|
HS Code |
884938 |
| Iupac Name | 4-[4-[4-(Trifluoromethoxy)phenoxy]piperidin-1-yl]phenol |
| Molecular Formula | C18H18F3NO3 |
| Molecular Weight | 353.34 g/mol |
| Cas Number | 139151-23-2 |
| Appearance | White to off-white solid |
| Melting Point | 140-142 °C |
| Solubility | Soluble in DMSO, methanol |
| Smiles | C1CN(CCC1OC2=CC=C(C=C2)OC(F)(F)F)C3=CC=C(C=C3)O |
| Inchi | InChI=1S/C18H18F3NO3/c19-18(20,21)25-15-4-2-13(3-5-15)24-12-6-8-22(9-7-12)14-1-10-16(23)11-17(14)26/h1-5,10-11,23H,6-9H2 |
| Storage | Store at 2-8 °C |
| Pubchem Cid | 9884343 |
| Synonyms | 4-(4-(4-(Trifluoromethoxy)phenoxy)piperidin-1-yl)phenol |
As an accredited Phenol, 4-[4-[4-(Trifluoromethoxy)Phenoxy]-1-Piperidinyl]- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed with a screw cap, labeled with hazard warnings. Contains 25 grams of Phenol, 4-[4-[4-(Trifluoromethoxy)phenoxy]-1-piperidinyl]-. |
| Shipping | Phenol, 4-[4-[4-(Trifluoromethoxy)phenoxy]-1-piperidinyl]- should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Package in accordance with local, national, and international regulations for hazardous chemicals. Use appropriate labeling and documentation. Recommended transport is via designated chemical courier, ensuring temperature control and secondary containment to prevent leaks or spills. |
| Storage | Phenol, 4-[4-[4-(Trifluoromethoxy)phenoxy]-1-piperidinyl]- should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Store in a chemical storage cabinet, preferably designed for organic chemicals, with appropriate labeling and access restricted to trained personnel. |
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Daily production lines buzz with the work of synthesis, control, and purification. Years spent perfecting heterocyclic chemistry have given us the tools to offer complicated intermediates like Phenol, 4-[4-[4-(Trifluoromethoxy)Phenoxy]-1-Piperidinyl] on consistent, actionable timelines. Unlike bulk phenols or readily available substituted aromatics, this compound brings a layered structure and distinct physical properties that require hands-on process knowledge. As an involved manufacturer, our team faces the details: stepwise coupling conditions, careful control over byproduct formation, solvent selections that keep purification simple, and batch-to-batch monitoring that keeps specifications tight.
What sets this phenolic piperidine apart can be traced to every choice made on the factory floor. Engineers calibrate equipment not just for output, but for reproducibility and trace impurity levels. On each production run, we evaluate melting point ranges to be certain of batch identity and stability, because this parameter affects storage, crystallization, and transportation. High-pressure reactors, specialty glassware, and inert-atmosphere techniques have become part of our workflow. With every batch, a barrage of in-process checks ensures the trifluoromethoxy substitution lands exactly where it belongs: para on the distal phenoxy ring. Small details like water content, which can creep in during storage, receive careful attention, since moisture can impact downstream reactions—especially Suzuki couplings, which several clients rely on.
Adherence to these hands-on controls results in a product that meets rigorous application standards. This is far from a casual substitution on a generic aromatic. Synthetic routes integrate demanding steps—such as nucleophilic aromatic substitution followed by piperidination. Only after the team verifies completeness at each step do we move forward. Scale-up poses its own hurdles, and our process chemists oversee every shift from pilot to full-scale. Between temperature ramp profiles and agitator speeds, it’s people, not just protocols, who ensure each kilogram remains uniform.
The unique molecular backbone of this phenol carries real weight in modern medicinal research and advanced material development. As more medicinal chemists scrutinize partition coefficients or seek improved solubility for lead optimization, the trifluoromethoxy motif finds itself in increasing demand. Unlike simple fluoro or methoxy substitutions, it brings electronic and lipophilic modulation in one group, driving decisions at the bench in real time.
