|
HS Code |
174073 |
| Chemical Name | 2-Hydroxy-3-methyl-5-nitropyridine |
| Cas Number | 16898-65-2 |
| Molecular Formula | C6H6N2O3 |
| Molecular Weight | 154.12 |
| Appearance | Yellow crystalline powder |
| Melting Point | 169-173 °C |
| Solubility | Slightly soluble in water |
| Smiles | CC1=C(C=NC(=C1O)[N+](=O)[O-]) |
| Inchi | InChI=1S/C6H6N2O3/c1-4-5(8(10)11)2-3-7-6(4)9/h2-3,9H,1H3 |
| Storage Conditions | Store at room temperature, keep container tightly closed |
As an accredited 2-Hydroxy-3-methyl-5-nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed, 25 grams, labeled with product name, CAS number, hazard symbols, and storage instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 12MT packed in 480 fiber drums, each containing 25kg net, suitable for export of 2-Hydroxy-3-methyl-5-nitropyridine. |
| Shipping | 2-Hydroxy-3-methyl-5-nitropyridine is shipped in secure, sealed containers to prevent moisture and contamination. It should be packaged according to regulatory guidelines for chemical materials. Transport occurs with proper labeling and documentation, using suitable protective measures to ensure safety and compliance with international shipping standards for laboratory chemicals. |
| Storage | Store **2-Hydroxy-3-methyl-5-nitropyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, moisture, and direct sunlight. Keep the substance away from incompatible materials such as strong oxidizing agents. Ensure proper chemical labeling and access for authorized personnel only. Use appropriate secondary containment to prevent possible leaks or spills. |
| Shelf Life | 2-Hydroxy-3-methyl-5-nitropyridine typically has a shelf life of two years when stored in a cool, dry, and dark place. |
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Purity 99%: 2-Hydroxy-3-methyl-5-nitropyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low impurity profiles. Melting point 170°C: 2-Hydroxy-3-methyl-5-nitropyridine with a melting point of 170°C is used in organic compound formulation, where it guarantees thermal stability during processing. Particle size <10 μm: 2-Hydroxy-3-methyl-5-nitropyridine with particle size below 10 μm is used in fine chemical production, where it enhances uniform dispersion and reactivity. Moisture content <0.2%: 2-Hydroxy-3-methyl-5-nitropyridine with moisture content less than 0.2% is used in API manufacturing, where it prevents unwanted hydrolysis reactions. Stability temperature up to 120°C: 2-Hydroxy-3-methyl-5-nitropyridine with stability temperature up to 120°C is used in catalyst development, where it maintains structural integrity under operational conditions. Assay 98% (HPLC): 2-Hydroxy-3-methyl-5-nitropyridine with assay 98% by HPLC is used in agrochemical formulation, where it optimizes desired biological activity and replicability. Residual solvent <50 ppm: 2-Hydroxy-3-methyl-5-nitropyridine with residual solvent below 50 ppm is used in electronics chemical processing, where it minimizes conductivity issues and contamination. |
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Chemistry keeps pushing the boundaries of what we think is possible, and among the small yet essential compounds, 2-Hydroxy-3-methyl-5-nitropyridine earns its place. This molecule has a knack for showing up right where researchers in pharmaceuticals, advanced materials, and organic synthesis want it most. You see, the subtlety of this compound—hydroxy and nitro groups placed just so on a pyridine ring—gives it a mix of reactivity and selectivity that's hard to beat.
People who've spent hours at the bench or pored over structure-activity studies recognize the value of a well-placed nitro group, not to mention how a hydroxy or methyl tweak can shift properties. Chemists choose 2-Hydroxy-3-methyl-5-nitropyridine because it brings both functionality and stability without demanding difficult handling or complicated purification steps. When you sit down with a synthetic route that calls for this compound, you expect something that fits seamlessly into a reaction sequence, lending itself to derivatization or stepwise transformation the way a trusted tool fits the hand.
Quality always stands as a top consideration, not just a tick box. Think about what happens if your starting material brings along stubborn impurities—suddenly, yields drop, downstream reactions misbehave, and analytical headaches begin. Here, experienced suppliers deliver 2-Hydroxy-3-methyl-5-nitropyridine with solid assurances on purity, often above 98%. That single percentage point can mean the difference between a successful run and a frustrating dead end. The best samples arrive as fine, yellowish crystalline powders, free of visible detritus or clumps, moving easily from bottle to balance to beaker without drama. No one wants to spend extra time grinding, filtering, or sorting out sticky masses, especially given the tight schedules facing most labs.
Storage presents another angle where practical experience counts. This pyridine derivative keeps best in cool, dry conditions with a tight seal, away from direct sunlight and away from oxidizing agents. I can remember a colleague losing a whole batch after sticking the substance on a window ledge; a harsh lesson in the power of slow degradation under mundane circumstances. Small errors add up over time, and a simple slip in storage can undercut weeks of planning.
