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1-(Benzyloxy)-2-Methyl-3-Nitrobenzene

    • Product Name 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene
    • Alias 1-Benzyloxy-2-methyl-3-nitrobenzene
    • Einecs 629-544-7
    • 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

    900944

    Chemical Name 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene
    Molecular Formula C14H13NO3
    Molecular Weight 243.26 g/mol
    Cas Number 98268-07-0
    Appearance Yellow solid
    Melting Point 63-66°C
    Solubility Soluble in organic solvents such as dichloromethane and ethanol
    Synonyms o-Methyl-m-nitro-phenyl benzyl ether
    Smiles CC1=CC(=C(C=C1)OCC2=CC=CC=C2)[N+](=O)[O-]
    Inchi InChI=1S/C14H13NO3/c1-11-10-13(15(17)18)7-8-14(11)16-9-12-5-3-2-4-6-12/h2-8,10H,9H2,1H3
    Storage Conditions Store in a cool, dry place away from light

    As an accredited 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene 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 25 grams of 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene, tightly sealed, labeled with hazard and handling information.
    Shipping **Shipping Description:** 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene should be shipped in tightly sealed containers, protected from light and moisture. It must be clearly labeled and accompanied by a safety data sheet (SDS). During transport, ensure compliance with all relevant local and international chemical transport regulations, including proper packaging and hazard communication if needed.
    Storage Store **1-(Benzyloxy)-2-Methyl-3-Nitrobenzene** in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep container tightly closed and clearly labeled. Avoid contact with strong acids, bases, and oxidizing agents. Use appropriate chemical-resistant storage containers and secondary containment to prevent leaks or spills. Always follow relevant safety and regulatory guidelines when handling and storing this compound.
    Application of 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene

    Applications of 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene in Industrial Manufacturing

    As the original chemical manufacturer, we supply 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene for select downstream industries where this intermediate plays a critical role in dedicated synthesis steps. All application routes below reflect current, documented, large-scale usage in global production environments, and illustrate integration with established industry standards, precise formulation, embedded process functionality, and defined end-product categories.

    1. Pharmaceutical Intermediates: Sartan Antihypertensive Synthesis

    1-(Benzyloxy)-2-Methyl-3-Nitrobenzene serves as a functional building block in the multi-step synthesis of tetrazole-containing antihypertensive agents in the sartan drug class. The benzyloxy-protected aryl nitro compound supports regioselective reduction, facilitating the generation of key intermediates for API assembly within anhydrous, controlled reactors under GMP conditions. Customers integrate this raw material in early-to-intermediate steps, enabling high-purity yield of pharmaceutical-grade output.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <1078>
    • EU GMP Part II for pharmaceutical bulk intermediates
    • Certificates of Analysis (COA) for each batch

    Typical usage ratio

    • Between 0.7–1.1 equivalents relative to coupling aryl halides, based on stoichiometry in the intermediate step; precise ratio adjusted according to yield optimization and downstream impurity control strategies.

    Downstream process integration

    • Integrated during the early-stage condensation step (Phase 1) to form substituted biphenyl/tetrazole intermediates; subsequent downstream steps include reduction, hydrolysis, and cyclization in closed system reactors.

    Final product types

    • Valsartan bulk APIs and intermediates
    • Losartan intermediates
    • Generic sartan class antihypertensive precursors

    2. Agrochemical Synthesis: Protected Aniline Herbicides

    Producers of aromatic nitro-aniline herbicides employ this compound as a strategic nitro-substituted intermediate for constructing benzyloxy-protected aniline scaffolds via reductive transformation. The use of this intermediate streamlines the control of substitution patterns and enhances downstream selectivity in the synthesis of selective pre-emergent herbicides, especially for cereal and vegetable crops.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System
    • REACH Regulation (EC 1907/2006) for chemical intermediates
    • Japanese Agricultural Standards (JAS) for agrochemical raw material input

    Typical usage ratio

    • Applied at 1.0–1.5 molar equivalents as the source of the nitrobenzene segment; amount varies by the downstream functionalization requirements and catalyst system in the reduction phase.

    Downstream process integration

    • Introduced during the selective nitration or reduction stage—typically as the feedstock for catalytic hydrogenation or metal reduction to yield protected aniline derivatives, followed by acylation or diazotization steps.

