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2-Fluoro-5-Nitrotoluene

    • Product Name 2-Fluoro-5-Nitrotoluene
    • Alias 2-Fluoro-5-nitro-1-methylbenzene
    • Einecs 211-996-1
    • 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

    446634

    Chemical Name 2-Fluoro-5-Nitrotoluene
    Cas Number 446-02-6
    Molecular Formula C7H6FNO2
    Molecular Weight 155.13
    Appearance Yellow to brown liquid
    Boiling Point 215-217°C
    Melting Point -7°C
    Density 1.31 g/cm3
    Refractive Index 1.548
    Flash Point 89°C
    Solubility Slightly soluble in water
    Smiles CC1=CC(=C(C=C1)[N+](=O)[O-])F
    Inchi InChI=1S/C7H6FNO2/c1-5-2-3-6(8)7(4-5)9(10)11/h2-4H,1H3

    As an accredited 2-Fluoro-5-Nitrotoluene 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 100 grams of 2-Fluoro-5-Nitrotoluene, tightly sealed, with hazard labeling and chemical identification details.
    Shipping 2-Fluoro-5-Nitrotoluene should be shipped in tightly sealed, clearly labeled containers, protected from heat and direct sunlight. It must comply with all applicable hazardous material transportation regulations. Proper documentation and safety data sheets should accompany the shipment. Use appropriate cushioning and package to prevent leaks or spills during transit.
    Storage **Storage of 2-Fluoro-5-Nitrotoluene:** Store 2-Fluoro-5-Nitrotoluene in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and bases. Keep the container tightly closed and properly labeled. Protect from sources of ignition, heat, and direct sunlight. Use appropriate chemical-resistant containers and avoid any conditions that may lead to the material’s decomposition or hazardous reactions.
    Application of 2-Fluoro-5-Nitrotoluene

    Applications of 2-Fluoro-5-Nitrotoluene in Industrial Manufacturing

    2-Fluoro-5-Nitrotoluene serves as a specialized intermediate in the synthesis of fine chemicals, agrochemicals, pharmaceuticals, and advanced materials. As the direct manufacturer, we focus on sectors where stringent process controls and consistent raw material quality are essential. Below, we detail real downstream industrial applications, highlighting critical compliance, integration points, and end products.

    1. Agrochemical Intermediate for Herbicide Synthesis

    Major agrochemical firms use this product as a fluorinated aromatic building block in selective herbicide synthesis. It enters key nitration and coupling steps, allowing formulation chemists to design molecules with enhanced weed selectivity and environmental stability. Its nitro and fluoro groups provide distinct reactivity channels, essential for tuning physicochemical behavior in modern crop protection agents. Production batches require trace impurity monitoring to ensure herbicide bioactivity and regulatory acceptance.

    Industry compliance standards

    • ISO 9001 Quality Management for chemical manufacturing
    • REACH Regulation (EC) No 1907/2006 registration for European markets
    • US EPA Toxic Substances Control Act (TSCA) registration
    • China Pesticide Registration standard (GB 3796, GB 4826)

    Typical usage ratio

    • Acts as 10–18% by weight in herbicidal active ingredient synthesis
    • Exact percentage depends on molecular target and desired activity spectrum

    Downstream process integration

    • Enters as a core substrate in nucleophilic aromatic substitution reactions
    • Used in subsequent reduction, coupling, or diazotization steps as required

    Final product types

    • Fluorinated phenylurea herbicides
    • Pyridine-based herbicidal compounds
    • Commercial weed control formulations

    2. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Leading pharmaceutical manufacturers incorporate this compound to produce certain anti-infective and anti-inflammatory APIs. The molecule’s dual electron-withdrawing substituents enable regioselective reactions for advanced intermediates. Process chemists optimize scaling parameters, including catalyst loading and solvent system, to ensure batch reproducibility and patient safety. Access to validated analytical methods assists in monitoring carryover in regulated environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF Monographs for relevant intermediates
    • EU EudraLex Volume 4, Part II
    • US FDA 21 CFR Part 211 (cGMP for drugs)

    Typical usage ratio

    • Ranges from 5–12% as a starting material in target API synthesis
    • Adjusted based on yield, process efficiency, and molecular complexity

    Downstream process integration

    • Included in multi-step organic reactions involving reduction and halogen exchange
    • Enters amidation or ring-closure stages downstream

    Final product types

    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Veterinary medicine precursors
    • Specialty antimicrobials

    3. Intermediate for Dye and Pigment Manufacturing

    Certified dye and pigment producers utilize the nitro-fluoro toluene structure for azo and disperse dye syntheses applied to synthetic fibers. Its unique electronic profile facilitates controlled diazotization, producing chromophores with targeted absorption and enhanced fastness properties. Downstream plants maintain analytical verification of residual aromatic amines to match both ecological requirements and end-user color consistency.

