|
HS Code |
291410 |
| Cas Number | 443-88-9 |
| Molecular Formula | C6H4F2O |
| Molecular Weight | 130.09 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 180-182 °C |
| Melting Point | −6 to −4 °C |
| Density | 1.329 g/cm³ |
| Flash Point | 66 °C |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.497 |
As an accredited 2,5-Difluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,5-Difluorophenol is packaged in a 100g amber glass bottle with a secure screw cap and clear hazard labeling. |
| Shipping | 2,5-Difluorophenol is shipped in sealed, chemical-resistant containers to prevent leakage and contamination. It should be handled as a hazardous material, protected from moisture and incompatible substances. Packaging must comply with local and international transport regulations, and appropriate hazard labeling is required to ensure safety during storage and transit. |
| Storage | 2,5-Difluorophenol should be stored in a tightly closed container in a cool, dry, well-ventilated area away from direct sunlight and sources of ignition. Keep it separated from incompatible substances such as strong oxidizers and bases. Store at room temperature, protected from moisture. Ensure proper labeling, and access should be restricted to trained personnel wearing appropriate safety equipment. |
Competitive 2,5-Difluorophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Decades spent on the chemical floor have taught us the difference between producing a nuanced fine chemical and simply offering it on a list. 2,5-Difluorophenol shines as one of those compounds where attention to synthesis, storage, and handling makes noticeable improvements for the chemist relying on it. We handle each batch from raw fluorobenzene through the fluorination and hydroxylation stages, monitoring every reaction for stability and purity. Nothing is left to chance during purification, as residual isomers or trace contaminations impact downstream yields in pharmaceuticals and agrochemicals.
We produce 2,5-Difluorophenol in colorless to slightly yellow batches, using high-purity reagents and inert atmospheres where needed. Our standard production route results in material boasting purity exceeding 99% by gas chromatography, with water levels kept below 0.10% on Karl Fischer titration. Residual solvents come in well below analytical detection limits—never left to guesswork. This consistency in specification means that R&D labs and pilot plants alike see reliable melting behavior, consistent reactivity, and minimum deviation in final product quality. The benefit extends to scaling from lab to kilo-work, avoiding extra purification cycles or headaches.
2,5-Difluorophenol finds value across synthetic organic chemistry. Many of our longstanding clients push for higher selectivity in aryl fluorination, better coupling yields, and scalable access to novel intermediates. Medicinal chemists use this molecule as a core building block for manufacturing advanced pharmaceutical intermediates, taking advantage of the aromatic hydroxyl for direct derivatization or protection, and of the fluorines to modulate both reactivity and metabolic stability. Several prominent crop protection projects rely on the unique behavior of the 2,5-difluoro substituent pattern, where steric and electronic effects support the creation of next-generation fungicides and herbicides.
Our in-house teams have run the compound through both Suzuki and Buchwald-Hartwig couplings, giving us real data about efficiency, by-product profiles, and workup considerations. These insights get shared with technical support calls—saving time and resources for colleagues outside our facility.
There is a marked difference between 2,5-Difluorophenol sourced straight from the synthesis line and lots held too long in substandard containment. Our storage protocols involve amber glass reactors and inert flushing to guard against gradual oxidative changes. We regularly see competitors deliver batches that display trace oxidation or unexpected yellow coloration, which can cause unwanted side-reactions or create additional purification steps. By using freshly manufactured lots and proper inert handling, yields stay high, and impurities are minimized at every stage—from pilot runs to process scale.
Someone familiar with monophenols or alternate fluorinated phenols will spot the core advantage here. The 2,5-regioisomer brings a combination of hydrogen bonding at the para position and fluorine deactivation on both sides. This impacts both acidity and nucleophilicity. Compared to less substituted phenols, such as plain hydroxybenzene, 2,5-difluorophenol resists oxidative coupling, so radical and electrophilic substitutions become more controlled. Furthermore, compared to 2,4-difluorophenol or 3,5-difluorophenol, the 2,5 isomer displays a different electronic environment that moderates both leaving group ability and metal insertion behavior under catalytic conditions.
We’ve observed, for example, that in copper-catalyzed arylations and nitrations, the difference between the 2,5- and the 3,5-isomers shows up in both conversion and selectivity rates. Chemists focused on late-stage fluorination often select 2,5-difluorophenol as their first phenolic candidate because the substitution pattern suppresses side-products seen with other isomers.
Years in large-scale chemical production have taught us that not all aromatic fluorinations are equal in safety or environmental impact. Our plant employs closed-loop systems and acid scavenging to minimize fluoride emissions, and workers receive routine training on safe neutralization protocols. Residues from each batch go through rigorous distillation and containment, steering clear of issues that arise with traditional waste handling. Our near-zero emissions record did not appear by accident but through attention to engineering and chemical process control.
