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HS Code |
994267 |
| Chemicalname | 1,3-Diamino-2,4,5,6-Tetrafluorobenzene |
| Molecularformula | C6H2F4N2 |
| Molecularweight | 178.09 g/mol |
| Casnumber | 2923-16-0 |
| Appearance | White to off-white solid |
| Meltingpoint | 182-185°C |
| Solubility | Soluble in common organic solvents |
| Purity | Typically >97% |
| Synonyms | 2,4,5,6-Tetrafluoro-1,3-benzenediamine |
| Smiles | C1(=C(C(=C(C(=C1N)F)F)N)F)F |
| Inchi | InChI=1S/C6H2F4N2/c7-1-3(9)5(11)6(10)4(1)8/h11H2,2H2 |
| Storagetemperature | Store at 2-8°C |
As an accredited 1,3-Diamino-2,4,5,6-Tetrafluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle, 25 grams, sealed with a PTFE-lined cap, labeled with hazard warnings, chemical name, and lot number. |
| Shipping | Shipping for 1,3-Diamino-2,4,5,6-Tetrafluorobenzene requires secure, sealed containers to prevent exposure. The chemical should be clearly labeled and handled according to standard hazardous materials protocols. Keep away from moisture and incompatible substances. Transport in compliance with local, national, and international regulations on hazardous goods shipping. |
| Storage | 1,3-Diamino-2,4,5,6-Tetrafluorobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, moisture, and incompatible substances such as strong oxidizers. Protect from light and store under inert atmosphere if possible to prevent decomposition. Properly label the container and ensure access is restricted to trained personnel only. |
Applications of 1,3-Diamino-2,4,5,6-Tetrafluorobenzene in Industrial Manufacturing1,3-Diamino-2,4,5,6-Tetrafluorobenzene supports several advanced material and chemical manufacturing sectors due to its unique aromatic diamine and tetrafluorinated structure. Our facility tailors this raw material for high-purity downstream production, supporting stringent compliance and technical performance in key industries. 1. High-Performance Polyimide Resin SynthesisAromatic diamines serve as building blocks for thermally stable and chemically resistant polyimides, heavily used in electronics, aerospace, and flexible displays. The tetrafluorinated structure reduces dielectric constant and moisture absorption. Polyimide resin formulators introduce this intermediate in diamine-dianhydride polycondensation to achieve targeted electrical, mechanical, and thermal properties for high-reliability applications. Industry compliance standards
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2. Organic Semiconductor IntermediateThe tetrafluoro-substituted phenylenediamine core supports synthesis of semiconducting polymers and small molecules for advanced organic electronics. Formulators utilize it in donor–acceptor polymer designs to tune electrochemical stability and charge mobility, vital for high-purity active layers in devices requiring precise energy level alignment. Industry compliance standards
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3. Fluorinated Aromatic Crosslinker in Specialty Epoxy SystemsEpoxy system designers employ the tetrafluorodiamine as a high-performance crosslinker to introduce dimensional stability, chemical resistance, and reduced moisture uptake, ideal for specialty adhesives and electronic encapsulants. The difunctional structure allows fine-tuning of glass transition temperature and dielectric behavior for demanding microelectronics and aerospace uses. Industry compliance standards
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4. Chemical Intermediate for Agrochemical SynthesisFine chemical producers leverage the diamino-tetrafluorobenzene as an intermediate for creating fluorinated heterocyclic structures. These targets serve as active ingredients for modern crop protection chemicals, thanks to enhanced bioactivity and metabolic stability provided by fluorine substitution in the aromatic system. Industry compliance standards
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5. Monomer for High-Temperature-Resistant FluoropolymersSpecialty polymer manufacturers use the tetrafluorinated diamine as a strategic monomer for copolymerizing with diacid or dianhydride partners to yield fluorinated polyamides or polybenzimidazoles. This application seeks to enhance flame retardancy, chemical durability, and low permeability in polymer films and engineered components. Industry compliance standards
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Competitive 1,3-Diamino-2,4,5,6-Tetrafluorobenzene 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 sales7@sinochem-nanjing.com.
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Tel: +8615371019725
Email: sales7@sinochem-nanjing.com
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Every batch of 1,3-diamino-2,4,5,6-tetrafluorobenzene we produce comes straight from our reactors. We work with real chemical synthesis, tuning process parameters ourselves and watching the transformations batch after batch. Over years handling aromatic fluorination, we've learned the finer points that turn a standard compound into a reliable building block. In the world of fluorinated aromatics, 1,3-diamino-2,4,5,6-tetrafluorobenzene stands out for combining high fluorine loading with reactive amino groups, and we see requests for this material continue to rise as advanced polymer and electronics labs look for trusted supply.
1,3-diamino-2,4,5,6-tetrafluorobenzene sits in a rare class of small molecules, carrying two orthogonal amino substituents and a fluorine at every other ring position. This unusual scaffold results from careful multi-step synthesis, usually involving selective halogenation and amination. From a manufacturing standpoint, this means regular instrumentation checks, especially to confirm complete substitution. Experienced chemists know that partial substitution or unreacted halides throw applications off course—so we go the extra mile in purification, using repeated crystallization and column techniques to ensure only the target structure remains.
