Anhui Liwei Chemical Co., Limited
Products

3-(2-Hydroxyethyl)Phenol


    • Product Name 3-(2-Hydroxyethyl)Phenol
    • Alias m-Tyrosol
    • Einecs 225-261-7
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    829004

    Chemical Name 3-(2-Hydroxyethyl)phenol
    Synonyms m-Tyrosol
    Molecular Formula C8H10O2
    Molecular Weight 138.17 g/mol
    Cas Number 501-94-0
    Appearance White to off-white solid
    Melting Point 73-75 °C
    Boiling Point 299.2 °C at 760 mmHg
    Solubility In Water Soluble
    Density 1.16 g/cm3
    Refractive Index 1.547
    Flash Point 133.5 °C
    Smiles CC1=CC(=CC=C1)CO

    As an accredited 3-(2-Hydroxyethyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 500g of 3-(2-Hydroxyethyl)Phenol, tightly sealed, labeled with chemical details, hazard symbols, and handling instructions.
    Shipping 3-(2-Hydroxyethyl)phenol is shipped in securely sealed, chemically resistant containers to prevent leaks or contamination. It is labeled according to regulatory guidelines, indicating the chemical name and hazard information. Shipping is conducted in compliance with relevant safety regulations, including temperature and handling requirements, to ensure safe transport and delivery.
    Storage **3-(2-Hydroxyethyl)Phenol** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances like oxidizers. Protect the chemical from light and moisture. Use secondary containment if necessary to prevent leaks and avoid prolonged exposure to air to minimize degradation or contamination.
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    Tel: +8615380400285

    Email: sales2@liwei-chem.com

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    Certification & Compliance
    More Introduction

    Introducing 3-(2-Hydroxyethyl)Phenol: A Core Ingredient in Modern Chemistry

    Direct from the Source: Our Experience with 3-(2-Hydroxyethyl)Phenol

    Every step in our production of 3-(2-Hydroxyethyl)Phenol reflects decades of hands-on know-how. This compound, known among chemists for its dual phenolic and hydroxyethyl group, brings distinctive versatility into the lab and down the line in industrial processes. Its molecular formula, C8H10O2, reveals a simple structure, but real-world performance tells the richer story. Our operators, chemists, and engineers have worked closely with this material from its raw sourcing to its precise refining and packaging, drawing on lessons earned batch after batch.

    We produce 3-(2-Hydroxyethyl)Phenol in a range of purities. Most demand centers around material above 99% by HPLC assay. Isomeric control is a must, as trace variants or unknown impurities skew outcomes—whether in polymers or fine chemicals. Instead of relying on off-the-shelf equipment, we've invested in both custom reactors and rigorous closed-loop purification. We never shortcut temperature control or filtration, since failed batches only create more waste and extra work for everyone. Consistent color and low residual water content do not just look good—they mean repeatable reactivity. Each drum we fill gets checked, because no one wants a reaction that stops half-way.

    Where It Performs: Broad Utility, Real-World Demand

    Ask our team where 3-(2-Hydroxyethyl)Phenol ends up, and you’ll get a range of real uses. Major clients put it to work as an intermediate for etherification and esterification in chemical synthesis, especially where other phenolic bases bring too much reactivity or not enough solubility. We've watched customers in specialty coating development leverage the hydroxyethyl side-chain for enhanced adhesion to metal and plastic surfaces, while fragrance formulators take advantage of its mild, non-intrusive aromatic scent. This dual utility—in both performance chemistry and polymer modification—keeps our line active year-round.

    Processability separates 3-(2-Hydroxyethyl)Phenol from older-generation alkylphenols. Our customers, especially those scaling up from lab to pilot, mention shorter dissolving times and easier handling thanks to its relatively low melting point. They often mention that it dissolves readily in typical organic solvents, such as ethanol and acetone, yet doesn’t foul up pumps or stick to filtration media. Bulk users in the textile and resin industries have run side-by-sides with standard cresols, reporting less gumming and improved reproducibility in emulsion dispersion. This real-life performance data has let us refine both storage and freight logistics, reducing on-site troubleshooting for downstream partners.

    What Sets It Apart: Not Just Another Phenol

    Field technicians working with 3-(2-Hydroxyethyl)Phenol often ask how it stands apart from 4-(2-hydroxyethyl)phenol or standard phenol. In practice, the ortho position of the hydroxyethyl group changes both its reactivity and compatibility. The molecule’s slight polarity tweak enhances miscibility with both aqueous and organic phases, proving especially valuable in surfactants and dispersants. For formulators shooting for stable blends—think epoxy hardeners or heat-resistant paints—this compound offers flexibility. The extra ethanol moiety disrupts stacking, so it’s less prone to untimely crystallization when stored under varying humidity or temperature. This is not theoretical: warehousing managers cite fewer caking issues and less degradation during extended holds, reducing write-offs.

