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4-Benzyloxy-3-Nitroacetophenone

    • Product Name 4-Benzyloxy-3-Nitroacetophenone
    • Alias NBENZ
    • Einecs 429-620-6
    • 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

    240404

    Name 4-Benzyloxy-3-Nitroacetophenone
    Cas Number 35049-72-4
    Molecular Formula C15H13NO4
    Molecular Weight 271.27 g/mol
    Appearance Yellow crystalline powder
    Melting Point 114-117°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents like DMSO and ethanol
    Smiles CC(=O)C1=CC(=C(C=C1)OCC2=CC=CC=C2)[N+](=O)[O-]
    Inchi InChI=1S/C15H13NO4/c1-11(17)12-7-8-14(16(18)19)10-15(12)20-9-13-5-3-2-4-6-13/h2-8,10H,9H2,1H3
    Storage Conditions Store at room temperature, protected from light and moisture

    As an accredited 4-Benzyloxy-3-Nitroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical, 4-Benzyloxy-3-Nitroacetophenone, is supplied in a sealed 25g amber glass bottle with tamper-evident cap and hazard labeling.
    Shipping 4-Benzyloxy-3-Nitroacetophenone is typically shipped in a tightly sealed, chemical-resistant container to ensure stability and prevent contamination. The package is labeled according to regulatory standards, including hazard information. It is handled and transported as a laboratory chemical, following all applicable safety and environmental guidelines to ensure safe delivery.
    Storage 4-Benzyloxy-3-nitroacetophenone should be stored in a tightly sealed container, protected from light, heat, and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and reducing agents. Ensure storage in accordance with local regulations and label the container clearly to prevent accidental misuse or exposure.
    Application of 4-Benzyloxy-3-Nitroacetophenone

    Applications of 4-Benzyloxy-3-Nitroacetophenone in Industrial Manufacturing

    4-Benzyloxy-3-Nitroacetophenone serves as an essential intermediate for downstream chemical transformation in fine chemicals and pharmaceuticals. We supply this material directly to leading manufacturers engaged in strict regulatory production chains. Below we outline key application sectors, providing detailed insights into compliance, ratios, process steps, and final product categories.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antimicrobial Drugs

    Our 4-Benzyloxy-3-Nitroacetophenone is a crucial starting compound in the synthesis of certain nitroaromatic-based antimicrobials. Process chemists rely on its reactivity for regioselective transformations during the assembly of complex aromatic pharmaceuticals, including precursors to dihydrofolate reductase inhibitors. Manufacturing lines introduce this intermediate during early-stage construction of the aromatic core, followed by hydrogenation, substitution, and acylation operations under cGMP conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) Category: Excipient and intermediate verification
    • European Pharmacopoeia (Ph. Eur.) Chapter 2.1.2 Purity of chemical substances
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • 5–20% by molar ratio, adjusted based on target yield and efficiency of key coupling reactions; purity requirements range from 98% to 99.5%

    Downstream process integration

    • Introduced as the primary aromatic intermediate during the initial synthesis step after raw material charging and prior to functional group modifications
    • Subjected to reduction or nucleophilic substitution before coupling with heterocyclic fragments

    Final product types

    • Nitroaromatic antimicrobial drug substances
    • Pharmaceutical intermediates for sulfonamide antibiotics
    • Dihydrofolate reductase inhibitor APIs
    • Specialty fine chemicals for advanced API synthesis

    2. Specialty Agrochemical Intermediate

    Agricultural chemical producers use this material as a structural building block for advanced herbicidal and fungicidal compounds. It enables selective introduction of benzyl and nitro groups essential for activity modulation in several proprietary agrochemical scaffolds. Production systems feed the compound into the process loop at controlled concentrations, ensuring compliance with international agriculture regulations and minimizing unwanted by-products.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA (US) 40 CFR, Part 169.2 (Agrochemical manufacturing standards)
    • ISO 9001:2015 (Quality management in agrochemical supply chain)
    • REACH Annex XVII (EU Restriction Protocols for Intermediates)

    Typical usage ratio

    • 3–10% by active ingredient weight in the synthesis batch; adjusted for conversion efficiency and regulatory residue thresholds

