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HS Code |
390059 |
| Chemicalname | Bis(4-Fluoro-3-Nitrophenyl) Sulfone |
| Casnumber | 101-40-0 |
| Molecularformula | C12H6F2N2O6S |
| Molecularweight | 360.25 g/mol |
| Appearance | Yellow crystalline powder |
| Meltingpoint | 168-172°C |
| Boilingpoint | Decomposes before boiling |
| Solubility | Insoluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Density | 1.67 g/cm³ (approximate) |
| Synonyms | 4,4'-Difluoro-3,3'-dinitrodiphenyl sulfone |
| Smiles | O=[N+]([O-])C1=CC(=CC=C1F)S(=O)(=O)C2=CC(=CC(=C2)F)[N+](=O)[O-] |
| Inchikey | GTMTBPZHYDJRNA-UHFFFAOYSA-N |
As an accredited Bis(4-Fluoro-3-Nitrophenyl) Sulfone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Bis(4-Fluoro-3-Nitrophenyl) Sulfone, 25g: Supplied in a sealed amber glass bottle with tamper-evident cap and printed product label. |
| Shipping | Bis(4-Fluoro-3-Nitrophenyl) Sulfone is shipped in tightly sealed containers, protected from moisture and light. The packaging complies with chemical safety regulations, ensuring minimal exposure during transit. It is transported under appropriate temperature conditions, with clear labeling for hazardous materials, and includes a safety data sheet (SDS) for reference during handling and delivery. |
| Storage | Bis(4-Fluoro-3-Nitrophenyl) Sulfone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong acids, bases, and oxidizing agents. Avoid exposure to direct sunlight and moisture. Store it under controlled room temperature and ensure proper labeling to prevent accidental misuse or contamination. |
Applications of Bis(4-Fluoro-3-Nitrophenyl) Sulfone in Industrial ManufacturingAs an experienced manufacturer, we supply Bis(4-Fluoro-3-Nitrophenyl) Sulfone for demanding applications in high-performance materials and electronics. Our material integrates into established downstream sectors under strict process controls and regulatory frameworks. Below, we outline the main application scenarios, with technical details across compliance, formulation, downstream usage, and final product outputs. 1. High-Performance Polyaryletherketone (PAEK) Resin SynthesisLeading polymer producers use this sulfone compound as a key monomer in the synthesis of polyaryletherketone specialty resins. It supports melt polymerization processes requiring high glass transition and high-temperature stability. Producers value the fluorinated structure for enhancing chemical resistance in demanding aerospace, oil & gas, and automotive components. Industry compliance standards
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2. Advanced Liquid Crystal Polymer (LCP) SynthesisManufacturers synthesize advanced liquid crystal polymers using this compound to achieve precise molecular alignment and high dielectric strength. The nitrogen and fluorine substituents offer tailored anisotropy and improved flame retardancy for microelectronics and automotive connector insulators. Process engineers control its addition to balance melt flow and crystallinity. Industry compliance standards
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3. Electronic Photoresist and Polyimide PrecursorsDownstream processors formulate high-performance negative-tone photoresists and specialty PI (polyimide) intermediates using this sulfone as a reactive crosslinking component. The nitro groups ensure controlled electron acceptor behavior for photolithography resolutions at nano-scale, targeting FPC, wafer-level packaging, and display manufacturing. Industry compliance standards
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4. High-Temperature Membrane Materials for Fuel CellsProducers of specialty membranes integrate this sulfone derivative during the backbone modification of aromatic polymeric ion-exchange membranes for proton exchange membrane (PEM) fuel cells. The molecular design helps create mechanically tough, chemically resistant, low-leach membranes for automotive and stationary fuel cell stacks operating at elevated temperatures. Industry compliance standards
Typical usage ratio
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Every batch of Bis(4-Fluoro-3-Nitrophenyl) Sulfone represents years of focused experience with sulfone chemistry. The compound, often identified by the abbreviation BFNPS or CAS number 356229-06-6, is no stranger on our production lines. As the ones directly involved in scaling its production and optimizing each reaction, we see firsthand what distinguishes this molecule from the wider family of sulfone intermediates. Our labs have driven improvements in methods that tackle reagent purity, manage exothermic steps, and tune particle morphology.
