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HS Code |
110457 |
| Cas Number | 403-15-6 |
| Molecular Formula | C6H7N2F |
| Molecular Weight | 126.13 |
| Iupac Name | 2,4-diamino-1-fluorobenzene |
| Appearance | Light yellow to brown solid |
| Melting Point | 55-58°C |
| Solubility In Water | Slightly soluble |
| Pubchem Cid | 94746 |
| Synonyms | 2,4-Fluorobenzene diamine |
| Smiles | C1=CC(=C(C=C1N)F)N |
| Inchi | InChI=1S/C6H7FN2/c7-4-1-2-5(8)6(9)3-4/h1-3H,8-9H2 |
As an accredited 2,4-Diaminofluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A sturdy, amber glass bottle containing 25 grams of 2,4-diaminofluorobenzene, clearly labeled with hazard warnings and chemical information. |
| Shipping | 2,4-Diaminofluorobenzene should be shipped in tightly sealed containers, protected from light and moisture. It must comply with relevant regulations for hazardous materials, ensuring proper labeling and documentation. Avoid extreme temperatures and physical damage. Transport by road, air, or sea must follow local and international chemical shipping guidelines to ensure safety. |
| Storage | 2,4-Diaminofluorobenzene should be stored in a tightly closed container, away from light, moisture, and incompatible substances like strong oxidizers. Keep it in a cool, dry, well-ventilated area, ideally in a flammables cabinet. Ensure proper labeling and restrict access to authorized personnel. Use secondary containment to prevent spills, and store away from food, drink, and animal feed. |
Applications of 2,4-Diaminofluorobenzene in Industrial ManufacturingAs a specialized manufacturer, we supply 2,4-Diaminofluorobenzene to chemical industries with strict process requirements. This compound serves as a key intermediate in advanced material synthesis, supporting production lines that prioritize regulated quality control and reproducibility. Below, we detail established downstream applications, highlighting critical compliance standards, formulation specifics, integration points, and the resulting finished products demanded by end-use markets. 1. Pharmaceutical API Intermediate SynthesisPharmaceutical companies utilize this material as a core intermediate during the multi-step synthesis of select active pharmaceutical ingredients, mainly where precise structural modification is essential for function. The aromatic amine structure enables targeted reactions in API manufacturing pipelines, facilitating pathway-selective modifications while adhering to stringent process and documentation controls during intermediate stages. Industry compliance standards
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2. Agrochemical Formulation IngredientFormulators of herbicides and related agrochemicals select this raw material for incorporation into molecular frameworks designed to provide high selectivity in crop protection agents. It supports pathways where electron-rich aromatic amino groups are required for further chlorination or fluorination, impacting the bioactivity and environmental persistence of the finished agrochemical product. Industry compliance standards
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3. High-Performance Dye Intermediate ManufactureSpecialty dye manufacturers employ this raw material in the synthesis of fluorinated azo and anthraquinone colorants, where incorporation of both amino and fluorine groups enhances chromophore stability and brightness under harsh processing conditions. Its controlled reactivity allows for fine-tuning of shade and light fastness in target pigment structures, critical for technical textile and polymer coloration. Industry compliance standards
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4. Specialty Polymer Fine Chemical Building BlockProducers of advanced specialty polymers integrate this aromatic diamine during the pre-polymerization stages to introduce defined substituents that modify polymer backbone flexibility, chemical resistance, and interaction with fillers or reinforcing agents. The presence of both amino groups and a fluorine atom provides designers with functional diversity to engineer specific polymer performance attributes for demanding technical applications. Industry compliance standards
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5. Electronic Material Intermediate for PhotoresistsManufacturers of advanced photoresist systems for semiconductor fabrication use this compound as a fine chemical precursor to engineer novel fluorinated moieties into diazo-based photoactive matrices. Its reactivity supports tight molecular weight distribution and functional group placement, directly influencing lithographic performance and etching resistance needed in next-generation transistor and MEMS device processing. Industry compliance standards
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As direct producers of 2,4-diaminofluorobenzene, we put a great deal of attention into every batch leaving our reactors. The core appeal of this aromatic amine lies in its molecular structure—two amino groups at the 2 and 4 positions and a fluorine atom at the 1-position. This layout creates a unique reactivity, making it a preferred choice in downstream synthesis, especially where selectivity and reliability matter. From our point of view, what stands out is how this compound streamlines development paths for key intermediates used in pharmaceuticals, agrochemicals, and advanced materials. Fluorinated aromatics like this one increase a molecule's stability, improve its metabolic resistance, and can fine-tune electronic properties, catering to needs not satisfied by non-fluorinated or monoamino analogs.
Realizing this product at scale involves high temperatures, tightly controlled atmosphere, and active monitoring to steer clear of unwanted byproducts. We invest in reaction controls, continuous analytics, and well-maintained purification columns to ensure our output reaches the level of purity required for further chemical transformations. Chemists choosing our 2,4-diaminofluorobenzene do not encounter off-odors or unexplained colors—a reflection of tight quality standards and careful selection of precursors. Specifications reflect a synthesis designed around practical feedback from our customers: powder consistency for reactivity, but also flowability, and a stability profile that reduces handling risks and waste.