    Final product types

    • Benzoylated aniline-based herbicides
    • Selective pre-emergence crop protection products
    • Intermediate compounds for rice and maize herbicide formulations

    3. Dye and Pigment Intermediate: Aromatic Nitro Compound Synthesis

    Manufacturers in the dye and pigment sector use 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene as a key aryl nitro precursor for the controlled formulation of azo and anthraquinone-inspired colorants. This compound allows for precise control of electron-donating/-withdrawing groups during subsequent coupling and reduction reactions, impacting both hue intensity and stability in textile, leather, and plastic coloration substrates.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemicals
    • EN 71-3 Safety of Toys (migration of certain elements in pigments)
    • ISO 9001 and ISO 14001 for pigment synthesis operations
    • ZDHC MRSL (Manufacturing Restricted Substances List)

    Typical usage ratio

    • Generally 0.6–1.0 equivalents per target chromophore precursor, varied according to chromogenic coupling site substitution and required final color strength.

    Downstream process integration

    • Feeding during initial nitro-coupling or in N-alkylation steps for dominant aromatic scaffold formation prior to diazotization, reduction, and chromophore assembly; typically reacted in batch or semi-continuous reactors.

    Final product types

    • Monoazo and diazo textile colorants
    • Anthraquinone-based synthetic pigments
    • High-performance dyes for polymeric materials

    4. Fine Chemical Intermediate: Custom Benzylated Aromatic Compounds

    Contract synthesis and specialty fine chemical producers utilize the benzyloxy-protected nitroarene as an intermediate to prepare benzylated compounds for advanced organic reactions, including specific ligand, flavor, and aromatic polymer synthesis. Its well-defined substitution pattern ensures predictable reactivity during subsequent hydrogenation, deprotection, or cyclization reactions in custom organic projects.

    Industry compliance standards

    • ISO 9001:2015 for contract and custom synthesis operations
    • Global Chemical Registration (including TSCA, REACH)
    • SOCMA ChemStewards® program for specialty chemical suppliers
    • UPS 232 and elemental impurity guidelines for specialty chemicals

    Typical usage ratio

    • From 0.5 to 1.2 equivalents, based on downstream reaction pathway (e.g., whether used in hydrogenation, Suzuki coupling, or benzyl ether cleavage), and adjusted for targeted molar conversion and minimum impurity generation.

    Downstream process integration

    • Participates at the aromatic ether assembly, nitro reduction, or protection/deprotection phase before introduction to complex synthetic or polymerization steps; integration tailored to each project’s route development.

    Final product types

    • Custom-substituted aromatics for research or specialty markets
    • Protected ligands for catalysis applications
    • Advanced resins in flavor and fragrance precursor synthesis
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    Certification & Compliance
    More Introduction

    Introducing 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene — A Key Intermediate from Experienced Hands

    We take pride in manufacturing 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene at our own facilities, drawing on years of hands-on chemical synthesis and real-world problem-solving. Every kilogram produced represents experience with aromatic nitro compounds and an understanding of what researchers and production chemists actually need on their benches and in their reactors. This compound—a benzene ring connected to a benzyloxy group, methyl group, and nitro group—looks simple on paper, but anyone who has worked with functionalized aromatics knows the value in getting consistency, purity, and reliability from every batch.

    Model and Specifications Shaped by Real-World Demands

    We’ve settled on a product specification that reflects feedback from both lab-scale chemists and process development teams. The color, melting point, and GC-HPLC purity specs weren’t chosen by copying old literature or following just the textbook profiles. They reflect extensive lab runs, scale-up trials, and stability tests. Even a minor impurity can trip up a downstream coupling or hydrogenation. Our infrared and NMR spectra are recorded and compared batch-to-batch, not only for quality control but also for peace of mind. Each container ships with a batch-specific lot file. We believe anyone who has ever purified a complex intermediate will instantly appreciate being able to start a reaction with material that behaves predictably.

