|
HS Code |
152164 |
| Iupac Name | 6-hydroxy-2-methyl-1H-pyrimidin-4-one |
| Molecular Formula | C5H6N2O2 |
| Molecular Weight | 126.12 g/mol |
| Cas Number | 5467-99-4 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 240-243 °C |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Pubchem Cid | 67970 |
| Smiles | CC1=NC(=O)NC(=O)C=N1 |
As an accredited 4(1H)-Pyrimidinone,6-hydroxy-2-methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle, labeled with hazard warnings, product name, purity, and manufacturer’s details. |
| Container Loading (20′ FCL) | 20′ FCL container loading maximizes bulk shipment efficiency for 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl-, ensuring safe, secure chemical transport. |
| Shipping | 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl- should be shipped in tightly sealed containers, protected from moisture and light. Transport in accordance with relevant chemical safety regulations, ensuring proper labeling and documentation. Use secondary containment to prevent leaks. Handle only by trained personnel, and avoid extreme temperatures during transit to maintain chemical stability. |
| Storage | 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl- should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture, light, and excessive heat. Store at ambient temperature unless otherwise specified, and ensure the storage area is designated for chemicals, following standard laboratory safety protocols. |
| Shelf Life | 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl- typically has a shelf life of 2–3 years when stored in a cool, dry place. |
Competitive 4(1H)-Pyrimidinone,6-hydroxy-2-methyl- prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
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Tel: +8615371019725
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As a company that has spent decades developing and refining production methods for heterocyclic compounds, we understand what it takes to deliver consistent quality at both laboratory and industrial scales. With 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl-, we're talking about a specialty heterocycle that supports the synthesis needs of pharmaceutical, agrochemical, and research enterprises worldwide. Customers depend on predictable traceability, reproducibility, and clear origins, especially in a marketplace where intermediates often change hands repeatedly before reaching the production floor. Manufacturing this compound in our own facilities lets us oversee every step—a difference that shows up in both physical purity and the confidence researchers place in each batch.
Many professionals in the chemical industry can recall times when supply interruptions or quality drift delayed crucial projects. Since we produce 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl- with direct control from raw material sourcing through to final packaging, our customers sidestep these frustrating hurdles. Every kilogram we supply is the result of in-house process development, purification, and real-world scaling experience.
Integrating this compound’s synthesis into our facility called for careful design of reaction stages and purification steps. Pyrimidinone derivatives, especially with both hydroxy and methyl modifications at defined positions, need tight process controls to prevent over-alkylation, isomer formation, and hydrolytic side reactions. That’s an ongoing hands-on challenge: adjusting temperature curves, optimizing solvents, monitoring yield losses at every stage. Problems get solved in the plant, not on a spreadsheet. Our technical staff—some with decades of background in nitrogen heterocycle synthesis—have actually run these reactors, sampled from bottom valves, and scrutinized the mother liquors. The accumulated know-how translates into stable output and sharp impurity profiles.
You won’t find us tossing out oversimplified claims or clipped data table summaries. The chemistry behind 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl- deserves direct explanation, especially if you’re tasked with developing next-generation pharmaceuticals or crop protection agents.
On the bench, this molecule typically appears as a pale solid, crystalline or powdered depending on drying methods. Its actual color and bulk properties reflect both synthesis conditions and lot-specific histories. For projects with sensitive end-uses, like regulated intermediates or screening for API scaffolds, we always recommend fresh analytical documentation. We regularly use proton and carbon NMR, HPLC, GC-MS, and melting point comparison under real-world ambient temperatures in our own laboratories.
This is not bulk commodity chemistry; batches tend to be smaller, and we see real value in flexibility. Many times, clients ask for particular particle size cuts, or seek lower residual solvent levels for subsequent coupling steps. We’ve built our operation around answering these calls, running post-synthesis refinement or custom packaging in direct dialogue with the end user. Because we own the entire manufacturing workflow, making these adjustments is part of daily business.
The substitution pattern on 4(1H)-Pyrimidinone—hydroxy at position 6, methyl at position 2—creates a building block with distinctive reactivity. Medicinal and agrochemical researchers reach for these frameworks when they’re mapping out new lead compounds because the patterning determines hydrogen bonding, solubility, and compatibility in different reaction schemes. Our team tracks downstream demand: nucleoside analogue synthesis, kinase inhibitor core construction, and base analogues all draw upon this unique scaffold.
Our own experience handling scale-ups has made it clear where other approaches can go wrong: sloppy drying conditions, lazy solvent selections, or compromised packing often introduce undetectable contaminants that only surface later down the pipeline. Since our analytical team works hand-in-hand with production—literally in the same building—we resolve problems and monitor drift at each scale-up stage. This has helped us navigate the bottlenecks that sometimes trip up contract manufacturers or trading companies, such as unwanted polymorphs in crystalline intermediates or batch inconsistency during long campaigns.
Veterans in synthetic organic chemistry will recognize that not all pyrimidinones behave alike. Isomers—distinguished only by the position of hydroxyl or methyl substituents—demonstrate sizable differences in their reactivity and application. One cannot simply substitute a 2,4-dimethyl or 4,6-dihydroxy variant in most route schemes. Our 6-hydroxy-2-methyl material yields specific regioselective advantages in nucleophilicity and tautomeric stability, relevant where base-pairing or hydrogen bond configuration plays a part in bioactivity assays.
