|
HS Code |
543171 |
| Iupac Name | 3,5-Difluorobenzaldehyde |
| Molecular Formula | C7H4F2O |
| Molecular Weight | 142.10 g/mol |
| Cas Number | 1013-63-0 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 188-190°C |
| Melting Point | 5-7°C |
| Density | 1.322 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 77°C |
| Smiles | C1=C(C=C(C=C1F)F)C=O |
| Refractive Index | 1.545 |
| Pubchem Cid | 156184 |
As an accredited 3,5-Difluorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle with a secure screw cap, labeled “3,5-Difluorobenzaldehyde,” with hazard and safety details. |
| Shipping | 3,5-Difluorobenzaldehyde is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be packed according to hazardous material regulations, typically under UN Hazard Class 6.1 (toxic substances). Ensure containers are clearly labeled, handled with suitable protective equipment, and accompanied by appropriate safety documentation during transit. |
| Storage | 3,5-Difluorobenzaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from moisture, direct sunlight, and heat. Store at room temperature and ensure proper labeling. Use appropriate chemical storage cabinets if available, and follow local regulations for hazardous chemicals. |
Applications of 3,5-Difluorobenzaldehyde in Industrial Manufacturing3,5-Difluorobenzaldehyde serves as a critical intermediate in advanced pharmaceutical synthesis, agrochemical production, fine chemical processes, and specialty material manufacturing. Its dual fluorine substitution pattern delivers distinctive reactivity, supporting multiple industrial value chains demanding high purity and consistent lot performance. 1. Active Pharmaceutical Ingredient (API) SynthesisOur material is widely used in the early-stage synthesis of complex APIs, including novel anti-infective agents and oncological therapeutics, where fluorinated aromatic building blocks are essential. It participates in structurally defining steps through condensation or coupling, influencing activity, bioavailability, and final compound metabolic profiles. Development and commercial production rely on validated GMP or Q7-compliant processes. Our production ensures reliable access and uniformity for multi-batch clinical and large-scale campaigns. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Intermediate ProductionThe compound enables synthesis of next-generation herbicidal and fungicidal agents, particularly those leveraging fluorine for environmental persistence and bioactivity. Upstream integration delivers high-purity intermediate lots for later formulation with diverse R-groups. Our supply supports both pilot process optimization and bulk agrochemical manufacturing for regulated markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Liquid Crystal Monomer SynthesisIn the specialty display materials sector, this raw material plays a pivotal role as a precursor in the production of difluorinated biphenyl or phenylbenzoate monomers for liquid crystal applications. Industrial processes selectively functionalize via formyl reactivity, shaping molecular order and dielectric properties demanded in advanced panel fabrication. Our clients rely on well-defined isomer ratios and purity for stable optical and electronic performance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Advanced Polymer Modifier ProductionThis compound acts as a functional modifier for fluorinated engineering polymers. Selective oxidation or cross-coupling installs aromatic aldehyde motifs, which enhance polymer chain rigidity, thermal resistance, or processability. Our production supports downstream companies in high-value electrical, electronic, and filtration materials markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Fine Chemical and Fragrance Intermediate ManufacturingWithin the fine chemical sector, producers use this intermediate for the controlled synthesis of perfumery aldehydes or functional aromatics, especially those demanding site-specific difluoro incorporation. Manufacture of such downstream intermediates requires precise stoichiometry and in-process analytical QC, supported by our material’s color and impurity profile consistency. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3,5-Difluorobenzaldehyde prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Chemical manufacturing anchors itself in accuracy—both in process and in the purity of what leaves our reactors. 3,5-Difluorobenzaldehyde sits among those select specialty chemicals where a small shift in substitution grants significant advantages. We prepare and ship this aldehyde in line with tighter controls compared to basic monofluorinated analogs, delivering a product marked by a two-fluorine signature that’s evident across its performance profile in downstream transformations.
