|
HS Code |
394612 |
| Chemical Name | 2-Methyl-3-hydroxypyridine |
| Cas Number | 1121-27-9 |
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.13 |
| Appearance | White to pale yellow solid |
| Melting Point | 81-84°C |
| Boiling Point | 265-267°C |
| Solubility In Water | Soluble |
| Density | 1.13 g/cm3 |
| Flash Point | 130°C |
| Smiles | CC1=C(C=CN=C1)O |
| Iupac Name | 2-methylpyridin-3-ol |
As an accredited 2-Methyl-3-hydroxylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Methyl-3-hydroxylpyridine is supplied in a sealed 100g amber glass bottle with a tamper-evident cap and clear labeling. |
| Container Loading (20′ FCL) | 20′ FCL container holds securely packed 2-Methyl-3-hydroxylpyridine, each drum or carton sealed, ensuring safe, efficient bulk transportation. |
| Shipping | 2-Methyl-3-hydroxypyridine should be shipped in tightly sealed containers, clearly labeled, and protected from moisture and incompatible substances. Transport in compliance with local, national, and international regulations. Use appropriate packaging to prevent leaks or spills, and handle with suitable personal protective equipment to ensure safety during shipping and handling. |
| Storage | 2-Methyl-3-hydroxypyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Proper labeling and compliance with chemical storage regulations should be ensured to maintain safety and prevent contamination or degradation. |
| Shelf Life | 2-Methyl-3-hydroxypyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and tightly sealed container. |
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Purity 99%: 2-Methyl-3-hydroxylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures consistency and efficiency in active ingredient formation. Melting point 106–110°C: 2-Methyl-3-hydroxylpyridine with melting point 106–110°C is used in organic synthesis applications, where predictable phase transitions facilitate controlled reaction processes. Molecular weight 109.13 g/mol: 2-Methyl-3-hydroxylpyridine with molecular weight 109.13 g/mol is used in medicinal chemistry development, where defined molecular weight supports precise dosage calculations. Low water content ≤0.5%: 2-Methyl-3-hydroxylpyridine with low water content ≤0.5% is used in sensitive catalyst preparation, where minimal moisture prevents unwanted side reactions. Particle size ≤50 µm: 2-Methyl-3-hydroxylpyridine with particle size ≤50 µm is used in formulation of high-dispersion blends, where fine particle size improves homogeneity and bioavailability. High thermal stability up to 180°C: 2-Methyl-3-hydroxylpyridine with high thermal stability up to 180°C is used in high-temperature pharmaceutical processes, where stability maintains molecular integrity under thermal stress. |
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Folks who spend time in chemical labs and manufacturing plants often know the challenge of tracking down reliable speciality compounds. 2-Methyl-3-hydroxylpyridine meets a need in pharmaceutical and chemical research that few other molecules fill as efficiently. With its molecular backbone built around a pyridine ring substituted with a methyl group at the second position and a hydroxyl group at the third, this compound doesn’t just catch the attention of chemists for its structure—it delivers real-world solutions in synthesis and research.
Its chemical formula, C6H7NO, places it squarely within a niche group of alkylated pyridines. This specific configuration, compared with plain pyridine or even its close relatives like 3-hydroxypyridine, grants a unique reactivity in organic synthesis. What sets it apart isn’t just academic; the functional groups open the door for targeted chemical transformations, allowing for faster reactions and cleaner results in many applications. Specialists appreciate the improved selectivity and yield when using 2-Methyl-3-hydroxylpyridine as a starting point or intermediate.
In medicinal chemistry, the structure of a molecule often determines whether a potential new drug is easy to produce on a large scale. With 2-Methyl-3-hydroxylpyridine in hand, chemists can explore new synthesis pathways for biologically active compounds. Many active pharmaceutical ingredients (APIs) rely on modifications made to the pyridine ring; this compound answers the call by providing both a handle for further substitution and a stabilizing methyl group that encourages favorable reaction kinetics.
Productivity and yield remain persistent concerns for pharmaceutical manufacturers. At my last position in a process chemistry group, we prioritized reagents that minimized waste while delivering strong batch yields. Using 2-Methyl-3-hydroxylpyridine, we shaved hours off certain reaction protocols and saw upward jumps in conversion rates. The methyl group at position two often dampened side reactions, which cut down on purification headaches and resource use. This efficiency not only saves time but reduces the load of hazardous byproducts heading for disposal, a concern both environmentally and financially.
The experience of running a clean, reliable synthesis hinges on purity. 2-Methyl-3-hydroxylpyridine supplied to research labs usually comes in crystalline or powder form, often reaching purities above 98 percent. This allows teams to skip extra purification steps, avoiding unnecessary labor and solvent use. Not all manufacturers keep that consistency, but the best ones subject each batch to HPLC, NMR, and sometimes even mass spectrometry, giving reassurance that the product won’t throw unwanted surprises during critical reaction steps.
