|
HS Code |
583706 |
| Chemicalname | 4-(Phenylmethoxy)Phenol |
| Casnumber | 822-36-6 |
| Molecularformula | C13H12O2 |
| Molecularweight | 200.24 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 105-108°C |
| Boilingpoint | 370°C at 760 mmHg |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.16 g/cm3 |
| Purity | Typically ≥98% |
| Smiles | C1=CC=C(C=C1)COC2=CC=C(C=C2)O |
| Inchi | InChI=1S/C13H12O2/c14-12-7-9-13(10-8-12)15-11-5-3-1-2-4-6-11/h1-10,14H,11H2 |
| Refractiveindex | 1.612 |
| Storagetemperature | Store at 2-8°C |
| Synonyms | 4-Benzyloxyphenol |
As an accredited 4-(Phenylmethoxy)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 4-(Phenylmethoxy)phenol; tightly sealed, labeled with chemical name, hazards, and CAS number. |
| Shipping | 4-(Phenylmethoxy)phenol is shipped in secure, airtight containers, clearly labeled and compliant with relevant chemical transport regulations. Packages are cushioned to prevent breakage and stored away from heat, moisture, and incompatible substances. Shipping is typically arranged via recognized couriers with tracking and material safety information provided to ensure safe handling and delivery. |
| Storage | 4-(Phenylmethoxy)phenol should be stored in a tightly sealed container, away from moisture and incompatible materials such as strong oxidizing agents. Keep in a cool, dry, and well-ventilated area, protected from direct sunlight and sources of ignition. Proper labeling and secure storage are essential to prevent accidental exposure, and it should be handled with appropriate protective equipment to avoid contact. |
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As a chemical manufacturer with decades on the production floor, our approach to specialty compounds has grown directly out of what research labs and industrial customers value most: consistent quality, transparent provenance, and materials built for complex modern synthesis. 4-(Phenylmethoxy)Phenol has become one of the more requested intermediates in our catalog—not because of marketing, but because its chemical properties make a visible difference where precision and reliability matter. Every step, from raw material sourcing to purification, reflects the focus our team brings in keeping the process direct and dependable.
Our standard offering delivers the molecular structure C13H12O2, more commonly labeled as 4-(Phenylmethoxy)Phenol or Benzyl 4-hydroxyphenyl ether. We manufacture this compound with a purity that matches the needs of high-sensitivity applications. Consistent melting point, precise solubility, and colorless crystalline appearance make it fit seamlessly into both pilot-scale research and full-scale commercial production. We understand how even the trace profile of side-products or residual solvents can set off unexpected hurdles, especially downstream in fine chemicals or pharmaceutical intermediates. Over repeated batch work, we take extensive steps to maintain tight control over these variables, so the end user spends less time filtering out unwanted variation.
Every production run brings its own practical lessons. Across industries, customers often compare 4-(Phenylmethoxy)Phenol to more typical phenolic ethers or unrelated ether intermediates. The real-world difference comes down to both the reactivity pattern and the balance between hydrophobic and hydrophilic properties. With 4-(Phenylmethoxy)Phenol, the para-directed substitution delivers a scaffold preferred for selective derivatization. Unlike basic phenol or unsubstituted ethers, the benzyl group consciously built into our molecule offers both steric protection and a ready handle for further chemical transformations, especially where selective O-benzyl deprotection is a step in the synthetic scheme.
Many traders miss that not every phenolic ether behaves the same way under process conditions. In pharmaceutical custom synthesis, we have supplied this compound for projects where the downstream step needed a clean, selective cleavage. The difference in workup yield and ease of purification has helped teams cut unnecessary steps and reduce both solvent use and purification time.
Some customers working on color developers or advanced monomer platforms choose 4-(Phenylmethoxy)Phenol because it integrates smoothly with aromatic couplers, often improving end-use stability. In contrast, simpler ethers show less predictable shelf-life and more susceptibility to discoloration or side reactions. In one client’s high-temperature polymerization, our manufacturing process—by careful exclusion of trace metal contaminants—reduced off-color formation. These subtleties show up repeatedly in process validation; it is less about the textbook structure and more about real-life behavior in the production plant.
As a direct manufacturer, we watch trends in related phenolic ethers. Some clients look to 2-(phenylmethoxy)phenol or 4-methoxyphenol in the hope of interchangeable results. Those structures depart swiftly from 4-(Phenylmethoxy)Phenol in both reactivity and selectivity; even small shifts on the aromatic ring can make or break the efficiency of a synthetic route. For instance, positional isomers change coupling constants and substitution patterns. These aren’t academic observations—they become plain during scale-up, where the difference between a 95% and a 70% step yield decides the process economics.