Progress in high-performance coatings, specialty polymers, OLED intermediates, and pharmaceutical intermediates depends on sourcing building blocks like 1,3-diamino-2,4,5,6-tetrafluorobenzene. Adding fluorine to the aromatic ring introduces amazing resistance to heat, chemicals, and environmental stress. Two amino groups give access to countless derivatizations: you can make polyamides, triazines, and diazabenzene compounds with thermal stability and low dielectric loss. We have seen our customers pivot away from non-fluorinated precursors where stability or hydrophobicity is crucial. Failures in electronic encapsulation or membrane performance often trace back to the wrong monomer—our job as manufacturers is to support the next innovation cycle by keeping quality consistent.
We keep specifications simple and achievable—purity above 99 percent (by HPLC), moisture below 0.2 percent (by KF), and color as close to light yellow as possible. Fluorine-NMR, proton NMR, and mass spec back every lot. Customers ask for certificate of analysis, but direct access to raw data means more in our shop than a stamped PDF copy. In process, our team checks melting points, but we focus on reactivity in key amide formation or electrophilic substitution tests for real feedback. Trace metal analysis has become more important as semiconductor customers demand even lower parts-per-billion impurity levels, so we now run ICP-MS for every major shipment. Specifications evolve as customer feedback comes in—flexibility only comes if you control the process end-to-end.
Batch-to-batch variability can derail a whole product launch. In fields like electronic chemicals and medical research, even a small fluctuation in purity, color, or particle size distribution can throw results off. Our reactors run at defined temperature and pressure regimes—not just because theory says so, but because we’ve watched off-spec batches end up in costly rework. Sometimes new team members ask why we run extra mid-batch GC checks. It’s because false economies in small-molecule manufacturing always turn out expensive in the long run; real savings come from fewer surprises.
Benzene derivatives cover a huge chemical landscape, but many lack the balance between reactivity and durability. Removing hydrogen from the ring and replacing nearly every position with fluorine makes this molecule hydrophobic and tough, but reactive amino groups make it click together with acyl or sulfonyl chlorides. Handling simpler tetrafluorobenzene or regular phenylenediamine just isn’t the same—the added fluorines shift the electronic map, making reactions cleaner or more selective. You end up with fewer side products, better color stability, and materials that handle heat and solvents far better. That’s why high-end membrane researchers and OLED teams have moved from using generic diaminobenzenes or plain fluorobenzenes to this molecule.
Most customers ask about solvent systems before anything else. As a powder, 1,3-diamino-2,4,5,6-tetrafluorobenzene dissolves in polar aprotic solvents like DMF or DMSO, and holds up under strong acid or base. We advise filtration to keep particulate out, especially in electronic or medical research. On rare occasions, light yellow color can darken if left exposed to air—simple inert atmosphere practice keeps it stable. We mill the product to a fine crystal size (typically 80-120 mesh), providing good dispersibility without excess dust. Excessive milling sometimes increases reactive surface, so we fine-tune this for each customer segment.
On the polymer side, we’ve shipped several hundred kilograms for use in synthesizing fluorinated polyamides and polyimides, which go directly into aerospace sealing or flexible electronics. For coatings, users often react it with perfluoroalkyl chlorides to build custom, low-surface-energy films. On the pharmaceutical side, only a small volume sees use, but the demand for high NMR purity is higher due to downstream transformations. We receive regular feedback from academic collaborators running cross-coupling chemistry or triazine synthesis, where small impurities have outsized impact on yields. We keep a running database of which solvents, catalysts, or protective groups give the best results, and we’re willing to share tips when customers reach out directly.
Early in our history, we depended on outside labs for much analysis, but long turnaround times and variable data accuracy led us to build out a full suite of in-house equipment. Our NMR, GC, and LC systems sit close to production, not in a distant R&D lab. Every production run spawns a wave of samples, which then go through head-to-head tests with historical batches. Issues like low-level halide residues or loss of reactive amino content can go unnoticed in a low-throughput distribution setup—our team sees every blip in real time, and we act on it. A surprising number of users have told us about contaminants detected only after delivery from distributors—direct sourcing from a manufacturer like us closes that gap.
Many in the specialty chemical space have faced hefty lead times and sudden price surges as global supply lines chafe under new constraints. By owning our synthesis process, we keep production local, secure, and traceable. We track inventory in real time and make scaling decisions based on real orders, not speculation. If raw material price swings threaten delivery, we communicate up front. That trust has kept us in long-term relationships with key electronics and polymer customers. Distributors can’t always promise supply continuity, especially for molecules with complex syntheses—direct manufacturing offers stability you just can’t get from third parties.
