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HS Code |
596561 |
| Iupac Name | 2,6-dihydroxy-3-cyano-4-methylpyridine |
| Molecular Formula | C7H6N2O2 |
| Molecular Weight | 150.14 g/mol |
| Cas Number | 4270-42-8 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 216-220°C |
| Solubility | Soluble in ethanol, slightly soluble in water |
| Smiles | CC1=NC(=C(C(=C1O)O)C#N) |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Synonyms | 4-Methyl-2,6-dihydroxy-3-cyanopyridine |
As an accredited 2,6-Dihydroxy-3-cyano-4-methyl Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2,6-Dihydroxy-3-cyano-4-methyl pyridine, sealed with a screw cap and labeled for laboratory use. |
| Container Loading (20′ FCL) | 20′ FCL: 13MT packed in 500kg jumbo bags, loaded on pallets, suitable for export-grade 2,6-Dihydroxy-3-cyano-4-methyl Pyridine. |
| Shipping | **Shipping Description:** 2,6-Dihydroxy-3-cyano-4-methyl pyridine is shipped in sealed, chemical-resistant containers to prevent moisture and contamination. It is transported as a solid under ambient conditions with appropriate hazard labeling. Package complies with relevant regulations for chemical substances. Handle with care, avoiding direct contact and inhalation. Store in a cool, dry place upon receipt. |
| Storage | 2,6-Dihydroxy-3-cyano-4-methyl pyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong acids and oxidizers. Protect the chemical from moisture and direct sunlight. Properly label the storage container and avoid excessive heat. Ensure appropriate safety measures and access is limited to trained personnel. |
| Shelf Life | 2,6-Dihydroxy-3-cyano-4-methyl pyridine remains stable for at least two years if stored in a cool, dry place. |
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Purity 98%: 2,6-Dihydroxy-3-cyano-4-methyl Pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product reliability. Melting Point 220°C: 2,6-Dihydroxy-3-cyano-4-methyl Pyridine with melting point 220°C is used in high-temperature chemical processes, where it maintains thermal integrity and process stability. Particle Size <50 µm: 2,6-Dihydroxy-3-cyano-4-methyl Pyridine with particle size less than 50 µm is used in catalyst formulation, where its fine dispersion improves reaction kinetics. Molecular Weight 150.13 g/mol: 2,6-Dihydroxy-3-cyano-4-methyl Pyridine with molecular weight 150.13 g/mol is used in analytical research, where it provides precise molecular calibration. Stability Temperature up to 160°C: 2,6-Dihydroxy-3-cyano-4-methyl Pyridine with stability temperature up to 160°C is used in polymer modification, where it enhances thermal resistance of materials. Solubility in Water 3 mg/mL: 2,6-Dihydroxy-3-cyano-4-methyl Pyridine with solubility in water 3 mg/mL is used in aqueous formulation development, where it allows for homogeneous mixing and distribution. UV Absorbance (λmax 310 nm): 2,6-Dihydroxy-3-cyano-4-methyl Pyridine with UV absorbance at λmax 310 nm is used in photochemical applications, where it provides effective UV shielding capability. Low Impurity (<0.5%): 2,6-Dihydroxy-3-cyano-4-methyl Pyridine with impurity content below 0.5% is used in electronic material synthesis, where it minimizes defect density in thin-film deposition. |
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You spend enough years in the chemical manufacturing business, and certain molecules start to leave an impression. 2,6-Dihydroxy-3-cyano-4-methyl pyridine, or just “DHCP” around here, is one of those compounds with both technical complexity and real utility. Unlike many standard pyridine derivatives, DHCP carves out its own spot as a specialty intermediate, mainly thanks to the cyano and dual hydroxy substitutions on the ring. Each batch we produce brings its own challenges, and I can tell you, making this molecule at a high purity isn’t just a matter of following a recipe.
In practical terms, DHCP offers a good combination of reactivity and selectivity that sets it apart from simpler pyridine derivatives. The two hydroxy groups activate positions on the ring, giving downstream chemists options they simply don’t get with mono-hydroxy or unsubstituted variants. That cyano group presents a handle for further functionalization, finding utility in pharmaceuticals, agrochemical synthesis, and specialty pigments. Getting the right substitution pattern is nontrivial, but we’ve adjusted our process over the years to boost selectivity and manage yields better than earlier methods from the literature.