BFNPS starts from carefully selected fluorinated and nitrated aromatic feedstocks. Its chemical backbone comes from linking two 4-fluoro-3-nitrophenyl units with a sulfonyl bridge. The manufacturing challenge centers on getting that linkage clean, controlling regioselectivity, and preventing contamination by structurally similar byproducts. In handling this process at scale, our engineers target conversion rates only possible by combining precise analytics with robust reactor controls.
Many customers ask what sets Bis(4-Fluoro-3-Nitrophenyl) Sulfone apart from other bis-aryl sulfones or conventional nitroaromatics. The impact starts at the atomic level. The dual presence of electron-withdrawing nitro and fluoro groups pushes this molecule into a specialized niche. Compared to unsubstituted bis(phenyl)sulfones, BFNPS offers a dramatically altered reactive landscape, featuring increased resistance to nucleophilic attack and higher thermal stability. We’ve observed that when plastics engineers or materials scientists in need of high-Tg properties try a basic phenyl sulfone, the result often falls short; BFNPS overcomes some of these classic limitations.
On the bench and on our line, the purification step never gets routine. Separating unreacted starting materials and traces of positional isomers challenges even skilled chemists. Through in-process monitoring and tailored crystallization cycles, we achieve purity levels that support demanding uses in polymer synthesis and electronic materials. Our dedication to these details saves downstream users many headaches: lower extractables, more predictable curing, and consistent dielectric performance are among the returns on this investment.
The value of BFNPS comes out most clearly in specialty polymers. Companies in high-stakes markets—membrane fabrication, light-emitting diodes, aerospace composites—turn to this compound when a performance gap appears in conventional monomers. Given the strong electron-withdrawing effect of its fluoro and nitro substituents, BFNPS supports the synthesis of polyarylsulfones and related polymers that retain mechanical strength and dimensional stability under aggressive service conditions. We’ve worked with project partners who need their finished products to survive sterilization, exposure to acids or bases, or extended high-temperature cycles, and standard aromatic sulfones won’t cut it.
One visible difference relates to processability. The high melting point and solubility profile of BFNPS occasionally pose a hurdle; to address this, we’ve spent years improving our particle sizing and drying practices. By delivering a powder that flows freely with minimal dust, formulators who add it to resin kettles get more consistent dispersion and, ultimately, tighter quality control in their final extrudates or cast films.
Electronic materials form another focal area. The requirements from PCB manufacturers and display engineers keep growing, especially where halogen content and dielectric loss become limiting factors. The structure of BFNPS, with its specific arrangement of fluoro and nitro groups, locks in polarity without swelling or degrading in most organic solvents. We tailor impurity profiles to guarantee trace-level ionic contamination remains well below industry thresholds, protecting sensitive circuits from corrosion or signal drift.
Direct experience with nitrated aromatics shapes our approach to both safety and continual improvement. The nitro groups within BFNPS require careful attention during reaction and recovery: any misstep in drying or temperature management can trigger hazardous decomposition. Over the years, our team has mastered these risks through persistent training, investment in reactor design, and a program of ongoing review. Operators follow strict protocols for transfer, ventilation, and waste management, and automated containment systems reduce human exposure when charging high-energy intermediates.
Customers relying on BFNPS often face their own environmental and process challenges. On the production floor, dust control stands out—persistent dust can clog filters, contaminate neighboring lines, or present a combustion risk. We address this upstream, offering customizable particle sizes and moisture content by adapting our finishing steps to each shipment’s specific target. Customer feedback on handling characteristics goes straight into process optimization: one batch of sticky, caked material produces more than frustration, it drives us back to improve drying efficiency and coordinate with logistics to reduce humidity swings during transit.
Unlike marketers, we face the realities of raw material sourcing and emissions control every day. The synthesis of BFNPS generates both organic and inorganic waste, including acidic filtrates and mother liquors with spent nitrate. Our early operations produced more waste per kilo of product than we care to admit, but constant iteration—switching to reusable process solvents, integrating closed-loop filtration, and onsite neutralization—reduced that burden by over half in recent years.
What improved environmental profile means for downstream users comes down to risk management and audit scores. Many of our customers contend with rising regulatory scrutiny, especially for materials shipping cross-border into the EU, Korea, or California. Supply chain partners now expect not only a certificate of analysis but also confirmation that each lot aligns with applicable waste reduction targets and conforms to hazardous substance declarations. Through periodic supplier audits, raw material traceability, and real waste treatment data, our plant meets these expectations, offering transparency that stretches from the production reactor to the delivery truck.