Anyone who has worked with aromatic amines or fluorinated organics knows handling practices can’t be an afterthought. Our manufacturing team keeps work areas under strict air handling, and we use local exhaust plus dedicated PPE. These are not just compliance exercises—minor skin or vapor exposure can cause health problems, and unlike dilute specialty chemicals, the concentrated powder moves through our facility every week. By training staff directly and updating SDS protocols with actual factory learnings, we reduce the risk of exposure incidents.
Straight from the chemical bench, fluorinated aromatic waste stands out as persistent. Standard organic solvents recover fairly easily, but any side products or incomplete intermediates require dedicated disposal. We’ve worked to minimize generation through precision synthesis, modest excess reactant, and early adoption of solvent recycling units. After a decade in specialty chemistry, we know that every kilogram of waste avoided at source saves thousands downstream. Our water treatment setup removes halide and amine traces, and we contract with vetted disposal partners for any regulated byproducts. Customers increasingly ask for life cycle data, and we are open about solvent recovery rates and waste minimization steps because they reflect the real costs and gains in the process.
We keep a regular pulse on literature trends and connect with research groups working on next-generation materials. This is more than a marketing strategy—it gives us early warning about shifts in purity needs or new transformations that legacy processes might not address. Several leading groups working on battery membranes or organic semiconductors have reached out for custom grades, and we’ve responded by tweaking parameters such as particle size, residual moisture, and specific anion counter-ion content. Sometimes a new customer will alert us to a previously unknown reactivity or stability challenge—the rapid communication between lab and production allows us to adapt without outside delay. Direct manufacturing gives us this feedback loop, missed by distributors feeding static product lines.
Regulatory frameworks for aromatic fluorinated chemicals continue to evolve, driven by rising concern about environmental and occupational health effects. With both industrial and academic clients, open sharing about our raw material sourcing and processing aids trust. We keep our registrations and certificates updated with agencies in major markets, and invest in toxicology reviews to deepen understanding of long-term risk. Being on top of governmental changes—not just for compliance, but for safety—gives both our team and our customers confidence.
Many buyers ask whether buying direct from a manufacturer matters—especially if a distributor can supply the same molecular formula. The lived reality is that synthetic history, purification path, and lot-specific verification all contribute to differences in performance. In our experience, even a molecule meeting generic HPLC purity specification can behave unpredictably when upstream trace impurities or altered crystal morphology slip through a less-controlled pipeline. Our on-site process control team catches subtle shifts that outside eyes can miss. The value for customers comes through fewer trial failures and more reliable results in application.
Some applications demand small but significant tweaks—different mesh sizes, alternate counter-ions, or lower moisture thresholds. Because we run all stages in-house, we adjust processes for qualified partners. This might look like two rounds of vacuum drying versus one, or a final sieving step to narrow the particle size. We work to understand not only what each customer intends to do, but how their process interacts with the source material. Our engineers and production chemists collaborate actively, shortening time from inquiry to shipment. We make these adjustments possible because we place real eyes and hands on the process at every stage.
Trends in technology—intelligent textiles, flexible electronics, and chemical-resistant membranes—all demand ever-better stability, processability, and long-lifetime performance. At the base of that evolution sits specialty building blocks like 1,3-diamino-2,4,5,6-tetrafluorobenzene. From our front-row seat in chemical manufacturing, we keep seeing designers and researchers move away from general-purpose aromatics toward more advanced, highly fluorinated and aminated compounds for superior utility. This isn’t a passing phase—the limits of older materials keep showing up in service life, weight reduction, and even regulatory hurdles. Our task is to follow and enable that push, never relying on legacy assumptions about “good enough” quality.
We understand that innovation rarely runs a straight line—feedback, trial runs, unexpected setbacks, and changing requirements all define our business. As a manufacturer, we align ourselves with these shifts. Our longest relationships come from years of open troubleshooting sessions and dogged follow-up when something doesn’t work right. The direct lines between our production leads and customer R&D groups mean issues are addressed early, and successes are celebrated together. While others may treat product like inventory, we know every batch is a part of a bigger picture—enabling better technology through chemistry, batch by batch.
As global pressures from regulation, supply chain complexity, and evolving green chemistry grow, our own business adapts in real time. Finding alternative greener reagents, cutting solvent usage, and moving toward zero-discharge operations are not just tasks for tomorrow—they shape our capital projects and daily operations now. We see opportunities for further innovation in catalytic cycle reuse and improved heat integration in fluorination steps. We’re open to collaboration and view every inquiry as a learning opportunity—the line between manufacturer and partner keeps getting thinner as markets shift.
Decades making and refining 1,3-diamino-2,4,5,6-tetrafluorobenzene have carved out more than just technical acumen—it’s informed every business process, every customer conversation, and every forward-looking investment. This is not a commodity product; it’s a specialty tool tuned by real-world needs. Customers rely on us to deliver reliability, transparency, and a degree of customization you can’t get elsewhere. Our team brings hands-on insight and continuous learning to every lot that leaves our plant. By sticking close to the science and never losing sight of practical challenges, we move chemistry—and our customers’ ambitions—a little further every year.