|
HS Code |
716434 |
| Compound Name | 3-Hydroxy-5-methylpyridine |
| Cas Number | 1121-22-8 |
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.13 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 65-70°C |
| Boiling Point | 265°C |
| Solubility In Water | Soluble |
| Density | 1.13 g/cm³ |
| Smiles | CC1=CN=CC(=C1)O |
| Iupac Name | 5-methylpyridin-3-ol |
| Pubchem Cid | 12088 |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 3-Hydroxy-5-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Opaque amber glass bottle containing 100 grams of 3-Hydroxy-5-methylpyridine, sealed with a screw cap and labeled with safety information. |
| Container Loading (20′ FCL) | Container loading (20′ FCL): 10MT packed in 200kg HDPE drums, securely palletized, suitable for 3-Hydroxy-5-methylpyridine export shipment. |
| Shipping | **Shipping Description:** 3-Hydroxy-5-methylpyridine is shipped in sealed, airtight containers suitable for laboratory chemicals. It is protected from moisture and light, with appropriate labeling for identification. Standard shipping practices for chemical materials apply, following relevant safety and regulatory guidelines to prevent accidental release or exposure during transit. |
| Storage | 3-Hydroxy-5-methylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Protect from moisture and incompatible materials such as oxidizing agents. Ensure proper labeling, and keep away from food and drink. Use appropriate personal protective equipment when handling and transferring the chemical. |
| Shelf Life | 3-Hydroxy-5-methylpyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and well-sealed container. |
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Purity 99%: 3-Hydroxy-5-methylpyridine with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low impurity formulation. Molecular Weight 109.13 g/mol: 3-Hydroxy-5-methylpyridine at a molecular weight of 109.13 g/mol is used in organic catalyst production, where precise molecular design enables selective catalytic activity. Melting Point 137°C: 3-Hydroxy-5-methylpyridine with a melting point of 137°C is used in solid-state drug development, where stable thermal properties support extended shelf life. Particle Size <10 μm: 3-Hydroxy-5-methylpyridine with particle size below 10 micrometers is used in fine chemical formulations, where enhanced dispersion increases reaction rates. Stability Temperature up to 100°C: 3-Hydroxy-5-methylpyridine stable up to 100°C is used in topical formulation processes, where consistent chemical integrity is maintained under process heating. Viscosity 1.2 mPa·s (at 25°C): 3-Hydroxy-5-methylpyridine at a viscosity of 1.2 mPa·s is used in injectable drug solutions, where low viscosity supports easy administration. Water Content <0.2%: 3-Hydroxy-5-methylpyridine with water content below 0.2% is used in anhydrous synthesis reactions, where minimization of hydrolysis increases product stability. UV Absorbance λmax 282 nm: 3-Hydroxy-5-methylpyridine with a UV absorbance maximum at 282 nm is used in analytical calibration standards, where accurate detection facilitates quality control. Residual Solvent <50 ppm: 3-Hydroxy-5-methylpyridine containing less than 50 ppm residual solvent is used in API manufacture, where low solvent ensures regulatory compliance. Assay ≥98%: 3-Hydroxy-5-methylpyridine with assay not less than 98% is used in laboratory research applications, where high assay guarantees reproducible experimental outcomes. |
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Sometimes, science brings us a compound that seems small on paper but carries a lot of weight in application. 3-Hydroxy-5-methylpyridine fits that description. With its core structure rooted in the pyridine family, its small tweak at the hydroxy and methyl positions means it’s not just another regular ring-based chemical. If you’re wondering what true versatility looks like in a single molecule, let’s take a closer look at why this compound matters, what sets it apart, and where it shows up across industries.
We’re talking about a six-membered ring, with a nitrogen atom sitting in as part of the aromatic core—classic pyridine territory. Add a hydroxy group at position three and a methyl group at position five and suddenly, you have a compound that both attracts new possibilities and dodges the limitations that pure pyridine brings. These subtle touches are not just decoration. They steer how this compound interacts with other substances, how it’s processed in labs, and where it fits into chemical syntheses.
Through plenty of lab hours, I've seen samples of 3-Hydroxy-5-methylpyridine that crystallize into a pale, off-white powder. It doesn’t take much to notice how easily it dissolves in water and a stretch of organic solvents. I recall running extractions and separations where this solubility cut straight through the usual bottlenecks. When purity hits above 99%, you notice that reactivity stays sharp, and there are fewer worries about byproducts derailing your synthesis. The melting point floats comfortably in the mid-temperature range, making it straightforward to store, handle, and transport. Those who have spent hours haggling with tricky chemicals that either evaporate too quickly or clump up know how much relief a stable, friendly melting point brings.
