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HS Code |
835471 |
| Chemical Name | 2-Hydroxymethyl-3,5-Dimethyl-4-Methoxypyridine |
| Molecular Formula | C9H13NO2 |
| Molecular Weight | 167.21 g/mol |
| Appearance | White to off-white solid |
| Melting Point | Approximately 80-85°C |
| Solubility | Soluble in organic solvents such as ethanol and DMSO |
| Purity | Typically >98% |
| Storage Conditions | Store at 2-8°C, protected from light |
| Smiles | COC1=NC(C)(C)C=C(CO)C1 |
| Synonyms | 4-Methoxy-3,5-dimethyl-2-(hydroxymethyl)pyridine |
As an accredited 2-Hydroxymethyl-3,5-Dimethy-4-Methoxypyridine 4-Methoxy-3,5-Dimethyl-2-Hydro 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, sealed with a screw cap, and clearly labeled with hazard and product information. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) involves securely packing 2-Hydroxymethyl-3,5-Dimethyl-4-Methoxypyridine in sealed, labeled drums or bags for safe transit. |
| Shipping | **Shipping Description:** 2-Hydroxymethyl-3,5-dimethyl-4-methoxypyridine is shipped in tightly sealed containers, protected from moisture and light. It is transported as a non-hazardous chemical under ambient conditions, with standard laboratory chemical handling precautions. Ensure proper labeling and documentation as required by local and international regulations for chemical transport. |
| Storage | Store 2-Hydroxymethyl-3,5-dimethyl-4-methoxypyridine (4-methoxy-3,5-dimethyl-2-hydro) in a tightly sealed container, protected from light and moisture. Keep at room temperature in a cool, dry, well-ventilated area away from incompatible substances, such as strong oxidizers and acids. Label the container appropriately and follow local regulations for chemical storage. Always wear suitable personal protective equipment when handling. |
| Shelf Life | Shelf life: Stable for at least 2 years when stored in a cool, dry place, tightly sealed, and protected from light. |
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Purity 98%: 2-Hydroxymethyl-3,5-Dimethy-4-Methoxypyridine 4-Methoxy-3,5-Dimethyl-2-Hydro with 98% purity is used in pharmaceutical synthesis, where it ensures high yield and reduced impurities during active ingredient formulation. Melting Point 88°C: 2-Hydroxymethyl-3,5-Dimethy-4-Methoxypyridine 4-Methoxy-3,5-Dimethyl-2-Hydro with a melting point of 88°C is used in solid-state API development, where it enables precise temperature-controlled processing. Molecular Weight 181.22 g/mol: 2-Hydroxymethyl-3,5-Dimethy-4-Methoxypyridine 4-Methoxy-3,5-Dimethyl-2-Hydro with molecular weight 181.22 g/mol is used in chemical research, where it allows for accurate stoichiometric calculations in reaction setups. Stability Temperature 120°C: 2-Hydroxymethyl-3,5-Dimethy-4-Methoxypyridine 4-Methoxy-3,5-Dimethyl-2-Hydro stable at 120°C is used in catalytic processes, where it maintains structural integrity under high-temperature reaction conditions. Moisture Content <0.5%: 2-Hydroxymethyl-3,5-Dimethy-4-Methoxypyridine 4-Methoxy-3,5-Dimethyl-2-Hydro with moisture content below 0.5% is used in electronic material synthesis, where it prevents hydrolytic degradation and enhances substrate compatibility. Particle Size ≤20 µm: 2-Hydroxymethyl-3,5-Dimethy-4-Methoxypyridine 4-Methoxy-3,5-Dimethyl-2-Hydro with particle size less than or equal to 20 µm is used in fine chemical formulation, where it achieves homogeneous dispersion in composite matrices. |
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Every chemist and formulator looking at heterocyclic compounds for pharmaceutical or fine chemical development knows the value of well-characterized pyridine derivatives. Over years of refining our processes, we have learned that 2-Hydroxymethyl-3,5-Dimethyl-4-Methoxypyridine consistently stands out due to its unique arrangement of methyl, methoxy, and hydroxymethyl functional groups on a stable pyridine ring. With a molecular formula of C9H13NO2 and precise batch-to-batch consistency, this compound enters reaction pathways where steric and electronic effects need careful balance.
What makes it distinct starts with the actual synthesis. We use direct methylation and selective hydroxymethylation instead of indirect methods, reducing byproducts and increasing selectivity. Our technicians confirm the structure and purity through NMR, HPLC, and mass spectrometry for every batch. The physical appearance—fine, crystalline solid with high chemical stability—makes storage and handling straightforward in most environments, even where humidity can pose problems for other pyridine analogues.
