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3-Ethoxyphenol

    • Product Name 3-Ethoxyphenol
    • Alias m-Ethoxyphenol
    • Einecs 221-975-0
    • 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

    242277

    Cas Number 621-19-6
    Iupac Name 3-ethoxyphenol
    Molecular Formula C8H10O2
    Molecular Weight 138.17 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 238 °C
    Melting Point 4 °C
    Density 1.08 g/cm³ at 25 °C
    Flash Point 105 °C
    Solubility In Water Moderate
    Refractive Index 1.532
    Synonyms m-Ethoxyphenol, 3-Hydroxyphenetole

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

    Packing & Storage
    Packing A 250 mL amber glass bottle with a secure screw cap, labeled "3-Ethoxyphenol,” displaying hazard symbols and handling instructions.
    Shipping 3-Ethoxyphenol is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be stored upright in a cool, well-ventilated area, away from sources of ignition or incompatible materials. During transit, appropriate labeling and hazard precautions are observed to comply with relevant chemical transport regulations.
    Storage Store 3-Ethoxyphenol in a tightly sealed container in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from direct sunlight and moisture. Label the container clearly and ensure proper secondary containment to prevent leaks or spills. Follow all applicable safety and regulatory guidelines for chemical storage.
    Application of 3-Ethoxyphenol

    Applications of 3-Ethoxyphenol in Industrial Manufacturing

    3-Ethoxyphenol is a high-purity aromatic compound serving as a critical intermediate in several specialized industrial verticals. Our manufacturing experience supports global clients in pharmaceuticals, agrochemicals, perfumery, polymer additives, and dye synthesis. See below for detailed application fields, compliance, processing steps, target ratios, and resulting end products, based on real downstream use.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical companies incorporate 3-ethoxyphenol as a building block in synthesizing complex drugs, particularly within analgesic, antipyretic, and anti-inflammatory compound families. It contributes significant electronic properties to core structures and enables functionalization during multi-step organic synthesis. Along with strict documentation, customers require traceable batch consistency for cGMP manufacture of active pharmaceutical ingredients.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals (FDA)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for APIs
    • USP General Chapters relevant to impurity testing and purity profile

    Typical usage ratio

    • 5–20% w/w in intermediate reaction steps; adjusted based on target API structure and process yield.

    Downstream process integration

    • Nucleophilic substitution or etherification in the active nucleus construction, directly preceding final API synthesis.
    • Often enters at Step 2 or 3 of total synthetic route, depending on the medicinal chemistry protocol.

    Final product types

    • Prescription pharmaceuticals (NSAIDs, antipyretics, custom candidates for clinical trial pipelines)
    • Research chemical libraries for drug discovery

    2. Agrochemical Synthesis (Herbicide and Pesticide Intermediates)

    Agrochemical formulators utilize 3-ethoxyphenol to construct specialized phenolic precursors for targeted pesticides and herbicides. Its physical properties support controllable reactivity and stability during scale-up. The compound enters either as a direct coupling partner or as a protection group modulator which later unlocks bioactivity in complex crop protection agents.

    Industry compliance standards

    • ISO 9001:2015 – Quality Management Systems for industrial chemicals
    • FAO/WHO Specifications and evaluations for chemical pesticides (JMPS)
    • REACH Regulation (EC) No 1907/2006 – Registration, Evaluation, Authorisation and Restriction of Chemicals
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 2–8% w/w as functional intermediate within total technical formulation; specifics set by each target molecule and local crop residue thresholds.

    Downstream process integration

    • Entry at coupling stage in the synthesis of diaryl ethers, selective phenolic esters or carbamates.
    • Applied following initial chlorination/halogenation activities, often as the phenolic ether component.

    Final product types

    • Herbicide active ingredients for selective weed management
    • High-performance insecticide intermediates for greenhouse and field use
    • Precursors for low-persistence, eco-profiled pesticides

    3. Fragrance and Flavor Ingredient Manufacturing

    Specialty chemical companies process 3-ethoxyphenol to synthesize stable aromatic ingredients for fine fragrances and high-grade flavorants. The compound imparts warm, earthy notes as part of musk, floral, and spicy-blend bases. Downstream users demand precise purity and strict control of olfactory profiles, with batch consistency and allergen declarations crucial for compliance.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for ingredient restriction
    • ISO 9001:2015 – Applied to fragrance manufacturing
    • EU Cosmetics Regulation (EC) No 1223/2009 – For fragrance application
    • FDA 21 CFR Part 172.515 (Flavoring Substances and adjuvants, United States)

    Typical usage ratio

    • 0.1–5% in fragrance concentrate or flavor blend; level set by target aroma impact and regulatory limit per finished product type.

