|
HS Code |
715454 |
| Chemicalname | 5-(m-Tolyloxy)-2(1H)-pyrimidinone |
| Molecularformula | C11H10N2O2 |
| Molecularweight | 202.21 g/mol |
| Casnumber | 33540-42-4 |
| Appearance | White to off-white solid |
| Meltingpoint | 148-151°C |
| Solubility | Slightly soluble in water; soluble in organic solvents like DMSO and ethanol |
| Structuretype | Aromatic heterocycle |
| Smiles | Cc1cccc(c1)Oc2cnc(=O)[nh]2 |
| Iupacname | 5-[(3-methylphenyl)oxy]pyrimidin-2(1H)-one |
As an accredited 5-(m-Tolyloxy)-2(1H)-pyrimidinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is supplied in a 25g amber glass bottle, sealed with a tamper-evident cap and labeled with chemical details and safety information. |
| Container Loading (20′ FCL) | 20′ FCL: Securely packed in sealed drums, 5-(m-Tolyloxy)-2(1H)-pyrimidinone loaded on pallets, moisture-protected, and properly labeled. |
| Shipping | The chemical **5-(m-Tolyloxy)-2(1H)-pyrimidinone** is shipped in a tightly sealed, chemically-resistant container, protected from moisture, light, and extreme temperatures. Transportation complies with standard hazardous material regulations. Packing ensures minimal risk of breakage or leakage, with all labeling reflecting proper chemical identification and safety requirements for secure delivery. |
| Storage | 5-(m-Tolyloxy)-2(1H)-pyrimidinone should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature (15–25°C) in a cool, dry, and well-ventilated area, away from incompatible substances such as strong acids or oxidizers. Ensure proper labeling and restrict access to authorized personnel only. Use appropriate safety measures during handling. |
| Shelf Life | **Shelf Life:** 5-(m-Tolyloxy)-2(1H)-pyrimidinone is stable for at least 2 years when stored in a cool, dry, and dark place. |
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Decades in chemical manufacturing have shown us that genuine breakthroughs often come through molecules that, on paper, seem uncomplicated. 5-(m-Tolyloxy)-2(1H)-pyrimidinone is one such substance: a pyrimidinone derivative that continues to reveal new value as research advances and market needs evolve. Formulated as a white to off-white crystalline powder, the product displays strong stability under typical storage conditions, and each batch leaves our site only after rigorous in-house quality control.
The chemical structure features a core pyrimidinone ring substituted with a meta-tolyloxy group, yielding a distinct physicochemical profile. Our team worked extensively with this molecule, iterating process steps until we reached optimal purity and reproducibility. Confirmed by multiple instrumental methods—HPLC, NMR, and FTIR—the typical purity of our product exceeds 98%, surpassing market expectations.
One lesson hard-learned on the manufacturing floor: purity isn’t a number, it’s the difference between a material that performs as intended and one that creates headaches down the line. The normal specification for our batches reaches or surpasses 98% on active compound, with controlled moisture to avoid caking and batch-to-batch fluctuations. This approach protects downstream reactions, gives formulators consistency, and supports robust applications requiring tight impurity profiles.
Physical characteristics are more than catalog details. We maintain particle size within a strict range for enhanced handling and to fit standard feeder systems. An experienced operator can tell the material’s handling quality by the way it flows from the drum. Trace impurity levels get monitored every production cycle to anticipate potential side reactions for sensitive synthesis work. The experience we’ve gathered allows us to preempt issues that customers of generalized, off-the-shelf material might not see until scale-up.
5-(m-Tolyloxy)-2(1H)-pyrimidinone serves most notably in pharmaceutical and agrochemical research. The molecule functions as a versatile intermediate, facilitating the creation of compounds with bioactive potential. Our partners in pharmaceutical R&D seek out this structure when synthesizing pyrimidine-based drug candidates. The m-tolyloxy modification gives this intermediate a unique electronic profile, which plays a critical role in reaction selectivity and yield.
Beyond early-stage drug discovery, this molecule advances agricultural research, underpinning the synthesis of certain fungicides and plant growth regulators. Chemistry teams benefit from its ease of functionalization and compatibility with various synthetic pathways, enabling rapid prototyping of analogues without re-optimizing entire protocols. Beyond strict synthesis, material scientists have explored this compound as a building block for specialty polymers with tunable thermal or photonic properties.
Years collaborating directly with scientists across industries taught us how the specifications of our product carry over into patentable innovation for our clients. When a batch runs clean, progress accelerates; when unknown peaks show up in the spectrum, months can be lost. We keep that risk top-of-mind with each drum that ships. Our QC approach is aligned with what principal investigators and formulation chemists confront in everyday laboratory decisions.
Countless pyrimidinone derivatives exist, but not all perform equally. Experience in this market forced our team to confront the subtle but real differences between meta, ortho, and para substituted isomers. The m-tolyl group gives this specific molecule a distinctive reactivity and solubility profile. For chemists, this often means smoother protection/deprotection cycles and better solubility in both polar and non-polar solvents as compared to other analogues.