Virtually every research team evaluating this compound begins by noting its reactivity. The presence of both electron-donating methoxy and methyl groups at the 3, 4, and 5 positions opens pathways for selective modifications that other alkylpyridines can’t handle as smoothly. For example, it has a reliable record as a synthetic intermediate in the development of advanced pharmaceutical actives—especially where functional group tolerance matters.
Chemists often choose our 2-Hydroxymethyl-3,5-Dimethyl-4-Methoxypyridine over comparable compounds when they face challenges like achieving regioselective functionalization or avoiding side reactions with sensitive groups. The compound’s solubility profile fits best in common polar organic solvents, especially methanol, ethanol, and DMF. In particular, its methyl and methoxy substitutions on the ring reduce susceptibility to oxidation, leading to fewer degradation products during multi-step syntheses.
Real-world feedback from customers drives our process optimization. Over the past decade, we received repeated requests for tighter controls on moisture and trace metal contaminants in pyridine derivatives. In response, our analytical team implemented advanced drying techniques plus inductively coupled plasma analysis. This extra step helps our clients avoid catalyst poisoning in pharmaceutical or fine chemical applications.
For traceability and compliance, our plant assigns production codes linking back to recorded process parameters for each lot. Not every supplier offers this level of assurance. From an environmental and workplace safety angle, the absence of hazardous byproducts or volatile impurities puts it in better standing with end-users who operate under stricter emission and waste constraints. Rather than shipping in generic drums, we use tamper-evident bags within high-density polyethylene containers, minimizing moisture ingress and physical contamination.
Scientists in R&D labs often contact us with concerns about pyridine ring activation or deactivation affecting downstream routes. We learned through collaborative pilot runs that the 2-hydroxymethyl group in this compound not only brings synthetic flexibility—it also influences hydrogen-bond formation in both small-molecule drugs and more complex frameworks. For example, medicinal chemistry teams rely on this property for creating prodrugs, or when they require a handle for future conjugation with bioactive ligands.
The pharmaceutical sector values this compound as a building block for kinase inhibitors and CNS-active molecules. Instead of scrambling for workarounds to mask unwanted functional groups, researchers use its tailored substitution pattern to streamline late-stage diversification, often reducing both timeline and cost risks. The fine chemical and agrochemical industries tap its reliable shelf-life and tolerance to process solvents. Scale-up from gram to kilogram quantities rarely encounters solubility or crystallization issues—a direct benefit of both careful process control and a deep understanding of the pyridine’s solid-state behavior.
Many laboratories experiment with generic 3,5-dimethylpyridine, but those often stall once reactions demand a high degree of selectivity or compatibility with sensitive intermediates. The methoxy group at the 4-position shifts the electron density of the entire ring, which can make a crucial difference in challenging cross-coupling or alkylation steps. Our direct feedback with synthetic chemists revealed that switching to this specific compound eliminates much troubleshooting on impurity formation and side reactions. This efficiency reduces the number of purification cycles, which often translates directly to higher overall yield by several percent—a significant factor in today’s competitive markets.
Process reliability stands out in industrial scale-up. Plenty of alternative pyridine derivatives cannot match the combination of low residual solvent content and reproducibility across large batches. Early on, we found that some competitors’ processes introduce more batch-to-batch variation, leading to irregular reactivity and extra qualification steps on the customer end. By addressing root causes such as temperature control during methylation or optimizing filtration protocols, we cut down on coarse particulate and other off-spec material often found in less rigorously produced options.
Anyone who has managed specialty chemicals at scale knows that supply consistency matters as much as molecular design. Over the years, we invested in raw material testing, not just at delivery but throughout storage. Peroxide traces or residual chlorinated solvents can linger from poorly controlled steps in upstream feedstocks; these often lead to downstream headaches. By reexamining every input and documenting every process deviation, our team reduced rework and customer complaints.
We learned through customer audits that clear, evidence-based specifications build trust. Personnel in QA labs value seeing detailed chromatograms attached to each batch, not broad “typical analysis” statements. This transparency provides end users with more confidence for critical path projects, letting them allocate more resources to innovation instead of troubleshooting supplier variation.
