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2-Bromo-4-Fluoro-6-Nitrotoluene

    • Product Name 2-Bromo-4-Fluoro-6-Nitrotoluene
    • Alias 2-Bromo-6-methyl-1-fluoro-4-nitrobenzene
    • Einecs 629-197-6
    • 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
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    Specifications

    HS Code

    579015

    Productname 2-Bromo-4-Fluoro-6-Nitrotoluene
    Casnumber 61097-18-9
    Molecularformula C7H5BrFNO2
    Molecularweight 234.02
    Appearance Yellow to brown solid
    Meltingpoint 39-42°C
    Density 1.75 g/cm3
    Purity Typically >98%
    Solubility Slightly soluble in organic solvents
    Smiles Cc1cc([N+](=O)[O-])cc(F)c1Br
    Inchi InChI=1S/C7H5BrFNO2/c1-4-2-5(10(11)12)7(9)3-6(4)8
    Storage Store in a cool, dry place

    As an accredited 2-Bromo-4-Fluoro-6-Nitrotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 2-Bromo-4-Fluoro-6-Nitrotoluene

    Applications of 2-Bromo-4-Fluoro-6-Nitrotoluene in Industrial Manufacturing

    2-Bromo-4-Fluoro-6-Nitrotoluene is a specialized intermediate widely integrated in advanced chemical manufacturing, particularly where halogenated aromatic compounds are essential. Our facility consistently supports pharmaceutical, agrochemical, dye, and specialty chemical sectors in developing finished goods that depend on precise halogen and nitro substitution patterns for performance and regulatory compliance.

    1. Pharmaceutical Intermediate Synthesis

    Drug substance manufacturers apply this compound as a starting material or intermediate for the synthesis of active pharmaceutical ingredients (APIs) within oncology, anti-infective, and central nervous system drug classes. The substrate delivers specific aromatic substitutions crucial for bioactivity and downstream transformations, such as nucleophilic aromatic substitution or reduction steps. In GMP environments, consistent purity, low metal content, and reproducible analytical profiles determine its suitability for inclusion in multi-step synthesis routes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA GMP regulations for pharmaceuticals)
    • Ph. Eur. General Chapters 2034 and 2035 (Pharmaceutical substance control)
    • USP/NF Monographs for relevant APIs

    Typical usage ratio

    • Ratio varies between 0.8–1.2 molar equivalents depending on API target
    • Adjustment considers side-reaction propensity and impurity thresholds
    • Specific charge calculation based on each process route mass balance

    Downstream process integration

    • Enters as a primary or secondary aromatic precursor in synthesis stages
    • Used in regiospecific halogenation or nucleophilic aromatic substitution steps
    • Feeds multi-step transformations before final API crystallization
    • Purified by column chromatography or preparative HPLC as required

    Final product types

    • Oncology treatment intermediates
    • Fluorinated anti-infective drug substances
    • CNS-active pharmaceutical compounds
    • Precursor blocks for branded and generic medicines

    2. Agrochemical Synthesis (Herbicides and Fungicides)

    Agrochemical producers rely on this compound as a halogenated aromatic building block to synthesize active substances for crop protection products. The material’s unique substitution profile enables precision coupling in condensation or cyclization steps, forming advanced intermediates or directly yielding functional agrochemical actives. Production environments demand process reproducibility and adherence to environmental risk assessments relating to halogenated by-products.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 9001:2015 Quality Management Systems
    • FAO Specifications for Plant Protection Products
    • EU Regulation EC 1107/2009 on plant protection product approval

    Typical usage ratio

    • Standard input of 0.5–1.0 molar equivalents per active ingredient molecule
    • Ratio determined by target compound structure and desired field stability
    • Optimized by crop safety studies and formulation shelf life requirements

    Downstream process integration

    • Feeds into early-stage aromatic coupling or halide exchange operations
    • Processed in solvent or aqueous medium with controlled temperature profiles
    • Key intermediate in the synthesis of high-value triazine, pyridine, or pyrazole herbicides
    • Residuals managed by in-process purification or adsorption

    Final product types

    • Pre-emergence and post-emergence herbicidal formulations
    • Fungicidal actives for cereals and row crops
    • Building blocks for next-generation seed treatment agents
    • Intermediates used in insect growth regulator design

    3. Advanced Dye and Pigment Intermediates

    Colorant manufacturers utilize this raw material as a key input for synthesizing halogenated nitroaromatic intermediates, which form the basis for high-performance dyes and pigments. The orthogonal halogen and nitro substituents enable controlled diazotization, reduction, and coupling reactions essential in producing stable, high-intensity pigments with resistance to light and chemicals. Batch records and analytical fingerprinting guarantee traceability and batch reproducibility for demanding textile, ink, and plastic pigment markets.

