|
HS Code |
394353 |
| Cas Number | 367-27-5 |
| Molecular Formula | C6H4F2O |
| Molecular Weight | 130.09 |
| Iupac Name | 2,4-Difluorophenol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | 8-10°C |
| Boiling Point | 171-173°C |
| Density | 1.271 g/cm3 |
| Solubility In Water | Moderately soluble |
| Flash Point | 72°C |
| Pubchem Cid | 95851 |
| Smiles | C1=CC(=C(C=C1F)O)F |
As an accredited Phenol, 2,4-Difluoro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Phenol, 2,4-Difluoro- is supplied in a 100g amber glass bottle with a secure screw cap, labeled with hazard warnings. |
| Shipping | Phenol, 2,4-Difluoro- should be shipped in accordance with hazardous materials regulations. It must be contained in tightly sealed, chemical-resistant containers, cushioned to prevent breakage. Label packages clearly with proper hazard warnings. Ship via authorized carriers, maintaining compliance with local, national, and international chemical transportation guidelines to ensure safety and legal conformity. |
| Storage | Phenol, 2,4-Difluoro- should be stored in a tightly closed container in a cool, dry, well-ventilated area away from heat, ignition sources, and incompatible substances such as strong oxidizers and bases. Keep container protected from physical damage and direct sunlight. Store under inert atmosphere if possible. Ensure proper chemical labeling and access to safety equipment like eyewash stations and spill kits. |
Competitive Phenol, 2,4-Difluoro- prices that fit your budget—flexible terms and customized quotes for every order.
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Every day in our plant, the production floor comes alive with the sharp bite of chemistry in motion. Phenol, 2,4-Difluoro-, known among our teams as 2,4-difluorophenol, holds a special spot in our lineup. Over the years, we have tracked the increasing demand for precise fluorinated building blocks. Among those, this compound stands out—balancing cost, utility, and performance in demanding applications.
Chemists who handle specialized phenols notice plenty of subtle but critical differences in reactivity, stability, and purity. Our experience shows that 2,4-difluorophenol’s two fluorine atoms placed at the ortho and para positions on the benzene ring do more than just slightly change its molecular weight. The added electronegativity tunes the compound's reactivity, often making it the preferred substrate over non-fluorinated phenols for targeted transformations. Traditionally in our facility, this variant sees more selection when reproducibility and tight product specifications matter. Over time, process engineers report they have fewer side reactions with this molecule than with many other difluorinated phenols, which translates into smoother downstream chemistry.
Our product routinely exceeds 99% GC purity, something we rigorously control from raw material selection right through to finished packaging. Quality assurance teams walk the lines, making sure every lot stays near colorless, with a crisp melting point and minimum residue. Labs tend to judge new suppliers based on year-to-year consistency—based on independent third-party analysis, ours delivers the reproducibility researchers and production managers expect.
The most common feedback from downstream users, especially in pharmaceutical and specialty materials sectors, comes down to two issues: ease of purification and reliability of performance under process conditions. 2,4-difluorophenol often leaves behind less troublesome impurities than non-halogenated phenols. This translates into cleaner reaction profiles and a clear benefit for anyone running scale-up trials or full-scale manufacturing. Process chemists appreciate not just purity but the way our product handles under variable humidity and temperature conditions, which often cause trouble in lesser materials.
In real terms, the majority of our 2,4-difluorophenol production makes its way into agrochemical intermediates and pharmaceutical research. Having watched the evolution of herbicide and fungicide design, we find that structural specificity at the aromatic ring level pays dividends. Fluorine atoms positioned precisely interact with biological targets, modifying metabolic stability and absorption characteristics.
The pharmaceutical world has sharpened its focus on halogenation since the late 1990s, not just for patents but to exploit the unique hydrogen-bonding and electronic effects fluorine brings. As an intermediate, 2,4-difluorophenol supports the manufacture of key active ingredients ranging from anti-infective to CNS compounds. In our shop, batch-to-batch quality isn’t theory—it’s the foundation that keeps multi-ton annual contracts on track, especially for customers running a narrow margin between success and costly process setbacks.
