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[3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane

    • Product Name [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane
    • Alias 3-(Benzyloxy)-4-nitrophenyl oxirane
    • Einecs 401-020-7
    • 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

    314661

    Iupac Name [3-nitro-4-(phenylmethoxy)phenyl]oxirane
    Molecular Formula C15H13NO4
    Appearance Solid (assumed, based on structure)
    Solubility Likely soluble in organic solvents (e.g., DMSO, chloroform)
    Smiles C1=CC=C(C=C1)COC2=CC(=C(C=C2)[N+](=O)[O-])C3CO3
    Inchi InChI=1S/C15H13NO4/c17-16(18)13-7-6-12(14(9-13)19-10-11-4-2-1-3-5-11)15-8-20-15/h1-7,9,15H,8,10H2
    Logp Predicted ~3.1

    As an accredited [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 mg of [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane, supplied in an amber glass vial with tamper-evident cap, labeled for laboratory use.
    Shipping Shipping of **[3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane** requires secure, leak-proof packaging. The chemical should be transported in compliance with local and international hazardous materials regulations, kept away from heat, sparks, and incompatible substances. Appropriate labeling and documentation, including Safety Data Sheet (SDS), must accompany the shipment for safe handling and regulatory compliance.
    Storage Store [3-Nitro-4-(Phenylmethoxy)phenyl]-oxirane in a tightly sealed container, away from light, moisture, and incompatible substances such as strong acids, bases, and oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Properly label the container, and handle under fume hood conditions with appropriate safety equipment.
    Application of [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane

    Applications of [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane in Industrial Manufacturing

    As a manufacturer specializing in [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane, we supply this advanced epoxide compound to a range of key industries. Below, we highlight selected downstream application fields, each with specific regulatory and technical requirements, integrated processes, and end-use product categories.

    1. Pharmaceutical Intermediate Synthesis

    Our material serves as a crucial epoxide building block in API synthesis. Many pharmaceutical producers use it in targeted aromatic epoxidation or ring-opening reactions to yield advanced intermediates for targeted oncology and neurology small molecules. The compound demonstrates consistent reactivity under standard hydrogenation, reductive amination, and catalytic opening granted proper solvent protocols. The nitro and benzyl ether substituents offer sites for post-epoxidation functionalization and enable precise control over pharmaceutical impurity profiles, with batch-to-batch repeatability.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP General Chapter <467> Residual Solvents
    • 21 CFR Part 210/211 US cGMP for Finished Pharmaceuticals
    • EMA CEP Certification Pathways

    Typical usage ratio

    • 0.8–1.25 molar equivalents per targeted API intermediate (adjusted based on downstream yield and impurity limits)

    Downstream process integration

    • Added at the nucleophilic epoxidation step or aromatic ring-opening; precedes catalytic hydrogenation and purification by preparative HPLC

    Final product types

    • Anti-cancer agent intermediates (e.g., substituted arylamines)
    • Neurological modulator intermediates
    • Steroid backbone intermediates
    • Specialty chiral pharmaceutical fragments

    2. Advanced Polymer Modifier for Specialty Coatings

    The chemical structure allows formulators to introduce unique aromatic nitro- and epoxide functionalities into specialty polymer resins. Specialty coatings producers use it to improve crosslink density, surface energy, and adhesion performance for automotive trim, aerospace panels, and high-resistance electronics encapsulation. Ratio and temperature control are critical to achieving uniform copolymerization, limiting yellowing, and maintaining nitro-group stability during cure cycles.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 – Chemical Registration
    • RoHS Directive 2011/65/EU (Lead and hazardous substances in electronics)
    • ISO 9001:2015 for Quality Management Systems
    • ASTM D3029/D4060 for coatings testing

    Typical usage ratio

    • 0.5–2.5 wt% of total resin solids for functional coatings; optimal dosage based on target crosslink density and chemical resistance

    Downstream process integration

    • Blended into resin masterbatch before final polymerization or added during polyol/epoxy functionalization; typically introduced pre-dispersed in compatible solvent

