|
HS Code |
697208 |
| Cas Number | 398-61-0 |
| Molecular Formula | C8H9FO2 |
| Molecular Weight | 156.16 g/mol |
| Iupac Name | 1-fluoro-2,3-dimethoxybenzene |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 211-213°C |
| Density | 1.140 g/cm3 |
| Melting Point | -17°C |
| Flash Point | 85°C |
| Refractive Index | 1.503 |
| Smiles | COC1=C(C=CC(=C1OC)F) |
| Solubility In Water | Practically insoluble |
| Synonyms | 1,2-Dimethoxy-4-fluorobenzene; 4-Fluoro-1,2-dimethoxybenzene |
As an accredited 1,2-Dimethoxy-4-Fluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 1,2-Dimethoxy-4-Fluorobenzene, tightly sealed, labeled with chemical name, formula, and warnings. |
| Shipping | 1,2-Dimethoxy-4-Fluorobenzene should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport in accordance with local, national, and international chemical regulations. Label as a chemical substance and handle with care. Ensure appropriate safety documentation, including SDS, accompanies the shipment, and avoid contact with strong oxidizing agents during transport. |
| Storage | Store **1,2-Dimethoxy-4-Fluorobenzene** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Clearly label the container, and access should be limited to trained personnel. Follow all appropriate safety protocols and local regulatory requirements for storage of organic chemicals. |
Applications of 1,2-Dimethoxy-4-Fluorobenzene in Industrial Manufacturing1,2-Dimethoxy-4-Fluorobenzene serves as a key intermediate in specialized organic synthesis due to its unique substitution pattern, which imparts targeted reactivity for downstream manufacturers. The following sections illustrate specific, authenticated downstream industrial applications where this raw material delivers distinct utility, focusing on ingredient ratios, compliance, technical integration, and the scope of finished products. 1. Active Pharmaceutical Ingredient (API) Synthesis: Fluoroarene Scaffold ConstructionPharmaceutical manufacturers leverage this compound as a crucial building block in the synthesis of selective serotonin reuptake inhibitors (SSRIs) and related CNS-active molecules. Its precise placement of methoxy and fluoro groups provides a route to fluorinated aromatic scaffolds, enabling medicinal chemists to modulate drug metabolism and targeting profiles. The compound enters multi-step routes after initial halogenation, dictating final molecule structure and pharmacokinetics for regulatory submission. Industry compliance standards
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2. Agrochemical Intermediate in Herbicide and Fungicide SynthesisMajor crop protection companies employ this compound as a functionalized aromatic starting point for the development of novel fluoro-containing herbicides and fungicides. Its electron-rich nature and substitution enable targeted halogenation, alkylation, or methylation reactions essential for tuning bioactivity against plant pathogens or weeds. Integration occurs prior to ring closure or heterocyclization in production lines focused on selectivity improvement for regulatory acceptance. Industry compliance standards
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3. Liquid Crystal Material Synthesis for Display TechnologySpecialty chemical manufacturers for advanced display segments utilize this compound as an electronic donor component in custom-designed liquid crystal mixtures. Its specific substitution allows for precise control of dielectric anisotropy and viscosity, supporting liquid crystal alignment and rapid switching essential for high-resolution, energy-efficient flat-panel displays. Manufacturers introduce this material during the pre-formulation of nematic or smectic base mixtures under inert gas to safeguard purity for ISO-certified flatscreen products. Industry compliance standards
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4. Fine Chemical Intermediate for Fluorinated Aroma CompoundsProducers of specialty aroma and flavor compounds employ this benzene derivative to construct fluorinated aromatics that impart unique notes and performance in consumers’ fragrances and flavors. The electron-rich and fluorinated profile allows for specific cross-coupling, etherification, or oxidation sequences directed at producing stable, heat-resistant volatile blends meeting contemporary safety requirements. The compound is introduced upstream, supporting controlled downstream tailoring for GC/MS-verified signature aromas. Industry compliance standards
Typical usage ratio
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In the chemical manufacturing business, trust in your raw materials forms a foundation that impacts every downstream process. Over the years, working with 1,2-Dimethoxy-4-Fluorobenzene, also known in our workshops as DMFB, has driven that point home for our team. The demand for this compound comes not just from its chemical structure, but from the reliability it brings to complex organic synthesis. Many of our partners in pharmaceuticals and advanced materials ask for DMFB by name, and for good reason: its specific profile makes it stand out among substituted benzenes.
We produce DMFB with a focus on high-purity grades, ensuring a consistent batch-to-batch experience. Chemists recognize 1,2-Dimethoxy-4-Fluorobenzene for its structure, combining two methoxy groups with a fluorine on a benzene core. This combination plays a key role in how the molecule behaves. Taking a closer look, the methoxy groups activate the aromatic ring for further substitution, while the fluorine delivers electronic influence that isn’t easy to replicate with other substituents.
