|
HS Code |
831046 |
| Iupac Name | 4-(2-Phenylpropan-2-yl)phenol |
| Molecular Formula | C15H16O |
| Molecular Weight | 212.29 g/mol |
| Cas Number | 13319-46-9 |
| Appearance | White to off-white solid |
| Melting Point | 107-110°C |
| Boiling Point | 334°C at 760 mmHg |
| Solubility In Water | Slightly soluble |
| Density | 1.09 g/cm³ |
| Smiles | CC(C)(C1=CC=CC=C1)C2=CC=C(C=C2)O |
| Pubchem Cid | 256974 |
| Logp | 4.06 |
| Refractive Index | 1.599 |
| Flash Point | 155°C |
| Synonyms | p-tert-Butylphenol, 4-(2-phenyl-2-propyl)phenol |
As an accredited 4-(2-Phenylpropan-2-Yl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed with a screw cap, labeled "4-(2-Phenylpropan-2-Yl)Phenol," hazard and safety symbols included. |
| Shipping | 4-(2-Phenylpropan-2-yl)phenol is shipped in tightly sealed, chemical-resistant containers to prevent contamination and ensure safety. It is transported in compliance with local regulations for hazardous chemicals, typically under ambient conditions, and accompanied by appropriate documentation, such as Safety Data Sheets (SDS), hazard labels, and emergency contact information. |
| Storage | 4-(2-Phenylpropan-2-yl)phenol should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight. Store away from incompatible substances such as strong oxidizing agents and acids. Ensure proper labeling and avoid sources of ignition. Use appropriate personal protective equipment (PPE) when handling and ensure storage complies with relevant safety regulations. |
Competitive 4-(2-Phenylpropan-2-Yl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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From the manufacturing floor, every new compound that enters our plant undergoes careful study. Years ago, 4-(2-phenylpropan-2-yl)phenol was just another name on the list of complex intermediates. Over time, as requests from research teams grew more frequent, this compound found its place in our regular production schedules. Its structure, combining a phenolic core with a bulky, branched aromatic side chain, makes it more than a standard lab reagent. In our daily experience with aromatic alcohols and substituted phenols, we noticed right away that 4-(2-phenylpropan-2-yl)phenol stands out.
Colleagues from pharmaceutical and specialty chemical routes mention its unique position during iterative optimizations. The extra bulk from the isopropyl-phenyl moiety on the phenol ring introduces steric hindrance, providing new selectivity in synthetic pathways. After producing ton-quantities and examining bench-scale trials, direct feedback from our partners points to applications in fine-tuning molecular scaffolds—especially those resistant to over-alkylation or unplanned side reactions.
Every seasoned chemist or operator working with substituted phenols recognizes the risks of contamination and batch inconsistency. Precise handling matters. Each run in our batch reactors starts with high-grade acetophenone derivatives, which we source directly. Our synthesis uses carefully controlled Friedel-Crafts alkylation, since we’ve learned that minor shifts in temperature or acidity can yield undesired isomers and reduce yield. Daily monitoring by our QC team picks up minute impurities—sometimes less than 0.1%. Only after drying, crystallizing, and careful purification does our material enter final packaging.
We've noticed requests for multiple purities, often aligned with either research needs or industrial production. Most clients choosing 4-(2-phenylpropan-2-yl)phenol use grades above 98%, colorless or faintly off-white, and require a moisture content below 0.1%. These standards came up after we found even slight trace solvents caused issues during etherification or acylation reactions. Our plant switched solvents and improved vacuum distillation processes as a result—real changes based on ground-level lab reports, not marketing hype.
Working closely with pharmaceutical companies, we’ve observed that 4-(2-phenylpropan-2-yl)phenol carves out a tangible role as a building block in the synthesis of non-steroidal anti-inflammatory drugs and new analogues. Some biochemists highlight its influence on tight selectivity and improved yield during transition-metal-catalyzed coupling reactions. For each order, we ask about the downstream process, which shapes how we filter and package the bulk product. A failed batch downstream, often traced back to a hidden contaminant or excessive residual solvent, wastes time and resources. These hard lessons have pushed us to invest in better in-process monitoring, high-performance liquid chromatography, and secure isolation facilities.