Synthesizing compounds for pharma pipelines, crop protection formulas, or base monomers for resin production often pushes standard aromatic amines beyond their limits. Our clients encounter situations where the stability of the molecule under harsh conditions—whether through aggressive reagents, catalytic cycles, or high-energy radiations—matters far more than just having an amino or a fluorine group present. In 2,4-diaminofluorobenzene, the electron-withdrawing character of fluorine at the para position tempers the nucleophilicity of the amino groups, allowing for more controllable reactivity. This trait helps avoid side-reactions, which can reduce yields or introduce persistent impurities.
Having handled alternatives like 2,4-diaminoanisole or 2,4-diaminotoluene, the differences come into sharp focus. Methoxy and methyl substitutions at the same loci shift electron density differently and come with distinct hazards or regulatory baggage. Fluorinated analogs, by contrast, often meet stricter environmental and safety expectations while pushing molecular characteristics into a new operational window. These changes only become clearer at production scale, where solvent compatibility, melting range, and crystalline nature impact not only chemistry but equipment cleanouts, scheduling, and throughput.
Scaling up 2,4-diaminofluorobenzene production, we focus equally on ensuring homogeneity and limiting lot-to-lot variability. We do not simply watch for the key peaks on a chromatogram — we look for subtle white-to-off-white appearance, manageable particle size distribution, and low residual solvent levels. Our teams are firsthand witnesses to how minor slips in temperature or drying time can affect not just specifications, but the real-world yield or downstream product quality in your hands. We welcome requests for pre-shipment samples because we know every process is unique, and we value feedback when a batch exceeds expectations or needs tweaking.
Uses for 2,4-diaminofluorobenzene vary. Medicinal chemists seeking to append a fluorinated ring to a lead scaffold get improved solubility and metabolic performance. Agrochemical innovators find a more robust building block that survives formulation stresses and outdoor application. Material scientists trying to boost thermal and chemical resistance in specialty polymers see tangible differences not just in lab settings, but in long-term field exposure. We talk directly with process chemists and bench teams to understand how changes we make upstream can reverberate through to catalyst loading, crystallization rates, or color development, supporting their search for efficiency and consistency.
From a manufacturer’s perspective, 2,4-diaminofluorobenzene faces comparison with old standbys as well as newer, high-specification alternatives. What truly elevates it over its methyl- or chloro-substituted cousins lies in how the fluorine atom’s small size and strong bond with the aromatic ring modify performance. It takes sustained process know-how to achieve the right mix of reactivity and stability, and even more to keep that balance across every metric that producers and end users both weigh—melting point, moisture sorption, and the freedom from unknown residuals.
A number of companies once struggled to produce consistent batches, especially at volumes above pilot scale. We invested early in in-line monitoring and extended drying cabins, as well as filter systems to catch trace colored byproducts. By de-risking the product at our level, customers can avoid surprises in their reactors and move forward in development timelines. The purity and specification gradients we offer are not marketing claims—they result from adjustments in filtrate recycling and reaction seeding, tuned specifically for the high standards demanded by regulated industries.
Real stories, shared with us from leading research labs and scale-up facilities, highlight why this molecule has become a staple. One pharmaceutical development team switched from a 2,4-diaminochlorobenzene precursor to our fluorinated variant and saw cleaner conversion profiles, a sharp drop in halide-related byproducts, and fewer purification challenges. In their feedback, the more predictable reactivity at the amino positions allowed for better yields, even when the reaction ran at the lower end of their temperature window. They also reported fewer problems relating to product color and downstream stability.
In the agrochemical industry, a customer developing a novel fungicide experienced clogging issues tied to inconsistent particle size from another supplier. Our strict control over granulation, verified by hands-on re-testing rather than just paperwork, allowed them to improve their blending process and hit a tighter release profile without investing in extra sieving or re-milling. They appreciated that the fluorinated backbone held up under harsh formulation processing, resisting degradation and reacting precisely at the required position.
Polymer experts, examining new backbone designs for electronic applications, cite our ability to provide larger lots with unchanging purity and moisture levels as a deciding factor. Moisture absorption may seem trivial on spec sheets, but in automated production systems, small upticks can throw off polymerization rates or generate unwanted foaming. Through active control over drying times and transport bins, we sustain less than 0.1% variability batch-to-batch, with actual logs to back it up.
Achieving repeatable purity with 2,4-diaminofluorobenzene calls for serious attention to line cleaning, reactor seasoning, and the timing of ingredient addition. Every step, from sourcing precursor fluoronitrobenzenes to the hydrazine reduction and careful crystallization, gets tracked and logged by our technical teams. We see firsthand that small slips mean big headaches at the next facility down the road—a little extra acidity or a trace of metal residue often cause color shifts or viscosity changes during further reactions.
