|
HS Code |
935566 |
| Iupac Name | 4-[4-(4-Nitrophenyl)piperazin-1-yl]phenol |
| Molecular Formula | C16H17N3O3 |
| Molecular Weight | 299.33 g/mol |
| Cas Number | 88112-50-5 |
| Appearance | Yellow solid |
| Melting Point | 174-177°C |
| Solubility | Slightly soluble in water, soluble in DMSO and ethanol |
| Storage Temperature | Store at 2-8°C |
| Pubchem Id | 10644048 |
| Smiles | C1CN(CCN1C2=CC=C(C=C2)[N+](=O)[O-])C3=CC=C(C=C3)O |
| Inchi | InChI=1S/C16H17N3O3/c20-15-5-1-13(2-6-15)18-10-8-17(9-11-18)12-3-7-14(16(19)21)4-12/h1-7,20H,8-11H2 |
| Hazard Statements | May cause irritation to skin, eyes, and respiratory tract |
As an accredited 4-(4-(4-Nitrophenyl)-1-Piperazinyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 10 grams of 4-(4-(4-Nitrophenyl)-1-Piperazinyl)Phenol, labeled with hazard warnings and storage instructions. |
| Shipping | This chemical, 4-(4-(4-Nitrophenyl)-1-piperazinyl)phenol, ships in secure, airtight containers compliant with chemical safety regulations. It is handled under controlled temperature and protected from light and moisture. Packaging includes clear labeling as a laboratory reagent. Transport follows all local, national, and international hazardous material transport guidelines to ensure safety. |
| Storage | Store 4-(4-(4-Nitrophenyl)-1-piperazinyl)phenol 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. Use corrosion-resistant containers and clearly label them. Handle under a chemical fume hood and avoid moisture and direct sunlight to preserve chemical stability and integrity. |
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In a chemical plant, every new process means mastering material down to its quirks, and 4-(4-(4-Nitrophenyl)-1-Piperazinyl)Phenol shows distinct behavior compared to simpler piperazine or nitrophenyl derivatives. Over the years, our teams have handled the full cycle for this compound—right from raw input to the finished fine powder or crystalline solid. There’s a difference in the way this molecule responds to processing conditions. The phenolic group brings a touch of sensitivity to temperature and pH shifts, demanding tighter process controls than you see in base piperazines, but it also offers a platform for selective transformations. The nitro group at the para position on the phenyl ring changes reactivity patterns and creates opportunities for downstream modification, while the piperazine linker introduces both flexibility and challenge, giving a non-planar structure that reacts differently under various solvent systems.
Production starts with rigorous quality checks on starting materials. Each batch of raw input can throw a curveball—some suppliers introduce slight shifts in impurity profiles. Even a trivial variance like residual solvent in the nitrophenyl starting material can alter the yield and color of the final product. Staff on the plant floor keep eyes open for subtle changes in reaction color or particle texture, since these often reveal more about purity than any textbook. These details, noticed by technicians with years of hands-on experience, matter in scale-up as much as in kilogram batches for research-scale orders.
We often get questions from pharmaceutical groups and specialty intermediates manufacturers about the difference between this compound and plain phenylpiperazines. On paper, it’s one more functional group, but that nitro substitution on the far end makes for a remarkably different reactivity in subsequent coupling reactions. That allows medicinal chemists to use it as a building block for structures where electron-withdrawing groups influence metabolic pathways or receptor binding. Plant operators know that controlling reaction exotherms in nitration or subsequent reduction steps shapes the purity and shelf-stability of the final product. This sort of feedback constantly sharpens our process parameters—steady agitation, slow temperature ramping, careful drying, all timed by the experience gained over batches run in every season.
The story of this molecule doesn’t stop at manufacturing. There’s always an eye on downstream application requirements. We keep open lines with project leaders in pharmaceutics, agrochemicals, and advanced coatings. A research team in oncology may need the compound for trialing new kinase inhibitors or receptor antagonists. Material scientists in electronics notice it as a precursor for specialty dyes or functionalized polymers. They ask about trace metal content, moisture levels, and even how it behaves under different storage conditions. These conversations drive continuous tweaks in the way we finish, dry, and package each lot. Silica gel drying may help moisture control, but customers sometimes prefer vacuum drying for use in sensitive synthetic steps. All this comes back to plant staff who understand why one batch runs longer in the dryer or why crystallization from methanol looks different from acetonitrile.