Manufacturers of specialty polymers also look for this compound when building block copolymers or resin systems need both chemical resistance and polarity. In our experience, the incorporation of 2,4-difluorinated moieties can enhance thermal stability and hydrophobicity in final materials by a measurable degree, which often marks the difference between commercial success and an expensive product recall.
Direct comparisons with other difluorophenols shed light on the value of correct isomer selection. Colleagues in research regularly flag 3,5-difluorophenol and its analogs for slightly different reactivity, but not every isomer suits all processes. Our product’s specific electronic pattern can influence coupling, oxidation, or substitution reactions in ways that are non-interchangeable—lessons we’ve learned both on the line and in troubleshooting customers’ glass-lined reactors.
We have seen clients switch away from generic chlorinated or methylated phenols in pursuit of tighter environmental targets, only to run into deposition issues or side reactions. Others choose between the 2,4 and 2,6 variants based on reactivity under strongly basic or acidic conditions. Experience shows the 2,4 isomer’s balance between electron density and steric effects helps avoid runaways and minimizes exotherm during scale-up. It’s hard to overstate the difference a single substituent position can make, and consistent process yields reflect the decisive impact of these choices.
Operating at plant scale sharpens perspective on raw material risks, waste management, and overall process safety. Each lot of 2,4-difluorophenol begins with closely monitored fluorination, distilled under reduced pressure to capture residual starting materials. Quality technicians regularly review spectral data for minor shifts, as the color and odor of off-spec material spot trouble long before analytical instruments confirm it.
Logistics matter too. This compound, a clear liquid at room temperature, requires special containment to prevent moisture uptake and maintain stability during shipment. Our facility’s drum-filling process uses inert atmospheres and automatic seals, steps that virtually eliminate air exposure. In transport, sealed drums reach customers with minimal loss and degradation, ensuring users receive product just as it left our line.
Consistency becomes real in day-to-day details. Operators rely on real-time process analytics, not just quarterly audits. By aligning staff training, materials handling, and calibration schedules, we meet the actual working needs of both research labs and commercial-scale customers. The feedback loop tightens with every completed batch and every customer validation report—demanding but rewarding work.
In today’s landscape, the push for molecular precision goes hand in hand with broader environmental accountability. Our technical team stays tuned to regulatory changes coming out of Europe, North America, and Asia-Pacific, especially concerning persistent organic pollutants and process residuals. 2,4-difluorophenol, with its relatively straightforward decomposition products, often replaces heavier halogenated phenols, aiding compliance with both emissions limits and stricter waste water standards.
We see research groups increasingly selecting fluorinated phenols for new synthetic routes, not only because of their functional advantages but also for their manageable risk profiles. Our in-house environmental team tracks emission trends and water discharge profiles, investing in continual process improvements that lower both solvent consumption and byproduct output.
On the client side, downstream users often request data packages showing the full impurity fingerprint. Clear documentation smooths regulatory submissions—an investment in transparency that helps avoid shipment delays and batch rejections. Transparency extends beyond paperwork; our teams participate in industry groups, sharing best practices and staying ahead of future scrutiny on trace impurities or handling risks.
From lab bench to metric ton reserves, the supply chain for fluoroaromatic intermediates remains vulnerable to both upstream bottlenecks and sudden demand spikes. Every member of our operations group remembers the volatility in raw hydrofluoric acid prices. Not all players make it through these swings with consistent product availability, but our vertical integration from precursor to finished intermediate provides steady supply and reasonable lead times for both recurring and spot orders.
Focused investments in onsite process automation, coupled with long-term supplier partnerships, make a measurable difference. Technician teams can reroute supply or re-blend finished product within hours, rather than days, if unexpected analytical drifts surface. For critical path users—often on tight project deadlines—this kind of flexibility translates straight to avoided downtime and finished product throughput.
Open communication between our plant teams and end users helps guide production adjustments, whether that means tweaking batch sizes, packaging formats, or delivery schedules. No automated system replaces knowledge gained by hands-on troubleshooting; our senior process engineers bring years of accumulated perspective when customers report unusual process challenges or new end-use specifications.