Working with aromatic systems that have multiple reactive sites like DHCP means we have no room to cut corners. The methyl group at the 4-position makes regioselectivity during synthesis more demanding. Trace impurities, even a slight over-alkylation or undesirable isomer formation, can derail sensitive downstream reactions. Our reactor setups with precise temperature control, staged addition protocols, and careful purification steps let us deliver batches with consistent purity—an essential requirement for high-value end uses.
Every time we produce DHCP, especially on scale, there are decisions to make. For instance, the choice of solvent goes a long way—selectivity shifts noticeably with small changes. Acetonitrile versus DMF as reaction media, or even changes in pH during the hydrolysis step, significantly impact impurity profiles. We’ve learned to never underestimate the value of stepwise monitoring (HPLC, NMR, and sometimes even simple TLC at critical junctures). From a manufacturer’s perspective, these hands-on insights influence process modification far more than paper protocols ever could.
It’s common to get asked why not skip the cyano or go with an all-hydroxy variant. The answer ties right back to performance in target applications. In crop protection, for example, interacting both through hydrogen bonding (from hydroxy) and π-π stacking (methyl and cyano groups) often gives the new molecules better selectivity for their targets. Pharma teams prize DHCP as a scaffold because the cyano group directs further synthetic modifications and offers metabolic stability—a rare combination. You don’t get that from plain 2,6-dihydroxy pyridine or methyl-substituted variants.
Competition exists, of course. Substituted pyridines have a huge market, but the demand for DHCP keeps growing. It’s never the biggest volume molecule in our portfolio, yet orders keep pulling us toward better, more efficient routes and higher analytical standards.
Over time, our standard DHCP comes in at a purity above 99%. The product’s particle size and moisture content are more stable now than ten years ago—hard lessons from the occasional mishandling saw to that. The yellowish powder seems innocuous, but the way it changes hue with air exposure tells you how reactive the molecule wants to be. That’s real chemistry in motion, not just an abstract spec sheet.
We don’t assemble generic product sheets; all the specifications we track grew from real process control and customer experience. Routine analysis—TLC, HPLC, NMR, IR—shows what’s really happening in each lot. The conversations we’ve had with end users in both pharma and agrochemical labs have taught us more than any standard ever could. If you ever see a batch with an unusual melting point, you can bet we caught it in the QC checks, not from some formality, but because downstream failures matter deeply to us. We know that even a small off-spec impurity can change a reaction’s profile or add days to a timeline in a tightly managed project.
Achieving repeatability isn’t luck. You start with trained operators who have seen the reaction go sideways and know how to fix it—sometimes that means tweaking the pH mid-run or stretching the drying phase to drive off that last bit of solvent. Watching the color and learning when the endpoint gets near—these may sound old-fashioned, but they beat any automation when something new sneaks in during scale-up. Documentation and analytical files are critical, but experience tells you what trends need action instead of just notes.
We hold sample retains from every batch. When a customer once questioned a minor IR peak in a sample after storage, we tracked the issue to shipping conditions. Our trial batches stay on shelves for months, helping us anticipate stability under real-world handling. That kind of diligence comes from decades of seeing where disruptions pop up and knowing that trust requires transparency.
In this industry, subtle changes in ring substitution make all the difference. The unique 2,6-dihydroxy, 3-cyano, and 4-methyl pattern of DHCP sets it apart. For instance, compare it to 2,4-dihydroxy or to mono-cyano analogs—solubility, stability, and bioactivity all pivot on those positions. The classic 2,6-dihydroxy-3-cyano pyridine lacks the methyl group at the 4-position and doesn’t plug into certain synthetic plans that DHCP enables.
From our earlier attempts to use related pyridines in the same applications, we’ve seen limitations firsthand. With only one hydroxy group, further functionalization isn’t as selective. Changing the cyano position results in less consistent coupling with many aryl halides or nucleophiles, which kills yields and clutters isolate purity. You save many headaches by starting from DHCP—especially when you need a clean result for clinical development or a patent-sensitive new compound.
Half of what we do, we learn from what people try on the other end. In the drug synthesis lab, DHCP gives medicinal chemists a reliable anchor for building out aryl or heteroaryl chains. It comes up in polymorph exploration. For pigment or agricultural chemistry, the dual reactivity of the hydroxy and cyano groups lets researchers customize molecules for light-fastness, water-resistance, or target specificity.
No batch leaves our site without application stories returning to us. One group mentioned that DHCP was key in the synthesis of an advanced herbicidal intermediate—they showed that the methyl group reduced oxidation during a late-stage reaction, compared to an unmethylated analog. In another case, the pharma team shared that the unique substitution lowered by-product formation. We didn’t plan every discovery, but we pay attention when the molecule outperforms expectations.