Outside pharma, our experience extends into high-performance coatings, where thermal stability matters. Certain end users require the compound as a monomer or additive, and expect consistency from drum to drum. We’ve assembled years of feedback noting that altered crystal habit, or slight color shifts, can affect performance in cross-linked networks. Hands-on process adjustments—like salt removal, controlled cooling, or gentle agitation—proved key for achieving the desired solid form and color.
Chemical formulas on paper simplify things, but reality inside a plant always brings complexity. Synthetic intermediates often look and behave differently from batch to batch, unless each step is rigorously managed. The branched bulk on the aromatic ring in 4-(2-phenylpropan-2-yl)phenol decreases its reactivity toward certain electrophiles, which sometimes helps avoid side reactions and over-alkylation—a valuable property not found in unbranched or less hindered analogues.
We track every run by spectral analysis, and small peaks in the NMR or traces on HPLC teach us more than any textbook. Early years, trial runs produced minor isomers or colored impurities. Regular meetings with our chemical engineers led to investments in analytical equipment. Our routine now involves tight control of reaction times, multi-stage filtration, and closed-loop feedback with QC, which keeps the final product locked to the specifications real-world chemists demand.
For anyone working with a broad range of phenols, differences show up quickly in practice. While phenol itself or para-substituted straight-chain alkyl phenols sometimes react too aggressively, 4-(2-phenylpropan-2-yl)phenol introduces substantial bulk on the para position, moderating its reactivity and imparting more control for stepwise reactions. We’ve fielded dozens of tech support calls from manufacturers struggling with unwanted polymerization or competing ring substitutions when using less hindered phenols.
By working hands-on with both 4-tert-butylphenol and other branched analogues, we see that the presence of the 2-phenylpropan-2-yl group not only adds steric blockage but also extends the hydrophobicity of the molecule, which modulates solubility and behavior in both organic and aqueous phases. For our partners developing new ligands or specialty resins, we often run side-by-side syntheses: less hindered phenols produce unwanted dimers and oligomers, while this compound keeps the process clean. Aromatic substitutions downstream appear much easier to control, minimizing costly purification steps.
Having processed thousands of kilograms over the years, our operators know the fine points of safe and efficient handling. Phenolic compounds often pose respiratory and skin hazards, especially under dusting or hot process conditions. All operations involving 4-(2-phenylpropan-2-yl)phenol take place under closed containment, using local exhaust and personal protective equipment to prevent workplace exposure.
Regular reviews of toxicity data reinforce the importance of training new hires and revisiting protocols before new runs. From experience, we see most incidents result from overlooked steps during drum loading or maintenance, not from mishaps in the main reactor circuit. We hold frequent practical safety discussions, reviewing each part of the handling train—storage, weighing, reaction charging, filtration, drying, and packaging. For large-scale handling, we use semi-automatic conveyors, which reduce manual exposure and product loss.
Maintaining product integrity is an ongoing process. Fluctuations in raw material quality, shifts in global supply chains, and changing regulatory expectations keep us vigilant. In the early days, supply disruptions of key starting materials sometimes forced us to tweak synthetic steps and analytical thresholds on the fly. Consistency became a discipline, not a catchphrase.
Our team double-checks every incoming raw lot, and we hold sample retentions for every batch shipped. Unexpected lab results or customer feedback push us to investigate immediately, shutting down new production until the root cause is identified and corrected. These events don’t become just statistics—they stretch across teams, from engineering to logistics.
Quality and safety are never static. After a particularly tough quarter—when a batch recall from a client traced back to a minor shipping document error—we overhauled our tracking systems. Now, every drum can be traced electronically by lot number, production date, and test data, straight from the synthesis bench to final customer delivery. Auditors and customers ask fewer questions when they see real-time documentation and rapid response to query.