Each batch leaves our plant as a clear, colorless liquid with a defined aromatic odor and a boiling point range our laboratory has measured and confirmed for years. The chemical community has catalogued the melting and boiling points, but what matters most to our technical team is matching real-world experience with the numbers. No surprises, no hidden impurities—our process remains open for customer audits and third-party verification.
We have seen steady requests from medicinal chemistry and crop science firms using DMFB as a starting point for synthesizing more complex targets. The electron-donating methoxy groups and the electron-withdrawing fluorine combine to provide a reactivity profile that others can’t quite match. This matters when projects hinge on controlling selectivity in aromatic substitution or tuning the electronic nature of intermediates. One client in the pharmaceutical sector told us the compound shaved weeks off a key route because they could dial in regioselectivity without juggling multiple intermediate steps.
That kind of feedback underlines something we see each day. The rise in demand for fine chemicals with fluorinated aromatics tracks with innovation across drug discovery, advanced polymers, and materials science. Our reaction vessels have seen countless fluorinated intermediates pass through them, but our team keeps coming back to DMFB when the challenge calls for high selectivity and reliable downstream chemistry. It's more than a matter of specification—it's about reproducibility and minimizing wasted runs.
Talk to the synthetic chemists and process engineers on our team and they’ll tell you, it’s easy to underappreciate the nuances of DMFB until you work with comparable compounds. Let's take 1,2-dimethoxybenzene as an example. With no fluorine in its structure, it behaves differently in electrophilic aromatic substitution and coupling reactions. Add the fluorine, and suddenly the reactivity toward nucleophilic aromatic substitution opens up, offering new openings for downstream reactions.
Chemists also reach for DMFB over 4-fluoroanisole or 2,5-dimethoxyfluorobenzene when positional selectivity matters. Each substitution pattern on the aromatic core influences both electronic effects and steric availability. During process optimization, we saw that switching to DMFB increased yields on certain Suzuki-Miyaura couplings where less hindered isomers struggled with conversion. Since our batches consistently meet needs for purity and trace-metal content, customers rarely need to stop and clean up side-products that sometimes plague alternative routes.
Upstream, many of the substituted benzenes we’ve produced have seen problems with stability or purity when exposed to certain process conditions. Through careful distillation and controlled atmospheres in our reactors, we repeatedly confirmed DMFB remains stable during both storage and reaction—even across multi-step syntheses. This stability reduces both lead times and on-site headaches for our customers.
In our plant, one can see 1,2-Dimethoxy-4-Fluorobenzene moving from bulk storage to precise dosing in both contract manufacturing and R&D batch production. The destinations? More advanced fluorinated building blocks, library compounds for pharmaceutical discovery programs, and intermediates for crop protection agents.
Pharmaceutical groups working on CNS-active molecules and anti-cancer scaffolds have requested this specific compound for its ability to introduce both electrons and fluorine into aromatic cores without resorting to more complicated protecting group strategies. Modern agrochemicals also tap into the unique electron balance of DMFB, seeing value in how the molecule’s profile influences both synthesis and environmental behavior.
Our engineering teams documented a marked reduction in reaction times for specific Buchwald-Hartwig and Ullmann coupling reactions using DMFB. Where traditional fluorinated aromatics required higher temperatures or longer dwell times in reactors, DMFB frequently streamlines those steps. This has cut energy usage and improved plant safety by lowering the time spent at high temperatures. Every step that improves efficiency without sacrificing quality gets noted here, from the lab scale up to full production campaigns.
Our roots as a chemical manufacturer go back decades. In that time, we’ve seen every possible sourcing and logistics bottleneck—from feedstock volatility to supply chain disruptions. These experiences shaped a procurement policy centered on reliability and control, especially for specialty aromatics like DMFB.
By investing in reactor capacity and analytical capabilities, we can respond to spikes in demand that pop up every time a major customer advances their project. On-site GC-MS, NMR, and HPLC keep batches in specification before they ever leave our gates. Our operators know that contamination at parts-per-million often spells failure for high-value synthesis, and we take extensive steps to avoid that. Internal protocols include routine checks for isomer content and trace metal contamination—each grounded in the sorts of challenges we faced scaling the product for real-world production.
Complaints about batch variation or handling problems don’t stick around for long on our shop floor. Our technical team remembers early process runs where a seemingly minor shift in temperature or catalyst made for a hard-to-purify side product. The answer wasn’t a one-size-fits-all fix; instead, it took careful in-process monitoring, refined distillation, and honest feedback from customers. Over time, that direct feedback loop fed into today’s process control logic, making DMFB one of the more robust products we run.