We’ve worked closely with discovery teams looking for ways to subtly influence metabolic stability or pass through biological membranes without excessive systemic retention. The piperidine ring, with its basic nitrogen, stands apart from more inert aryl ethers, supporting solubility in both polar and nonpolar solvents. Several client formulations exploit this duality—often in the context of CNS-active library projects, where logD shapes both potency and selectivity. On our floor, attention to these downstream needs keeps us dialed-in to the purity and physicochemical profiles that matter.
Having walked through hundreds of batch records and years’ worth of QC logs, the difference between actual manufactured material and off-the-shelf alternatives feels stark. Fluctuating supply chains, vague origins, and spotty documentation can derail both regulatory and research programs. Our in-house routes build in multi-tiered checks and stability monitoring, right down to storage safeguards with argon blankets or controlled-humidity vaults for long-term holding. What arrives on the client’s bench comes straight from a controlled process run by chemists who can discuss every exotherm, every solvent exchange, and every minor variance.
In the real working world, numbers always beat claims. For our production lots, we support exact NMR, HPLC, LC-MS, IR, and melting point data. As a manufacturer, hands-on methods trump generic certificates: spectroscopic overlays help us support client verification, and side-by-side comparisons with reference standards back up each lot. Instead of hiding behind regulatory generalities, we invite partners to review anonymized batch records, impurity profiles, and full chromatograms. Tank sizes, reactor capacity, cycle times—each is factored into projected timelines, not just inventory pulses. Purity levels gauge above typical 98% standards; we chase down minor byproducts and rework any outlier until agreed targets are met.
Unlike stock intermediates where supply and fits-and-starts often dictate what gets shipped, we manage the workflow. This means better control of appearance (white to off-white solid, not “yellowish,” not variable), known particle morphology for better dispensing, and real data about thermal stability, not just bullet points from a catalog. Ambient storage recommendations follow from actual experience with shipment spoilage and stability testing over quarters, not just weeks. All this stems from making, handling, and watching the product move from vessel to flask week after week—not just third-party reselling.
Making a high-end heterocycle always starts with the fine details. Reproducible output means competent technicians, round-the-clock maintenance, and hands ready to adapt on the fly. Trifluoromethoxy arylations demand carefully staged additions and real-time sensor feedback. Density fluctuations across reaction phases spool out during scale-up, triggering adaptive approaches to mixing and agitation. Trace water can catalyze unwanted hydrolysis; the team keeps continuous Karl Fischer titrations in play. Vacuum dryers and nitrogen-purged vessels help guarantee each drum heads out with consistent dryness. Each output order generates fresh analytics, not recycled certificates.
Our plant supervisors have learned the hard way how even simple physical shifts—ambient temperature changes, new lots of piperidine, or minor tweaks in supplier solvents—can influence yield and byproducts. Regular troubleshooting and team huddles cut response time. Our policy stays rooted in rapid root-cause identification, not finger-pointing or speculative fixes. From years spent on the production floor, we know exactly how one small variation can echo through the pipeline, and we spare no effort to keep these effects minimized for our clients.
Research teams don’t want surprises in their reaction streams. Medicinal chemists have told us directly how a slightly out-of-spec melting point, or an extra unassigned NMR signal, can halt an entire SAR campaign. Agencies examining regulatory data require traceable origins and granular detail. From this feedback, we keep updating both protocols and documentation practices, offering up full audit trails, SDS transparency, and real-world support. Actual answers matter more than generic assurances.
We treat every lot as a discrete milestone, not just an “item.” Our teams track changes in raw material provenance, run stability samples to assess shelf-life, and provide repeat analysis for stored materials. Analytical teams calibrate instruments frequently, benchmark against pharmacopeial standards, and run routine cross-validation with outside labs for larger projects. The outcome is not just paperwork, but real, actionable confidence for clients aiming to use the product in multi-step synthesis or as part of lead development campaigns.