Its solubility marks another practical advantage. In water and most common organic solvents, 2-Methyl-3-hydroxylpyridine dissolves well enough for quick dissolution in both bench-top and large-scale operations. Researchers in analytical chemistry will recognize the benefit here, as better solubility smooths out assay workflows and helps when preparing standards for calibration curves. Several academic studies have noted that the spectral properties of the compound—such as its UV absorption—make it suitable for monitoring in-process development with standard analytical equipment.
The pathways to drug development grow more complex every year. 2-Methyl-3-hydroxylpyridine carves out a reliable role by acting as more than just a raw material. Medicinal chemists reach for it during the discovery of new central nervous system agents, especially when a subtle tweak to the electronic properties of a molecule can make the difference between an inactive compound and a promising candidate. In anti-inflammatory and neuroprotective compounds, for instance, the addition of the methyl and hydroxy groups unlocks new metabolic profiles without significantly raising toxicity risks.
Outside the pharmaceutical world, specialty chemical companies have found other uses. Its reactivity allows for the preparation of corrosion inhibitors and antioxidants for industrial applications. In agrochemical research, molecules like 2-Methyl-3-hydroxylpyridine help design safer, targeted pesticides and plant-growth regulators; the ability to modify both the aromatic ring and the side-groups encourages the design of compounds that break down more predictably in the environment.
Materials science sees similar trends. When functionalized polymers and advanced coatings demand building blocks that offer both reactivity and stability, this compound has found its place. The free hydroxy group can react with various cross-linkers, enabling the design of resins and adhesives with tailored mechanical and chemical properties.
Chemists familiar with pyridine chemistry often compare 2-Methyl-3-hydroxylpyridine to its close cousins: pyridine itself, 3-hydroxypyridine, and other methylated isomers. Here’s where real, tangible differences emerge. Pyridine, the simplest in this family, acts as a basic nitrogen heterocycle, but lacks functional handles for fine-tuning. 3-Hydroxypyridine introduces polarity and reactivity, yet it remains more prone to unwanted side reactions during synthesis or scale-up.
The combined presence of both the methyl and hydroxy groups in the two and three positions, respectively, shifts the molecule’s electronic structure. This subtle change guides reactions to preferred products, especially under mild conditions. In my own work optimizing Suzuki-Miyaura couplings, adding that methyl group delivered higher yields with fewer impurities compared to plain 3-hydroxypyridine—no small success when deadlines tick closer and grant funding feels tight. For anyone in scale-up chemistry, this reliability means smoother regulatory review and less risk of process bottlenecks.
This compound’s unique profile influences more than reactivity; it changes how end products perform. Biologically, the substitution pattern makes a difference in metabolic stability, often translating to different pharmacokinetic profiles in drug candidates. In materials science, functional coatings built from this building block often last longer under UV or chemical exposure compared to those made with unsubstituted pyridine analogs.
Responsible sourcing of chemicals forms the bedrock of any safe and sustainable operation. The growing concern about counterfeit or off-spec specialty chemicals makes transparency from suppliers a top priority. Companies that supply 2-Methyl-3-hydroxylpyridine carry a duty to back up quality claims with batch-level data and certificates of analysis, verified through reliable analytical methods. A few years ago, our team saw first-hand the fallout when a lesser-known supplier delivered a batch contaminated with 3-methylpyridine. That misstep cost us several weeks as we tracked down the problem and re-qualified our samples.
Storage and handling practices carry significant weight. The powder form generally settles in sealed containers under dry, cool conditions. Given the compound’s reactivity, especially that free hydroxy group, it reacts with strong oxidizing agents and acids—failing to segregate leads to hazardous conditions or waste of expensive reagents. Teams running process chemistry lines or scale-up work align storage and inventory controls tightly to avoid mishaps that could halt production.
Waste management matters just as much. Green chemistry principles push for recovery and recycling where feasible. With careful process design, both unused reagent and by-products can be captured and reprocessed; in our department, switching to closed-loop solvent and reagent systems cut chemical waste down by double-digit percentages, providing both ecological benefits and real cost savings. Regulatory compliance grows easier when waste streams stay clean and predictable.
Stringent regulatory environments demand that compound suppliers follow best practices from production through delivery. The modern relevance of 2-Methyl-3-hydroxylpyridine lines up with the trend toward sustainable production—especially since downstream products often end up in consumer-facing pharmaceuticals or high-tech coatings. Traceability and documentation have become part of daily life in chemical labs. Distinctive labeling and digital batch records now tie every shipment to its origin and purification route.
On the environmental front, chemists and quality managers aim to reduce lifecycle risks. Unlike some pyridine derivatives notorious for volatility or soil persistence, 2-Methyl-3-hydroxylpyridine shows moderate aqueous solubility and doesn’t hang around as long as chlorinated isomers. This means that proper handling mostly prevents environmental release, and any accidental spills get remediated with standard in-lab protocols.
