|
HS Code |
858251 |
| Chemicalname | 4-Nitro-3-(Trifluoromethyl)Phenol |
| Casnumber | 19895-67-3 |
| Molecularformula | C7H4F3NO3 |
| Molecularweight | 207.11 |
| Appearance | Yellow to orange solid |
| Meltingpoint | 70-74°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1O)[N+](=O)[O-])C(F)(F)F |
| Inchi | InChI=1S/C7H4F3NO3/c8-7(9,10)4-1-2-5(11)6(3-4)12(13)14/h1-3,11H |
As an accredited 4-Nitro-3-(Trifluoromethyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 25 grams, labeled with chemical name, CAS number, hazard symbols, batch number, and safety precautions. |
| Shipping | 4-Nitro-3-(Trifluoromethyl)Phenol is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be handled as a hazardous chemical, following all regulatory guidelines, including labeling and documentation. Transportation should be in accordance with local and international regulations for hazardous materials, ensuring safety throughout transit. |
| Storage | 4-Nitro-3-(Trifluoromethyl)phenol should be stored in a tightly sealed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Clearly label the container, and keep it away from sources of ignition or heat. Use appropriate chemical storage protocols to prevent contamination and degradation of the compound. |
Competitive 4-Nitro-3-(Trifluoromethyl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Every day in our manufacturing plant, teams handle a vast range of specialty chemicals, but among these, 4-Nitro-3-(Trifluoromethyl)Phenol stands out because of its distinct molecular attributes. Many years of refining reaction processes have given us a close familiarity with this phenolic compound. Its unique structure, carrying both a nitro group and a trifluoromethyl group on the aromatic ring, doesn’t just make it distinct—it gives rise to reactivity patterns that chemists in research, pharma, and advanced materials deeply appreciate.
In laboratories and industry, the need for phenolic derivatives with electron-withdrawing groups continues to rise. Users look for consistency, purity, and a solid supply chain. We produce 4-Nitro-3-(Trifluoromethyl)Phenol as a pale yellow to yellowish solid, and careful batch control keeps the impurity profile tightly within standard. Every drum leaving our site meets the specification for assay, moisture, and residue.
Over the last decade, we have brought the manufacturing up to a reproducible model that holds tight to purity and minimizes by-products. The finished product comes regularly at assay values above 98%, with trace-level moisture and low impurities, thanks to a controlled synthesis and robust purification steps. Experienced operators, not just machines, oversee the critical phases. By running our reactors at optimal temperatures and monitoring real-time chromatograms, we maintain product properties that downstream chemists can rely on.
Raw material quality goes under the spotlight each week. When batches of meta-nitrophenol and trifluoromethylating agents show even slight shifts, finished product quality can be impacted. Over years of volume production, adjustments to reaction timings and quenching procedures made a clear difference to particle consistency and filtration rates. We’ve adapted by using fine-tuned stirring speeds and carefully chosen solvents, which help the crystallization steps run predictably each cycle and keep batch-to-batch results reliable.
Our approach differs from those who chase speed at the expense of impurity control. Early on, ignoring subtle temperature spikes led to unpredictable dimer formation in our runs. Proper insulation, precision temperature monitoring, and regular line cleaning mean we’ve kept by-product contamination to a minimum, lessening purification burdens. All finished batches depart in lined, sealed containers, and everyone on the team signs off after a double check of sampling documents, not just an automated line signature.
Most of our partners source this compound for its value in medicinal chemistry and agrochemical discovery. There’s real excitement whenever new leads in fluoroarene research demand functionalized building blocks with electron-withdrawing nitro and trifluoromethyl groups together. The combination boosts metabolic stability and changes bioactivity profiles in ways simpler phenols cannot achieve. Those groups grab attention for SAR work, where researchers probe how chemical modifications affect activity.
Beyond the laboratory, it has a place as an intermediate for specialty dyes and high-performance resins. Aromatic substitution enabled by its unique substitution pattern makes it a tool for developing UV-stable polymers and optical brighteners, as well as nitro-activated trifluoromethyl building blocks for follow-up couplings. Chemists find it valuable for producing analogs where traditional phenols do not survive nitration or fluorination conditions cleanly. Our reliability in delivering this compound lets process chemists experiment with scale-up and pilot runs without hold-ups.
Specific feedback from our customers shapes our production approach. Years ago, a customer encountered downstream filtration pains due to slightly off-target melting behavior. That led us to take a closer look at crystal form and packing during both batch-drying and cooling, modifying both oven protocols and the timing of agitation. The adjustments not only solved their issue but helped us reduce bottlenecks elsewhere. Direct dialogue between plant operators and end-users is the only way to catch these kinds of chain reactions early.
The performance of 4-Nitro-3-(Trifluoromethyl)Phenol cannot be swapped 1-to-1 with general nitrophenols or mono-fluorinated phenols. The combination of nitro and trifluoromethyl groups on the ring provides a distinct balance of electron deficiency and steric shielding. In real terms, this influences both reactivity in coupling reactions and solubility in polar solvents during workup. We have had cases where customers tried using 4-nitrophenol or 2,4-dinitrophenol, but the subtle electron pull and size of the CF3 group here mean those analogs don’t give comparable results. The chemistry must match the exact substitution pattern.
