|
HS Code |
573982 |
| Chemical Name | 3,4-Difluoro-6-Nitrophenol |
| Molecular Formula | C6H3F2NO3 |
| Molecular Weight | 175.09 g/mol |
| Cas Number | 64325-64-6 |
| Appearance | Yellow solid |
| Melting Point | 100-104°C |
| Solubility | Slightly soluble in water |
| Smiles | c1c(c(c(c(c1F)O)F)[N+](=O)[O-]) |
| Inchi | InChI=1S/C6H3F2NO3/c7-3-1-4(8)6(10)2-5(3)9(11)12/h1-2,10H |
| Synonyms | 3,4-Difluoro-6-nitro-1-hydroxybenzene |
| Pubchem Cid | 3085837 |
As an accredited 3,4-Difluoro-6-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3,4-Difluoro-6-Nitrophenol, 5g: Supplied in an amber glass bottle with a white screw cap, labeled with hazard and identification details. |
| Shipping | 3,4-Difluoro-6-Nitrophenol is packaged in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is shipped according to relevant hazardous materials regulations, with appropriate labeling and documentation. The shipment is handled by trained personnel and often transported as limited quantity or as per specific local and international safety guidelines. |
| Storage | 3,4-Difluoro-6-Nitrophenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible materials like strong oxidizers and bases. Protect from moisture and direct sunlight. Store in a chemical storage cabinet designated for hazardous substances, and properly label the container to ensure safe handling and prevent accidental exposure. |
Competitive 3,4-Difluoro-6-Nitrophenol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.
We will respond to you as soon as possible.
Tel: +8615380400285
Email: sales2@liwei-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Over the years, the pursuit of selective fluorination has opened up pathways that drive both pharmaceutical and materials chemistry. Our team works hands-on with these compounds every week, and 3,4-Difluoro-6-Nitrophenol stands out. Physically, this compound presents as a light crystalline powder, and in our facility, every batch shows consistent color and purity. We manufacture under tightly controlled environmental and process conditions, with each run dialed in for the right moisture content and minimal residual solvents—because those details matter down the line.
Our production batches of 3,4-Difluoro-6-Nitrophenol run in the hundreds of kilograms. We maintain strict tolerance ranges for melting point and residual solvents. On the analytics bench, we use NMR, GC-MS, and HPLC to track product quality. From hands-on experience, we’ve learned that batch crystallization and precise temperature control separate a top-tier product from the rest. It comes in various mesh sizes based on customer feedback, not theoretical standards, since certain steps in pharmaceutical synthesis work better with a coarse or a fine grade. Technical documentation comes bundled with actual batch data, not just the regulatory minimum.
Every time we talk to medicinal chemists, requests for fluorinated intermediates keep growing. The 3,4-difluoro substitution increases metabolic stability in advanced intermediates, and the nitro group at the 6-position serves as a versatile functional handle. We have delivered this compound for small molecule drug development and for specialty polymers. One customer used our material to build moieties that needed both electron-withdrawing and activating properties in a single scaffold.
This dual functionality—created by careful ortho-fluorination and para-nitration—produces marked reactivity differences compared with mono-fluorinated phenols or standard dinitrophenols. Over the years, we’ve seen that side reactions drop on scale, with cleaner downstream transformations, when using this molecule instead of traditional phenolic starting points. This keeps chemists focused on project progress, not troubleshooting unapparent impurities.
Colleagues in process development reach out for our 3,4-Difluoro-6-Nitrophenol most often as an intermediate. In preparing fluorinated benzoxazoles, for example, this product acts as the key ring precursor for cyclization steps that demand high ortho-selectivity. We’ve also heard from agrochemical researchers who use it to optimize lead compounds for better bioactivity profiles—small fluorine atoms tend to drop the logP, improving soil mobility and environmental tolerance of actives.
Early on, we fielded calls about solubility. Over several campaigns, we mapped out solubility limits in acetonitrile, DMF, and dichloromethane, since those are the go-to solvents for scale-up. Some direct competitors list theoretical values, but we’ve run continuous assessment with actual product. What we found proved useful: the compound dissolves especially well in polar aprotic solvents, leading to improved handling in both automated dosing and batch setups.
Comparison with close analogs is frequent in our work. Many process chemists mention 3-fluoro-4-nitrophenol or standard dinitro phenol as alternatives. The difference comes out in practice. The careful placement of fluorine atoms on both sides of the aromatic ring affects acidity, reactivity, and subsequent substitution. Our synthetic team has observed cleaner conversion to downstream products like fluoroaryl ethers. The di-fluoro substitution also means superior shelf stability—no creeping discoloration or oxidation during extended storage, which plagues some mono-fluorinated nitrophenols.
We field a lot of questions regarding extractability and purification. The dual fluorine often reduces polarity, so liquid-liquid extractions work differently compared to mono-fluorinated products—we relay this tip to partners tackling purification. One frequent user told us his yields in Suzuki coupling improved when moving from 3-fluoro-4-nitrophenol to our material, not just because of higher purity but because of predictable electronic effects across the ring during metal-catalyzed steps.