    Industry compliance standards

    • EN 71-3:2019 (Safety of Toys – migration of certain elements)
    • REACH Regulation (EC) No 1907/2006 — substance registration, evaluation, and authorization
    • OEKO-TEX® Standard 100 (Textile chemical safety)
    • ISO 18451-1:2015 (Pigments and extenders – Terminology)

    Typical usage ratio

    • Loaded at 0.7–1.1 equivalents per structural unit of final dye or pigment
    • Ratio varies based on chromophore extension length and substitution pattern
    • Adjusted to optimize color fastness or spectral absorbance properties in the end product

    Downstream process integration

    • Introduced in primary nitration, halogenation, or diazotization units
    • Forms azo or anthraquinone intermediates for further coupling and modification
    • Diversifies pigment grain structure via selective reduction or substitution
    • Monitored by HPLC and GC-MS for residual nitro or halogen byproducts

    Final product types

    • Reactive and disperse dyes for textiles
    • High-performance pigments for automotive coatings
    • Printing ink pigment concentrates
    • Colorants for engineering plastics and masterbatches

    4. Synthesis of Specialty Fluorinated Aromatic Compounds

    Producers in specialty chemicals and materials science sectors integrate this compound for elaborating fluorinated aromatic molecules where rigid control over electronic and steric effects is required. The raw material’s structure allows for advanced nucleophilic substitutions, Suzuki couplings, and cross-coupling applications to build functional units involved in electronics, liquid crystals, or advanced polymer additives. Application requires compliance with international chemical inventory and notification standards, as well as rigorous QC on trace impurity content.

    Industry compliance standards

    • Toxic Substances Control Act (TSCA, USA) chemical inventory regulations
    • Japan Chemical Substances Control Law (CSCL) notification and registration
    • EU CLP Regulation (1272/2008) for classification, labeling, and packaging
    • ISO 9001:2015 for specialty chemical process control

    Typical usage ratio

    • Usage level 0.6–1.7 equivalents based on degree of fluorination in target molecule
    • Process optimization driven by downstream material performance criteria
    • Loaded in proportion to anticipated coupling efficiency and cost environment

    Downstream process integration

    • Acts as aryl halide substrate in Pd/Cu-catalyzed coupling reactions
    • Introduced prior to final substitution or redox stages
    • Critical for electronic fine-tuning in advanced functional material design
    • Real-time purity and transformation rate tracked by LC-MS and NMR

    Final product types

    • Fluorinated aromatic monomers for specialty polymers
    • Functional materials for display technologies
    • Liquid crystal intermediates for panel manufacturing
    • Electronic-grade fine chemicals
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    More Introduction

    2-Bromo-4-Fluoro-6-Nitrotoluene: Advancing Synthesis with Precision

    A New Age Tool for Modern Organic Chemistry

    Organic synthesis always pushes for more precision, less waste, smarter pathways, and better yields. Some intermediates stand out not for their celebrity status, but because they simplify hard problems for chemists aiming at efficiency and selectivity. 2-Bromo-4-Fluoro-6-Nitrotoluene fits this bill. The structure seems simple — a toluene ring, holding the halogens bromine and fluorine as well as a nitro group, all in finely tuned positions. Getting the placement right changes everything about its reactivity. While some folks only see another yellow crystalline compound, anyone digging into pharmaceuticals, crop protection, or specialty polymers sees a solution to their trickiest cross-coupling or nucleophilic aromatic substitution challenges.

    Back in grad school, I struggled with the limitations of basic aromatic compounds. Trying to stitch together a multi-step synthesis, I hit a wall on selective halogenation. Either everything reacted at once, or nothing did. Later, stumbling across an aryl halide like 2-Bromo-4-Fluoro-6-Nitrotoluene was like unlocking a cheat code. Its electron-withdrawing nitro group, pulled into the ring with surgical precision, encourages high selectivity in reactions that’d otherwise blanket the benzene with junk. The ortho-positioned bromine opens doors for Suzuki and Buchwald-Hartwig couplings. The para-fluorine resists unwanted side-reactions, and the methyl group quietly tunes reactivity without getting in the way.

