Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
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O-Ethylphenol

    • Product Name O-Ethylphenol
    • Alias 2-Ethylphenol
    • Einecs 202-507-8
    • 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

    309943

    Chemical_Name O-Ethylphenol
    CAS_Number 90-00-6
    Molecular_Formula C8H10O
    Molar_Mass 122.16 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling_Point 215-217 °C
    Melting_Point -27 °C
    Density 1.025 g/cm³ at 20 °C
    Solubility_in_Water Slightly soluble
    Refractive_Index 1.5280
    Flash_Point 90 °C (closed cup)
    Odor Phenolic, medicinal

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

    Packing & Storage
    Packing O-Ethylphenol is packaged in a 500mL amber glass bottle with a secure screw cap, featuring hazard labeling and product details.
    Shipping O-Ethylphenol should be shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. Transport in accordance with local and international regulations for hazardous chemicals, ensuring proper labeling and documentation. Avoid exposure to heat, sparks, or open flame. Handle with appropriate safety measures to prevent leaks or spills during transit.
    Storage O-Ethylphenol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizers. Keep the container tightly closed and protected from direct sunlight. Use approved containers made of compatible materials. Ensure proper labeling and maintain storage away from heat and moisture to prevent decomposition and ensure safety.
    Application of O-Ethylphenol

    Applications of O-Ethylphenol in Industrial Manufacturing

    O-Ethylphenol serves as a crucial intermediate and functional additive in several industrial sectors. As a direct manufacturer, we support global enterprises that require consistent purity, batch reliability, and regulatory support for this material in high-value downstream processes. Below we outline focused, real-world industrial applications derived from proven manufacturing partnerships and feedback from quality-led production environments.

    1. Agrochemical Intermediates – Herbicide and Fungicide Precursor

    O-Ethylphenol is widely integrated as a key intermediate in the synthesis of selective herbicides and fungicides, valued for its performance in producing active ingredients used by large-scale agricultural chemical manufacturers. Our clients rely on stringent quality management to support downstream registrations and compliance for crop protection chemistries.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for agrochemical intermediates
    • REACH Regulation (EC) No 1907/2006 for registered chemical substances
    • China National Standard GB 2763 for pesticide residue control
    • BPR (EU Biocidal Products Regulation)

    Typical usage ratio

    • 3–8% of precursor mass during target synthesis; adjustment depends on yield optimization and active ingredient conversion efficiency

    Downstream process integration

    • Added as a specific reactant during condensation and alkylation steps; reacts under controlled conditions to form core biocidal scaffolds

    Final product types

    • Triazole-based fungicides (e.g., propiconazole derivatives)
    • Phenoxyalkyl herbicides
    • Seed treatment actives
    • Leaf-applied operational concentrates

    2. Fragrance and Flavors – Aroma Chemicals Production

    Our high-purity O-Ethylphenol supports the specialty chemicals sector as an essential intermediate in the synthesis of select aroma compounds. It functions as a building block for formulations that demand strict aromatic character and compliance with international flavor regulations, predominantly for the fragrance and flavor ingredient supply chain.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • FEMA GRAS (Flavor and Extract Manufacturers Association, Generally Recognized as Safe number #3207)
    • US Food Chemicals Codex (FCC)
    • EU Regulation No 1334/2008 on Flavorings

    Typical usage ratio

    • 0.02–0.12% in finished perfumery/fragrance compound batches, titrated for odor threshold and component balance

    Downstream process integration

    • Introduced in the aroma chemicals synthesis stage, typically by etherification or acylation routes, or as a precursor in custom molecule synthesis for proprietary fragrance bases

    Final product types

    • Animalic and smoky note aroma chemicals
    • Flavoring agents for food-grade products
    • Creamy, spicy notes for fine fragrance blends
    • Fragrance raw materials for detergents and personal care

    3. Dye and Pigment Manufacturing – High-performance Colorant Synthesis

    The phenolic structure of O-Ethylphenol makes it suitable for use in dyestuff and pigment production, especially for developing high-fastness organic colorants used in textiles, plastics, and ink formulations. Professional manufacturers utilize its reactivity to achieve targeted molecular structures and colorfastness requested by global OEM clients.