    Downstream process integration

    • Charged at the aromatic derivatization step, prior to the conjugation of amide or ester groups
    • Tested for residual solvents before use in the synthesis pipeline

    Final product types

    • Pre-emergence and post-emergence herbicide intermediates
    • Systemic fungicide precursors
    • Advanced pesticide actives with enhanced selectivity profiles
    • Crop-specific agrochemical raw materials

    3. Fine Chemical Intermediate in Dye and Pigment Synthesis

    The benzyl and nitro substitution pattern of this compound enables its application in the production of high-purity synthetic dyes and organic pigments. Textile chemical manufacturers employ it for selective oxidative reactions and coupling processes to create pigments with improved color fastness and brightness. It enters dye synthesis during the formation of azo or anthraquinone frameworks, undergoing precise process monitoring in compliance with environmental controls.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile chemical safety for dye intermediates)
    • REACH Annex XIV (EU candidate list of substances of very high concern)
    • ISO 14001:2015 (Environmental management systems for dye plants)
    • German Hazardous Substances Ordinance (GefStoffV) Section V for colorant manufacture

    Typical usage ratio

    • 5–15% by weight, adjusted for chromophore formation and batch color uniformity; higher ratios applied for deep tone pigmentations

    Downstream process integration

    • Added after the initial aromatic etherification, prior to diazotization or coupling reactions
    • Critical junction in scale-up where batch traceability and impurity control are enforced

    Final product types

    • Reactive and disperse dyes for textile and leather finishing
    • Organic pigments for inks, plastics, and coatings
    • Intermediate colorants for specialty print chemicals
    • High purity pigments for technical and automotive applications

    4. Intermediate for Liquid Crystal Material Synthesis

    Electronics material manufacturers use 4-Benzyloxy-3-Nitroacetophenone to produce advanced intermediates required in the tunable refractive index segment of liquid crystal materials. It facilitates precise introduction of polar and electron-withdrawing groups, supporting the formation of mesogenic structures suitable for high performance displays. The feed material integrates into the esterification or cyclization stage in the synthetic process, controlled under stringent non-contamination protocols.

    Industry compliance standards

    • IEC 61249-2-21 (Materials declaration for electronic components)
    • RoHS directive 2011/65/EU (Restriction of hazardous substances relevant for electronics)
    • JEITA ET-7304A Guideline (Quality assurance in electronic material production)
    • ISO 9001:2015 (Material supply to electronic component sectors)

    Typical usage ratio

    • 2–6% by weight of total key intermediates in the mesogen assembly batch; adjusted for final LC blend compositions and purity requirements

    Downstream process integration

    • Input prior to key cyclization step for core liquid crystal assembly
    • Functionally tested for UV absorption and impurity profile prior to integration

    Final product types

    • Liquid crystal intermediates for TFT-LCD and OLED display manufacturing
    • Phase stabilization additives for advanced display panels
    • Specialty mesogenic compounds for adaptive optics and smart windows
    • Intermediates for high clarity and contrast display chemicals

    5. Intermediate in Fragrance and Aroma Chemical Manufacturing

    Within the specialty fragrance sector, chemists use our material as an intermediate to construct aromatic ketones and ethers found in high-end perfume bases. Its specific structural features allow for efficient transformations essential for producing long-lasting musk and floral notes. The aromatic intermediate enters at the alkylation or Friedel–Crafts acylation stage, followed by purification and final blending.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association, purity and traceability)
    • ISO 9001:2015 (Quality management for aromatic intermediates)
    • REACH Regulation (EC) No 1907/2006 Annex XVII for fragrance intermediates
    • RIFM Standards for raw material safety and usage thresholds

    Typical usage ratio

    • 2–8% of total synthetic batch as a building block; ratio depends on target fragrance strength and volatility profile

    Downstream process integration

    • Added at the initial synthesis phase as a precursor to complex aromatic ketone formation
    • Purified by fractional distillation before incorporation into the aroma blend

    Final product types

    • Musk and floral fragrance ingredients
    • Aromatic ketone and ether intermediates
    • Perfume base concentrates for fine fragrance houses
    • High value aroma chemicals for consumer product formulations
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    Certification & Compliance
    More Introduction