Cultivating a stable supply chain for fluoro-aromatics means not cutting corners. Our operational journey with 3,5-difluorobenzaldehyde began by partnering with process chemists pushing for consistent outcomes in challenging reactions. Handling difluorinated compounds brings extra hurdles—from fluorination safety protocols to the arrangements in glassware that resist halogen degradation over multiple runs. By refining batch purification steps and investing in multi-stage distillation, we keep typical impurity levels low and recover high yields with each campaign. Analytical checkpoints—GC, NMR, and moisture content tested every lot—allow us to release material that serves both lab scale and production expansion without nasty surprises.
Our 3,5-difluorobenzaldehyde matches the structural formula C7H4F2O, a clear pale-yellow liquid or crystalline solid, depending on ambient temperature and storage cycle. We have converged on specifications where assays run over 99%, and residual moisture and acidity remain minimal. Each delivery arrives in thick-walled amber glass to shield sensitive aldehydes from stray UV and oxidation, which help maintain a long shelf life past a typical fiscal year. We gravitated toward these details after hearing from teams whose work fell apart from slow trace degradation during storage and transit. By anchoring our shipping protocols to observed failure points, we have carved out confidence in every bottle that moves from our loading dock to the customer’s bench.
Chemists working with benzaldehydes quickly notice the difference between ortho-, meta-, and para- substitution. Adding fluorine at the 3 and 5 positions creates an electron distribution that behaves much differently from 2,4-difluoro- or unsubstituted benzaldehyde. Functional group tolerance in oxidative couplings, for example, improves because the deactivating effect slows down unwanted side reactions. In pharmaceutical R&D, this precision matters when tuning reactivity or seeking consistent intermediate purity. Our own teams adopted 3,5-difluorobenzaldehyde as a test bed, running head-to-head trials against mono- and di-substituted cousins. Yields, melting points, and byproduct profiles consistently showed an edge for the two-fluorine setup when softer nucleophiles or sensitive amines appeared in the workflow. This opens doors for scale, wasted hours drop, and downstream isolation becomes far more straightforward.
Other benzaldehydes in the catalog—whether bearing chlorine, single fluorines, or bulkier electron-withdrawing groups—deliver value in their contexts. Yet few compounds bridge the aromatic reactivity window the way 3,5-difluorobenzaldehyde does. That’s the finding echoed by customers engaged in everything from liquid crystal synthesis to sharply tuned pharmaceutical intermediates. The balanced electron profile of our product delivers resilience to oxidation and shelf stability, while its purity provides a platform that doesn’t leave you guessing about side impurities or variable response with catalysts.
Producing and handling aromatic aldehydes always brings safety and environmental stakes to the table. With difluorinated series, volatility and inhalation risk raise further concerns. We set up our plant lines to minimize ambient loss: closed reactor trains, double-vented containers, and real-time air sampling by in-plant EHS techs. Community trust depends on careful waste stream handling, especially since fluorinated byproducts persist in water and soil environments. For every extraction run, scrubbers and acid quench tanks operate in parallel with emission logs tracking each filtration and phase separation batch. The difference isn’t just regulatory; it’s about maintaining a social license with those living next to our facilities.
Greener approaches to fluorination and waste minimization have gained traction across specialty chemicals. While traditional routes have leaned heavily on selectfluor or DAST in halogenation, more sustainable oxidative procedures and flow chemistry setups have let us cut down on reagent excess and energy footprint. Adopting alternatives is not a matter of keeping up with buzzwords but of sustaining access to skilled operators and keeping insurance costs manageable. Our commitment runs through continuous process reviews, staff training, and direct dialogue with research groups who wind up running scale-outs years after our first production run.
Synthesis chemists bring a pragmatic eye to the bench. Rarely do they want another variable complicating a scale-up. Our usual contact starts with a request for precise material information—certificate of analysis, impurities, shelf life, the works. But after that, the focus shifts: Will this aldehyde hold up in high-throughput screening? Can it stand a two-step condensation followed by Grignard or Wittig work without generating ghosts in LCMS? Over repeated cycles with process partners, what we noticed was that 3,5-difluorobenzaldehyde held tight under cross-coupling and condensation protocols, where mono-fluorinated or chlorinated benzaldehydes stumbled with batch-to-batch purity shifts.