Routine customer inspections and third-party audits are part of our normal workflow, not special events. Production logs, analytical records, and staff training certificates are verified regularly. If changes in process or starting materials require documentation, plant-wide notifications and retraining follow. These practices didn’t come from policy manuals—they grew from ground-level production team experience, where one small slip undermines years of reputation.
Most product improvements at our facility originate outside the meeting rooms. Synthetic chemists at client sites, academic collaborators, and internal R&D provide ongoing insight. Recently, a project in agrochemical synthesis revealed trace side-products below the limits of routine detection. Joint analysis with a customer’s advanced analytical team identified the culprit—an overlooked secondary byproduct from a minor shift in catalyst choice. Our team immediately piloted new purification and switched to a more selective catalyst, which removed the impurity below quantitation. We distributed improved samples for confirmation before scaling up new production runs.
Learning from users helps us better understand which specifications matter. Some customers require higher melting point product due to integration in high-temperature transformations, while others value even lower residual solvent levels for downstream bioactivity screening. We regularly adjust crystal size, drying cycles, and solvent traces, depending on feedback and application nuances. Every year, we roll out small process adjustments tied directly to specific customer use cases, not just theoretical improvements.
No batch leaves our site without thorough analytical work. NMR, GC, HPLC, and FTIR testing come as standard. In our experience, robust in-house analysis eliminates guesswork and shortens troubleshooting. Once, a modest peak in the chromatogram flagged a cross-contaminant from a previous unrelated run. Instead of dismissing it as a fluke, our QA team traced it to a faulty gasket in a filter press, swapped equipment, and started fresh. That incident underlined the real necessity of deep batch analysis, especially on scale-up runs.
User demands for greater transparency about process impurities, trace elements, and heavy metals have grown sharper. We keep reference standards and co-test with select customer labs before weekly bulk shipments. This effort has decreased return rates and smoothed out repeated business. Analytical rigor builds mutual trust, and gives us early warning on shift trends, especially as new regulations roll out or end users shift application requirements.
Proper storage and shipping safeguard the compound’s properties. Moisture, heat, or air exposure can degrade phenolic products or alter their appearance. Over years of exporting shipments, we refined our packaging approach to seal against environmental change. High-barrier liners, nitrogen blanketing, and tamper-evident closures protect each drum from loading to end-user receipt.
We developed custom packaging protocols after noticing that prolonged transoceanic shipping sometimes shifted product color or introduced minute moisture traces. Our logistics team tracks each shipment’s route, weather exposures, and customs delays to flag trouble early. Special shelf-life studies guide product lot rotation, holding window, and re-testing cycles. Logistics isn’t an afterthought; it’s the last barrier standing between our plant and the results clients see in their own processes.
Manufacturing chemistry always demands more than paperwork and formulas. Factory noise, the aroma in the air, late-night alarms—these fill the view of real practitioners. Through the life cycle of 4-(2-phenylpropan-2-yl)phenol production, we’ve learned to expect surprises. Sometimes a speculative process improvement fails, other times a minor tweak saves enormous labor on the filling line. The best lessons flow from repeated cycles: mistakes, smart adjustments, and shared practical knowledge.
Beyond the technical files and published literature, our team’s daily work shapes the reliability that customers count on. Operators, engineers, and analysts work side-by-side, constantly improving safety, reducing waste, and upholding a product quality standard that stands up to third-party review. Every time an end user points out drift or improvement opportunity, we treat it as a springboard, not a setback.
Current developments in global chemical trade, environmental regulations, and supply chain transparency press on every manufacturer’s planning. Over many years producing 4-(2-phenylpropan-2-yl)phenol, we’ve built routines that respect each shift in expectation. Customers seeking audit trails for compliance, green chemistry credentials, or reduced environmental impacts receive clear, fact-based communication about our processes and sourcing.
Our factory experience keeps us grounded, clear-eyed about both current performance and needed improvement. When quality concerns surface, resolution draws from shared knowledge and real data instead of slogans. By valuing truth from production to delivery, we support chemists, R&D, and global industrial innovators who rely on our work. Each batch, large or small, reflects years of feedback, boots-on-the-ground diligence, and technical pride.