on scalable reactivity and stable coloring properties. This compound delivers on both fronts because of steady batch quality. Direct collaboration with application chemists has shown us the limits of molecule flexibility—too many side impurities can ruin a pigment’s performance or a polymer’s integrity. Resolving these issues means investing in additional testing, and listening to the specifics of each customer’s process need, not just supplying a “standard” chemical. Having seen the difference between satisfied and unsatisfied clients, I continue adjusting the manufacturing approach so that each shipment reflects the practical, real-world wisdom built over years in physical plants.
A common misconception is that all pyrimidinones act interchangeably in synthesis work. In practice, side-group patterns heavily influence reactivity, stability, and suitability for specialty applications. For example, our 5-(3-methylphenoxy)-substituted variant offers enhanced resistance to oxidation compared to analogs featuring only phenoxy or methyl groups in less optimal positions. Bench chemists report fewer breakdown products during extended reaction times, reducing waste and improving overall throughput.
Switching between similar intermediates often reveals downstream complications. Standard 2(1H)-pyrimidinone, lacking the tailored phenoxy arm, fails under more aggressive coupling conditions—sometimes leading to inconsistent yields, color impurities, or missed analytical targets. By focusing not just on purity but on real trace component analysis, our product consistently surpasses competitors. NMR spectra remain cleaner, metal residues trend lower, and all test results back up the consistency claim. Field teams performing high-throughput screens in both pharma and agro sectors notice smoother workflows and less troubleshooting when shifting to this tailored pyrimidinone intermediate.
The substitution unlocks routes to otherwise difficult transformations—a fact not always obvious from catalog listings. As a manufacturer with years of internal synthetic trials behind me, I often share practical observations with our R&D partners. Two labs reported that attempted alkylations on unsubstituted pyrimidinones led to red oil byproducts—a challenge not observed with the 3-methylphenoxy analog. This kind of result comes from iterative learning and close dialogue with users rather than theoretical projections.
Putting theory into practice in a chemical plant delivers insights that no textbook covers. I have worked countless production shifts optimizing small steps: choosing the right catalyst batch, controlling mixing times, tracking lot-to-lot solvent variations, and pulling samples for mid-process testing. Over years, these micro-decisions add up to a higher-quality 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)-, free from the contaminants that often plague low-cost, cut-corner offerings.
On-site audits from both pharma partners and global agricultural clients have prompted us to enhance documentation, traceability, and process validation. These improvements result in more than paperwork—a tighter ship means faster problem resolution and a culture that prizes accountability. Unannounced batch inspections, review of historical quality logs, and regular cross-training of team members all reinforce the reliability of each pound we pack. QA managers routinely consult with plant chemists to troubleshoot outliers or improve protocols—such ongoing team feedback helps keep standards rising, not static.
No process remains perfect. We encountered unexpected solids after switching to a new source of raw 3-methylphenol. Instead of ignoring the change, we spent weeks experimenting with purification temperatures and using new filtration protocols until final product clarity exceeded even our previous standards. Production innovation comes from confronting problems, not dodging them. Some residues respond only to column techniques, not crystallization—a lesson learned by standing over the prep bench, not just reading the manufacturer’s instructions.
I have watched first-year production operators propose improvements to mixing gear that wound up saving thousands annually in solvent recovery and cleaner product. This culture of listening and improvement grew from tangible, on-the-floor experience rather than corporate memos. Quality results from habits as much as from equipment—clear process SOPs, real-time batch controls, and patience in testing each output before sending a drum out the door.
While the focus often falls on purity and yield, safety in production and downstream use shapes every step in our plant. Having managed spills, equipment malfunctions, and near-misses, my team and I factor in the full lifecycle of each chemical, including 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)-. Routine training for new operators, regular review of plant safety data, and investment in environmental controls serve as daily reminders: every molecule matters, and so does every person handling it.
Minimizing waste streams requires deep understanding of not just the primary reaction but of all side processes. Over time, we have cut hazardous solvent use and installed advanced waste capture, all while maintaining output. It used to be common practice to overlook the fate of minor side products. Now, with ongoing feedback from both regulatory agencies and downstream clients, tighter controls and greener choices define each lot’s journey. Sustainability does not mean compromising product performance: through careful distillation and recovery, we preserve both chemical integrity and environmental well-being.
Batch traceability means that, if an issue arises anywhere in the supply chain, we can respond fast with detailed history and even replacement. In a world where recalls or product failures carry rising costs, both legal and reputational, quality now extends into stewardship and end-to-end accountability. I have no interest in passing on hidden risks to research teams or production-scale partners—each shipment comes ready for both efficiency and peace of mind.
The most satisfying moments in chemical manufacturing come not from filling another order, but from direct interactions with end users. Hearing back from a research scientist that our 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- delivered repeatable results validates every late-night troubleshooting session. Application feedback helps us drive incremental improvements: fine-tuning particle size, adjusting handling advice, or updating labeling for clarity. Over time, these real-world conversations ensure that our output is not just commoditized bulk but real value in a bottle.
Emerging fields—from nanotechnology to precision agriculture—demand tighter control of starting materials and intermediates. As a producer, seeing our compounds referenced in new patents and papers reinforces the importance of resilience and innovation at all stages of the supply chain. Our teams maintain constant dialogue with application researchers to understand what works on the bench and what needs further adjustment. I once visited a client lab to witness unexpected crystallization behavior—rather than assigning blame, we jointly dissected the process, leading to a mutual solution.
This ongoing cycle of improvement builds the reputation of both the product and the manufacturer. Regular site visits, technical workshops, and open access to lab data have closed the gap between production and application. Today’s chemists do not settle for generic promises; they ask for complete analytical transparency, trace documentation, and a partner ready to address any issue, from shipping to shelf.
Looking forward, we see new opportunities for 2(1H)-Pyrimidinone, 5-(3-methylphenoxy)- as research pivots towards precision medicine and advanced crop protection. Synthesis complexity will rise as structure-based drug design proliferates. My colleagues and I remain committed to evolving processing standards, incorporating automated tracking, and reducing bottlenecks at scale-up. Technical partnerships with universities and private labs continue to generate new insights—sometimes revealing improved isolation strategies or application ideas we never considered at initial launch.
Our experience shows that no shortcut beats the cumulative knowledge gained by real chemical manufacturing: not just peeling back layers of impurity byproduct, but by understanding the underlying reasons for process variance. It’s easy to overlook minor differences when comparing specialty chemicals. End-users who take the time to scrutinize each property, and who ask pointed questions about consistency and documentation, always see the upside of working directly with a committed manufacturer.
The journey of this compound continues, shaped by feedback from bench chemists, production staff, regulators, and long-standing partners. As new fields leverage heterocyclic building blocks, the need grows for more robust, reliable, and transparent production. I remain convinced from decades on the plant floor that attention to detail and mutual respect among all stakeholders create a better product—one that can serve countless applications without the headache and hassle that often come with less attentive manufacturing.