Anyone who spends long enough shipping chemicals knows that what happens outside the plant matters as much as anything inside. DHCP tolerates standard storage conditions, but we’ve found that moisture uptake over time can change handling properties—a lesson learned from a sticky sample a few years ago. Adjustments to internal packaging and desiccant use have since solved the problem, but we still advise partners to store the product in tightly sealed containers and avoid excess heat or direct sunlight.
Those practical steps may not sound revolutionary, but they count. Bulk chemical totes or fiber drums can let in humidity in certain climates. Small-batch users might see clumping or color shifts if the product isn’t transferred into glass or lined containers after delivery. Sharing these experiences saves everyone time and helps keep outcomes predictable.
Reliable chemistry needs both people and numbers. On the QC side, our staff checks every DHCP batch with both chromatography and spectroscopy. We rarely rely on a single metric, because narrow focus blinds you to creeping impurities. Visual inspections still have a place—color and texture tell experienced hands much about a batch’s fate. Over the years, this blend of effort pays off, because problems that make it past one filter don’t get through the rest.
If a batch ever underperforms in a partner’s hands, we trace every variable, from raw material lot to reactor run logs. That process uncovered a subtle issue with a particular solvent lot last year, which we fixed by tightening purchasing standards. Everyone expects high standards, and we do too, not for compliance, but because we know what’s at stake when an intermediary fails to meet expectations.
Regulatory agencies in our markets have grown more strict about trace contaminants, especially for intermediates headed into pharmaceuticals or food-contact applications. We’ve retrofitted lines, upgraded air monitoring, and reformulated some procedures over the past five years. Doing so wasn’t a strictly legal requirement—it’s what the standards in our field demand. These investments add cost, but they also protect our relationship with companies down the chain who depend on our reliability.
Raw materials, like pyridine and certain nitriles, can fluctuate in quality and cost. Our purchasing team works in close sync with lab heads to check quality on arrival, not just on paper. Input stocks have to hibernate in climate-controlled rooms if shipping time runs long—a lesson taught by storms that delayed railcars once and briefly dented quality before we built in that safeguard.
The inquiries we field today come from both researchers seeking a 5-gram test batch and plant chemists scaling up to a ton. Each shift in production scale teaches us something—the way heating ramps at small scale sometimes fail to match the dynamics in a thousand-liter mixer, or the way product isolation turns up different side products as volumes increase. There’s no substitute for this direct learning curve, and every adaptation feeds back into the next round of deliveries.
Researchers bring new asks yearly—higher purity targets, non-standard packaging, unique blends of particle size distribution. We respond by testing altered crystallization protocols, adding dedicated sieves, or working with packaging suppliers to try fresh liners or barrier films. Everyone expects adaptability, but our factory history shows how necessity drives process updates faster than mandates or trends. Real manufacturers embrace that pace.
The market for specialty pyridine derivatives grows more sophisticated each year. We see research steering toward greener chemistry and bio-based synthons. DHCP already fits well within several streamlined synthetic plans. We’re tracking literature on step reduction and catalytic processes that could offer cleaner, lower-waste manufacturing. Pilots are in the pipeline to test recyclable catalysts and solvent remediation, not to tick boxes, but to keep output cost-effective while anticipating changes in environmental expectations.
Being in production for as long as we have, trends in molecule demand don’t surprise us much. Yet, the recurring need for DHCP tells us its utility isn’t fading. End uses keep expanding—into specialty dyes, advanced polymer intermediates, and more targeted agrochemical actives. Every one of these fields challenges us to keep process robustness high while tailoring supply for experimenters and industrial plants alike.
The difference between a good molecule and a dependable one lies in details. Factories staffed by veterans know to watch for subtle signals that precede a batch going off track. Documentation keeps everyone aligned, but no protocol replaces accumulated memory—the dozens of times a subtly slower slurry filtration signaled a change upstream; the years learning that certain glassware types might trigger surface-catalyzed side reactions. Those experiences combine to teach what numbers can only partially capture.
Every kilogram of DHCP that leaves our factory reflects hands-on choices at every step—inputs, process timing, troubleshooting, packing, and above all, quality checks that take both data and judgment. We stand by our product not because it fits a template, but because its ongoing real-world use feeds back into its manufacture every day. No one needs to remind us what’s at stake: in every flask and every drum, we know our partners rely on more than just a molecule—they rely on all of us behind it.