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Ethyl 4-Hydroxy-3-Nitrobenzoate

    • Product Name Ethyl 4-Hydroxy-3-Nitrobenzoate
    • Alias Ethyl 4-hydroxy-3-nitrobenzoate
    • Einecs 223-568-7
    • 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

    824869

    Cas Number 22762-64-1
    Molecular Formula C9H9NO5
    Molecular Weight 211.17 g/mol
    Appearance Yellow crystalline powder
    Melting Point 142-146°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.43 g/cm³ (approximate)
    Purity Typically ≥98%
    Synonyms Ethyl p-hydroxy-m-nitrobenzoate
    Smiles CCOC(=O)C1=CC(=C(C=C1O)[N+](=O)[O-])
    Inchikey ZVPIBBJVRREXIX-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of Ethyl 4-Hydroxy-3-Nitrobenzoate, labeled with chemical information, hazards, and expiry.
    Shipping **Shipping Description for Ethyl 4-Hydroxy-3-Nitrobenzoate:** Ships in a tightly sealed, chemical-resistant container. Store and transport under dry, cool conditions, away from heat and incompatible substances. Compliant with relevant chemical transport regulations. Handle using appropriate personal protective equipment. Label container with chemical name, hazard information, and safety precautions. Not regulated for transport by most standard agencies.
    Storage **Storage Description for Ethyl 4-Hydroxy-3-Nitrobenzoate:** Store in a tightly sealed container in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and bases. Keep away from sources of ignition and moisture. Ensure proper labeling, and avoid prolonged exposure to air. Use secondary containment to prevent spills. Handle according to standard laboratory safety protocols.
    Application of Ethyl 4-Hydroxy-3-Nitrobenzoate

    Applications of Ethyl 4-Hydroxy-3-Nitrobenzoate in Industrial Manufacturing

    Ethyl 4-hydroxy-3-nitrobenzoate sees specialized use in targeted sectors demanding high-purity intermediates for organic synthesis, including pharmaceutical active ingredients, advanced pigment manufacturing, and the development of specialty functional materials. As an established input in these fields, the substance offers consistent reactivity and formulation predictability, meeting strict process control standards. Our ongoing supply supports both batch and continuous production, helping downstream partners maintain regulatory and operational certainty throughout complex synthesis chains.

    1. Pharmaceutical Intermediate for Antimicrobial Agents

    Pharmaceutical manufacturers regularly rely on this raw material in the multi-step synthesis of nitrophenolic core intermediates for antibacterial agents. Its unique substitution pattern provides the structural basis necessary for targeted functionalization steps, directly contributing to the bioactive scaffold construction. Consistency in purity and processability remains vital due to the stringent regulatory controls governing APIs, especially for oral and topical dosage forms. Users commonly tune the ratio by batch process control depending on the required intermediate throughput and target impurity profile for subsequent coupling, reduction, or esterification steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph.Eur., USP, and Chinese Pharmacopoeia monograph alignment for nitrobenzoate-type intermediates
    • FDA 21 CFR Part 211 (US cGMP regulations for finished pharmaceuticals)
    • Current Good Laboratory Practice (cGLP) guidelines for analytical monitoring

    Typical usage ratio

    • 0.4%–2.8% of reaction charge, variable according to specific molecule yield requirements and downstream target API
    • Exact amount refined based on desired purity profile and conversion efficiency in stepwise synthesis

    Downstream process integration

    • Charged during the nitro-ester intermediate buildup stage, often post-nitration but pre-coupling or reduction
    • Purified using crystallization or chromatographic separation in pilot and production scale flows

    Final product types

    • Semi-synthetic antibacterial active pharmaceutical ingredients
    • Intermediate scaffolds for further transformation into anti-inflammatory compounds
    • Pharmaceutical-grade nitrophenolic building blocks for downstream modification

    2. Precursor in High-Performance Organic Pigments

    Producers of advanced azo and anthraquinone pigments use this compound as a precision-controlled secondary reactant, primarily leveraging its nitro and hydroxyl functionalities to introduce chromophore modulations at the molecular level. Its role is especially pronounced in the fine-tuning of color shade, intensity, and lightfastness for pigments used in demanding automotive, plastics, and specialty inks applications. End-users benefit from granular adjustment of precursor feed, optimizing both coverage and stability per finished product requirements.

