|
HS Code |
110328 |
| Cas Number | 553-16-6 |
| Molecular Formula | C8H10O2 |
| Molecular Weight | 138.17 g/mol |
| Iupac Name | 2-(2-hydroxyethyl)phenol |
| Synonyms | o-(2-Hydroxyethyl)phenol; 2-Hydroxyethylphenol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 264 °C |
| Melting Point | 20-22 °C |
| Density | 1.146 g/cm3 at 20 °C |
| Solubility In Water | Soluble |
| Flash Point | 127 °C |
| Refractive Index | 1.546 |
| Purity | Typically ≥98% |
| Storage Temperature | Store at room temperature |
| Inchikey | KFWYYESCSPLQFW-UHFFFAOYSA-N |
As an accredited 2-(2-Hydroxyethyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 500 mL of 2-(2-Hydroxyethyl)phenol, sealed with a screw cap, safety label, and hazard symbols. |
| Shipping | 2-(2-Hydroxyethyl)phenol should be shipped in tightly sealed containers, away from heat, sparks, and open flames. Ensure proper labeling and compliance with local regulations. Handle with gloves and safety goggles. Transport as a chemical substance, protecting from physical damage and moisture. Follow all applicable hazardous material and safety guidelines during shipping. |
| Storage | 2-(2-Hydroxyethyl)phenol should be stored in a tightly sealed container, away from light, heat, and sources of ignition. Store in a cool, dry, well-ventilated area, separated from incompatible substances such as strong oxidizers. Avoid moisture and prolonged exposure to air. Label the container clearly, and ensure access is restricted to trained personnel. Always follow appropriate chemical safety protocols. |
Competitive 2-(2-Hydroxyethyl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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At the core of fine chemical synthesis in the laboratory and on production lines, small but critical choices define how efficiently each batch delivers for downstream users. Over the past decade, our process chemists and plant operators have dealt hands-on with thousands of tons of 2-(2-Hydroxyethyl)phenol, known informally in some settings as o-(2-Hydroxyethyl)phenol or by CAS number 706-35-0. Every drum and tank we ship reflects years of process refinement responding to what manufacturers, formulators, and R&D scientists require from this midweight phenolic alcohol.
We manufacture 2-(2-Hydroxyethyl)phenol to support both standard and customized technical requirements. Most clients require material with purity not less than 99%, since even minor byproducts—typically from over-oxidation or unreacted phenol—can impact final product consistency in adhesive, resin, or surfactant formulations. In our process, tight in-process control maintains byproduct levels well below 0.5%, and every lot ships with full assay and chromatographic profiles. Moisture and color remain equally vital. Without careful thermal management, moisture creep influences storage and handling, so we routinely hold water content under 0.1%. The color on the Gardner scale rarely drifts above 2 in our finished lots, minimizing downstream yellowing.
Customers who handle end uses like epoxy hardeners or custom surfactant blends tell us that particulate-free liquid form is essential for uninterrupted feed during mixing, so filtration and clarity checks reach a higher standard here than with typical phenolic intermediates. Consistent viscosity and a pourable, low-crystallization-point form broaden storage and shipping windows for distributors and on-site tanks—less time spent on drum warming or line purges, more reliability in continuous dosing equipment.
People outside chemical plants picture specialty ingredients like 2-(2-Hydroxyethyl)phenol as a simple building block. For us, every shipment has to prove it adapts to customer workflows that are often cost-sensitive, time-sensitive, and at the mercy of batch-to-batch variations. This molecule’s key value traces to its dual hydroxyl and benzene moiety—factories put it to work in epoxy resin modification, textile treatment agents, and custom surfactant packages. Each application places its own stresses on purity and handling.
For instance, in epoxy resins, this compound often enters as a chain extender or toughening agent. Operators expect it to react smoothly, without gelling or causing unwanted color development during high-temperature curing. Consistent melting point and purity translate directly to lower scrap, predictable curing, and robust mechanical properties in finished plastics. We see similar themes with textile auxiliaries. Here, trace iron or copper in the raw material can cause staining or degrade dye uptake across thousands of meters of fabric. Feedback from textile finish producers taught us early that even low ppm levels of residual metals cause headaches. As a result, we batch-test not just for organic specification, but also for trace metals, continuously improving the filtration and material handling chain.
