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HS Code |
863726 |
| Name | 3,5-Bis(Trifluoromethyl)Anisole |
| Cas Number | 328-70-1 |
| Molecular Formula | C9H6F6O |
| Molecular Weight | 244.13 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 164-166°C |
| Melting Point | -6°C |
| Density | 1.44 g/mL at 25°C |
| Refractive Index | 1.413 |
| Purity | Typically ≥98% |
| Smiles | COC1=CC(=CC(=C1)C(F)(F)F)C(F)(F)F |
| Synonyms | 3,5-Bis(trifluoromethyl)-1-methoxybenzene |
| Solubility | Insoluble in water, soluble in organic solvents |
| Flash Point | 63°C |
| Ec Number | 206-403-6 |
As an accredited 3,5-Bis(Trifluoromethyl)Anisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 grams, tightly sealed with PTFE-lined cap, labeled with chemical name, hazard symbols, and handling instructions. |
| Shipping | 3,5-Bis(Trifluoromethyl)Anisole is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is packed according to standard hazardous material regulations, clearly labeled, and transported at ambient temperature. Ensure compliance with local, national, and international shipping guidelines for safe handling and delivery of this chemical compound. |
| Storage | 3,5-Bis(Trifluoromethyl)Anisole should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Keep the container in a cool, dry, well-ventilated area, and segregate from incompatible materials such as strong oxidizers. Store at room temperature and avoid moisture. Properly label the container and ensure access is restricted to authorized personnel only. |
Applications of 3,5-Bis(Trifluoromethyl)Anisole in Industrial ManufacturingOur manufacturing expertise with 3,5-Bis(Trifluoromethyl)Anisole enables consistent supply to specialized industrial customers operating in advanced market segments. The following sections detail verified and compliant downstream applications, real-world processing ratios, core process integration points, and representative end products in well-established industries. 1. Agrochemical Intermediates for Selective Herbicide SynthesisIn agrochemical manufacturing, 3,5-Bis(Trifluoromethyl)Anisole acts as a key intermediate for synthesizing fluorinated aromatic building blocks. Major herbicide producers incorporate this compound as a core feedstock in multi-step synthesis routes for active ingredients targeting broadleaf weed species. Integration focuses on nucleophilic substitution and coupling reactions under mild to moderate conditions, supporting tracked lot traceability and impurity control throughout the process chain. Industry compliance standards
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2. Pharmaceutical Intermediate for CNS-Active Molecule Manufacture3,5-Bis(Trifluoromethyl)Anisole plays a technical role in producing advanced pharmaceutical intermediates, particularly for central nervous system (CNS) drug scaffolds where aromatic fluorination is required. Manufacturers use it for early-stage synthesis steps, combining it with other halogenated or methoxylated aromatics in controlled environments that demand high traceability and GMP-level documentation. End-use producers monitor stage-specific purities using validated analytical methods as part of regulatory submission batches. Industry compliance standards
Typical usage ratio
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3. Liquid Crystal Compound Synthesis for Display Technology3,5-Bis(Trifluoromethyl)Anisole sees significant use as a performance modifier in liquid crystal (LC) chemistry. Major LC producers rely on its unique electronic and steric properties to generate mesogenic core units for advanced display segments, including IPS and TFT-LCD technologies. Usage is closely monitored for purity, and multi-step routes require validated reaction parameters to ensure batch-to-batch reproducibility and optical performance stability in subsequent panel applications. Industry compliance standards
Typical usage ratio
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4. Fluorinated Aromatic Monomer for Polymer and Resin ModificationWithin advanced polymer manufacturing, 3,5-Bis(Trifluoromethyl)Anisole is integral to the development of specialty resins such as high-gloss coatings, engineered adhesives, and PFPE-modified epoxies. The compound introduces fluorine moieties to increase thermal stability and chemical resistance, while maintaining controlled polymerization kinetics in the matrix. Quality control teams monitor integration at the oligomer or monomer input stage, with rigorous downstream testing for surface energy and durability metrics. Industry compliance standards
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5. Performance Additive in Electronic Chemical FormulationsManufacturers of electronic-grade chemicals utilize 3,5-Bis(Trifluoromethyl)Anisole as a functional additive to improve the dielectric profile and wetting properties of formulations for semiconductor, photoresist, and wafer cleaning markets. Processing demands extremely low metal and ionic contaminant levels, with integration controlled via metered feed systems and in-line QA sampling consistent with microelectronics specification requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
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Years on the plant floor, evaluating each drum as it rolls off the line, build a certain relationship with specialty aromatic ethers. 3,5-Bis(Trifluoromethyl)Anisole—sometimes referenced as 1-Methoxy-3,5-bis(trifluoromethyl)benzene—has grown from textbook curiosity into a sought-after staple. The product carries the CAS number 328-84-7 and a molecular formula of C9H6F6O, details worth knowing but not the heart of what’s beneficial in practical application.