    Industry compliance standards

    • Oeko-Tex® Standard 100 for textile safety
    • EN 71-3 (Safety of Toys – Migration of certain elements) for pigment preparation
    • ISO 9001:2015 Quality management for colorant manufacturing
    • EU REACH for dye registration and classification

    Typical usage ratio

    • 1–5% w/w as a coupling or modification agent in dye intermediate synthesis; varied according to shade, substrate, and performance requirements

    Downstream process integration

    • Fed into azo coupling or condensation reactions to yield specialized dye chromophores, integrated in batch or continuous reactors according to dyehouse protocols

    Final product types

    • Disperse and acid dyes for synthetic and natural fibers
    • Organic pigments for plastics and printing inks
    • High-stability textile colorants
    • Eco-labeled fabric dyes

    4. Resin and Polymer Industry – Phenolic Resin Modifier

    O-Ethylphenol acts as a critical phenolic modifier or monomer in the development of specialty resins, enhancing thermal properties and providing distinct performance attributes for industrial-grade thermosets. Our OEM clients in resin formulation demand strictly controlled phenolic content and low residual impurity levels to meet manufacturing and application standards.

    Industry compliance standards

    • UL 94 Flammability Standards for phenolic resins
    • RoHS Directive (2011/65/EU) Restriction of Hazardous Substances
    • ISO 14001:2015 Environmental management for resin plants
    • ASTM D1610 (Phenolic Resin Test Methods)

    Typical usage ratio

    • 0.5–3% of total resin composition; adjusted based on modulus and curing profile targets

    Downstream process integration

    • Charged during prepolymerization, either by direct addition to the phenolation step or post-condensation blending, according to the specific resin system (novolac, resol, or polyethers)

    Final product types

    • Heat-resistant molded components
    • Laminates for electronics (PCB substrates)
    • Bonding and insulation resins
    • Aerospace and automotive composite matrices

    5. Pharmaceutical Intermediate – Drug Synthesis Precursor

    Manufacturers employ O-Ethylphenol as a pharmaceutical-grade intermediate during the synthesis of specific APIs and intermediates in fine chemical drug manufacturing. It provides targeted alkylation sites for forming active molecular scaffolds, with quality and traceability controlled per GMP guidelines in regulated markets.

    Industry compliance standards

    • EU GMP (ICH Q7) for active pharmaceutical ingredients
    • U.S. FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • Japanese Pharmacopoeia (JP) & European Pharmacopoeia (Ph. Eur.) for intermediates
    • ISO 9001:2015 for fine chemical manufacturing

    Typical usage ratio

    • 0.8–2.5% relative to total reaction charge in key alkylation and etherification steps; proportion refined via process development QbD

    Downstream process integration

    • Introduced at route-defining transformations; typically in the initial etherification step or as a blocking group within the multi-stage process scheme

    Final product types

    • Targeted cardiovascular and CNS API precursors
    • Pharmaceutical building blocks
    • Compounded intermediates for custom syntheses
    • Contract manufacturing output for finished drug substances
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    Certification & Compliance
    More Introduction

    O-Ethylphenol: Direct from the Manufacturer

    Working with O-Ethylphenol on the Factory Floor

    Every batch of O-Ethylphenol that leaves our facility reflects years of focus, learning, and hands-on problem-solving. Start with the raw material—phenol, itself a building block in chemical manufacturing for over a century. We put it through a controlled ethylation reaction, pressing precision and consistency at every step, to craft O-Ethylphenol. Chemists at our plant monitor purity using proven analytical methods—primarily gas chromatography paired with mass spectrometry. That detail allows us to keep up with the shifting expectations that partners in pharmaceuticals, agrochemicals, and fine chemicals demand.

    Understanding Specifications: Beyond the Label

    Purity sits at the center of most discussions. We continually monitor for possible contaminants, including trace para- and meta- isomers. Typical output clocks in above 99% O-Ethylphenol, well within the standards requested by regulated markets. Water content, acidity, and color all matter, too. Even small changes in any of these parameters can create headaches for downstream processing; synthetic yields can stall or purification costs climb faster than anyone likes to admit. We label each drum with a batch number. Every lot matches an archived certificate of analysis; nothing leaves our site without that check.

    The Backbone of Many Industries

    O-Ethylphenol slots into many pipelines as more than just an intermediate. Customers building active pharmaceutical ingredients trust it for its predictable reactivity. In agrochemical plants, it finds a place in crop protection formulations, where reliable performance and low impurity levels cut the risk of regulatory setbacks. Fragrance and flavor houses blend it into complex aroma profiles. We have seen growing interest from developers of high-performance resins and specialty plastics as well. Each sector brings its own quirks: some want ultra-low trace metals, others need tight control on oxidation byproducts.