    Industry compliance standards

    • OEKO-TEX Standard 100 restricted substances list
    • DIN EN ISO 105 color fastness testing standards
    • EU REACH Annex XVII restrictions on aromatic amines
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturer Restricted Substances List)

    Typical usage ratio

    • Applied at 7–14% by mass during batch azo dye coupling
    • Ratio varies by color intensity and substrate type

    Downstream process integration

    • Used during diazotization, then combined with phenol or aniline derivatives
    • Participates in post-coupling treatments for dye particle stabilization

    Final product types

    • Disperse dyes for polyester textiles
    • Azo pigments for industrial inks
    • Special effect colorants for plastics

    4. Intermediate for Fluorinated Polymer Additive Preparation

    Producers of engineered plastics and coatings turn to this compound as a monomer precursor for fluorinated functional additives. The strong C–F bond imparts desirable hydrophobic and chemical-resistant qualities when introduced during polymerization or masterbatch production. Product managers monitor the additive’s distribution to achieve precise mechanical and barrier performance for challenging application environments such as electronics encapsulation or automotive coatings.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical processing
    • RoHS Directive 2011/65/EU for electrical/electronic components
    • REACH SVHC checks for persistent organic pollutants
    • UL 94 flammability specification for plastic materials

    Typical usage ratio

    • Used at 2–8% loading in fluorinated additive masterbatches or prepolymers
    • Adjusted based on final polymer application and target barrier characteristics

    Downstream process integration

    • Incorporated during initial monomer blending or reactive extrusion phases
    • Co-formulated with other specialty monomers for copolymer formation

    Final product types

    • Hydrophobic coatings for electronics
    • Fluorinated engineering plastic compounds
    • Barrier resins for packaging and automotive interiors
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    Certification & Compliance
    More Introduction

    Introducing 2-Fluoro-5-Nitrotoluene: Crafted for Today’s Synthesis Demands

    Meeting the Modern Synthetic Challenge

    Across the chemical industry, practical solutions drive progress. Take a closer look at 2-Fluoro-5-Nitrotoluene: its molecular structure, C7H6FNO2, forms an important building block for a variety of advanced molecules. Every batch starts with a clear target—reliable performance in real-life synthesis. As a direct manufacturer, we handle each step ourselves, from raw material sourcing to purification and quality reassurance.

    Most clients select 2-Fluoro-5-Nitrotoluene for its dual-reactivity: a nitro group at the 5-position and a fluorine at the 2-position on the toluene ring. This pairing balances electronic effects and sets it apart from simple monofluorotoluenes or dinitrotoluenes, opening more room for creative organic transformations on the aromatic framework. It serves as a starter for pharmaceutical intermediates, specialty dyes, and agricultural research. Through hands-on production, we don’t just consider theoretical yields; feedback from bench-scale to pilot plant runs influences our consistency checks.

    Detailing the Specifications That Matter

    Technicians and R&D chemists focus on what influences their reactions most: purity, moisture, and isomeric precision. Our process delivers a material purity of at least 99%. Every lot undergoes GC and NMR controls; we watch for typical impurities—such as unreacted toluene, alternative halogenated isomers, and residual starting acids—since these can cause unwanted side-products downstream. Minor process tweaks over the years taught us which solvents, reaction times, and workup protocols most reliably eliminate carry-over.

    Product comes as a pale yellow to off-white crystalline solid at ambient temperature, with melting points checked batch by batch. Each specification sheet lists water content, but by drying carefully after each synthesis, moisture rarely exceeds 0.2%, ensuring fewer hydrolysis issues for reactive downstream chemistry. We steer clear of packaging bulk in ambient air; sealed drums under inert atmosphere maintain stability and shelf-life.

    Applying 2-Fluoro-5-Nitrotoluene: Beyond Bench Reactions

    Toluene derivatives like this one often set the stage for more elaborate active ingredients. Fluorinated aromatics in particular contribute unique electronic characteristics—stabilizing certain intermediates, shifting reaction selectivity, or modifying biological activity in drug candidates. The addition of a nitro group increases its versatility further.

