|
HS Code |
299898 |
| Iupac Name | 4-chloro-3,5-difluorophenol |
| Molecular Formula | C6H3ClF2O |
| Molecular Weight | 164.54 g/mol |
| Cas Number | 195628-79-2 |
| Appearance | White to off-white solid |
| Melting Point | 56-60°C |
| Solubility In Water | Slightly soluble |
| Density | 1.52 g/cm³ (approximate) |
| Smiles | C1=C(C=C(C(=C1F)Cl)F)O |
As an accredited 4-Chloro-3,5-Difluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Chloro-3,5-Difluorophenol is supplied in a 25g amber glass bottle, sealed and labeled with hazard and identification details. |
| Shipping | 4-Chloro-3,5-Difluorophenol should be shipped in tightly sealed, chemical-resistant containers, compliant with international hazardous material transport regulations. It must be labeled clearly, packed with appropriate cushioning and absorbents, and kept away from incompatible substances. Shipping should be done via certified carriers, preferably under cool, dry conditions to ensure stability and safety during transit. |
| Storage | 4-Chloro-3,5-difluorophenol should be stored in a tightly sealed container, protected from light, heat, and moisture. Keep in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers, acids, and bases. Proper labeling and secure shelving are essential to prevent accidental spills or exposure. Personal protective equipment is recommended during handling. |
Competitive 4-Chloro-3,5-Difluorophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Producing specialty chemicals is not a matter of pumping out intermediates and hoping they fit someone’s needs. Quality, traceability, and practical performance drive us. In the field of fluorinated aromatic compounds, 4-Chloro-3,5-Difluorophenol stands out for handling modern industrial challenges and demanding research projects. Over years of working directly with engineers and chemists, we've learned where products falter and where they excel. This particular compound, often known by the shorthand 4C3,5DFP, offers a clear set of advantages for those who need distinct molecular reactivity, consistent purity, and streamlined downstream processing.
Let’s look at what goes into the production of this molecule and why careful manufacturing matters. This isn't just another phenol with two fluorine atoms and a chlorine atom. We’ve fine-tuned our process for clean halogenation and precise substitution at the para and meta positions, minimizing side reactions and contamination. Every step reflects direct communication with formulators and synthetic chemists. Practically, this means you get a white to off-white crystalline material with consistent melting behavior and chemical stability.
Take specification seriously — people in the lab and on the plant floor do. Our typical batches of 4-Chloro-3,5-Difluorophenol have a purity above 99%, measured by GC and confirmed by NMR. Moisture content is controlled right from the raw material intake to the final packaging. We do not cut corners by blending off-spec material or adding unknown stabilizers; the molecule you receive matches the molecular weight and structure expected on your COA, and every drum comes from a well-documented batch history.
Modern phenolic compounds occupy a key role in pharmaceuticals, agrochemicals, and specialty materials. Our clients use 4-Chloro-3,5-Difluorophenol for applications where both reactivity and structure matter. The two fluorines at the 3 and 5 positions bring unique electronic effects, pushing down electron density, lowering the pKa, and altering reactivity compared to regular phenol. Customers tell us that these differences lead to selective coupling and cleaner derivatization, especially when building active pharmaceutical ingredients or high-performance coatings.
Direct chlorination at the 4-position influences both the physical properties and downstream chemistry. In synthesis, this substitution pattern often means a unique platform for making aryl ethers, esters, or activated intermediates. Folks developing novel crop protection compounds have come to us looking for specific halogen patterns because even small changes can make or break a product’s function, persistence, or toxicity profile. It’s never simply about filling a bucket with a chemical; it’s how those atoms and bonds steer molecular recognitions in the real world.
Synthetic pathways have become more creative in recent years. More often, we see multi-step sequences where the phenolic component acts as a linchpin. For example, several pharmaceutical development teams turn to fluorinated phenols when seeking compounds with improved metabolic stability or enhanced binding affinity. Fluorine is not a mere substitution—it changes the game at the molecular level. They’ve told us that 4-Chloro-3,5-Difluorophenol works particularly well as a precursor for certain diaryl ethers and heterocyclic scaffolds that resist metabolic breakdown or oxidative stress, traits valued both in clinical candidates and materials science.
Our experience supplying grams for research, kilograms for development, and tons for commercial operations has taught us where quality failures occur. Impurities in halogenated intermediates trigger yield drops, messy chromatograms, or regulatory headaches. By maintaining strict in-process controls—monitoring everything from reaction time, temperature, and post-synthesis purification—we limit such surprises. Customers in fields as varied as crop protection, pigments, liquid crystal display production, and performance adhesives benefit from this attentive approach.
Many ask how 4-Chloro-3,5-Difluorophenol differs from similar phenolic compounds, either mono- or di-fluorinated, or from those with altered halogen placement. The edge comes from the specific electron distribution imparted by its structure. For chemists, the substitution pattern guides not only the positioning for follow-on reactions but also determines acidity, volatility, and interaction with catalysts or reagents. This molecule’s balance of hydrophobicity and modest reactivity provides just enough resistance to unwanted side reactions, while still opening up sites for alkylation or acylation.
