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2,4-Dinitro-5-Fluoroaniline

    • Product Name 2,4-Dinitro-5-Fluoroaniline
    • Alias 2,4-Dinitro-5-fluoroaniline
    • Einecs 251-837-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 2,4-Dinitro-5-Fluoroaniline

    Applications of 2,4-Dinitro-5-Fluoroaniline in Industrial Manufacturing

    As 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 APIs

    Major 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP directives (EudraLex Vol 4, Part II)
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • Chinese Pharmacopoeia, Section for Intermediates

    Typical usage ratio

    • Used at 0.8–3.5% (by mass) in targeted stage reactions, depending on the specific synthesis route and desired fluorination yield

    Downstream process integration

    • Introduced in early-to-intermediate stage Buchwald–Hartwig amination or nucleophilic aromatic substitution, then fully converted and removed via aqueous work-up and chromatographic purification

    Final product types

    • Fluorinated quinolones
    • Novel oncology drug APIs
    • Antimicrobial API intermediates

    2. Herbicide Intermediate for Fluorinated Nitroaniline Derivatives

    Global 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

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC 1907/2006) Registration & Evaluation
    • China National Standard GB 20665/GB 2763 (Maximum Residue Limits for Pesticides)
    • EPA FIFRA (40 CFR Parts 150–180) for pesticide manufacturing

    Typical usage ratio

    • Applied at 2.0–6.0% by weight in the formation of target nitroaniline intermediates, with precision scaling according to batch size and targeted specific activity in the resultant herbicide

    Downstream process integration

    • Added during the nitration or condensation stage, then carried through catalytic hydrogenation or halogen exchange to tailor the final herbicide molecule structure

    Final product types

    • Fluorinated pre-emergent herbicides
    • Selective weed control agents for grain crops
    • Intermediate compounds for sulfonylurea-class herbicides

    3. Dye Intermediate for Synthesis of High-Performance Organic Pigments

    Producers 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

    • OEKO-TEX® Standard 100 (Textile Substance Regulations)
    • EN 71-3:2019 (Safety of Toys—Migration of Certain Elements, for pigments in consumer goods)
    • REACH Annex XVII (Restriction on Certain Hazardous Substances)
    • ZDHC MRSL (Manufacturing Restricted Substances List for textiles)

    Typical usage ratio

    • Used at 1.2–5.8% (pigment synthesis stage), adjusted for target molecule molecular weight and specific shade intensity requirements

    Downstream process integration

    • Charged into azo coupling or cyclization reactors, then isolated after pH neutralization, washed, and processed through filtration/spray drying steps

    Final product types

    • Fluorinated azo textile dyes
    • High-stability pigments for automotive coatings
    • Industrial-grade colorants for plastics and inks

    4. Specialty Fine Chemicals for Advanced Material Synthesis

    Materials 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

    • ISO 9001:2015 (Quality Management for Fine Chemical Production)
    • OECD GLP Principles (for test and laboratory chemical synthesis)
    • RoHS (EU 2011/65 Restriction of Hazardous Substances for electronics intermediates)
    • Japanese Industrial Standard JIS K 0557 for electronic material evaluation

    Typical usage ratio

    • Typically employed at 0.5–2.0% (mol/mol vs. core reactant), with laboratory screening guiding scale-up ratios for pilot and commercial runs

    Downstream process integration

    • Inserted during arylamine substitution, then advanced through functionalization, crystallization, and vacuum drying to achieve high-purity end products

    Final product types

    • Key intermediates for OLED/OPV materials
    • Liquid crystals for display manufacturing
    • Specialty monomers and polymer additives for research and commercial electronics applications
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    Competitive 2,4-Dinitro-5-Fluoroaniline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,4-Dinitro-5-Fluoroaniline: Experience from the Manufacturing Floor

    What We’ve Seen in the Production and Application of 2,4-Dinitro-5-Fluoroaniline

    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.

    Specifications that Matter on the Shop Floor

    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.

    Why 2,4-Dinitro-5-Fluoroaniline Draws Attention in Synthesis

    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.

    How It Differs from Other Dinitroanilines—Not Just a Subtle Shift

    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.

    From Raw Materials to Final QC: Challenges We’ve Had to Fix

    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.

    Customer Insights: What Matters Most to People Downstream

    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.

    Environmental and Safety Considerations

    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.

    Regulatory Landscape: What Affects Daily Decision-Making

    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.

    Looking Ahead: What Still Needs Solving

    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.

    Conclusion Is in the Process, Not the Pitch

    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.