|
HS Code |
973845 |
| Iupac Name | 3-methyl-4-hydroxypyridine |
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.13 g/mol |
| Cas Number | 603-80-5 |
| Appearance | White to off-white solid |
| Melting Point | 150-154°C |
| Solubility In Water | Soluble |
| Density | 1.15 g/cm³ (approximate) |
| Pka | 9.7 (for the hydroxyl group) |
| Structure | Pyridine ring with a methyl group at position 3 and hydroxy group at position 4 |
| Smiles | CC1=CN=CC(=C1)O |
As an accredited 3-methyl-4-hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, sealed with screw cap; labeled with chemical name, CAS number, hazard symbols, and manufacturer details. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL):** 3-methyl-4-hydroxypyridine packed in 25kg drums, totaling 8,000kg per 20′ FCL, safely secured for transport. |
| Shipping | 3-Methyl-4-hydroxypyridine is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with safety regulations to prevent leaks or contamination. Labels indicate chemical identity, hazard information, and handling instructions. Shipping adheres to international and local transport guidelines for chemicals, ensuring secure and safe delivery to the recipient. |
| Storage | **3-Methyl-4-hydroxypyridine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it away from incompatible materials such as strong oxidizers and acids. Ensure the storage area is clearly labeled and restrict access to authorized personnel. Follow all relevant chemical safety regulations. |
| Shelf Life | 3-methyl-4-hydroxypyridine is stable for at least 2 years when stored in a cool, dry place, tightly sealed. |
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Purity 99%: 3-methyl-4-hydroxypyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures consistency in drug formulation. Molecular weight 109.13 g/mol: 3-methyl-4-hydroxypyridine with molecular weight 109.13 g/mol is used in organic synthesis research, where precise molecular composition supports reproducible reaction outcomes. Melting point 140°C: 3-methyl-4-hydroxypyridine with melting point 140°C is used in thermal processing applications, where stable phase behavior enhances process control. Particle size <50 µm: 3-methyl-4-hydroxypyridine with particle size less than 50 µm is used in fine chemical manufacture, where small particles improve solubility and reactivity. Stability temperature up to 180°C: 3-methyl-4-hydroxypyridine with stability temperature up to 180°C is used in high-temperature synthesis protocols, where thermal stability prevents decomposition and maintains product integrity. Water content <0.5%: 3-methyl-4-hydroxypyridine with water content less than 0.5% is used in moisture-sensitive reactions, where low water presence reduces unwanted side reactions. UV absorbance 254 nm: 3-methyl-4-hydroxypyridine with strong UV absorbance at 254 nm is used in analytical calibration standards, where reliable detection enables accurate quantification. Assay ≥98% (HPLC): 3-methyl-4-hydroxypyridine with assay not less than 98% by HPLC is used in active ingredient preparation, where verified content ensures product efficacy. |
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Some chemicals quietly transform modern research, medicine, and applied science, slipping into toolkits without fanfare. 3-methyl-4-hydroxypyridine is one of those behind-the-scenes champions in chemistry labs and industrial circles. From my visits in pharmacology settings to discussions with plant biochemists, its value is clear: reliability, specificity, and an ease of integration that advanced users appreciate. Its structure—a methyl group attached to the third carbon of a pyridine ring, and a hydroxyl group at the fourth—lends all sorts of advantages when customizing reactions or searching for unique biological responses.
Let’s lay out what this really means, not just for chemists in lab coats, but for anyone curious about innovation. 3-methyl-4-hydroxypyridine doesn’t show up on ingredient lists for your favorite snacks, but it often plays a subtle role when researchers need a precise foundation for synthesis and testing. It’s a kind of anchor: a material shaped for accuracy, whose chemical behavior offers both stability and flexibility. One major plus that stands out from years of industry exchanges is the way this compound fits into complex environments—whether as a raw material, an intermediary in more layered reactions, or in analytical studies where accuracy shapes outcomes.