Scale-up introduces hurdles that can derail even the best pilot runs. Minute impurities, non-uniform heating, or trace moisture expose hidden risks that might not emerge during small-scale experiments. In fluoroaromatic chemistry, the difference between a smooth multi-kilogram run and a failed batch often lies in the raw material’s gas chromatography profile.
Our staff approach each process transfer with caution and a long list of historical batch data. Regular cross-checks between lab results and full-scale production prevent recurring deviation; we publish typical ranges for residual starting material, water content, and UV-Vis absorbance to help customer QC teams adapt methods quickly. When something drifts, a dedicated troubleshooting group responds, sharing root cause analysis and new handling protocols—ensuring our partners don’t repeat past missteps.
Some clients working in combinatorial chemistry or parallel synthesis require hundreds of similar batches with identical profiles. To meet these standards, each reactor setup runs with validated parameter sets and redundant real-time monitoring. Over the years, we have found that taking extra time on initial method validation pays dividends in reduced rework and faster project timelines on the customer’s end.
Every chemical with volatile tendencies or specific storage requirements brings challenges in logistics. The storage and transport of phenol derivatives, especially lightly colored, volatile fluids like 2,4-difluorophenol, need just as much care as the core synthesis steps. Our filling hall uses closed-loop vapor recovery and temperature control, keeping vapor phase loss low and product exposure almost nonexistent.
Staff training includes spill drills, drum inspection, and ongoing refresher courses—tools that make a difference every year on safety dashboards. Packaging in lined steel drums or amber glass bottles is standard but is always chosen in conversation with each client. If an R&D lab requests a custom packout, process staff work cross-functionally to minimize losses and keep the material compatible from transit to storage to final usage.
Clients sometimes ask for pre-ground material or other special formats. Through pilot trials, we’ve found that in most cases, the standard format suits both benchtop and continuous production, but for those who need unique particle sizes or solvent-wetted material, our teams can deliver, provided enough lead time for relevant stability and compatibility testing.
Over years of supplying a variety of fluorinated aromatics, it becomes clear that each structural variant leaves its own mark on both process chemistry and the character of final products. Phenol, 2,4-difluoro- carves out its niche for reasons rooted in tangible benchwork: The ortho and para fluorine atoms guide reactivity in ways that can’t be exactly mimicked with other isomers or halogen patterns.
Feedback from the field underscores this. Contract manufacturers working on pharmaceutical APIs report more robust coupling yields and less troublesome byproduct formation when switching to this compound from trifluoromethylphenol analogs. The difference often boils down to the balance of electron-rich versus electron-deficient centers on the ring, something synthetic chemists exploit for regioselective functionalization or cross-coupling reactions.
In coatings, adhesive, and advanced material applications, the use of 2,4-difluorophenol correlates to gains in polymer backbone stability. Properties such as oxidative resistance, glass transition temperature, and chemical durability show measurable improvements, confirmed both by outside testing labs and our own in-house evaluation team. For clients building performance claims into their finished goods, these differences move beyond theoretical—real-world warranties and certifications depend on such aggregate benefits.
Every day in the plant brings unexpected questions. Despite a decade-plus of producing phenolic intermediates, each market, each new synthesis requirement, pushes us to adjust both technique and mindset. The rigorous, sometimes repetitive quality controls give a foundation for confidence—yet it’s regular feedback from users that teaches us where incremental improvements matter most.
The reputation of phenol, 2,4-difluoro- in today’s chemical landscape is earned, not given. Consistency isn’t an accident or just a matter of good specifications—it’s built on trained eyes, tuned instrumentation, and a willingness to revisit every parameter when a customer challenge emerges. In this way, the product evolves from a commodity into a specialty tool, matched to the increasingly exacting demands of modern synthesis.
As a company built by hands-on staff and real-world process challenges, we see every batch as both a technical achievement and a promise kept. Through changing regulatory climates, evolving customer needs, and relentless internal improvement, phenol, 2,4-difluoro- remains a reliable tool in the hands of chemists, formulators, and manufacturers building the next generation of pharmaceuticals, materials, and more.