Comparisons with commercial piperazine derivatives make clear that 4-(4-(4-Nitrophenyl)-1-Piperazinyl)Phenol stands in its own category. Piperazine itself feels straightforward—stable, forgiving, and highly soluble. Link a p-nitrophenyl group, and you see lower solubility in basic water, slower filtration, often more tendency to oil out if cooling rates aren’t controlled in the final crystallization. In-process analytics catch shifts in purity, color, and melting range earlier than any written protocol could predict. Staff learn to expect slight yellowing if the reaction goes too warm, which reflects in UV absorbance and—importantly—can point to batch-specific side-products that impact final usage. That kind of real-time knowledge is woven into our process book and updated with every run, not just in yearly audits.
There’s a regulatory angle that shapes this work, grounded in hard lessons from years spent managing GMP and ISO inspections. The regulatory field never sleeps, especially with phenolic nitro compounds, which come under closer scrutiny for potential toxicological hazards. Our teams spend time collecting, cataloging, and reviewing every batch record, confirming traceability from start to finish. In-process sampling for residual solvents meets ICH Q3C guidelines, and heavy metal remediation strategies change as standards evolve. Local wastewater limits force periodic redesign of side-stream purification to remove even negligible phenolic traces before discharge. These compliance tasks might look invisible to those focused only on the product, but they shape daily decisions across engineering and quality control alike.
Mixing and handling operations matter more than textbooks hint. Phenolic groups often cause sticking or caking in standard blending equipment, so we schedule more frequent cleaning and swap out contact parts as needed. The nitrophenyl moiety can release dust or odor under certain conditions, prompting plant operators to monitor air handling equipment with calibrated sensors. The result of all this tinkering is a material that arrives at the customer end with consistent particle size and purity, even when humidity or ambient temperature outside the plant swings wildly from week to week.
Packaging this compound might sound trivial, but plant managers know each step can impact a sensitive application. Our lines use antistatic liners in drums and bags, since both the nitro group and phenol functionality can make for slightly hygroscopic behavior, particularly in finely divided powders destined for high-precision R&D. The move to tamper-evident packaging came after a customer noticed trace oxygen ingress in standard drums was enough to alter color and reactivity months after delivery. Those field reports, coming back from chemists or plant supervisors, close the loop between production and real-world performance.
Every step in the chain—handling, drying, packaging, documentation—rests on practical chemistry. Bench chemists who spend years fine-tuning coupling reactions involving this scaffold pass along insights that land in every updated SOP. For instance, the cold-start reflux never works as well as a staged ramp in building the piperazine-phenol linkage. That means less batch-to-batch variability downstream. These habits, learned by doing, drive reliability that can’t be captured by paperwork alone. Newer staff pick up this knowledge by confronting unexpected blips—hard lumps in the mixer, or an off-yellow product—and learning how to troubleshoot instead of starting over.
Procurement teams at research labs and manufacturers often ask about the availability of higher-purity or custom modification of this compound. A broad spec sheet won’t answer their real requirements—many want ultra-low water, or a defined polymorphic form, or batches produced using certain solvents due to trace impurity concerns. Some request explicit confirmation of the starting material lineage for regulatory filings, requiring detailed batch histories. Our staff handle these inquiries with direct reference to in-plant logs, not just quoting catalog numbers, since real trust comes from knowing which run produced that lot and how it tracked through the system.
Customers often weigh 4-(4-(4-Nitrophenyl)-1-Piperazinyl)Phenol against products integrated with different linkers or fewer functional groups. Each choice means new safety profiles, reactivity under coupling, and process risk management. While a simple piperazinylphenol feels easier, this nitro-containing variant creates space for advanced work in medicinal chemistry, catalysis, and material science. The electron-withdrawing effect, distinct color properties, and handling dynamics open or close avenues for downstream modification, so we work closely with project scientists to match not just spec sheets, but actual lab requirements.
