Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Bromo-6-Fluorotoluene

    • Product Name 2-Bromo-6-Fluorotoluene
    • Alias 2-Bromo-6-fluoro-1-methylbenzene
    • Einecs (EINECS) 401-120-7
    • 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

    517341

    Cas Number 19960-58-4
    Molecular Formula C7H6BrF
    Molecular Weight 189.03 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.527 g/cm3
    Boiling Point 178-180°C
    Melting Point -11°C
    Refractive Index 1.548
    Flash Point 66°C
    Purity Typically ≥98%
    Smiles CC1=C(C=CC=C1F)Br
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 2-Bromo-6-fluoromethylbenzene
    Storage Temperature Store at room temperature
    Ec Number 606-994-0

    As an accredited 2-Bromo-6-Fluorotoluene 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 mL, sealed with a red screw cap, labeled with chemical name, hazard pictograms, and batch number.
    Shipping 2-Bromo-6-Fluorotoluene is shipped in sealed, chemical-resistant containers compliant with international transport regulations. It is handled as a flammable liquid and may require labeling for hazardous materials. Shipments should be protected from heat, direct sunlight, and physical damage, with appropriate safety documentation and packaging to prevent leaks or spills during transit.
    Storage Store 2-Bromo-6-fluorotoluene in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Use appropriate chemical storage cabinets or flammable liquid storage areas if possible, and ensure proper labeling. Personal protective equipment should be used when handling this chemical.
    Application of 2-Bromo-6-Fluorotoluene

    Applications of 2-Bromo-6-Fluorotoluene in Industrial Manufacturing

    As a core intermediate with bromine and fluorine functionality, 2-Bromo-6-Fluorotoluene enables efficient construction of advanced molecules in fine chemical synthesis. Below we outline specialized downstream manufacturing scenarios, based on our plant’s client integration experience and established industry pathways.

    1. Agrochemical Intermediate Synthesis

    Manufacturers producing modern herbicides and fungicides frequently rely on aromatic halogenated toluenes to build complex active ingredients. 2-Bromo-6-Fluorotoluene participates in Suzuki coupling and nucleophilic aromatic substitution stages, delivering the critical aryl fluorine-bromo motif. Precision in molar ratio controls impurity formation, vital for regulatory compliance. Our technical support ensures batch-to-batch consistency aligns with process specifications, meeting the demands of scalable agricultural chemical production.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • REACH Registration (EC No. 1907/2006) for hazardous chemical intermediates
    • Global Crop Protection Guidelines (FAO/WHO specifications)
    • Applicable national environmental protection laws for plant effluents

    Typical usage ratio

    • Ranges from 0.6 to 1.2 molar equivalents per target aromatic fragment, adjusted according to coupling partner reactivity and desired impurity threshold control

    Downstream process integration

    • Fed into the early intermediate formation stage preceding heterocycle construction
    • Charged to multi-step reactors under nitrogen blanket for controlled substitution or palladium-catalyzed cross-coupling
    • Post-reaction, the toluene moiety anchors further derivatization or sulfonation

    Final product types

    • Selective herbicide actives for cereal and broadleaf crops
    • Fungicidal precursors targeting soil and foliar pathogens
    • Seed-treatment additive intermediates

    2. Pharmaceutical Building Block

    The compound serves global pharma manufacturers as an advanced halogenated scaffold in small molecule R&D and scale-up. Medicinal chemists employ it for rapid access to fluorinated aromatic drugs, with lab documentation covering full traceability. Regulatory filings require impurity profiling and stringent solvent residuals tracking, for clinical and commercial use. We provide full batch records and documentation for regulatory submissions, supporting API synthesis from preclinical scale through cGMP manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR 211 for finished pharmaceuticals
    • European Pharmacopoeia / USP for starting materials if applicable
    • GMP documentation and Certificate of Analysis (CoA) aligned to pharma specifications

    Typical usage ratio

    • Typically between 0.95 to 1.05 molar equivalents per step, precision based on desired API target and avoidance of bromo or fluoro-impurities

    Downstream process integration

    • Introduced during early-stage benzene ring elaboration
    • Reacted under controlled temperature for regioselective substitution or metal-catalyzed coupling
    • Employed for in-situ fluorination or bromination extension where further derivatization needed

    Final product types

    • Key pharmaceutical intermediates for oncology, CNS, or antiviral APIs
    • Reference standards for analytical method development
    • Synthon units for lead molecule customization in contract drug research

