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2-Fluoro-6-Nitrotoluene

    • Product Name 2-Fluoro-6-Nitrotoluene
    • Alias 2-Fluoro-6-nitro-1-methylbenzene
    • Einecs 221-063-7
    • 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

    754542

    Chemical Name 2-Fluoro-6-Nitrotoluene
    Molecular Formula C7H6FNO2
    Molecular Weight 155.13 g/mol
    Cas Number 2048-52-6
    Appearance Pale yellow liquid
    Boiling Point 208-211 °C
    Melting Point -10 °C
    Density 1.319 g/cm3
    Refractive Index 1.544
    Flash Point 90 °C
    Solubility Insoluble in water
    Smiles CC1=C(C=CC=C1F)[N+](=O)[O-]
    Inchi InChI=1S/C7H6FNO2/c1-5-2-3-6(8)4-7(5)9(10)11/h2-4H,1H3

    As an accredited 2-Fluoro-6-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, 100 g, tightly sealed with a screw cap and safety label displaying hazard symbols, chemical name, and purity.
    Shipping 2-Fluoro-6-Nitrotoluene should be shipped in accordance with relevant chemical safety regulations. It must be securely packed in airtight, chemical-resistant containers, labeled appropriately, and handled as a hazardous material. During transport, it requires secondary containment to prevent leaks, and may require temperature control, ventilation, and documentation compliant with DOT/IATA/IMDG standards.
    Storage **2-Fluoro-6-nitrotoluene** should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and reducing agents. Protect from moisture and direct sunlight. Properly label the container, and keep it away from food and drink. Use appropriate personal protective equipment when handling.
    Application of 2-Fluoro-6-Nitrotoluene

    Applications of 2-Fluoro-6-Nitrotoluene in Industrial Manufacturing

    As a direct manufacturer of 2-Fluoro-6-Nitrotoluene, we deliver this specialized chemical intermediate to large-scale producers working in advanced pharmaceutical synthesis, agrochemical formulation, and specialty dye development. Our production experience enables us to supply consistent quality material suited for highly controlled, specification-driven downstream processes. The following section details real industrial applications where this raw material plays a critical role, with a focus on compliance, formulation, process integration, and finished product types.

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

    Downstream pharmaceutical manufacturers rely on 2-Fluoro-6-Nitrotoluene for constructing fluorinated aromatic building blocks used in the synthesis of APIs such as anti-inflammatory and central nervous system agents. The compound enters multi-step reactions, typically in Suzuki or Buchwald couplings, providing a source of both nitro and fluoro functionalities necessary for targeted molecular modifications. API projects often require rigorous traceability and validation, with material purity and reactivity directly impacting final compound yield and compliance with international pharmacopeias.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia, relevant monographs for fluorinated intermediates
    • WHO Good Manufacturing Practices (GMP) guidelines

    Typical usage ratio

    • Ranges from 0.05 to 0.22 molar equivalents per API target batch, adjusted based on synthesis route and yield optimization.

    Downstream process integration

    • Charged during the early halogenation or nitration steps in multi-step organic syntheses, proceeding through hydrogenation, coupling, or cyclization stages under controlled reaction temperatures and pH.

    Final product types

    • Prescription drug APIs such as non-steroidal anti-inflammatory agents (NSAIDs)
    • CNS-active pharmaceutical substances with aromatic fluorine residues
    • Fluorinated pharmaceutical intermediates supplied to contract manufacturers

    2. Agrochemical Active Ingredient Manufacturing

    Major agrochemical producers incorporate 2-Fluoro-6-Nitrotoluene into targeted herbicide and fungicide synthesis, exploiting its synergistic effect in generating nitro-fluorinated aromatic cores essential for selective bioactivity. The raw material acts as a precursor in nitration and fluorination sequencing, contributing to product specificity and regulatory compliance for crop protection products where molecular uniformity is strictly policed.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO)
    • ISO 9001:2015 Quality Management for Chemical Manufacturing
    • REACH Regulation (EC 1907/2006) for agrochemical precursors
    • EPA FIFRA standards for pesticide ingredient traceability (US)

    Typical usage ratio

    • 0.5–5% by total reactant mass per batch synthesis, with dosage refined per target molecule and active concentration requirements.

