N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine

    • Product Name: N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine
    • Chemical Name (IUPAC): 3-cyano-1-methyl-4-methyl-6-hydroxypyridin-1-ium
    • CAS No.: 884495-22-5
    • Chemical Formula: C8H8N2O
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    957152

    Chemical Name N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine
    Molecular Formula C8H8N2O
    Molecular Weight 148.16 g/mol
    Appearance Solid (likely crystalline powder)
    Color Typically off-white to light yellow
    Solubility Soluble in organic solvents (e.g., DMSO, methanol)
    Functional Groups Pyridine ring, cyano, methyl, hydroxy, N-methyl
    Iupac Name 1-Methyl-6-hydroxy-4-methylpyridine-3-carbonitrile
    Storage Conditions Store in cool, dry place
    Synonyms N-Methyl-3-cyano-4-methyl-6-hydroxypyridine

    As an accredited N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g amber glass bottle, sealed with a tamper-evident cap; labeled with chemical name, hazard warnings, and batch information.
    Container Loading (20′ FCL) 20′ FCL can load approximately 12 metric tons of N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine, packed in 25kg fiber drums.
    Shipping Shipping of **N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine** requires packaging in tightly sealed, chemical-resistant containers. The container should be clearly labeled, handled with appropriate PPE, and shipped in compliance with local, national, and international hazardous materials regulations, including documentation and temperature control if necessary. Avoid exposure to heat, moisture, and direct sunlight during transit.
    Storage Store **N-Methyl-3-Cyano-4-Methyl-6-hydroxypyridine** in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep the chemical away from incompatible substances such as strong oxidizing agents and acids. Ensure proper labeling and limit exposure to moisture. Follow all relevant chemical storage regulations and safety guidelines.
    Shelf Life N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine has a typical shelf life of 2 years when stored in a cool, dry place.
    Application of N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine

    Purity 99%: N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine with 99% purity is used in pharmaceutical intermediate synthesis, where high chemical purity ensures optimal reaction yields.

    Melting Point 157°C: N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine with a melting point of 157°C is used in organic compound formulation, where thermal stability enables precise processing conditions.

    Particle Size <10 µm: N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine with particle size under 10 µm is used in fine chemical manufacturing, where uniform particle distribution enhances dispersion in solvents.

    Solubility in Ethanol: N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine with high ethanol solubility is used in solution-phase synthesis, where rapid dissolution improves batch homogeneity.

    Stability up to 120°C: N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine stable up to 120°C is used in catalytic reaction environments, where resistance to thermal degradation extends catalyst lifespan.

    Assay ≥98% HPLC: N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine with assay ≥98% by HPLC is used in analytical research, where high assay values provide reliable quantification.

    Moisture Content ≤0.5%: N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine with moisture content at or below 0.5% is used in moisture-sensitive synthesis, where low water content prevents unwanted side reactions.

    Molecular Weight 163.17 g/mol: N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine with a molecular weight of 163.17 g/mol is used in precise stoichiometric calculations, where accurate molecular mass ensures correct formulation.

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    Certification & Compliance
    More Introduction

    N-Methyl-3-Cyano-4-Methyl-6-hydroxy Pyridine: Critical Building Block for Modern Synthesis

    In our work as a chemical producer, one compound that draws constant interest from researchers and manufacturers is N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine. This molecule reflects how careful synthesis can open doors for downstream chemistry—especially for those in drug discovery, agrochemical development, and advanced material research. Its structure carries functional groups that help bridge the gap between basic pyridine chemistry and more elaborate, high-value end uses.

    The Chemical Structure and Why It Matters

    N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine stands out for a simple reason: the combination of its methyl, cyano, and hydroxy groups attached to the pyridine ring. Synthesizing this compound requires attention to moisture levels, choice of solvents, and temperature control. Every batch follows strict steps to check for the right purity, since even tiny amounts of contaminants can change how it reacts in the next step. Our teams avoid shortcuts during workup and isolation, because downstream users demand consistent, reproducible material.

    Other pyridine derivatives in the market often lack the synergy between these groups. You’ll find that the cyano functionality leans towards nucleophilic substitution or cyclization in API synthesis, while the hydroxy group opens pathways for etherification or esterification. The methyl group, though simple, adds to the stability and lipophilicity of the molecule—making it viable in several biochemical routes where bulkier or less-polar groups would create solubility headaches.

