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4-(5-(3-(Trifluoromethyl)Phenylamino)-4H-1,2,4-Triazol-3-Yl)Phenol

4-(5-(3-(Trifluoromethyl)Phenylamino)-4H-1,2,4-Triazol-3-Yl)Phenol


    • Product Name 4-(5-(3-(Trifluoromethyl)Phenylamino)-4H-1,2,4-Triazol-3-Yl)Phenol
    • Alias FCN-437c
    • Einecs NA
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    414376

    Iupac Name 4-[5-(3-(Trifluoromethyl)phenylamino)-4H-1,2,4-triazol-3-yl]phenol
    Molecular Formula C15H11F3N4O
    Cas Number 1254121-31-9
    Appearance White to off-white powder
    Melting Point 221-225°C
    Solubility Slightly soluble in DMSO; poorly soluble in water
    Storage Temperature 2-8°C (Refrigerated)
    Purity Typically ≥98% (HPLC)
    Smiles C1=CC(=CC(=C1)O)N2C=NN=C2NC3=CC(=CC=C3)C(F)(F)F
    Inchi InChI=1S/C15H11F3N4O/c16-15(17,18)10-2-1-3-12(8-10)21-14-20-13(9-4-6-11(23)7-5-9)19-22-14/h1-8,23H,(H,19,20,21,22)
    Logp Approximate 3.5

    As an accredited 4-(5-(3-(Trifluoromethyl)Phenylamino)-4H-1,2,4-Triazol-3-Yl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass vial, 5 grams, sealed with a PTFE-lined cap, labeled with chemical name, purity, batch number, and hazard warnings.
    Shipping This chemical, 4-(5-(3-(Trifluoromethyl)Phenylamino)-4H-1,2,4-Triazol-3-Yl)Phenol, is shipped in sealed, high-quality containers to ensure stability and prevent moisture exposure. It is packaged according to applicable chemical transportation regulations, with appropriate hazard labeling and documentation, ensuring safe and secure delivery to the customer’s specified location.
    Storage Store 4-(5-(3-(Trifluoromethyl)phenylamino)-4H-1,2,4-triazol-3-yl)phenol in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep at room temperature or as specified by the manufacturer, in a well-ventilated, dry area. Use appropriate personal protective equipment when handling. Avoid sources of ignition and store away from strong oxidizing agents and acids.
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    Certification & Compliance
    More Introduction

    Direct from Our Plant: 4-(5-(3-(Trifluoromethyl)Phenylamino)-4H-1,2,4-Triazol-3-Yl)Phenol

    Refining the Craft of Triazole Chemistry

    Every chemical we introduce to the market starts out as a lab-scale curiosity, a molecule promising enough to push through all the disturbance of scale-up, flow monitoring, reaction tweaking, and quality control. Our 4-(5-(3-(Trifluoromethyl)Phenylamino)-4H-1,2,4-Triazol-3-Yl)Phenol has earned its place in the portfolio after extensive work in our pilot reactors and downstream optimizing. Our synthetic teams have spent months determining how to convince this particular triazole-based compound to yield consistently clean, powdery batches without complications such as byproduct contamination or inconsistent melting profiles.

    At the bench, triazole chemistry asks for steady attention. The amination step, the handling of the trifluoromethyl aromatic fragments, and purification through each wash present their own lessons. Each part shapes the final product, beyond what any datasheet ever summarizes.

    What Sets this Product Apart

    A lot of folks who see "triazole" think of the tried-and-true fine chemical families powering antifungals, crop protection, or specialty coatings. But when you add a 3-(trifluoromethyl)phenylamino group at the 5-position and a para-hydroxyphenyl at the 4-position of 1,2,4-triazole, you’re in different territory. It’s not just about wedge-shaped molecules locked by trifluoromethyl stability or the homogeneous appearance under HPLC—though those features make a difference on the production floor.

    Most of the triazole derivatives out there don’t combine this aromatic amine with the electron-rich phenolic group at para. That means you get different physical properties at the molecular level. Solubility profiles change. Recrystallization behaves in a distinct way. The aromatic substitution affects stacking interactions—something that matters when you try to dissolve or blend concentrated batches during downstream processing.

    From the reaction vessel’s perspective, adding a trifluoromethyl group isn't a simple swap. It influences reactivity under heat and solvent phase, and gives the molecule an edge in terms of thermal stability and volatility. Trifluoromethyl works as a resistor against unwanted side reactions, which keeps batches cleaner and translates to less extra work for our operators. These unique fragments matter as much on the plant floor as they do in journals.

    Every Batch Tells Its Own Story

    No chemical plant runs on paperwork or protocols alone. Each kilogram of this phenol-triazole product has a history, from the earliest runs where yields teetered on the edge to the modern lots that easily surpass what we thought possible five years ago.

