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HS Code |
649283 |
| Cas Number | 372-39-4 |
| Molecular Formula | C6H5F2N |
| Molar Mass | 129.11 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.282 g/cm³ |
| Melting Point | 14-16°C |
| Boiling Point | 173-174°C |
| Flash Point | 68°C |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.535 |
| Pubchem Cid | 151002 |
| Smiles | c1cc(N)cc(F)cc1F |
As an accredited 3,5-Difluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 250g amber glass bottle labeled “3,5-Difluoroaniline,” features hazard symbols, chemical details, and a secure screw cap. |
| Shipping | 3,5-Difluoroaniline is shipped in tightly sealed containers, protected from light and moisture. It should be transported according to regulations for hazardous materials, typically under UN 2810 (Toxic Liquid, Organic, N.O.S). Ensure proper ventilation and labeling, and handle with gloves and eye protection to prevent exposure. Store separately from incompatible substances. |
| Storage | 3,5-Difluoroaniline should be stored in a tightly sealed container, away from light, heat, and sources of ignition. Store in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as oxidizing agents and acids. Ensure proper labeling and access to appropriate spill containment. Personal protective equipment should be available for handling accidental leaks or spills. |
Applications of 3,5-Difluoroaniline in Industrial ManufacturingAs a direct manufacturer, we supply 3,5-Difluoroaniline to key sectors where high-purity fluorinated aromatic intermediates shape advanced materials and specialty chemicals. Below, we detail core downstream applications based on proven industry practice, each with dedicated formulation standards, integration steps, and compliance requirements. 1. Agrochemical Active Ingredient SynthesisCrop protection formulators use 3,5-Difluoroaniline as a primary precursor for the synthesis of difluorinated phenyl-based herbicides and fungicides. Its electron-withdrawing fluorine atoms enable targeted modifications in new actives, increasing selectivity and metabolic stability in final agrochemical agents. Our manufacturing partners incorporate this intermediate under tightly controlled conditions to ensure batch traceability, minimize contamination risk, and precisely adjust functional group reactivity for patent-specific pesticide molecules. Industry compliance standards
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2. Pharmaceutical Intermediate ManufacturingRegulated pharmaceutical manufacturers employ this intermediate to assemble difluoroaryl structures in various small-molecule APIs, particularly for anti-inflammatory, oncological, and CNS drug categories. The precise fluorination of the aniline ring directly impacts bioavailability, metabolic pathway selectivity, and patentable novelty. Integration into GMP pharmaceutical synthesis requires strict impurity control, validated cleaning, and batch records to comply with international drug regulations. Our facility ensures full origin traceability and documentation to support submitted Drug Master Files (DMF) and investigational applications worldwide. Industry compliance standards
Typical usage ratio
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3. Specialty Polymer and Liquid Crystal Material ProductionManufacturers in the electronics and advanced coatings sectors deploy 3,5-Difluoroaniline as a functional monomer for specialty polyimides and aromatic ethers. The difluoro units impart increased dielectric stability, thermal endurance, and resistance to ion migration—crucial for liquid crystal displays, flexible OLED substrates, and high-reliability electronic films. Precise molarity control in monomer preparation ensures material performance meets both end-use electronics reliability criteria and strict cleanroom purity requirements. Industry compliance standards
Typical usage ratio
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4. Dye and Pigment Intermediate in High-Performance ColorantsProducers of specialty dyes and pigments incorporate this difluoro-substituted aniline into nitro- and azo-dye synthesis. It advances the hue stability and lightfastness of finished products by reducing photooxidative decomposition. Such dyes are tailored for technical textile, industrial inkjet, and UV-curable printing markets, where regulatory and performance cross-checks demand strict lot consistency and regulatory-compliant trace impurities. We supply this intermediate with supporting CoA and impurity profiles aligned to end-user analytic protocols. Industry compliance standards
Typical usage ratio
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As a chemical manufacturer with years of hands-on experience, I believe every compound tells a story. 3,5-Difluoroaniline stands out not only on paper but in real-life production for its steady reliability and simple, straightforward reactivity. The chemistry behind this compound brings a layer of flexibility for innovation in both research and commercial settings. Our long-running commitment to both purity and consistency finds a reliable touchpoint in 3,5-Difluoroaniline, a product shaped as much by its users’ needs as by its molecular structure.
We designed our process to yield 3,5-Difluoroaniline in a way that goes beyond meeting numbers on a spec sheet. Consistency in melting point and GC purity is not just about compliance — it makes a difference in downstream synthesis. For typical shipments, our analytical data confirm GC purity regularly over 99%, water content below 0.2%, and minimal mono and trisubstituted byproducts. These values are not random; they are the result of process optimization over successive batches, careful raw material qualification, and control at every step from hydrogenation to work-up.