    Downstream process integration

    • Acts as a modifying agent during molecular distillation or chemical recombination stages in fragrance formulation.
    • Added post-headspace analysis to calibrate blend profiles for perfume and food uses.

    Final product types

    • Fine fragrances for personal care and cosmetics
    • Flavor preparations for baked goods, confectionery, and non-alcoholic beverages
    • Specialty aroma chemicals for industrial perfumery

    4. Dye and Pigment Intermediate Manufacturing

    Textile and specialty dye manufacturers employ 3-ethoxyphenol for advanced azo dye and anthraquinone pigment synthesis. Its substitution pattern allows color tuning during coupling reactions, directly affecting hue, solubility, and lightfast characteristics. Quality control focuses on trace metal content and purity for high chromatic performance in technical textiles and inks.

    Industry compliance standards

    • OEKO-TEX® Standard 100 – For raw materials used in textiles
    • REACH (EC) No 1907/2006 substance evaluation
    • ZDh (German Dye Association) purity protocols for technical dyes
    • ASTM D2619 – Standard Test Method for Hydrolyzable Chloride in Aromatic Compounds by Potentiometric Titration

    Typical usage ratio

    • 3–15% of dye batch synthesis; modifications aligned with target pigment shade and substrate compatibility.

    Downstream process integration

    • Introduced at the diazotization or coupling step for reactive and direct dye manufacture.
    • Used as a coupling component influencing light stability and wash fastness in the final pigment.

    Final product types

    • Reactive and direct textile dyes for cotton, wool, and blended fibers
    • Organic pigments for printing inks, coatings, and plastics coloration
    • Specialty color concentrates for polymer processing

    5. Polymer Additive and Stabilisers

    Producers of high-performance polymers integrate 3-ethoxyphenol as a stabilizing additive, particularly for polyesters, epoxy resins, and specialized engineering plastics. The phenolic ether group enhances resistance against oxidative degradation and improves aging properties in polymers exposed to elevated temperatures or strong UV light.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management) compliance for additive use
    • UL 94 Standards for polymer flammability
    • RoHS Directive (2011/65/EU) compliance on restricted substances
    • FDA 21 CFR 177.2420 (Polyester Resins for food contact applications, if applicable)

    Typical usage ratio

    • 0.05–1% by mass in finished polymer formulations; increased or decreased depending on matrix type, target UV stability, and final product exposure profile.

    Downstream process integration

    • Added at masterbatch preparation or compounding phase for polymer pellets and granules.
    • Incorporation occurs before extrusion or injection molding.

    Final product types

    • Engineering plastics for automotive and electronics
    • Packaging films and sheets
    • Epoxy systems for circuit boards and adhesives
    • Construction polymer additives
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    Competitive 3-Ethoxyphenol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3-Ethoxyphenol: Practical Know-How from a Chemical Manufacturer

    Experience with 3-Ethoxyphenol

    In our day-to-day operations, chemistry relies on both reliable raw materials and an understanding of what separates them. Among our aromatic ethers, 3-Ethoxyphenol deserves discussion—not just as another compound on the order sheet, but for what its structure brings to both our shop floor and the industries we supply.

    Why Is 3-Ethoxyphenol Worth Attention?

    The appeal of 3-Ethoxyphenol, known chemically as m-Ethoxyphenol and with the CAS Number 620-17-7, starts with its structure. The ethoxy group at the meta position of the phenol ring influences how this compound behaves in organic synthesis and in downstream formulations. On our line, we control moisture, color, and purity with a clear understanding these factors impact reaction performance and end-product quality. Batch after batch, tiny deviations in residual moisture or trace color can push results off-spec, so strict process oversight keeps us on target.

    We see 3-Ethoxyphenol used widely in the making of pharmaceutical intermediates, specialty resins, and certain agrochemical syntheses. The preference comes especially in processes looking for predictable O- and C-alkylations that depend on the right reactivity profile. Agrochemical producers have pointed us toward 3-Ethoxyphenol’s stability when scaling bromination or nitration steps. They return for lots that offer tight melting range and low impurities, highlighting that not all sources of this compound meet those marks.

    Specifications That Matter in Real-World Manufacturing

    Much of the talk about raw chemical quality can only be separated with direct results over time. We produce 3-Ethoxyphenol typically as a pale yellow to colorless liquid or low-melting solid, with a purity above 99%. Every shipment includes NMR and GC data from our own in-house QC lab, where we check for low phenolic resin content, organic base residue, and minimal volatiles. Our own data suggests that even low levels of residual starting materials or byproducts create headaches in syntheses that demand high selectivity. This leads to batch failures, which waste time and raw materials down the chain.