    3. Electronic Chemical Synthesis (Advanced Materials)

    Fabricators of liquid crystal and organic semiconductor materials use 2-Bromo-6-Fluorotoluene as a customizable precursor for molecular engineering. Its unique bifunctional halogen profile aids in constructing robust molecular wires, OLED emitters, and high-K dielectrics. Downstream processes demand controlled introduction of the raw material to minimize oligomeric byproducts. Our supply chain supports just-in-time delivery for integrated multi-step synthesis in confined cleanroom conditions.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive 2011/65/EU)
    • ISO 14001:2015 Environmental Management System
    • SEMI S2, S8 for electronic chemical manufacturing
    • Cleanroom production documentation as per contract requirements

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents per coupling reaction; ratio depends on electronic property targets and minimization of halogen residue in the matrix

    Downstream process integration

    • Charged into Grignard couplings or Yamamoto polymerizations
    • Used as a monomer feed in small-batch high-purity processes for display-grade precursors
    • Subsequent steps include purification and size exclusion for device compatibility

    Final product types

    • OLED blue/green emitters and hole/electron transport layers
    • Liquid crystal alignment layers for LCD panels
    • Polymer semiconductors for flexible electronics

    4. Specialty Dye and Pigment Preparation

    Producers of specialty dyes and pigments for high-value plastic and fiber coloration utilize 2-Bromo-6-Fluorotoluene as a halogenated precursor. The aromatic substitution enables tight control over chromophore assembly, brightness, and lightfastness. Manufacturing incorporates precision color matching and downstream purification to meet end-customer shade requirements. Our material tracking supports continuous in-process quality control and waste minimization practices.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile applications
    • EN 71-3 Safety of Toys (Europe) for colorants in consumer applications
    • ISO 9001 Quality Management for pigment processing
    • Local chemical control laws for environmental discharge

    Typical usage ratio

    • 0.75–1.10 equivalents per pigment batch, depending on desired color depth and chromophore yield; ratio adjusted for batch-to-batch pigment shade uniformity

    Downstream process integration

    • First step in diazo-coupling or aromatic fusion for new chromophore synthesis
    • Substrates charged under controlled temperature and solvent selection for nucleophilic aromatic substitution
    • Post-synthesis, integrated into finisher’s pigment paste dispersions or solid concentrates

    Final product types

    • Fiber-reactive dyes for polyester and polyamide spinning
    • Specialty yellow/orange pigments for plastics molding
    • Functional colorants for high-performance inks
    Free Quote

    Competitive 2-Bromo-6-Fluorotoluene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Bromo-6-Fluorotoluene: Behind the Drum of a Modern Synthesis Partner

    Introduction to 2-Bromo-6-Fluorotoluene

    Walking through our plant on a typical day, the smell of halogenated aromatics is familiar—clean, brisk, and tinged with an almost metallic sharpness. Among the reactors, there are certain compounds that consistently earn their keep through reliability and versatility. 2-Bromo-6-Fluorotoluene has played a quiet, important part in our production line for over a decade, standing out for its consistent physical and chemical behavior. As both manufacturer and long-term handlers of this compound, we’ve seen its growing significance, especially in active pharmaceutical ingredient (API) synthesis and advanced materials. Over years of batches, we’ve come to know its preferred conditions, its quirks, and its limitations.

    Model, Grade, and Physical Character

    In our facility, 2-Bromo-6-Fluorotoluene goes by its CAS number, 429-62-7, but the details matter more than labels. We run two reactor setups for this molecule: one with a single-batch process yielding the standard grade, favored by downstream halogen-exchange chemists, and another with column purification that removes minute impurities, requested by clients needing consistent signals for analytical use. Both exhibit an off-clear to pale yellow liquid, with the denser feel characteristic of bromo-fluoro compounds. This subtle color tells us about trace levels of oxidation or residual starting material—details we constantly refine. At room temperature, its stable liquid form (mp below ambient) avoids the bottlenecks we see in more crystalline substituted toluenes, letting us keep material flowing out without seasonal interruptions.

    Why Usage Goes Beyond a Simple Toolbox Molecule

    Chemists working with this compound usually pursue more elaborate molecules, but there’s no skipping the basics: reliable halogen sources underpin much of modern drug and crop-protection work. As manufacturers, we’ve heard stories from both campfire meetings and conference panels about challenging couplings, where other bromotoluenes under-delivered due to side reactions or splitting issues. 2-Bromo-6-Fluorotoluene’s tight tolerance for side-chain oxidation keeps those headaches to a minimum. We’ve seen it feed directly into palladium-catalyzed cross-couplings—Suzuki, Stille, and Buchwald-Hartwig reactions all benefit when starting halogenated toluenes don’t smuggle in unwanted isomers or unreacted toluene.