    Downstream process integration

    • Fed into intermediate nitroarene synthesis prior to sulfonation or reduction, followed by condensation or cyclization reactions under high-shear agitation and temperature control.

    Final product types

    • Selective herbicidal active compounds for broadleaf and cereal protection
    • Contact and systemic fungicidal ingredients for pre-emergence and post-emergence formulations
    • Raw materials for further downstream processing into formulated pesticide blends

    3. Specialty Dye and Pigment Synthesis

    Producers of high-performance dyes and pigments use 2-Fluoro-6-Nitrotoluene to obtain colorants with defined chromatic and fastness properties through nitration and electrophilic aromatic substitution. The dual functional groups improve dye substantivity and stability on technical textiles and plastics. This material fits processes demanding chemical purity and batch-to-batch reproducibility due to tight color and performance parameters mandated in automotive and textile coatings.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for dye and pigment ingredients (Textiles)
    • EN 71-3 European Toy Safety Standard (Colorant migration limits)
    • ISO 9001:2015 Quality Management for Pigment Synthesis
    • GHS SDS Compliance (Globally Harmonized System)

    Typical usage ratio

    • Employed at levels from 1–8 wt.% relative to primary aromatic substrate, contingent on targeted color intensity and application substrate.

    Downstream process integration

    • Dosed during controlled aromatic substitution as a nitro-fluoro source, typically under catalytic conditions in batch or flow reactors, followed by purification and microfiltration.

    Final product types

    • High-fastness dyes for polyester and polyamide fabrics
    • Specialty pigments for plastics and engineered coatings
    • Automotive and industrial-grade colorant dispersions

    4. Chemical Synthesis of Custom Fluorinated Building Blocks

    Synthesizers of advanced intermediates for fine chemical and material science applications deploy 2-Fluoro-6-Nitrotoluene to introduce both nitro and fluoro groups into aromatic structures, enabling downstream diversification via reduction, aminolysis, or metal-catalyzed cross-coupling. This usage supports research and production for liquid crystals, OLED materials, and high-value functional coatings, requiring reliable supply of highly pure, specification-certified inputs under controlled handling and traceability protocols.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for Chemical Synthesis
    • REACH Registration (EC 1907/2006) for specialty chemical raw materials
    • Local chemical management regulations for process intermediates
    • GMP for Fine Chemicals (where supplied to pharma-adjacent industries)

    Typical usage ratio

    • From 0.1 up to 3.5 mol% per synthetic step, with specific adjustment per target molecule architecture and process scale.

    Downstream process integration

    • Added during initial building block construction, usually in stepwise nitration, reduction, or halogen-metal exchange processes; followed by further derivatization or polymerization for electronic or coating applications.

    Final product types

    • Fluorinated aromatic intermediates for high-purity material synthesis
    • Performance additives for electronic displays (OLED, LCD)
    • Custom functional monomers for specialty polymers and advanced coatings
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    Certification & Compliance
    More Introduction

    2-Fluoro-6-Nitrotoluene: Manufacturing Insight and Application Commentary

    Years in the Trenches: Crafting 2-Fluoro-6-Nitrotoluene on the Manufacturing Floor

    Our experience making 2-Fluoro-6-nitrotoluene comes from deeply rooted chemical process know-how. Day in and day out, batches of this niche aromatic compound emerge from reactors under tightly monitored conditions. The chemical structure—fluorine at the ortho position, nitro at the para to methyl—defines how the molecule moves in reaction schemes and how it holds together through processing. We don’t just know those substitutions on paper. Our teams confront the thermodynamic quirks of fluorinated nitroaromatics, handling their volatility and reactivity in large-scale vessels. Each batch goes through precise controls: checking melting points, GC purity, isomer absence, and water content. Small variations in raw fluorotoluene feeds shift the recrystallization process—these lessons come only through hands-on production.