Shipping larger quantities of a compound like this raises logistical and storage challenges. Maintaining purity from drum to drum—whether over ocean freight or during weeks in long-term inventory—requires more than just sealing and labeling. Over the past ten years, incremental improvements like air-tight transfer equipment and non-reactive linings helped our clients cut down on out-of-spec returns or moisture-related caking, especially during hot, humid seasons.
Pharmaceutical chemists and process engineers relay frequent stories of failed reactions with generic pyridines, especially under sensitive coupling or acylation conditions. By choosing this specific substituted pyridine, clients report avoiding search for exotic purification strategies, and they benefit from reduced need for protective groups. Anticipating needs in the lab, we keep technical support organic—offering not just product data, but troubleshooting insight from years of hands-on experience.
This compound’s stability under light and moderate temperature variation lowers concerns about decomposition during both day-to-day handling and extended storage. Customers who previously encountered issues with light-induced degradation in other pyridine derivatives now move projects quicker. Repackaging and reselling never replace the direct benefit of knowing our material retains its chemical identity for years, not just months.
During process development for a new CNS-active pharmaceutical candidate, an external team approached us for help resolving persistent low yields in late-stage alkylation. After reviewing their process, our chemists suggested an equipment cleaning tweak and supplied a higher-purity batch, free of traces of residual base that can catalyze unwanted side reactions. The difference was tangible—an overall 8% yield boost with a single synthetic step, as well as fewer isolation steps to meet purity specifications. This result exemplifies why deeply understanding not just what’s in the drum but how it interacts with sensitive chemistries sets manufacturers apart from mere suppliers.
Another customer working on agricultural actives faced regulatory scrutiny over unknown impurities in final formulations. Drawing from our batch records and analytical data, we worked closely to track the impurity’s origin to a specific feedstock. Through consultation and process adaptation, both teams reduced those levels to below regulatory thresholds. This kind of technical partnership doesn’t happen with off-the-shelf intermediates; it requires a transparent approach and an ongoing commitment to process quality.
Markets never stand still, and neither do chemists looking for new synthetic shortcuts or better regulatory profiles. Over the past years, feedback from product development teams led us to adjust not only product purity criteria but also documentation. Responding directly to requests, we created more accessible digital datasheets and proactively disclosed impurity profiles above 0.1%. Attentiveness to evolving needs saves time, lowers project risk, and speeds new commercial launches.
Our manufacturing teams regularly review process data and new literature to identify opportunities for further improvement. Smaller details—down to crystallization solvent ratios—often make the difference between a product that easily integrates into a customer’s workflow and one that causes days of reformulation. By gathering post-delivery feedback and acting on customer suggestions, we shortened the development cycle for several top clients.
Producing specialty pyridine derivatives opens up questions about worker safety and environmental responsibility. We track every reagent and byproduct through disposal and emission controls. Adopting solvent recovery, air scrubbing, and up-to-date waste management has lowered our plant’s environmental impact even as production scaled. Chemists and operations staff work under guidelines that combine real-world risk assessment and industry best practice, reducing unplanned releases and exposure even under tough production schedules.
Clients with green chemistry initiatives increasingly value suppliers who prioritize lifecycle thinking. Feedback from multinational customers led us to invest in safer on-site effluent treatment and more efficient purification systems, which also deliver better energy and solvent utilization. The result shows not only in a better ecological footprint but also in lower process costs.
Talking with end-users in academic, industrial, and pilot plant settings highlighted an overlooked reality: technical support from a true manufacturer offers more than just the compound itself. Each customer environment brings different challenges, whether it’s lab-scale material loss at bottling or production downtime from equipment incompatibility. Because our team knows exactly how this compound behaves in practice—not just in a datasheet—troubleshooting happens faster and with greater precision.
Chemists who have made the jump from off-the-shelf intermediates to our dedicated manufacturing support report fewer costly surprises and greater process reliability. The expertise drawn from decades of chemical synthesis and customer collaboration drives ongoing product improvements, never standing still as new challenges and applications arise. Consistently high-quality, reliable intermediates remain the foundation on which innovation in pharmaceuticals, fine chemicals, and agriculture continues to build.
Each year brings new demands for pyridine derivatives that do more than just meet basic specifications. With regulators tightening oversight and markets demanding ever-higher purity and reproducibility, only a manufacturer with real process insight and long-running experience can rise to the challenge. By prioritizing proven sourcing, rigorous analytical standards, and genuine customer collaboration, we see projects get to market quicker and with fewer obstacles. As tighter timelines and more challenging syntheses become the standard, customers continue to share their success stories, motivating our ongoing commitment to quality and responsiveness at every batch and every shipment.