    Industry compliance standards

    • EN 71-3 (Safety of Toys—Migration of Certain Elements, relevant for pigment residues)
    • ISO 1248 (Pigments—Requirements and Test Methods for Industrial Colorants)
    • REACH Regulation (EC) No. 1907/2006, Annex XVII restrictions on azo colorants
    • GMP for food-contact colorants where applicable (EC 2023/2006)

    Typical usage ratio

    • 1.5%–6% of pigment precursor charge, typically set according to target tinting strength and desired chromatic properties
    • Adjusted by substrate compatibility or dilution grade during masterbatch formulation

    Downstream process integration

    • Introduced post-primary condensation or diazotization, forming stabilized pigment complexes
    • Integrated within milling and finishing stages for pigment dispersion and purification

    Final product types

    • High-stability organic pigments for industrial coatings
    • Colorant masterbatches for plastics and polymers
    • Specialty printing ink pigments required for UV resistance

    3. Key Intermediate in Liquid Crystal Material Synthesis

    Manufacturers engaged in producing advanced liquid crystal compounds for display and sensor applications adopt this raw material as a structural intermediate, relying on its precise substitution for subsequent etherification or ester coupling steps. The chemical purity and batch-to-batch reproducibility ensure proper integration into the liquid crystal backbone, directly affecting alignment, viscosity, and electro-optical performance in finished products. The downstream process demands strict stoichiometry and environment controls, especially where optical-grade clarity is required.

    Industry compliance standards

    • ISO 9001 and IEC 61747 (Quality and safety for LCD and electronic display components)
    • RoHS Directive (2011/65/EU) for restriction of hazardous substances
    • REACH chemical registration and safety data verification for advanced materials
    • IECQ QC 080000 (Hazardous Substance Process Management)

    Typical usage ratio

    • 0.2%–1.1% by mass in reaction feed, calculated based on liquid crystal precursor chain length and required phase transition temperature
    • Ratio adjusted for targeted viscosity and birefringence properties of the final material

    Downstream process integration

    • Introduced in early aromatic core modification, prior to final esterification or etherification
    • Followed by rigorous distillation and purification to electronic-grade standards

    Final product types

    • High-performance liquid crystal display (LCD) mixtures
    • Optoelectronic active layers for sensors
    • Advanced photoalignment materials for display technologies

    4. Intermediate for Synthesis of Specialty Plasticizers

    Within the specialty chemicals sector, compounders utilize this molecule in the manufacture of advanced non-phthalate plasticizers, leveraging its aromatic nitro-ester backbone for imparting tailored flexibility and migration resistance in high-demand polymer systems. Its function as a bridging intermediate within esterification and condensation reactions enables formulators to fine-tune plasticizer performance across temperature, volatility, and compatibility ranges. Consistent input quality ensures reliable process outcomes and reduces downstream purification steps for sensitive applications.

    Industry compliance standards

    • FDA 21 CFR 177.2600 (Elastomers and rubber articles intended for repeated use)
    • European Regulation (EU) No 10/2011 (Food contact plastics—Plasticizers and additives)
    • ISO 9001 for plasticizer formulation quality control
    • REACH Annex XIV compliance for non-phthalate substitutes

    Typical usage ratio

    • 0.6%–3.5% of total precursor mass, based on backbone modification needs and targeted migration limits within finished plasticizer
    • Adjustable per required thermal or mechanical performance profiles of downstream polymer blends