Years of hands-on trial and error taught us that, for this specific aromatic amine, even minor temperature fluctuation during the reduction phase impacts solubility, downstream filtration, and long-term storage. Details like vessel lining material, mixing blade geometry, and wash protocols for filter cakes matter. Our engineers participate directly in production runs, not just overseeing from a control room but physically sampling, checking particle size under the microscope, and adjusting drying time by touch when needed to achieve the ideal condition.
Placing our product next to non-fluorinated diamines, our production observations make the difference plain: fluorinated crystals show stronger resistance to caking in humid conditions, and the product has a longer shelf life both on-site and in sealed drums at customer sites. This means fewer returns, less lost time on reprocessing, and a smoother journey from the warehouse to the final formulation step.
Our team’s proximity to the manufacturing process gives us an edge in anticipating and addressing potential handling problems. 2,4-diaminofluorobenzene holds up well under ambient storage, provided it is kept free from unnecessary humidity and direct sunlight. We have observed that improperly sealed containers complicate downstream systems through clumping or slow dissolution, so our shipping and logistics staff double-check not only product quality but also packaging integrity.
Clear labeling and batch tracking help customers trace any deviations quickly, and our documentation matches what users encounter in actual plant settings. We do not depend on computers to tell us what works or doesn’t—we rely on collective experience from years of running, maintaining, and optimizing these systems. Whether the product is heading into a glovebox for synthesis, or being loaded into bulk feeders for resin modification, those expecting prompt flow and rapid solution formation for further use notice the care taken at the packing stage.
Years of operating plants taught us the habits that support trouble-free use—such as proper grounding for powder transfer to avoid electrostatic hazards and routine verification of the liner seals before shipment loading. Our recommendations stem from concrete events, not generic procedures. For large-scale users, we offer direct support and, where needed, provide technical feedback if unusual phenomena crop up. We approach every customer’s process as a partnership, not just a transaction.
In chemical manufacture, trust gets built over repeated good outcomes, not by resting on data sheets alone. We remain accountable for our product throughout its life in the supply chain. Customers tell us when even a single drum appears subpar, and we never brush off issues as isolated events. Instead, we trace back, identify root causes, and if necessary, refine the process or adjust the packaging protocol for future batches. This approach shapes not just the reputation of our 2,4-diaminofluorobenzene, but also the willingness of clients to take on bigger projects and new product applications.
Our technologists, support team, and plant operators work closely, ensuring every query receives an informed answer—often paired with practical advice learned through direct practice rather than theoretical compliance. This ensures that each customer, large or small, receives not distant call-center boilerplate, but a clear explanation based on real operating context.
Over the years, sustainability shifted from a box-ticking exercise to a key plank in daily operations. We cut solvent use and improved heat recovery systems to minimize the environmental footprint associated with every kilogram of 2,4-diaminofluorobenzene. Scrubber upgrades, recovery units, and smart feedstock sourcing reflect not just regulatory expectations but also pressures from clients seeking to shrink their own carbon accounting. Feedback from end users guides how we manage waste, package materials, and monitor emissions. This ongoing dialogue impacts product design and builds loyalty among innovators looking to meet global standards without compromising performance.
Restriction of hazardous substances and transparent reporting means customers can answer downstream audits with evidence. Our willingness to open the books, so to speak, results in trust and reduces risk in long product rolls and strategic developments. Taking advice from the plant floor, we continually upgrade safety and emissions systems, giving operators concrete buy-in and responsibility. This dynamic, responsive approach filters through into both product quality and customer satisfaction.
With greater industrial digitization and data capture, we integrated digital batch records and real-time analytics, sharing key data points when requested so client audits and technical validations become straightforward. Yet, the value lies in the intersection of these tools with the hard-won experience of long-serving production staff. As producer, we see novel uses for 2,4-diaminofluorobenzene surfacing each season. Whether as the starting point for PET-trackers in diagnostics, or in next-generation solar cell coatings, there is always the challenge to refine, scale, or customize based on changing technical requirements.
Knowing expectations will continue to rise, and that new regulations and technical hurdles will shape demand, we treat each lot as a chance to reinforce our reputation for reliability and technical rigor. We welcome input from academic labs, start-ups, and established global corporations alike. In each case, we bridge the gap between on-paper specs and real-world results, building on every customer conversation to drive ongoing improvements in the way our 2,4-diaminofluorobenzene serves the chemical community.
By remaining closely involved at every step—from raw material acquisition through plant operations, loading, and shipment—we ensure that our 2,4-diaminofluorobenzene meets not just technical benchmarks but also the hands-on demands of R&D and production environments. Decades of accumulated know-how shape the product more than spreadsheets or brochures ever could. For those designing, scaling, or fine-tuning advanced chemical synthesis, partnering with a manufacturer committed to quality, transparency, and responsiveness can save weeks or months lost to trouble-shooting, reformulation, or compliance reviews. Our open-door philosophy, rigorous standards, and willingness to innovate alongside our customers help explain why 2,4-diaminofluorobenzene produced here stands the test of time and changing industry needs.