Pharmaceutical groups tell us they see less need for extensive pre-purification, allowing teams to move directly into amine condensation or heterocycle-forming sequences. Each hour saved on column or distillation translates to dollars kept in-house and fewer headaches during regulatory signoff. Agrochemical firms point toward the reduced risk of over-reaction during heteroatom incorporation—another trait unique to the 3,5-fluorine motif.
Academic groups, working at the front line of discovery, depend on documented batch homogeneity. Many have flagged how fine distinctions in fluorine placement alter both NMR signals and downstream reactivity, affecting everything from analytical clarity to reproducibility in catalytic applications. Across feedback cycles, chemists stress that stable purity, packaging, and honest dialogue about what’s in each bottle matter more than any downloadable product spec sheet.
Our own internal R&D team treats 3,5-difluorobenzaldehyde as more than an intermediate. Screening reactivity trends and new fluorinated building blocks starts here. During recent exploratory work, we fed 3,5-difluorobenzaldehyde through novel cross-coupling—both Suzuki-type arylation and modern copper-catalyzed protocols—watching for unanticipated byproduct formation or yield dips. This hands-on approach shows the real-world backbone of chemical manufacturing, not lost in paperwork or buzzword abstraction.
Structural reliability over repeated syntheses lets us adapt to shifting customer demands, such as scaling up to pilot plant runs or small kilo-lot production for pharmaceutical and materials companies. Equipped with real process feedback, we tweak upstream fluorination and downstream aldehyde isolation when a trend—higher water content, for instance—creeps in. We have found, time and again, that early investment in characterization, from multi-nuclear NMR through to HRMS and GC-FID, pays out in trust, not just cost savings.
Every successful lot of 3,5-difluorobenzaldehyde that leaves our site carries lessons from collaborative troubleshooting. If a customer flags a drifting melting point or unexpected color change, our technical support team audits not just batch records, but every touchpoint—from flask cleaning through to bottle cap torque. Adjusting protocols and raw material sourcing follows from these deep dives. It’s how the product found its current balance of purity, stability, and cost.
We partner with global companies and smaller start-ups alike. These relationships often involve exchanges of in-process data, which helps both groups anticipate challenges in reaction optimization or scale-up. Open lines mean both sides share in the upside of improved manufacturing, whether it’s reduced solvent use or more robust isolation techniques.
This compound’s demand cuts across sectors. In pharmaceuticals, it serves as a synthon for fluorinated benzyl alcohols, hydrazones, and various heterocycles. In crop protection, the molecule lands as a backbone in new active ingredients, often leveraging fluoro-aromatic scaffolds to hit modern regulatory and biological targets. In advanced materials, the impact shows up in the world of liquid crystals and specialty polymers, where the electron-withdrawing power of two meta fluorines supports reliable downstream functionality. For research labs, the compound behaves as a versatile entry point—reactive, selective, and consistent—supporting new catalyst discovery, metal-organic frameworks, and custom dye synthesis.
Some users lean on predictable reactivity, some prioritize ease of purification, others focus on regulatory paperwork. What unites all users is a pressing need for batch-stable, contamination-free chemicals. Substitution patterns like 3,5-difluorination minimize side-product formation in oxidation and condensation reactions, streamlining project timelines and easing up the regulatory signoff that often bogs down late-stage programs.
Producing aromatic aldehydes on scale can grind to a stop from unexpected shelf instability if oxygen or light find their way into the container. We have set up dry pipelines, revised our glass selection, and now routinely add a tight margin to our fill weights so customers don’t experience shortfall from slow evaporative losses.