    Specifications Shape Results

    Every batch of 2-Bromo-4-Fluoro-6-Nitrotoluene owes its utility to more than purity. Particle size, moisture content, and even packaging walnut play their part. In research settings, the compound comes typically as a yellow powder or crystals — but tiny impurities make a world of difference. There’s no use talking up a molecule if the assay dips below 98%, or if trace metals throw off palladium catalysis. Chemists grew wise over the years to the quirks of organohalogens: a hint of water can crash a reaction, while dust-sized metal traces can poison otherwise healthy transformations. Reliable suppliers vouch for consistent melting points, NMR spectra, and HPLC traces, giving bench scientists confidence. Not every manufacturer maintains this vigilance, which explains the reluctance many labs show towards bulk, unverified materials.

    In fieldwork, I’ve seen some extraordinary applications for this building block. The big pharma companies use it to craft intermediates for drugs that target cancer, infection, or even metabolic disorders. It features prominently in the synthesis of heterocyclic cores — structures that drive the pharmacological punch of many treatments. Crop science teams rely on it for the fine-tuned preparation of new classes of agrochemicals, chasing herbicidal activity with lower environmental impact. Polymer chemists use it to carefully anchor fluorine atoms onto new backbones, tweaking surface energy or resistance to heat and solvents.

    2-Bromo-4-Fluoro-6-Nitrotoluene Offers Options, Not Headaches

    In the world of halogenated toluenes, you get differences that show up not just in theoretical papers but in Monday morning lab work. Swap out the positions of the nitro or the halogens, and you wind up with an entirely different beast: maybe less reactive, maybe slower to couple, maybe more prone to unwanted by-products. Regular 2-Bromotoluene, for example, lacks the electron-withdrawing nitro and the uniquely placed fluorine. It becomes unruly in Buchwald couplings, and shouldn’t be asked to perform in the same clean, high-yielding way. The introduction of the nitro group drops the electron density, making aromatic substitutions crisper and more predictable. Fluorine — a tiny atom but a force in medicine and materials — brings metabolic stability and often improves the bioavailability of lead compounds.

    Among the subtle yet potent advantages, chemists can exploit the multiple halogens present for strategies like selective removals or exchanging groups under mild conditions. Medicinal chemists like having handles for late-stage diversification, tweaking the structure to dodge patent landmines or to probe new biological space. From a green chemistry point of view, handling fewer steps, less waste, and clearer reactions means both better cost control and a smaller environmental footprint.

    Practical Considerations — Why This Molecule Beats Others

    Bench experience shows countless reactions ruined by unreliable counterparts: poor solubility, unanticipated byproducts, overreactivity, and a shelf life that fizzles before your project finishes. 2-Bromo-4-Fluoro-6-Nitrotoluene manages to sidestep some of these headaches. It dissolves in solvents like dichloromethane, acetonitrile, and THF, fitting classical protocols for aromatic substitutions and cross-coupling. The molecule doesn’t throw off nasty odors typical of some halogenated benzenes, a small mercy in crowded labs. It stores well under inert atmospheres, avoiding slow decomposition that plagues more labile intermediates.

    Safety always carries genuine weight. The nitro group raises the bar — chemists know to avoid open flames or extreme heat. Gloves and goggles are standard, but awareness matters because even so-called benign intermediates introduce risk in skilled hands. In my time working in academic and industrial settings, I’ve observed the best labs invest in training that keeps the focus on the details — eye-wash stations, clear labelling, thoughtful disposal — especially with toxic or combustible compounds. Accidental releases impose burden on air quality and lab cleaning, so packaging with sturdy containers and clear hazard information helps all the way from shipping to waste collection.

    Scaling Beyond the Flask: Bridging Research and Industry

    Scaling reactions brings new headaches: exotherms, stirring issues, and the perennial battle with purification. Slight tweaks in the toluene ring structure mean tweaks in every variable of the process. 2-Bromo-4-Fluoro-6-Nitrotoluene doesn’t guarantee a plug-and-play experience, but it regularly outperforms its less sophisticated siblings. Batch production frequently leans on proprietary crystallization to hit purity goals, and companies monitor trace elements with modern spectral tools. Documentation matters too — from MSDS to lot-specific certificates — as legal and regulatory reviews demand transparency.