On the scale-up front, m-tolyloxy substitution tends to reduce unwanted byproducts in bromination, acylation, and selective hydrogenation steps. That means cleaner reactions downstream, improving both yields and purity in subsequent transformations. Side by side, the differences with 5-(p-Tolyloxy)-2(1H)-pyrimidinone or 5-phenoxy-2(1H)-pyrimidinone go beyond nomenclature: they reflect how slight modifications in structure can dramatically shift work-up times, reactivity, and overall cost-effectiveness of an industrial synthesis.
We regularly run pilot reactions to map out how shifts in functional groups impact isolation and yield. This continuous R&D approach, bolstered by customer feedback, helps improve standard operating procedures to favor the m-tolyloxy variant in complex, multi-step workflows. In our facility, the reduced formation of trace tars and uncontrolled color formation means less downtime for reactor cleaning and faster changeovers.
Manufacturing pyrimidinone derivatives isn’t a series of check-boxes. Each kilo we produce reflects a closely managed process, from raw material inspection to careful crystallization and packaging. Impurities, moisture content, and storage conditions must be tightly controlled, not only for compliance, but to ensure smooth integration into research and commercial pipelines.
Many clients shared war stories: prior attempts sourcing from traders led to inconsistent batches and unpredictable solubility profiles. With direct manufacturing control, troubleshooting moves quickly. When a chemist needs documentation on the most recent impurity profile or updated COA, we’ve already tracked the relevant analyses, and can provide full transparency. Third-party actors aren’t always prepared to offer this level of detail, leaving gaps that only appear at scale or under regulatory scrutiny.
The drive to adapt to changing synthetic demands led us to invest in custom small-batch capabilities. Researchers testing new modifications asked for tighter specification on residual solvents and granulation. By integrating modular reactor setups, our team ramped up pilot-scale production with turnaround times tailored for rapid feedback. That flexibility has kept us relevant to startups and multinational partners alike.
Certain customers approached us needing modifications for solvent, trace catalyst, or alternative counterions. Open communication with their technical teams drove incremental improvements to crystallization and drying steps, ensuring the compound fits downstream applications. This approach creates value far beyond “commodity” status; it builds deep relationships rooted in process understanding, delivering more than just consignment.
Scaling production of 5-(m-Tolyloxy)-2(1H)-pyrimidinone taught us to navigate a set of recurring challenges. Maintaining high purity requires vigilance against contamination—mineral acid residues, solvent traces, or incorrect temperature programming can quickly degrade performance. Years of process optimization led our operators to focus on robust local exhaust, proper material transfer, and automated cleaning cycles. Setting up a closed-system workflow lowered both worker exposure and batch-to-batch variability.
Striking the balance between throughput and control posed one of the tougher operational puzzles. Rushing the reaction sometimes caused unwanted oligomerization, shaving points off purity or clogging filtration units. By updating protocols around stepwise addition and reaction monitoring, we raised yields and improved crystalline uniformity. The hands-on experience of seeing product behavior in different reactors, at different scale, informed our approach better than any readout from a remote partner could.
Fielding technical queries from customers requires our chemists to stay constantly engaged with upstream and downstream science. If a customer observes an issue with material dissolution, precipitation, or color during formula preparation, we dive into retrospective analysis of production logs and batch records. Being both manufacturer and scientific collaborator sharpens accountability and protects project timelines.
Many customers base critical research or commercial launches on our supply chain. Delivering product that meets published standards is a baseline, yet advancing to ICH, cGMP, or local regulatory benchmarks demands even closer attention. The audit processes for pharmaceutical and agricultural intermediates often require full traceability of each raw material lot, reaction record, and analytical method. Since our team manages the full lifecycle from sourcing to shipment, our documentation stands up to the scrutiny of global clients and regulators.
We’ve seen how end users rely on repeatable impurity signatures. Variability burns time—not least by forcing chemists to revalidate their own synthetic steps. Applying best practices in statistical process control, we keep key release parameters well within confidence limits, reducing risk for product development and commercialization timelines. Our experience shows that quality isn’t maintained by edict, but by thousands of accumulated process improvements, born from mistakes as well as successes.
Supply reliability stands on equal footing with technical performance. The past few years challenged even established suppliers thanks to logistical disruptions, raw material shortages, and growing regulatory expectations. Because we control our raw material pipelines and maintain local inventory buffers, clients have ridden out surges in demand more smoothly. Close communication and transparency about potential delays let users plan ahead rather than scrambling for alternatives at the last minute.
Environmental pressures and regulatory expectations in the chemical sector press us to innovate continuously. Handling pyrimidinone intermediates like 5-(m-Tolyloxy)-2(1H)-pyrimidinone creates unique challenges—trace solvent emissions, process water contamination, and byproduct management all feature prominently in our everyday decision-making. Working directly as a manufacturer, we remain well aware of the scrutiny applied to our sector, not just by authorities, but by end-market clients and the communities we serve.