Once you spend enough time dealing with the pyridine family, subtle differences jump out. With 3-Hydroxy-5-methylpyridine, the location of the hydroxy group creates a new set of hydrogen-bonding opportunities. In my experience, this really matters in pharmaceutical research, where you want a compound that can hook onto a specific target and hang on just tight enough to get the job done—without blowing up the rest of the reaction pathway. The extra methyl group adds some bulk and shifts the compound's electronic properties, making it more stable in certain conditions and less prone to breakdown than plain old pyridine or even its 3-methyl cousin.
Colleagues working on the synthesis of catalytic intermediates noticed that 3-Hydroxy-5-methylpyridine resists unwanted oxidation better than its siblings. That’s worth gold on a lab bench where oxygen sensitivity can ruin hours of work. You’ll also spot the difference in terms of toxicity; this compound often lands with a safer profile due to the methyl group’s steric effect shaping metabolic routes in biological systems.
Many years back, I watched a med chemist use 3-Hydroxy-5-methylpyridine as a key intermediate for creating cardiovascular agents. The compound’s ability to donate and accept hydrogen bonds paved the way for making structures that lock onto enzyme sites involved in vital metabolic pathways. Outside of drug discovery, it also takes a place in the world of vitamins and nutritional supplements, since derivatives exist as active forms of vitamin B6. Those who have worked in foods or feed additives can appreciate how this molecule often becomes the backbone for tailored compounds—its subtle tweaks to the ring system offering just enough tuning to boost stability and bioactivity without sacrificing safety.
There’s another layer in its value for agrochemicals and fine chemicals. The functional groups can take multiple synthetic hits—nitrations, alkylations, oxidations—without falling apart. In chemical manufacturing, this means recipes can run with fewer side reactions and less expensive cleanup. When designing ligands for metal chelation, 3-Hydroxy-5-methylpyridine binds with a mix of selectivity and strength, giving metallurgists more options in separating rare metals from ores or electronic scrap. Over the years, I’ve seen the difference such refinements make on process efficiency and environmental impact.
Quality control isn’t just about ticking boxes. In regulated sectors like pharma and food, I’ve seen inspectors trace impurities down to the parts per million. 3-Hydroxy-5-methylpyridine stands up well to that scrutiny. Analytical profiles by HPLC and NMR come out clean—no ghost peaks or odd residues. This means less downstream worry about unpredictable reactions, off-target effects, or legal headaches. Suppliers that treat purification with care—going for extra crystallization rounds or employing advanced distillation—deliver a product that shows up to work every time.
Comparing this to less-refined versions of related pyridine derivatives, the headaches become clear: more frequent recalls, more reanalysis, and more time troubleshooting at the bench instead of advancing science. As a chemist who has watched project timelines slip due to avoidable ingredient mishaps, I don’t discount the cost savings and risk avoidance that comes with a high-spec compound.
Some may wonder if there is enough difference to justify the switch when there are so many pyridine derivatives on offer. Technical facts say yes, but experience in the field confirms it time and again. Enzymatic studies sometimes call for a pyridine base that can either play nice in a reaction or throw a curveball to tease out a mechanism. 3-Hydroxy-5-methylpyridine is a point of reference in mechanistic enzymology partly because its substituents provide specific sites for enzyme catalysis to latch onto.
Stepping outside the lab, the compound gets folded into the real world. Developers crafting formulations for animal health find that it serves as a bridge to more bioavailable B6 analogs. Farmers who rely on smarter, safer crop protection chemicals might not see the name on their invoices, but they benefit from its stability in the intermediates upstream. Supply-chain reliability gets tied back to how easily this compound resists degradation during transport and storage. Having spent time supporting companies through change controls and audits, I’ve found that stakeholders relax when the backbone chemistry is this robust.
Those coming at this from a background in synthesis might be tempted to treat all pyridine derivatives as roughly interchangeable, but hands-on work proves the gaps. 3-Hydroxy-5-methylpyridine resists base and acid hydrolysis better than related structures. This came into focus for me during a project attempting multiphase extractions at different pH ranges. Where 3,5-dimethylpyridine broke down under mild acid, the hydroxy/methyl combo on 3-Hydroxy-5-methylpyridine held firm. Because the compound absorbs less water vapor, batches ride out humidity swings without caking or forming unwanted hydrates.
In pharmaceutical salt formation, this matters more than theory suggests. The ability to form salts that dissolve easily in both organic and aqueous systems boosts oral drug absorption. Medicinal chemists aiming for improved pharmacokinetics can start with better raw ingredients. Even though regulatory frameworks like REACH and the FDA recognize a broad class of pyridine derivatives as safe under certain use patterns, the data suggests that downstream reaction profiles are far less variable with this compound in the mix.