    In my industrial years, technical transfer between R&D and pilot-plant folks often came down to trace impurities and the batch reproducibility of stepping stones like 2-Bromo-4-Fluoro-6-Nitrotoluene. One poorly documented batch led to weeks of chasing ghosts in the scale-up, missing timelines, and blowing out budgets. Smart procurement teams make a habit of verifying analytical data, even running orthogonal tests, because the real cost arrives only after a project stalls over failed crops or unexplained low yields.

    Global Impact: More Than Just a Lab Chemical

    What gets exciting is watching how this intermediate connects with broader trends in chemistry. The pharmaceutical arms race for smarter, safer drugs depends on sharp intermediates. New cancer therapies or antiviral agents break ground, in part, because earlier steps land smoothly with minimal fuss. As regulatory eyes turn toward lowering solvents, waste, and energy use, efficient couplers like this one gain more value. The nitro, bromo, and fluoro pattern is proving flexible in constructing next-generation molecules for imaging, diagnostics, and even material science — think fluorinated coatings or advanced battery materials.

    In tough markets — where regulatory and ecological scrutiny peak — a compound’s synthetic profile matters more than ever. Waste minimization and careful supply chain management matter in both regulated pharma and high-end polymers. Many firms now use 2-Bromo-4-Fluoro-6-Nitrotoluene as a safer alternative to less predictable aromatic precursors, as it helps lower process risk and reduce undesirable byproducts that are tough to remove. Clean chemistry reduces downstream headaches and shrinks the risk of environmental liabilities.

    Supporting Claims with Experience and Evidence

    The march toward more selective and robust syntheses is no empty promise. A review of recent medicinal chemistry literature shows increased adoption of multifaceted aryl halides. Both the Journal of Medicinal Chemistry and Organic Process Research & Development publish papers touting intermediates that mimic 2-Bromo-4-Fluoro-6-Nitrotoluene’s blend of groups. Markets for active pharmaceutical ingredients and their intermediates each run to billions of dollars, as documented in the Global Specialty Chemicals Report. Leading companies openly credit their supply chain wins to intermediates that work across multiple steps with fewer failures, and to the cost-savings that come from avoiding extra purifications. Regulatory filings from the last decade flag more attention on trace impurities, especially residual catalysts and solvent residues in key intermediates. Having control at the intermediate level saves untold sums during late-stage clinical evaluations, where impurities can delay or derail entire programs.

    Facts stack up outside pharmaceuticals too. The US EPA and European Chemicals Agency routinely update guidance for halogenated aromatic compounds, focusing on process safety and environmental management. Safe storage, traceability, and waste reduction are more than regulatory hoop-jumping — they shield workers and communities. 2-Bromo-4-Fluoro-6-Nitrotoluene’s solid state and stability outshine more volatile family members, making it less likely to vaporize or spill. Professional experience matches with published case studies — facilities handling it report fewer evacuation drills and lower insurance premiums compared to less stable analogs.

    Sustainability: Green Chemistry and Engineering Solutions

    Anyone discussing specialty intermediates needs to talk sustainability. The industry’s carbon footprint depends heavily on cutting down by-products, solvent use, and hazardous waste. 2-Bromo-4-Fluoro-6-Nitrotoluene streamlines steps and reduces chances for mishaps, often bypassing the need for protecting-group gymnastics or harsh reagents. In process design meetings at my former employer, conversations shifted to molecules like this because halide/nitro combinations offer such clear handles for transition-metal catalysis without side journeys into messier protection/deprotection cycles. That means less solvent, less energy burned in purification, and less scrap. These savings show up directly in plant operating costs and the environmental reporting that every publicly traded company faces.

    Solid intermediates mean less chance of air and water emissions. Plant engineers sleep better knowing their floor techs handle less toxic or flammable material. As more chemical makers invest in safer packaging, automatic transfer systems, and smaller, more precise batch sizes, the footprint shrinks incrementally year over year. It matters — both for boardroom reporting and for real risk on the ground. Technically minded chemists share their best protocols in places like the ACS Green Chemistry Institute, and molecules like 2-Bromo-4-Fluoro-6-Nitrotoluene show up again and again as go-to solutions for greener methodology.

