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4-(Benzyloxy)Pyridine N-Oxide

    • Product Name 4-(Benzyloxy)Pyridine N-Oxide
    • Alias BPO
    • Einecs 629-646-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    525327

    Chemical Name 4-(Benzyloxy)Pyridine N-Oxide
    Molecular Formula C12H11NO2
    Molecular Weight 201.22 g/mol
    Cas Number 61890-47-9
    Appearance White to off-white solid
    Melting Point 83-86 °C
    Solubility Soluble in organic solvents such as DMSO and methanol
    Purity Typically ≥98%
    Smiles C1=CC=C(C=C1)COC2=CC=[N+](O-)C=C2
    Inchi InChI=1S/C12H11NO2/c1-2-4-11(5-3-1)9-15-12-6-8-13(14)10-7-12/h1-8,10H,9H2
    Storage Conditions Store at 2-8 °C, protected from light
    Synonyms 4-Benzyloxypyridine N-oxide

    As an accredited 4-(Benzyloxy)Pyridine N-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 containing 10 grams of 4-(Benzyloxy)Pyridine N-Oxide, labeled with chemical name, CAS number, and hazard information.
    Shipping 4-(Benzyloxy)Pyridine N-oxide is shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. Packaging complies with chemical safety regulations, ensuring the compound remains stable during transit. Typically, it is dispatched via priority courier with full documentation, and handling instructions are provided for safe receipt and storage upon arrival.
    Storage 4-(Benzyloxy)Pyridine N-oxide should be stored in a tightly sealed container, protected from light and moisture, and kept at room temperature (20–25 °C). Store it in a cool, dry, and well-ventilated area away from incompatible substances such as strong acids or oxidizers. Ensure proper labeling and avoid exposure to heat or open flames. Always follow standard laboratory safety protocols.
    Application of 4-(Benzyloxy)Pyridine N-Oxide

    Applications of 4-(Benzyloxy)Pyridine N-Oxide in Industrial Manufacturing

    4-(Benzyloxy)Pyridine N-Oxide serves critical synthetic roles in advanced chemical production environments that require precise reactivity harnessed for specialty chemical, pharmaceutical, and agrochemical sectors. As the original manufacturer, we supply this intermediate for technical processes with tightly regulated requirements, where consistency, traceability, and compliance are essential.

    1. API Intermediate Synthesis for Antiviral Drugs

    This intermediate is integral during the late-stage functionalization steps for certain pyridine-based antiviral actives, contributing to regioselective N-oxidation and downstream heterocycle construction. Major pharmaceutical manufacturers utilize it in controlled, validated cGMP environments, with inclusion tightly linked to maintaining psycho-chemical purity and regulatory acceptability of target APIs for human use.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7 guideline)
    • European Pharmacopoeia (Ph. Eur.) Monograph 2.9.40 on Residual Solvents
    • US FDA 21 CFR Part 210 & 211
    • ICH Q3A/B for Impurities and Residuals

    Typical usage ratio

    • Used at 0.8–1.5 molar equivalents relative to the nucleophilic pyridine substrate, with adjustment based on process yield and impurity profile during scale-up campaigns.

    Downstream process integration

    • Introduced after ring closure steps in multi-step synthesis, followed by reaction work-up and isolation via preparative chromatography or crystallization. QC analysis ensures competing side products remain within regulatory thresholds.

    Final product types

    • Crystalline antiviral APIs (e.g., nucleoside and non-nucleoside reverse transcriptase inhibitors)
    • Pyridine-based prodrugs for clinical development pipelines

    2. Agrochemical Active Ingredient Building Block

    Formulators of selective herbicides and plant growth regulators use this intermediate to construct dipyridine-based active moieties. The compound’s presence ensures site-specific N-oxide introduction, required for generating herbicide selectivities across different crop applications. Agricultural synthesis runs rely on strict traceability and environmental compliance from raw material input to finished product registration.

