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2-(4-Nitrophenoxy)Ethanol

    • Product Name 2-(4-Nitrophenoxy)Ethanol
    • Alias 4-Nitrophenoxyethanol
    • Einecs EINECS 242-830-9
    • 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

    567091

    Chemical Name 2-(4-Nitrophenoxy)Ethanol
    Cas Number 4209-67-4
    Molecular Formula C8H9NO4
    Molecular Weight 183.16
    Appearance Yellow solid
    Melting Point 51-55°C
    Solubility Soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CC(=CC=C1OCCO)[N+](=O)[O-]
    Inchi InChI=1S/C8H9NO4/c10-5-6-13-8-3-1-7(2-4-8)9(11)12/h1-4,10H,5-6H2
    Storage Temperature Room temperature
    Synonyms 4-Nitrophenoxyethanol

    As an accredited 2-(4-Nitrophenoxy)Ethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 grams, tightly sealed with screw cap; labeled with chemical name, formula, hazard warnings, and storage instructions.
    Shipping 2-(4-Nitrophenoxy)Ethanol should be shipped in accordance with applicable chemical transport regulations. Package securely in tightly sealed containers, protected from light, moisture, and heat sources. Label as a potentially hazardous chemical and include appropriate hazard symbols. Ensure shipping documentation complies with local and international safety standards for organic compounds.
    Storage 2-(4-Nitrophenoxy)ethanol should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers or acids. Keep the storage area clearly labeled and secure, and avoid exposure to moisture. Personal protective equipment should be used when handling to prevent skin and eye contact.
    Application of 2-(4-Nitrophenoxy)Ethanol

    Applications of 2-(4-Nitrophenoxy)Ethanol in Industrial Manufacturing

    2-(4-Nitrophenoxy)Ethanol plays a critical role in specialized chemical synthesis across several key sectors. Our facility ensures full traceability and process control, supporting downstream manufacturers in high-value applications where quality, compliance, and process integration are essential. Below, we highlight established industrial use cases that leverage the unique properties of this intermediate.

    1. Synthesis of Liquid Crystal Monomers for Display Technologies

    Manufacturers in the electronics sector use 2-(4-Nitrophenoxy)Ethanol as a precursor during the molecular customization of phenyl-based monomers, which are essential for the formulation of advanced liquid crystal mixtures. This compound enters syntheses as a controlled reactant, contributing to the fine-tuning of dielectric anisotropy and viscosity parameters required for precision display applications such as TFT-LCD panels and high-contrast monitors. Accurate documentation and analytic characterization of each step are necessary due to strict industry requirements.

    Industry compliance standards

    • IEC 61290-1 (International Electrotechnical Commission standards for liquid crystal materials)
    • RoHS Directive (2011/65/EU) for hazardous substances restrictions
    • ISO 9001:2015 for quality management during component manufacturing
    • REACH Regulation (EC 1907/2006) registration for chemical intermediates

    Typical usage ratio

    • 3.5%–6.8% by weight in custom liquid crystal monomer batches; adjustments depend on targeted mesogenic core structure and downstream blending requirements

    Downstream process integration

    • Incorporated at the aryl etherification or ether cleavage step before final monomer purification and blending

    Final product types

    • TFT-LCD liquid crystal mixtures
    • Passive/active matrix display fluids
    • Temperature-compensated display fluids for instrumentation panels

    2. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Producers of APIs employ 2-(4-Nitrophenoxy)Ethanol as a core intermediate in multi-step syntheses of certain nitrophenyl-substituted agents, notably those targeting specific aromatic etherification steps within proprietary patent-protected chemical entities. Strict batch-wise quality testing and impurity profiling are enforced at every stage, ensuring regulatory traceability and downstream process safety from pilot through commercial scale.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) guidelines (ICH Q7)
    • USP–NF (United States Pharmacopeia–National Formulary)
    • European Pharmacopoeia (Ph. Eur.)
    • 21 CFR Part 210/211 (US FDA cGMP for finished pharmaceuticals)

    Typical usage ratio

    • Used stoichiometrically as required by each synthetic pathway; generally 1.0–1.2 molar equivalents relative to target substrate per reaction sequence

