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2-Fluoro-6-Nitrobenzoic Acid

    • Product Name 2-Fluoro-6-Nitrobenzoic Acid
    • Alias 2-Fluoro-6-nitrobenzoic acid
    • Einecs 242-646-8
    • 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

    544268

    Cas Number 403-25-6
    Molecular Formula C7H4FNO4
    Molecular Weight 185.11 g/mol
    Appearance Yellow solid
    Melting Point 150-154 °C
    Solubility In Water Slightly soluble
    Purity Typically >98%
    Smiles C1=CC=C(C(=C1F)C(=O)O)[N+](=O)[O-]
    Inchi InChI=1S/C7H4FNO4/c8-5-3-1-2-4(7(10)11)6(5)9(12)13/h1-3H,(H,10,11)
    Synonyms 2-Fluoro-6-nitrobenzenecarboxylic acid
    Ec Number 609-019-4
    Storage Temperature Store at room temperature
    Hazard Statements Irritant

    As an accredited 2-Fluoro-6-Nitrobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with secure cap, white label displaying product name, hazard symbols, and quantity: 25 grams, from certified supplier.
    Shipping 2-Fluoro-6-Nitrobenzoic Acid is shipped in tightly sealed containers to prevent moisture and contamination. The chemical is handled under standard hazardous material guidelines and typically transported via ground or air, compliant with regulatory safety standards. Packaging includes clear labeling and documentation for identification, storage, and safe handling throughout transit.
    Storage 2-Fluoro-6-nitrobenzoic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases and oxidizing agents. Protect from light, moisture, and sources of ignition. Use appropriate chemical storage cabinets and ensure proper labeling. Personal protective equipment should be used when handling the compound.
    Application of 2-Fluoro-6-Nitrobenzoic Acid

    Applications of 2-Fluoro-6-Nitrobenzoic Acid in Industrial Manufacturing

    As a direct manufacturer of 2-Fluoro-6-Nitrobenzoic Acid, we supply this aromatic building block for essential chemical synthesis pathways across several specialized industries. Below we outline the verified technical applications, usage recommendations, compliance mandates, integration points, and final products that result from large-scale industrial adoption.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical companies use this compound as a critical intermediate in the synthesis of select APIs, particularly within certain fluoroquinolone and nitroaromatic drug classes. The material’s fluorine and nitro groups serve as reactive sites to introduce specific pharmacophores during multi-step synthesis. Its incorporation occurs typically at the stage of aromatic modification or amidation before final ring closure and purification, directly affecting impurity profiles and batch reproducibility. Downstream partners rely on precise analytical release profiles and traceability from this raw material to finished tablets or parenterals.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (ChP) monograph requirements
    • European Pharmacopoeia (Ph. Eur.) process validation guidelines

    Typical usage ratio

    • 0.2–0.5 molar equivalents relative to API core in staged reaction blocks; actual concentration set by API structural scaffold and batch scale, with higher ratios for double-substitution or secondary nitration steps.

    Downstream process integration

    • Step 2–3 in multi-stage intermediate coupling
    • Input to nitration, esterification, or amide formation reactors
    • Subjected to filtration, crystallization, and in-process QC prior to downstream conversion and purification

    Final product types

    • Fluorinated anti-infective drug substances (e.g., quinolone antibiotics)
    • Specialty nitroaromatic APIs
    • Intermediates supplied for generic formulation manufacturing

    2. Agrochemical Synthesis Precursor

    The agrochemical industry integrates this compound in the controlled synthesis of advanced herbicide and fungicide molecules. Its electrophilic aromatic system permits targeted substitutions required for assembling complex active moieties. The intermediate introduces both electron-withdrawing and activating effects enabling regioselective derivatization, particularly effective in triazole or pyridine-based crop protection agents. Production facilities dictate reagent charge according to desired field efficacy and residual tolerance profiles for regulated markets.