This all sounds optimistic, but anyone in production knows that even standout molecules face scaling hassles. Multiple-step syntheses, solvent use, and byproduct management present ongoing environmental and economic headaches. Some routes to 3-Hydroxy-5-methylpyridine still require steps that generate waste or call for solvents, like chloroform or benzene, that industrial users strive to avoid. Instead of settling, several outfits have begun to chase greener chemistry: flow synthesis, biocatalysis, and solvent recovery loops. Success here trims footprint and cost, turning a good molecule into a socially responsible one.
I have worked at the bench during scale-up, where each hazard or inefficiency multiplies in risk from gram-scale to tons-per-year. Finding catalysts that cut energy demands or recycling reaction media without excessive purification is a personal mission for many in process chemistry. Reports from leading journals point toward new catalysts based on iron or bio-inspired ligands that could transform the process, removing the need for precious metals and noxious reagents. Progress is slow but ongoing. Every breakthrough trickles down to lower prices, wider access, and less environmental strain.
I’ve seen trends wax and wane in both pharma and specialty chemicals, but not every substance gets to stick around after the initial buzz wears off. 3-Hydroxy-5-methylpyridine anchors itself by remaining useful in both mature and developing fields. In microbiological media, it sometimes serves as a growth factor analog, contributing to experiments guiding antibiotic discovery. In catalyst research, those fine details in its structure give researchers another branch to climb in the search for selectivity and yield.
Even its molecular weight and manageable volatility mean that those assembling chemical libraries get a compound that performs predictably in automated processes—an underrated but real advantage. For startups and universities trying to do more with less, every saved purification step or extended shelf life matters. Those savings multiply through each link in the supply chain, pushing innovation forward even when funding tightens.
Plenty of chemical suppliers throw their weight behind promises, but users know that trust is built on clear sourcing, honesty about batch consistency, and genuine customer support. As someone who’s had to pinch pennies for grant-funded research, I can’t overstate the relief that comes from opening a bottle and finding it matches last month’s stock—same powder, same performance, same outcome.
Open disclosure about analytical certificates and residual solvents serves everyone. Researchers and production managers who feel confident about what’s in the drum pass that peace of mind along to their clients, regulators, and patients. And with globalized supply chains, this level of transparency stands as much protection for small labs as for multinational producers.
Production methods keep evolving. A decade back, most 3-Hydroxy-5-methylpyridine landed in batches produced by batchwise chemical synthesis. Newer synthetic biology platforms may soon offer fermentation-based alternatives. The learning curve will be steep, but the payoff—fewer petrochemical byproducts, less hazardous solvent, and a clearer supply chain—aligns with rising demands for sustainability.
I believe the path forward lies in linking process improvements with product stewardship. Why go backwards to dirtier, clunkier chemistry when the industry proves, time and again, that cleaner pathways exist? Collaboration between academic chemists, production-scale engineers, and customers encourages quicker proof-of-concept trials, leading to better, cleaner commercial supply.
No single sector can claim full ownership over 3-Hydroxy-5-methylpyridine. Every application contributes to a richer understanding of its value. In materials science, its unique electronic characteristics draw interest as modifying agents for advanced polymers and coatings. In analytical chemistry, specialized reagents built on its skeleton bring added resolution and selectivity for samples where standard dyes fall short.
Having watched teams from pharma, agriculture, and energy gather at the same conferences, I’m encouraged by how knowledge, data, and even supply networks cross boundaries. The molecule’s centrality to so many disciplines suggests it will continue to evolve as researchers and manufacturers demand more from their materials.
Drawing from years spent in both research and industry, a few truths have emerged that solve recurring challenges with 3-Hydroxy-5-methylpyridine:
The best outcomes I’ve seen grow from supportive professional networks. Whether you’re designing a new synthesis or just trying to replace a hazardous intermediate, the collective expertise built around compounds like 3-Hydroxy-5-methylpyridine moves the needle for everyone involved.
It’s not hard to spot short-term trends or ephemeral chemical fads. Longevity in the field often comes from quietly filling essential roles, adapting as the science changes, and keeping one’s nose clean in terms of safety and compliance. In all these ways, 3-Hydroxy-5-methylpyridine remains a reliable performer.
No wonder it stays on the shopping list for research labs, production plants, and quality control outfits worldwide. As the push for sound science and cleaner industry shapes the next decade, chemicals like this—practical, proven, and adaptable—set the bar for what’s possible. Whether in the hands of a seasoned chemical engineer or a curious graduate student, the tools for progress often look a lot like 3-Hydroxy-5-methylpyridine: precise, approachable, and ready for more.