We constantly hear chatter about new synthetic tricks and green chemistry approaches for difluoroaromatic building blocks, but walk the shop floor, and you see which methods hold up at scale. Our teams have experimented with both traditional halogenation steps and novel electrochemical fluorination routes. The newest advances have cut reaction times and cut down on solvent loads, but maintaining product identity and consistent profile remains the guiding metric. Every time batch data tells a different story, we adapt by tuning parameters—be it temperature profile, phase transfer reagents, or post-reaction crystallization. Results go directly into the next production run, not into marketing copy.
Demand for specific building blocks never stays static. Pharmaceutical partners regularly send requests for different lot sizes, custom packaging, twin samples for method validation, or even microbatches for high-throughput assay screening. Our direct role in synthesis makes it possible to fulfill specialized requests quickly. Clients who ran into bottlenecks with bulk traders or long supply chains come to us for direct technical feedback. For example, when a large-scale customer hit unexpected trouble with dehalogenation during formulation, in-person troubleshooting at the reactor helped dial in solution conditions and eliminated impurities.
It’s this hands-on troubleshooting and process adjustment that makes a true difference on the manufacturing side. Chemists at the lab bench or scale-up line value this level of cooperation, knowing they can pick up the phone and speak with someone who has literally handled the material and understands its properties under pressure, temperature, or storage shifts.
Raw material markets for fluorinated aromatics have become complicated by logistics and geopolitical shifts. We’ve recently shifted toward regional sourcing of starting materials and have expanded in-house capabilities for critical fluorination reagents. That makes it possible to weather delays and fluctuations that stop others in their tracks. Storage capacity for intermediates, robust process documentation, and an onsite analytical lab keep lead times tight and deliveries reliable. There is no mystery about origin or quality with every shipped lot. Our customers see the benefit during rush orders or unplanned scale-ups, when the need for truly on-demand synthesis becomes obvious.
Any laboratory methodology that dumps its troubles onto the end user stops being useful after the first few runs. We’ve learned from hard experience not to send out lots that haven’t been pressure-tested in actual application. Material shipped from our factory comes with real technical support—everything from advice on solvent selection during recrystallization to optimal metal scavengers for post-coupling cleanup. It’s common for our chemists to share real-world NMR, HPLC, and GC/MS data, making it possible for end-users to replicate results instead of struggling with unknowns.
This feedback loop links actual manufacturing knowledge with the demands of medicinal chemistry, agrochemical innovation, or even custom dye and pigment synthesis. Especially when users ask about trace metal content or specific impurity challenges, our technical team has the answers—not just a data sheet, but hard-won information about what truly works.
Choosing a source for specialized fine chemicals goes well beyond cost-per-gram calculus. We’ve fielded too many calls from buyers who learned the hard way that not all sources for 2,5-Difluorophenol deliver the promised consistency. We get requests for analyses beyond simple COA values—think long-term impurity tracking, stability under transport, batch-to-batch reproducibility, and tailored storage solutions. As the actual producer, meeting these needs comes built-in, not as afterthoughts or add-ons.
Many products appear similar at a glance: white powder, clear liquid, list of ingredients. Step into a full-scale manufacturing shop and you see the difference in how materials behave—under heat, in different solvents, after months sealed or unsealed. We track every signal deviation and intervene before it leaves the building. The result is a compound that performs as predicted, even at demanding scales where surprises cause downtime and lost product.
Over the last decade alone, our process has delivered material for hundreds of projects that span everything from advanced materials chemistry to veterinary APIs. Each time, user feedback—whether glowing or critical—filters straight back into the way we conduct our work. Problems faced by a bench scientist in Singapore or a plant chemist in Germany improve batch quality for every future output. Everyone downstream benefits from one manufacturer taking responsibility for every step between order and delivery.
The fundamental difference in sourcing 2,5-Difluorophenol directly from a chemical manufacturer rests with ongoing attention to process, product, and user need. Each kilogram of material comes with the quiet assurance that it has passed not just analytical checks, but real-world handling tests. This goes beyond a simple metric or purity percentage and becomes visible during every step of use—from dissolution in polar or nonpolar solvents, to purification, to late-stage derivatization.
Specialty projects call for more than commodity chemistry. We stand behind every batch because we know what went into it, who oversaw the critical steps, and how it performs under stress. There are no shortcuts here, no reliance on vague promises or untraceable lots. The users who entrust their research or production line to 2,5-Difluorophenol from our shop get more than a product—they get a partner for technical progress.
Every year brings new challenges, from regulatory changes on fluorinated compound handling to evolving client expectations about sustainability or molecular design. Regulatory demands push us to audit processes and invest in safer, cleaner synthesis routes, trimming all non-essential waste and ambiguous material streams. Through dialogue with our users, we have redesigned packaging, adjusted batch sizes, and fine-tuned shipping procedures to fit real project timelines.
By maintaining a close loop between those who make the compound and those who use it, chemical manufacturing gains efficiency and reliability. The circle completes itself with every informed improvement, whether in yield, impurity control, or user guidance. Anyone seeking 2,5-Difluorophenol—whether for next-generation medicinal scaffolds, performance materials, or tailored precursors—can trust a manufacturer who understands these needs from experience, not guesswork.