Where regulations tighten—across Europe, North America, and parts of Asia-Pacific—producers invest in greener synthesis routes. Catalysis, process intensification, and biomimetic transformations see growing use in specialty chemical plants, and 2-Methyl-3-hydroxylpyridine’s efficiency as a synthetic intermediate keeps it top of mind among R&D managers. Government audits focus on cradle-to-grave documentation, requiring thorough recordkeeping covering everything from source materials to final waste streams.
Bringing a product like 2-Methyl-3-hydroxylpyridine from lab curiosity to high-value industrial staple doesn’t happen by accident. Ongoing collaboration between product developers, bench scientists, and regulatory agents supports the kind of reliable supply chain that protects both end-users and the general public. Whether the application demands small, research-grade batches or steady, drum-scale shipments, the same principles—traceability, purity, and waste minimization—come into play.
Fact-based risk assessment never takes a vacation in chemical industries. The vertical integration seen with some of the world’s top manufacturers helps bring supply and demand in line, meaning fewer price shocks and delivery delays for downstream partners. Meanwhile, periodic third-party audits and marketplace reviews help keep operations on the level. When quality dips, word travels through professional networks fast. In tight-knit R&D teams, switching suppliers mid-project brings more disruption than most people expect.
From my seat as both a buyer and a user, the best suppliers treat end-user feedback seriously. Companies that gather needs from both the pharmaceutical and specialty chemical markets adjust their product specs over time, offering higher-purity lots or modified particle sizes to match evolving tech. This two-way street—where users openly describe successes and bottlenecks—spurs incremental product improvements, pushing chemistry forward. It’s the collective pursuit of better compounds, not the short-term chase for profit, that builds reputational capital in specialty chemicals.
Each year brings new hurdles for specialty chemical buyers and end-users. Supply chain shocks—whether sparked by geopolitical tension, public health challenges, or climate events—necessitate better risk management strategies. Resilience grows by qualifying multiple reliable suppliers and embracing local sourcing, which shortens lead times and decreases the carbon footprint of global distribution.
Information sharing also plays a growing role. Encouraging open channels between researchers, production managers, and regulatory agencies helps identify quality or safety issues early, well before they spiral into regulatory fines or product recalls. Peer-reviewed publications and conference proceedings covering reliable production methods of 2-Methyl-3-hydroxylpyridine and best handling practices build an ecosystem where less experienced users come up to speed quickly, improving safety and performance at all levels.
Digital transformation stands poised to address persistent documentation and quality-tracing problems. With blockchain-backed chain-of-custody systems, end-users gain confidence that each shipment matches specs, and regulators gain an easier path to verification. Early adopters in the fine chemicals sector have already shown improvements in transparency and efficiency, allowing lab teams to spend more time on research rather than regulatory paperwork.
The evolution of specialty chemicals reflects changing expectations from society and industry. Customers demand greener, safer, and higher-purity products, and 2-Methyl-3-hydroxylpyridine serves as a prime example of how those expectations play out. Companies that succeed in this arena routinely revisit production technology, invest in employee training, and seek third-party validation of their safety protocols.
Continuous improvement requires feedback not just from managers but from hands-on chemists who witness firsthand both the successes and the frustrations of product use. In survey after survey, chemists rank batch-to-batch consistency, clear documentation, and responsive customer service as their top needs—well ahead of cost savings or even speed of delivery. Suppliers who close this feedback loop end up gaining market share over time, especially as regulations tighten and end-users grow more sophisticated.
Training contributes to safe, effective use of specialty chemicals. Regular safety briefings, hands-on demo sessions, and transparent accident reporting mean that users of 2-Methyl-3-hydroxylpyridine rely less on luck and more on practiced skill. Smaller teams can partner with universities and industrial associations to keep up with the latest protocols, preventing accidents and safeguarding long-term success.
Whether in the research lab or on the manufacturing floor, 2-Methyl-3-hydroxylpyridine creates versatility and opportunity. Its structure positions it for use both as a backbone in new pharmaceuticals and as a source of functional groups in materials science. Each time it contributes to new discoveries or better-performing products, it demonstrates the value of smart product design and responsible sourcing.
In my years of working both at the bench and on procurement teams, the difference made by reliable specialty chemicals rarely gets enough attention. When compounds like 2-Methyl-3-hydroxylpyridine show up with consistency and the right paperwork, teams feel more confident to plan ambitious projects. This culture of reliability soaks into every phase—R&D, scale-up, routine production—and creates a foundation for breakthrough success.
Future gains will depend on blending experience with innovation. Companies that keep listening to both the marketplace and their own technical teams will set the standard for years to come. Whether you’re mixing a new pharmaceutical precursor or building advanced coatings, investing in high-quality, reliable intermediates like 2-Methyl-3-hydroxylpyridine serves as a blueprint for enduring success.