    How Our Process Differs from Generic Supply

    Working directly as the manufacturer lets us act on feedback overnight. If a customer reports color shift or a change in solubility, plant crews can pull archived samples and run a side-by-side comparison. Trading houses and distributors rarely have this kind of access to the root process. Over years, we have modified our reactors to minimize hot spots that drive unwanted side reactions. We use nitrogen blanketing to keep oxidation risks low, fighting offtrace product formation. These process tweaks add cost and complexity, but cascading quality failures later in the supply chain cost everyone much more. The knowledge we gather from each improvement builds a stronger foundation for future partnerships and product launches.

    Comparing O-Ethylphenol and Other Phenol Derivatives

    Ethylphenols show up in three isomers: ortho, meta, and para. We focus on the ortho isomer for a reason. Ortho substitution makes the ethyl and hydroxyl groups crowd one side of the benzene ring, which creates reactive sites that are favored in selective syntheses. Customers often approach us wondering if a blend of isomers would perform the same way. The answer: rarely. Even a modest amount of para-ethylphenol can throw off chiral catalyst systems or poison an enzyme during a synthetic step. Some applications use blends of isomers really well, but precise biological and pharmaceutical processes reward single-isomer specificity. That guides much of our ongoing R&D work.

    Tackling Industry Challenges Head-On

    Sourcing O-Ethylphenol often hits roadblocks that traders downplay—periodic shortages of base phenol, rising cost of ethylene, and the ever-tightening regulatory grip on aromatic compounds. We consistently source feedstock from vetted suppliers and regularly invest in storage infrastructure to buffer against market swings. Some customers bring us stories from other suppliers: one month, batch purity reaches the required standard; next month, background odor from decomposition products creeps in and throws a wrench into flavor libraries or crop safety profiles. With roots in manufacturing, we push back on inconsistency by folding every bit of feedback into our batch logbooks. Each operator’s firsthand notes help us spot rare or emerging trends before they can grow into real problems.

    Quality from Start to Finish

    No shortcut replaces vigilant daily oversight. Raw materials come through tracked supply chains, and every new lot faces a short quarantine. Visual inspection catches the occasional outlier; gas chromatography and titration provide a hard safety net behind it. On the production floor, crew leaders trace every shift and handoff. Minor issues—like a subtle color hue or a slight drop in refractive index—kick off a deeper review. After distillation, material cools under inert gas and goes straight into high-integrity drums. Each barrel matches up with records back to its origin. Customers have a standing invitation to visit our sites and see these processes for themselves. We encourage it. Direct trust goes a lot further than paperwork ever does.

    Environmental Impact and Compliance

    As public pressure grows to reduce emissions and hazardous waste, every manufacturer faces hard choices. We take recycling and energy recovery as non-negotiable parts of our operation. Distillation residues are routed into an in-house recovery stream, not dumped. Process water cycles through multi-stage treatment before re-entering the environment. Regulators check these efforts often. Staff run regular training sessions on chemical handling and emergency drills, keeping everyone sharp and grounded in safety-first practices. These are not just claims checked off for audits. Down the line, these habits protect products and people alike. Customers see the benefit in fewer product recalls, steadier supply, and a confidence in regulatory submissions supported by transparent records.

    Technical Support Direct from Source

    Much of the value comes from access to people who actually run the process. If a formulation chemist calls us about a solubility issue or an unexpected chromatographic peak, our technical teams can jump in and track the origin. We keep research chemists, analytical staff, and plant engineers under the same roof—so solve problems quickly. Some buyers appreciate the ability to request one-off specifications. R&D batches with tighter limits on metal content, custom blending ratios with ortho/para isomers, or even alternative solvents have left our packing lines, each reflecting a context-specific tweak guided by hands-on contact with customer tech teams. For many projects, this collaboration changes the landscape—reducing lead times, simplifying regulatory submission, and delivering proof-of-origin records that hold up under close scrutiny.

    Continuous Improvement Drives Value

    Chemical synthesis never sits still. New regulations in one region or a shift in the accepted impurity profile for a pharmaceutical ingredient can ripple back to raw material standards. We keep two-way communication with several downstream partners, watching for early signs of change. No two production runs end up completely identical, but closing that gap builds resilience. Plant teams respond to even small process upsets, logging results, and pivoting on the fly. Some of our most valued process improvements—like switching to a new grade of catalyst or tightening distillation fractions—came direct from field requests when a customer’s application reached a new scale.