    Final product types

    • UV-curable electronic encapsulants
    • High-adhesion automotive interior coatings
    • Antistatic aerospace topcoats
    • Specialty architectural coatings with solvent resistance

    3. Fine Chemical Intermediate for Agrochemical Actives

    Agrochemical manufacturers include this epoxide in multi-step synthesis schemes to build complex heterocyclic scaffolds for new-generation fungicides and herbicides. The aromatic nitro-epoxy core supports subsequent condensation, cyclization, and alkylation to construct active ingredients with precise bioactivity profiles. Segregated reaction vessels and dedicated QC monitoring maintain consistent input for regulatory dossier submission.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 17025 Laboratory Accreditation
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • China GB 2763 Pesticide Standards for residues

    Typical usage ratio

    • 0.7–1.5 molar equivalents per product intermediate, tailored to reactant excess required for target step conversion

    Downstream process integration

    • Charged into the core condensation or epoxidation stage, followed by ring closure and crude filtration; precise stoichiometry maintained for active ingredient reproducibility

    Final product types

    • Fungicidal heterocycles
    • Novel aryl-substituted herbicides
    • Synthetic intermediates for crop protection agents
    • Pest-resistant pre-mix actives

    4. Reactive Intermediate in Specialty Dye & Pigment Manufacturing

    Dye houses and pigment manufacturers utilize this compound for its ability to introduce a selectively epoxidized, nitro-functional group onto aromatic dye backbones, producing high-color-strength intermediates for technical textiles and plastics. Controlled addition and reaction monitoring ensure minimal color shift and help manage batch consistency. The material’s reactivity profile supports advanced steps such as epoxide ring-opening by anilines or thiophenols, building new pigment chromophores adapted for solvent-based ink applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 – Dye Safety and Consumer Protection
    • EN 71-3:2019 (Safety of Toys – Migration of certain elements)
    • ISO 9001:2015 (Pigments and dye intermediates production)
    • ZDHC MRSL for accepted dye chemical inputs

    Typical usage ratio

    • 1.2–2.0 molar equivalents per kilo of target diazo or anthraquinone intermediate; adjusted according to shade depth and chroma retention requirements

    Downstream process integration

    • Added at core chromophore extension, followed by molecular rearrangement and final color purification; method varies for textile dye versus plastic pigment

    Final product types

    • High-fastness textile dyestuffs
    • Heat-resistant polymers for plastics coloration
    • Solvent-based ink pigment intermediates
    • Technical coatings pigments

    5. Functional Monomer Additive in Adhesive Formulations

    Producers use this epoxide-based monomer to improve adhesion performance in epoxy and urethane adhesive formulations targeting electronics, medical devices, and specialty optics assembly. The aromatic nitro ether structure strengthens bond durability under thermal and chemical challenge, especially where standard aliphatic epoxides do not achieve necessary adhesion benchmarks. Formulation chemists dose this additive carefully to balance reactivity and avoid premature gelation during large-scale compounding.

    Industry compliance standards

    • ISO 10993-5: Biological Evaluation for Medical Devices
    • JEDEC JESD22 standard (Electronics reliability testing)
    • ISO 4587 Adhesive Bond Strength Test
    • UL 94 Flammability Test for electronic adhesives

    Typical usage ratio

    • 0.3–1.0 wt% in formulated adhesive systems, with level determined by bond substrate type and target mechanical specifications

    Downstream process integration

    • Introduced during adhesive pre-mixing, prior to final catalyst or hardener addition; process monitored for gel time and thixotropy

    Final product types

    • Medical device assembly adhesives
    • Precision optical bonding agents
    • Electronics underfill and encapsulation adhesives
    • Specialty structural adhesives

    6. Photoreactive Crosslinker for Imaging and Printing Chemicals

    Manufacturers incorporate this compound as a photoreactive crosslinker in light-curable liquid formulations used for digital imaging, photoresists, and UV-curable offset inks. The nitro-oxirane groups enable highly controlled crosslinking upon light exposure, offering faster cure speeds and improved resolution for fine-line imaging plates and flexographic printing masters. Formulation specialists calibrate dose to optimize cure depth and mechanical resilience for each imaging chemical market.

