|
HS Code |
217808 |
| Cas Number | 364-76-1 |
| Molecular Formula | C6H4FN3O4 |
| Molecular Weight | 201.11 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 153-155°C |
| Solubility In Water | Slightly soluble |
| Density | 1.65 g/cm³ (approximate) |
| Purity | Typically >98% |
| Synonyms | 5-Fluoro-2,4-dinitroaniline |
| Smiles | CC1=CC(=C(C(=C1[N+](=O)[O-])F)[N+](=O)[O-])N |
| Inchi | InChI=1S/C6H4FN3O4/c7-3-1-4(9(11)12)2-5(6(3)10(13)14)8/h1-2H,8H2 |
| Storage Temperature | Room temperature |
| Hazard Statements | Harmful if swallowed; Irritant |
As an accredited 2,4-Dinitro-5-Fluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2,4-Dinitro-5-Fluoroaniline, with tamper-evident cap and hazard-warning label. |
| Shipping | **Shipping Description for 2,4-Dinitro-5-Fluoroaniline:** 2,4-Dinitro-5-Fluoroaniline should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Appropriate labeling as a hazardous chemical is required. Comply with regulations for toxic and potentially combustible substances; use secondary containment and ensure transport by licensed hazardous materials carriers. Handle with suitable PPE. |
| Storage | 2,4-Dinitro-5-Fluoroaniline should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sunlight, heat sources, and incompatible materials such as strong oxidizers and reducing agents. Protect from moisture and physical damage. Use appropriate secondary containment and clearly label the storage area to prevent accidental exposure or mixing. Handle with appropriate personal protective equipment. |
Applications of 2,4-Dinitro-5-Fluoroaniline in Industrial ManufacturingAs a specialized manufacturer of 2,4-Dinitro-5-Fluoroaniline, we supply this advanced intermediate directly for leading downstream chemical syntheses. We focus solely on its established, industrially validated roles across pharmaceutical active ingredient synthesis, agricultural herbicide development, specialty dye formulation, and advanced materials research, with each segment requiring strict compliance, controlled usage ratios, and well-defined integration into their production pipelines. 1. Pharmaceutical Intermediate for Fluorinated APIsMajor pharmaceutical firms incorporate this intermediate in the multi-step synthesis of specific fluorinated active pharmaceutical ingredients, particularly for anti-tumor compounds and advanced anti-infectives. Production lines require full traceability of raw input ratios and robust purification control to achieve regulated residue levels dictated by regional GMP requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Herbicide Intermediate for Fluorinated Nitroaniline DerivativesGlobal agrochemical manufacturers rely on this material to construct key building blocks in selective herbicide formulations. The fluorine-nitro functionality imparts enhanced weed control profiles and environmental stability, requiring precise ratio balancing and controlled reaction monitoring to meet both yield and environmental emission standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Dye Intermediate for Synthesis of High-Performance Organic PigmentsProducers of specialty dyes select this compound to synthesize high-chroma, fluorine-modified azo and anthraquinone pigments, valued for their durability and brilliance in textiles and industrial coatings. Stringent batch QC, solvent selection, and ratio calculations ensure target color indices and environmental discharge limits are met consistently. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Fine Chemicals for Advanced Material SynthesisMaterials science R&D centers and specialty chemical producers use this molecule to introduce fluorinated aromatic motifs into advanced functional materials, such as liquid crystal compounds and organic semiconductors. Laboratories and pilot plants carefully tailor input ratios and process parameters to optimize substitution and purity levels according to published and proprietary methods. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,4-Dinitro-5-Fluoroaniline 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!
Every batch of 2,4-Dinitro-5-Fluoroaniline (model: 5-Fluoro-2,4-dinitroaniline) tells its own story. We started synthesizing this compound over a decade ago, and its role in chemical synthesis continues to stand out because of its unique structure. Working directly with nitroanilines, you come to realize that changing the position or type of substituent makes a significant impact, not only in the reactivity but also in downstream uses. Introducing a fluorine atom at the 5-position gives chemists a versatile handle. Coming from the manufacturing side, purity always draws our attention; even a slight deviation during reaction opens the door for impurities, so our process never cuts corners with raw material quality or filtration.
