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HS Code |
360503 |
| Cas Number | 1535-38-4 |
| Molecular Formula | C10H6F6 |
| Molecular Weight | 240.15 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 142-144 °C (at 760 mmHg) |
| Melting Point | -13 °C |
| Density | 1.393 g/cm³ at 25 °C |
| Refractive Index | n20/D 1.449 |
| Purity | Typically ≥98% |
| Synonyms | 1-Ethenyl-3,5-bis(trifluoromethyl)benzene |
| Smiles | C=CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 |
| Inchi | InChI=1S/C10H6F6/c1-2-7-3-8(4-7-9(11,12)13)5-10(14,15)16/h2-5H,1H2 |
| Solubility | Insoluble in water, soluble in organic solvents |
| Hazard Information | May cause skin and eye irritation |
As an accredited 3,5-Bis(Trifluoromethyl)Styrene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, securely sealed, labeled with chemical name, CAS number, hazard pictograms, and manufacturer details. |
| Shipping | 3,5-Bis(Trifluoromethyl)Styrene is shipped in tightly sealed containers, protected from moisture, heat, and light. Transportation complies with relevant chemical safety regulations, ensuring proper labeling and documentation. The chemical is classified as a hazardous material; therefore, handling by trained personnel and the use of appropriate personal protective equipment are required during shipping and receiving. |
| Storage | 3,5-Bis(Trifluoromethyl)styrene should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Store under an inert atmosphere if possible to prevent polymerization. Ensure proper labeling and follow all relevant safety protocols for handling flammable and potentially hazardous chemicals. |
Applications of 3,5-Bis(Trifluoromethyl)Styrene in Industrial Manufacturing3,5-Bis(Trifluoromethyl)Styrene serves as a key raw material for industrial synthesis across specialized chemical sectors. Our direct manufacturing output is tailored for advanced technological, electronic, and polymer industries, with strict regulatory and process controls in every vertical. 1. Specialty Fluorinated Polymer SynthesisThis compound functions as a prominent comonomer in developing high-performance fluorinated polymers and copolymers. Chemical engineers introduce it to increase hydrophobicity and chemical resistance in specialty materials for demanding environments such as semiconductor and aerospace applications. Production often involves controlled radical or catalytic copolymerization with styrenic or acrylic monomers under precisely monitored reaction conditions to achieve target molecular weight and desired microstructure. Quality management protocols require continual analytical verification throughout the process. Industry compliance standards
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2. Advanced Electronic Photoresist MonomerManufacturers use this intermediate in producing advanced photoresist formulations required for micro-patterning in semiconductor wafer fabrication. The compound features high electronic stability and fluorine content, enabling precise etch selectivity and enhanced contrast during UV lithography steps. Strict traceability and purity control prevent contamination, supporting high-yield and reproducible patterning. Industry compliance standards
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3. Chemical Intermediate for Fluorinated Aromatic CompoundsOrganic synthesis laboratories and custom chemical producers select this styrenic compound as an intermediate for building more complex fluorinated aromatic structures. It forms the basis for many agrochemical, pharmaceutical intermediate, and liquid crystal precursor syntheses. The electron-withdrawing trifluoromethyl groups facilitate subsequent functionalization such as halogenation, cross-coupling, and ring substitution with predictable yields, under controlled moisture and temperature conditions to maintain batch purity. Industry compliance standards
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4. High-Performance Surface Treatment AdditivesIndustrial formulators incorporate this styrenic derivative into additive packages for engineered surface coatings to improve hydrophobicity, anti-fouling, and solvent resistance. The material supports controlled grafting onto polymer backbones or direct blending into sol–gel processing. Regulatory and technical protocols require full additive traceability, with consistent performance across manufacturing lots. Application development routinely includes accelerated aging and abrasion testing as part of customer validation. Industry compliance standards
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5. Performance Monomer for High-End Adhesive SystemsChemical formulators rely on this compound when developing adhesives requiring extreme chemical and thermal stability. Its unique trifluoromethyl groups reduce surface energy and increase bonding performance in aggressive conditions. Production processes demand tight quality control in raw material blending and reaction conditions, particularly for adhesives destined for electronics, automotive, and aerospace assembly, where reliability testing is mandatory. Industry compliance standards
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Hands-on experience has taught us that not every fluorinated styrene delivers the same performance in advanced material synthesis. 3,5-Bis(Trifluoromethyl)Styrene, often called 3,5-bis-TFM-styrene among our team, has repeatedly shown its value, particularly for R&D groups and specialty polymer producers who run into bottlenecks with less reactive or less stable styrene derivatives. We have worked side-by-side with chemists exploring new monomers for demanding applications such as liquid crystal materials, high-performance coatings, and custom-designed specialty polymers.