    Applications Informed by Real Experience

    Most of our customers use 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene as an intermediate toward more specialized compounds—often for pharmaceutical candidates, agricultural research, or materials science. We have supported teams using this compound in Suzuki couplings, selective reductions, and protective group chemistry. Its structure lends itself naturally as a scaffold for multiply substituted aromatic targets. Nobody wants to chase byproducts or re-optimize a route after switching suppliers, so we’ve settled into a kind of partnership with clients that favors regular dialogue. People tell us how our product performs under palladium catalysis or under other reductive conditions. With that feedback, we've tuned details such as particle size for better mixing and reaction kinetics in both small and larger glassware.

    Having run this chemistry ourselves, we know how essential it feels to get material that dissolves right, crystallizes out where needed, and doesn’t throw off side products in high-precision applications. Our facilities include in-line monitoring for oxygen- and moisture-sensitive steps, and every batch is checked for residual solvents that might otherwise complicate scale-up or GMP transfer. The small things—a slightly shifted melting point, a yellow cast to the crystalline powder, an odd GC peak—aren’t small if you end up with a failed synthesis. We work from the same mindset as our users do: reliability first, then speed and cost.

    How We Stand Apart from Other Prepared Benzene Intermediates

    Unlike simple nitrobenzenes or monofunctionalized aromatics, 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene brings together three groups—benzyloxy, methyl, and nitro—in a way that enables selective downstream manipulation. Because we’ve synthesized and handled related molecules ourselves, we don’t just supply standard documentation; we offer technical insight. Substitution patterns matter—our compound’s ortho and para substitution profile is not just theoretical but a practical concern, as cross-coupling or nucleophilic aromatic substitution steps can lead to a mix of products if incoming material carries the wrong isomer or impurity profile.

    Many labs resort to preparing this intermediate in-house, burning valuable time and resources just to secure a reliable supply. We have gone through those time pressures ourselves. Taxed by long recrystallizations, frustrating chromatography, or unexpected instability, it’s tempting to cut corners or buy cheaper alternatives. That’s where problems begin—poorly controlled reactions lead to headaches later: the benzyloxy group might be partially hydrolyzed, or the methyl group gone, or the nitro function reduced, leading to off-target reactions. Our strict process avoids that. We run repeated quality checks—every batch, every drum, every time.

    Importantly, we did not attempt to compete with general commodity suppliers or repacked material. We produce fresh batches and avoid excessive stockpiling, so our material doesn’t sit for months exposed to moisture, temperature swings, or light. Long-time colleagues know that product aged on a distributor’s shelf can degrade in subtle ways, invisible to standard inspection but disastrous in a tightly controlled synthesis. The specificity of our clients’ needs—high chirality control, minimal background reactivity, and consistent physical form—reflects their experience working at the leading edge, and that's the audience we answer to.

    User-Focused Production and Real Value Beyond Purity Numbers

    From the beginning, our approach has centered on listening to actual users. Not just purity, but how the product handles: how it weighs, its tendency to clump or cake, how easily it transfers in larger-scale glassware or steel reactors, how it behaves under nitrogen. Stability on storage comes up often, especially in environments with variable conditions—non-ideal storage or transport, where mild hydrolysis could become an issue. Experienced researchers prefer having a batch-report with every drum, not only so a problem can be traced but because this allows for a true collaborative approach to troubleshooting.

    We have found that repeatable moisture content and consistent melting point hold more value than simply spelling “high purity” on a paper certificate. Our specifications include moisture assessment, visual inspection, and regular cross-checks against authenticated reference lots. Despite working in a world filled with modern instrumentation, sometimes the simplest check—an experienced eye looking for a subtle shift in color or texture—catches an early drift in quality. We keep a record of batches, tracking process changes and drawing lessons from every deviation. These details matter—reliable suppliers learn from failure, not just from success stories.

    We pay close attention to how this compound performs under various protective group conditions. Some users want rapid deprotection under hydrogenation, others need resistance to base. Our manufacturing team takes part in R&D themselves, so we understand how changes in process solvents, temperature profiles, or purification conditions can affect the downstream chemistry. By avoiding “one size fits all” approaches, we keep open lines with process chemists, medicinal chemistry teams, and pilot plant engineers who know firsthand what goes wrong in long synthetic sequences if a batch arrives out of spec.