No one pays for guesswork. Research and manufacturing only keep advancing if their core supplies meet consistent targets. A high-purity 3-methyl-4-hydroxypyridine loads confidence into each stage of use. In my experience with analytical workflows in academic and industrial groups, reliable supply means a product should meet a purity of at least 98 percent by HPLC, with a clear, pale crystalline powder that mixes well and dissolves readily in most polar solvents. Lab staff have remarked about its sharply defined melting point, tracking in at about 164–166°C—a useful check for anyone confirming batch identity by hand.
Trace metals and organics, ever the troublemakers, can clog up data and derail sensitive experiments. This is why good batches of 3-methyl-4-hydroxypyridine feature heavy metal concentrations measured in mere parts per million or less. People who monitor environmental or pharmacological contamination appreciate this tight control; their entire confidence in results sometimes rests on minutiae.
Packaging also makes a difference. Glass bottles with PTFE lining keep the compound uncontaminated and dry, which matters after the seal breaks on the warehouse floor or beneath fume hoods. This consideration may seem secondary, but if you’ve witnessed a dozen spilled powders and swollen plastic jars, you know it influences productivity and safety just as much as data sheets.
Even with a reputation for reliability, chemicals don’t stay relevant unless they solve new problems. In the pharmaceutical industry, chemists know 3-methyl-4-hydroxypyridine as a valuable intermediate, a base for building more complex and bioactive compounds. Some colleagues speak about its use as a scaffold, a starting point for molecules that eventually show up in advanced drug candidates.
Beyond big pharma, enzymologists and neurochemists look at its structure and see possibilities in metabolic studies, receptor targeting, or antioxidant development. Having worked alongside research teams using oxidative stress models, I’ve watched this compound teased into test solutions to track cellular resilience—or, just as often, to calibrate sensitive analytical devices. Each batch, so long as its purity holds, becomes a consistent ruler for measuring subtle biological changes.
The value extends into fine chemical synthesis. Teams pushing for green chemistry or more efficient synthetic methods sometimes mention how this derivative reacts cleanly, delivering high selectivity when hooked up with electrophiles or coupled in Suzuki or Buchwald reactions. This reliability speeds up troubleshooting and reduces waste—a point that earns quiet approval from cost-conscious operations managers and overworked waste disposal crews alike.
Hundreds of pyridine derivatives fill catalogs, many offering unique features. Here, 3-methyl-4-hydroxypyridine stands apart for a few reasons. First, its dual substituents—methyl at the third position, hydroxyl at the fourth—shape both reactivity and solubility in unique ways. From routine observation, you’ll find it participates in hydrogen bonding more strongly than most plain pyridines. This can make it a more sensitive tool in spectroscopic or binding studies.
Some similar molecules, including 4-hydroxypyridine or 3-methylpyridine, offer part of the picture: maybe a similar size, or a comparable reactivity at one site. Still, neither matches the distinctive interplay you find when both substituents work together. Research chemists and formulation engineers appreciate this “Goldilocks” zone—a balance that can nudge reactivity or selectivity just enough to open new possibilities. There’s something satisfying about a chemical that’s not too basic, not too hydrophobic, and not too expensive, but reliably productive in the right context.
In the world of analytical chemistry, selectivity matters more than price per gram. Years of peer-reviewed journals show this molecule is versatile: suitable as a marker in redox studies, an intermediate in multi-step synthesis, and a reference sample in fine-tuned calibration routines. Its spectral signature, clean and sharp across NMR, FTIR, and UV-Vis, beats out close analogs and saves hours otherwise wasted cross-referencing ambiguous peaks.
High demand for clean, traceable compounds doesn’t come without its own headaches. As research budgets contract or supply chains tangle, sourcing pure 3-methyl-4-hydroxypyridine takes extra vigilance. More than once, I’ve seen teams stuck with backorders, scrambling to swap in less suitable alternatives that add time or confusion to projects. The solution starts with building relationships—trustworthy suppliers, open communication with distributors, and a willingness to audit samples before each new round of research. Results may cost more, but the downstream savings in efficiency and data integrity usually pay off.
