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2-Hydroxy-3-Nitroacetophenone

    • Product Name 2-Hydroxy-3-Nitroacetophenone
    • Einecs 225-004-1
    • 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

    480165

    Chemical Name 2-Hydroxy-3-Nitroacetophenone
    Molecular Formula C8H7NO4
    Molar Mass 181.15 g/mol
    Appearance Yellow crystalline solid
    Melting Point 120-124°C
    Boiling Point No data available (decomposes)
    Cas Number 1162-55-8
    Smiles CC(=O)C1=C(C(=C(C=C1)O)[N+](=O)[O-])
    Solubility Slightly soluble in water; soluble in organic solvents such as ethanol and DMSO
    Density 1.45 g/cm³ (approximate)
    Iupac Name 1-(2-hydroxy-3-nitrophenyl)ethan-1-one

    As an accredited 2-Hydroxy-3-Nitroacetophenone 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 2-Hydroxy-3-Nitroacetophenone, tightly sealed with a screw cap and labeled with safety information.
    Shipping 2-Hydroxy-3-Nitroacetophenone is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported according to regulations for hazardous chemicals, typically under ambient temperature, with clear labeling for chemical identification and hazard information. Appropriate documentation and safety data sheets accompany each shipment to ensure safe handling and compliance.
    Storage 2-Hydroxy-3-Nitroacetophenone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and reducing agents. Protect from light and moisture. Properly label the container and ensure it is kept away from direct sunlight and any heat sources to maintain stability.
    Application of 2-Hydroxy-3-Nitroacetophenone

    Applications of 2-Hydroxy-3-Nitroacetophenone in Industrial Manufacturing

    As a specialized producer of 2-Hydroxy-3-Nitroacetophenone, we supply this intermediate for key chemical processes across several specialized industries. Our focus is on markets and manufacturing stages where this compound directly impacts performance, output quality, and compliance outcomes. Below, we outline the primary application channels with detailed context for leading downstream producers.

    1. Pharmaceutical Intermediate for Antifungal Agents

    Downstream pharmaceutical companies utilize 2-Hydroxy-3-Nitroacetophenone in the multi-step synthesis of imidazole-based antifungal actives. The compound acts as a specific starting reagent, where its nitro and hydroxy groups drive selectivity in targeted condensation and cyclization stages. Process chemists prefer this intermediate for its reliable reactivity profile, which helps achieve strict purity and yield requirements in final APIs. The handling and integration at various purification steps support full traceability and robust quality assurance practices throughout regulated pharma manufacturing.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Part 210/211, US FDA)
    • European Pharmacopoeia monographs for antifungal APIs
    • ICH Q7: Good Manufacturing Practice for API
    • China GMP for APIs and intermediates (NMPA)

    Typical usage ratio

    • Ranges from 0.6 to 1.5 molar equivalents as required for specific antifungal actives; process chemistry optimization depends on target molecule design and downstream step conversion efficiency

    Downstream process integration

    • Introduced in early-stage condensation and cyclization reactions as a key electrophilic component; isolated as a crystalline intermediate before successive hydrogenation, halogenation, or ring closure steps

    Final product types

    • Active pharmaceutical ingredients for treating dermatophytosis and systemic fungal infections (e.g., miconazole, econazole family APIs)
    • Bulk pharmaceutical intermediates for export and contract manufacturing

    2. Synthesis of UV-Absorbing Monomers for High-Performance Coatings

    Producers of specialty coatings rely on 2-Hydroxy-3-Nitroacetophenone to synthesize advanced benzophenone derivatives, essential for creating UV-absorbing resin monomers. By introducing the intermediate at early condensation stages, formulators precisely tune photostability and yellowing resistance in high-durability clear coat systems. The compound’s specific functionality enables covalent incorporation into polymer chains, meeting performance targets for automotive, aerospace, and architectural finishes exposed to intense sunlight.

    Industry compliance standards

    • REACH Annex XVII (EU) for chemical safety in coatings
    • ISO 12944 for protective paint systems
    • RoHS Directive (2011/65/EU) for restricted substances in coatings on electronics
    • ASTM D3022 for UV stability testing of automotive finishes

    Typical usage ratio

    • Used at 0.5–2% by weight in monomer batch reactions, adjusted based on target molecular weight and required UV absorbance index

    Downstream process integration

    • Reacted via acylation or etherification with phenolic modifiers during resin pre-polymer synthesis; the resulting UV-absorbing monomer feeds directly into emulsion, solution, or powder coating polymerization

    Final product types

    • UV-resistant automotive clear coats and topcoats
    • Weatherable architectural powder and liquid coatings
    • Protective finishes for composite substrates and outdoor metalwork