    In our comparison trials, standard phenol reacts under less specific control and introduces brittleness in high molecular weight polymers. 3-(2-Hydroxyethyl)Phenol, on the other hand, participates in chain extension without the usual trade-off of yellowing or spontaneous gelation. Among our more quality-focused partners in electronics encapsulants, the cleaner workups they achieve stem directly from the chemical’s balanced reactivity profile. No need for excessive washing or downstream pH adjustments. This is borne out by yield data from resin plants operating both automated and manual lines—our product performs reliably.

    Safety, Handling, and Practical Observations from the Floor

    In our own facility, material safety constantly shapes workflow. 3-(2-Hydroxyethyl)Phenol, like other substituted phenols, requires thoughtful handling. Liquid batches release a mild, phenolic scent; ventilation prevents overexposure. Operators suit up with proper gloves and splash protection, not because we've ever let up on containment, but because no one wants skin irritation or chronic exposure. Leaks or spills clean easily with common absorbents, much less hassle than many halogenated aromatics. In over a decade, we've recorded no persistent storage issues, provided containers remain sealed and shielded from direct sunlight.

    Transport stands out for its straightforwardness. Unlike some phenolics that clump or oxidize under ambient air, our 3-(2-Hydroxyethyl)Phenol remains stable through domestic and export shipping cycles. During monsoon season, we check each inbound for moisture ingress, but even with longer sea legs, customer complaints about off-spec cargo remain rare. That proven track record matters to both our compliance managers and to end-users, who count on predictable physical and chemical properties.

    Consistency and Quality Control: Practices Earned from Production

    An often-unspoken truth in specialty chemicals is that raw material quality varies by batch, sometimes by the day—something no technical data sheet ever fully reveals. We’ve implemented a closed feedback loop from our packing line, through customer labs, and back into our process control charts. Out-of-lot samples get tested weekly, not just at QC signoff. Our in-house chromatographers don’t shy away from reporting impurities detected at 200 ppm or less. The full traceability chain—from base feedstock pre-approval through end-of-run analytics—sets a higher bar than minimum spec sheets.

    This extra attention pays off where it counts: end-users handling coatings, adhesives, or custom monomers have submitted fewer claims for unexpected polymerization or odor drift since we raised our assay target three years ago. Comparison data from overseas partners points to reduced downtime, with fewer incidents of line purges required due to off-color or errant boiling points. As a manufacturer who has seen the costs of poor consistency—not just financial but in lost trust—this feedback drives our next improvements.

    Environmental Stewardship: Responsible Production of Phenolic Derivatives

    Manufacturing phenolic intermediates brings a responsibility to minimize both emissions and waste. We operate with multi-stage scrubbing and closed water flows, so that caustic byproducts don’t leave our plant untreated. Our distillation residues feed directly into an energy recovery loop. Compared to traditional open-kettle operations, these investments have lowered not only our regulatory footprint but also the total chemical oxygen demand in plant outflow. Our environmental audits—both by local authorities and international clients—inspect not only paperwork but hardware integrity and incident logs. Anything less would endanger both our community and valued contracts.

    Within the industry, 3-(2-Hydroxyethyl)Phenol compares favorably to certain nonylphenols or cresols, which draw tighter restrictions due to toxicity concerns or persistent bioaccumulation. Our internal risk reviews prioritize reactant selection and solvent recovery at every scale. Customers building toward green chemistry certifications see benefit in our detailed compliance reporting as well as our willingness to engage in dialogue about formulation substitutions. We collaborate with both regulators and application engineers to pilot less hazardous processes when substituting legacy alkylphenols, sometimes with this molecule as a safer, less persistent lead-in.

    Process Improvements from Firsthand Experience

    It’s easy for outsiders to gloss over the grinding, repetitive work that goes into scaling a new molecule. Anyone can point to yields on paper. From our experience, every new production run reveals hidden pinch points—metals leached from pump housings, ring-closing exotherms, or discoloration tracing back to minor impurities. Technical fixes, tested not just by R&D but in pilot kettles, keep these hurdles in check. Tuning reaction times or swapping out base catalysts doesn’t make headlines, but improves safety, consistency, and costs over dozens of cycles.