Our product provides not just the correct molecular skeleton but repeatable physicochemical traits. Once, a customer found that using a competitor’s batch from a different synthesis route led to more colored impurities after hydrogenation. We tracked the reason to starting material variance and the quality of hydrogen source used. With careful feedstock management and using only corrosion-resistant, lined equipment for the nitro introduction, our version of 4-Nitro-3-(Trifluoromethyl)Phenol gives predictable work-ups and color profiles.
Aromatics with a trifluoromethyl group often create volatility in purification or storage. We have fine-tuned drying and storage practices to extend shelf-life and minimize moisture uptake, which some competing products face due to residual solvent or poor packaging. Storage tests at both low and high humidity showed our compound’s resistance to discoloration, a property linked to full drying and the use of thick, gas-tight liners. All batches receive a moisture test before shipment, something that’s saved more than one overseas customer costly rejections at their receiving dock.
Every manufacturing run shows us something new. A little over a year ago, examining microscope shots of crystal habit revealed a small fraction of clumped, twin crystals that influenced both dissolve time and process flow. We reformulated our post-crystallization dispersion protocol to avoid agglomeration, which cut handling time at customer sites. These real-world process tweaks don’t happen spontaneously in a vacuum—they come from daily operator vigilance and feedback.
As research applications shift, the demand for higher-purity, lower-residue phenolic intermediates grows. Research groups developing new small molecules and enzyme inhibitors often ask for even stricter limits on residue-on-ignition and heavy metal content. To answer these needs, our quality control group runs extra tests on every outgoing lot, including more sensitive detection for trace metals. That effort, though more demanding, has become a selling point—pharmaceutical clients want to avoid delays performing double tests on third-party samples.
Handling safety is no less important. The trifluoromethyl and nitro functionalities both carry process risks if uncontrolled. Every member of our crew receives regular hazardous material handling training. The plant uses explosion-proof reactors and full venting to keep any exotherms from causing field incidents. Over the years, partnerships with local emergency response groups and government auditors have kept our safety record clean. It is not just compliance; it is responsible chemistry from one run to the next.
Pressure for lower costs and speedy delivery is a fact of the chemical sector. That said, experience teaches not to cede ground on quality or safety for quantity. Raw materials often fluctuate in price and supply, but shortcuts in sourcing cause headaches later. Several years ago, partway through a large-lot order, a supplier tried to switch to a lower-grade trifluoromethylating reagent—deals that look attractive upfront led directly to a spike in trace impurities. That sparked changes to our vendor qualification and random-access sampling routines.
Sometimes, buyers ask for modified physical forms of 4-Nitro-3-(Trifluoromethyl)Phenol for easier weighing, dissolution, or feeding to their processes—whether as spray-dried powders, finer crystallized forms, or free-flowing granules. Our operations team runs controlled screens and drying cycles to fulfill these needs when possible. Each adjustment means another round of compatibility and stability checks, but the results are tailored to true process requirements—not just one-size-fits-all claims.
Countries updating their regulations on fluorinated aromatics and nitroaromatics mean compliance checks must be rigorous. Across Asia, Europe, and the Americas, we work through pre-shipment documentation and secure the right certifications, ensuring customs and regulatory passage with less red tape for our partners. Once, a delay at an overzealous customs inspection led to supplies drying up for a key customer’s pilot program—since then, shipping batches leave only after thorough checks and full paperwork assemblies.
New application areas keep arising as research into fluorinated phenols broadens. While pharmaceutical applications remain the main driver, sensors, specialty plastics, and diagnostic reagents increasingly turn to these building blocks. Staying ready for new requirements—higher purity, different form, or guaranteed traceability—requires our plant to remain nimble. When requests arrive for ultra-low halide content or non-detectable heavy metals, our analytical lab expands batch release criteria, running longer tests to catch potential outliers. These investments pay off as customers encounter stricter regulatory hurdles.
In production, sustainability claims are not made lightly. Waste minimization remains a constant goal. Waste streams high in spent acid or solvent are neutralized and recycled on-site, minimizing environmental impact. Teams participate directly in local government audits. Recovering and treating spent trifluoromethylating agents reduces emissions and aligns with stewardship goals, not just avoiding fines but staying accountable for what we put out.
Our workforce carries knowledge from years on the line. New chemists, operators, and maintenance teams train under senior staff who carry long memories of both triumphs and lessons learned. Regular safety briefings and performance reviews keep the group’s standards high, engraining quality habits that translate into each outgoing kilogram of finished product.
Customers come with increasingly sophisticated demands, whether that’s for longer shelf life, certified low-impurity supplies, or documentation for global regulatory routes. Our plant stands ready for new synthesis tweaks, better purification steps, and the continued rise of automation in certain packaging lines. But no amount of automation replaces real oversight—every batch signs off with hands-on checks from production, QC, and shipping together.
With new generations of chemists driving research on fluorinated aromatics in medicine, materials, and diagnostics, our responsibility as a manufacturer centers on supplying the right product with unwavering integrity. Feedback from end-users guides us—every missed target and every successful downstream outcome gets discussed in daily plant meetings.
The market for 4-Nitro-3-(Trifluoromethyl)Phenol reflects broader shifts in specialty chemistry. As technology advances and regulatory environments tighten, producers with firsthand process knowledge, robust quality control, and consistent customer dialogue will continue to meet these evolving needs. For us, that’s a challenge worth meeting head-on, with every shift, every batch, and every kilogram that ships out the door.