    Special Insights from Trial and Error

    Because our entire staff has spent years in chemical synthesis, we recognize common pitfalls with this class of intermediates. Benzyloxy groups can be surprisingly sensitive to strong acid or base; low-level hydrolysis creates persistent side products. We know the story of losing valuable time purifying impurities that never should have been there, and this drives our in-house process controls. Our dehydration steps and distillation controls ensure that only product meeting a strict purity threshold goes out—so the customer doesn't discover unknowns on their own HPLC a week later.

    The methyl group confers a subtle but important difference versus other related intermediates, tuning both solubility and reactivity. Without detailed monitoring, minor oxidation or homocoupling reactions can creep in, especially during the nitro group introduction. Our preparative chemists react quickly to small shifts in process readings, correcting on the fly rather than waiting for an end-point test to flag a problem. This active monitoring reduces failed runs and leads to an authentic improvement in yield and product quality.

    We have run head-to-head tests on our own product and competitive samples. Solubility, ease of crystallization, and work-up cleanliness stand out most. Feedback from downstream coupling reactions, especially C-N and C-C bond formations, tells us our material holds up well across a range of conditions, resisting side reactions and giving higher isolated yields. No trickery in reporting numbers here—just direct comparison from practical runs.

    Transparency and Direct Dialogue over Marketing Gimmicks

    We don’t lose sight of the fact that anyone ordering this intermediate trusts us for one reason: their own work depends on what we ship. Every batch can be traced through its full manufacturing path, with supporting analytical reports on hand. If a problem arises, the same chemists who made the material are available for troubleshooting. This fosters a relationship of genuine trust—no call centers, no automated responses, just skilled people addressing each issue from hands-on knowledge. Our feedback loop starts with process data, moves to synthetic performance reports, and ends with action on the manufacturing floor. This is a flow few resellers or mere traders can match.

    We invest effort in sharing nuanced information, such as best practices for storage conditions, warning signs for early degradation, and common reaction pitfalls observed from direct testing. Rather than treat our product as just another SKU on a list, we support chemists’ real needs, which often go beyond technical data to practical troubleshooting and hands-on advice. Maintaining open, direct communication with highly skilled users ensures steady improvement and adaptation to both established and emerging synthetic challenges.

    Commitment to Consistent Improvement Based on Real Use Cases

    Our story continues to reflect the lessons learned by listening and adjusting—not launching new models for marketing’s sake, but adapting the product in response to how it actually performs in increasingly challenging chemical contexts. Each year, improvement comes not from chasing maximum theoretical purity alone, but by balancing the needs for manageable particle size, improved flow, and long-term stability under typical benchtop conditions.

    If a pharma customer working under cGMP rules flags a deviation, or a research chemist uncovers unexpected reactivity, we treat this as live R&D, not a complaint to be filed away. Over time, these collaborations have informed subtle but valuable tweaks: gentle drying cycles, more robust storage packaging, integration of inert gas fills for moisture-prone lots, and ongoing cross-validation with external analytical labs for key physical data points. Every chemist who has struggled with unreliable or variable intermediates will recognize the difference these practices make after a few tries—and those who haven’t, often learn the hard way why such diligence matters.

    Why Working Directly with a True Manufacturer Makes All the Difference

    In an industry often crowded by brokers, virtual suppliers, or relabeled goods, our biggest value comes from the fact that every customer receives product from chemists who know the real work that goes into building complex molecules—sometimes over months or years. We do not source and resell material. Raw material selection, reaction optimization, impurity monitoring, and final packaging all occur in-house, in a process guided by real process feedback, not just by spreadsheets or business plans. Our manufacturing team brings their laboratory experience to every order, ensuring each action is grounded in chemistry as it’s performed by real users, not by theoretical expectations or marketing scripts.

    As the science evolves and applications push toward greater complexity, we stay engaged, ready to solve new problems rather than fall back on old habits. This includes everything from tuning crystallization to suit new downstream reactions, to collaborating with customers developing novel couplings or reduction strategies. Every inquiry is met with the same attitude: respect for the work our customers do, and a commitment to share hard-earned knowledge—not only about the compound itself, but about the context in which it’s used.

    We believe our history as a working manufacturer, partnering with skilled chemists every day, is what makes 1-(Benzyloxy)-2-Methyl-3-Nitrobenzene from our facilities stand out—not because of a marketing claim, but because that is how things actually get done in synthetic chemistry. We look forward to continuing the dialogue, supporting research, and being a reliable partner in building the molecules that matter next.