    Process chemists use nitrated-fluorotoluenes as stepping stones in nucleophilic aromatic substitution, the nitro activating the ring for further modification, while the fluorine’s presence lets them introduce substitution at positions otherwise inaccessible. In dye and pigment research, its profile supports the development of molecules that meet new brightness or fastness requirements. Agricultural labs reach for it when screening new classes of herbicides or pesticides—often those with specific action modes needing a delicate balance of hydrophobic and electron-withdrawing groups.

    As a manufacturer working closely with formulation chemists and academic groups, we’ve watched our product’s role grow from a specialty intermediate to a regular fixture in combinatorial libraries. Last year, several clients in the pharma sector began using it for early-stage SAR studies, citing its track record for conversion and its behavior during scale-up.

    Direct Manufacturing Control: How We Keep Quality Consistent

    Many buyers ask about batch-to-batch reliability. By running everything in-house—reactor loading, solvents, crystallization, and final packing—we have the visibility needed for proactive adjustments. All steps, from fluorination to nitration, use only high-purity reagents and dedicated glass-lined equipment. This investment aims to ensure minimal contamination and a cleaner, more reproducible output.

    Routine revalidation of procedure steps—every few campaigns—lets us catch small drifts in yields or impurity levels that long-term outsourcing could easily miss. Our technical team pulls random samples at both the crude and polished stages, compares spectra, and inspects AQ/QC trends. Direct relationships with end-users mean rapid feedback: if something falls below expectation for solubility or conversion rate, that information returns to the production floor.

    We also learned from clients that physical consistency matters: no one wants needle-like crystals in one lot, heavy clods in the next. By refining crystallization solvent choice and cooling profiles, we provide uniform, easy-to-handle product, improving weighing accuracy and dosing.

    Real Differences from Other Aromatic Intermediates

    What draws manufacturers to 2-Fluoro-5-Nitrotoluene arises from its particular substitution pattern. Run-of-the-mill nitrotoluenes—without fluorine—miss out on the rearrangement possibilities in certain heterocycle syntheses. In contrast, adding fluorine at the ortho-position gives chemists a unique reactivity lever, especially welcoming when exploring new scaffolds in medicinal chemistry.

    Compared to chlorinated or brominated analogs, fluoro-substitution leads to different leaving group properties, making it more suitable for SNAr applications at milder conditions with fewer side products. Environmental and regulatory matters lean in its favor too: no heavy metal residues and little halogenated waste complicating post-reaction workups, especially at kilo-scale.

    Project managers benefit: less downtime optimizing purification or tweaking base equivalents. In actual downstream applications, our clients report cleaner conversion rates when introducing amines or protected alcohol groups onto the aromatic ring. Those switching from monochloronitro or dibromonitro variants often mention time savings during method development.

    Safety and Handling Realities

    Anyone familiar with nitroaromatics knows their hazards. We stress accurate labeling for flammability and toxicity during all internal movement. Long experience—hundreds of tons over the last decade—taught us the routines that minimize risk: bonded containers, spill control trays, regular ventilation checks in the warehouse. Strict separation from acids and oxidizers avoids runaway reactions.

    Data sheets provide all relevant thresholds, but in everyday practice, double-wrapped lined drums reduce vapor loss and minimize staff exposure. Efforts pay off through low loss rates in transit and steady shelf stability when stored below 25°C. Over years, continuous monitoring delivers data on long-term product integrity, supporting customers with shelf-life records for their own batch protocols.

    Working with solvents, one learns to chase down every potential residue. We employ GC-MS screening on outgoing stock, paying attention to not only process solvents but also unanticipated byproducts, which could impact reaction selectivity for sensitive pharmaceutical projects.

    Practical Experiences: Synthesis, Packing, and Delivery

    Over the years, we found that genuine interaction between operator and product cannot be replicated by automated distribution alone. We welcome questions from formulation teams about specific packing sizes. Our plant can switch between bulk and laboratory-scale packaging with quick turnaround, thanks to dedicated buffer storage and batch segregation. For international shipments, robust packaging standards match freight requirements, with custom documentation supporting regional compliance.

    Clients sometimes ask how we verify purity mid-delivery. Along with every shipment, we include a full analytical profile—chromatograms, NMR, and FTIR. We hold reference samples for at least three years, letting end-users double-check any concerns. Feedback loops evolve our process: recently, feedback about caking during high-humidity shipping led us to develop an improved desiccant protocol.