The field regularly compares it to 4-chloro-2,6-difluorophenol and other isomers. Our takeaway? Subtle shifts in ring substitution create marked changes in product outcome. The 3,5-fluorine layout gives a practical advantage for Suzuki or Ullmann coupling, and often reduces competitor byproduct formation. This real-world feedback, from process optimization and analytical review, drives our desire to continually tweak conditions, solvents, and catalysts in production—something not every supplier considers worth their time or cost.
As a chemical manufacturer, day-to-day hurdles can be underestimated. Handling reactive intermediates, preventing cross-contamination, and ensuring reliable logistics takes more than textbook knowledge. Over years in industrial synthesis, we developed tailored reactor setups for halogenation, using lined vessels and temperature controls that prevent both decomposition and offtarget substitution. It’s the difference between delivering a consistent product every shipment, versus one that causes angry phone calls from the customer’s QC lab.
Packaging and storage matter just as much. We select packaging to prevent moisture pickup or accidental static-borne contamination, always validating long-term stability. There’s constant back-and-forth between lab and plant to ensure the process translates as scale increases, avoiding surprises like unexpected byproducts or purity loss that were invisible at the gram scale. This depth of experience comes through every time a client receives exactly what was ordered, batch after batch.
Health and safety aren’t box-ticking exercises for us. Handling chlorinated and fluorinated aromatic compounds can pose real risks to operators, the community, and downstream users. We have in-house training, respirator programs, and always favor ventilation setups that go beyond regulatory basics. Waste management never stops at the legal minimum; waste streams containing chloride and fluoride get carefully neutralized and sequestered before any disposal occurs. Our experience has shown that taking shortcuts here just creates legacy problems—regulators and local communities alike expect long-term responsibility, and so do we.
Customers increasingly ask about regulatory track records and sustainability. Regulatory requirements have shifted, but our approach to compliance and documentation always aims ahead of the curve. We maintain comprehensive raw material traceability, batch records, and certified analytical data. No matter the industry—pharma, electronics, or agriculture—traceability now counts as much as chemical reactivity. That’s why we keep up-to-date on evolving REACH, TSCA, and EPA frameworks.
Supplying chemicals is as much about the relationship as the molecule. Research groups sometimes contact us with complex multi-step synthesis challenges; what’s on paper doesn’t always translate to what works on a larger scale. Our technical team engages early, reviewing target specifications, possible impurities, and even offering guidance on purification if a rare contaminant emerges. The process isn’t just transactional. Shared know-how and open communication solve more problems than spreadsheets ever can.
We have adapted both synthesis and logistics for large-scale requirements, including custom packaging or documentation modifications. Pharmacopeial requirements and global shipping paperwork add layers of complexity, but experience has honed our ability to manage these without missing deliveries or causing headaches for procurement teams. This focus on ground-level reality—from synthesis steps to warehousing—supports not just the molecule's delivery, but the long-term success of each project our product enters.
Demands don’t stand still. Each year, R&D teams in pharma and agrochemical sectors set new bars for purity, structural requirements, and analytical verification. Recognizing this, we invest in pilot plant modifications and analytical technology upgrades. Mass spec, advanced chromatography, and rapid NMR scans aren’t just buzzwords—they let us spot and resolve problems well before shipment. Any deviation from standard, whether due to a new impurity or a sudden customer request, gets handled through process adjustment, not wishful thinking or data fudging.
Some of our recent customers challenged us with requests for green synthesis or reduced solvent use. These conversations produced process optimizations that lowered emissions and, just as importantly, reduced cycle times and improved operator safety. Green chemistry is not a slogan for us—it’s built into each equipment upgrade and operator briefing. When working with halogenated aromatics, every improvement counts. This willingness to invest and adjust arises out of long-term engagement, not just chasing short-term procurement wins.
Deciding on a starting material or intermediate has far-reaching implications for cost, regulatory compliance, waste, and downstream yield. Many products on the market claim similar quality; the difference shows up in production line stoppages, unexpected analysis results, and lost development time. Our experience with 4-Chloro-3,5-Difluorophenol—how it reacts, stores, and moves through logistics—helps partners avoid these risks. No other isomer or single-fluorinated phenol quite gives the same range of applications or exacting performance in both traditional and cutting-edge processes.
The future belongs to those who learn and adapt. Each gram of 4-Chloro-3,5-Difluorophenol that leaves our site reflects not only skilled synthesis but years of troubleshooting, listening, and direct experience with the needs of scientists, plant operators, and innovators worldwide. From highly consistent supply to the ability to tweak and improve based on field reports, we see our product as a tool to unlock progress in fields as diverse as life sciences, materials development, and environmental engineering.
End users have taught us the most. Success stories often start with thorough preparation, clear requirements, and open lines of communication. Perhaps a customer wants to reduce residual chloride in their final active ingredient, or seek an intermediate that eliminates a troublesome high-boiling byproduct. The details matter—whether through improved filtration, better solvent selection, or pinning down shipping schedules to avoid material degradation. Our history producing 4-Chloro-3,5-Difluorophenol is filled with moments where real-world experience turned near-misses into achievements.
Direct engagement means fewer unknowns, fewer interruptions, and faster progress. For us, it comes down to pride in what leaves our gates. Our track record is built on long-term partnerships, not quick deals. Each kilo reflects a promise that the next one will perform just as well, with the same documented pedigree and field-proven reliability. This approach shapes every stage of making and moving 4-Chloro-3,5-Difluorophenol, and will continue to set the bar in specialty chemical supply.