    Downstream process integration

    • Fed into condensation or direct esterification reactors following aromatic system activation
    • Subjected to vacuum distillation for removal of unreacted intermediates and byproducts

    Final product types

    • High-stability plasticizers for specialty PVC, PUR, or elastomer formulations
    • Plasticizer components in wire & cable coatings with stringent migration limits
    • Plastic additives for flexible automotive and construction components
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing Ethyl 4-Hydroxy-3-Nitrobenzoate: From Manufacturer’s Experience

    A Chemical with Proven Experience in Synthesis and Application

    Standing in the manufacturing lab as we blend and crystallize Ethyl 4-Hydroxy-3-Nitrobenzoate, the process tells us more than any catalog entry ever could. From the sharp scent lingering over the reaction kettle, the way the solution shifts clarity at just the right temperature, and the dry, fine powder left in the centrifuge, this compound reminds us of how many steps in synthesis offer their own signature challenges and successes. We don’t just know this molecule; we know how it responds to the touch, to pH, to those moments where a degree or two changes everything. This gives us confidence that every lot, every batch, reflects reliable consistency. Anyone working with this material–sitting at our benches or opening their own fresh drum across the world–should expect nothing less than what our own chemists trust for their own projects.

    Identity and Model

    Ethyl 4-Hydroxy-3-Nitrobenzoate stands out among benzoate derivatives for its unique combination of an ethyl ester, nitro, and hydroxy substituents. Chemically expressed as C9H9NO5, this compound embodies the subtle green-yellow color that signals both high purity and precise synthesis. We categorize our main grade under the in-house model ENB-459, a shorthand our clients have learned to recognize for consistent processing yield and minimized impurity levels. Experience has taught us that even trace contaminants will interfere with downstream chemistry; therefore, we continue to improve purification through additional recrystallization and chromatography steps. On the benchtop, our ENB-459 powder resists humidity pick-up longer than comparable grades, which gives formulators a tangible window for handling and weighing without worrying about caking or clumping.

    Key Specifications as Understood in Real Manufacturing

    Checking the chromatogram for ENB-459, we routinely see purity exceeding 99.5 percent, a threshold that stems from careful attention to every detail in the reaction. The melting point remains sharp, between 153 and 155°C, which reflects not just molecular structure but rigorous removal of isomers and side products. We test for color through spectrophotometry, but our chemists, with years behind them, often notice a subtle shift in hue before the meter does—suggesting micro-impurities that we follow up with targeted purification. Water content rests well below 0.2%, and we tightly limit heavy metal traces using modern ICP detection. Reproducibility seems simple on paper; in the plant it means fighting for consistency, whether scaling from a few kilos to several tons, or changing water sources and seasonal environmental factors. We keep a direct line from synthesis to quality control, drawing samples at every crucial step. That persistent search for improvement shapes the performance of ENB-459 in real end-user applications.

    Application Strength and Role in Synthesis

    Many industries rely on rare intermediates, and Ethyl 4-Hydroxy-3-Nitrobenzoate sits squarely where precision matters in synthesis routes. Respected as a building block for pharmaceuticals and agrochemicals, this molecule reacts predictably in esterification and reduction steps, opening doors for further substitution or transformation. Medicinal chemists favor it for its selectable reactivity; the ortho orientation of hydroxy and nitro groups allows complex ring modifications. In anti-inflammatory or antimicrobial candidate molecules, this benzoate sets up core skeletons that can withstand tough conditions during downstream reactions. We’ve watched both large and small R&D outfits return for ENB-459 after evaluating lab-scale reactions, often noting that our product’s low residual acidity lets them skip pre-reaction basification.

    The color and particle size profile contribute directly to its suitability in solid formulations—an insight that surfaced after several major customers struggled with flowability and dissolution issues using off-brand equivalents. By ensuring a uniform size range, we help partners avoid variability in dissolution and content uniformity. For dye intermediates and specialty pigment work, the azo-coupling and reduction steps benefit from ENB-459’s sharp purity, translating to better yield and clearer color resolution in finished products. In the realm of chemical research, we hear feedback from project leads about minimizing NMR “ghost peaks” and unexplained HPLC retention times thanks to our approach to trace impurity monitoring.