Everything about this product’s molecular design complicates and enriches its application. The presence of the trifluoromethoxy group provides strong electron-withdrawing effects without causing the harsh deactivation often seen with nitro or cyano analogs. Our QC chemists have run many reaction screens—Suzuki couplings, Buchwald-Hartwig aminations, O-arylations—tracking reactivity shifts and yielding direct guidance on practical handling. The piperidine nitrogen further broadens the chemistry, opening up alkylation, acylation, and salt formation options. That flexibility doesn’t come easily: only a few plants commit to the specialized conditions needed for full, clean conversion, and as a manufacturer, our fingerprints can be traced in every decision and outcome.
Working closely with customers, we’ve documented how our process materials outperform resold or repackaged alternatives: cleaner baseline in reverse-phase HPLC, slower color change under accelerated storage, fewer unknown signals on NMR expansion. Relationships with users inform future improvements, but also sharpen our sense of what “good manufacturing” actually means, right down to how it impacts the next phase of the client’s work.
As chemical makers, we believe that product stewardship doesn’t end at the loading dock. Every step, from raw material procurement to spent solvent disposal, falls under strict internal review. The chemical’s handling profile—low vapor pressure, real but controlled exposure potential, clear labeling, and responsible waste transfer—receives continuous compliance attention. SDS documents fit the reality of our process, not a one-size-fits-all template. Safe handling echoes through every room and every shift-change briefing.
Environmental obligations shape day-to-day choices. Solvent recovery circuits, closed-system transfers, and minimal use of regulating agents anchor our operations. We report to local safety authorities, maintain a transparent greenhouse gas assessment, and follow documented spill containment procedures. In-house teams conduct risk and exposure training quarterly, boosting everyone’s comfort with both the “what” and “why” of safe production and handling. The specifics of each plant, each run, each team member’s record matter—a perspective only a manufacturer can provide.
Years of compound handling have given us more than familiarity; they’ve taught us where incremental changes in process and analysis drive reliability and quality. Our researchers collaborate with both clients and internal R&D, pursuing new routes for waste minimization, greener solvents, and routine yield optimization. Small equipment upgrades—photoreactors for specific oxidations, newly jacketed vessels for improved exotherm control—arise from the lived experience of making intricate phenols, not from vendor wish lists.
Product thermograms, early warning flags on batch trends, and direct operator feedback inform even subtle tweaks. We’ve learned to anticipate not just routine lab successes but also the operational quirks that emerge on 200-kg scales. That’s how each drum, flask, or packaged vial has the backing of real people, process, and partnership, rather than layers of vendor intermediaries.
Market trends are clear: demand for highly-functionalized, selective intermediates climbs alongside progress in therapeutic targets and advanced polymers. In many fields, especially pharmaceuticals and advanced coatings, purity, homogeneity, and clear documentation beat price. We keep lines of communication open with purchasers, technical leads, and R&D groups in order to respond not just to one-off samples but to program-scale needs—whether this means smaller, faster runs for discovery, or sustained tonnage supply to bridge from pilot to validation.
Every piece of feedback is scrutinized. Supply chain interruptions elsewhere have prompted us to expand documentation, build more flexible production lines, and certify multiple upstream vendors for key starting materials. Downstream users rely on our openness: real delivery forecasts, transparent lot histories, and the capacity to discuss specific batches with someone who’s actually been in the reaction blockroom.
Manufacturing Phenol, 4-[4-[4-(Trifluoromethoxy)Phenoxy]-1-Piperidinyl] brings constant reinforcement to the idea that real value comes from experience, interaction, and the willingness to put work behind each claim. Each lot stands as a result of decisions made by chemists, operators, and engineers who carry forward lessons from every challenge. For clients seeking molecular complexity, product performance, and direct manufacturing relationships, every batch represents trust in human effort as much as technical process—a partnership built on real, continuous commitment.