    We take a close look at particle morphology with optical microscopy. Sometimes, batch-to-batch differences arise: crystal habits shift if the solvent evaporation curve drifts by just a few degrees. That feeds back into how filtration feels—not all powders move through a Buchner funnel with the same ease. Operators’ hands-on feedback leads us to fine-tune stir rates or solvent choices, right alongside our chromatographic analyses.

    Each batch cycle also offers a new perspective on aging and long-term integrity. We run real-time and accelerated stability on retained samples. The presence of both a phenolic OH and a trifluoromethyl aromatic group holds up well in the face of humidity, but learning that first-hand saves plenty of heartache down the road. Practical shelf life isn’t just about molecular theory, it’s about what’s survived the heat, air, and time on real storage racks.

    Applications Driven by Close Collaboration

    We get direct inquiries about where this molecule really shines. Most users interested in triazole cores already know their way around specialty chemistry. They come looking for this structure not by accident, but by a purpose that’s often shaped by patent filings, new active candidates, or process patents in agricultural or pharmaceutical fields.

    With its paired trifluoromethyl-phenylamino and hydroxyphenyl architecture, this compound attracts attention from researchers focusing on bioactive leads. Electron-withdrawing groups like CF3 on the aromatic ring increase metabolic stability, and that pays dividends in drug discovery workups involving oxidative stress tests in the lab. The hydroxy substituent changes hydrogen bonding in comparison to a plain phenyl. This additional anchor opens routes for further derivatization downstream, with less drift in product purity during scale-up. That translates to real advantages for custom synthesis groups or in full-scale pharmaceutical ingredient development.

    Some customers are looking further afield. In the materials world, triazole derivatives serve as intermediate building blocks for advanced polymers, ionophore ligands, or coordination complexes. The balance of aromaticity, electron-rich and -poor fragments, and overall pKa profile puts this molecule in a class suited for specialty resin syntheses. Whether in research or pre-commercial development, our engineers occasionally help users troubleshoot solubility or reaction yield issues when incorporating this compound into proprietary platforms.

    Production Insights: Chemical Reliability Every Step of the Way

    There’s no substitute for firsthand experience in production-scale chemistry. One lesson that stands out: The difference between a smooth production day and one lost to rework often comes down to details few outsiders suspect—like the grind size after final drying, or whether a batch’s color shifts slightly on the rotary evaporator.

    In our facility, we keep open books on every lot’s full analytical trace. We’ve had batches surprise us: a slightly damp filter cake here, a subtle shift in melting range there. When your own staff stirs the reactor and runs the columns, you pick up more than just numbers—you notice how solvent changes result in easier washing, how small alterations in the base-to-acid ratios increase final throughput, and how quick feedback loops improve the next run.

    We have invested in in-line monitoring systems, not because it is trendy, but because it cuts down the number of times we need to rework batches for trace impurities. Tight control over process variables, paired with real operator knowledge, minimizes off-spec lots and reduces chemical waste. That’s good business, but it’s also basic respect for both the molecules and the people who handle them.

    Real Comparisons: How This Molecule Differs from Related Products

    Our catalogue today includes a series of related triazoles, each built around the 1,2,4-triazole core, but with distinctive functional groups tagging the aromatic systems. The inclusion of a 3-(trifluoromethyl)phenylamino substituent on this molecule carries real consequences for both handling and downstream chemistry compared to a plain phenylamino group. Those fluorines shift electron density, influence final pH in solution, and lead to improved stability against hydrolytic degradation.

    In lab-scale testing, you can taste the difference in the reactions: plain phenylamino triazoles react more readily with electrophiles, but show less metabolic stability. Add trifluoromethyl, and you slow down certain unwanted reactions, meaning less yellowing or byproduct buildup during storage. In practical terms, this means less lost inventory for our customers, as fewer lots drift off-color or lose potency over time on their shelves.

    Positioning the phenol group at the para location instead of ortho or meta grants this molecule distinctive resonance behavior. We discovered over several production campaigns that these electronic shifts matter. They influence not only how the compound interacts with solvents and downstream reactants, but also how it blends with active ingredients or excipients in composite formulations—a difference that shows up clearly under HPLC but also in how powders disperse or settle in solution tanks.

    Another point to note: handling properties during drying and packaging. The combination of the bulky trifluoromethyl group and the polar hydroxyphenyl ring yields a product that flows more predictably on packing lines. We spend less time clearing bridging or powder hang-ups during drum filling compared to related compounds with more symmetrical substitution, which in practice speeds up deliveries and reduces delays.