    Downstream process integration

    • Integrated during aromatic nucleophilic substitution or O-alkylation steps in the API synthesis route

    Final product types

    • Nitrophenyl-based active pharmaceutical ingredients
    • Research-grade small-molecule intermediates for clinical candidates
    • Reference compounds for analytical standards

    3. Urethane and Polycarbonate Additives for Performance Polymers

    Polymer compounders utilize 2-(4-Nitrophenoxy)Ethanol as a functional chain extender or as a structural modifier in the synthesis of specific aryl ether–containing polyurethanes and polycarbonates. By influencing polymer flexibility and thermal stability, it produces specialty engineering plastics well-suited for high-impact and optical applications, where molecular dispersity and reproducibility are critical. Production lines require trace impurity control and on-line color testing to meet industry specs.

    Industry compliance standards

    • ASTM D638 for tensile properties of plastics
    • UL 94 (Underwriters Laboratories) for flammability of plastic materials
    • ISO 10993-5 for biocompatibility (where applicable)
    • RoHS compliance for electronic and automotive applications

    Typical usage ratio

    • 1.2%–4.5% by weight as a co-monomer or chain extender, determined by targeted degree of polymerization and mechanical properties

    Downstream process integration

    • Blended during pre-polymer formation or introduced directly into the polycondensation reactor before final extrusion or molding

    Final product types

    • Impact-resistant optical polycarbonate sheets
    • High-performance polyurethane elastomers
    • Polycarbonate-based device housings for electronics

    4. Agrochemical Synthesis: Herbicide Intermediate

    Major agrochemical companies select 2-(4-Nitrophenoxy)Ethanol in the multi-step preparation of herbicidal active ingredients, leveraging its aromatic ether and nitro functionalities for selectivity engineering. This intermediate introduces specific substitution patterns, modulating the target molecule’s physicochemical and degradation profile to meet crop protection standards. Downstream processes include continuous-flow reactors and stringent effluent monitoring to ensure both yield and environmental compliance.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • ISO 23119 for agrochemical intermediate purity
    • OECD Good Laboratory Practice (GLP) for field trial substances
    • EU Regulation (EC) No 1107/2009 for plant protection products

    Typical usage ratio

    • Typically between 1.8%–3.0% by weight of total synthetic intermediates per batch, calculated for stoichiometric conversion relative to the subsequent coupling agent

    Downstream process integration

    • Reacted in the initial aromatic etherification step of the target herbicide’s synthesis pathway

    Final product types

    • Nitrophenyl-based post-emergence herbicide formulations
    • Intermediate bulk concentrates for further derivatization
    • Tested actives for field efficacy evaluation

    5. Synthesis of Specialty Dyes for High-Fidelity Printing

    Producers of industrial colorants employ 2-(4-Nitrophenoxy)Ethanol in the tailored synthesis of nitrophenoxyaryl dyes, optimizing hue intensity and lightfastness for advanced inkjet and security printing applications. This material enters the azo coupling phase, providing electron-withdrawing properties that stabilize color strength and resistance. Stringent in-process chromatography and shade-matching protocols ensure consistent end-product quality demanded by high-volume print runs.

    Industry compliance standards

    • ISO 2846-1 (Printing ink color and transparency)
    • EN 71-3 (Safety of toys: migration of certain elements in printed materials)
    • REACH Regulation (Annex XVII for colorant safety in printing)
    • ISO 9001:2015 for ink manufacturing process traceability

    Typical usage ratio

    • 2.5%–5.0% by weight in intermediate dye syntheses; determined by the desired color index and dye performance targets

    Downstream process integration

    • Added during azo coupling or ether formation prior to final dye isolation and standardization

    Final product types

    • Nitrophenoxy-based pigment dyes
    • Industrial inkjet inks
    • Anti-counterfeiting security inks
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    Certification & Compliance
    More Introduction

    Understanding 2-(4-Nitrophenoxy)Ethanol: Practical Benefits from a Chemical Manufacturer’s Perspective

    What Sets 2-(4-Nitrophenoxy)Ethanol Apart?