    Pharmaceutical teams ask for it not just because it’s technically reactive—the ring fluorine gives just enough electron-withdrawing sway to favor selectivity in aromatic substitutions, hitting a nice medium between sluggish multi-halos and the over-eager single-substituted cases. We’ve seen it feed libraries of substituted benzylamines, pyrazoles, and even more ambitious heterocycles. Material science clients often target functionalized liquid crystals or fluorinated building blocks; they count on our repeatable specification for blending consistency and batch-traceability. Compared to our 2-bromo or 2-fluoro-toluenes, the dual substitution profile offers a more direct path to specific regioisomers, shaving weeks from iterative synthetic campaigns.

    Practical Issues We See, Day In and Day Out

    In manufacturing, knowing the pain points is as important as knowing the recipe. Unlike lighter halogenated aromatics, 2-Bromo-6-Fluorotoluene brings logistical challenges due to its mass and tendency for minor phase separation in long-term storage. We routinely test for subtle hydrolysis or slow decomposition, especially for clients moving product overseas, where containers linger in unpredictable climates. From our cold-room logs, we know exposure above 30°C for extended times can yield faint acidity, so we pack and recommend transport in tightly sealed HDPE containers with desiccant linings. A big difference from working with purely brominated or fluorinated toluenes: 2-Bromo-6-Fluorotoluene resists light-induced polymerization surprisingly well. In the mid-2000s, several batches of other bromo-toluenes polymerized during warehousing, leading to shipment delays. We saw significant savings moving sensitive conversions to our dual-substituted stock, minimizing last-minute rework.

    We keep a running dialogue with clients who run continuous-flow syntheses, since 2-Bromo-6-Fluorotoluene’s low melting point—staying liquid through most normal operating ranges—pairs well with automated dosing systems, eliminating the clogging seen with higher-melting analogs. That alone can drive up batch yields by preventing line fouling and downtime.

    Handling, Experience, and Quality Assurance

    There’s a learning curve with halogen-aromatics. When we first set up for 2-Bromo-6-Fluorotoluene over ten years ago, we spent months fine-tuning distillation columns to avoid co-distillation of lighter fluoro-toluenes and nip contamination issues early. These incremental improvements aren’t glamorous, but the consistency in product profile means our phone rings less with last-minute crisis calls from demanding formulators.

    Clients relying on precise NMR profiles have told us that our product’s purity, confirmed through every batch run by multidimensional chromatography, has saved precious days on downstream purification. We measure batch-to-batch consistency in more ways than just GC or HPLC purity—moisture pickup, UV-absorbance windows, and storage stability all factor into whether a drum quietly ships or triggers a bottleneck in a client pipeline.

    Working hand-in-hand with compliance and safety teams taught us early on the need for responsible production. We regularly consult updated regulatory status for every market, since 2-Bromo-6-Fluorotoluene sometimes falls under local export controls or registration in downstream applications. Audits from global pharma and electronics firms push us to maintain both traceability and transparency.

    Key Differences: 2-Bromo-6-Fluorotoluene vs. Related Aromatics

    Daily hands-on work with the molecule reveals clear differences compared to single-halogen or other polysubstituted toluenes. The bromine atom brings leaving group strength for metal-catalyzed cross-coupling, while the ortho-fluorine affects reactivity and selectivity without substantially raising handling risks. In comparison, 2-bromotoluene or 6-fluorotoluene alone often require additional steps in multi-stage synthesis to install a second substituent with sufficient selectivity. We see our dual-substituted product provide a shortcut—bypassing regrettable protecting group detours—especially prized by companies racing to patent space or speed up process chemistry.

    On the environmental front, our waste stream control benefits from the inherent stability of 2-Bromo-6-Fluorotoluene. Its robust structure allows for straightforward neutralization and solvent recovery—an easier outcome compared to more reactive trihalogenated series, which tend to create more persistent byproducts in quench steps.

    Process safety earns regular attention on our shop floor. Comparative experience shows 2-Bromo-6-Fluorotoluene generates less aggressive vapor pressure under standard use scenarios than its lighter or higher-branched analogs, fewer inhalation or exposure alerts, and lower fugitive emission incidents.

