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HS Code |
158659 |
| Chemical Name | 2,4-Dimethyl-6-Hydroxypyrimidine |
| Molecular Formula | C6H8N2O |
| Molecular Weight | 124.14 g/mol |
| Cas Number | 27347-49-5 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 138-142 °C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Pka | Approx. 9 (hydroxyl group) |
| Smiles | CC1=NC(=C(C(=N1)C)O) |
| Iupac Name | 2,4-dimethyl-1,6-dihydropyrimidin-6-one |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 2,4-Dimethyl-6-Hydroxypyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle with a secure screw cap, labeled with chemical name, CAS number, safety icons, and storage instructions. |
| Shipping | 2,4-Dimethyl-6-Hydroxypyrimidine is typically shipped in sealed, chemical-resistant containers to prevent moisture ingress and contamination. It should be handled as a non-hazardous material under normal conditions but must be stored in a cool, dry place, away from strong oxidizers. Shipping must comply with local chemical safety and transportation regulations. |
| Storage | 2,4-Dimethyl-6-hydroxypyrimidine should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents. Label the container clearly and ensure access is restricted to trained personnel. Follow appropriate safety and chemical hygiene protocols during handling and storage. |
Applications of 2,4-Dimethyl-6-Hydroxypyrimidine in Industrial Manufacturing2,4-Dimethyl-6-Hydroxypyrimidine serves as a specialized intermediate in several advanced chemical sectors. Its unique structural features enable targeted functionality in pharmaceutical synthesis, crop protection, specialty material production, electronic chemicals, and fine chemical intermediates. Below are the key downstream application scenarios supported by market-verified demand and manufacturing integration. 1. Pharmaceutical Intermediates for Antiviral Drug SynthesisPharmaceutical manufacturers deploy 2,4-Dimethyl-6-Hydroxypyrimidine as a core building block for the synthesis of heterocyclic antiviral drug intermediates. It enables nucleoside analogue development by facilitating selective ring modification and further derivatization. Strict traceability, impurity management, and batch consistency are required throughout cGMP operations and regulatory inspections. Industry compliance standards
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2. Agrochemical Building Block for Herbicide SynthesisChemical crop protection producers utilize this pyrimidine derivative to construct selective herbicide actives through advanced heterocyclic chemistry. The material enters as a key core reactant for ring-closure reactions in the creation of pre- and post-emergence herbicidal actives, demanding tight process monitoring and trace impurity management under agrochemical registration protocols. Industry compliance standards
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3. Specialty Material Intermediate in UV-Absorbing PolymersManufacturers of specialty polymers select this compound for functionalizing polymer chains with enhanced UV absorption and stability. It supports copolymerization and grafting in the intermediate stage, providing performance improvements in films, coatings, and optical-grade plastics. Manufacturing runs employ strict controls to minimize extractables and maintain transparency standards for high-spec applications. Industry compliance standards
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4. Electronic Chemical Precursor for Photoresist Additive SynthesisLeading semiconductor and microelectronics chemical suppliers use the compound as a precursor for synthesizing pyrimidine-based photoactive additives. These additives enhance lithographic pattern resolution and developability in high-resolution photoresists. Clean room supply chain qualification and electronic grade impurity specifications are critical to ensure film-forming reliability and device yield. Industry compliance standards
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5. Fine Chemical Intermediate for Laboratory ReagentsProducers of reference standards and analytical reagents incorporate this building block into the synthesis of specialty chemical standards. Used for the preparation of analytical controls, impurity markers, and HDX-MS reference compounds, the material requires tight specification compliance and reliable batch certification for accredited laboratory use and third-party proficiency testing programs. Industry compliance standards
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Over the last decades, effort, skill, and investment have shaped how we manufacture 2,4-dimethyl-6-hydroxypyrimidine. Speaking from the production floor, this compound is not just another pyrimidine derivative—its reliability matters at every stage, from the earliest pilot batches through full-scale delivery. Our daily goal isn’t to hit numbers for inventory’s sake; it’s to give formulators and researchers a dependable, high-purity intermediate for their innovations.
Our 2,4-dimethyl-6-hydroxypyrimidine, offered as a crystalline solid, delivers consistent purity above 99%. In practice, the feel, flow, and clarity of this material reveal a lot about batch quality. Each inspection—whether for moisture pick-up, trace color, or byproduct content—anchors real accountability. Even minor changes in these parameters can influence downstream processes. We've seen it: A handful of ppm in impurity can disrupt a whole synthesis, and some solubility quirks can throw off process yields or spectral analysis. We test more than just HPLC and NMR, because shipping a flawless certificate doesn’t always tell the whole story. Satisfying the paper doesn’t always mean the chemistry holds up in real-world conditions—after months in storage, after rough handling, and after scaling-up.