    Industry compliance standards

    • ISO 9001:2015 Quality Management (agrochemical supply chain)
    • FAO/WHO specification 283/2022 for Technical Active Ingredients
    • European Union Regulation (EC) No 1107/2009 for Plant Protection Products
    • REACH (Regulation (EC) No 1907/2006) substance registration if market >1 tonne/year

    Typical usage ratio

    • Applied at 3–5% wt/wt of core reaction mass in the synthesis of active ingredient precursors, scaled according to batch size and required yield in pilot or commercial runs.

    Downstream process integration

    • Dosed during the controlled oxidation phase after initial coupling/reaction, with in-process GC and HPLC tracking to ensure specification adherence when transitioning to isolation and formulation steps.

    Final product types

    • Pre-formulated herbicide technical concentrates
    • Plant growth regulator actives for branded agrochemical products

    3. Specialty Catalysis Ligand Precursor for Fine Chemical Synthesis

    Producers of homogeneous catalysts for precision organic transformations select this intermediate to prepare N-oxide-based ligand scaffolds. It is favored for its influence on electronic density of ligand systems, supporting process intensification and high catalytic selectivity in downstream applications involving oxidations and cross-couplings.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management (chemical processing)
    • Responsible Care® Global Charter for specialty chemicals
    • GMP for Specialty Chemicals (custom chemical tolling environments)
    • Local wastewater and air emission standards (EU BREF, EPA National Emission Standards for Organic Chemicals)

    Typical usage ratio

    • Typically 0.5–2.0 equivalents versus halogenated aryl substrates, quantity adjusted to optimize ligand formation and minimize unreacted N-oxide residuals.

    Downstream process integration

    • Added during ligand assembly synthesis before coordination to transition metals; downstream purification includes column chromatography or solvent extraction, validated by NMR and HPLC for batch release.

    Final product types

    • Homogeneous catalyst complexes (e.g., for Suzuki coupling or aerobic oxidation)
    • Custom ligands for fine chemical manufacturing and research reagents

    4. Intermediate for Advanced Material Surface Modification

    Manufacturers of functionalized polymer materials and specialty resins integrate this intermediate when engineering nitrogen-containing surface functionalities. Its controlled reactivity tailors surface charge, hydrophilicity, and chemical durability in advanced composite and filtration media. Strict quality protocols govern its integration to maintain reproducibility and application-relevant performance parameters.

    Industry compliance standards

    • ISO 10993-5 for cytotoxicity (when targeting medical-grade polymers)
    • ASTM D638 for physical and mechanical polymer properties
    • ISO 9001-certified quality control on batch release
    • RoHS Directive (2011/65/EU) for electronic material markets

    Typical usage ratio

    • Introduced at 0.1–1.2% by weight of polymer mix, with precise dosing dependent on target surface loading as verified by XPS or FTIR analysis post-modification.

    Downstream process integration

    • Charged during post-polymerization modification stage or melt blending, with subsequent extrusion, molding, or lamination according to end product specification. Final QC includes contact angle measurement and leachability testing.

    Final product types

    • Specialty filtration membranes (e.g., for solvent purification)
    • Functionalized composite sheets for high-performance assemblies

    5. Photoreactive Intermediate in Electronic Material Synthesis

    Electronic material producers incorporate this compound in the synthesis of nitrogen-containing photoresist additives and molecular electronic layers. The N-oxide structure enables stable electron-donating groups pivotal for photopattern definition and charge transport modulation. All manufacturing steps operate under strict cleanroom and quality controlled systems to ensure device grade reliability.

    Industry compliance standards

    • JEITA ET-7302 (technical requirements for photoresists)
    • ISO 14644-1 cleanroom standards in semiconductor fabrication
    • IEC 62474 material declaration for electronic applications
    • Restriction of Hazardous Substances (RoHS) and REACH applicable to microelectronics

    Typical usage ratio

    • Formulated at concentrations of 0.5–3.0% within photoresist or electronic solution polymer blends, proportion tuned for lithography method and target device architecture.

