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2-Ethoxy-4-Nitrobenzoic Acid

    • Product Name 2-Ethoxy-4-Nitrobenzoic Acid
    • Alias 2-Ethoxy-4-nitrobenzoic acid
    • Einecs 223-653-5
    • 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

    376195

    Iupac Name 2-ethoxy-4-nitrobenzoic acid
    Cas Number 6108-45-2
    Molecular Formula C9H9NO5
    Molecular Weight 211.17 g/mol
    Appearance Yellow crystalline powder
    Melting Point 155-157 °C
    Solubility In Water Slightly soluble
    Density 1.41 g/cm³ (approximate)
    Pubchem Cid 24979904
    Smiles CCOC1=C(C=CC(=C1)[N+](=O)[O-])C(=O)O
    Inchi InChI=1S/C9H9NO5/c1-2-15-9-5-6(10(13)14)3-4-7(9)8(11)12/h3-5H,2H2,1H3,(H,11,12)

    As an accredited 2-Ethoxy-4-Nitrobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled “2-Ethoxy-4-Nitrobenzoic Acid, 25g,” sealed with a screw cap; features hazard and safety information.
    Shipping 2-Ethoxy-4-Nitrobenzoic Acid is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported according to chemical safety regulations, typically under ambient conditions, and accompanied by a safety data sheet. Ensure appropriate labeling and handle with gloves and eye protection during receipt and transfer.
    Storage 2-Ethoxy-4-nitrobenzoic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong bases and oxidizing agents. Ensure the storage area is free from moisture. Properly label the container and keep it away from food and drink. Handle with suitable protective equipment.
    Application of 2-Ethoxy-4-Nitrobenzoic Acid

    Applications of 2-Ethoxy-4-Nitrobenzoic Acid in Industrial Manufacturing

    2-Ethoxy-4-Nitrobenzoic Acid serves as a key intermediate in advanced organic synthesis, with its functional groups making it suitable for specialized use in pharmaceutical research, high-performance dye manufacturing, speciality agrochemical synthesis, and polymer additives. Each downstream sector requires precise control over purity, ratio, and integration within established quality systems. We support industrial partners through direct, application-focused supply and technical guidance specific to each manufacturing segment.

    1. Pharmaceutical Intermediate for API Synthesis

    This material enters pharmaceutical manufacturing as a core building block in the assembly of certain active pharmaceutical ingredients, particularly within antipyretic and anti-inflammatory agent classes. It is selected for its defined reactivity and low impurity profile, supporting cost-effective, high-yield synthesis under GMP standards. Formulators rely on batch consistency due to strict regulatory audits and material traceability requirements.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for Active Pharmaceutical Ingredients
    • USP and EP Monograph Reference Testing (where applicable for intermediates)
    • FDA 21 CFR Part 210/211 (cGMP for Drug Products)
    • ISO 9001:2015-certified QC Framework

    Typical usage ratio

    • 0.3–1.2 molar equivalents per API batch, adjusted according to specific synthesis route and target yield; stoichiometry is optimized based on reaction efficiency and downstream purity requirements.

    Downstream process integration

    • Charged at the condensation or acylation stage during multi-step API synthesis; purification occurs via crystallization before the subsequent transformation or coupling reactions.

    Final product types

    • Bulk intermediates for antipyretic pharmaceuticals
    • Key intermediates in custom anti-inflammatory or analgesic synthesis
    • Non-steroidal drug precursor compounds produced for multinational generic manufacturers

    2. High-Performance Dye Manufacturing

    Downstream formulators in dye and pigment production use this acid as a diazo component for synthesizing specialized azo, disperse, and acid dyes. Its unique ethoxy and nitro substitution pattern ensures color consistency and fastness properties critical for textile and plastics coloration. Extensive documentation and trace lot data support customer regulatory submissions and end-use certifications.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Restricted Substance List for textiles)
    • REACH (EC) No 1907/2006 registration and substance evaluation for dyes
    • ISO 14001 for environmental monitoring during dye synthesis
    • ZDHC MRSL compliance

    Typical usage ratio

    • 5%–20% by weight relative to total dye precursor blend, depending on final color strength, shade, and application method (pad-dyeing vs. exhaust dyeing).

    Downstream process integration

    • Introduced during coupling reactions with aromatic amines, directly influencing the chromophore structure of the finished dye molecule; supplied as purified crystalline powder to minimize color defects and batch inconsistency.