    Industry compliance standards

    • FAO Specification for Plant Protection Products
    • ISO 9001:2015 certified quality management
    • REACH registration requirements for agrochemicals (EU)
    • China National Standard GB 2763 residue analysis protocol

    Typical usage ratio

    • 0.5–1.8% (w/w) relative to the total synthetic batch weight; adjusted for target purity, reaction yield, and evolving application needs for selectivity in downstream derivatization processes.

    Downstream process integration

    • Direct addition in nucleophilic aromatic substitution steps
    • Functional group integration prior to copper-catalyzed cross-coupling
    • Monitored by HPLC and GC-MS for endpoint determination

    Final product types

    • Novel herbicide actives for rice and wheat
    • Fungicide precursors for seed treatment formulations
    • Synthons for environmental fate improvement in crop protection agents

    3. Advanced Materials for Liquid Crystal Display (LCD) Monomers

    Manufacturers of liquid crystal materials utilize this compound in designing high-performance mesogenic monomers for next-generation display films and optical substrates. Strict control over the fluorine positioning and nitro functionality enables production of liquid crystal mixtures with improved response times and thermal stability. Processing facilities introduce the compound at oligomer-building stages, precisely controlling feed purity to prevent downstream optical defects. Demand in this segment is driven by panel makers seeking custom alignment layers and anisotropic films with reproducible molecular orientation.

    Industry compliance standards

    • RoHS Directive (EU 2011/65/EU) for electronic chemical substance use
    • IEC 61249-2-21 halogen-free specification
    • TQC LC material migration testing protocols
    • ISO 9001:2015 certified production quality

    Typical usage ratio

    • 0.8–2.0% by weight in mesogen synthesis blends; customized ratio based on viscosity, birefringence, and dielectric offset targets established by display panel engineering

    Downstream process integration

    • Early-stage input for monomer condensation reactions
    • Intermediate for azomethine or biphenyl derivative assembly
    • Controlled crystallization and film casting into LCD cell layers

    Final product types

    • High-clarity nematic and smectic liquid crystal mixtures
    • Anisotropic films for LCD and OLED displays
    • Alignment layer specialty coatings for electronic panels

    4. Dye and Pigment Intermediate for Specialty Colorants

    Producers of fine dyes and pigments incorporate this compound as a core intermediate in the manufacturing of select azo and anthraquinone colorants. Its electron-withdrawing substituents facilitate diazotization and coupling, yielding colorants with tuned chromatic stability and improved fastness properties. Integration occurs at the key intermediate synthesis stage, where precise control of stoichiometry and side reactions ensures batch consistency—integral for applications demanding strict color uniformity such as textile or industrial ink production.

    Industry compliance standards

    • EN 71-3 migration standards for colorants in toys and textiles
    • Oeko-Tex Standard 100 chemical safety restrictions
    • REACH SVHC (Substances of Very High Concern) exclusion rules for pigments
    • ISO 1248 pigment purity/identity norms

    Typical usage ratio

    • 1.2–2.7% of dye or pigment mass formulation, with variations tailored for desired absorption maxima and application substrate (fibers, plastics, print media)

    Downstream process integration

    • Input to azocoupling or nitration units prior to chromophore assembly
    • In situ feed for continuous-flow pigment coating reactors
    • Post-reaction isolation and standardization for final dye blending

    Final product types

    • High-performance azo textile dyes
    • Color-stable printing ink pigments
    • Specialty plastics and synthetic fiber colorants
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    Certification & Compliance
    More Introduction

    Introducing 2-Fluoro-6-Nitrobenzoic Acid: A Manufacturer’s Perspective

    Making Real Chemistry: Our Journey with 2-Fluoro-6-Nitrobenzoic Acid

    In the world of specialty chemicals, the story behind every compound carries more weight than just numbers on a datasheet. From the first barrels to today's kilo-lot production, 2-Fluoro-6-Nitrobenzoic Acid (2F6NBA) has grown into a trusted key building block for those tackling advanced synthesis. Based on our hands-on experience running multi-step routes and working with demanding pharmaceutical partners, the conversation around 2F6NBA isn’t about hype or market buzz. It’s about reliability, purity, and knowing your upstream chemistry inside and out.