    Downstream process integration

    • Blended during additive synthesis step prior to the preparation of photoreactive co-polymers, followed by casting, spin-coating, or printing on microelectronic substrates, with in-process monitoring via UV-Vis and conductivity measurements.

    Final product types

    • Nitrogen-rich photoresist films for IC fabrication
    • Specialty organic electronic layers for advanced display and sensor components
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    Certification & Compliance
    More Introduction

    4-(Benzyloxy)Pyridine N-Oxide: Experience-Driven Quality for Researchers and Innovators

    In the past decade, research labs and process chemists have welcomed a wave of highly functional N-oxides into their experiment routines. Among all the specialty chemicals we've been trusted to produce, 4-(Benzyloxy)Pyridine N-oxide stands out for its unique role in synthetic routes and fine chemicals development. Drawing from years on the plant floor, handling both pilot and production-sized syntheses, I’ve seen why this molecule finds consistent value among both bench researchers and scale-up teams in pharmaceutical and materials research.

    What Defines Our 4-(Benzyloxy)Pyridine N-Oxide?

    For our current model, we manufacture a compound with the molecular formula C12H11NO2. Chemically, the structure brings together features from the benzyl-protected oxygen group and the electron-rich pyridine N-oxide nucleus. The batch process at our site delivers a fine white to off-white solid, free-flowing and ready for use in organic synthesis; particle control and moisture exclusion count for a lot in maintaining shelf stability. We produce lots ranging from grams to dozens of kilograms, a strategy that helps us support custom orders and meet spikes in demand without raising lead times. Spectroscopic purity sits above 98%, confirmed by NMR and HPLC, so material comes ready for even the most sensitive synthetic protocols.

    Why Chemists Choose This Molecule

    Batches of 4-(Benzyloxy)Pyridine N-oxide get picked up by both medicinal chemistry teams and academic groups seeking selective N-oxide reactivity. Looking back on projects where this molecule made the difference, I see three big reasons for its steady popularity. The benzyloxy group serves as a protecting group, masking reactive sites until a specific step demands their unveiling. The pyridine N-oxide framework displays gentle nucleophilicity, which can be fine-tuned via benzylic protection. Working with this molecule in our reactors, we saw how predictable chemistry and good bench handling permit precise modifications down the line. A veteran synthetic chemist might reach for this compound while designing C–H activation reactions, orchestrating oxidations, or building more complex scaffolds for further functionalization.

    Some years back, a pharmaceutical project relied on this N-oxide when exploring late-stage functionalization of aromatic systems. We saw the team quickly converting it to achieve chemo- and regioselective substitution, yielding key intermediates blocked by traditional approaches. As a manufacturer, seeing our product do heavy lifting in late-phase R&D feeds back into how we optimize for batch consistency and purity.

    Model and Specifications, Developed Through Practical Experience

    While we avoid overcomplicating process controls, precision plays a role throughout. Raw material selection, temperature staging, solvent choice, and reaction time all influence the resulting quality. Based on years operating reactors, I can say that controlling water content and limiting basic impurities pays off in downstream vessel cleaning, not just purity numbers. Our process brings typical batch purities up to 98.5% minimum by HPLC; this fits most needs of process chemists and academia, who rarely want to spend extra time purifying intermediates when a reaction is challenging. Appearance may seem cosmetic, but minimizing fines during post-reaction workup keeps product losses down and makes lab handling far less stressful.

    Particle size and powder flow can shift from supplier to supplier. We keep median size in a user-friendly range by optimizing crystallization, aiming for smooth transfer and minimal clumping during standard weighing routines. Once a major project required a micronized variant: we modified our entire downstream crystallization to match those specs, because matching the end-user’s workflow mattered more than flexibility. Our customers appreciate not having to mortar and pestle or sieve. This practical feedback forms the backbone of why we settle on certain specs.