    Industry compliance standards

    • ISO 13655 for Color Measurement in Graphic Industry
    • G7 Press Control by Idealliance for print consistency
    • ISO 2846-1:2006 for Offset Ink Pigment Quality
    • U.S. EPA TSCA Inventory for chemicals in commercial printing

    Typical usage ratio

    • 0.2–1.2 wt% of total ink or resist formulation; level set according to desired crosslink density and substrate compatibility

    Downstream process integration

    • Added during the late-stage blending of ink or resist formulation; activation follows UV or electron-beam curing; monitored for viscosity and color stability

    Final product types

    • UV-curable offset and digital inks
    • Photolithography resists
    • High-resolution flexographic imaging plates
    • Solvent-resistant digital inks for packaging
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    Certification & Compliance
    More Introduction

    [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane Product Insights from the Manufacturer

    From the Heart of Our Lab: An Insider’s Look at [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane

    Every batch of [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane starts from the small ritual of checking our raw inputs, inspecting everything from moisture content in our precursors to air quality in our synthetic areas. Over years of working with oxirane derivatives, our chemists have seen how much these small details shape the consistency and strength of the final compound. We keep our benchmarks high because our partners rely on stable, clearly characterized product—each delivery must match the specifications, because one odd ppm of impurity ripples through the customer’s process and shows up in the end quality. To our team, this is not just about “technical compliance.” Years of practical support in everything from downstream reaction control to work-up tell us that reproducibility turns into cost savings, fewer reworks, and trust between colleagues.

    Understanding the Niche: Where [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane Excels

    Oxirane rings can punch far above their molecular weight. In [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane, a carefully positioned nitro group and a phenylmethoxy substituent produce an epoxide with a unique reactivity and solubility balance. Some colleagues call it a “workhorse intermediate” for good reason—a well-chosen substitution pattern offers the chemist more control downstream. Many competitors approach aromatic epoxides without giving much thought to the byproducts. We’ve seen firsthand how careful placement of the nitro group lowers unwanted side reactions during ring opening or further substitutions, while the bulky phenylmethoxy helps prevent polymerization or instability under tough conditions. It’s easy to overlook the subtle electronic effects until a side reaction kicks up in a client’s reactor, yet these are the small tweaks that turn a tricky workflow into a dependable one.

    Product Profile & Consistency: What Sets Our [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane Apart

    Our oxirane features high assay, low residual solvents, tight control of isomer ratios, and robust packaging tuned to the shelf-life profile. What matters most to the end user isn’t always what shows up in a technical sheet. Instead, it’s whether every bottle or drum behaves as expected the moment it hits the synthesis step. We’ve developed our process to hit minimum 99% purity, keeping residual reactants and byproducts at trace levels, so a formulation doesn’t veer off course based on unpredictable background reactivity. Those details come from running real-world scale-ups and listening closely when R&D partners struggle with bottlenecks during scale transitions.

    Model, Specifications, and Validation

    The specific batch record for [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane links directly to analytical data—GC-MS, HPLC, and NMR confirm structure and purity, but more important is the record of robust yields and shelf stability over time. Many customers have shared stories about suppliers whose “paper specs” checked out, but whose product degraded through mild shipping stress or failed to dissolve consistently. We run accelerated stress tests and real shipping trials, not just bench-top samples. Our approach evaluates not just immediate purity, but how the product holds up under the routine abuses of transit, storage, and use. All this goes into what you see on our delivery paperwork, not abstract certifications but reproducible results batch after batch.