    We maintain traceability for each lot, and customers come back to us describing how our consistency cuts their process troubleshooting. We do not believe color or purity specs alone distinguish materials. Instead, we look at how our 3-Ethoxyphenol behaves in pilot trials, where delayed solidification, unexpected odor, or poor filtration signal upstream problems that ripple through to finished product quality. Our team has learned to tie feedback on boiling point and odor directly to process conditions and batch handling, not just what comes out of the distillation column.

    Where 3-Ethoxyphenol Sits Versus Other Phenolic Ethers

    Seasoned formulators and synthetic chemists compare 3-Ethoxyphenol with related compounds like 2-ethoxyphenol and 4-ethoxyphenol. The position of the ethoxy group changes not just reactivity, but also physical properties—boiling point, solubility in polar and nonpolar solvents, and stability under UV or heat. These differences matter in processes like polymerization, dye manufacturing, or when creating custom antioxidants for lubricants or plastics. Some customers switch between meta, ortho, and para isomers when adjusting reaction selectivity or downstream solubility.

    Our experience tells us that, while 2-ethoxyphenol often appears in fragrance blends for its sharp, slightly sweet aroma, 3-ethoxyphenol fits more industrially robust synthesis due to its moderate electron-donating effects. The meta orientation imparts a different electron density profile, impacting both ring substitution rates and patterns. Where 4-ethoxyphenol might encourage faster side-chain introduction under certain conditions, 3-ethoxyphenol gives more deliberate, controllable reactivity, useful in multi-step syntheses with little room for error.

    What often gets overlooked is that minute changes in isomeric purity can tilt the scales between a viable process and wasted product. We monitor for these isomeric impurities using HPLC and NMR, as downstream failures in pharmaceuticals sometimes get traced back to poorly defined aromatics at the front end. More than once, we have fielded customer complaints triggered not by absolute purity, but trace cross-contamination between ethoxyphenol isomers that disrupts formulation stability or introduces regulatory compliance issues in final goods.

    Why Purity and Trace Impurity Control Remain Critical

    Looking at historical data, problems in scale-up rarely trace to gross errors—rather, they come from low-level impurities in starting materials. Phenolic ethers like 3-Ethoxyphenol, when poorly refined, may hold onto oxidation byproducts or micro-traces of unreacted phenol. During catalyst-driven steps or downstream oxidations, these compounds sometimes poison the catalyst bed or promote color formation in resins.

    Over the past decade, we’ve seen environmental and pharmaceutical regulation grow far stricter. Customers now request detailed impurity profiles—showing not just what we remove, but what remains below quantifiable limits. Sophisticated users run their own GC-MS screens on delivery and circle back quickly if a new peak appears. Our in-house policy now tracks impurity drift across production runs, linking every lot back to the conditions in our reactors and distillation systems. This means hands-on process monitoring and, as a manufacturer, this translates directly to smaller process upsets and fewer rejected customer shipments.

    End Uses Shaped by Reliable Supply

    The end-users manufacturing resins, drugs, and specialized coatings depend on regular, reliable deliveries. Our customers making UV-curable adhesives and high-performance monomers often cite not just price, but our documented performance records. A dependable source of 3-Ethoxyphenol avoids scrambling for alternatives that may alter downstream processing and regulatory declarations. For pharmaceutical intermediates in particular, a consistent aromatic ether source forms the backbone of their validated supply chains. Audits from their QA teams frequently focus on our batch records, in-house environmental and safety controls, and evidence of rigorous impurity testing.

    Some applications require relatively small amounts of 3-Ethoxyphenol, but those grams need to perform predictably. An example comes from a custom dyes producer, who struggled with batch-to-batch variability in hue strength and solubility. Their feedback showed that minor shifts in our process (such as slightly changed residence time in the final purification) impacted their end use more than overall purity. This contribution to real-world R&D means that we tune our manufacturing approach to fit not just high-volume commodity demands, but also small-batch specialty use.

    Understanding Demand and Scalability

    Bulk chemicals like phenolic ethers need a different production and supply mindset compared to high-value, low-volume materials. Large customers might take multiple drums per month, requiring us to maximize run sizes and minimize product changeover. Yet our operation retains the flexibility for smaller campaigns and R&D grade production, using parallel reactor suites and dedicated purification lines to cut cross-contamination. This reduces expensive quarantines and rework, especially on tight deadline jobs.

    We continually invest in process intensification, automation, and batch monitoring, not only to hit tighter impurity specs but to ensure plant reliability. Shutdowns from pump failure or fouling feedstock cost everyone time and trust. The customers in the coatings and resin world—where 3-Ethoxyphenol often forms the core of phenolic resin precursors—demand this operational focus because their lines stop when upstream chemicals are missing or inconsistent.