3,5-Bis(Trifluoromethyl)Styrene carries the CAS number 57749-52-7, a detail those in the laboratory will appreciate for clear referencing. In our facilities, purity isn’t just a spec on a datasheet—it underpins every batch's consistency and performance. Our process routes ensure a consistent purity of 99% and above, with controlled residual solvent content and negligible color. Visual inspection, NMR, and GC analyses form our daily routine, and we’ve noticed tiny departures in impurity profile can result in changes to reaction kinetics when customers are pushing the limits of new polymer designs.
Traditional styrene monomers might cut it for basic plastics, but the demands of today’s electronics, coatings, and performance materials raise the bar. The bis(trifluoromethyl) groups at the 3 and 5 positions on the aromatic ring significantly increase electron-withdrawing character, which changes both polymerization behavior and finished material performance. We’ve stood at the reactors and watched how this modification leads to sharper thermal stability, and it often opens new solubility windows for polar and nonpolar chemistries.
Customers return because this product bridges a gap where standard para-, ortho-, or mono-substituted fluorinated styrenes simply can’t keep up. The intense CF3 electronic effect brings new routes to tuning dielectric properties. We recall one project where a multinational lab worked for months on RF-resilient polymer films and the simple introduction of 3,5-bis-TFM-styrene into their backbone design pushed dielectric loss rates well below their old benchmarks.
Every manufacturer touts their controls, but day-to-day experience reveals which process tweaks matter most. With 3,5-Bis(Trifluoromethyl)Styrene, temperature, catalysts, and solvent choices during both production and end-use polymerization take center stage. Compared to mono-substituted trifluoromethyl styrenes, small exotherms during addition polymerization have a different profile; the bis-substituted ring changes the initiation and propagation pathways.
We routinely see better control over glass transition points in copolymer production when using this molecule compared with unsubstituted or mono-trifluoromethyl-styrenes. Labs have commented back that material batches remain stable in solution for longer—no random gelation, no off-odors from side reactions. The difference isn’t just anecdotal. Consistent purity and less batch-to-batch variation translate to better QC numbers for the end customer. Anyone racing to get pilot-scale or full-scale materials through regulatory and commercial testing knows small surprises in material performance can mean months lost.
Over the past decade, we’ve worked closely with polymer scientists adapting materials for microelectronics, OLED displays, and demanding optical coatings. One distinct customer in Japan shared results where polymer resins built around 3,5-bis-TFM-styrene showed sharper refractive index control and outperformed traditional matrix polymers for light-guiding efficiency. The unique electronic effects lower cross-linking densities under standard curing, making fine feature creation easier, which is vital for precision photolithography.
Feedback from battery and sensor developers motivates our own R&D team. We had three different groups approach us last year—each building thin-film sensors for different end uses. They needed a fluorinated monomer that could produce polymers with low permeability to moisture yet maintain functional group compatibility for further surface grafting. The 3,5-bis-trifluoromethyl substitution achieved this balance, and not just on paper. Pilot polymer runs showed breakage resistance and chemical inertness that exceeded results from earlier generations built from mono-CF3 or non-fluorinated styrene units.
Plant engineers like to see how theory plays out at scale. 3,5-Bis(Trifluoromethyl)Styrene isn’t as volatile or air-sensitive as some fluorinated monomers. Stability under typical storage conditions is a real asset. In warm climates or high-throughput facilities, the material resists premature polymerization, especially compared to more active ring-substituted alkenes. Our operators check for peroxide formation and maintain batch freshness, advising storage under nitrogen and away from excessive UV just as a precaution, but we haven’t had disaster stories. Even in large drums, the product moves well and pours with minimal residue.
We invest in consistent quality control because repeated feedback suggests even trace contaminants from old packaging or reactive metal surfaces can start unwanted side reactions. That’s why our drums use specific linings and low-leach transfer tubing. The small operational tweaks make it practical to scale from 1-kg trial runs to several tons without changing product quality.
Many customers first ask “what’s the practical difference between 3,5-bis-TFM-styrene and the regular 4-trifluoromethylstyrene?” In some reactions, the difference shows up only as subtle changes to free radical reactivity. In more advanced applications, the story’s different. Two CF3 groups, especially positioned at 3 and 5, drive down the electron density on the aromatic ring and open up unique reaction pathways. In custom copolymer systems, this creates room for new strategies—block copolymer self-assembly, tuning phase separation, pushing temperature flexibility.
We’ve learned that smart material designers often aren’t content matching legacy specs. They need new property windows. The additional fluorine content improves both hydrophobicity and chemical resistance, making the derived polymers last longer in acid-rich or base-rich conditions. For outdoor coatings, the improved UV stability has allowed some formulators to extend warranty periods, and we field weekly questions about weatherability performance.