2,4-dimethyl-6-hydroxypyrimidine rarely makes headlines on its own. Instead, its role sits squarely at the crossroads of innovative chemistry, especially in pharmaceutical and agrochemical research. This pyrimidine core finds demand in the synthesis of crop protection agents, certain pharmaceuticals, and specialty intermediates where electron-rich, robust heterocycles are needed. We have watched small biotech teams and global companies alike find value in the unique properties this molecule brings to their lead compound libraries. The dimethyl substitution increases lipophilicity; the 6-hydroxy group – when handled correctly – influences reactivity in follow-up derivatizations. That difference can determine whether a project clears a development hurdle or stalls in a test tube.
Unlike simpler pyrimidine compounds, the dual methyl groups and the single hydroxy handle together result in enhanced selectivity for certain coupling or alkylation steps. In early research campaigns, chemists sometimes substitute similar analogues, only to circle back to this exact scaffold for its balance of reactivity and manageability. Years ago, we worked with a team trying to optimize activity in a bench-scale series of kinase inhibitors. Batch after batch, alternatives gave them solubility headaches or stability issues—they needed clean, reproducible 2,4-dimethyl-6-hydroxypyrimidine, and we learned the hard way how a little inconsistency at our end could disrupt whole weeks of carefully planned work.
Production-scale chemistry often reveals the difference between real manufacturing control and trading chemistry by catalog or spreadsheet. At our facility, each shipment reflects a network of process controls painstakingly refined across many campaigns—this isn’t a bring-it-in, ship-it-out warehouse mentality. Careful temperature control, optimized crystallization, and purification are not slogans. Our team tracks trends in physical properties, employs multiple analytical techniques, and always watches for subtle signs of batch drift.
We repeat extra steps in drying cycles on humid days, and track solvents residue clearance at every batch, not just when customers ask. Year after year, we have seen the advantage a true manufacturer brings—especially for chemists running kinetics, working in heat-sensitive regimes, or scaling up to make pilot lots for registration batches. Uniform melting point, consistent powder density, low residual water, and absence of color bodies benefit every downstream user. If you have ever had to troubleshoot an unexpected side reaction or batch failure, you know that source reliability makes a difference. No trader or reseller understands the messy details—the tiny crystals clogging a filter, or small lots blending poorly, or material that cakes and doesn’t dissolve as expected.
We have been called at odd hours by customers who bought alternate material elsewhere for a “cost save”, only to find their HPLC chromatograms a mess, or their reactors fouled by residues. For them, the difference isn’t theoretical. These stories shape our belief: chemistry remains a craft as much as an industry, and the more hands-on you stay, the better your product gets.
The numbers matter, but numbers must be earned at every lot. For us, batch purity consistently exceeds 99%, with controlled losses on drying and trace metals managed in tolerances suitable for pharmaceutical synthesis. Melting point sits tightly within expected limits. Packing avoids waxy residues that can creep in from certain solvents. Granule size stays within the narrow bounds that industrial batch reactors or automated dosing systems demand. A spec sheet often gets read once—but repeated, verified quality makes reputations.
We put the work in at the ground level, vetting every drum before it leaves—running not just NMR and IR, but also real-time solubility and stability checks in common solvents and buffers. These are time-consuming steps, but they save headaches later. A technician might spend hours gently coaxing out clumps or evaluating flocculation under heat, because we’ve seen what bad powder flow or off-odors can do in a busy plant. There is simply no shortcut for the hands-on, batch-by-batch scrutiny that keeps surprises out of your workflow.
Not every batch lives up to the highest standard. We never hide from this reality. Real manufacturing creates opportunities for drift—raw material quality, seasonal temperature swings, water content in local air, a slightly worn filter cloth. Years ago, a shift in one solvent distillation run resulted in a faint shift in powder color. It triggered days of root-cause investigation. Tracking down these details isn’t glamourous—or cheap. But resolving them builds resilience and a deeper understanding that only comes from repeated, direct experience. We have learned to anticipate certain “trouble signs” and plan extra controls during seasonal switchover.
Every new campaign gets a batch-specific logbook. Instead of chasing minimum spec, we record aberrations and anomalies in real time, using both digital records and hands-on physical checks. This diligence matters especially for 2,4-dimethyl-6-hydroxypyrimidine, where inconsistencies in hydroxyl content or methyl substitution ratios lead to costly errors in complex synthesis regimes. Not everything shows up in a chromatogram. The seasoned operator knows to watch for subtle textural changes, invisible to an external auditor, but unmistakable to someone who has handled thousands of kilos of the same molecule.
Many of our long-term customers are small to midsize chemistry teams with ambitious targets and limited time. They bring real pressure for rapid iteration. For them, sourcing from a direct manufacturer means not only reliable material but tailored support. We have supported users who need documentation for regulatory filings, and others who require technical advice on solvent compatibility, reactivity under microwave conditions, or behavior under inert gas flows.
Chemists are creative problem solvers—not just number crunchers. When one client needed to modify the classical synthesis route, our team provided both technical feedback and material for feasibility runs that supported a successful pivot. In another situation, a team adapting a high-throughput screen encountered caking in their feed hoppers from previous suppliers. Our extra drying and twin-screw blending solved it. This kind of back-and-forth—manufacturer and end-user aligned on real problems—drives better outcomes for everyone.