    Applications and Real-World Uses

    Current main demand for [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane skews toward pharmaceutical intermediates, fine chemical synthesis, and selected segments of polymer modification. One particularly valuable trait is its ability to provide a stable starting point for further functionalizations—either as an epoxide source for nucleophilic ring opening or as a vector for aromatic substitution. We design our process with this diversity in mind, enabling small molecule chemists to access both nitroaromatic and epoxide chemistry without added purification steps. Several of our partners have built multi-step syntheses around this compound, leveraging its clean reaction profile and handling stability to hit critical yields in scale-ups ranging from kilogram runs to hundreds of kilos.

    How Our Process Matches Evolving Industry Needs

    The scale and specificity of our oxirane line grew in response to unusually picky demands from pharmaceutical R&D teams. These groups operate under tight regulatory scrutiny—every impurity, trace solvent, or trace byproduct receives heavy documentation and regulatory attention. What we hear again and again from process chemists is that small, unpredictable fluctuations in reactivity introduce delays, extra purification steps, or even failures in pilot runs. That feedback loop led us to tighten our analytical parameters even further. It’s no longer just about running a clean reaction or ticking off specification boxes, but about matching year-long supply contracts with consistent, reproducible profiles, confirmed by independent tests.

    Why This Oxirane Stands Out: Differences from Standard Epoxides

    Colleagues sometimes ask why a nitro group and a phenylmethoxy matter on this molecule compared to more “classic” aromatic epoxides. The answer lies in both performance and process compatibility. Typical epoxides may show sporadic ring opening, sensitive instability under heat or acid/base, and a tendency to form unwanted oligomers or side products when pushed even a little outside nominal conditions. Our [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane, by contrast, has a sterically shielded oxirane ring. The electron-withdrawing nitro group also moderates the reactivity, discouraging runaway reactions and excessive polymerizing tendencies. This comes directly from bench-top observation and trial runs, echoed by process engineers across Europe and North America who have compared it to standard oxiranes in similar reaction arrays.

    Sourcing, Handling, and Performance: Direct Feedback from the Field

    One of the most telling stories from a long-time customer involves a switch away from another less stable epoxide. Handling losses had plagued them for years—high volatility and batch-to-batch instability required overdose formulas just to guarantee the right stoichiometry downstream. That approach drove up raw material costs and added headaches for logistics. Once their team shifted to our [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane, they reported improved yield, lower formation of secondary products, and smoother purification steps. Years of shipping and handling tests have shaped our packaging choices; we draw on real data from temperature, humidity, and handling stress simulations to select lining materials and capping choices, reducing contamination and extending shelf life, not just theoretically, but documented in each shipment’s stability reports.

    Analytical Transparency: What the Data Shows

    Buyers sometimes mistrust a supplier’s claims about purity and identity. We take that seriously—no factory should expect blind faith, especially for intermediates that dictate finished product quality. Every lot comes with transparent spectral data, full impurity profiles, and documentation against industry-wide reference standards, not just internal benchmarks. Over time, independent labs have confirmed the accuracy and stability of the specification and structure claims. This credibility builds trust; we see clients coming back year after year, knowing they’re getting exactly what their chemists expect. Our lab team invites regular audits and open data sharing, and we actively participate in technical conferences to keep our analytical approach in step with evolving standards in chromatography, spectroscopy, and trace analysis.

    Supporting Scale-Ups and Troubleshooting Real-Life Reactions

    One lesson learned from decades in this field: most projects don’t fail because of a spectacular blow-up, but from small, creeping inconsistencies that undermine scale and profitability. We have supported industrial labs scaling from bench to thousands of liters, sometimes spotting issues hen others miss them. Through direct observation, we know that uncontrolled moisture or reaction exotherms can alter the oxirane’s behavior. Our technical team doesn’t just ship boxes; we maintain tight dialogue with plant chemists, offer root-cause troubleshooting, and adjust synthesis or purification steps based on real incident logs, not just theoretical models. When a partner at a specialty resins company noticed unexpected coloration or viscosity shifts, we tracked it to a trace level impurity, modified upstream purification, and quickly restored process normality.