Not every innovation comes without its puzzles. Increasing demand for high-purity, specialty monomers has pushed us to rethink older reactor materials to prevent trace metal or byproduct contamination. For example, we discovered that certain grades of stainless steel introduced low-level iron impurities, which only became obvious when polymer batches changed color or showed odd molecular weight distributions. Direct experience forced us to shift to specialty reactors and refine our purification setup, a lesson that still pays dividends for our quality numbers.
Handling waste management and emission controls requires constant vigilance. Regulatory landscapes, particularly for fluorinated organic compounds, keep evolving. Rather than only chasing greener credentials, we took to heart the practical concern—avoid operator exposure and minimize atmospheric loss. Closed-system handling, local scrubbers, and intensive staff training form the backbone of keeping our plant safe and our emission numbers below the legal radar.
In conversations with procurement teams, sometimes the focus rests too narrowly on cost per kilogram and current lead times. But most users of 3,5-bis-TFM-styrene are not just spec buyers. Researchers, development chemists, and new materials engineers frequently approach us with formulations, analytical questions, and requests for application-specific support. It’s a two-way street. We garner feedback on how the monomer performs in real-life applications and, in turn, pass along our own learnings—such as optimum addition rates for UV-initiated copolymerizations or tricks for getting cleaner conversion in cross-coupling reactions.
Some groups explore this monomer for use in medicinal chemistry, but its impact is clearest in the advanced materials sector. We’ve supported pilot plant scale-ups where the customer needed not just the kilogram-scale material but predictive information on how our product might behave in full reactor runs, with every tiny impurity tracked. That cooperative problem-solving ensures few surprises at scale, which protects everyone’s bottom line.
Raw material reliability drives every batch we produce. Trifluoromethyl starting materials have experienced supply spikes due to global plant outages, and styrenic intermediates sometimes dry up when broader petrochemical markets hiccup. We keep our inventory buffers healthy and maintain a robust supplier matrix for both main and backup sources. Over the years, this discipline has helped several customers avoid painful delays, especially those with tight annual project timelines.
Scrutiny over upstream supply chains of fluorinated materials has risen since regulatory concern over perfluorinated byproducts emerged. We monitor and document each batch’s origin, and regularly audit our own environmental practices along with those of major suppliers. Being transparent about these checks reassures our partners who must answer tough questions from regulatory auditors and multinational procurement boards.
From a manufacturer’s standpoint, actual usage patterns tell the story. Research centers and industrial labs gravitate toward this monomer for projects targeting properties beyond commodity plastics. Epoxy and acrylate formulators depend on our 3,5-bis-TFM-styrene to achieve low shrinkage and resilience against abrasion or chemical wear. The polymer’s stability and its ability to maintain high optical clarity over time have mattered in optics and display sectors.
The bis(trifluoromethyl) substitution depth means the final polymers resist staining, survive aggressive cleaning cycles, and maintain dielectric performance across temperature extremes. In one project, an electronics company developing flexible circuit board materials reported fewer defects and scrap batches when switching from standard fluorostyrenes to our material. These everyday wins and headaches shape our commitment to maintaining not just purity, but reliability lot after lot.
Every region brings its own preferences and regulatory needs. Our teams in Europe and North America share regular updates with Asian partners on process tweaks, especially since reaction kinetics can vary with local catalyst grades and water quality. Years spent fielding morning, midday, and late-night calls with researchers means we share methods for sample analysis, safe handling practices, and optimum storage routines.
We have learned from application failures just as much as successes. A project in Germany hit a snag when polymerization protocols lifted off-gassing byproducts—something we traced to micro-residues in an uncleaned reactor. Sharing those lessons prevented similar headaches for another customer scaling a high-gloss outdoor coating product a few months later. This kind of knowledge transfer only happens through transparency and long-term partnership.
Materials science never stands still. We see ongoing development in fluorinated monomers, particularly as emerging electronics, battery, and biomedical sectors press for new features: lower water permeability, less environmental persistence, easier recyclability. In collaboration with outside labs, our own chemists are exploring process improvements to lower residual solvents to near-zero and use less energy-intensive purification steps. We test continuous-flow synthesis on pilot lines and benchmark against batch runs for both impurity profile and yield stability.
We encourage open research partnerships to help devise safer, more circular downstream usages for polymers built from advanced monomers like 3,5-bis-TFM-styrene. Whether that means chemical recycling, post-consumer collection, or design tweaks for easier material separation, any new insight passes quickly into our in-house training and outbound guidance for our global customer base.
Our firsthand experience as the actual chemical producer—rather than a distributor or third-party—lets us offer genuine insights into what makes 3,5-Bis(Trifluoromethyl)Styrene a strategic choice for material innovators. Its unique substitution pattern opens doors to performance unachievable with older monomers. Continued tweaks to process and quality control—born out of both our own trials and feedback from the global development community—mean every kilogram reaches the customer with all the properties they expect, ready for the next breakthrough in material design.