We’ve trialed reactions in-house to verify outcomes: for example, this compound’s selective participation in acylations and ring-closure steps often surpasses other similar scaffolds. In solution, its solubility profile and resistance to oxidative breakdown means longer shelf-life—an outcome our clients appreciate, especially in high-value drug discovery projects. Direct conversation with formulation and process chemists in our client’s R&D teams has made clear that these subtle differences streamline development, especially when time pressure around patent filings or regulatory submissions is high.
Many suppliers today market blends, technical grades, or isomer-containing materials. Since we manage our own crystallizations and have developed reliable chromatography cleanups, our delivered product typically maintains higher chemical purity and isomeric definition. We don’t view high purity as a marketing term, but as an operational safeguard. Too many production mishaps elsewhere have started from accepting lower-clarity intermediates.
Colleagues in pharmaceuticals ask about the molecule’s history as a core structure in nucleoside analogues, certain antiviral candidates, and synthetic work linking to natural bases. Its methyl and hydroxy groups lend themselves to stepwise derivatization, and our team regularly supports partners with route development, impurity profiling, and alternate salt forms. The compound’s role as a proven intermediate links directly with downstream documentation and regulatory filings. Supplying consistent documentation—batch COA, analytical spectra, and insight on handling—comes from direct manufacturing experience.
Agrochemical researchers look for pyrimidinone derivatives when designing new plant health agents and fungicide candidates. In these cases, consistency in impurity profiles is critical, particularly as field trials can be invalidated by batch-to-batch drift. Since our senior chemists work directly with scale-up teams, we offer informed answers on potential storage and formulation questions, practical advice drawn from shipping and storing hundreds of kilograms of related heterocycles under varied global conditions.
University and industrial labs often rely on our material as a reference compound. These research settings demand certainty both in chemical structure and chain of custody—a certainty enabled by factory-direct shipments and traceable internal yields.
Over the years, our facility has navigated the ups and downs of raw material shortages, custom synthesis bottlenecks, and evolving regulatory standards. Rather than chase every market trend, we’ve maintained a focus on process stability and compliance. Our analytical documents come from instruments calibrated and managed by on-staff experts—it’s not just a matter of passing a spec, but of anticipating what end users will actually find useful. These reports include routine NMR, MS, and HPLC data, but may also—on request—cover more specialized needs such as residual metals analysis or thermal degradation profiles.
Clients sometimes share stories about unexplained color variation or erratic solubility in competitor batches. We encourage open, rapid communication and operate as a real partner when such situations arise. By providing access to technical leaders and synthesis teams, no one is left puzzling over answerless support emails or impersonal ticketing systems.
Shipping logistics, particularly for moisture-sensitive compounds, require thoughtful packaging and a realistic view of global transit conditions. Every packed drum or flask reflects our own team’s experience with what has gone right—and wrong—in prior deliveries. We monitor feedback, address real-life warehousing problems, and adapt packaging and labeling based on how users actually handle the compound across continents.
Having control over the plant means adaptation is mostly a matter of rebalancing reactors and purification schedules. Unlike sales-driven third parties, we have every reason to prioritize workable yields and prevent cross-contamination. Our production staff, often career-long employees, carry direct responsibility for each shift. With fluctuating project loads and occasional urgent requests, this foundation helps us meet needs from tens of grams for pilot work up to multi-hundred kilogram campaigns.
We’ve invested in redundant process trains and analytical redundancy, letting us swap between equipment with minimal downtime. Stored samples from historical batches form our own internal archive, helping us track any evolving subtle issues and answer customer questions about shift-level details without resorting to guesswork.
Where customer specs demand extra polishing—say, for preclinical use or field trial qualification—our technical and QC teams address requests in real time. This is where pure manufacturing experience outweighs trading expertise; process tweaks and documentation updates happen in the same building, overseen by senior chemists with practical exposure to everything from oven drying to final product sealing.
Staff in our facility know from hard-earned experience that handling derivatives like this one calls for respect—open containers and high humidity spell trouble. Our teams organize storage by compound class, minimize airborne exposure during transfer, and test through multiple material splits prior to packaging outbound shipments. Each step in the workflow benefits from people who have lifted the barrels, measured the solvents, and seen the impact of minor temperature skew on storage stability.
Since 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl- often heads for further derivatization, we document moisture content, particle morphology, and thermal stability for every production lot. This detail resonates in every customer conversation, whether the focus is pilot plant transfer or planning a new downstream reaction.
Too many projects stall or backtrack because raw material origins are murky. We dedicate real effort to documentation, batch traceability, and prompt technical responses. Chemical manufacturing isn’t glamorous, but our focus has always been on helping partners, not just making a sale. Customers trust us to deliver products like 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl- because each lot reflects real-world experience, a direct synthesis pathway, and day-to-day problem-solving by people who care about chemical integrity.
From our side, reliability means more than matching numbers on a certificate. It means listening to feedback, reworking processes when field experience calls for it, and delivering not just molecules, but honest support over decades of service in the chemical industry.