Modern supply chains encounter enough surprises. We regularly talk with process chemists and purchasing managers who have lost valuable development time because of batch-to-batch variability. Since we produce the compound in-house, all analytical documentation comes straight from our own QA team. Full batch records, chromatographic fingerprints, and detailed impurity profiles are available with every shipment. The absence of middlemen avoids miscommunication, especially regarding subtle purity questions that come up at the regulatory or audit stage.
Our year-to-year stability in specification—rather than chasing after slightly cheaper alternatives—has allowed several long-term customers to standardize their protocols, cutting down on unnecessary retesting. Real value lies in the absence of unwelcome surprises; when a compound passes every purity assay, color check, and residual solvent specification, end users can spend more time developing their products rather than troubleshooting their starting materials.
It’s not uncommon for labs to call with unusual analytical requests. A large multinational wanted us to provide additional chiral impurity testing on a recent batch, driven by their evolving regulatory requirements. Because we control the full route from starting material to finished product, our technical team responded with both the raw analytical data and supporting validation. In contrast, customers relying on traders or generic bulk suppliers found slow answers and less confidence in the veracity of the information.
We ship 4-(Phenylmethoxy)Phenol as a stable solid, tightly packaged to guard against unnecessary moisture or light exposure. Real experience teaches that even a few weeks of careless storage can show up in discoloration or subtle hydrolysis, especially in humid environments. Our facilities invest in climate-controlled packaging and regular stock rotation to avoid the “old-batch” pitfalls more common among intermediary resellers.
From small research lots of under a kilogram to full drum orders, our process scales with every customer’s immediate need. We watch out for the most common pitfalls associated with high-purity aromatic ethers—seasonal weather variation, inconsistent freight conditions, minor packaging damage. Our warehouse-to-doorstep control has translated into fewer damaged shipments, and a much lower return or complaint rate compared to importers who never see the inside of a packaging room.
Academic synthetic chemistry laboratories have relied on this compound as a key intermediate in total synthesis projects, including both natural product analogues and pharmaceutical candidates. In-house experiences show its role as an intermediate stands out most clearly in multistep sequences calling for an aryl ether that can be deprotected under mild conditions, sparing other sensitive functionality present in complex targets. A classic example is the use of O-benzylphenol derivatives for protecting phenolic hydroxyl groups during stepwise synthesis; these protecting groups can be removed under hydrogenolysis, allowing synthetic teams to time their unveiling as late as possible in convergent routes. Our product’s clean deprotection profile has repeatedly supported high-value routes where byproduct formation needs to be minimized.
Some downstream partners apply 4-(Phenylmethoxy)Phenol in specialty polymer synthesis. For certain advanced materials, the phenylmethoxy substituent imparts better handling and improved processability. In the development of thermosetting resins and specialty adhesives, our customers have reported improved crosslinking performance compared to base phenol derivatives, noting a lower tendency toward resin yellowing and enhanced mechanical stability after cure. Process chemists appreciate the compound’s non-hygroscopic solid form, which simplifies weighing, metering, and feeding into reactors with less risk of clumping or caking.
A major photography developer firm turned to our formulation. Here, the electron-donating benzyl ether group supported higher sensitivity and faster developing times in their proprietary chemistry. Our batch-to-batch consistency gave them confidence scaling from pilot to production, minimizing failed runs and reducing the risk of substandard end product reaching critical client projects. We have observed that compounds of similar molecular structure fail in their process because of less robust solvent compatibility or more persistent side reaction pathways.
Customers in the flavor and fragrance industry use 4-(Phenylmethoxy)Phenol as a masked phenolic note in certain aroma intermediates. The benzyl ether moiety softens the typically sharp phenol edge, creating a more rounded aromatic impression in the final product. This direct feedback has steered our continued investment in better purification and odor minimization, which matters especially for those downstream who cannot tolerate a single stray off-note in their formulations.
Research teams in the agrochemical sector have explored the intermediate as a building block in selective herbicide candidates, utilizing its predictable reactivity profile in multi-step syntheses. Our technical support staff frequently partners with industrial chemists optimizing reaction conditions, providing solid data on solubility and compatibility with a spectrum of organic bases and acids. The value here comes in not just the reactivity, but the way that the para-substituted ether lets clients design new candidates with predictable transformation pathways.