    Final product types

    • Azo dyes for cellulose fiber textile printing
    • Disperse dyes for synthetic polyester fibers
    • Speciality pigments for industrial plastic extrusion
    • High-fastness dyes used in automotive textile applications

    3. Agrochemical Intermediate for Herbicide Synthesis

    Agrochemical formulators incorporate this compound as a controlled-source intermediate for the selective synthesis of nitrobenzoic acid-derived herbicides. Its role as a regulated input necessitates verified documentation chains and analytical conformity to minimize crop protection agent contamination risks. Downstream, production plants require consistency in reactivity and impurity profile to avoid off-target side reactions, especially during scale-up.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001 process traceability and batch record documentation
    • Chinese GB 20810-2006 for pesticide raw material quality
    • European Regulation (EC) No 1107/2009 approval for active ingredient registration

    Typical usage ratio

    • 0.07–0.35 molar fraction within technical concentrate blending, depending on targeted herbicide yield and product-specific purity standards.

    Downstream process integration

    • Reacted at the nitration and subsequent esterification phase of herbicide precursor production, with in-line QC monitoring via HPLC to ensure target intermediate concentration and control of process impurities.

    Final product types

    • Selective post-emergence herbicide intermediates
    • Formulated herbicidal active concentrate (technical grade)
    • Raw materials for finished crop protection mixtures

    4. Functional Monomer/Additive in Polymer Industry

    The chemical structure enables its use as a functional monomer or additive to enhance specific properties in specialty resins and engineering plastics. Formulators in the polymer sector value its precise melting and reactivity profile for proprietary end-use applications, such as UV-curable resins or high-durability thermoplastic polymers. Controlled addition and traceable sourcing support QA/QC documentation for certification by end users in regulated industries.

    Industry compliance standards

    • ISO 9001 quality management during polymer compounding
    • UL 94/V-0 (for flame retardant testing, as relevant)
    • RoHS Directive 2011/65/EU (for restricted substance content)
    • EN 71-3:2019 for migration of certain elements in plastic toys, if used in consumer applications

    Typical usage ratio

    • 0.1%–0.8% by polymer resin weight, adjusted after pilot runs to achieve target thermal or UV resistance properties without negatively impacting processing viscosity or extrusion flow.

    Downstream process integration

    • Pre-mixed with base resin during melt blending; dosage fine-tuned before compound pelletization or extrusion, ensuring homogeneous distribution for property enhancement.

    Final product types

    • UV-curable high-durability coatings
    • Specialty engineering thermoplastic compounds
    • Custom-formulated flame retardant resin masterbatches
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    Certification & Compliance
    More Introduction

    2-Ethoxy-4-Nitrobenzoic Acid: Practical Perspectives from the Manufacturer’s Bench

    Grounded Chemistry for Real-World Applications

    Over the years, we have handled plenty of benzoic acid derivatives. Some get all the attention in classic esterification projects or as standards for analytical methods. Among them, 2-Ethoxy-4-Nitrobenzoic Acid definitely has its own way of working inside the lab and on the production line. From a practical angle, its appeal lies in a steady blend of stability, manageable handling properties, and targeted reactivity. As a manufacturer invested in process consistency, I value this compound’s straightforward profile—both in bulk and in-use.

    Model Details and Reliable Characteristics

    Looking at the most requested grade, we supply 2-Ethoxy-4-Nitrobenzoic Acid as a white to pale yellow crystalline powder, following strict QC for purity usually exceeding 99 percent by HPLC. The molecular formula reads as C9H9NO5, and it weighs in at 211.17 g/mol. Melting points for our standard batch hover between 161 and 165°C. These details might sound routine, but from experience, subtle shifts can muddy downstream synthesis, so we focus on giving each batch the same reliable profile every time.

    How End Users Tap Into This Compound

    From customers in fine chemical labs to those feeding intermediates into actual pharmaceutical lines, the demands for this product rarely stray too far from a few core uses. I have seen it serve as a direct intermediate in active pharmaceutical ingredients, especially where ethoxy groups create the right molecular spacers or where the nitro group opens a path for reduction. In agrochemical projects, the same framework gives starter molecules for handling crop protection syntheses. Users aiming at pigment development and advanced materials sometimes draw on its properties for building block chemistry as well—though this feels more niche in terms of volume.