    Distinctiveness Compared to Other Benzoates

    Manufacturing Ethyl 4-Hydroxy-3-Nitrobenzoate means we see fine differences among similar benzoate compounds up-close. Unlike simple ethyl benzoate, the presence of both hydroxy and nitro substituents demands tighter control over reaction milieux and purity. Here, process nuances separate high-performing material from the merely adequate: incomplete nitration or poor hydrolysis introduce byproducts that downstream users end up troubleshooting. We found this difference in cross-checking batches synthesized using generic nitrobenzoic acid – those often introduce minute levels of dinitro or unreacted starting materials, leading to reduced conversion or product discoloration. By starting from highly vetted raw materials and running extra in-process checks, we maintain color fidelity and assurance against runaway side-reactions.

    What sets ENB-459 apart isn’t just the parent chemical but the hands-on effort behind it. For formulations in advanced pharmaceutical intermediates, our product shows higher batch-to-batch reproducibility than most 3rd-party lab-scale offerings. Substitution on the aromatic ring increases both the chemical’s potential and its sensitivity; this is where our manufacturing controls protect both yield and downstream product quality. We have observed end-users reporting rapid saponification with some imported lots, often linked to excess moisture or alkaline residues. Our extra drying and neutralization steps may require added time and tighter planning, but they reward both the manufacturer and end-user with reliable outcomes.

    Reliability through Process and Quality Mindset

    Our operations reflect more than completing a synthesis. Every bag and drum passes through environmental monitoring, with tight logs kept on every degree and atmospheric variable. Operators calibrate sensors before every campaign, not because an auditor forces the workflow but because minor temperature drifts mean less material delivered in range. On the packing line, every team member inspects batch documents by hand, crosschecking equipment records and in-house reference spectra. We don’t rely on “one-size” quality specs copied from textbooks—our benchmarks draw on decades of test data and field experience, building up a resistance to shortcuts or easy fixes. Research teams who have compared alternative products note a lower occurrence of failed validation runs or lost production days due to unexpected out-of-spec results when using ENB-459. The production logbooks tell the same story—a focus on detail at one end multiplies downstream confidence manyfold.

    Health, Safety, and Environment—A Realistic Outlook

    Like most nitroaromatics, Ethyl 4-Hydroxy-3-Nitrobenzoate deserves respect in handling. On the plant floor, spill drills and regular airflow checks remind our staff that even minor exposures can cause irritation. Gloves and local exhaust never become afterthoughts; we select materials for containment with actual field trials, not default recommendations. Wastewater undergoes staged neutralization and photo-reactive treatment—the goal lies not just in compliance but in minimizing trace nitro content at discharge points. Operators have flagged the distinct, slightly sweet odor as a useful early warning for leaks—something that end-users in R&D settings have learned to appreciate, especially when working late into the night with small-scale glassware. Environmental responsibility doesn’t start with a memo—it unfolds through repeated walks around the plant perimeter, tracking stormwater flow, reviewing air monitor readouts, and working the line with every new hire. The lessons we learn turn straight into updated safety practice, not after an incident but from routine vigilance.

    Continuous Improvement as a Reality, Not a Slogan

    One shift’s batch record sometimes reveals more than weeks of planning forecasts. We notice changes in yield when outside humidity spikes, or when a subtle tweak in re-flux timing brings cleaner phase separation. Rather than locking into old recipes, our process development teams welcome feedback—whether it comes as a customer’s complaint about trace yellowing, or a colleague noticing excess filter clogging in colder months. Adjustments don’t trickle down from management memos—they land directly at the workbench in the hands of those who know the material best. Customer returns of ENB-459 are rare, but our log of actions from those cases reads longer than any product catalogue. Field samples kept from every lot offer a real record for backtracking quality or troubleshooting unexpected results, bridging the gap between scheduler, chemist, and client.