    How Our Product Stands Out

    Unlike commodity-grade pyridine N-oxides or more generic building blocks, 4-(Benzyloxy)Pyridine N-oxide demands a tailored synthetic path. Many lower-grade products arrive with problematic byproducts, such as unreacted benzyl halides or residual pyridine. These reduce predictability in downstream chemistry. We spent several seasons refining our workup to address these concerns: selective extractive washes, high-vacuum drying, and filter cake refluxing, each borrowed from problems seen at scale when a less rigorous process was followed. This type of attention to contaminant profile brings clear value when used as an intermediate for pharmaceuticals, where even low levels of bench contaminants create analytical headaches.

    Compared to similar N-oxides with different substituents, the benzyloxy group gives researchers a controlled handle for further manipulation, unlocking a wider range of transformations. I watched a team leverage this structural feature in photoredox catalysis, achieving radical-based couplings previously out of reach with other N-oxides. Other analogues might bring quicker reaction times but usually lack this balance of stability and tunability. This product, which we originally optimized for one custom project, has since enabled entirely new reaction sequences in more than a dozen different customer workflows.

    Reliability in Supply Chain and Operation

    From a manufacturing perspective, consistency does more than smooth out research hurdles. It prevents loss at bench-scale and de-risks process transfers. We set up our production to align with changing order volumes, because exploration in research doesn’t follow strict timetables. Twice in recent years, global regulatory pressure on chemical imports brought sudden interest in local sourcing; our ability to respond with quality-assured, reproducible material made a difference for teams facing tight development windows. This same flexibility strengthens collaborations with multinational clients, where traceability across batches assures valid data submission in regulatory dossiers.

    Handling requirements pop up in conversations: careful packing to exclude humidity and minimize static soiling, and recommending cool, dark storage. Shipments reach researchers ready to use, not needing further adjustment or drying. This is something only a manufacturer tracking their own process from start to finish can promise. Several global labs flagged problems with inconsistent flow and crystallinity from third-party suppliers, and our team invested in new milling and sieving equipment as a direct response. We don’t just check boxes for documentation; each step reflects roadblocks researchers have shared with us. Working with product every day, in kilogram batches, highlights where subtle adjustments improve overall lab experience.

    Supporting New Chemistry and Emerging Applications

    Creative chemists find novel uses for this molecule almost every year. Beyond classic synthetic transformations, 4-(Benzyloxy)Pyridine N-oxide steps in as a ligand scaffold, oxidant, and transient directing group. Our own collaborations with academic partners brought up interesting catalytic phenomena—especially in metal-catalyzed arylations and heterocyclic functionalizations. Keeping these conversations open helps us see which future specs or variants researchers expect next. Once, a project required an enantiomerically enriched derivative; getting feedback early let us build that feature into the next development cycle and test various prep and resolution methods right on our pilot plant equipment.

    Materials science teams run their own flavor of process, sometimes looking for a tweak in crystallinity, sometimes purity, sometimes just delivery timing. We're set up to adapt because long-term clients have shaped our synthesis, packaging, and QC. Rather than focusing on 'high throughput' alone, we put in extra man-hours to ensure trace contamination—especially trace metal and halide—is kept well below the limits needed for future tech like OLED materials, specialty polymers, and high-value imaging agents. In each of these growth areas, the molecule’s combination of stability, solubility, and reactive site accessibility keeps finding new value.

    Comparison With Related Chemical Building Blocks

    Some colleagues ask how this product stacks up against other protected pyridine N-oxides or even against the unprotected parent compounds. In my view, regular pyridine N-oxide often brings more problems than solutions to custom syntheses: more sensitivity to moisture, unpredictable crystallization, and less straightforward downstream deprotection. The benzyloxy variant finds a sweet spot—stable enough for storage, yet reactive when nudged under the right conditions. We’ve fine-tuned the benzylic protection dynamics, supported by end-user feedback describing smoother deprotection with hydrogenolysis, and observed better compatibilities in one-pot, multi-step processes.

    Comparisons with para-methoxy or alkyl-substituted N-oxides highlight further tradeoffs. The benzyl-protected oxygen endows both steric effects and a modicum of lipophilicity, opening options in hydrophobic media. Those small process details have cropped up in customer trials using greener solvents or continuous-flow reactors, where partitioning or mass transfer issues matter more than in classic batch chemistry. Our teams ran side-by-side trials and watched the difference as soon as the solvent was switched or the synthesis scaled up.

