|
HS Code |
623281 |
| Iupac Name | 4-(Piperazin-1-yl)phenol |
| Cas Number | 2553-46-6 |
| Molecular Formula | C10H14N2O |
| Molecular Weight | 178.23 |
| Appearance | White to off-white solid |
| Melting Point | 150-153°C |
| Solubility In Water | Slightly soluble |
| Pubchem Cid | 156331 |
| Smiles | C1CN(CCN1)C2=CC=C(C=C2)O |
| Inchi | InChI=1S/C10H14N2O/c13-10-3-1-9(2-4-10)12-7-5-11-6-8-12/h1-4,11,13H,5-8H2 |
| Synonyms | 4-Hydroxy-1-phenylpiperazine; p-Hydroxyphenylpiperazine |
| Storage Conditions | Store at 2-8°C |
As an accredited 4-(Piperazin-1-Yl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a secure screw cap, labeled "4-(Piperazin-1-Yl)Phenol," including hazard and handling instructions. |
| Shipping | 4-(Piperazin-1-yl)phenol is shipped in tightly sealed containers, protected from moisture and light. It is packed according to standard chemical transport regulations, ensuring safety during transit. Appropriate labeling, documentation, and hazard warnings are provided. The chemical is shipped via trusted carriers, with temperature and handling requirements maintained as specified by safety data guidelines. |
| Storage | 4-(Piperazin-1-yl)phenol should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from moisture, direct sunlight, and sources of ignition. Keep the storage area clearly labeled and access limited to authorized personnel. Ensure appropriate spill containment measures are in place. |
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Years of hands-on chemistry work have shown me the value of smaller molecules that pack versatility and reliability into their structures. 4-(Piperazin-1-Yl)Phenol stands out in our production halls—not because it shouts the loudest, but because it delivers steady utility to a wide array of industrial customers. As the backbone of several intermediate syntheses and the subject of so many process refinements, this compound always draws discussion among chemists who keep production lines moving.
At its core, 4-(Piperazin-1-Yl)Phenol bears the molecular formula C10H14N2O. The combination of a phenol ring and a piperazine moiety opens the door to both reactivity and stability. Years of in-process trials and customer applications have driven us to dial in the optimal purity and crystal form, since small shifts in impurity levels or isomer content can swing downstream reactions in unpredictable ways.
For most of our customers, ‘model’ tends to mean one thing only—consistency batch to batch. Ours comes as an off-white crystalline powder, typically with HPLC purity above 98%, minimizing headaches for formulation teams and maximizing synthetic yields. Dense feedback from pharmaceutical, agrochemical, and specialty polymer teams keeps us pushing the analytical boundaries here, confirming identity and ensuring trace contaminants never trip up regulatory dossiers further down the chain.
Standing on the manufacturer’s side of the fence, I encounter every upstream and downstream pressure firsthand. Research firms or custom chemical suppliers often want a hands-free, turn-key solution. They won’t tolerate inconsistencies in moisture content or particle size—these small things sabotage solubility or reactivity, wasting hours of method development. We invest in controlled drying and careful packing not out of formality, but because nobody wants to get that phone call about a process stalling due to a caked-up drum.
Documentation and transparency keep trust alive in every repeat order. Spectra, chromatograms—these are more than paperwork; they anchor every purchase order to a proven history. We back samples and full shipments with batch-specific data, tracking impurities and degradation markers down to the parts-per-million level. Customers building APIs or advanced polymers lean heavily on this rigor, especially as audits and international registrations get ever more demanding.
Over the years, I’ve walked more than a few plant floors and talked shop with hundreds of production chemists and engineers. The first thing they flag about 4-(Piperazin-1-Yl)Phenol is its role as a key intermediate for selective syntheses. Much of its value comes through the piperazine ring, serving as a vector for further N-substitution or cross-coupling, while the phenolic hydroxyl opens up alternative activation steps for linking into larger frameworks.
Take pharmaceuticals as an example. Many innovators target the piperazine motif for biological activity—antipsychotics, antihistamines, kinase inhibitors, and even experimental oncology agents. Where scaffold modifications are needed, our phenolic version gives the flexibility for late-stage functionalization. Medicinal chemists can use this specific linkage to fine-tune solubility and receptor selectivity. The benzylic position resists oxidation compared with straight phenols or unprotected piperazines, which has saved some projects from early termination during stability trials.
The agrochemical industry brings its own constraints. Formulators demand solubility in a tight range as they seek new insecticide or fungicide backbones. Using the 4-(Piperazin-1-Yl)Phenol structure, they can create hybrid agents by selective alkylation or acylation. Our technical team spends more time than one might guess discussing byproducts and yield losses with these users, supporting iterative synthesis as their regulatory hurdles grow more daunting.
Outside of direct product applications, this compound crops up in specialty polymer work. Rigid-rod polyamides and modified polyaryletherketones draw strength and processability from heterocyclic spacers. The thermal and hydrolytic stability of 4-(Piperazin-1-Yl)Phenol makes it a favorable candidate, especially when electrical or flame-retardant properties are crucial.
Across the spectrum of phenol derivatives, the piperazine-substituted variant maintains a unique balance of reactivity and benign handling. Unlike 4-aminophenol or other common electron-rich phenols, the piperazine group moderates both basicity and hydrogen bonding. This moderation, evident in kinetic studies and batch reactivity logbooks, translates into fewer surprises during scale-up.
Comparing this to N-methyl or N-ethyl piperazine phenols, our 4-(Piperazin-1-Yl)Phenol wins out with a lower melting point and better crystalline stability, which eases bulk handling and formulation. Chemists developing new coupling reactions often report a smoother purification path, thanks to the signature UV absorbance profile at different pH levels. Qualitative differences show up, too: reactions run with unprotected piperazines sometimes require tougher downstream workups, while those built from our version allow easier extraction and higher reactivity selectivity.