Market shifts, regulatory changes, and new application spaces constantly alter what’s needed from the plant floor. Moves to tighten nitro-aromatic controls for worker safety or environmental discharge will always force us to rethink handling protocols. Process engineers stay ahead by retooling air capture, improving dust controls, and working up alternative cleaning strategies based on real feedback from day and night shifts. Training focuses not just on safety compliance, but on recognizing subtle shifts—like a faint tart odor or slow settling in the centrifuge—that signal the need for intervention before a deviation spins out of control.
Innovation isn’t just a motto in this field; it’s the day-in, day-out challenge of chemistry at scale. Starting from a well-known backbone, we work with contract partners in drug discovery and advanced materials to create offshoots tailored to end-use. Sometimes the changes are small—altering substitution patterns, purification strategies, or drying schedules. Other times, projects call for hybrid forms with specific solubility profiles or reactivity with unusual nucleophilic partners. The manufacturing teams build up hefty process notebooks, cross-referencing runs for the same project across seasons, suppliers, and subtle differences in incoming materials. These notebooks become lab bibles, shaping how the next batch is made and what new solution gets tried when old tricks don’t fit the new challenge.
Plant chemists gain expertise not just by running batches, but by solving the unexpected. A stuck filtration or crystallization refusal means a day adjusting solvent ratios, swapping in fresh filters, or pausing for fine-tuned temperature control. The sense of satisfaction comes not from reading about success stories, but from beating back unforeseen problems—ensuring material with five nines purity lines up with both analyst data and customer performance expectations. Our crew understands not just how to execute an SOP, but how to adjust in real time, keeping the process on track even under shifting market demand or input costs. That’s where factory-grown expertise shines.
Quality by design is no idle phrase in the context of 4-(4-(4-Nitrophenyl)-1-Piperazinyl)Phenol. Each stage—from receiving raw chemicals to final drum sealing—includes planned and unplanned checks. Visual inspection catches color nuances missed by HPLC, and operators log changes in texture or pourability with as much attention as analytical numbers. These observations, built up batch after batch, mean we catch drifts in quality before they escape the plant, upholding both compliance and end-use reliability.
Listening to customer feedback creates a feedback loop that benefits both plant and end user. When a polymer lab describes the need for a specific hydrate form, manufacturing teams collect historic process data and tweak neutralization or drying conditions. When a pharmaceutical group reports improved yields with our low-Na batch, process logs and equipment cleaning records backtrack to ensure we can repeat and scale the same outcome. This practical commitment to continuous improvement keeps our product line both consistent and capable of meeting new challenges.
Shipping and logistics aren’t just about moving boxes—they form an extension of precise process control. Moisture, temperature, and transit timing all affect how this sensitive chemical arrives at the next bench or production line. Each shipment includes documentation from people who understand not just the law, but the practical impact that slow customs or a stacked container can have on a critical organic synthesis run. A full logistics team, working hand-in-hand with quality and plant operations, handles unexpected events on the road to make sure what leaves the plant meets the same specs that guided the process at home.
People talk about supply chain transparency. In our plant, that means weekly meetings where supervisors, line workers, and quality control review every incident—unexpected yield drop, color change, or packing issue. Root causes get uncovered and new protocols written into the daily routine. This culture, born of daily hands-on work, respects both the expertise of the plant floor and the innovation needs of chemistry teams downstream. That’s what actually translates into trust when a customer orders their next batch.
4-(4-(4-Nitrophenyl)-1-Piperazinyl)Phenol is more than a chemical name; it represents years of learning how a multi-functional compound fits into modern organic synthesis, scale-up, and specialty applications. It stands apart from more basic derivatives by requiring and inspiring greater process adaptability, tighter controls, and a deeper understanding of how even minor process tweaks translate to major differences in end-use reliability. Our commitment at the plant is rooted in decades of experience—a belief that process knowledge passed down day by day builds products that succeed for every new challenge, application, and evolving market.