    The Model That Works: A Closer Look at What Sets 2F6NBA Apart

    We produce 2-Fluoro-6-Nitrobenzoic Acid with a focus on consistent batch reproducibility. Each production run gets tracked by its lot, not just for traceability, but to ensure a repeatable, high-quality output. Over years of process improvement, we’ve refined our fluorination and nitration steps to minimize byproduct levels—those small details make a difference in later reactions. Our analysts watch for even minor shifts in melting point and appearance, as these can flag irregularities that impact downstream conversion rates for our customers using the acid in complex syntheses.

    Specifications That Go Beyond the Label

    People ask why we put so much energy into true analytical control. In reality, it’s a direct result of working on tight timelines with pharmaceutical crews, where every hour counts for pilot trials and gram-to-kilo transitions. We routinely achieve a purity of 99.5% or higher by HPLC, and our water content typically falls well below 0.5% by Karl Fischer. While some chemical intermediates allow more slack, our clients’ reaction yields often hinge on clean, well-characterized acids.

    We ship material in glass-lined chemical drums or bags—as dictated by sensitivity to atmosphere and cross-contamination—based on our understanding that some benzoic acid derivatives react to trace amounts of iron or moisture. Careful drying under inert gas and immediate sealing follows every batch. It’s not just routine; it saves money and headaches for downstream users struggling with ghost peaks or color bodies in their actives.

    Real Use Cases: The Role of 2F6NBA Across Labs and Production Plants

    From the lens of a hands-on producer, 2-Fluoro-6-Nitrobenzoic Acid earns its keep in multi-step synthesis routes. Researchers in medicinal chemistry regularly come to us for this molecule to access fluorinated aromatic cores, which cannot be substituted with more common acids like 2-Fluorobenzoic or 6-Nitrobenzoic alone. The paired substitution unlocks reactivity patterns in Suzuki or Buchwald–Hartwig couplings; the resulting fragments build into active pharmaceutical ingredients, specialty agrochemicals, and advanced polymers.

    One client found that their borylation of the 2F6NBA ring gave much higher yields, and fewer purification headaches, than with less pure or mixed-regioisomer material sourced elsewhere. Time after time, these stories anchor our investments into higher-end analytical verification and process tuning.

    What Makes 2-Fluoro-6-Nitrobenzoic Acid Different in Practice

    Compared to other nitrobenzoic acids or mono-fluorinated analogs, 2F6NBA brings a very defined set of reactivity and electronic characteristics. The ortho-fluorine both activates and directs many coupling reactions, allowing users to build up dense substitution patterns on the ring that remain difficult when starting from a less tailored intermediate.

    Some chemists try to replicate the same results starting from multipurpose acids, or by blending separate nitro and fluoro substituents onto the aromatic ring. They usually see dead-ends or low conversions. Our 2F6NBA, with guaranteed regioselectivity, saves the back-and-forth optimization and delivers specialty performance. This translates into fewer wasted batches, reduced column work, and higher certainty in scale-up. Our regulars often cite that this compound cuts weeks off their project timelines, running smoothly in both bench-top glassware and mid-scale reactors.

    Consistency as a Working Principle

    The world of chemical manufacturing rarely tolerates surprises. In our facility, repeatability means running the same process over dozens of batches and building a true statistical picture of impurity backgrounds, melting points, and reaction profiles. We track initial raw materials by supplier lot and demand detailed impurity lists before committing to a vendor. Each batch faces a battery of checks, from NMR to HPLC and trace-metal by ICP, reflecting a culture that rarely leaves quality to trust alone.

    Deviations turn up as early as the first recrystallization or filtration; any change in crystal habit, or a shift in color, prompts immediate investigation and process recalibration. Over years, the investments in these checks earned customer loyalty from process chemists who come back for peace of mind, not just a lower price.

