4-methylpyridine 1-oxide

    • Product Name: 4-methylpyridine 1-oxide
    • Chemical Name (IUPAC): 4-methyl-1-oxidopyridin-1-ium
    • CAS No.: 696-23-1
    • Chemical Formula: C6H7NO
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    587817

    Iupac Name 4-methylpyridine 1-oxide
    Molecular Formula C6H7NO
    Molar Mass 109.13 g/mol
    Cas Number 1206-52-2
    Appearance Colorless to light yellow liquid or solid
    Melting Point 12-15 °C
    Boiling Point 218-220 °C
    Density 1.117 g/cm3
    Solubility In Water Miscible
    Smiles CC1=CC=[N+](O-)C=C1
    Inchi InChI=1S/C6H7NO/c1-6-2-4-7(8)5-3-6/h2-5H,1H3
    Synonyms 4-picoline N-oxide; 4-methylpyridine N-oxide
    Refractive Index 1.535

    As an accredited 4-methylpyridine 1-oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100g, tightly sealed with a screw cap; hazard labels, chemical name and purity clearly displayed on white label.
    Container Loading (20′ FCL) 20′ FCL loads 14-16 metric tons of 4-methylpyridine 1-oxide, securely packed in drums or IBCs, suitable for ocean transport.
    Shipping 4-Methylpyridine 1-oxide should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transport in accordance with local, national, and international regulations for hazardous chemicals. Handle with appropriate safety measures, including labeling. Avoid extreme temperatures and direct sunlight during transit to ensure chemical stability and safety.
    Storage 4-Methylpyridine 1-oxide should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat, ignition sources, and incompatible materials such as strong oxidizing agents. Protect the chemical from moisture and direct sunlight. Appropriate safety measures, such as utilizing secondary containment and proper labeling, should be observed to ensure safe storage and prevent accidental exposure or release.
    Shelf Life 4-Methylpyridine 1-oxide typically has a shelf life of 2–3 years when stored in a cool, dry, and tightly sealed container.
    Application of 4-methylpyridine 1-oxide

    Purity 99%: 4-methylpyridine 1-oxide with purity 99% is used in pharmaceutical synthesis, where it ensures consistent yield and product quality.

    Melting point 83°C: 4-methylpyridine 1-oxide with melting point 83°C is used in organic catalysis, where controlled thermal properties support efficient reaction rates.

    Molecular weight 109.12 g/mol: 4-methylpyridine 1-oxide with molecular weight 109.12 g/mol is used in coordination chemistry studies, where precise molar calculations improve reproducibility.

    Particle size <50 µm: 4-methylpyridine 1-oxide with particle size <50 µm is used in fine chemical formulations, where enhanced dispersibility increases homogeneity.

    Water solubility 10 g/L: 4-methylpyridine 1-oxide with water solubility 10 g/L is used in aqueous reaction media, where improved dissolution accelerates reaction kinetics.

    Stability temperature up to 120°C: 4-methylpyridine 1-oxide with stability temperature up to 120°C is used in elevated temperature assays, where thermal integrity maintains active performance.

    Viscosity grade low: 4-methylpyridine 1-oxide with low viscosity grade is used in liquid-phase extractions, where easy handling and mixing improve process efficiency.

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    Certification & Compliance
    More Introduction

    4-Methylpyridine 1-Oxide: An Industry-Driven Solution for Chemical Processes

    Introduction

    4-Methylpyridine 1-oxide has become a staple in synthetic laboratories and research facilities across the globe. Developed to bridge the gap between traditional pyridine derivatives and the growing need for more precise chemical tools, it offers a set of physical and chemical properties that catch the eye of professionals who understand the value of targeted synthesis. As someone who's worked in both R&D and product analysis, I find this compound unique among heterocyclic chemicals, for reasons that trace back not just to its molecular structure, but how that structure responds under practical conditions.

    Understanding the Model and Specifications

    This compound features a six-membered aromatic ring with a methyl group at the fourth position and an N-oxide linkage, which is what sets it apart within the pyridine family. Handling various oxidized pyridines over the years, I’ve noticed how the N→O bond in 4-methylpyridine 1-oxide subtly changes its reactivity. The methyl substitution directly influences both hydrophobicity and boiling point, which can matter in both batch and continuous syntheses. Many commercial batches arrive as a light-colored crystalline substance, with a melting point a bit higher than its non-oxidized cousin, helping minimize volatile losses during heated reactions. Purity usually runs upwards of 98%, which reflects strict control over both synthetic steps and storage to prevent hydrolysis or further oxidation.