Our most recent production upgrades integrated solvent recovery units designed for this molecule’s boiling point and polarity. Recovering and reusing solvents brings down cost and cuts environmental footprint, delivering a clear win for both sustainability targets and operational margins. The specifics of our closed-loop system limit operator exposure and enable better compliance with local discharge regulations. These modifications grew out of direct experience, field data, and dialogue with environmental monitors.
We stay committed to exploring new, less hazardous solvent systems, both for core synthesis and purification. Partnering with academic researchers and industry peers, we’ve piloted replacements for more toxic agents, aiming for greener chemistry that meets evolving global compliance standards. Our credibility comes not only from successful product releases, but from the willingness to acknowledge setbacks and adapt accordingly.
Digitalization has transformed many core processes. By rolling out real-time batch monitoring and data aggregation, plant managers catch deviations more rapidly and fine-tune processes with evidence rather than guesswork. Our new dashboard reporting captured key insights on how shift changes or raw material sourcing can ripple through final assay results. This sort of direct data feedback—a reality only for those close to the process—translates to actionable results for client-facing teams.
We’ve seen over time that direct lines between our production team and customer scientists foster stronger outcomes than long relay chains of distributors. Each technical question or quality complaint becomes not just a service issue, but a chance for both sides to learn and improve. Whether the challenge involves solubility oddities or tighter particle size control, hands-on engagement reveals practical solutions far removed from generic datasheets or sales claims.
A manufacturer’s long-term health depends on trust. Missteps in delivering specifications or addressing problems can erode confidence faster than any price shift or new entrant. We take pride in a culture of root-cause investigation, not quick excuses—backed by the willingness to document findings and pursue corrective action when needed. By sharing detailed production and analytical logs, we help customers unlock hidden efficiency in their own formulations.
Many of our collaborations extend beyond a simple transaction. We’ve worked with academic teams developing novel synthetic routes, providing test quantities for feasibility studies, and assisting with process troubleshooting along the way. Commercial partners developing proprietary formulations value the added insight of experienced manufacturing chemists, able to interpret analytical results, flag potential hazards, and recommend tweaks to improve yield or reduce waste.
The pace of global change in specialty chemicals keeps us humble. Shifts in regulation, new patent filings, and changing application demands force a constant process of adaptation. We watch the entry of generic competitors and changing cost structures as closely as the latest advances in reaction chemistry. While it’s tempting to focus on volume and throughput, our experience demonstrates that agility, feedback, and close dialogue with users produce more sustainable wins.
As niche markets for pyrimidinone derivatives diversify, we continually reassess whether our standard process fits emerging applications or if upstream modifications are warranted. Feedback from pilot partners and research teams informs both incremental improvements and major investment decisions. Our management holds regular technical reviews not just to improve yield, but to identify new application fields—from advanced materials to pharmaceutical intermediates previously unserved by current catalogues.
Developments in AI-assisted synthesis and high-throughput screening have changed the volume and timeliness of orders. With bench scientists able to generate hundreds of analogues in days, supply chains orient around rapid, repeated shipments of high-spec product. Our focus on flexible batch sizes, rapid quality confirmation, and streamlined logistics positions us to serve these more dynamic R&D environments far better than purely commodity producers.
Working close to the source of innovation has shown us how little separates success from frustration, both on the shop floor and in the lab. Many synthetic routes depend on the reliability of core intermediates—delivering consistent 5-(m-Tolyloxy)-2(1H)-pyrimidinone remains both a technical challenge and a point of pride for our team.
Years in chemical manufacturing have taught us to value precision, accountability, and transparency. Every batch of 5-(m-Tolyloxy)-2(1H)-pyrimidinone tells a story of deliberate choices—reaction pathways, purification challenges, technical collaborations, and regulatory dialogues. As market demands grow more sophisticated, being an engaged partner rather than a remote supplier proves decisive.
Through direct connections between plant, lab, and customer site, we refine not only the product but the practices that sustain both innovation and safety. In supporting our clients, we consistently advocate clear data, honest feedback, and hands-on problem-solving. For research teams driving the edge of drug and agrochemical innovation, reliability cannot be an afterthought. Deep knowledge of 5-(m-Tolyloxy)-2(1H)-pyrimidinone’s synthesis, behavior, and potential enhances both our operation and the products our clients bring forth.
Continuous improvement governs our mindset—each production cycle, customer request, or regulatory development offers a new opportunity to adapt. By investing in robust process control, environmental responsibility, and rapid response capabilities, we help ensure that the next breakthrough molecule, formulation, or application isn’t held back by the details of the supply chain.
Our perspective as manufacturers—bridging detail-oriented chemistry with the broader goals of progress—grounds the value we offer to every collaborator seeking a reliable, high-performance 5-(m-Tolyloxy)-2(1H)-pyrimidinone.