    Practical Handling and User Experience: What Matters to Chemists

    From packing to shipping, we target issues that real lab teams face: material caking during storage, changes in particle size, unwanted static, or micro-contamination. A freshly dried batch of 2-Fluoro-6-Nitrobenzoic Acid resists clumping due to our vacuum drying and sifted sieving steps, while inert-gas padding carries through shelf life out to one year. Our technical team answers questions on storage, transfer losses in process, and best practices for scaling up—drawing on years of direct-use feedback, not just textbook wisdom.

    Some partners run continuous flow reactors and demand exact dosing; others scale kilo lots with batch-cooling crystallizations. We’ve learned that while certain issues—like oxidative discoloration—rarely surface in pure lots of 2F6NBA, they can snowball fast if exposure or minor contamination creep in before or during use. By sharing protocols and our error logs, we help new users avoid pitfalls that would otherwise appear only after pilot or commercial trials.

    Environmental Responsibility on the Manufacturer’s Side

    With regulatory eyes on synthetic intermediates, we find it crucial to minimize residual waste and solvent use right from the factory floor. Our nitration process runs at carefully monitored temperature regimes, with continuous pH and emissions tracking to limit NOx output. Fluorination steps rely on state-of-the-art containment, and all aqueous and organic waste streams head to licensed third-party treatment to avoid untracked chemical releases.

    Years ago, disposal meant trucking out tons of spent acid and organics. Today we’ve switched over to in-house pre-neutralization and solvent recovery, cutting waste output by more than a third. These investments aren’t greenwashing; they come from watching local regulations tighten and from firsthand meetings with downstream partners who require REACH compliance and a firm supply chain audit trail.

    Our customers benefit: cleaner product, less risk of regulatory snags, and strong documentation for their own compliance reviews. Requests for Life Cycle Assessment (LCA) or carbon footprint data meet with real, audited numbers. That kind of credibility is only possible for firms that control their own manufacturing end-to-end, not just trading warehouse stocks.

    Supporting Real Users: From University Labs to Fine Chemical Producers

    Having built a customer base including academic research teams and major pharma, we see how the demands change across different sectors. University labs often push for fast turnarounds on small packages with high analytical depth, wanting real spectra and full CoAs instead of generic PDFs. The feedback loop is immediate: if a batch underperforms—say, unexpected side reactions or purity drift—we hear back in days and investigate from both sides.

    Larger fine chemical manufacturers or contract synthesis groups look for long-term, multi-kilo supply arrangements. Trust in the reliability of material is everything. We give site visits, open up our QA/QC records, and co-develop control strategies for sensitive applications. Some of our most experienced customers use 2-Fluoro-6-Nitrobenzoic Acid as a performance benchmark for their own purification trains, knowing it tracks well with “difficult” intermediates used in later steps.

    Lessons Learned: The Hidden Importance of Purity and Traceability

    Years ago, we fielded calls from partners who had run high-throughput fragment couplings using off-spec 2F6NBA from unnamed suppliers, only to struggle with impurity cascades and fouled reactors. The experience drove home the fact that a complex intermediate, even at “fine chemical” grade, can throw off entire downstream routes if handled casually. We created a feedback program for customers to share details on unsuccessful or problematic reactions, using their insights to tweak both our QA and our shipment procedures.

    It’s not about chasing paperwork or boasting certificates—traceability makes every batch a reference point in the larger process landscape. Our chemists track isotope ratios, minor regioisomer populations, and residual solvents at a level that supports not just audits, but real chemical predictability for anyone using the material in critical synthesis.

    Staying Ahead: Refining What Works in a Fast-Moving Industry

    The worldwide demand for niche building blocks like 2-Fluoro-6-Nitrobenzoic Acid keeps climbing, driven by innovation in medicinal chemistry and more complex active molecules. Process intensification, continuous flow chemistry, and green chemistry now move from pilot to production in record time. Experienced buyers and technical teams expect more than just stock on hand—they need manufacturing partners who keep pace with changing requirements.