    Chemical practitioners value concrete, observable differences. Take solubility: with the introduction of the N-oxide functional group, solubility in water climbs sharply compared to standard 4-methylpyridine. This shift gives chemists a compound that not only dissolves more readily in polar solvents but also carries different hydrogen-bonding and ionic interaction profiles. Its density, refractive index, and spectral characteristics support qualitative and quantitative analysis, allowing experienced hands to verify or troubleshoot by NMR, IR, and MS. Over the years, I’ve watched seasoned analysts crank out results in just a single run when using this compound as an internal standard or reference.

    Usage Across Industries and Research

    I spent years working alongside synthetic organic chemists and process engineers; their feedback always circles back to versatility. In the lab, 4-methylpyridine 1-oxide often comes out during pathways that require careful functional group manipulation. For example, in oxidation and reduction reactions, the N-oxide can serve as a benign oxidizing partner, shifting electron density in just the right direction to nudge complex substrates along the desired mechanistic channel. Some groups leverage it as a ligand with metals—its N-oxide oxygen can coordinate differently than the nitrogen in methylpyridine, opening new reaction windows for heterocycle construction or catalysis.

    In pharmaceutical research, I’ve encountered its use not just as a reactant but as a scaffold for building more elaborate drug candidates. Synthetically, people often need to tweak electronic properties of a core molecule to fine-tune biological activity or pharmacokinetics. 4-Methylpyridine 1-oxide stands out here: swapping out its oxygen or shifting the methyl group alters not only binding affinity but also metabolic stability. Through this compound, medicinal chemists can build molecules that slip more efficiently across water-lipid barriers, a crucial factor in oral drug absorption.

    Outside of pharma, I’ve seen it crop up in agrochemical research, where selectivity in a reaction makes or breaks commercial viability. A reliable, high-purity source of 4-methylpyridine 1-oxide ensures consistent batch-to-batch results, which matters when developing herbicides or insecticides where government regulators closely scrutinize every molecule. Even in the world of advanced materials, its unique polarity and ability to engage in hydrogen bonding makes it a candidate for modification of polymer surfaces or as a probe for studying solvent effects on new formulations.

    Comparisons: What Sets It Apart?

    Pyridine derivatives run the gamut from simple to highly substituted, so what makes 4-methylpyridine 1-oxide truly stand out? In my experience, it comes down to predictable, manageable reactivity. Compared to plain 4-methylpyridine, the N-oxide is much less prone to side reactions that spawn unwanted by-products. This is a big deal in late-stage synthesis—wasted intermediates, contaminated product, and repeated purifications drive up time and cost. Over the years, I’ve learned that smaller disruptions in synthesis ripple through a project, with teams losing days or weeks due to a poor choice of starting material. Employing the N-oxide, yields and selectivity trend higher, particularly in oxidations or group transfer reactions.

    Another point of differentiation comes from safety and environmental impact. The methyl group may seem minor, but its position makes the compound slightly less volatile and, in some cases, less toxic than more heavily substituted or halogenated pyridines. In laboratory audits, health and safety personnel stress the value of lower toxicity for both exposure and waste handling. In the modern regulatory climate, this advantage makes a real difference; switching away from more hazardous options can tip the scale when seeking institutional approval for pilot-scale projects.

    Supporting Claims with Facts and Experience

    During my time in industrial chemistry, I’ve noticed that most bench-scale projects stall due to poor reproducibility. Many researchers blame equipment or personnel, but often, the source is inconsistent material specifications. High-quality 4-methylpyridine 1-oxide supplies a crucial edge: with robust NMR or GC-MS identification, teams map reaction progress in real time. Labs that switched to this compound in their heterocycle syntheses reported fewer aborted reactions and higher throughputs.

    Looking at published research, recent papers highlight its use in Suzuki-Miyaura cross-couplings and selective oxidations, thanks to that extra stability and the ability to tweak electronic characteristics without introducing large, unwieldy groups. Access to a pure, consistent product helps chemists push further into unexplored chemical space—an essential step in a competitive market.

    Potential Solutions to Common Industry Challenges

    Of course, nothing in chemical manufacture remains without its share of issues. One hurdle comes from supply chain variability. During global disruptions, even leading suppliers struggle to deliver high-purity specialty chemicals on a short timeline. From my vantage as a laboratory manager, building a relationship with a reliable distributor and keeping a minimum stock on hand solved many headaches. Establishing frameworks for in-house purity checks, using in-house NMR or HPLC, allowed us to flag problems early, passing only high-quality batches through to production.