In daily lab life, good technique underpins safe and responsible use. 3-methyl-4-hydroxypyridine carries low acute toxicity based on current safety data, but smart researchers never take shortcuts. Common-sense measures—protective gloves, eye shields, ventilated hoods, secure labeling—form the backbone of safe procedures. As with almost every small organic molecule, users keep Material Safety Data Sheets within reach and avoid pouring anything down the sink. Disposal processes take priority. Collecting waste in dedicated containers prevents cross-contamination. Some labs coordinate with certified haulers who can thermally break down or neutralize such waste, keeping hazardous load off wastewater treatment plants and the environment.
Environmental concerns stretch further than the end of a single bottle. It’s tempting to forget about what happens after shipping crates leave vendors or glass bottles empty out. Yet, tracking accountability—from synthesis to use to disposal—matters. More labs participate in green chemistry audits now, double-checking that input chemicals, including pyridine derivatives, arrive from operations using less solvent or reduced toxic byproducts. Some manufacturers adopt circular supply systems to reclaim containers or unused products. This kind of stepwise responsibility gets noticed by both funding agencies and regulatory inspectors.
With any substance this specialized, clear guidelines and shared best practices help avoid small disasters. Research consortia often develop shared protocols for 3-methyl-4-hydroxypyridine. Internal working groups keep logs on batch numbers, use rates, and synthesis outcomes. Digital tracking and automated storage systems quietly ensure only fresh, verified material goes into experiments. This prevents the common misstep of mislabeling or accidental cross-mixing, which can cost a week’s data or set timelines back even further.
Real innovation comes from people who ask “what if?” after mastering the basics. A medicinal chemist may tweak the reaction conditions to pull new derivatives from this core molecule, chasing better biological activity. Environmental labs train technicians to spot trace residues in larger sample pools, leveraging its spectral properties to project contamination or transformation rates downstream. High school chemistry clubs experiment with small analogs of pyridine to see the impact of just one methyl or hydroxyl substitution; these lessons form a bedrock for deeper understanding later on.
From here, future advances depend on nimble partnerships. Collaboration between manufacturers, safety experts, academic groups, and end users builds a deeper, more responsive knowledge base. This in turn trickles back to packaging changes, new applications, and better waste handling. I’ve seen firsthand how these relationships speed up everything from response to recalls, to testing greener synthesis, to reducing operational disruptions when external factors—natural disasters, economic shocks—hit chemical supply lines.
It’s easy to focus on the good news, but real credibility comes from seeing the setbacks too. Not every batch lives up to its certificate of analysis. Sometimes weak points in a manufacturer’s process show up as off-odors, discoloration, or out-of-range melting points—clear flags for batch rejection. Vigilant teams rapidly screen for such inconsistencies by baking in regular spectroscopic checks, microanalyses, and retention of reference standards in well-organized cold storage. Skipping these minor steps turns into a major headache down the line, especially in regulated industries where documentation must stand up to outside audits.
Counterfeit or “clone” versions of high-value research chemicals have popped up more often. These can look, feel, even smell legitimate, until subtle differences in impurity levels or spectral profiles derail experimental outcomes. Purchasing direct from known suppliers with auditable sourcing and tracking systems short-circuits many such headaches. The rise of digital inventories and QR-coded batch tracking has further insulated big labs from fraud—small steps that help keep results reproducible and funds well spent.
Long-term storage presents its own challenges. While unopened bottles stored in cool, dry, light-protected places can last for years, I’ve seen real-life cases where labs lose product quality after repeated opening, exposure to air, or simply the wear and tear of day-to-day access. Implementing smarter storage schemes—dividing main stocks into smaller aliquots, using fresh utensils for each access, and consistent logging—keeps active material fresh for each new run.