    Lessons Learned from Real Manufacturing

    Anyone manufacturing small molecules at scale faces the reality that each process step teaches something new—with every lot, minor adjustments can make significant longitudinal improvements. In the early days of producing this triazole-phenol, our team noticed that using higher purity starting materials led to tighter analytical specs in the final API. Low-level metal contamination from impure triazole sources tends to amplify in downstream steps, showing up as hard-to-remove specks in the final powder under electron microscopy, which QC detected and quickly flagged. Upgrading starting materials cut reprocessing by over 20 percent over two years.

    Dealing with solvent recovery not only reduces waste but also keeps costs in check, which gets passed on to our customers. The phenolic group in this molecule introduces additional hydrogen bonding sites that made early extraction steps inefficient when using unsuitable solvents. After repeated trials, moving to a binary solvent system dialed in a cleaner split between aqueous and organic phases, reducing solvent losses by a measurable margin.

    Our operators learned to watch out for pH swings during neutralization steps, which could crash out fine suspensions or induce clumping, impacting physical handling and filtration. Adjusting stir speed, impeller type, and the timing of quench additions all contributed to achieving a consistent and manageable product every time. Regular training and steep experience curves across the team help keep production running smoothly, and batch histories feed directly into future process improvements.

    Quality Control and Confidence In-House

    Quality doesn’t result from testing alone—it comes from real accountability on the line and from knowing the raw materials, solvents, and intermediates personally. We set retention samples aside for each lot, run full chromatographic profiling, and cross-check every analytical result against our own reference spectra. We have seen competitors skip these steps, only to wrestle with unexplained out-of-spec findings later.

    Handheld IR devices might give a rough confirmation, but real trust comes from long-form NMR, LC-MS, and particle imaging—work performed by our in-house team, not handed off to anonymous third parties. Knowing how materials look and smell at each point along the way helps pick out early indications of problems, such as solvent carryover or trace impurity buildup. Consistent documentation helps root out variations that crop up, whether through upstream supply changes or minor equipment wear.

    Batch-to-batch variation matters more in products like this, where purity affects how chemicals perform in others’ complex syntheses or formulations. The presence of a single outlier in melting range or color can derail a whole downstream campaign, so our standards reflect not just regulatory requirements, but the feedback and real-world stories from those working at the bench.

    What Our Customers Really Value

    The customers we work with want more than just a bulk chemical—what they need is reliability, transparency, and continuous improvement. Many come back after trialing small orders, reporting feedback from their own lab and pilot runs. If a powder comes rougher than expected, or a solubility profile drifts, our technical team gets directly involved, troubleshooting in partnership with end-users. This approach leads to long-standing relationships that outlast the typical transactional model.

    We've seen cases where a pharma developer or material scientist ran headlong into roadblocks tracing to inconsistent chemical supply from third parties. That’s part of the reason our plant focuses on full vertical integration, keeping synthesis, purification, and packing under our own roof. Direct oversight reduces the risk of surprises, and lets us respond quickly if any issue arises. The knowledge flows both ways: feedback from the field shapes future process changes and helps us keep improving product quality.

    Safer, Cleaner, and More Responsible Manufacturing

    Producing a molecule like 4-(5-(3-(Trifluoromethyl)Phenylamino)-4H-1,2,4-Triazol-3-Yl)Phenol demands more than rote procedure. It takes commitment to sustainability and responsible waste handling at every stage. We use dedicated containment and solvent recycling systems to keep environmental impact in check. Waste streams—whether solvent residues, washings, or off-spec material—are handled by qualified staff, ensuring compliance with the strictest standards.

    We replace outdated equipment to further reduce fugitive emissions and implement best practices in chemical stewardship. Modern filtration and scrubber systems have reduced the plant’s overall waste burden, helping to ensure both the safety of our employees and minimal footprint in the surrounding community. These improvements result from ongoing audits and the drive to exceed regulatory minimums, not just meet them.

    Building for the Future: Innovation and Growth

    Investing in optimum production of 4-(5-(3-(Trifluoromethyl)Phenylamino)-4H-1,2,4-Triazol-3-Yl)Phenol forms part of our long-term commitment to supporting diverse innovation streams. As research pushes into new chemistries—targeted molecular therapies, plant health agents, or specialty performance materials—we want to supply a building block whose provenance and batch history are documented and trustworthy.

    We partner with customers developing derivatives or integration-ready intermediates, supporting projects from exploratory R&D to the edge of commercial production. Keeping core competency in synthetic chemistry lets us offer consistent material supply as research transitions out of lab scale. Our experience navigating challenging regulatory landscapes around CF3 chemistry gives added comfort to those managing hazardous goods in their future pipelines.

    Every Molecule Counts

    Delivering each consignment of this product stands as a testament to the work of every chemist, operator, and engineer who has touched the process. Across years of refining our approach, every improvement comes from attention to both the smallest molecular features and the broad impact each shipment has on researchers and industrial users around the globe. This is practical chemistry, grounded in craftsmanship, constant learning, and steady resolve to deliver only the best.