    Specifications Shaped by Practical Needs

    In our reactors, the real-world specs evolve around reliability. We target purities greater than 99% by GC, because customers in pharmaceuticals and agrochemical intermediates find that even slim impurities risk their downstream catalysts or enzyme steps. Our plant team routinely pushes for single-digit water content, since lingering moisture leads to hydrolysis risks both during transport and in customer-side reactions. We monitor and control particulate contamination and color, since off-odor or tint—often a sign of oxidation or trace metal pickup—undermines high-value transformations later. Our product weighs in near a density of 1.3 g/cm³ in liquid form and transitions to a crystalline solid that packs easily for larger-scale usage. Fluctuations in melting point or color catch our attention, since they often reveal upstream batch control flaws that rip down the supply line if left unchecked.

    The work doesn’t stop after the reaction: purification takes center stage. Compared to similar products on our line, 2-Fluoro-6-nitrotoluene requires extra vigilance in vacuum distillation and drying. The nitro group readily absorbs trace water or ambient oxygen, and subpar purification leaves telltale yellowing or instability. Years back, we overhauled our filtration protocols and brought in advanced chemical-resistant seals to block cross-contamination, learning from a costly episode where a single gasket breakdown tainted more than a ton of product. Now, every batch we produce not only meets but beats common purity standards, shaped by the harsh lessons from scaling up.

    Real-World Applications: Stories from the Field

    We do not approach this molecule simply as a set of numbers or a generic intermediate. In practice, most requests come from synthetic chemists driving toward specialty pharmaceuticals or high-value crop protection agents. 2-Fluoro-6-nitrotoluene kicks off reactions leading to complex benzimidazoles, anilines, and fluoro-aryl scaffolds. Its nitro group holds up under reductive conditions, making it a versatile jumping-off point for coupling and substitution routes. Chemists choosing between ortho-fluoro, para-fluoro, or unsubstituted nitrotoluenes care about reactivity. In the case of ortho-fluoro substitution, the electron density around the ring shifts, nudging favor toward certain SNAr transformations. Our technical support often discusses these details directly with R&D chemists at pharmaceutical labs or agrochemical plants, where the reactivity fingerprints determine project outcomes.

    Compared to its close cousin 4-Fluoro-2-nitrotoluene, the 2-position fluorine changes both the physical handling and reactivity. Its boiling point differs by enough to influence distillation setups. In some catalytic hydrogenations, our clients report better yields or selectivity, especially when constrained by sensitive functional groups elsewhere on their molecules. Others find better solubility in their preferred solvents, due in no small part to the position and influence of fluorine. We often invest in customer trials with both isomers, supporting pilot-scale runs to help confirm which version delivers on commercial process economics. Rarely do we see a one-size-fits-all winner; instead, the ortho-fluoro product tends to shine in routes requiring pronounced ring activation or where regioselectivity downstream makes or breaks process efficiency.

    Contrast with Related Products: Design and Handling Differences

    Our plant routinely produces several monofluorinated nitrotoluenes, and 2-Fluoro-6-nitrotoluene stands apart for more than a simple difference in substitution. Production-wise, it presents more exotherm during nitration, requiring close operator vigilance and staged addition of reactants. Colleagues who once worked exclusively with the para-fluoro variant quickly learn to dial back reactor rates and adjust stirring protocols, since runaway heat undermines batch quality or, in rare cases, safety. Storage habits also differ. The ortho-fluoro compound shows slightly greater sensitivity to prolonged exposure to high humidity. To counter this, our packaging and bulk containers always feature high-barrier linings that safeguard the product all the way to the client’s tank farm or synthesis bay.