    One repeat challenge: water content at pack-out. 3-(2-Hydroxyethyl)Phenol’s affinity for hydrogen bonding can attract trace moisture from high-humidity storage. Rather than wait for downgrades, we invested in nitrogen-blanketed filling and metallic liners. Trouble tickets dropped and shelf-life chalked up to months, not weeks, especially for export lots. Partners mixing high-grade epoxy resins or UV-cure systems have come to rely on this rigor, with fewer side reactions and more predictable end-product appearance. This is the result of dozens of iterative tweaks, not a one-off equipment upgrade.

    Technical Support and Real World Troubleshooting

    Offering technical support on 3-(2-Hydroxyethyl)Phenol takes more than reading back a data sheet. Our application team fields requests spanning abnormal color shifts, batch-to-batch response changes, and unexpected viscosity increases in polymerizing blends. Troubleshooting often uncovers root causes ranging from minor batch pH drift to incompatibility with stabilizers that performed adequately with alternate phenolics. Fielding those issues does not just help the current user; it deepens our in-house knowledge—letting us proactively fine-tune process and improve yields for the next round.

    On several occasions, composite manufacturers reported gel point shifts after changing their hardener supplier. Joint investigation traced the issue to a subtle surfactant buildup, rather than the core 3-(2-Hydroxyethyl)Phenol. This back-and-forth, sharing of process data, pictures, and even retained samples, goes far beyond what any technical bulletin could offer. It cements trust in manufacturer-partner relationships—where fast fixes based on real experience keep delays to a minimum.

    Regulatory Compliance and User Considerations

    Anyone working with substituted phenols knows the landscape of global regulations changes year to year. We track new standards in both Asia and Europe, conducting annual dossier reviews and compiling full REACH-style reports for our supply chain partners. Customers often ask about food safety, allowable migration, or VOC status for their end-use. Our analytical team provides not just purity certifications but contaminant profiles and maximum residual limits, drawing from validated methods and experience with regional labeling norms.

    This readiness removes hurdles for formulators introducing new consumer products or scaling up medical adhesives. We supply updated certificates after each process change, with full backward documentation. As scrutiny on phenolic chemicals rises, transparent, up-to-date compliance systems position us to ensure long-term viability, both for our own operation and for everyone who relies on our material.

    Improving Through Feedback: Listening to Customers and Colleagues

    Direct insight from users shapes continuous improvement more than any top-down directive. Field reports, ranging from faster dissolving rates to runoff color changes in cured resins, filter straight back to our production chemists. Test batches for emerging applications, like fuel cell adhesives or high-strength laminates, progress through our pilot plant in close partnership with target users. Their feedback—good or bad—drives entrants on the floor and informs both our upstream sourcing and downstream logistics planning.

    Regular site visits keep the cycle of improvement turning. When a customer’s line reported unexpected frothing during mixing, a visit confirmed that a mild adjustment in agitation speed and order of addition solved a months-old issue blamed on a supposed contaminant. This close-loop communication streamlines future introductions and cuts learning curves not just for us, but for anyone moving from sample to scale.

    Innovation Through Collaboration

    Sustained innovation with 3-(2-Hydroxyethyl)Phenol involves working alongside downstream chemists trying to stretch formulation boundaries. New requests come in for lower halogen residuals, or tighter color targets for clear resins. Some of the best lessons come from off-label uses, where creative users adapt our material outside traditional markets. We don’t just observe—our technical teams trial alternative purification steps, test for new potential catalysts, and adjust feedstock routes to support these out-of-the-box applications. Every conversation with a formulation scientist opens a new avenue for both product development and process optimization.

    Our partnership with academic labs and industrial think tanks continues to uncover fresh analytical perspectives. Ongoing work involves fine-tuning supports for green chemistry applications, where pressure mounts to replace more toxic alkylphenols. Collaboration strengthens every link in the chain, accelerating both creative breakthroughs and practical improvements in cost, safety, and utility.

    Looking Ahead: The Evolving Role of 3-(2-Hydroxyethyl)Phenol

    As industries evolve—whether toward greener chemistry, advanced electronics, or specialized surface coatings—the role of high-purity, consistent 3-(2-Hydroxyethyl)Phenol will deepen. We stay committed not just to supplying a specification, but to sharing technical wisdom and troubleshooting expertise that come only from direct manufacturing experience. Our production scales up to meet changing demands without compromise in quality control or environmental management.

    Sourcing directly from the manufacturer removes guesswork and aligns with user needs for reliability. We invest in both technology and people so that every new drum, tote, or tanker brings both certainty and the cumulative benefits of experience earned through years in the field. As challenges in processability, compliance, and performance continue to shift, we remain ready to adapt and deliver, grounded in the everyday realities of chemical manufacturing and customer engagement.