    Support and Partnership Beyond Shipping

    Many think of a manufacturer as a faceless entity moving drums from one address to another. For us, the job starts before the purchase order arrives. Our technical team holds regular sessions with users, sharing specific tips for preparation—how to dissolve ENB-459 in organic solvents without clumping, or pre-treating glassware to avoid film deposits. In some projects, our chemists collaborate directly with process engineers at customer sites, diagnosing reaction stalling via shared data packets and live video from lab benches. One client facing repeated trace iron contamination in their synthesis found relief when we re-examined our drum liner sourcing, tracing back a problem that only hands-on partnership could resolve. Every technical inquiry—from solubility questions to batch variation troubleshooting—feeds our own process database, informing not just future runs but the design of new production lines.

    On more than one occasion, collaborative troubleshooting has uncovered unexpected advantages; a modified filtration protocol developed for a custom client ended up raising yield across several campaigns. Our approach spills over into shared process validation as well; we routinely provide not just a Certificate of Analysis but a deeper batch narrative when requested—outlining the specific control points, interventions, and in-process test results for full transparency. This way, users building regulatory submissions or running critical toxicology studies can pull not just a product spec, but a partner’s record of every step that shaped their material.

    Challenges, Solutions, and Looking Ahead

    No batch line stays trouble-free. Even with every SOP and checklist in place, unforeseen process variations crop up: reactant lots shift character, power surges trip monitoring sensors, seasonal temperature swings alter solvent evaporation rates. We respond by keeping extra diagnostic tools at hand, from handheld GC-MS units to rapid on-line pH monitors. In cases where we see a trend toward higher residues or side-products, cross-departmental rapid response groups assemble—pulling expertise from R&D, quality, maintenance, and supply logistics. These fast-moving teams operate by open discussion, chasing down every variable from glassware cleaning protocols to vacuum sealing failures. Solutions get field-tested, iterated, and logged; if a fix works consistently, it goes straight into both our process guide and client advisory notes.

    Regulatory shifts demand their own pace of adaptation. As governments worldwide tighten limits on nitroaromatic emissions or move to harmonize safety thresholds, we track pending requirements, often preempting enforcement deadlines. Our site’s investment in waste gas abatement outpaced regional mandates by several years—partly from anticipating stricter compliance, partly because our teams pursue lower-impact synthesis for its own rewards. Raw material traceability, high on regulators’ lists, comes naturally due to our embedded batch recording protocols. Client audits confirm not just our document flow but the visible care across each department—audit teams often cite staff engagement and willingness to discuss “off-script” process details as a standout trait. These habits build trust not only in product quality but in long-term reliability.

    Reflections from the Manufacturing Floor

    Working with Ethyl 4-Hydroxy-3-Nitrobenzoate for years, from bench experiments to large-scale campaigns, we understand firsthand what makes a compound dependable or difficult. The subtleties—how the powder settles in a scoop, which solvent clears it fastest, or which stirring speed prevents local crystallization—matter more than standard specs can capture. Our process reflects accumulated stories, incidents, and small innovations. Each feedback cycle shapes the next improvement.

    So, when end-users ask why ENB-459 delivers better reproducibility, cleaner outcomes, or smoother processing, we answer not with a marketing line, but with stories and records from our own plant. The proof rests in the product we use ourselves, the batches we trace back for root-cause analysis, and the shared troubleshooting that backs up every shipment. We know the substance and its behavior because we see it, handle it, and refine it with every campaign. This commitment, born from direct experience, carries forward into every drum, every bag, and every support call. That’s the standard we hold, the difference behind our Ethyl 4-Hydroxy-3-Nitrobenzoate, and the partnership we extend to everyone using it in their next synthesis or innovation.