We produce 2,4-Dinitro-5-Fluoroaniline mainly as a pale yellow crystalline powder. Our customers expect moisture content below 0.5%, as excessive water leads to clumping and complicates further reactions. The melting point typically falls within 130 to 135°C, a narrow range indicative of product consistency; outliers often hint at contamination or incomplete reaction, both of which our lab checks can pick up early. HPLC purity over 99% isn’t just a sales point; it emerges from carefully selected reagents, slow temperature ramps, and proper post-reaction washing cycles. Inconsistent blending in reactors quickly becomes apparent in the NMR spectra. On occasion, we notice buyers ask for optical clarity data—most organic chemists don’t need it for this class of compound, but in specialty fields like pigment intermediates, subtle coloration differences still get flagged.
Few compounds with a single fluorine atom change the course of a synthetic pathway quite like this one. Manufacturers of pharmaceuticals and agrochemicals lean on it as a cornerstone intermediate for heterocyclic assembly. Through years of customer feedback and collaboration, we’ve watched the role of this compound move from curious experiment to process staple. Electrophilic aromatic substitution proceeds with more control thanks to the electron-withdrawing effects of both the nitro and fluoro groups. Our partners in research often reflect that this reactivity translates to fewer byproducts and more efficient step economies, which matters as regulatory pressures grow tighter on waste disposal.
In dyes, including certain azo and disperse dyes, we see 2,4-Dinitro-5-Fluoroaniline serve both as a coupling component and a building block that shifts absorption bands in finished molecules. Some manufacturers in the east Asian textile sector shared data with us showing deeper hues and better stability in dyed fabrics compared to analogous anilines lacking the fluorine substituent. It’s more than a laboratory curiosity: these properties steer long-term production choices, especially when customers demand higher lightfastness and color strength.
A routine question in client meetings asks how 2,4-Dinitro-5-Fluoroaniline stacks up against 2,4-dinitroaniline or even 2,4-dinitro-6-chloroaniline. Structurally, the para and ortho nitro groups already pull electrons, but adding fluorine at the 5-position sharpens that withdrawal, producing a molecule less reactive toward nucleophilic displacement yet more tailored for making particular heterocycles under milder conditions. This translates to more selectivity when it undergoes further substitution or cyclization—something chemists working on pharmaceuticals regularly confirm back to us.
Practically, differences show up not just on the bench but out in the plant. Fluorinated derivatives tend to volatilize less than their chloro or non-halogenated peers at the same temperatures, reducing emissions during solvent recovery. Handling protocols reflect this; containment design changes, and personal protective equipment recommendations get tweaked. The toxicity profiles change as well: animal studies point to lowered acute toxicity compared to compounds with bulkier halogens, though all dinitroanilines require careful handling. With fluorine, finished products often pass stricter impurity specification than those synthesized from the non-fluorinated variant, especially in regulated markets.
Anyone working at a manufacturing scale knows the devil hides in process consistency. Our team struggled early on with incomplete nitration when upscaling from gram to kilogram batches, particularly if mixing efficiency slipped or temperature control lagged. In one instance, a faulty sensor cost us yield and, more importantly, introduced side products that complicated purification. Customers picking up even faint traces of 2-fluoro or 3-nitro regioisomers appreciate our transparency about such issues. Our chemists now monitor exothermic peaks and solvent evaporation closely, shutting down a batch if temperature or pH readings drift. We’ve built redundancy into all pilot reactors, knowing from long experience that human error is difficult to root out completely.
On filtration and drying, we learned not to rush. Dinitro compounds, especially fluorinated ones, can retain solvent in caked crystals, and we’ve thrown out product that failed Karl Fischer water testing even after overnight drying. Labeling and sampling both inside and outside our warehouses ensure traceability; it always seems like a paperwork hassle at first, but sudden customer audits or transport mishaps highlight its value. For example, after a minor spillage during loading, clear batch coding helped us prove full compliance—something which can never be guaranteed by guesswork.