It is tempting to focus only on the chemical structure, but keeping batch quality high depends much more on repeatability and process control. From the earliest manufacturing campaigns, human oversight and real-time monitoring became our greatest assets. Any variation in precursor quality—be it nitrosylation or fluorination—shows up in finished product consistency. We tested various purification paths including vacuum distillation, column chromatography, and crystallization. With each, we discovered that sloppiness in crystallization lets in trace contaminants that haunt further steps.
In one particularly tight deadline, we managed back-to-back production runs—hundreds of kilos passed QC without a single outlier, a milestone for our group. Our plant operators, chemists, and QA team all share accountability; we track historical process deviations and run root cause analyses immediately if measurements stray. This keeps impurity profiles tight and saves our partners headaches in downstream manufacturing.
The question of traceability always comes up. For regulated markets, we've built systems that assign unique lot numbers and maintain retention samples beyond minimum requirements. Materials destined for drug synthesis follow strict change control—any shift in input reagents or suppliers gets reviewed and documented, so our customers always know the complete history of what they receive.
We routinely supply validation data and audit trails for partners who need assurance beyond paperwork. During the last round of facility audits, several QA teams complimented the way we record both in-process and finished product results, not just COA summaries. The feedback loop between manufacturing, QA, and client labs ensures no surprises—people can trace every drum back to a single lot with full supporting data.
Securing stable access to raw materials has required considerable effort. Early in our production, we met bottlenecks due to limited availability of high-quality fluoro aromatics. We now rely on long-term relationships with upstream producers and perform regular incoming QC. Environmental regulations are not just checkboxes. Output of spent acid, for example, receives onsite neutralization, and solvent recycling makes both environmental and financial sense.
Our team invested in closed system handling for byproducts, reflecting a commitment to safe operations and regulatory compliance. Any emission readings are checked regularly, not only during scheduled audits. We train new operators extensively, so process deviations are caught before they cause safety or quality problems.
The combination of difluoro and nitro substitution delivers a compound fit for a range of challenging transformations. We learned from one longtime partner in Japan that his yields on challenging nucleophilic substitution went up by more than 10 percent with our material compared to single-fluorinated competitors. Batch reliability meant he could run longer syntheses with fewer interruptions.
Polymers and specialty additives teams also turn to 3,4-Difluoro-6-Nitrophenol when looking to modify electrical or thermal properties in engineered materials. Our product blends smoothly into multi-step processes, from pilot to full-scale manufacturing. In each case, repeat purity and homogeneity helped avoid unwanted byproducts and simplified later purifications.
Direct communication with end users—rather than just shipping out batches—has shaped our workflow. Every chemist knows: the real challenges show up on the floor, not in the catalog. Over years of feedback, we optimized packaging to prevent caking in humid climates and offered technical troubleshooting for users struggling with minor solubility or recovery issues.
On-the-ground insights helped us create several grades, with adjustments tailored for either high-throughput screening or larger scale reactor loads. By keeping field feedback at the center, our adjustments come from practical needs, not marketing hype.
Our finished drums and kegs come with real traceability documents, not just batch numbers. The quality laboratory cross-checks every drum and holds retention samples from every order. Quality comes not only from in-process analytics but from continual staff training and real-time checks.
Detailed attention to shipping integrity also became important after feedback from partners working in variable climates. Our material now arrives with extra moisture protection and inner lining as needed, depending on the destination. It’s all aimed at removing the small frustrations that often slip past in standard supply lines.
Markets shift quickly. Where a decade ago demand centered on simple mono-fluorinated phenols, we see today’s needs rapidly transition toward high-functionality building blocks for targeted synthesis. As one of the few manufacturers who scale and supply this difluoro-nitro phenol directly, we accept the pressure to keep standards high and adapt processes to meet tomorrow’s regulatory or technical hurdles.
Our chemistry team collaborates with outside labs, exploring new routes to maintain tight quality and stable pricing. Each campaign lets us fine-tune conditions—modulating fluorination protocols and purification sequences based on yield observations, field use, and evolving compliance landscapes. This spirit of adjustment and accountability keeps us in sync with both heritage processes and the next wave of technical asks.
Anyone can list purity on a sheet. Reliability grows out of real production, real troubleshooting, and keeping sight of every step from raw materials to delivered batch. Our own lab-scale and pilot reactors run daily, so every quality detail feeds back into future batches.
For each lot, the people making it are the same ones who answer follow-up technical questions. Continued field input—whether from pharma labs, polymer formulators, or agrochemical developers—drives our improvements. No process is static, and as regulatory environments evolve, so do our technical and documentary practices.
The compound we deliver today draws on continuous hands-on experience. Every crystal, analysis, and batch record tells its own story, and each order reflects not just chemistry but years of incremental refinement and real-world collaboration.