    3. Dye Intermediate in Synthesis of High-Fastness Azo Pigments

    Large-scale pigment and dye manufacturers process 2-Hydroxy-3-Nitroacetophenone as a key coupling component in production of azo-based colorants with advanced lightfastness. The electron-withdrawing nitro group enhances bathochromic shifts and pigment stability, enabling coloration used in automotive, plastics, and industrial inks. Controlled reaction with diazonium salts yields target azobenzene structures supporting high opacity and solvent resistance, meeting demanding requirements for both mass coloration and specialty print inks.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted dye substances
    • EN 71-3:2019 for safety of toys (migration of certain elements in pigments)
    • ISO 105-B02: Methods for determining color fastness to light
    • FDA 21 CFR 178.3297 for colorants in plastics that may contact food

    Typical usage ratio

    • Applied at 1.2–2.3 parts per 10 parts coupling agent, with adjustments based on batch scale and target pigment dispersion consistency

    Downstream process integration

    • Dissolved in alkaline solution prior to controlled diazotization and subsequent azo coupling, followed by filtration and grinding for micronization of pigment particles

    Final product types

    • Colorfast azo pigments for engineering plastics
    • Solvent-resistant printing inks for packaging
    • Pigment dispersions for high-wash textile applications

    4. Chemical Intermediate for Agrochemical Synthesis (Herbicides and Fungicides)

    Crop protection synthesis lines incorporate 2-Hydroxy-3-Nitroacetophenone as a building block in multi-stage synthesis of select herbicide and fungicide actives. Its tailored reactivity with halogenating or nitrating agents supports the formation of target substitution patterns critical for mode-of-action specificity and environmental breakdown. The compound assists in producing active ingredients with tightly controlled residue profiles and required stability for global field deployment.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) guidelines
    • ISO 9001: Quality management for agrochemical manufacturing
    • US EPA 40 CFR Part 180: Tolerances and exemptions for pesticide chemicals
    • Directive 91/414/EEC (EU approval of active substances)

    Typical usage ratio

    • Varies from 0.8 to 1.7 molar equivalents based on route and catalyst selection in key active synthesis; process adaptation targets conversion efficiency and downstream purification yield

    Downstream process integration

    • Integrated in key condensation or aromatic substitution steps, followed by targeted reduction, halogenation, or side-chain assembly required for generating the bioactive scaffold

    Final product types

    • Herbicide actives in post-emergence weed control formulations
    • Fungicidal agents for cereal and horticultural crop protection
    • Active intermediates for pesticide custom synthesis contracts
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    Certification & Compliance
    More Introduction

    Understanding 2-Hydroxy-3-Nitroacetophenone: Experience from the Manufacturer’s Floor

    Introduction to 2-Hydroxy-3-Nitroacetophenone

    Every day, the push for more reliable and consistent intermediate chemicals comes from those who use these compounds to build anything from pharmaceuticals to specialty dyes. At our facility, the journey with 2-Hydroxy-3-Nitroacetophenone (sometimes referenced as 2H3NAP) is marked by continual adaptation. There is no shortcut to a thorough grasp of this compound—a molecule built on the backbone of acetophenone, with the addition of hydroxy and nitro groups that open a door to new reactivity.

    Model and Specifications as Crafted on the Line

    Our standard process for manufacturing 2-Hydroxy-3-Nitroacetophenone reflects not only technical know-how but countless hours spent refining yield and consistency. We produce this product with a focus on purity—often exceeding 98 percent by HPLC—all the way down to residual solvent traces, which routinely land below detectable thresholds for those running sensitive downstream syntheses. The yellow-to-pale-yellow crystalline solid that results from our runs offers good handling stability with a melting range typically falling between 117 °C and 121 °C. Over time, we have learned that every degree in melting point drift says something about batch variation, so routine, open discussions between QA and production keep the product on target.

    Dust formation once frustrated many teams at the recrystallization step; one of the most persistent challenges in working with nitro aromatics. After repeated handling trials, we settled on a crystallization and drying protocol that gives crystals easy to handle during bulk transfers, with reduced airborne dispersion. Moisture absorption is rarely an issue, but packaging still reflects the need for stability—double-layer polyethylene or inert-gas-purged liners, not out of excess caution but from direct experience with extended warehouse holdings and the threat of unseen humidity.

    Real-World Usage Insights from Those Who Handle It

    Chemists see value in 2-Hydroxy-3-Nitroacetophenone as a versatile intermediate. The balance of electron-withdrawing and electron-donating groups sets up this molecule as a key player for building heterocycles—many of those used in active pharmaceutical ingredients or advanced organic pigments. Product developers in our client network rely on its performance in C–C coupling strategies, and more than once have told us how its substitution pattern avoids side reactions common when starting from less optimized derivatives.