    Differences Beyond Chemistry: Service and Accountability

    One feedback that stands out: customers appreciate dealing direct with a team structured to solve problems, not shuffle paperwork. If a shipment gets stuck at customs, local logistics staff step in—bringing real answers, not empty apologies or automated emails. This approach came from years adapting to global export climates. As manufacturers, we also manage product stewardship. Safety data, regulatory filings, and customer-specific documentation all update with each process change. Stakeholders in regulated industries, from pharmaceuticals to food, rely on up-to-date records to keep projects moving. Partnerships that last years—not just purchase cycles—grow from this kind of accountability.

    The Future of O-Ethylphenol in Emerging Markets

    Demand continues to spread geographically. Asia’s contract manufacturing organizations now call for O-Ethylphenol at scales matched only by established European and North American groups. Compliance standards diverge: Japanese customers may request lower residual solvents; Indian partners weigh cost and local REACH alignment; North American buyers check for direct approval under EPA or FDA frameworks. Our adaptive approach means shifting process details and documentation at short notice, not clinging to a “one size fits all” model. Direct feedback from these varied markets shapes our technical and regulatory playbook over time.

    Adapting Our Operations for Tomorrow’s Standards

    Shifts in the market—be it regulatory change or customer-driven specifications—require that our team stays close to the floor. We invest in new analytics, train operators to spot subtle changes, and keep maintenance tight on critical systems. Sometimes, this means pausing production to avoid a deviation; sometimes, it means rolling out a process change to remove a newly regulated impurity or cut greenhouse gas emissions further. Never static, our process reflects the realities of a living, responsive manufacturing environment.

    Practical Applications: Getting Specific

    Custom resin producers look for high-purity O-Ethylphenol to drive targeted cross-linking reactions. Their material specs ask for low isomeric cross-contamination; minute amounts of meta or para structural variants can slow polymerization or foul reactors. Pharmaceutical syntheses use O-Ethylphenol as a reactant, but the story usually goes deeper—a shift in crystalline form, a tweak to an impurity threshold, or a need for a unique solvent profile. At our plant, a process tweak to meet these demands might come from major retooling or just a tighter sampling protocol. New market entries—bioplastics, sustainable fine chemicals—test out O-Ethylphenol for specialty performance, stretching the standards ever higher.

    Supporting Innovators and Legacy Users Alike

    Long-time users—those whose specs for O-Ethylphenol haven’t changed in decades—continue to rely on batch reproducibility and documentation. We respect legacy specifications but continually suggest process and quality upgrades that enhance reliability or regulatory alignment. Meanwhile, newer customers trialing experimental processes challenge us as much as we challenge them. They push for lower trace impurities, alternate packaging, or a creative fit into greener chemistries. Our operator teams and chemistry staff meet these requests head-on, using every lesson and data point from past batches to predict, adapt, and deliver.

    What Sets Manufacturer Supply Apart

    Traders often only see what’s on the analysis sheet. At our end, every batch brings a combination of process data, field feedback, and technical adaptability. The ability to back up a sales promise with archived analytical data, historical process control records, and direct access to formulation staff is something only a hands-on manufacturer provides. Regulatory agencies call for a direct audit trail back to source. Having in-house expertise lets us deliver – no back and forth or unanswered questions.

    Learning from Every Order

    Each outgoing shipment carries more than just product; it carries process experience, teamwork, and a lesson for the next run. Our view is that steady, quality O-Ethylphenol supply comes from continuous dialogue with users. Issues—be they a subtle off-odor, an unplanned bottle leak during transit, or a shift in haze—feed new controls and process tweaks. Facilities remain open to customer inspection. Analytical records update in tandem with regulatory and technical advances.

    The Human Element: Operator Wisdom on the Line

    An analytical instrument can track impurities to the part-per-million, but only experienced eyes catch some early warning signs. Plant staff who have followed a product journey from raw material truck to shipping pallet know what a healthy batch looks like and what to flag in real time. Customer calls reporting a drift in processing parameters get routed to these staff, who investigate not just the numbers but the story behind them—a running log of environmental, technical, and human variables.

    Summary of Distinctives

    Our process stands out for its transparency and responsiveness. Our commitment to environmental responsibility, technical innovation, and open communication makes us a trusted partner in O-Ethylphenol supply. We act on experience gained from the factory floor, not from third-party reports. Product leadership comes from this front-line engagement with chemistry, compliance, and customer needs.