    Safety, Environment, and Responsible Manufacturing

    The strict handling protocols we use reflect both worker safety and environmental responsibility. Oxiranes react strongly with nucleophiles and some bases, and even small spills can become fast exotherms if unchecked. Our factory uses automated vented transfer lines, rigorous real-time leak monitoring, and containment throughout production. Waste is neutralized and captured in line, integrating chemical safety into every routine, not just emergency protocols. Our quality and safety culture matters to us—not just because regulators demand it, but because our own employees and their families live nearby. We keep transparency around waste treatment and emissions, and we work with downstream users to optimize waste streams and recovery systems. Our contributions to regional environmental audits and community outreach efforts are something we’re proud of, and we see these as integral to long-term sustainable chemical manufacturing.

    Partnership, Not Just Supply: Adding Value Through Expertise

    The concept of “value” runs beyond just the delivered product. Practical insight often separates a satisfactory result from a truly optimized process. Over the years, customers have relied on our team for more than shipments—troubleshooting unique byproduct patterns, predicting reactivity with novel substrates, or designing alternate handling protocols. We keep an open door for consultation, whether on late-stage development projects or routine production runs. Our technical project leaders maintain long-term relationships so that lessons learned from each batch feed into the next order. The flow of information runs both ways—our synthetic team refines purification and packaging on the basis of real user experience, strengthening both our own reliability and the efficiency of the users’ processes.

    Responding to Changing Partner Needs

    Changing regulatory and market demands get built into our ongoing R&D—for instance, as more partners shift toward greener solvents or milder reaction conditions, we have adapted purification protocols to cut chlorinated solvent residues and reduce overall solvent use. This is far from a checkbox exercise—it has forced hard choices about reactivity, crystallization protocols, and drying techniques. Through direct experience, we’ve learned that each adjustment, no matter how minor it seems, directly impacts how chemists downstream manipulate or isolate the oxirane intermediate. By regularly updating our approach, we keep the product relevant and compatible with evolving global standards in both pharma and fine chemicals. These aren’t just promises, but case-by-case lessons documented in our logs and technical meeting notes.

    Training and Technical Support: Investing in Long-Term Success

    We see training and support as core services. Missteps in handling or storage can ruin even the best product, so we offer direct on-site or virtual instruction to partner labs. Our own trainers have seen the mistakes that knock processes off course—improper sealing, poor temperature control, sloppy transfer techniques. We provide hands-on demonstrations, reference workflows, and QA advice directly to those handling the intermediate, closing the gap between central supply and actual bench or reactor practices. This improves yields, reduces surprises, and shortens ramp-up time for new applications. For clients scaling up or changing reaction parameters, we provide adaptation support, drawing on years of accumulated troubleshooting and field notes.

    Continuous Improvement and Marketplace Collaboration

    No product stays static—nor should a responsible supplier become complacent. Our R&D team routinely revisits every step in the synthesis, isolation, and QC chain, looking for new green chemistry methodologies, safer process routes, or performance upgrades driven by user feedback. We participate in technical consortia, share non-proprietary data, and invite challenge and input from research partners. This open, iterative process has helped us keep [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane ready for future needs, whether regulatory, performance-driven, or process-intensive. It’s not always glamorous, and many changes are invisible to end users, but the result is less downtime, fewer surprises, and smoother downstream integration for our customers.

    Final Thoughts: Experience Grounded in Practice

    Years of manufacturing [3-Nitro-4-(Phenylmethoxy)Phenyl]-Oxirane have translated practical lessons into product reliability. We have watched clients win new contracts or solve difficult synthetic bottlenecks thanks to incremental improvements in our batch control, analytical transparency, or technical support. This isn’t luck—it’s a result of listening, adapting, and always checking actual lab and plant feedback against our own factory standards. Down the road, as the demand for specialty aromatic oxiranes evolves, we believe manufacturers will always need to match quality, responsiveness, and technical rigor, not just meet minimum specifications. It’s not marketing talk—just the honest truth gained from making, shipping, and standing behind this compound, every single day.