Discussions with purchasing teams have opened our eyes to evolving raw material costs, which impact specialty intermediates like difluorinated aromatics. By securing multi-year supply agreements and directly sourcing fluorination reagents, we smooth out cost spikes. Over the last couple of years, the broader industry saw price pressure on fluorinated compounds linked to upstream raw material shortages, but reliability in shipment pushed us ahead of global disruptions. We believe close relationships with both upstream and downstream partners cement long-term resilience in the supply chain.
Maintaining transparency with every batch—whether that’s through open batch records or expanded trace impurity analysis—fosters customer trust. We see less product returned, fewer disputed invoices, and quicker onboarding for structural changes in our production lines. These small victories accumulate, translating to time saved, risk avoided, and teams freed up to invent the next molecular breakthrough.
The people handling 3,5-difluorobenzaldehyde matter as much as any reactor or tank. From reactor charging through packing bottles for shipment, every operator sees basic training but also ongoing refreshers in handling hazardous materials. Aldehyde fumes—especially fluorinated derivatives—demand reliable hoods, monitoring, and a practiced response to minor leaks or spills. Our protocols extend beyond plant gates through regular community drills and emergency planning with local agencies, giving both operators and neighbors a direct voice in facility operations.
Equipment upgrades—designed flushing, real-time vapor detection, and a robust maintenance plant—cut downtime and protect staff health. Regular feedback from technical operators often drives investments that don’t show up on spreadsheets but do show up as line reliability and low turnover. Skilled operators, empowered to flag unsafe conditions or suggest procedural tweaks, benefit not just our workplace but customer outcomes, as quality control runs upstream from finished bottle to raw material drum.
Looking past the immediate—hundreds of grams or a drum shipment—chemists increasingly see difluorobenzaldehydes as a way to probe deeper reactivity. Many routes in medicinal chemistry exploit the two-electron-withdrawing fluorine groups to drive condensation, cyclization, or electrophilic activation without heavy metal catalysis. Modifying this parent core grants further access to chiral centers or fluorinated building blocks. New polymer development programs have leveraged the resilience of 3,5-difluorinated scaffolds to tune thermal, chemical, and optical properties, often outpacing legacy materials on cost and performance. What’s clear after thousands of bottles produced: well-characterized, reliable intermediates anchor programs where every small detail can mean progress or a roadblock.
Fluorinated aromatics, and particularly 3,5-difluorobenzaldehyde, continue to see expanded usage as regulatory trends favor selective, less reactive, and environmentally considerate chemistry. Our direct connections with evaluation labs and innovation hubs spill over into custom support, tailoring purification or packaging when a new regulatory barrier or supply chain pinch arises. Through steady conversation with researchers and production leads, the product itself evolves—becoming more than just an intermediate on a list, but a versatile tool recognizing the unpredictability and ambition driving modern chemical development.
Production of specialty organofluorines will only grow more demanding as regulations tighten, and new applications emerge. Our commitment draws from the deep well of accumulated operational experience, shaped equally by hands-on batch work, customer feedback, and evolving best practices. Continuous investment in process intensification and greener fluoro-chemistry supports not only stable supply for existing partners, but also delivers resilience against market and regulatory shocks.
Through all stages—development, manufacture, testing, and support—our goal stays simple: reliability in supply, consistency in quality, and responsiveness to customer needs. Whether a customer runs a small discovery batch or a multi-ton production campaign, the assurance that each delivery matches expectations cements long-term partnerships. Every improvement, every adaptation to process or market shifts, comes from the synthesis of experience—ours in the plant, and our customers at the bench or on the production floor.
Pragmatism, not polish, defines daily operations. We measure success not in abstract metrics, but in stories from chemists whose projects move forward, thanks to a steady, predictable supply of 3,5-difluorobenzaldehyde. This compound’s unique substitution pattern, practical handling attributes, and established track record across diverse industries set it apart from competitors. We’ll keep refining, listening, and supporting the work of teams that trust us to get their chemistry right, batch after batch.