    Room to Improve: Addressing the Downsides

    Every tool has a downside. Nitro groups sometimes mean higher sensitivity to impact or extreme heat. That brings restrictions for airlines, couriers, and customs agencies. Some facilities need special licenses to handle aromatic nitro compounds in bulk. Waste disposal must follow rules for both toxic organics and for halogens. On the lab bench, students and new hires will hear warnings early and often. Spills on benchtops or clothing demand more attention and better hygiene than simpler toluenes. Chemistry instructors and industrial trainers devote precious time not just to reactions, but to storage and safe handling, reinforcing old lessons to new generations.

    The cost per kilogram may run higher than commodity chemicals like toluene or xylene. Users prioritize value by selecting steps where the added selectivity justifies the investment; trying to save pennies on feedstock often blows dollars on failed scale-ups or ruined downstream purification. Investments in dedicated storage and staff training balance out against improvements in throughput and reduction in batch failures.

    Potential Solutions and Smart Strategies

    Smart labs and manufacturers adapt by building comprehensive risk assessments into their process development. Advanced training helps teams identify not just the obvious hazards — explosive potential and toxics — but tricky dangers like trace impurity carryover. Solutions include tighter engineering controls, materials compatibility checks, and staggered workflow layouts to avoid accidental mix-ups. In one pharma plant I visited, batch tracking technology got implemented with barcoded intermediates, preventing costly cross-contamination during nights and weekends when turnover is highest.

    Supply chain partners respond, too. Certifications, third-party audits, and transparent documentation keep trust high. The world learned tough lessons during the last decade’s shortages and recalls: buyers now demand full access to NMR, GC-MS, ICP, and other data before purchase orders clear. No one wants to learn about a failing batch the hard way, with wasted time and delayed deliverables. Smart organizations also stay close to transport and regulatory partners — a sure way to avoid late-stage customs blocks or compliance headaches.

    Some of the most effective programs tackle problems at the molecule’s source: investing in greener synthesis, shifting routes to use bio-based reagents, and partnering with universities to develop milder, less hazardous methods. Several research groups — as documented in reputable journals — now report scalable protocols that lower the atom economy, using smarter catalysts and simpler solvent systems. Longer term, many are watching to see whether fluorinated intermediates like this one can take the spotlight in green transformations that cut fossil use and byproduct formation. Product stewardship teams, in turn, share safety data, handling tips, and waste management plans to help labs meet ambitious sustainability goals.

    At the researcher level, ongoing education and peer mentoring make all the difference. New hires need real-world stories — not just policy binders — telling why labels matter, how to spot hidden hazards, and what to do when things go off-script. My best mentors in industry showed leadership not only by running tight syntheses but by championing a culture of accountability: prepping reagents before the shift, double-checking cargo lots, and keeping emergency plans not just posted but practiced.

    Moving Forward: The Role of 2-Bromo-4-Fluoro-6-Nitrotoluene in Tomorrow’s Chemistry

    In a landscape where every choice affects downstream yield, safety, and price, each intermediate plays an outsized role. 2-Bromo-4-Fluoro-6-Nitrotoluene leverages small, precisely chosen modifications to upgrade inventiveness and reliability. From the bench chemist fending off byproduct headaches, to the manufacturing manager balancing safety, cost, and compliance, the advantages stand up to scrutiny. The world keeps pushing for cleaner, safer, and more affordable pharmaceuticals, smarter agriculture, lighter and tougher polymers, all while responding to tougher environmental scrutiny.

    What stands out most every time this intermediate replaces clumsier or less reliable building blocks is a simple fact: there’s value in getting the basics right. Careful substitution, a wise blend of halogen and nitro, clever engineering, and robust supply chain support add up to fewer disruptions, clearer compliance, and better science. In the end, the difference between lost weeks and a successful scale-up often comes down to choices made far upstream, in the silent details of one yellow powder, carefully packaged and equally carefully used. 2-Bromo-4-Fluoro-6-Nitrotoluene may not make headlines outside a handful of chemical journals, but for those building the treatments, materials, and technologies of tomorrow, it’s a small investment with major payoffs.