    Differentiating 2-Ethoxy-4-Nitrobenzoic Acid from Other Benzoic Acids

    We often field questions about the real benefit of this compound over other nitrobenzoic acids. From my vantage point as a maker—someone standing next to reactors, not behind a desk—the clearest difference is in how the ethoxy group tunes reactivity. Straight nitrobenzoic acids or methyl analogs respond differently during coupling or reduction steps. The ethoxy chain can introduce a degree of solubility or shift the electron density just enough to offer selectivity, changing yields and purification efforts in actual campaigns. That shift makes or breaks a process at centigram scale when high-value or high-specificity work is underway.

    For those handling substitutions at scale, the subtle shift from a methyl or propoxy to an ethoxy chain impacts not only the chemistry but also the downstream storage—ethyl ethers resist hydrolysis just a bit longer under warehouse conditions, especially in climates with variable humidity. These practical details matter after a few months, long after the spec sheet left the inbox.

    Steps Behind Consistent Quality

    Day in, day out, manufacturing 2-Ethoxy-4-Nitrobenzoic Acid means watching out for all the telltale signs—off-color, residual solvent, errant melting point shifts. The route we follow leverages direct nitration and ethoxylation, not post-modification. Why? The nitro group in para-position relative to the carboxylic acid avoids over-reaction risk and keeps batch quality high, cutting waste downstream. We confirm structure with NMR and IR spectra, checking against previous production runs. In this business, drifting specs increase costs and frustration, neither of which lead to long-term partnerships.

    Experience reminds me that on paper, many suppliers claim the same purity numbers. What sets one source apart is the everyday grind: clean glassware, trained operators, prompt line maintenance, and honest reporting. Benzene-derivatives, especially those with activation groups such as nitro or ethoxy, don’t leave room for half-measures in process hygiene. When the customer gets a batch that runs clean, it is not by accident—it’s from deliberate follow-through.

    Key Application Areas and Insights from the Field

    We see most of our 2-Ethoxy-4-Nitrobenzoic Acid go toward pharmaceutical intermediates. Reagents working downstream—usually in reduction and amide coupling steps—benefit from the precise substitution pattern. Research chemists emphasize selectivity over speed these days, and the well-defined ethoxy group helps with regioselective modifications without triggering too many side reactions.

    In one instance, a client scaled up an antihypertensive candidate, reporting back that the ethoxy group promoted clean conversion with minimal tarring—contrasting their previous results with a methyl analog. We rechecked our own samples for residual byproducts and found that the route held up. Years of messy reductions with other nitrobenzoic acids made it clear: the right substitution, however subtle, can prevent headaches for everybody on the project.

    Agrochemical clients lean into similar features. Here, the goal is less about ultimate purity and more about cost-effectiveness and solid yield. Having a consistent starting material shaves days off pilot runs, and the ethoxy group’s effect on downstream esterification or amidation routes can change formulation costs. We learned this the hard way after shipping a batch with a slightly wider melting range—customers immediately flagged less-than-ideal process results. They wanted material with tight, predictable characteristics so their own products could remain competitive.

    Raw Material Sourcing and Impact on Performance

    One nagging question we face as a producer: how much does the origin of early-stage raw materials affect batch outcomes for this compound? Anecdotally, differences appear clearer in products with multiple electron-donating or withdrawing groups, like this one. The type of ethanol, its water content, even the acid scavenger profile during ethoxylation—these matter for downstream uses. For example, small tweaks in the base used can swing the impurity profile and influence the final solubility, which becomes obvious in fine-tuned pharma formulations.

    We have ended up working with a few specific ethanol suppliers to rule out variable denaturants and traces of aldehydes. Some customers ask for detailed impurity tracking, and we provide batch-level transparency on these data. The reassurance goes both ways—the customer gets reliability, and we get fewer complaints or rejections later on.

    Handling inbound nitrobenzoic acid raw material with tight assay data is another safeguard. Our experience tells us that cutting corners at this stage cascades into headaches across purification, yield, and product stability. We move away from recycled solvents and favor fresh reagents where possible. The small premium pays off as predictable quality, especially for high-consequence batches heading to pharma plants under regulated oversight.

    Handling, Storage, and Downstream Compatibility

    For a manufacturer, storing and dispensing 2-Ethoxy-4-Nitrobenzoic Acid boils down to practical measures over theory. We use airtight liners inside drums, avoid exposure to ambient moisture, and rotate stock on a regular schedule. Extended storage usually doesn’t create issues if these steps get respected. A handful of customers told us their product caked in storage; feedback like that informed later improvements in our own warehouse, and now we monitor humidity as closely as temperature.