Anyone who’s worked on the shop floor in chemical manufacturing learns one lesson quickly: documentation only matters if your colleagues trust the safety controls in place. 1,2-Dimethoxy-4-Fluorobenzene, like many aromatic ethers, requires careful handling. We’ve enforced closed transfers, dedicated PPE, and rigorous ventilation in our own plant long before outside standards caught up. On site, every shift team gets safety updates on new findings in the literature—practical advice drawn from real incidents and near-misses, not just from manuals.
Environmental management matters here, too. Our waste and emissions controls draw on years of on-the-ground troubleshooting. Instead of batch-neutralizing spent DMFB or worrying about open air emissions, our plant routes residues and wash streams through closed-loop recovery and thermal treatment. This isn’t about box-checking; minimizing environmental impact supports both local community health and long-term business stability. Calls from regulatory agencies and neighbors confirm that a proactive approach pays off in trust.
New entrants to the market bring a range of substituted benzenes advertised with a focus on cost or “universal application.” What our technical partners care about, though, is dependability at scale—consistent product, smooth process, and transparent data. For us, high-purity DMFB delivers this. We exclude off-spec batches before they reach packaging, documenting every deviation and every corrective step internally. Over time, fewer surprises show up, and our teams rest easier knowing that end-users aren’t spending overtime fixing impurities or batch-to-batch inconsistencies.
Working with many multisite R&D teams has taught us how tiny differences in product quality translate into massive headaches in route scouting, or worse, full-scale campaigns stopped by column fouling or unplanned rework. It is routine for customers to send comparative feedback about materials sourced elsewhere—they notice differences in color, purity on NMR, and ease of dissolution. DMFB from our plant consistently rates high for clarity and reproducibility, translating directly to cost savings and confidence in further applications. We don’t take that lightly; our reputation rides on every drum that goes out the door.
Even in academic and early-stage research, details make all the difference. Because of its substitution pattern, DMFB serves as a workhorse for constructing more complex, functionalized aromatics. The challenge usually comes when moving from milligram scale to kilograms or more. Our technical support teams have advised on dozens of process transfers where an R&D group moving to pilot scale needed insight on solvent choices, impurity profiles, or isolation techniques. We share our own plant findings—what works, what doesn’t, how process tweaks at scale bear out long-term safety and cost implications.
For contract manufacturing partners, the story gets more complicated as throughput and reproducibility start to matter more than theoretical yield percentages. We’ve streamlined our QC workflows to make release testing fast and transparent, without hidden delays or vague explanations for out-of-spec results. Materials supply is only as good as the people who stand behind it; our chemists and engineers take pride in their direct line to customer labs and project managers, offering real advice honed by mistakes, fixes, and successes over generations.
Changing industry dynamics drive us to find better, cleaner, and more sustainable ways to manufacture fluorinated aromatics. In the early days, DMFB production sometimes led to more waste alongside the product. Lessons learned drove significant upgrades in catalyst recovery, solvent recycling, and batch scheduling. By now, our solvent plan focuses on reusability and minimal residue—a far cry from the throwaway mindset that marked earlier years in the chemical industry.
Our R&D collaborations remain a major source of new insight. Projects in green chemistry and flow processing increasingly lean on DMFB because it’s easy to incorporate in modular syntheses while still allowing downstream complexity. Reactions that once took hours now finish in a fraction of the time, with less energy and lower risk of side reactions. A critical part of improving the industry’s footprint involves supporting these projects not just with product, but with real-world knowledge about process robustness and reduction in waste.
Our team’s experience tells us that the best solutions come from dialogue—months, sometimes years, spent in partnership with customers exploring new process routes or fixing hard-to-isolate impurities. We keep our technical documentation open and encourage feedback about anything our partners encounter in their own labs. Mistakes turn into learning only if there’s transparency. Our longest-running customers tend to be the ones who value that, just as we do.
DMFB sits at the intersection of reliability and versatility in organic chemistry. For many customers, a successful project comes down to predictability: will every shipment meet their standards, will process scale-up stay headache-free, will unusual side-products slow down discovery or production pipelines? Our business—our reputation—rests on answering those questions with confidence and experience.
Over the years, we’ve changed or improved nearly every step in our process for producing 1,2-Dimethoxy-4-Fluorobenzene by listening to the daily realities faced by chemists at the bench and engineers at the plant. From our first batches to our current production volumes, we have seen how quality, transparency, safety, and long-term partnerships keep this compound at the core of countless successful syntheses. As demand for high-purity aromatic building blocks grows, our approach remains grounded: do the work, keep standards high, and never lose sight of the real outcomes for our customers.