    Comparing 2-Fluoro-6-nitrotoluene to standard 2-nitrotoluene, the presence of fluorine lowers the rate of side reactions in some aromatic nucleophilic substitutions. Synthetic teams working on fluorinated APIs often tell us the ortho-fluorine clears away possible ortho/para-ambiguities in electrophilic aromatic substitutions, streamlining multi-step syntheses. This gives development chemists an edge in building out drug candidates and lead structures. We know these stories not through spec sheets, but by fielding samples, testing reactivity in our own labs, and walking through scale-up headaches with customers.

    Quality Experience—Bridging Plant Practice and Customer Demands

    Quality assurance isn’t a checkbox on our batch records. Many a time, solvents, ambient air, and even operator handling influence the finished product in ways hard to predict from desk-based SOPs. Over the past decade, we’ve adopted in-line analytical monitoring and batch-feed controls tailored to fluorinated aromatic chemistry. Each new synthesis campaign brings its curveballs: fluctuations in upstream aniline or fluorotoluene quality, or even changes in drum storage practices that shift water ingress rates. We document each deviation and tune our process controls—errors logged, fixed, and lessons passed to new shift chemists.

    Customer feedback loops shape the product just as much as our own QC. When one pharmaceutical client’s catalytic cycle stalled due to trace metallic contamination, our investigations led to overhauling certain condenser materials at our site. That case led to a routine—every customer claim triggers an on-site and in-lab root cause analysis. Through these cycles, we’ve developed a stable, handled product with fewer shock surprises. Reliability in delivery, batch-to-batch purity, and shipment timing often matter as much to customers as the product itself. Our bulk customers, with multimillion-dollar processes riding on timely feedstock, trust that our logistics and plant teams answer phone calls after hours, chase carriers, and solve hiccups without kicking blame.

    Sustainability and Worker Safety: Day-to-Day Realities in Manufacture

    2-Fluoro-6-nitrotoluene challenges our sustainability and safety practices. The nitration step, in particular, demands rigor: nitric acid, water treatment, exothermic runs, and tight air management. For years we juggled waste acid streams, learning the balance between throughput, neutralization chemistry, and scrubbing tower design. Each environmental audit, every new wastewater permit, sharpened our response and upgraded our abatement methods. Operators wear out gloves and aprons faster than on many other lines, since nitroaromatics demand more than routine PPE.

    On one occasion, ambient temperatures spiked during a summer run, pushing the reaction rate. The lessons from that incident led us to automating more of our temperature control and introducing new alarms that catch deviations before they go critical. Worker training covers more than theoretical drills; crew spend days shadowing seasoned operators, learning from hands-on troubleshooting—because an hour in the plant reveals more than a day in a classroom.

    Research Connectivity: Supporting Evolving Use Cases

    Every so often, synthetic chemistry groups develop new transformations or routes that shift the demand for 2-Fluoro-6-nitrotoluene. We keep our pilots and kilo-lab lines flexible, ready to scale up proof-of-concept batches that explore new coupling chemistries or environmental catalysts—often before the wider market catches on. In recent years, fluorinated building blocks have surged in importance, driven by drugs and specialty agrochemicals demanding precise metabolic profiles. Fluorine can mask positions from oxidative metabolism or modify binding profiles in bioactive molecules—details that researchers bring to us long before commercialization.

    We’re not outsiders to these projects. Our technical team not only reads the latest literature but also replicates emerging reactions in our own labs, confirming reactivity profiles and uncovering pitfalls in recovery or workup. Academic teams sometimes discover that their published conditions don't translate to larger reactors; our engineers step in, design custom feeds, or troubleshoot heat transfer bottlenecks. We recognize that real progress in the use of 2-Fluoro-6-nitrotoluene often comes from closing the gap between benchtop discoveries and production-scale realities.