    Specification and Consistency: The Core of Our Offering

    The current demand for N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine covers a spectrum from milligram-scale research trials to bulk production. We generally supply this product in purity levels above 98%, since substandard material disrupts both analytical and preparative progress for our clients. Our routine QC panels use HPLC and NMR as benchmarks for every production lot. Water content—often overlooked—can be a dealbreaker for certain reactions, causing side products or unwanted hydrolysis. That’s why our drying and packaging lines focus on minimizing exposure to moisture from start to finish.

    Differences from Other Pyridine Variants

    There’s no shortage of pyridine-based intermediates in the market. Each variant caters to a unique slice of the synthetic spectrum. Some lack functional handles such as the cyano or hydroxy groups, limiting their downstream value. Others pack in reactive groups that require protection or extra purification, adding both time and cost to multi-step syntheses.

    N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine balances reactivity with selectivity. Drugs and agrochemicals built from this intermediate tend to show better process yields and simpler workups. We’ve watched clients replace halogenated pyridine analogues with this compound purely to sidestep costly environmental scrubbing and waste management. The compact size of this molecule fits neatly into high-throughput screening and combinatorial chemistry platforms, unlike bulkier pyridine derivatives which complicate miniaturized workflows.

    Practical Usage in Research and Scale-Up

    Our customer base routinely explores new synthetic routes, and we listen closely when they describe process bottlenecks. In medicinal chemistry, the adjustable positions of the cyano and hydroxy substituents on the pyridine core simplify the synthesis of diverse libraries. The electron-withdrawing cyano group enables robust cross-coupling or condensation without unwanted aromatization or loss of functionality. Researchers appreciate how this stability aids purification, letting them skip additional steps.

    Scaling from lab bench to production floor, the compound’s behavior under various conditions, such as temperature and pH, proves reliable. Unlike some ortho-substituted pyridines, our product resists decomposition during standard hydrogenation or oxidations. Customers tell us this feature alone can turn an experimental protocol into an industrially viable one. Waste reduction in these cases translates directly to lower production costs and reduced regulatory scrutiny.

    Meeting Regulatory and Documentation Standards

    Every step of production and storage considers regulatory frameworks in different countries. Audits focus on traceability, which covers everything from raw material origin to finished product packaging. We record every part of the process, not to satisfy bureaucracy, but because our partners—especially those in pharmaceuticals and crop-protection—need airtight data trails for both patent filings and ongoing monitoring.

    Shipping and storage require real-world robustness. We use chemical-resistant packaging that handles humidity and light—essential for maintaining quality from our facility to the end user’s lab or plant. We regularly test stability against both time and transport vibration since even low-level degradation reduces batch-to-batch reproducibility.

    Supporting Innovation with Consistent Supply

    In the competition-heavy worlds of pharma and fine chemicals, project timelines shrink every year. Interruptions in the supply of specialty intermediates like N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine cost more than just lost days—missed deadlines can derail patent applications or new product launches. We’ve structured our manufacturing schedules to strike a balance between just-in-time responsiveness and inventory depth. This strategy keeps our regular clients covered during unpredictable demand spikes.

    Production flexibility comes from longstanding investments in raw material sourcing and process optimization. Our facility isolates production lines handling pyridine intermediates from those that handle sulfur or halogenated compounds, warding off cross-contamination. Real-time feedback loops between downstream users and our technical team tighten the process window and yield more robust products.

    Challenges and Solutions in the Synthesis Process

    Making N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine involves more than simply reacting a handful of starting materials together. Our team navigates sensitive steps where timing, temperature, and reagent quality work together for optimal yield. The introduction of the cyano and hydroxy functions demands precise control, since overreaction or byproducts waste precious time and materials. In the past, we tried alternative manufacturing approaches, such as single-pot condensations or extended hydrolysis, which introduced inconsistent impurities.

    Through this experience, robust process control systems have been incorporated. Our reactors feature programmable dosing controls and in-line monitoring of pH, allowing us to adjust on the fly and catch any drift before a batch moves outside specification. Whenever a new impurity shows up, its fingerprint is tracked through advanced chromatography and MS techniques, giving us insight into how to tweak our purification protocols further.