In the modern regulatory landscape, documentation supporting both safety and traceability stands alongside product purity itself. Our team bridges the needs of R&D, QA/QC, and scale-up managers by collaborating at every project phase. We keep a close watch on regional regulatory updates, including REACH and other global frameworks. Requests for impurity mapping and advanced analytical support have surged over the past five years, with users wanting ever-more granular insight into their raw materials. Our chemists share real data from production runs: precise impurity levels, spectroscopic confirmation, and stability under light, temperature, and storage stress testing.
Being hands-on in manufacturing means we can tune the production parameters to accommodate special requests or unusual formulation needs. Sometimes a project calls for the lowest possible levels of a particular contaminant—whether halogenated organics or specific residual metals. Our lab capabilities flex to deliver these tight specs, reporting complete heavy metal panel results and residual solvent screenings on every batch. No guesswork, no vague promises—just real numbers that laboratories can trust in their process validation.
The difference between theory and real plant-floor experience becomes evident in the way we support researchers under non-standard conditions. For example, a major pharmaceutical account requested a non-standard packaging size, tailored to match automated meter-feeder load. Our logistics responded within the week, cutting down the customer's repackaging time and reducing dusting risk. We treat these requests not as burdens, but as insights into the shifting needs of the field. Direct manufacturers have the agility to do this; traders and brokers simply cannot provide that level of customization or fast response.
Direct input from customer labs guides our continuous improvement. One customer asked for a modification to our standard process after observing mild batch-to-batch odor variability in their own QC. Together, our teams pinpointed a minor variation in drying time post-reaction as the cause. Adjustments to our protocol resolved the issue permanently, turning what could have been a recurring headache into a process advantage. It’s only through this open technical dialogue that compounds like 4-(Phenylmethoxy)Phenol consistently meet exacting modern standards.
Efficiency in manufacturing makes a measurable difference as market demand fluctuates in response to shifts in global procurement and research focus. Over the past decade, we have optimized our reaction protocols for better atom economy, more controlled reagent dosing, and simplified waste streams. Making these improvements does more than cut costs; it reduces both environmental burden and storage of unused intermediates. Batch reproducibility remains paramount, especially as the customer base shifts toward more regulated end-use markets—pharmaceuticals, agrochemicals, and advanced electronic materials.
One critical improvement grew out of observed moisture pickup in our original storage containers. After documenting mild hydrolysis in a control sample stored over several months, investments went into more robust sealed packaging, traceable shipment conditions, and routine environmental monitoring during handling. This direct feedback loop has driven our quality higher and reduced the time our customers spend running unnecessary secondary purity tests.
As process chemists ourselves, we recognize that the devil hides in the details. It’s easy for a non-manufacturer to overlook minor points—particle size consistency, residual catalyst traces, the specific geometry of the substitution pattern. Our production staff monitor these everyday operational details because, in the end, a missed adjustment on a single filtration or drying step echoes downstream as lost time or lower yield for customers. These learnings, built up over years, distinguish direct manufacturing expertise from off-the-shelf trading.
4-(Phenylmethoxy)Phenol’s growing importance in both established and emerging fields has kept us vigilant about keeping stocks available and quality protected as new challenges arise. As fields such as medicinal chemistry and electronic materials press for ever tighter purity windows, our lab teams are pushing new boundaries in analytical technique—LC-MS, chiral chromatography, trace ion analysis—all incorporated into our real world batch documentation. Researchers moving into uncharted synthesis adventures bring us fresh challenges: new downstream reactivities, compatibility with the next generation of smart polymers or advanced monomers, and shelf-life performance under unfamiliar climates.
We view our role as more than a supplier; years of direct production mean we carry broad institutional knowledge. A single bottle of 4-(Phenylmethoxy)Phenol isn’t just a commodity—it represents technical expertise, attention to detail in handling, and confidence built on thousands of prior batches supporting projects small and large. By investing in people and process at the plant, we keep the production robust and the knowledge base growing in step with industry requirements.
Direct manufacturing brings its own pressures, but also opens up more meaningful partnerships with researchers and industry alike. With a product like 4-(Phenylmethoxy)Phenol, the true distinction emerges not only from abstract purity numbers, but from how well the material lets the next user work—how many process steps become smoother, how many headaches about storage or compatibility fade quietly into the past, how many research hours are directed toward discovery rather than troubleshooting.
As customer expectations evolve and applications diversify, we see every batch as another chance to demonstrate that manufacturing is more than a process—it’s a commitment to clarity, continuity, and genuine progress in chemical science.