    In chemical manufacturing, each compound tells a unique story. 2-(4-Nitrophenoxy)Ethanol brings more to the table than just its molecular formula. Over the years, as raw material availability shifts and industrial needs evolve, we've seen how small changes in chemical structure can influence outcomes in production. This particular compound, with the nitrophenyl ether backbone and accessible ethanol side chain, has become a steady performer in our product portfolio. Not every compound can handle the scrutiny of technical staff, but 2-(4-Nitrophenoxy)Ethanol rarely falls short in practice, especially where fine-tuned chemical reactivity, solubility, and stable performance matter.

    There’s a practical reason our team continues to refine the process for producing this chemical. We have learned from first-hand experience that consistency between batches matters; problems don’t show up immediately but rather after repeated runs in customers’ reactors. 2-(4-Nitrophenoxy)Ethanol often finds its way into fine chemicals synthesis, particularly as a building block for pharmaceutical intermediates, specialty resins, and various custom molecules. Whether a customer is scaling up a pilot project or running high-volume operations, reliable quality makes a big difference. It’s about reassurance that starting material impurities won’t come back to bite stages down the line or throw off a tightly controlled synthesis.

    Model and Specifications Informed by Years on the Floor

    Manufacturing goes beyond lab results. In the plant, routine means something different; you hear about pump fouling, resin discoloration, and off-odors before any academic paper catches up. For 2-(4-Nitrophenoxy)Ethanol, we worked to tame the nitro group’s sensitivity during scale-up, settling on a robust preparation method we monitor from the raw material tank to finished drum. Typical purity levels hover above 98.5% by HPLC, not because it’s a marketing bullet point, but because underlying impurities can throw off downstream functionalization reactions. We learned through close communication with R&D partners that even minor amounts of related impurities change the reactivity profile, especially where catalytic hydrogenation or further substitution steps are involved.

    Moisture content stays low — usually less than 0.2% — not only as a nod to GMP standards but to prevent caking and unexpected side reactions during processing or long-term storage. Color sometimes gets lost among the numbers, yet a pale yellow, clear liquid helps our customers avoid problematic tars that accumulate when the compound sits in dispensers or dosing pumps. The model most often requested by the industry matches a molecular weight of 199.17 g/mol, and the standardized batch size scales comfortably for both small-batch creators and high-volume users.

    Why Usability and Handling Are More Than Checklist Items

    As a manufacturer, you see patterns in customer requests. Users working in small-molecule development pay close attention to viscosity, ease of transfer, and how the substance behaves under ambient and slightly elevated temperatures. 2-(4-Nitrophenoxy)Ethanol remains manageable: it pours without excess foaming and stays within acceptable viscosity ranges at standard warehouse temperatures. We focus storage recommendations on stability, knowing real-world warehouses sometimes stray beyond the classic 20°C target. Our logistics partners test drums exposed to temporary heat during summer or cold snaps in winter to ensure the product does not polymerize, form unwanted residues, or separate in solution.

    Handling practices reflect on-the-ground reality. Laboratory staff report back that the product doesn’t cling to glassware after rinsing, saving cleaning effort—an advantage over stickier analogs. In manufacturing operations, the compound proves less volatile than lower-weight methyl or ethyl ethers, reducing fugitive emissions and associated health risks. Packaging standards evolved from years of feedback: tight-sealing HDPE drums prevent both moisture ingress and potential cross-contamination with other stored reagents, something that plagued open-head barrels years ago.

    Application Experiences in the Real World

    We don’t just supply 2-(4-Nitrophenoxy)Ethanol; we see the ways it makes a difference in cost savings for formulators and research teams. In the custom synthesis of pesticide intermediates, the compound’s ether linkage makes it a sturdy oxygen donor, while the nitro group is ripe for selective transformations. One of our long-term collaborators switched from a related para-nitrophenol derivative due to repeated problems with unwanted oxidation during scale-up. After replacing it with our ethanol analog, they documented measurable reduction in side-product formation—and cleaner finished lots.