Chemists in the lab notice tiny variances that shift a reaction. One batch is off by a fraction, and new side products appear, or the reaction takes longer to finish. That’s why from reaction vessel maintenance to solvent selection, nothing is left to habit. Each lot carries our in-house batch number; its journey from raw material receipt to packed drum comes with a full trail of data. Our standard packaging runs from 25 kilogram drums to custom options for scale-up feasibility studies. Shelf stability has been tested up to two years in typical warehouse environments without loss of quality for the majority of applications.
Requests for 3,5-Difluoroaniline come from a broad set of industries. Some of our customers use it to develop agrochemical active ingredients – we see its two fluorine atoms at the 3- and 5- positions acting as electron-withdrawing groups, altering the reactivity for downstream functionalization. This isn’t just academic theory: small tweaks in the aromatic ring let chemists adjust the metabolic stability of molecules, fine-tuning how they work in the field. Pharmaceutical intermediates also pull from our inventory. We have seen 3,5-Difluoroaniline play a role in crafting fluorinated heterocycles and coupling reactions, taking advantage of its defined substitution pattern for clarity and specificity in SAR studies.
Other firms approach us for material used in dyes and pigments. Stability in color and performance in varied environmental conditions often starts with carefully chosen aniline derivatives. The placement of the fluorine atoms on the aromatic ring in this grade makes a difference in final product performance—less susceptibility to oxidation and no strange hues or unexpected decomposition even after long-term use. Each application comes back to fundamentals: purity, consistency, and clear analytical signatures that inform every run, trial batch, or scale-up.
I often get questions comparing our 3,5-Difluoroaniline to 2,4-Difluoroaniline or more traditional unsubstituted anilines. The analogy isn’t direct because the substitution pattern of the fluorines really does shape both the electron density on the aromatic ring and the selectivity in further reactions. For instance, 3,5-Difluoroaniline introduces a unique electronic effect. Fluorine at the meta position withdraws electrons differently than at ortho or para sites; this can favor certain coupling or acylation reactions and influence yields or byproduct profiles. In polymer research or the design of novel ligands, this subtlety means less second-guessing and more predictable results.
Compare this to monofluoroanilines, which retain more classic nucleophilicity and thus act up in some condensation or nucleophilic aromatic substitution reactions. Having two fluorine atoms in these positions opens up pathways for selectivity in halogen-lithium exchange when building up more elaborate chemical scaffolds. Multi-step routes benefit from lower reactivity of certain positions, giving chemists space to operate. More heavily fluorinated anilines tend to show even higher melting points and can be waxy solids, complicating processing, while our 3,5-Difluoroaniline remains manageable at room temperature and sits as a crystalline solid, making for easy weighing and dissolution.
Solubility is another topic that often gets overlooked until it matters. Users working with more substituted rings sometimes deal with hard-to-dissolve powders. Here, standard organic solvents like toluene, ethyl acetate, and dichloromethane pick up 3,5-Difluoroaniline with ease across research and production setups. This practical feature cuts down on fiddling and wasted man hours.
Our relationship with this compound isn’t theoretical. On production days, the smell—a sharp, distinctive aniline note with a hint of the familiar—but less persistent compared to classic anilines. Handling crystalline 3,5-Difluoroaniline is straightforward. It resists clumping, pours without static build-up, and dusting is less of a nuisance because the particle size sits in a practical middle range: not too fine to cake up filters, not too coarse to feel gritty in automated feeding lines.
Operators and lab techs quickly notice the difference. Less downtime cleaning clogged reactors. Fume hoods don’t get overwhelmed, and most spills scoop up fast without residue. We maintain MSDS and REACH-compliant documentation for our shipments, but we also train crews directly on site in every aspect of handling and spill response, because safety comes from more than paperwork.
Some customers spot a cheaper offer elsewhere, but the real cost shows up after the drum arrives. Impurities in aromatic amines result in more labor and waste after the reaction stage. We've spent years working out trace control, even for minute residual acids or solvents, because they don’t go unnoticed in follow-up chemistry. We run trace ionic and metals tests quarterly, not just to satisfy regulation, but to catch trends before they cause problems. Regular feedback from long-term partners tells us that this upstream diligence saves them cash and time.
A chain is only as strong as its weakest link. We trace every raw material batch, so knock-on effects don’t slip through the cracks. This means if there’s a transient impurity spike, we know before anyone else does, and can pull or retest drums before shipment. Unannounced audits from overseas customers never come as a surprise, because we face the same numbers every day ourselves.