    Industry Trends: A Shifting Demand for Specialty Intermediates

    The landscape for aromatic building blocks is changing fast. Generic intermediates see commoditization; specialized derivatives such as 2-Fluoro-5-Nitrotoluene grow popular among innovators chasing new patents, advanced agro technologies, and targeted pharmaceuticals. Over the last five years, more process teams have migrated away from unmodified nitrotoluenes, taking advantage of the unique reactivity this molecule enables.

    Our experience reflects this shift. Requests for kilo-lots and flexible shipping windows multiplied, especially from mid-sized biotech and new materials startups. These clients appreciate rapid parallel screening, enabled by aromatic frameworks that accommodate efficient downstream transformations. High-purity aromatic intermediates no longer serve only large-scale manufacturers—small labs with advanced characterization capabilities expect consistent, reproducible material on short notice.

    Environmental Responsibility and Compliance Commitments

    Manufacturing fine chemicals, especially nitro and fluoroaromatics, places special obligations on producers. Over the last decade, environmental controls tightened—driven by regulatory updates and customer priorities. We invested in recovery and treatment systems: vapor scrubbers and solvent reclamation prevent significant fluorinated and nitrated emissions from reaching the environment.

    All process water passes through multi-stage neutralization, protecting downstream users and meeting discharge requirements. As a producer conscious of global supply chain developments, we provide transparency into sourcing and waste management. Each customer receives traceable batch histories, which proves crucial for regulatory audits.

    Efforts also extend to refining reaction protocols, reducing reliance on halogenated solvents, and exploring new reagent choices when feasible. The feedback loop from customers manages to point out opportunities that might not emerge from in-house QA alone. In discussion with downstream partners, we developed take-back programs for non-specification or expired material, closing the loop and reducing hazardous waste.

    Troubleshooting Common Application Issues

    Not every batch transfers perfectly from the production plant to the customer's bench or reactor. Over time, frequent concerns include unusually slow reactivity during nucleophilic substitution, or rare issues with unanticipated byproducts after extended storage or transit during humid seasons. To address these, we collaborate closely with customers, exchanging analytical data and running parallel reactions in our own application labs.

    We've seen how tightening up moisture control during final drying results in improved conversion rates for SNAr transformations, while more stringent in-process filtration lessens the load of side products that tend to complicate downstream chromatography. To further support varied application demands, our technical support responds rapidly to questions about compatibility with new reagents, solvent systems, or temperature protocols.

    When users shift from laboratory to pilot scale, we step in to offer process recommendations: whether adjusting dissolution rates, recalibrating dosing protocols, or tweaking carrier solvent blends. Our experiences allow for practical suggestions on stirring speeds, addition timeframes, and impurity monitoring at each transfer point.

    Advantages of Close Supplier-Manufacturer Relationships

    Real progress often grows from dialogue rather than catalog transactions. Our team offers direct access to the actual chemists and engineers behind every lot. Whether resolving questions about storage life, testing blending protocols, or providing documentation for regulatory clearance, fast responses backed by real production experience make the difference.

    On several occasions, project managers shifted synthetic routes mid-campaign. Ready communication let us accelerate new batch synthesis or adjust specifications. We treat every inquiry as a step in building confidence—a practice reflected by repeat collaborations and new requests spurred by word-of-mouth among fellow producers.

    By owning the manufacturing chain from start to finish, we drive short feedback cycles and quick adaptation. Insights gained in one application area inform improvements in another, closing the loop faster than distant procurement models.

    Supporting the Next Wave of Discovery

    Shifts in chemical manufacturing always come with uncertainty. Reliable access to specialty building blocks like 2-Fluoro-5-Nitrotoluene gives downstream innovators flexibility to push boundaries. As regulatory standards and performance targets climb, the upstream input—shaped by consistent production, adaptable logistics, and a real understanding of lab-to-plant transition—lets researchers keep pace.

    Our experience shows that the greatest success comes not just from what’s in the drum, but from the expertise that travels alongside it. Questions evolve: from singular focus on purity or cost-per-kilo, toward broader concerns like environmental impact, application utility, and practical troubleshooting. We keep learning, responding, and adapting.

    Whether supporting established process plants or emerging research teams, the aim remains steady: provide a solid link in the supply chain that pushes technical progress forward. 2-Fluoro-5-Nitrotoluene, as we produce it, isn’t just another item on a product list—it reflects years of experience and the evolving needs of each user who puts it to work.