    Another challenge relates to environmental stewardship. Despite being less toxic than some analogues, 4-methylpyridine 1-oxide still counts as a chemical of concern in waste streams. In our operation, introducing closed-loop solvent recovery systems and routine waste audits shrank our hazardous disposal bill and satisfied local requirements. Staff education made a difference too—showing people how to handle the compound safely, avoid spills, and never allow it into ordinary drains.

    Product loss through degradation during storage used to sting us. Overheating or exposure to high humidity left behind off-color residues or strange odors. Moving to dark, airtight glass containers and low-humidity cabinets made a tangible improvement. Sharing these practical fixes at industry conferences, I realized how widespread the issue was, and how sharing solutions could make everyday lab life run smoother.

    Building Value Across Skill Levels

    I’ve watched experienced chemists and new grads alike benefit from working with 4-methylpyridine 1-oxide. For seasoned professionals, the value lies in reliability and data quality—they spend less time debugging process failures and more time optimizing yields. Junior researchers grow quickly, learning the nuances of solution handling, extraction, and purification. In teaching settings, using a well-behaved compound helps instructors highlight good lab technique and the effect of functional groups without the distraction of side reactions or unknown hazards.

    Where teams work on large-scale syntheses, process engineers track performance metrics like reaction rate and product purity. Small improvements here translate directly to cost savings at scale. Over several projects, I tracked how using this compound instead of less reliable alternatives kept material costs down, limited plant shutdowns, and made the case for further investment in synthetic development.

    Making Informed Choices: The Bottom Line

    Access to specialty reagents empowers chemists, engineers, and researchers to design smarter, safer, and more productive processes. The experience using 4-methylpyridine 1-oxide has convinced me that not all refinements in chemical supply are equal. Its unique chemical character—thanks to the N-oxide functional group and the shield of the methyl substituent—provides a controlled, flexible tool for diverse applications. Chemistry may never be simple, but working with a compound that delivers predictable results takes much of the guesswork out of discovery and innovation.

    Looking to the Future: Sustainability and Responsible Use

    Continued progress in chemical manufacturing relies on smart stewardship. As industry trends move toward reduced waste, lower toxicity, and energy-efficient syntheses, compounds like 4-methylpyridine 1-oxide open up new approaches to greener processes. My colleagues and I have debated the future of synthetic intermediates—whether bulk chemicals or boutique reagents will drive the next breakthroughs—and across both camps, there's agreement: adaptability, safety, and documented performance will take priority.

    Investment in renewable feedstocks offers promise, as does the development of recycling streams that reclaim value from every process. In working groups focused on green chemistry, I’ve encountered proposals that leverage the unique properties of N-oxides to mediate milder, catalytic transformations, cutting down on harsh reagents and wasteful steps. The trajectory suggests that 4-methylpyridine 1-oxide will play an important role not just as a workhorse reagent, but also as a model for how functional molecules can drive sustainable growth in chemicals, pharmaceuticals, and materials science.

    Supporting Team Growth and Knowledge Sharing

    Teaching and knowledge transfer remain essential for any lab looking to get the most out of their reagents. I've seen firsthand how open dialogue, from troubleshooting sessions to informal lab talks, can bring out fresh ideas for better handling, novel applications, or risk reduction. For those starting new research lines or scaling up existing protocols, feedback from people who’ve tackled setbacks or fine-tuned reaction conditions with 4-methylpyridine 1-oxide can save time, material, and frustration.

    Sharing practical tips—like the importance of controlling light, temperature, and moisture, or how to use spectral data to diagnose batch variability—turns a simple chemical into a reliable instrument. As more information emerges from published case studies and collaborative projects, teams learn not just what the compound can do, but how best to deploy it across fast-evolving fields.

    Conclusion: The Choice for Forward-Thinking Chemists

    Practical experience, documented results, and a keen eye for innovation mark out 4-methylpyridine 1-oxide as a key player in contemporary synthesis. From streamlining standard transformations to powering cutting-edge pharmaceutical or materials chemistry, it makes life easier for anyone looking to deliver reliable outcomes. Over the years, I’ve learned that investing in high-quality reagents and sharing expertise pays out in fewer errors, more robust data, and an environment where safety and creativity can flourish side by side. As demands increase and laboratories push for both performance and sustainability, compounds like 4-methylpyridine 1-oxide will continue to earn their place at the center of smart industry practice.