Compared to pyrimidine compounds missing one or both methyl groups, or featuring only an amino substitution, this molecule delivers distinct reactivity. The dimethyl pattern alters electron density, tuning coupling preferences and reactivity during heterocycle formation, Suzuki couplings, or stepwise oxidations. The 6-hydroxy group both adds polarity and supplies a unique anchor for downstream derivatization steps. Some chemists try similar structures, hoping to find a cheaper or more available substitute. Their feedback lands with us—lower solubility, inconsistent yields, or unstable intermediates push them back to our product.
Beyond reactivity, texture and flow matter more for real-world use than catalog claims. Fine control over moisture, granulometry, and solvent compatibility allows our 2,4-dimethyl-6-hydroxypyrimidine to perform more predictably in powder handling systems, sealed reactors, or open-bench scales. Smoother flow means fewer interruptions in feeding processes, and predictable solubility prevents downtime for forced dissolutions or last-minute tweaks in process solvent selection.
We engage in technical exchanges with researchers working on new routes in medicinal chemistry and crop science. Sometimes, small changes in the product’s physical parameters have meaningful effects in these investigations. We adjust, provide custom samples, and track feedback, because in process chemistry, the real world always intervenes.
Producing high-purity pyrimidines isn’t only about chemistry—it’s about responsibility. Over years of operation, we have upgraded waste treatment, cut solvent loss, and refined containment systems to minimize environmental burden. Process improvements are more than marketing—they cut real costs, reduce regulatory headaches, and protect worker health. In our daily work environments, strict control measures keep dust and vapors in check, and ongoing sampling monitors for traces outside work zones.
Every campaign means careful tracking of starting material origins, batch-level traceability, and end-to-end records. We have implemented digital tracking for inventory at every stage, ensuring any anomaly can be traced backward in minutes, not days. Experienced engineers refine protocols, and maintenance teams ensure no leaky seals or aging equipment threaten either product quality or personnel safety. This integrated mindset is what stands behind a stable supply of 2,4-dimethyl-6-hydroxypyrimidine—not a warehouse, but a living, working factory where every employee owns a share of the process.
Reality-based innovation starts with listening. Customers—both longtime users and new clients switching from competitors—share frontline reports. These include practical insights from batch failures, yield shifts, or new process adaptation. We have shaped our campaign flows around this feedback, not top-down mandates. Switching a solvent to minimize off-odors, altering drying protocols to trim caking risk, and developing grading on powder format for streamlined feeding, all grew from such practical advice.
Real quality comes from closing that feedback loop fast. Direct access between users and manufacturing teams—skipping traders—enables diligent troubleshooting, frequent small-scale adjustments, and priority shipment support for urgent needs. The more open the conversation, the less likely users are to be left struggling with unknown variables or late-night production delays.
In the last few years, chemical customers have learned hard lessons about the risks in fragmented supply chains. During periods of raw material scarcity or logistics disruption, traders and resellers often found themselves out of the loop—or powerless in the face of upstream issues. As direct manufacturers, our team holds real sway over production timelines and order fulfillment. We understand the volatility of both raw material pricing and transport cost structures.
Each successful campaign reinforces the trust our partners place in us. We carry buffer capacity, diversify upstream sourcing, and keep redundant ordering systems in place. When inevitable disruptions pop up, open and immediate communication ensures that a customer planning a campaign involving 2,4-dimethyl-6-hydroxypyrimidine will not be left guessing. Advance warning and open alternatives are standard practice; that kind of transparency only comes from hands-on production, not marketers who handwave away problems.
Demand for specialized heterocyclic building blocks grows every year alongside new advances in discovery chemistry. Regulatory changes, greener protocols, and end-user preferences drive us to invest in cleaner, more efficient process routes. Continuous process improvement shapes the future of 2,4-dimethyl-6-hydroxypyrimidine production. Our investment in real-time analytical tools, expanded containment, and waste minimization gives customers confidence that the product they depend on will remain available, even as external rules evolve.
New applications continue to emerge, especially in more demanding roles where predictable reactivity and low impurity count carry even greater weight. Every project that pushes at the edge of what pyrimidines can do gives us the chance to strengthen our own knowledge and production expertise. By staying alert to small-scale feedback and fostering direct technical dialogues, we keep ahead of shifting needs—always refining, always listening.
From our perspective as hands-on chemical manufacturers, 2,4-dimethyl-6-hydroxypyrimidine is more than just a supplied molecule. It represents years of knowledge, layered process refinements, and direct technical support. Chemists who rely on it know the difference that transparency, batch-by-batch accountability, and long-term partnership make. Every shipment leaves our plant carrying that commitment—not as an abstract principle, but as the sum of careful production, real-world troubleshooting, and mutual respect for creative, demanding work in modern chemistry.