    4-Benzyloxy-3-Nitroacetophenone: Experience from the Production Floor

    What Years of Manufacturing Reveal About 4-Benzyloxy-3-Nitroacetophenone

    Our story with 4-Benzyloxy-3-Nitroacetophenone began in the late 2000s when we noticed a steady rise in demand for specialty aromatic intermediates in pharmaceutical and advanced material industries. By then, more clients wanted products with clean reaction profiles, easier purification, and better yields in their downstream syntheses. Over the last decade and a half, our team has gained hands-on experience refining this compound’s production, understanding its quirks, and learning where it fits best in customer projects.

    This isn’t one of those commodity chemicals filling up containers by the ton at ports. Each batch of 4-Benzyloxy-3-Nitroacetophenone starts with our control over raw material sourcing. We insist on strict assay specifications for the benzyloxy precursor and only work with stabilized nitroacetophenone streams. Years ago, we struggled with inconsistent oxidation states in our nitro intermediates; repeated troubleshooting led us to retrain staff and implement a more reliable inline monitoring system. These steps cut down unknowns and introduced more predictability in reactivity and yields.

    Why Synthetic Chemists Keep Coming Back

    At first glance, 4-Benzyloxy-3-Nitroacetophenone doesn’t look very different from its close siblings—take the para or ortho-substituted versions, for example. But ask any contractor who’s spent hours coaxing stubborn nitroaromatics into compliance, and they’ll tell you the difference lies in how this compound handles in multistep synthesis. Its benzyloxy group responds reliably to common hydrogenolysis conditions. The nitro group at the 3-position is less likely to interfere with ring substitutions, especially for companies working on heterocycle construction or targeted reduction. We have seen CRO teams running parallel reactions and reporting significantly higher clean-up efficiency compared to 3-benzyloxy variants, which sometimes leave sticky byproducts after scale-up.

    Our product, identified by the industry-standard CAS number, features a practical melting range and minimal residual solvents, verified by GC and HPLC—anything above trace levels means a batch won’t leave our warehouse. We often receive questions about residual palladium or tin levels after hydrogenolysis: our analytical data confirms metals are either undetectable or well below regulatory thresholds.

    Specification Isn’t Just a Checklist—It’s the Result of Hard-Learned Lessons

    One of the biggest surprises newcomers face is the color consistency and purity level of 4-Benzyloxy-3-Nitroacetophenone. Years ago, we struggled with faint ivory or straw-colored batches, hinting at trace oxidized byproducts. Some customers found these suitable, but advanced users, especially those in agrochemical intermediate synthesis, reported unpredictable reactivity unless color was uniform. The breakthrough came with small tweaks in re-crystallization using fractioned ethanol—heat ramps matter more than many realize. Nowadays, every product leaving our line passes visual and HPLC checks for color and purity, reflecting experience that has translated into fewer complaints and virtually zero rejections in the last five years.

    We keep the product particle size in the 60-100 mesh range. Some clients once requested finer material, hoping for faster dissolution in non-aqueous solvents. After testing, our group found that grinding below this range risked static charge buildup and challenged downstream blending, leading to unpredictable dispersal. Delivering a slightly coarser cut has greatly reduced customer complaints about clumping and accelerated batch turnaround in their R&D labs.

    Reliability in Applications—A Manufacturer’s Real-World Lens

    Over the past decade, 4-Benzyloxy-3-Nitroacetophenone has become indispensable for researchers fine-tuning their libraries of potential active pharmaceutical ingredients. The compound doesn’t just serve in the making of advanced intermediates—it helps get complicated benzanilide, diaryl ketone, or heterocycle facsimiles off the bench and into real-world testing. Many labs focus on the flexibility of the benzyloxy group, which breaks cleanly under mild hydrogenolysis or acidic conditions. That makes it a favorite for chemists layering in selectivity or testing scaffold modifications.

    We’ve spoken with process engineers who tried swapping in para-substituted analogs or standard acetophenones. Their results often included trace byproducts that drained time and labor during analysis. One customer in a mid-sized pharma company found that using our 4-Benzyloxy-3-Nitroacetophenone product led to a 15% higher isolated yield, slashing their purification time. That result saved them weeks over the course of a campaign aimed at developing a new antimicrobial scaffold.