    End-User Applications and Real-World Value

    Most inquiries for N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine center on drug development, particularly as a scaffold for kinase inhibitors or CNS-active compounds. Its compatibility with Suzuki and Buchwald coupling methods brings down the cost per API candidate, since fewer steps mean less solvent, fewer consumables, and shortened cycle times. We see similar patterns in plant protection, where rapid access to new active ingredients keeps pace with resistance management in the field. Years of feedback from these industries point to one lesson: even minor variations in sample purity or reactivity lead to scale-up failures, so upstream reliability makes or breaks downstream innovation.

    Outside large-scale industries, this compound finds use in specialty polymer work and in the preparation of chelating agents. Both applications benefit from a clean hydroxy group, which acts as a site of modification. Because the cyano group resists most ambient conditions, researchers get a chance to push their reactions further without frequent rework. As a result, even academic and government labs starting novel lines of inquiry turn to this intermediate instead of betting on less well-traveled options.

    Environmental Responsibility and Sustainable Manufacturing

    Producing pyridine derivatives at scale brings environmental obligations, not just technical ones. Waste from cyanation or methylation steps has the potential to introduce nitriles or other persistent compounds into effluent streams. We address this risk through a closed-loop solvent recovery system and on-site waste neutralization. Both measures shrink the carbon footprint per kilogram of finished material and reassure clients who themselves operate under tightened environmental permits.

    Solvent selection and energy use have changed, too. Instead of relying on traditional chlorinated solvents or high-temperature reflux, our process designers have shifted towards greener alternatives and energy-efficient batch processing. The adoption of these methods brought initial skepticism—efficiency and safety rarely go hand in hand on the first try. Only through iterative improvements did the process stabilize without any drop in product quality.

    We regularly audit our approach to raw material sourcing, mindful of both cost and sustainable credentials. Violations of this standard by upstream suppliers result in immediate loss of business, because we cannot risk a breakdown in compliance that follows the product all the way to its application in regulated industries.

    Partnership and Feedback from Downstream Users

    Quality isn’t only about the compound—it’s about how it fits into each customer’s broader purpose. We maintain technical support lines that connect research chemists and process engineers with our own manufacturing teams, not just a faceless sales channel. Detailed feedback from project pilots or even failed scale-ups leads directly into our next round of process improvements. Some years ago, a customer flagged a troublesome low-level impurity—one we hadn’t caught in our panel since it only showed up during a multistep cyclization. The ensuing collaboration helped us zero in on the formation mechanism and fine-tune reaction quenching in subsequent runs. This type of exchange turns a good product into a crucial tool for those betting company success on a few grams of consistency at a time.

    We make a point of keeping up with changes in regulations and published scientific literature, not to ride trends, but to stay ahead of changes that directly alter what’s required of our product. When new uses emerge in high-throughput biology or materials science, we run trials in parallel to see how small tweaks to synthetic conditions better suit those applications. Our batch-to-batch documentation, which has grown from simple certificates of analysis to full traceability maps, reflects this feedback cycle. For clients, this means quicker troubleshooting and less time lost navigating compliance paperwork.

    Forward-Looking Perspectives for N-Methyl-3-Cyano-4-Methyl-6-hydroxy Pyridine

    Industrial chemistry never stands still, and neither does our own process toolbox. Ongoing research into more selective catalysts for cyclization, or greener methods for introducing the methyl group, keeps our team on its toes. Each advance shortens timelines for bringing a new process from lab bench to commercial scale, with payoffs for everyone in the supply chain. We evaluate emerging analytical techniques such as real-time NMR and advanced mass spectrometry both to assure product purity and to anticipate new impurity issues before they show up in client labs.

    Customers now ask us to prepare custom modifications of this intermediate, betting that even a single atom change can bring a breakthrough in bioactivity or solubility. We’re adding modular synthesis steps to meet these needs—an extra functional group here, a different protecting group there—all with the goal of keeping process hazards manageable and performance high. For us, these requests aren’t burdens; they’re reminders of why close communication and relentless process refinement push chemistry forward.

    Final Thoughts on Collaboration and Reliability

    N-Methyl-3-Cyano-4-Methyl-6-hydroxy pyridine is more than a compound on a shelf—it’s the result of years of chemical expertise brought to bear on real manufacturing challenges. Every adjustment improves not just the purity or availability, but the confidence end users feel as they build complex molecules on top of our foundation. Succeeding in pharmaceutical or specialty chemical projects means trusting that each intermediate will live up to its promise on every scale, in every application. Our doors remain open to those who care as much about quality, reliability, and real-world results as we do on the production floor.