    Challenges Unique to 3-Ethoxyphenol

    Any manufacturer familiar with phenolic ethers will recognize recurring production challenges. Phenols, in particular, encourage color formation if exposed to trace metals, high temperature, or oxygen for even short periods. Our team observes that keeping a low-oxygen environment and using deionized water for washes helps maintain a clean, pale product. We’ve also found that certain batches require in-line filtration to remove fine particulates picked up during transfer. Even minor vessel fouling can reduce color quality, with the result visible immediately upon distillation.

    Shipping also brings its own constraints. 3-Ethoxyphenol solidifies near room temperature, so packaging and storage play a role in maintaining product flow. Bulk deliveries in colder climates need brief warming on arrival to avoid delays in unloading. We supply both metal drums and HDPE containers, chosen for inertness and protection against moisture. Labelling errors or storage near incompatible chemicals create safety concerns or alter product properties, so close attention to filled packaging and warehouse conditions keeps supply reliable.

    Working With Regulatory and Sustainability Pressures

    The modern chemical world cannot ignore regulatory scrutiny. Phenolic ethers draw attention in many regions due to environmental fate and toxicity questions. Our compliance team closely tracks REACH registration in the EU and US EPA reporting for chemicals like 3-Ethoxyphenol. Supporting customers means providing transparent documentation—from synthesis route details to regular safety data updates. A technical team prepares full batch histories and impurity profiles, allowing quick answers to customer audits and spot checks.

    Over the last five years, more customers insist on supply chain transparency and risk management evidence. Our response relies on good process controls rather than excessive documentation. We cut batch variance at the source, keep detailed root-cause records, and involve the production crew in hidden loss investigations. Most sustainability improvements, in our experience, come from process energy savings and tighter cut point optimization in distillation. These improvements do not only keep us in regulatory good standing but reduce waste and improve our competitiveness.

    We’ve responded to customer pushes for greener chemistry by reviewing the sourcing of our starting materials and reducing process solvents where possible. This means choosing suppliers that themselves face third-party audits, and shifting away from legacy purification agents with high environmental tolls. In the grand scheme, each improvement compounds: greener chemistry translates to a stronger business, fewer regulatory headaches, and longer customer loyalties.

    Supply Challenges and Industry Solutions

    Changes in global logistics over the past few years highlighted the risk in long supply chains for all but the most basic chemicals. 3-Ethoxyphenol does not escape these effects. Everything from port slowdowns to container shortages can disrupt just-in-time operations. We have learned to work closely with logistics partners, maintaining safety stocks in key locations, and rehearsing contingency plans for both raw material and finished goods blockage.

    We run regular review meetings with our shipping and sales teams to flag potential disruptions early. Customers appreciate up-front communication and rapid rerouting options in case of delays. Where needed, we’ve developed tolling relationships with chemical processors in other regions, able to swing short-run production to alternate facilities within weeks rather than months. In one particularly tight supply stretch, advance planning and joint raw material purchasing with a major partner helped stabilize both our production and the supply for several downstream resin makers.

    Supporting End User Innovations

    We do not simply supply a list of chemicals. Working as a manufacturer, our staff holds deep knowledge in aromatic ether chemistry and downstream formulation. Our R&D group supports customer trials, troubleshooting color, solubility, or reactivity deviations traced back to even subtle process shifts. More than once, feedback about reaction optimization, purification failures, or product stability led us to detect process drift and correct future batches.

    We also invite regular customer visits and audits. Seeing our process up close adds trust, and we learn about how our material actually performs at the customer’s hands. One manufacturer of specialty coatings described subtle yield boosts after identifying a previously undiagnosed impurity, leading us to revise our post-distillation polishing step. These collaborations strengthen the end product and build the kind of supply chains that weather global shocks and shifting regulations.

    Learning from the Field

    Experience has taught us that successful chemical manufacturing blends technical discipline with hands-on adjustments. 3-Ethoxyphenol, with its dependence on purity, consistency, and trace impurity control, offers a clear example of how operational vigilance pays off. Our team remains committed to in-plant process development, rigor in quality control, and active customer support. The lessons learned from decades of handling phenolic ethers shape not just this product but every batch rolling out of our units.

    In today’s demanding environment, no one in manufacturing can afford shortcuts. Customers are right to demand tight specification control, transparency, and responsive supply. Our approach with 3-Ethoxyphenol comes down to the basics: strong process knowledge, full attention to the details, and honest communication. Whether the material goes into a high-value pharmaceutical intermediate or a specialty resin project, we follow the same guiding philosophy. Meeting these expectations is what keeps our products at the center of many successful chemical supply stories.