Manufacturers creating surfactants and emulsifiers rely on this molecule’s hydrophilic character and aromatic backbone. The ethylene side-chain adds flexibility, important for synthesizing ethoxylated derivatives and specialty esters. Our partners in daily chemical production have flagged thermal stability during storage and blending as a recurring concern. Because this phenolic intermediate can begin oxidizing or darkening if exposed to air or iron over months, we invest in lined containers and inert-atmosphere packaging at scale. Compared to simpler mono-phenols, this compound handily tolerates processes that elevate temperature and pH, reducing side reactions even in tightly wound batch reactors or heated transfer lines.
Many users first approach us with a list of candidates: various cresols, basic phenol, or other hydroxyethyl derivatives. Why do major paints and adhesives producers specify 2-(2-Hydroxyethyl)Phenol over simpler alternatives? From our experience on the manufacturing floor, the chemical structure matters at every stage. Mono-phenols react rapidly, but lack the flexibility and high boiling point needed for tougher reaction regimes. 2-(2-Hydroxyethyl)phenol stands apart because of its balance—the benzene core provides reactivity and rigidity, while the hydroxyethyl tail grants solubility and moderates handling risks.
Cost may attract some buyers to basic phenol or para-cresol, but downstream issues—such as worker exposure and the need for more rigorous clean-up after batch reactions—often end up neutralizing any savings. With 2-(2-Hydroxyethyl)phenol, the higher boiling point and stability reduce loss during distillation and minimize process interruptions from volatilization or decomposition. For continuous processes, that stability is a cornerstone; resin kettles run smoother, with less gum buildup and fewer filter changes.
Within the segment of hydroxyethyl-substituted phenols, other isomers—like 4-(2-hydroxyethyl)phenol—show subtle but critical differences. In the real world, isomeric purity matters more than most buyers initially realize. During pharmaceutical intermediate synthesis, trace amounts of positional isomers give rise to separation headaches later. We structure our production routes to control isomer ratio as tightly as possible, not just for regulatory assurance, but to deliver practical value at bench and ton scale.
From an operator’s outlook, working with 2-(2-Hydroxyethyl)phenol can mean troubleshooting batch color, resolving rare solidification, or adjusting process water content. Every season brings lessons: summer brings concerns about evaporation or tanker warming, winter exposes storage drums to crystallization at low ambient temperatures. By integrating jacketed bulk tanks and always finishing each batch with closed-system cooling, we’ve learned to deliver across climate zones worldwide.
Long-term commercial buyers often audit our process, seeking evidence for the reliability of each run. Batch histories matter more than glossy datasheets. Our control records show not only assay and appearance logs, but yield trends, catalyst loads, and specific corrections applied during scale-up. Any consistent blip in GC spectra becomes grounds for process review—years of refinement have brought rework rates for this product down to less than 1% of total output.
Handling feedback from both technical managers and plant floor operators brings perspective. Multinational adhesive firms have shared stories of cross-contamination affecting UV stability in end-use systems. Local formulators use the same base compound for two-step ethoxylate synthesis, reporting huge batch loss when input purity dips below established thresholds. These conversations shape how we select raw materials and determine shipment packaging—stainless, lined, and inert-gas sealed.
Every so often, a new client approaches with a problem encountered in practice: unexpected color shifts, lower-than-expected conversion in amine reactions, or high viscosity at cooler ambient conditions. Knowing this is a molecule prone to minor oxidative darkening, our plant team designed feed lines with reduced headspace and implemented oxygen scrubbing in the holding tanks. Fine particulate or color body formation prompted us to shift filtration to sub-micron modules and intensify column fractionation.
In regions where logistics stretch over weeks or cross multiple climate bands, product stability under varying temperature and light becomes key. We’ve tested both drum and IBC packaging over long routes, tracking product oxidation, crystal formation, and vapor evolution. Now, most lots ship in custom-lined containers, minimizing iron leaching and oxygen penetration. Communication with customer plants handling high-throughput blending lines encouraged us to switch to lower-headspace closures, preventing both air ingress and premature darkening.
We’ve also wrestled with the tendency of this compound to thicken at low temperatures, particularly in northern warehouses. While some intermediates manage winter storage without fuss, 2-(2-Hydroxyethyl)phenol benefits from periodic gentle warming and circulation in cold climates. Our largest clients monitor tank temperature and use recirculation loops or immersion heaters set well below the compound’s decomposition point, preventing degradation while restoring full liquidity. The right packaging and handling instructions, based on firsthand feedback, deliver fewer customer complaints and decrease lost material.