Applied chemists know the compound doesn't live its life as a static entity. It shows up as a starting material, intermediate, or sometimes even as a target in synthesis projects. Medicinal chemists appreciate its track record as a scaffold for drug development, ready to be functionalized into libraries of analogues. Those working on dyes, advanced polymers, or agrochemical products also find themselves reaching for this molecule thanks to its balanced electronic properties and reliable performance in coupling and substitution reactions.
Walking through a typical synthetic sequence, you might see this compound undergo O-acylation, N-alkylation, or take part in the construction of heterocyclic rings. Its reactivity profile means you can trust the position of those substituents—no dance of random byproducts or wandering methyls. The versatility demonstrates why this compound rarely sits on the shelf for long. For teams facing the pressure of patent timelines and cost controls, avoiding protracted optimization is not just preferable; it is often essential.
Comparisons with other pyridine derivatives shed light on what makes 2-Hydroxy-3-methyl-5-nitropyridine unique. Some might ask, why not reach for something like 2-hydroxypyridine or 3-methyl-5-nitropyridine? The difference comes down to the electronic balance and hydrogen bonding opportunities provided by the exact substitution pattern. A single shift in group position throws off reactivity. The presence of both hydroxy and nitro groups, aligned with a methyl team, gives a distinct set of characteristics, separating it from simpler or more crowded analogues.
I once worked on a library of nitrogen-based heterocycles and ran up against the tricky selectivity offered by nearby methyl and nitro groups. A similar structure substituted at the four-position simply couldn’t offer the same combination of reactivity and synthetic resilience. Try pushing a nitration step too far down the route and you risk decomposing precious intermediates; instead, starting with a molecule like 2-Hydroxy-3-methyl-5-nitropyridine sidesteps such pitfalls. It brings strategic control to the hands of the chemist, leading to cleaner routes and less waste.
Let’s talk about what happens in practice. Research labs and manufacturing lines need compounds they can trust, particularly as projects scale. Imagine running a gram-scale reaction where yield matters less than the ultimate purity of a drug candidate. This compound performs in chromatography, crystallization, or extraction steps without unpredictable behavior. In kilogram quantities for industrial production, chemists start to care a lot about material flow, batch consistency, and shelf-life. Experience tells me that a stable, crystalline powder saves many headaches over sticky oils or amorphous solids that tend to pick up water and degrade.
For those optimizing pharma intermediates, speed matters. Route scouting can chew up budgets if intermediates become tricky to make or purify. 2-Hydroxy-3-methyl-5-nitropyridine typically avoids such complications, offering a safe middle ground between overly sensitive and overly stubborn molecules. Even where regulatory filings set demanding specifications, this intermediate tends to meet them without heroic effort. In contrast, lesser-known relatives or makeshift substitutes might introduce subtle isomeric impurities or color issues that trigger lengthy investigations.
The analytical profile—the sharp NMR peaks, reliable mass spectrum, and solid melting range—gives further peace of mind. Nobody has time to troubleshoot oddities where a simple choice of starting material can head off entire sets of problems.
Across my own experience, and in conversation with others in the field, I’ve noticed recurring themes around product grades. Sigma, research, and industrial classes offer different balances of purity and cost. Research labs aiming to push boundaries with minute quantities often spring for the highest-grade powder to guarantee clean results and easy compliance. Larger pilot plants lean on bulk purchases, trusting a proven supplier’s consistency and transparency around trace metals or residual solvents.
It’s easy to overlook little differences in supplier documentation, but these matter. Batch traceability, patient handling instructions, and solid support channels separate reliable partners from risky bets. Even if the molecule itself remains unchanged, the people backing it—and their level of transparency—can make or break an entire project. Suppliers willing to publish data from independent testing and verification help build the kind of trust that keeps entire teams running smoothly, especially in regulated industries where audit trails are not optional.
Some might ask if other forms—liquid, suspension, or pre-blended mixtures—bring advantages. Based on what I’ve seen, chemists and engineers still want the powder either for its storage properties or flexibility in metering. Those rare times someone considers an alternate form usually relate to special process requirements or downstream blending. Still, the standard crystalline form stands out for a reason: it works time and again across different applications and scales.
Any seasoned chemist knows that structural elegance doesn’t guarantee total safety. As with many aromatic nitro compounds, a measured respect is vital. Eye and skin contact pose the usual risks, and inhalation of fine dust is better avoided through simple PPE and good ventilation. In my own lab work, I’ve seen what happens when small spills go unreported—a gentle yellow staining on the benchtop that hints at the robust color this compound brings. Cleaning up spills quickly, labeling containers clearly, and double-checking disposal protocols all feel routine at this point. The best habits develop after bitter experience reminds us what slips through the cracks when under pressure.