End users remind us, both directly and subtly, of their biggest priorities: purity, reliability, and documented sourcing. Some of our pharmaceutical clients require extensive impurity profiling; minor isomers, even in the hundreds of parts per million, trigger process reviews on their end. Agrochemical customers care about stability during formulation, reporting back when off-spec batches affect dispersibility in final product mixes. Our dyes industry partners send us feedback on everything from color inconsistency to flowability from bulk shipping containers—sometimes a small difference in particle size means headaches in their automated feeders.
We added an extra sieve step for one long-term customer who found intermittent clumping in 200kg drums. Their automated line kept jamming, pausing their operations and costing thousands. After on-site troubleshooting with their engineering team, we now pass every production lot through a calibrated mesh before final packaging. Another customer from the specialty intermediates sector asked about trace chlorinated byproducts. Our analysis, along with collaborative dialogue, prompted a review and mild change in acid washing protocol. Partnerships built on open communication consistently drive quality improvements.
No discussion about any nitroaniline compound is complete without addressing environmental and safety realities. 2,4-Dinitro-5-Fluoroaniline stands out for its lower volatility and comparatively friendly thermal decomposition profile, but it remains a regulated chemical requiring only experienced handlers. From day one, our safety training involves everyone on the line, backed up by visible reminders in all chemical area workstations. We’ve adjusted our production spaces with improved ventilation and advanced solvent scrubbing, after internal and regional environmental reviews indicated airborne exposure risk above accepted minima at peak production hours.
Spill protocols receive real-life tests regularly—not because they happen often, but because readiness avoids disaster. We’ve chosen double skin steel drums for all shipping, based on earlier issues with minor leakage in HDPE liners over long sea voyages. Effluent from purification is treated via neutralization and carbon adsorption, a process verified by our local environmental compliance partners. These measures stem from years of incremental improvements, often forced by the learning curve of real incidents rather than optimistic projections.
Changing environmental and workplace safety rules shape nearly every move we make. Import and export documentation reflect both customs requirements and chemical-specific transport guidelines, and our QC logs endure their own cycles of update in response to changing standards. Some years ago, a new national environmental code required every operator to rotate respirators after 90 minutes of open charging duty—old routines needed breaking, but our records now show lower absenteeism from respiratory complaints. In the EU, REACH registration and constantly evolving hazard labeling have forced updated SDS formats and stricter batch segregation.
We’ve observed increasing requests from customers for full analytical documentation—HPLC chromatograms, NMR spectra, GC-MS traces—even for routine shipments. Several major clients run their own incoming QC, comparing against these reports and rejecting anything not matching claimed specifications. The cost of one batch failing this process can amount to lost contracts. Our in-house laboratory now produces parallel testing and spot auditing on every lot, and this scrutiny pays off with fewer returns and stronger relationships.
Raw material sourcing continues to be more than just a supply chain concern. While fluorobenzenes and nitric acids remain accessible, recent fluctuations in commodity prices expose the dangers of single-source supply. Several times in the last five years, we’ve felt the pinch as suppliers in one region halted due to regulatory changes or shipping disruptions. Our strategy now involves qualifying alternative vendors, often running side-by-side trials to guarantee input consistency before committing to changes at scale.
Reducing process waste and improving energy efficiency present ongoing challenges. Nitro group installation inevitably produces acidic and oxidizable effluents, and our continuous improvement team works with outside process consultants to minimize associated byproducts. Utility metering on all major equipment spots areas where cooling demand spikes or heat exchangers run out of spec, prompting rapid corrective maintenance. Chemical synthesis is never a set-and-forget operation; vigilant operators and a culture that listens to feedback make a real difference on the ground.
We don’t look at 2,4-Dinitro-5-Fluoroaniline as just another commodity. Its specific combination of functional groups—two nitros and a fluorine—sets unique demands from both a chemistry and a manufacturing standpoint. Success in this business hinges on keeping every detail, from temperature gradients in reactors to proper drum sealing, under constant review. It takes close relationships with customers to truly understand changing requirements, and even closer attention to what happens in day-to-day production. We draw on decades of process refinements and end-user dialogue to make sure each batch lives up to expectations, and each improvement is logged for the next cycle. That ongoing work matters just as much as any technical specification.