    Another customer, producing UV-curable coatings, needed a raw material that could contribute not just flexibility, but predictable reactivity in photopolymerization. The phenoxy-ether structure of 2-(4-Nitrophenoxy)Ethanol fit the bill, blending with acrylate systems without the slow, tacky curing sometimes seen with bulkier plasticizers. End users noticed improved clarity and a sharper cure endpoint, especially under variable production line speeds where minor delays matter. Each production trial led to small tweaks—reaction time, initiator dosage, even drum turnover protocols. Over time, production managers reported fewer batch failures and less downtime from cleaning tanks fouled by incompatible residues.

    Pharmaceutical innovation asks for flexibility without unknown risks. In our experience, 2-(4-Nitrophenoxy)Ethanol finds a niche as both a linking group and as a reversible protection element for more reactive sites. Researchers working on heterocyclic libraries saw consistent yields, especially in multi-step synthesizes where other possible intermediates brought unpredictable color changes or harder-to-remove by-products. Operators value the compound for its straightforward quenching and extraction behavior, reducing the headaches of tricky separations that eat up time in pilot plants.

    Differences Compared to Similar Chemicals

    Out in the field, not every product suits every downstream program. Some customers start by comparing 2-(4-Nitrophenoxy)Ethanol to its predecessor, 4-nitrophenol, or to standard alkoxy ethanol derivatives. On paper, differences look subtle, but daily outcomes tell another story. We saw that swapping to our compound often lowered off-gassing and waste treatment load, attributable to the increased molecular weight and reduced volatility of the nitrophenoxy ethanol framework. Even simple things like the less pungent smell compared to their methyl or ethyl equivalents count during tank charging shifts, sparing operators from unnecessary discomfort.

    Customers sometimes test our material’s limits against even more specialized reagents—alkyl nitrophenyl ethers or heavier glycol analogs. Results depend less on spec sheets and more on how the chemistry performs at scale. One ink manufacturer described how switching to 2-(4-Nitrophenoxy)Ethanol stabilized color fastness over a six-month shelf-life for solventborne formulations; previous attempts with diethylene glycol mononitrophenyl ether had led to pigment migration and uneven aging. We regularly discuss real trial data with process chemists, not just lab anecdotes, as so many variations aren’t obvious until you’re troubleshooting a live production line.

    Environmental, Health, and Safety Priorities

    Good stewardship starts on our end, so we design production processes that minimize hazardous waste and recover solvents where possible. 2-(4-Nitrophenoxy)Ethanol isn’t classified among the highest-risk chemicals, but our team doesn’t take shortcuts on containment. In the past, we encountered issues with seasonal humidity causing surface discoloration and raised the alarm internally; now, we monitor humidity more tightly in both packaging and transit hubs.

    We consistently update SDS and transport documents based on the latest local and international regulations as chemicals like these sometimes change classification in different markets. In-house training goes beyond written protocols: operators receive hands-on demonstrations, including emergency neutralization and spill response, to anchor safety routines in muscle memory. Lab-scale and drum-upscale staff both participate since incidents can occur at any stage. We’ve found that running short debriefs after minor incidents helps everyone learn collectively and avoid any recurrence.

    Our on-site wastewater treatment facility underwent upgrades to specifically handle traces of nitrophenolic compounds. Recirculation loops and monitoring programs track effluent purity, reducing the impact of inadvertent discharges to well below permissible regulatory thresholds. Sharing these improvements doesn’t just meet norms—it builds trust with community stakeholders and international buying teams alike. By investing in these systems, we've improved not only plant safety but overall product consistency.

    Troubleshooting and Continuous Improvement in Production

    Even the best-designed processes run into snags. Early batches of 2-(4-Nitrophenoxy)Ethanol sometimes presented with faint orange hues or a resinous by-product that made drum transfer difficult. Rather than blame packaging or shipping, we traced the problem back to a solvent purity issue upstream. Over time, we changed solvent grades, swapped filtration media, and adjusted distillation vacuum levels until the color and purity dialed in under real-world conditions. These adjustments didn’t just benefit bulk buyers; even one-liter recipients, often specialty labs, reported easier handling and fewer downstream purification steps.