Heeding MSDS guidance matters, but so does the real-world context: storing away from acid chlorides or strong reducing agents, keeping containers capped tight, and training every new team member to recognize what safe handling looks like. I cannot overstate the peace of mind that comes with these basics, which ensure both person and product hold up under scrutiny—whether from health inspectors or your own conscience.
The global landscape for specialty chemicals like 2-Hydroxy-3-methyl-5-nitropyridine brings its share of frustrations and workarounds. Long lead times and fractious shipping conditions can bottleneck entire research programs. Price swings and vendor shortages only add to the strain. From direct experience, diversifying sources and working with local suppliers when possible beats putting all your hopes on a single import. Even the most established companies can hit snags—port slowdowns, regulatory hold-ups, or sudden changes in trade policies. Keeping a modest stock on-hand helps avoid last-minute scrambles and protects research momentum.
Open communication with suppliers proves indispensable. Asking straight up about future availability or flagging upcoming larger orders lets everyone in the chain prepare, and can spare labs from unpleasant surprises. I’ve seen teams improvise with alternate intermediates only to double their purification workload. Often, the effort to source the original compound, even at a premium, pays off in time saved down the line.
Quality control means more than ticking a box for most experienced researchers. Before committing to a large batch, most chemists run small-scale pilot reactions to confirm expected reactivity and product profile. A new lot of 2-Hydroxy-3-methyl-5-nitropyridine gets checked by TLC, NMR, and sometimes HPLC—especially if it needs to be registered in a tightly controlled environment. Over my career, I’ve come to accept an extra half-day spent upfront as a small price to avoid lost weeks chasing mystery contaminants.
This approach pays off when unexpected changes slip through. Sometimes a benign change in hue points to a deeper issue, such as minor impurities carried through by an altered synthetic route at the supplier. Direct communication with trusted suppliers helps resolve these quickly; open channels avoid finger-pointing and foster the kind of collaboration that solves problems instead of just documenting them.
Community sharing of batch experiences and crowd-sourced reviews bridges individual knowledge gaps. Platforms or networks where chemists compare notes have dramatically improved confidence in specialty chemical sourcing, driving up overall standards simply by making problems harder to hide.
Science and technology thrive on reliable building blocks. As fields like medicinal chemistry, green manufacturing, and advanced materials research stretch boundaries, foundational compounds like 2-Hydroxy-3-methyl-5-nitropyridine keep processes grounded. Their reputation for reliability isn’t accidental—it’s built on years of real-world performance, subtle improvements in batch processing, and genuine responsiveness to research community needs.
For organizations pursuing greener synthesis routes or lower-cost alternatives, this compound still plays a foundational role. It’s compatible with greener solvents and milder reagents, broadening where and how it can be used. Newer synthetic strategies often incorporate this molecule in early stages, banking on its sturdiness to unlock more complex modifications downstream.
Some innovators explore modifications to the pyridine ring, but demand for the specific 2-hydroxy, 3-methyl, and 5-nitro substitution pattern remains robust, as it delivers a hard-to-replicate combination of chemical and physical traits. Research teams continue to find new uses, not out of habit, but because the unique layout of substituents anticipates the needs of ever-evolving chemistry challenges.
Rather than disappearing as new molecules gain favor, 2-Hydroxy-3-methyl-5-nitropyridine sustains relevance across decades—proving that certain core structures enable new fields, time and again.
Long hours in the lab and countless reaction flasks have taught me a healthy respect for the foundational chemistry that these specialty intermediates make possible. 2-Hydroxy-3-methyl-5-nitropyridine stands as a case in point—not just a tool on a shelf, but a resource that underpins progress from startup benches to industrial production lines. Its reputation travels ahead of it, built on the real-world benefits of purity, consistent handling, and broad application. For the scientist, engineer, or scale-up manager, the right choice of intermediate becomes a quiet but critical part of success.
Every compound earns its place by delivering on its promises, not just in theory but in repeated, hard-fought wins at the workbench. Asking the right questions about origin, form, and function takes the guesswork out of a process that too often leaves teams repairing avoidable mistakes. The streetwise chemist trusts the proven value of 2-Hydroxy-3-methyl-5-nitropyridine for that very reason—hard lessons translate into wise purchases, and reliable molecules keep the machinery of science running at top speed.
What comes next? As research shifts and industrial demands evolve, having stable, trusted building blocks isn’t a luxury; it’s a necessity. This compound will continue to anchor future breakthroughs because its story is woven from proof, performance, and experience—not just the fine print in a catalog or the bounds of a chemical structure. I wouldn’t bet against it becoming even more important as the world’s science problems grow in size, scale, and complexity.