Decades on the manufacturing line have taught us the difference practical safeguards make. Most customers focus on the efficiency and performance side of the product, yet safety governs the real world of handling and disposal. 2-(2-Hydroxyethyl)phenol’s moderate toxicity and phenolic nature mean regular training on PPE, careful drum sealing, and aggressive spill containment. We invest in closed transfer systems not just for compliance, but to reduce everyday worker exposure and batch loss. Fume capture at drum filling stations and routine monitoring inside tank farms match the regulatory guidelines but also prove essential through each shift.
Solvent use during purification traditionally sparked process safety reviews. Over the years, we transitioned away from chlorinated solvents toward greener extraction and purification routines, well before regulatory deadlines mandated the change. This switch delivered marked improvements: reduced emissions, simpler waste management, and lower operator turnover in the purification bay. Downstream, these steps mean buyers face less stringent VOC management and lower total input costs.
Disposal and waste minimization shape production planning. Strong pushback from clients deploying large-scale surfactant or plasticizer lines led us to cut phenol and organic solvent residues well below default thresholds, and internal recycling now reclaims off-spec batches wherever feasible. By keeping these figures transparent, we let long-term clients consult their own compliance directors, saving time across audits and third-party certifications.
Global demand for 2-(2-Hydroxyethyl)phenol shifts in response to changes in epoxy resin design, environmental regulation, and customer demand for safer, more durable materials. Over recent years, as end-users in electronics, automotive, and coatings industries pursue higher heat resistance and lower emissions, our R&D teams face ongoing requests for tighter specifications and cleaner supply chains.
Recent upgrades in our own synthesis lines—prompted by feedback from quality engineers working in silicone and isocyanate development—allow us to deliver larger, more consistent lots, increasing predictability for high-throughput factories. Our analytical labs now run full impurity fingerprinting across each lot, highlighting even trace byproducts that could affect high-performance applications. We continually publish benchmark purity and color data for key clients to integrate into their own project files; transparency often smooths project planning and regulatory submissions overseas.
Increasing demand for lower environmental impact has prompted us to reduce energy consumption per ton through both reactive distillation steps and better heat recovery from exothermic reactions. Our operators collaborate closely with logistics providers willing to use cleaner transport modes for bulk cargoes, and our customers in the coatings and electronic resin sectors have responded positively to these documented improvements in cradle-to-gate carbon intensity.
Answering day-to-day technical queries, troubleshooting process delays, and handling the rare but critical batch complaint shapes our workflow each season. Direct calls from customer plant engineers often reveal details hidden behind basic specification sheets—unexpected filter blockages, subtle product yellowing over storage, or off-odors arising in scale-up. Decades in manufacturing taught us that, while standardized documentation satisfies procurement, it is the rapid response to technical field problems that distinguishes a fine chemical manufacturer from a casual supplier.
We keep a line open to chemists and maintenance teams in each region we serve. Many improvements—new filtering protocols, alternate drum linings, and modified shipping practices—trace directly to field requests. Iterative improvement underpins not just our process, but our reputation in industrial segments running multi-million-dollar resin and surfactant lines.
The pressure on specialty chemicals is growing. Tighter environmental regulation, evolving material performance standards, and higher customer expectations challenge every producer to step up. As more end users look to reduce emissions, increase product lifespans, and phase out legacy solvent systems, the demands on intermediates such as 2-(2-Hydroxyethyl)phenol only grow.
Staying ahead requires more than meeting current standards. Our plant teams focus on preemptively scanning for risks, finding opportunities to reduce byproducts at the source, and building robust traceability into each production campaign. Feedback from global partners guides everything from minor tweaks—more informative batch labels, refined handling protocols—to larger systemic changes, including the move toward closed-loop handling and lower energy inputs. The value added for each customer begins long before the product leaves our filling lines; it originates in the ability to listen, adapt, and deliver precisely what the process needs, not just what the specification requests.
This long-term commitment, grounded in decades of on-the-ground learning and constant technical dialogue with users at every level, separates commodity trading from true manufacturing partnership. Reliable 2-(2-Hydroxyethyl)phenol supplies help keep the world’s adhesives, resins, surfactants, and functional materials lines moving smoothly—one batch, one improvement at a time.