Our own batches of 3,5-Bis(Trifluoromethyl)Anisole reach an assay greater than 99%. Years of tweaking distillation times and working through quirks in the fluorination stage have delivered a transparent, water-white liquid with no trace of colored impurities. Beyond the number on a certificate, it’s the clean GC traces and consistent boiling point profiles that reassure a process chemist or development scientist.
Some buyers look for a technical grade in bulk. Research teams sometimes care more about minimizing trace non-aromatic side products. Through hands-on monitoring — chromatography, NMR, and FT-IR quantification — we’ve learned every batch shows its true character under scrutiny. Whether in kilograms or ton-lots, this chemical demands attention to the smallest production variables to guarantee reproducibility year-round, barrel after barrel.
3,5-Bis(Trifluoromethyl)Anisole stands out structurally, owing to trifluoromethyl groups at the 3- and 5-positions of the aromatic ring, with a methoxy group at the 1-position. These features aren’t just academic points. The electron-withdrawing nature of the –CF3 groups, combined with the oxygen of the methoxy substituent, brings about an unusual mix of chemical stability and reactivity. In practice, this unique profile makes it a strong choice where both steric hindrance and electronic effects can benefit further functionalization.
A product’s purity is only one part of the story. Those with years in fine chemical production know that batch-to-batch reproducibility, distillation residue, and the strict separation from close-boiling fluorinated impurities often tip the scale when a purchasing choice needs to be made. Each of these aspects turns up in the laboratory downstream, whether in complex pharmaceutical research or the design of fluorinated agrochemicals. Poor separation or trace contamination may not flag on routine checks, but they will surface in the catalyst or when advanced analytics dig further.
Chemists working within pharmaceutical synthesis seek scaffolds that allow for precise substitution and late-stage modification. 3,5-Bis(Trifluoromethyl)Anisole fits right into these contexts. Its high degree of fluorination lowers metabolic vulnerability and can alter physicochemical profiles, such as lipophilicity or bioavailability, in lead compounds. Our customers often share stories about how small changes—swapping a hydrogen for a fluorine or adding another –CF3 group—unlock new behavior or pharmacokinetics.
Academic researchers find value in the bench-tested predictability of its reactivity, which supports studies ranging from fluorinated material design to novel ligand development. This single molecule sometimes becomes a seed for an entire research campaign, not just a one-off reagent. Every milliliter has a role, whether contributing to the investigation of new pesticides, high-performance polymers, or as part of intermediate libraries destined for further derivatization.
There’s no strict limit to where this aromatic ether finds itself. Its use isn’t just driven by an esoteric demand for fluorinated compounds. Researchers in electronics, for example, have shown increased interest in 3,5-Bis(Trifluoromethyl)Anisole due to its high dielectric properties, influencing how materials for high-frequency applications or insulation are formulated. The importance of tight control over trace ionic and conductive impurities in such fields only underscores why direct-from-manufacturer supply becomes critical.