Process engineers at our site have scaled 3,5-Difluoroaniline production from gram-level pilot batches up to metric ton lots without a hitch. Reproducibility between batches isn’t an abstract concept; it represents hours saved in troubleshooting and rework downstream. We have experience shipping custom volumes to support both early-stage R&D programs and full-scale continuous process runs. As researchers push boundaries in the pharmaceutical, agrochemical, and materials sectors, our production methods keep pace. Modern reactor controls automate addition, sampling, and temperature profiles, but experienced operators catch deviations far earlier than the best instrument can.
From a manufacturing standpoint, minimizing exposure of fresh product to atmospheric moisture and oxygen improves both the handling and shelf life of 3,5-Difluoroaniline. We store the compound under inert gas during transit between steps and pack under nitrogen. After years testing stability in various packaging, we shifted from older lined drums to new HDPE variants—delivering better product integrity after weeks on the ocean or months in storage.
Concerns about sustainable production and safety drive regular updates to our manufacturing practices. We recover and recycle solvents from every batch, reducing environmental load as well as operating cost. Energy usage is tracked and steadily improved. We’ve worked to reduce process waste by implementing closed-loop purification and more effective filtration that cuts down on solid disposal.
Our team regularly updates process documentation to reflect global compliance needs—not just to secure a shipment, but to ensure every employee can trace what happens at each stage, and why. This builds trust with regulators and keeps us ahead of new legislation, particularly for aromatic amine emissions and waste handling. We keep an open-door policy with local regulators, which means fewer surprises and more constructive, forward-thinking improvements on both ends.
Feedback from synthetic chemists, development scientists, and process engineering teams has shaped our product development. Requests for improved color or stricter impurity limits drove us to overhaul filtration steps, switch to food-grade HDPE liners, and implement more liberal sampling for homogeneity checks. Requests from academia prompted us to adapt kilogram-scale packaging without raising cost, supporting groups running multiple experiments in parallel. Whether defining new standards for coupling reactions or simply clearing up documentation, we translate customer challenges into process changes—because our jobs don’t finish once drums leave the plant.
We regularly receive direct data from formulation labs, reporting how batches perform in their unique applications. These field reports guide us in tightening specs where it actually counts. If a pigment developer sees off-profile fading after accelerated testing, we know it before mass distribution starts. If a pharma group raises a flag on minute N-alkyl byproducts, QA gets to work on new protocols.
Years of collaboration teach that most problems come not from the molecule itself, but from unnoticed micro-variables: tank contamination, aging of storage vessels, variable seal integrity in packaging, or even small shifts in analytical calibration. Keeping a dialog open helps us work towards solutions that matter on the ground.
Manufacturing is not just routine repetition. Each process run brings fresh variables. Solvent supply may vary between lots. Sometimes weather or humidity shifts during key steps. We integrate new analytical technologies as they prove their worth—faster HPLC methods, automated NMR runs. We also believe in people. Many of our operators started as apprentices years ago; their hands-on familiarity with not just 3,5-Difluoroaniline but all its analogues means subtle problems get flagged fast.
Every new challenge—a different impurity profile, a request for a more restrictive residual solvent specification—pushes us to adapt. We document every process tweak, keep training up to date, and see robust internal debate on trial runs. Mistakes happen, and we treat them as lessons rather than setbacks. This honest learning culture leads to superior batches with fewer surprises for our customers.
Having the direct link between production floor and application chemists brings practical benefits. Issues get solved in real time. Technical questions reach operators and lab analysts who’ve handled the product in all its forms, not just sales staff or resellers downstream. Understanding what happens after a drum leaves our warehouse builds our process knowledge as much as QC data.
Customers who engage early in their project planning share the specifics of an intended reaction or formulation. This partnership lets us preempt possible issues, whether it’s solubility in a new solvent blend or compatibility with other intermediates. Pre-shipment test samples, custom packaging, or split shipments—all these grow out of two-way conversations, not mass-market guesswork.
The demand for high-purity fluorinated intermediates continues to grow. More researchers recognize how the right substitution pattern on aniline affects not just reactivity but downstream safety, pharmacokinetics, and even regulatory profiles. Our role as a manufacturer goes beyond the drum—offering a platform for innovation and creative synthesis. By staying ahead in process control, traceability, and end-user support, we help push boundaries in what makers, researchers, and industrial chemists can accomplish.
Sharing years of insight, working with real people, and adapting to new scientific frontiers keeps manufacturing rewarding. 3,5-Difluoroaniline is just one piece in the larger puzzle, but it is a piece we know well. Chemistry is built as much on practice as on theory; manufacturing brings that into sharp, practical focus.