    Outside pharmaceuticals, several materials scientists come to us for bespoke runs intended for OLED or advanced resin applications. They use our compound as a building block in the synthesis of performance additives, thanks to the stability of the aromatic core. Each time, they ask for the fine details on impurity levels, especially residual nitro or aldehyde groups. Our technical sheets directly reflect our test records and small tweaks from years of hands-on improvement.

    Safety and Handling: Lessons Earned Through Direct Work

    A factory floor can be an unforgiving place for assumptions. During our early campaigns with this compound, team members noticed the powder’s mild dustiness in humid conditions. Standard ventilation worked, but extra localized suction at the weigh-in stage made a bigger difference than any PPE adjustment. As a manufacturer, we emphasize keeping scoops and utensils bone-dry to avoid clumping or losses to glassware. Staff members receive thorough training, and monthly drills ensure protocols remain fresh. No script or checklist replaces the sense of readiness that comes from watching this product handled up close.

    Our packaging strategy grew out of trial and error. Early users asked why we didn’t ship in plastic bags—one humid summer, a large customer found their batch absorbing odors and growing lumpy during air transit. Now we use inner glass jars or lined drums for quantities above 10 kg, and we have received positive feedback about batch consistency even after several weeks of storage.

    How We Manage Purity and Traceability—A Detailed Process

    Traceability goes beyond sticking a lot number on the label. Our production records stretch back over a decade, tying raw material lots to reactor conditions and all final test results. Several pharmaceutical clients ask for retrospective batch histories during regulatory filings. That means every crystallization run, vacuum distillation, and melt point check finds its place in a database, updated within hours of batch close-out. This approach provides unparalleled confidence and is the result of long evenings spent reconciling hand-written notes from the early days with digital records.

    Every shipment includes a detailed certificate and a brief technical bulletin written by our chemists—not a copy-paste of old literature, but a summary with the latest batch’s specifics. Customers repeatedly mention that our results match their own internal QC checks, which helps them cut through the noise and focus on getting their synthesis running smoothly.

    What Sets 4-Benzyloxy-3-Nitroacetophenone Apart—Through a Manufacturer’s Eyes

    Similar-sounding products sometimes tempt buyers with lower prices, but the consistency gap shows up during multi-kilogram campaigns. Years of listening to feedback from reaction-scale and kilo-scale customers have taught us that differences in product uniformity can lead to hours—sometimes days—of lost optimization time. We have spent years tightening controls on residual solvents, particle size, and impurity spikes, learning to catch small deviations long before they show up in customer test results.

    Repeated internal testing has shown that close relatives such as 3-benzyloxy-4-nitroacetophenone introduce subtle shifts in reaction selectivity and post-reaction clean-up. Our clients in peptide chemistry have expressed how the precise placement of the nitro group in our product keeps side-chain protection predictable and straightforward. We have received feedback from teams who ran parallel tests and found our product produced sharp, well-defined peaks by both LC and NMR.

    On the service side, rapid batch turnover isn’t just marketing talk. Our average delivery window tracks at 6–10 days for custom quantities, not because of any specialized courier arrangement, but due to the planning in our production pipeline. After years of balancing long-term contracts with custom one-off runs, we can shift between kilo-scale and multi-gram production without quality slippage.

    Meeting Evolving Demands from the Lab and Pilot Plant

    From the first time we took a close look at the evolving demands of pharma and specialty chemical labs, we realized that shelf-stable, reproducible intermediates would only become more important. Our 4-Benzyloxy-3-Nitroacetophenone keeps pace with these trends by offering both scale and consistent quality control, addressing batch reactivity, and helping fine-tune complex routes.

    A common scenario involves researchers launching an exploratory program with small batches, later moving to pilot scale on tight timeframes. By keeping records on past orders and providing batch-specific advice, our technical staff assist with everything from dissolving selectivity challenges to navigating unanticipated reaction stalling. Each new use case adds to our shared body of knowledge, strengthening the product and our own manufacturing know-how.