    On the pharmaceutical side, the compound slots into multi-step syntheses where selective functionalization of either the hydroxy or nitro group paves the way to new scaffolds. In dye chemistry and pesticide innovation it features as an entry point to more complex systems, often through reduction, acylation, or alkylation reactions. We have spent years talking to process engineers in these fields, and the feedback is consistent: reliability in purity and melting profile means the downstream reactions run clean, avoiding contaminant peaks and troublesome byproducts that cut into yields and force tedious rework.

    What Sets It Apart: From Lab-Scale Beginnings to Large-Batch Consistency

    There are other nitroacetophenones, each with its own substitution landscape. Some vendors point to 4-Hydroxy-3-Nitroacetophenone or 2-Hydroxy-5-Nitroacetophenone as alternatives. We began producing 2-Hydroxy-3-Nitroacetophenone because our synthesis pathway gives us a higher yield from common acetophenone feedstock, and the hydroxy-nitro placement on the aromatic ring proves more forgiving during downstream derivatization.

    From years spent troubleshooting plant bottlenecks, our staff have seen how slight differences in molecular substitution turn into major roadblocks on the production floor. For example, moving the nitro group even a single position changes the solubility in industrial solvents, making it noticeably harder to separate batches from process impurities. Our current manufacturing setup allows us to sidestep many of these pain points; customers recognize quick filterability and superior solid-state purity, which means less stress on their own purification systems.

    Cheaper products from bulk traders, often without full traceability, find their way into the market. We have fielded calls from new clients who tried those batches and ran into runaway exotherms due to inconsistent impurity levels. It costs more to remediate a tank of failed product than to source a reliable standard—but sometimes that lesson only sinks in after the fact. For those in regulated sectors, a well-documented chain of custody and consistent batch analysis reports are not optional luxuries but foundation stones.

    Practical Challenges and How Real Manufacturing Responds

    Nothing about 2-Hydroxy-3-Nitroacetophenone’s production process invites complacency. As a chief operator recalls, uncontrolled temperature shifts during nitration quickly degrade yields and encourage side-products, something tolerable at the gram scale but catastrophic when working with reactors holding hundreds of kilograms. Our control room keeps data logs going back years; even seemingly minor excursions or changes in feedstock quality raise flags. The result is a running dialogue—not just digital records, but face-to-face engagement with reactor operators about pressure drops, stirrer speeds, or even subtle changes in the foam over a reaction batch.

    Scaling up chemical manufacture always reveals issues hidden at the bench. Overheard in breakrooms: “It looked clear in the lab, but blocked filters tell a different story.” Many iterations of process control, feed rates, and downstream isolation steps now carve out a path through these problems. For example, past experience with sticky intermediates forced us to change our filtration media and backflush cycles. That detailed tweaking means our teams avoid costly downtime—a margin that matters in industries where restart times eat into customer delivery windows.

    Waste management remains a running priority. Byproduct management, including nitroaromatic residues, stokes ongoing conversations with regulatory consultants to keep all waste streams within permits. Our investment in modern scrubber circuits and compliant storage protects both the workforce and the neighborhood. Lessons on the cost of overlooking a single valve or underestimating a reactor heel are not soon forgotten; we keep these stories active in training sessions so new staff pick up the hard-earned realities.

    Responsible Manufacturing: The Environmental and Safety Reality

    Producing 2-Hydroxy-3-Nitroacetophenone demands vigilance. Aromatic nitro compounds require close emissions tracking and robust worker protection. Recent upgrades in our air-handling system cut organics to parts-per-billion levels around sensitive job posts. We moved to continuous real-time monitoring with benchtop PID detectors instead of relying solely on periodic spotchecks. The real driver behind these changes has not only been compliance but the people who staff the reactors, storage sheds, and drum filling stations.

    Wastewater has risen to the same level of scrutiny. Piloting a novel treatment train, we found that high-strength organic loads can drop below regulatory thresholds without excessive chemical neutralization if oxidative pre-treatment is dialed in precisely. Upgrades like these follow years of review after batches with more than usual organic carryover. Through in-house testing and strong communication with local authorities, we’ve reduced non-conforming discharges, meeting our obligations to the community and legal requirements at the same time.

    Supply Chain Stability: Direct Producer Value

    As a direct manufacturer, our supply chain never strays far from our production scheduling and inventory planning. Investing in raw material quality checks reduces mid-campaign surprises. Unloading staff reinforce this by immediately sampling every incoming drum. We keep redundant qualified vendors for sensitive reagents, which softens shocks from regional shortages or port slowdowns—no last-minute scrambles to substitute reactants.