    Process Understanding Drives Quality

    While the science of N-oxide synthesis gets plenty of literature coverage, the day-to-day reality of reliably making high-quality material takes hands-on knowledge. Over the years, our crew saw how sources of failure—sub-optimal stirring, off-ratio feeds, carryover of trace metal, or inconsistent drying—led to head-scratching results for customers. We document each tweak, validate with fresh spectroscopy, and feed those data back into future runs. If a bench chemist mentions slight yellowing or clumping, we track raw material lots for possible changes upstream and share insights with the QC team. This process handling discipline makes a difference in when customers count on our material to work each time, not just for a lucky batch.

    Customers sometimes seek variants: extra low-water content, custom blending, or finer granulometry. We adjust our process parameters because our role goes beyond simply shipping a jar. One particular lot destined for a photochemistry project needed micron-grade sizing; after retooling our crystallization and filtration, that customer reported more consistent results, and we incorporated the new process as an option for similar customers. That kind of interplay between user need and factory practice brings home what chemical manufacturing looks like today: it’s about agility and feedback, not simply scale.

    Engagement With the Community of Practice

    Regular engagement with R&D chemists, project managers, and process engineers shapes the ongoing refinement of this product. Lab visits, supplier audits, and phone conversations leave us with a constant stream of feedback—new reaction conditions, alternate purification demands, and updated regulatory compliance. We monitor shifts in best practices, and stay prepared to offer full traceability and custom documentation accompanying every batch. This open loop builds credibility, and keeps us a trusted partner for innovators and established companies alike.

    Beyond the technical, relationships guide continual improvement. We run benchmarking studies against market alternatives, sharing side-by-side NMR, HPLC, and performance data with clients who want evidence, not just claims. Occasionally, a project has been won or lost by just a fraction of a percent higher purity or better controlled melting profile. Each time, our commitment to hands-on improvement puts us in a place to meet that need, so new projects get underway confidently using our product as a launchpad.

    Environmental and Safety Considerations: Doing Better by Knowing Better

    Running a manufacturing site involves constant vigilance about best practices in safety and environmental stewardship. Our production routes have shifted over the years toward greener oxidants, better solvent recovery, and minimized waste. On the floor, this translates to smaller environmental footprints—fewer air emissions, reliable recycling of solvents, and batch documents that satisfy internal and external audit. These practices matter because many end users care as much about responsible sourcing as they do about chemistry; our shared progress in this area started long before it became an external requirement.

    Recommendations for safe handling, packing, and shipping stand as practical advice learned through real mishaps and solution sharing. We avoid overpacking, instead relying on solid primary containment, desiccant usage, and safe stacking rules. Customers regularly provide feedback on package resilience and consistency; we factor this into both product protection and disposal ease. From firsthand experience, mitigating dust exposure and routine PPE recommendations reflect not just compliance, but common sense built on years of operating actual facilities.

    The Path Ahead: Adapting to an Evolving Chemical Landscape

    Looking forward, the market’s appetite for customized and high-integrity building blocks is only growing. 4-(Benzyloxy)Pyridine N-oxide, by virtue of its utility and flexibility, sits well positioned as a foundation for new chemical space exploration. Newer synthetic methods (photoredox, flow chemistry, biocatalysis) all stand to benefit from predictable, tunable intermediates like this one. Keeping manufacturing agile, responsive to both regulatory and technical trends, remains central to our approach.

    Direct dialogue with researchers keeps us accountable and spurs ongoing product evolution. As new analytical benchmarks arise, or as specialty requirements enter the mainstream, we adapt. Open sharing of technical data, batch documentation, and a focus on real-world problem solving keep our product delivering value beyond base molecular identity. Whether the goal is novel aryl functionalization, safer batch operation, or a greener synthetic process, we support this chemical community with continuously improved supply and solutions.