Healthcare innovation—especially in targeted small-molecule therapy—never really pauses. 3-methyl-4-hydroxypyridine’s reputation as an intermediate with just enough reactivity sets it up to feed new lines of research. Peers in drug development mention projects where this core molecule, after a few tweaks, anchors vital building blocks for drugs targeting neurodegenerative disease. There’s also interest in custom ligand systems for catalysis, where the fine-tuned electron distribution of this compound promises more efficient, selective transformations.
Looking beyond strict laboratory confines, there’s untapped ground for deployment in agrochemical synthesis and diagnostics. In sustainable agriculture projects, scientists experiment with derivatives of pyridines, including 3-methyl-4-hydroxypyridine, to optimize nutrient absorption or pest resistance. Here, the compound’s background in reliable, traceable chemistry matters as much as any flashy headline material. Clear supply routes and established safety protocols protect both workers and the food chain itself.
In environmental science, this compound’s presence in advanced analytical setups drives big questions. Monitoring organic pollutants, tracking microbial transformations, or sizing up real-world exposure to environmental contaminants—here, every microgram measured counts. Again, the specificity 3-methyl-4-hydroxypyridine offers is a key advantage that speeds up studies and tightens error margins.
Even as the world speeds up, end users and decision-makers recognize the value of slow, careful verification. Data integrity relies not just on the numbers but on the confidence that test materials—3-methyl-4-hydroxypyridine included—arrive pure, documented, and ready to perform. Good suppliers regularly release audit trails, showing everything from starting raw materials to analytical confirmation of each batch. This high standard of transparency serves more than regulatory compliance; it actively builds trust across the supply chain.
Professional networks help as well. Technical committees in pharmaceutical, food safety, and chemical manufacturing industries rotate best practice updates, rolling in the latest learnings from years of hands-on work. Some forward-looking research institutions now pre-register and publish their raw material profiles alongside final publication, giving readers and reviewers added insight into sourcing, handling, and verification steps. This push for clarity keeps the whole ecosystem honest, making it harder for poor practices to persist.
On paper, 3-methyl-4-hydroxypyridine reads like chemistry: formulas, weight calculations, diagrams. In practice, it stands as a point of comparison—helpful for calibrating instruments, training young chemists, and double-checking that bigger, glossier projects rest on solid technical ground. When working with undergraduates or onboarding new research assistants, I’ve handed out vials of this material as a baseline: test its solubility, run its NMR, compare notes, see what happens if you substitute a closely related analog. The lessons stick better than a slide presentation ever could.
Batch variability can throw off even the most careful user. This reality shapes a reliance on secondary verification—running side-by-side tests with known standards before committing resources to big experiments. Failing early and small is much better than failing big and late. In my own collaborations, a few well-documented pilot runs with 3-methyl-4-hydroxypyridine resolve inconsistencies and sync techniques before scaling up to more ambitious targets.
When I step back and consider the broader landscape, 3-methyl-4-hydroxypyridine emerges—quietly, perhaps, but undeniably—as one of the unglamorous pillars of scientific practice. Its reputation for steady performance isn’t hype; it comes from years of practical use in diverse fields, from brain biochemistry to materials science. What’s made it stick over the years? Not flashy marketing, but a pattern of doing its job without fuss, leaving the real innovation and discovery up to the humans running the show.
Researchers can count on it to behave predictably in complex reactions, while still permitting enough chemical “elbow room” to innovate. From every inspection of its crystal form to its presence in complicated spectra, you get the sense that this molecule isn’t just another name in a catalog. It’s a part of the invisible infrastructure that supports real progress, the kind that makes breakthroughs possible.
Looking forward, responsibility sits with everyone involved in sourcing, using, and ultimately retiring every batch. Fair pay for reliable suppliers, disciplined handling, regular safety updates, smart disposal: these don’t just protect workers or increase output—they directly safeguard the trustworthiness of data and the safety of people who depend on this work, even if they never glimpse the inside of a laboratory. By focusing on longer timelines, deeper accountability, and a willingness to share new practices, the community around 3-methyl-4-hydroxypyridine—and molecules like it—can keep enabling the best of today’s science while clearing the path for whatever comes next.