    Troubleshooting and Ongoing Improvement

    Every manufacturing campaign brings new problems. Instrument drift, tank leaks, raw material swing—you name it, we’ve faced it. Sometimes the problems show up as off-spec batches, others as customer phone calls from a stalled pilot run. We don’t shy from these moments. Instead, our leadership encourages direct dialogue between plant shift leads, QC chemists, and technical account managers. Early in our production history, a recurrent problem with polymeric residue in the distillate threatened to sideline the whole 2-Fluoro-6-nitrotoluene line. Working in cross-functional teams, we tracked the impurity to a subtle side reaction in one of our aged reactor linings, learned the right cleaning cycle, and built more robust SOPs.

    We log each technical troubleshooting episode in a cumulative archive, cross-referencing batch records and root causes in monthly stand-downs. The most effective solutions spring from team-wide brainstorming—often someone from maintenance or packaging, not just the front-line chemists. These tweaks, large and small, mean fewer surprises for us and smoother, more consistent product for those relying on our deliveries.

    Packaging and Transit: Lessons Learned on the Road

    Transporting 2-Fluoro-6-nitrotoluene involves more than tossing drums on a truck. We’ve learned that subtle temperature and humidity fluctuations during transit can nudge the product toward instability or minor decomposition, especially if storage beyond a week or two occurs in humid zones. Early on, a careless loadout resulted in water ingress and product complaint from a major pharma customer. That single event overhauled our drum specification to require even tighter-sealing, multi-layer protection—not just for regulatory compliance, but for process reality.

    Now, we maintain a supplier partnership network that tracks the shipping environment and logs temperature swings in transit, allowing rapid intervention if conditions veer out of range. Distribution channels can introduce delays or raw material swaps at handlers—another reason we supply full CoAs and reference batch histories. Customers on tight process schedules rely not just on a chemical, but on detailed knowledge of what happened from kettle to dock.

    Regulatory Landscape: Working within a Broader System

    Operating under global regulations for nitroaromatic production, our team faces routine environmental permitting, chemical registration, and occupational health inspections. For 2-Fluoro-6-nitrotoluene, clear labeling, traceability, and updated SDS documents travel with every shipment. Each region, from the Americas to Asia Pacific, layers on compliance paperwork, storage mandates, and emission tracking. Over the years, we developed dedicated compliance teams that ensure no detail slips during audits or regulatory renewals.

    Regulations also push us to optimize process yields and minimize emissions. Early process development revealed avoidable solvent losses and higher-than-anticipated vent releases. By streamlining batch sequences and updating degassing scrubbers, we cut losses and improved environmental scores. Our shift toward more closed-loop systems directly stemmed from regulatory tightening. Through all this, we keep open lines to local and international agencies, recognizing they form part of the landscape where specialty chemicals like ours make their way into critical applications.

    Customer Collaboration: Building Trust through Shared Progress

    Decades in this industry have taught us that close technical partnership with customers makes or breaks the success of 2-Fluoro-6-nitrotoluene in applied settings. Challenges often show up mid-project, after an initial process transfer or during pilot-plant scaleup. We visit customer sites, run joint troubleshooting, and adapt QA routines to emerging requirements—be it new impurity thresholds, process safety, or logistics documentation. In doing so, we develop a shared language and a foundation of trust, insulating both parties from supply chain strains or R&D roadblocks.

    Sometimes this means producing a custom lot with tighter specs, or supporting a validation run with onsite technical advisors. True partnership comes when problems—real or anticipated—land on our desk as soon as they show up in the customer’s plant. We’ve shipped emergency lots across continents, sourced alternate drum supplies at midnight, and retooled batch schedules at short notice. These are not anecdotes, but the daily reality of manufacturing specialty intermediates for fast-moving sectors.

    Conclusion: Experience at Every Step

    Producing 2-Fluoro-6-nitrotoluene involves technical expertise, constant adaptation, and hands-on troubleshooting at every stage. Our ongoing dialogue with customers, regulators, and internal crews shapes our approach to manufacturing and supply. No product, including this fluorinated nitroaromatic, stands apart from its process realities and real-world usage stories. Every improvement, safety practice, and customer collaboration builds on the last, shaping what we deliver today and how we refine our processes for tomorrow.