    To meet this, we are not static. Our development engineers review every new customer use case, looping in suggestions for analytical upgrades, tweaks to standard operating procedures, and new packaging configurations. Recently, one client required micro-sized flakes for a microfluidic screen; another wanted ultra-low moisture for a high-temperature amide coupling. We responded with tailored batch runs, supported by custom endpoints in drying and particle milling, proving our willingness to engage in problem-solving instead of “one size fits all.”

    Getting 2-Fluoro-6-Nitrobenzoic Acid Right—From Raw Input to Final Shipping

    Every lot starts with a documented source of starting material, examined for trace elemental content and consistent morphology. Since trace iron and heavy metals can catalyze unwanted decomposition, our QA team runs all inputs through standardized checks prior to synthesis. Real-time monitoring of the reaction, closely watched by experienced operators and digital control systems, means fewer surprises and a tighter yield curve.

    The steps after pure acid formation require as much discipline as the upstream chemistry. Material heads through controlled crystallizations, followed by thorough washing and drying. Each drum receives its own bar-coded identity, linking physical inventory to digital batch records. We run confirmatory analysis on random samples before release, matching spectral and chromatographic data from the lot against historical controls.

    Shipping logistics round out the chain, focusing on matching right-fit packaging to route, climate, and handling risk. Transport partners train in our specific procedures for handling sensitive aromatic acids, including rapid transfers to minimize atmospheric uptake and avoiding situations where packages might linger in hot or unregulated warehouses.

    The Value of Direct Manufacturing: Keeping the Chain Transparent

    We manufacture our own product from start to finish, cutting out the confusion and layer-cake problems that can trouble the distributed model. Customers often approach us after challenges with multi-tiered sourcing, finding trace impurities or mismatched analytical data despite purchasing a “nameplate” chemical. Our work brings them into direct connection with the team that actually understands what came out of the reactor, and who stands behind the data—answering questions about synthetic pathway, packing material, or analytical method with practical, first-hand insight.

    Supply chain disturbances, regulatory shifts, and tightening user requirements keep raising the bar. We see our job as more than just shipping drums of acid. Our focus remains on anticipating production issues, improving our analysis, and thinking through the full impact of every change—because a missed detail in our plant turns into a lost week, or a failed trial, for someone down the line in the field of molecular innovation.

    Reflections from the Factory Floor: Into the Future

    As demand for advanced benzoic derivatives grows, we see 2-Fluoro-6-Nitrobenzoic Acid gaining even greater relevance. Technical challenges evolve. New applications appear as drug discovery heads into ever-tougher molecules. The feedback loop between user and manufacturer tightens: the days of “anonymous intermediates” are fading.

    For us, every kilogram reflects both a technical achievement and a relationship. We treat our role in the chain as a partner, troubleshooting unusual reactivity patterns, squashing batch-to-batch variance, and troubleshooting unforeseen storage or handling issues. Blending analytical rigor with a willingness to listen makes a compound like 2F6NBA into more than just a chemical identifier. It becomes a cornerstone for chemists searching for that reliable, no-drama building block that performs as expected—not just the first time, but every time.

    The Real Difference: Putting Experience Into Every Drum

    With the growing sophistication of chemical synthesis, the days of “good enough” material recede. By trusting their advanced routes to genuine manufacturers, not third-party aggregators, customers find sustainable advantage. The edge lies not just in purity numbers printed on a report, but in day-to-day technical support, swift reactions to feedback, and years of iterative improvement built into every batch.

    As the landscape evolves, we stay committed to improving alongside it. Whether tackling unusual reactivity, troubleshooting trace impurity effects, or refining our analytical depth, our journey with 2-Fluoro-6-Nitrobenzoic Acid remains one of constant learning and dialogue. Product by product, shipment by shipment, we focus on reliability, openness, and deep respect for the chemist’s craft.