Some wonder how 3,5-Bis(Trifluoromethyl)Anisole compares with standard anisole, or with mono-trifluoromethylated derivatives. On the production side, synthesizing this doubly fluorinated version requires more meticulous temperature and pressure controls. Distillation fractions must be sharper, and columns work harder to resolve closely related by-products. In the finished material, those two CF3 groups push its boiling point higher and alter solubility in both polar and nonpolar solvents.
In downstream application, a regular anisole shows little of the blocking or inductive effects that benefit advanced synthesis—its electron density and interaction with catalysts is entirely different. Mono-substituted versions can sometimes suffice where slight fluorine presence is enough, but experience teaches that in many cases, the higher degree of fluorination from the ‘3,5’ arrangement strengthens both the stability and the impact on end-use properties. Researchers may save time on tedious protection/deprotection cycles or avoid unexpected breakdowns when using the doubly fluorinated compound under demanding conditions.
Looking sideways to non-fluorinated or chlorine/bromine-substituted anisoles, environmental and safety profiles start to diverge. While all aromatic ethers need care in handling and disposal, the chemical inertia imparted by –CF3 makes this anisole much less prone to environmental transformation, which has both benefits and responsibilities for downstream users making decisions around residue fate or regulatory clearance. This aspect often weighs heavily in sustainable process design or compliance audits, so supplying material without extra complicating trace impurities helps simplify both paperwork and validation runs.
Years of running batch processes for high-fluorine aromatics have taught us the value of rigorous feedstock selection and real-time process control. Not all samples of trifluoromethylating agents deliver predictable results, so close supplier relationships and on-site analysis avoid unpleasant surprises mid-campaign. Pressure reactors must be regularly validated for both integrity and cleanliness, or else trace metallic catalysis can rear its head during production.
Consistency in 3,5-Bis(Trifluoromethyl)Anisole goes far beyond a “pass” result on a handful of specifications. Each drum records its story in trace water residuals, UV-absorption shoulders, and background NMR peaks. Downstream, these details spill into customer labs, showing up in melting points and chromatographic retention times. In pharmaceutical manufacturing and agricultural R&D, those slight shifts can mean extra work for purification or even regulatory scrutiny.
Our approach relies on using glass-lined reactors to prevent iron contamination, drying towers for both solvents and intermediates, and continuous monitoring for residual acidic or basic impurities. Gas chromatography matched to internal standards, not just reference peaks, helps us lock down profiles. No batch moves past QA without at least two orthogonal purity checks, because, in our experience, no single method ever tells the whole truth about organic purity at these complexity levels.
International shipping regulations on high-fluorine organics keep tightening each year. We’ve navigated evolving safety data requirements and container compatibility tests, noticing notable differences in stability with different packaging types. For drum shipments, vapor permeability must be quantified or else trace atmospheric moisture can cause hydrolysis or even formation of micro-impurities over months in storage. Smaller packs destined for academic labs sometimes call for argon or nitrogen overlays to further safeguard quality.
Product scarcity hits hardest when fluoroaromatic building blocks, especially those dependent upon irregular global supply of raw fluorinated feedstocks, face production or logistics hiccups. By maintaining diversified sources and ample reserves for critical intermediates, we have managed to weather most disruptions. Longstanding relationships with hydrofluorination plants abroad give us clear lines of sight on supply risks, letting us adapt rather than be forced into last-minute bidding or speculative purchases of unknown pedigree.
Traceability and rapid documentation have grown in demand from end users. Every dispatch includes detailed product history, not only a batch certificate. Trace metals, halogen balance, t-butyl and isopropyl isomer content, and radiopurity (when relevant) form part of the background data—most of this is possible only because each production run is logged from reactor load to package dispatch in a digital system. This transparency adds costs, but we’ve learned that informed buyers treat documentation as integral as actual product quality.
New projects tend to begin at gram or multi-gram scale. Academic labs and development chemists report back which impurities hinder reactions, which solvents dissolve the chemical best, and how the material behaves in stacking within combinatorial libraries. Only by listening closely and returning detailed feedback from multiple runs can a manufacturer adapt batch conditions to minimize odorous or colored contaminants and improve ease of handling—often by minor tweaks to isolation or filtration steps.