    Our Role in the Industry Chain

    As manufacturers, the feedback loop never stops. From the upstream sourcing of the cleanest toluene and halogen sources, to the final batch sign-off, we interact with every input along the way. Over the years, we’ve adopted fully closed-transfer systems for charging reactors, avoiding worker exposure and contamination risk. Our partnerships extend from bulk API plants to materials specialists working on the next generation of organofluorine electronics.

    We know 2-Bromo-6-Fluorotoluene’s real power lies in predictability. Pharmaceutical labs look for minimal side product burden—and we see our product’s characteristic splitting and coupling constants translate to easier lab work and more rapid project progression. Advanced material groups value its clean trace element profile, with no detectable heavy metal contamination—a point we routinely verify using atomic absorption and ICP-MS on outgoing lots.

    With the regulatory climate tightening worldwide, there’s more scrutiny than ever. Our regular audits and transparent logging systems close the loop for quality-minded buyers, reducing their own reporting stress and facilitating regulatory submissions.

    Common Challenges and Problem Solving

    We’ve encountered a recurring worry among formulators regarding long-term color stability, especially as trace oxidation products sometimes tint large batches over time. Our solution focuses on dual-layer drum linings and nitrogen blanketing from the point of filling to shipment. Ongoing stability testing has guided our shift to specialty lined drums, which has cut color drift calls by over half in the last three years.

    In large-scale plant runs, scale-up sometimes uncovers impurity knock-ons from unseen side reactions—this was especially true during our early years of continuous production. Once we started regular in-process monitoring by in-line FTIR, those missteps diminished. We’ve shared these insights candidly with partner plants, quantifying how trace methylbromo or trifluorotoluene content can predict downstream route viability and prevent headaches at the kilogram scale.

    Sometimes, less expected uses pop up. A few years ago, a solar material developer asked about batch-specific absorbance—concerned it might interfere with device performance. After a handful of experiments in our own labs, we supplied detailed absorption spectra on every subsequent batch. This let the customer maintain device consistency and gave us another metric for batch release, sharpening our control standards another notch.

    Continuous Improvement and Relationship Building

    We see every run of 2-Bromo-6-Fluorotoluene as both a technical challenge and a trust exercise. Our technical team meets weekly to review any deviations, documentation flags, or client feedback—no matter how minor. This feedback finds its way into our next scale-up or purification tweak, and clients often notice the difference. One client’s comment about sulfur trace in an unrelated compound prompted us to improve inert gas sweeps across all aromatic lines.

    Our daily work includes ongoing learning. Techniques like ultrafast GC, in-line UV monitoring, and remote temperature logging have made material quality more predictable. We invest every quarter in equipment upgrades and operator training, which pay dividends in smooth, reliable operation and batch integrity. These investments aren’t optional if we want to keep up with global expectations for supply security, process transparency, and safety.

    Partnerships and Future Directions

    Close relationships with our synthetic chemistry partners have revealed new directions for 2-Bromo-6-Fluorotoluene’s application. Researchers in advanced monomer design and pharmaceuticals sometimes stretch our process abilities by requesting custom solutions—whether that's tighter specification ranges, specialty purification requests, or alternative solvent carriers. We collaborate directly on feasibility, pilot runs, and ultimately production-scale shipments that deliver on the performance they require.

    Looking ahead, we anticipate more pressure to document and minimize environmental impact. Early adoption of process mass-intensity metrics has shaped our approach to waste reduction, especially now with growing scrutiny from both regulators and eco-conscious clients. By analyzing every input and output—recycling halogen sources, capturing organic residues, and optimizing solvent use—we lower end-to-end impact and stay well ahead of tightening standards.

    Conclusion: The Everyday Value of Direct Manufacturing Experience

    From the plant floor, we see that delivering a high-value building block like 2-Bromo-6-Fluorotoluene takes more than quick reactions or a shelf full of reference standards. It takes thorough knowledge—from solvent and reagent selection to analytical troubleshooting and downstream customer support. Regular dialogue with users, commitment to ongoing process improvements, and transparency in documentation all strengthen the relationships that move projects from concept to completion.

    We take pride in how reliably our 2-Bromo-6-Fluorotoluene empowers advanced chemistry applications, lets R&D teams work with confidence, and enables streamlined, modern manufacturing. With each order, we share more than a chemical—we deliver tried-and-tested experience that stands behind every drum, every batch, and every project deadline.