Scalability stands as a daily trial for any chemical manufacturer. BFNPS belongs to a chemical sector more susceptible to raw material shocks than most commodity aromatics. The sourcing of high-purity fluoroaromatics and nitration agents remains subject to global price swings and occasional logistical bottlenecks. During pandemic-era disruptions, we watched costs for precursor materials shoot up by a factor of three, squeezing margins and forcing us to redesign scheduling to maintain promised lead times.
Planning around these realities, we established long-term supply contracts whenever possible. Our purchasing team balances cost with reliability, sometimes sourcing from multiple continents to reduce risk. Relationships with upstream suppliers matter as much as own process controls; a two-week shipment delay from a nitrate supplier in Japan might ripple through the entire downstream schedule. Here at the factory, we keep buffer stocks, monitor market movements daily, and adjust batch sizes quickly to respond to swings in customer demand.
Everyone talks about quality, but for us, every batch of BFNPS tells a story. We track how minor variations in input purity, temperature curves, or agitation speed can shift outcomes. In our experience, the difference between “good enough” and “zero-failures downstream” starts in how we train plant staff, calibrate sensors, and adjust lot-specific parameters based on real feedback.
Beyond basic purity, we test for trace solvents, metallic contaminants, and unwanted isomers. Polymer and electronics customers have pressed for increasingly tight specs—parts-per-million levels in some cases—even in lots that exceed baseline industry expectations. To meet this challenge, we invested in industry-leading chromatography and spectroscopy tools. These don’t just generate certs for paperwork; pinpointing and fixing problems at trace levels keeps returns and product recalls rare.
The difference between BFNPS and other bis-aryl sulfones comes down to the specifics of molecular tailoring. For instance, plain bis(phenyl)sulfone lacks the polarizing effects of nitro and fluoro substituents, leading to a loss of chemical resilience and diminished compatibility with next-generation engineering plastics. We’ve fielded more than a few requests to replace older monomers or “stretch” blending formulas, only to find that substituting BFNPS leads to immediate property gains—whether it’s flame retardance, increased glass transition, or resistance to oxidative stress.
Compared to trisubstituted phenyl sulfones, BFNPS presents a balance of stability and reactivity that benefits both polymer scientists and formulating chemists. Its difluoro structure blocks sites vulnerable to side reactions, which means polymers built on this core display less discoloration and longer service lifetime in exposed environments. While some sulfone intermediates are tuned for price, BFNPS focuses on performance, especially in premium segment applications where small differences cascade into bigger product gains.
Continuous improvement keeps this compound competitive. Advances in catalysis and green chemistry drive our future R&D. Through in-house trials, we’re experimenting with lower-temperature coupling reactions and less hazardous nitration protocols, seeking to maintain performance while shrinking environmental impact. We’re close with polymer customers in scaling up new blends that feature BFNPS, especially where novel thermoplastics or membranes demand even higher thermal or chemical tolerance.
Requests for custom solutions—altered morphology, impurity profile refinement, or granular adjustments to crystalline form—continue increasing. Each new challenge yields practical insights we reinvest in our systems. As regulatory landscapes change and end-user requirements evolve, our team stays in close contact with downstream partners, making proactive adjustments to both documentation and production decisions.
Every lot that moves out of our facility reflects a network of decisions: raw material selection, operator skill, equipment investment, and customer engagement. Over decades, the direct line between practice and product defines our reputation. Many users in technical and academic settings return to BFNPS for repeat applications, citing not just its technical merits but the reliability and technical support that come with a direct-from-manufacturer relationship.
Internally, we encourage our staff to record both successes and learning points with each batch, feeding experience back into training modules and process refinements. Quick incident reviews for any deviation or customer complaint have taught us more than a thousand routine runs. Taking this hands-on approach, we see our product not as a static commodity but a result shaped by attention at every stage: from a raw benzene ring to a tailored specialty sulfone ready for advanced chemistry.
Making, refining, and selling Bis(4-Fluoro-3-Nitrophenyl) Sulfone is less about moving units and more about problem-solving, reliability, and mutual advancement. Each customer application—whether as a building block for high-performance polymers, a component in sensitive electronics, or a tool for materials scientists—reflects a concrete solution built on a foundation of technical mastery and transparent, responsive manufacturing practice. Trust, both internal and external, grows from what happens on our shop floor, not from distant marketing promises. That’s been our core principle since the first kilo left our factory.