    Continuous feedback loops drive our progress. Our technical team spends time visiting user sites and bringing back detailed process notes. One food chemistry client noted minor flavor taints in a precursor batch not tied to obvious contamination. Instead of dismissing the issue, our analysts mapped out trace side-reactions with the customer’s exact thermal cycle, narrowing the problem to a tank agitation setting. Fine-tuned agitation protocols led to tangible improvements, reducing spurious flavor formation in downstream batches of unrelated compounds.

    Customer follow-up shines a light on overlooked details. A large order destined for a specialty coatings manufacturer led us to customize drum closures with gas-impermeable seals after staff complained about trace oxidant ingress during long ocean freight. They tracked even minor deviations in coating performance back to barely-detectable product changes caused by prolonged transit. Now, we score shipments based on post-delivery sampling, and quality assurance teams coordinate closely with forwarders and customers alike to verify the product remains unchanged.

    Market Shifts and Adapting to Changing User Demands

    Durable partnerships stem from flexibility and listening. Over the last decade, end-users in both pharma and specialty chemicals requested options for smaller runs with tight release requirements. Short lead times and smaller drum lots once dragged down both productivity and profitability, but we adapted. On-site small-batch reactors allow us to support research parks and start-ups as fluidly as larger manufacturers.

    Every year, industry expectations shift, with more interest in lifecycle analysis and product traceability. More buyers ask about the environmental impact per kilogram of final product. In response, we implemented batch-level tracking and provide optional sustainability reports. We track the carbon footprint of 2-(4-Nitrophenoxy)Ethanol from raw material receipt through final QC, offering data transparency for audits or compliance purposes. The material itself meets the needs of a range of end users, but knowing where it came from and how it was made has become equally important.

    Supply interruptions bring their own challenges. Global disruptions tested our sourcing channels, but on-hand inventories, backup supplier vetting, and direct relationships with logistics partners ensured ongoing shipments. We don’t overpromise lead times yet regularly handle rush orders by drawing on both established inventories and collaborative planning with customer teams. Each rush order is reviewed by both logistics and quality supervisors to make certain that expedience never compromises quality.

    Supporting Research and Custom Synthesis

    We see a growing need for flexibility in technical support. Research groups designing new active compounds often need custom purity selections or specific packaging. Our development lab can deliver tailored lots, verified by enhanced NMR and mass spectrometry analysis for those investigational programs needing documentation beyond standard COAs. Our staff stays available for call-ins or site visits if unanticipated challenges come up.

    We’ve found that standard-grade 2-(4-Nitrophenoxy)Ethanol suffices for many base-level programs, but as work progresses to pilot plant or early commercial samples, customers often seek tighter analytical data. Our in-house team takes this seriously, providing detailed impurity profiles, retained samples for reference, and open access to batch chromatograms. For particularly sensitive applications involving chiral intermediates or trace-level activity, we work with clients to specify target impurity cut-offs and even design special filtration or addition protocols.

    Collaborative problem solving always leads to better results. Several exploratory programs in material science used our compound as a starting material for novel adhesives; challenges around curing time and mechanical strength prompted weeks of exchange between our process chemists and the user’s technical staff. Joint testing and in-process sampling closed the gaps, uncovering small but meaningful adjustments in addition rate and storage procedure that saved downstream troubleshooting for all involved.

    Lessons Learned and Looking Ahead

    After years of producing 2-(4-Nitrophenoxy)Ethanol, we understand that no one batch, customer, or application is quite like another. Quality starts early, long before raw materials reach our gate. Each drum that leaves our facility represents hundreds of hours of behind-the-scenes planning, collaboration, and honest troubleshooting. Even compounds as reliable as this one bring new challenges as users find unexpected applications that test its limits. Our teams remain committed to learning from setbacks and sharing successes.

    Markets will always chase novelty. New synthetic pathways and regulatory pressures may shape future iterations of this compound. For now, confidence comes from each successful delivery and a track record of open communication. 2-(4-Nitrophenoxy)Ethanol earns its place in our offering not through abstract promise, but through the accumulated testimony of process chemists, engineers, and researchers who rely on it to solve specific problems every day. As needs change, we stand ready to adapt, leveraging hands-on experience and honest feedback, continuing the work of refining both the product and the partnership that supports it.