    Another practical factor: cross-contamination with similar nitrobenzoic acids or off-grade batches. We mark production days carefully and avoid shared cleaning streams for critical lots. Over time, these habits reduce rework, scrap, and—most importantly—customer frustration when they need to trace a lot number or validation run.

    Regulatory and Analytical Challenges in the Real World

    Compliance carries its own set of pressures. Even though 2-Ethoxy-4-Nitrobenzoic Acid doesn’t appear on many hazardous lists, a changing regulatory climate means more detailed documentation. For markets in Europe and North America, batch records now include not only purity and melting point but also GC-MS impurity fingerprints. It used to be that a brief COA satisfied everyone; those days have passed.

    Analytical methods also change over time. We transitioned from TLC checks and basic IR to HPLC and mass spectrometry as customer requirements evolved. The main goal: provide enough data so clients can incorporate the batch into their own compliance systems without bottlenecks. We log certificate numbers, archival spectra, and secure backup samples—an approach shaped by a decade’s worth of trending toward tighter documentation in pharma and advanced material supply chains.

    Technical Questions from the Field

    Anytime we restock, experienced clients raise questions around reaction compatibility and handling. In nitration or reduction steps, they want to know how the ethoxy group affects process safety. The biggest challenge lies in controlling not just temperature but also solvent ratios—our tech support team knows the practical implications of using higher pressure or alternate hydrogenation catalysts compared to those on benzoic acids with no alkoxy substitution.

    Customers who use the compound as a coupling intermediate have pointed out changes in crystallization patterns during scaling. Never assume a bench-scale solvent system will hold up at a hundred-kilogram run. We share our laboratory insights—sometimes tweaking antisolvents or adjusting cooling curves transforms six-hour filtration headaches into reliable cake formation and easy isolation.

    Lessons Learned and Solutions for Supply Chain Hiccups

    Running a synthesis line for this compound means running into hurdles—supply crunches for high-grade ethanol, shipping delays for specialty acids, or upturns in regulatory paperwork. Each snag forced concrete adjustments. We built dual-source supply contracts for vulnerable intermediates. On shipping bottlenecks, working with regional logistics partners over international giants gave more reliable transit times—customers got product on shelf days earlier and could keep their own schedules intact.

    Batch failures rarely happen in a vacuum. Dumping off-spec material isn’t just wasteful; it affects long-term trust. After two consecutive off-grade shipments to one customer in the late 2010s, we added in-process controls, with checkpoints after each main synthetic step, not just at final blending. The extra analysis takes time (and cost), but the bounce-back in performance—and customer satisfaction—proves its worth.

    Learning from End-User Feedback

    Field feedback drives much of our incremental improvement. If a customer finds a better deprotection protocol, spots batch-by-batch variation, or has compatibility issues, they share those insights. In turn, we refine our purification process, storage handling, and even packaging options. The back-and-forth with repeat users feeds real data into our process improvements—instead of making changes based on market rumors or assumptions, we use actual user input.

    For example, after learning some research teams struggled with static buildup in dry climates, we adjusted our powder micronization steps to reduce fines, cutting down on both handling loss and dust hazard. Shipping to customers with solvent-recycling programs led us to pre-wash drums more meticulously. Over time, this kind of fluid adjustment means we waste less material, streamline user workflows, and strengthen mutual trust in the product lifecycle.

    Continuous Improvement and Looking Ahead

    Every production run is a learning opportunity. In the case of 2-Ethoxy-4-Nitrobenzoic Acid, the challenges are neither show-stopping nor trivial—they’re the daily realities of balancing chemistry, logistics, and customer priorities. Our energetic group of operators, QC analysts, and process engineers trades knowledge regularly, translating recurring issues into standard practice updates.

    We keep up with market shifts. If tighter residual solvent controls or new analytical methods come into play, we adapt. Experience tells us: ignore these signals, and we risk losing relevance. Embrace them, and we strengthen our reputation for consistency, reliability, and grounded technical support.

    Conclusion: Manufacturer-Client Collaboration Moves the Needle

    At the end of the day, this isn’t a popularity contest between benzoic acid derivatives. It’s about finding the right material for the real-world process—from tablets to coatings to specialty reagents. 2-Ethoxy-4-Nitrobenzoic Acid has earned its spot for a set of reasons honed through experiments, line audits, and tough feedback from real clients. We don’t just ship out a powder; we provide backing when an unexpected problem arises at scale. Through the push-pull of regular demand, feedback, and nimble problem-solving, we keep moving production quality forward—not just for this product, but for every molecule that passes through our plant.