    Transparency runs deep. Every outgoing shipment comes with the full analytical trace each customer expects in tightly regulated industries. Our long-term relationships mean feedback arrives on packed form, solids color, particle grit, and three-month stability—details that matter much more than the “purity percent” leading so many third-party brochures. Our involvement doesn’t end at the loading dock. Application chemists and scale-up engineers ring us up directly, sometimes long after the purchase, to troubleshoot what looks like a manufacturing issue but often traces back to something as simple as storage temperature drift or an unexpected formulation interaction.

    Certification, Compliance, and End-to-End Documentation

    Documentation isn’t busywork; our release criteria and batch records have shut down more than one potential mishap before shipment. Working with international clients, experience teaches that bureaucracy sometimes outpaces the chemistry. Customs queries over restricted chemicals, or requests for impurity profiles in new jurisdictions, add days—not hours—to lead times. We keep audit-ready records, including full synthetic pathway documentation and impurity rationales for each batch number, which smooths these snags most of the time.

    Supporting standards compliance, such as REACH or US FDA precursor rules, takes sustained investment. Rapid reference crosschecks, certificate of analysis issuance, and chemical hazard communication stay linked to lot numbers tracked from raw material intake all the way through finished product drumming. Actual practice on the floor must match paperwork—no shortcuts on batch hold and release can survive auditing from external partners, as our field team has seen during many unannounced checks.

    Physical and Chemical Handling: Lessons from Years on the Plant Floor

    Handling nitroaromatic intermediates reliably means planning for their quirks. Over-packing or under-packing product drums in the past led to avoidable compaction or shifting of product, so now crews check fill levels against batch size, not theoretical drum weight. Airborne dust, particularly right after drying, is controlled at the station, with in-line air extraction updated to keep operator exposure low.

    Logistics, too, brings its own lessons. Where summer humidity spikes threaten product stability, scheduled shipments pivot to insulated storage quickly. Cross-continental delivery routes rarely follow textbook timelines; insurance and inspection teams now check not just container seals but shock and vibration logs recorded during transit. At the receiving end, clients relay their own on-site observations to us, which feed back into adjustments on batch density and crystal fraction—one client's bottleneck often triggers a process tweak across the floor.

    Supporting Advanced Applications: Beyond the Intermediates Shelf

    Clients using 2-Hydroxy-3-Nitroacetophenone for specialty fields like API synthesis demand more than bulk supply. Small changes in side component concentrations push or block key transformations; troubleshooting with their process chemists looks like side-by-side examination of chromatograms and hands-on sample workups, not distant spreadsheet exchanges. These partnerships shape ongoing revisions to our routine impurity exclusion rules, often accelerating change faster than internal reviews alone would allow.

    New industrial uses arise. For instance, custom projects in polymer development introduced batch-by-batch optimizations of melting point, aimed at ensuring compatibility with solvent casting or spin-coating procedures that tolerate little batch drift. Collateral benefits have even shown up in pigment chemistry, where tighter control over hydroxy positioning on the aromatic ring produces improved lightfastness and color consistency—a request that appeared thanks to a single customer’s pattern of repeated feedback.

    Improvements and Adaptation: Listening and Responding

    The intersection of process refinement and customer feedback drives most of our adaptation. Once, complaints about hard-to-dissolve lots led to an overhaul in the solvent exchange phase, including an extended vacuum strip that lowered residual DMF levels by over 90 percent. Post-implementation, customer batch acceptance rates ticked upward, and internal rework costs dropped. This open channel between application needs and production not only keeps the end product at spec but delivers tangible value to partners relying on us to provide foundational materials for their own high-value products.

    By seeing firsthand how minor contamination or mislabeling events can unravel weeks of customer planning, our staff treat every filled drum as a potential line-stopper—not just another number on a ledger. Solutions, whether process or packaging, come from the people who know the product most intimately. Real improvements stem from deep engagement, not surface-level box-checking.

    Long-Term Perspective: Building Reliability and Trust

    Year after year, we have seen the same reality play out: people who depend on dependable intermediates cannot afford deviation. Trust forms when problems are addressed head-on, not explained away or deferred. Everyone from the synthesis bench to the QA office lives with a clear understanding that their hands, their signatures, and their observations have direct impact not just on today’s batch, but on next quarter’s supply chain reliability for partners worldwide.

    Few things bring satisfaction like hearing back from a longtime partner that their production campaign ran without a hitch—thanks to a grade of 2-Hydroxy-3-Nitroacetophenone that delivered exactly what they needed batch after batch. Reliability in chemical manufacturing is not a slogan on a website but the outcome of every small decision, from choice of filtration media to how a drum is loaded onto a truck. As direct manufacturers, we feel the weight of those decisions, every day.