Larger scale synthesis—ranging from pilot groups to full plant-scale production—demands consistency within tighter tolerance. Automated fraction collection, in-line moisture detection, and hands-on distillation management together reduce batch variability, ensuring each ton has the same reliability as the smaller research-grade lots. Some customers request further controls—extra filtration, longer drying cycles, lower allowable content for certain non-volatile residues. These are achievable only for those willing to adjust schedules, modify cleaning protocols, and keep the conversation open with users willing to share what works best in their own syntheses.
3,5-Bis(Trifluoromethyl)Anisole often ends up as a key intermediate, where late-stage diversification (functional group manipulations, coupling reactions, nitration/sulfonation) brings out its full value. Having silenced the variability at the source, research and production chemists alike gain the confidence to undertake experiments and multistep processes with fewer setbacks from unexpected raw material quality swings.
The world of fluorinated aromatics comes under strict environmental review. Both regulatory drivers and stewardship principles demand that every shipment meets not just purity standards but also documentation for residual contaminants and sustainable sourcing. Customers working with large-scale equipment discharge face tight effluent limits for organofluorine content, so our own attention to minimizing non-essential fluorinated by-products in manufacturing steps makes their own operations smoother.
Waste management matters at every stage. As manufacturers, we pay particular attention to on-site recycling and solvent recovery. Fluorinated compound waste cannot go out with regular organic residues, and any bleed into off-gas streams or water calls for immediate remediation measures. Working with permitted hazardous waste handlers and regularly updating internal protocols, we help safeguard both our environment and the long-term runnability of global fluorinated industries.
End-to-end communication with users ensures that new regulatory measures, such as restrictions on certain persistent organic pollutants or updates to chemical inventory lists, are flagged ahead of time. Our position has always been transparent: disclose full process details where material leaves our site, and support customers through their own compliance reviews, up to and including detailed breakdown of reaction residuals, listing of all secondary reagents, and supporting documentation for regulatory submissions.
Relationships with buyers are rarely one-off. The best feedback comes when research partners or industrial clients keep an open line, sharing not only praise for a batch that ran smoothly but also the detection of an off-odor, an unexpected yellow tint, or low-level impurity that skews analytical results. Each of these observations feeds back into the ongoing improvement of our process.
Repeatability is a cornerstone of chemical supply. Process changes are implemented with care and shared in advance, even if only trace changes to solvent grade or minor temperature ramps. This level of collaboration helps large pharmaceutical teams or advanced materials groups avoid downtime mid-campaign. Tracking every key performance indicator from the point of raw material entry to the final packaged product ensures accountability and fosters mutual trust—no supplier can afford surprises when deadlines and quality are on the line.
Purchasing 3,5-Bis(Trifluoromethyl)Anisole direct from the manufacturer allows scientists and engineers access to both material and expertise. The nuances of multi-stage distillation, feedstock selection, and impurity management are learned only hands-on, across countless production cycles. Rather than guessing what lurks behind a lot number or relying on blind redistribution, our team’s close association with every aspect of production ensures each package reflects a commitment to the details that make or break advanced research and reliable scale-up.
Having fielded calls from chemists caught off-guard by anomalous GC peaks, or development groups troubleshooting a bottleneck caused by subpar intermediates, we’ve learned that transparency, solution-oriented support, and technical rigor ensure that new research projects, pilot studies, or commercial productions can move forward unimpeded by uncertainty over starting material. True product knowledge, cultivated from years in the lab and plant, enables a relationship far richer than what a simple commodity exchange offers.
At the core, manufacturing 3,5-Bis(Trifluoromethyl)Anisole is about reliability, technical dialogue, and hands-on involvement from the first raw material delivered to the final batch shipped. Each challenge along the way shapes both process and product, keeping us dedicated to quality and partnership with every kilogram that leaves our gates.