    Recent years have seen chromophore exploration and ligand manufacturing teams requesting more detailed impurity breakdowns and requiring not just the total organic impurity content, but specifics on isomeric contamination. Our in-house QA team keeps pace by running expanded analytical panels—HPLC, GC-MS, and on request, qNMR and optical rotation measurements. The purpose is always the same: to offer peace of mind that the material they’re running through preparative columns or reactors behaves just as anticipated batch after batch.

    Supporting Smarter Synthesis from Start to Finish

    Customers sometimes share their process designs and ask for feedback—what solvent compatibility should they expect, which protective groups come off most reliably? As people invested directly in producing 4-Benzyloxy-3-Nitroacetophenone, we bring practical answers that save time, such as recommending preferred solvents (ethyl acetate and toluene dissolve the compound efficiently), or sharing which filtration methods will keep purity levels top-notch.

    Teams working in process development have noted that switching to our product decreased filtration time by about 20% compared to similar products, due to more predictable crystallization and solid handling properties. This wasn’t an accident—after several trials, we adjusted our drying cycles and invested in new vacuum filtration technology. Sharing these lessons directly benefits clients taking their first steps with new reaction routes.

    The world of fine chemicals isn’t static; every month brings new process tweaks, evolving customer standards, and regulatory shifts. Our long-term commitment comes through ongoing improvements—reprioritizing reactor loads for emergencies, proactively reaching out to customers about supply changes, or tweaking our QA procedures to reflect the latest analytical technologies. Every improvement finds its root in direct observation and dialogue with our buyers and our production teams.

    Environmental Considerations—Sustainable Practices on the Production Line

    Clean chemistry matters—on both sides of the supply chain. Early production runs generated organic residues and excess waste streams, but we responded by implementing solvent recovery loops and dedicated waste neutralization facilities. Our teams manually monitor emissions during critical reaction steps, optimizing catalyst recovery, and have reduced solvent waste by nearly a third in the last three years.

    Local regulations have prompted us to move more aggressively in energy efficiency and worker safety. That means heat exchangers for solvent condensation, routine audits of HVAC efficiency, and regular updates to material handling training. By putting in these safeguards and reduction plans, we support cleaner operations and better long-term results for downstream users. Customers consistently mention our transparent reporting of environmental impact during supplier audits.

    Navigating Challenges—What Decades of Problem-Solving Have Taught Us

    No product reaches maturity without facing its share of snags. During one year of global transport disruptions, a raw material shipment sat delayed for weeks. Our backup plans—diversified supplier pools and strategic on-site storage—enabled us to keep all orders on track. The experience reinforced the need for redundancy and flexibility, not blind reliance on schedules.

    We have learned the critical importance of ongoing skills development for our staff. The stepwise assembly of 4-Benzyloxy-3-Nitroacetophenone isn’t automated; it still calls for skilled chemists to recognize subtle color changes during crystallization or rework a filtration setup when the viscosity doesn’t line up with expectations. Annual training cycles, cross-functional ‘deep dive’ meetings, and knowledge-sharing between junior and senior staff keep us ahead of avoidable mistakes.

    Customer feedback remains our best quality lever. When a pilot client in Japan reported slightly higher than expected moisture content, we re-examined our drying cycle. The tweak—doubling vacuum drying time—resolved the issue and improved overall consistency. It’s this give-and-take with end users that keeps standards high and builds lasting trust.

    Where Experience Matters Most—Partnering with Real Manufacturers

    There’s no substitute for the day-in, day-out commitment to refining a single specialty chemical. Our direct connection to the production floor means that every insight, improvement, and success story gets incorporated right back into our processes. For our team, 4-Benzyloxy-3-Nitroacetophenone isn’t just a catalog number—it’s a project that has grown with us from uncertain beginnings to a product that supports innovation in fields as diverse as pharmaceuticals, electronics, and advanced resins.

    Each request for custom batch sizes or expanded impurity panels adds another layer to our understanding and drives further improvement. It’s that commitment to hands-on problem solving, transparency, and technical support—not just meeting product specs on paper—that keeps customers returning. By investing in long-term relationships and technical collaboration, we provide a consistent product that keeps up with the most demanding research and production needs.