Substituted phenols used solely as antioxidants or polymer stabilizers rarely match up on versatility. Those applications typically need bulk volumes and minimal reactivity. Our 4-(Piperazin-1-Yl)Phenol serves best in dynamic settings—where selective transformations matter, and where the downstream application is unforgiving of minor impurities.
Scaling up a molecule means living through the aches and pains that lab-scale processes hide. We’ve overhauled batch reactors and changed extraction procedures to scrub out batch-to-batch variability. During early pilot runs, solvent residues dogged our quality team, demanding longer drying times and new filtration steps. Over time, tweaking crystal seeding protocols delivered smaller particle size distribution, critical for fast and complete re-dissolution.
Our teams scrutinize not only immediate process safety but also long-range storage stability. The phenolic portion can oxidize under abusive conditions, so we purge vessels with nitrogen and pack under low-oxygen atmosphere. These precautions have paid dividends, especially for customers with long inventory cycles or distant shipping routes.
Quality assurance, as practiced by our crew, means tracking every intermediate and documenting how each change in input and process shifts the fingerprint chromatogram. Customers who once doubted sourcing from outside multinational giants now trust our agility and documentation. This sense of partnership drives us to address issues directly: from off-odors picked up during inspection, to slightly off-target melting points traced back to small solvent carryover at the centrifuge stage. Every incident, every fix, stays in our process notes and informs the next troubleshooting session.
End-users pushing molecules into clinical or environmental use place heavy demands on manufacturers. Every new batch pours through our quality, environmental, and safety tracking systems. We see firsthand how a single unnoticed impurity spells weeks of delay down the regulatory path. Process engineers and regulatory affairs teams pore over our analytical updates, and some customers request split production batches for their own reference labs to test.
Handling comes up often in technical calls. Pure 4-(Piperazin-1-Yl)Phenol features low volatility under ordinary temperature and pressure, easing in-plant air quality control compared to more volatile phenol derivatives. Its limiting factor often lies in dust formation, which we address by compacting or granulating larger shipments and using liners resistant to static buildup.
Long transport hauls raise questions about stability, especially to warm or humid regions. Years of troubleshooting have taught us how moisture uptake degrades product quality, so we use desiccant linings for every drum headed across climate zones or stored at unregulated sites. An in-house stability chamber runs ongoing retention samples, helping us flag issues or fine-tune our recommendations before they affect customer operations.
Sustainability is no longer a buzzword at the factory gate; it’s built into every stage of our sourcing and waste management. Classic chemistries generate more solvent waste than modern standards tolerate. We work to minimize solvent consumption at extraction and washing stages by recycling filtration mother liquors and reusing water in initial wash cycles. Analytical tracking after every tweak assures us—and our customers—that product purity or contaminant risk never slips.
Pressure mounts industry-wide over trace contaminants like heavy metals and aromatic amines. Our lab harmonizes detection techniques at low thresholds, tuning synthetic methods to avoid precursor overlap. Most of our improvements start with small-batch optimization—tweaking reagents or replacing aged catalysts—before pushing changes to daily production. These steps, though incremental, translate into fewer customer batch rejections and less landfill waste, benefits we track carefully and report upon request.
Growing demand for more flexible molecules for combinatorial libraries and new synthetic scaffolds drives us to keep evolving 4-(Piperazin-1-Yl)Phenol's possibilities. Getting clean, well-documented lots to early-stage researchers helps them move quickly through hit-to-lead efforts. Each time a partner publishes or files a patent using our output, that result builds momentum, helping us prioritize which analytical standards and process adjustments deserve the most attention.
Trust between manufacturer and end user doesn’t grow overnight. The most successful projects often come from open, sustained dialogue. Beyond standard purity profiles or per-batch analyses, we find value in working through the entire downstream process with our partners—understanding solubility hiccups, characterizing byproducts, or redesigning package sizes to match on-site transfer equipment.
Years of supporting R&D and pilot projects have shown us that providing technical data early and responding frankly to analytical queries delivers better results for everyone. We pull feedback from failed experiments and process deviations, pin down the cause (even if it lies outside our walls), and refine both our synthesis and communication. Our experience tells us that users of 4-(Piperazin-1-Yl)Phenol value not just a reliable supply stream, but also shared learning from every challenge or technical snag along the way.
A reputation for quality grows from steady small actions: keeping clear records, honoring commitments, and speaking openly about setbacks. The close-knit nature of chemical manufacturing means word about batch consistency or documentation lapses travel quickly through technical networks. We have built our name by facing these moments candidly, answering the tough questions, and bringing solution-oriented suggestions to the table—whether in the form of supply chain tweaks, packaging redesigns, or synthetic route modifications to support cleaner outcomes.
Each new synthetic demand—tighter impurity specs, alternate packing formats, or audit-friendly documentation—reminds us that delivering 4-(Piperazin-1-Yl)Phenol means responding to a dynamic market. The work never stands still: we test innovative drying or isolation methods, vet renewable feedstocks, and pursue higher recovery yields, not for show, but from constant pressure from labs and plants depending on our output every day.
Our drive isn’t only about staying ahead in the market, but also about making sure that every batch of 4-(Piperazin-1-Yl)Phenol leaving our plant reflects the lessons learned from years at the intersection of synthesis and application. This approach has shaped how we solve complex process issues and how we help customers unlock the next steps in their development pipeline. The outcome—a refined, dependable, versatile intermediate—follows from the resolve of everyone on the shop floor, in the lab, and at customer sites, all dedicated to getting the chemistry right and building real trust, batch after batch.