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4-Bromo-2-Fluoro-5-Methylbenzaldehyde

    • Product Name 4-Bromo-2-Fluoro-5-Methylbenzaldehyde
    • Alias 4-Bromo-2-fluoro-5-methylbenzaldehyde
    • Einecs 841-064-7
    • 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
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    Specifications

    HS Code

    221815

    Chemical Name 4-Bromo-2-Fluoro-5-Methylbenzaldehyde
    Molecular Formula C8H6BrFO
    Cas Number 886372-60-1
    Appearance White to pale yellow solid
    Melting Point 48-52°C
    Density 1.63 g/cm³ (approximate)
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Smiles CC1=CC(Br)=C(F)C=C1C=O
    Solubility Soluble in organic solvents (e.g., dichloromethane, ethanol)
    Synonyms 4-Bromo-2-fluoro-5-methylbenzaldehyde; Benzaldehyde, 4-bromo-2-fluoro-5-methyl-

    As an accredited 4-Bromo-2-Fluoro-5-Methylbenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 4-Bromo-2-Fluoro-5-Methylbenzaldehyde

    Applications of 4-Bromo-2-Fluoro-5-Methylbenzaldehyde in Industrial Manufacturing

    4-Bromo-2-Fluoro-5-Methylbenzaldehyde serves as a key intermediate in several specialized industrial synthesis chains. Our manufacturing expertise supports clients across multiple mature downstream sectors with precise integration of this raw material according to international quality and regulatory demands.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use this compound as an essential building block in the synthesis of targeted API precursors, particularly those based on substituted aromatic aldehydes for oncology and central nervous system applications. Stringent quality assurance controls require documented traceability and impurity profiling throughout the aldehyde coupling, condensation, and reduction stages. Compliance-driven documentation supports new drug applications and regulatory filings in regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • EU EudraLex Vol. 4 GMP Annex
    • USP-NF monograph reference (where structure applies)
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Introduced at 0.8 to 1.3 molar equivalents relative to the downstream core scaffold. Specific ratio adjusted based on desired substitution patterns in the targeted API intermediate.

    Downstream process integration

    • Charged directly into reaction vessels during the formylation or aromatic coupling stage. Purity (≥98%) critical for reaction yield and minimizing downstream purification.

    Final product types

    • Anti-cancer API intermediates
    • CNS drug precursors
    • Specialty amide pharmaceuticals
    • Custom synthesized small molecules for clinical trials

    2. Agrochemical Intermediate Production

    Major agrochemical companies incorporate this benzaldehyde derivative for the preparation of selective herbicide and fungicide scaffolds, including pyridine and triazole structures. Downstream manufacturers require strict raw material quality traceability, including compliance with international chemical safety and environmental regulations. Reactions are conducted in closed-batch or continuous flow reactors to maintain batch reproducibility and regulatory labeling.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH regulation (EC) No 1907/2006 pre-registration/authorization as applicable
    • Globally Harmonized System (GHS) for chemical labeling
    • OECD guidelines for chemical testing

    Typical usage ratio

    • Employed at 0.5 to 1.1 molar equivalents based on downstream pesticide core requirements. Adjustments depend on target active moiety and waste minimization goals.

    Downstream process integration

    • Loaded during the aromatic nitration, alkylation, or cyclization synthesis phases in herbicide or fungicide development. Quality control requires confirmation of active aldehyde content prior to introduction.

    Final product types

    • Triazole fungicide intermediates
    • Selective herbicide actives
    • Pyridine-based pesticide cores
    • Seed treatment components

    3. Advanced Dye and Pigment Intermediate Manufacturing

    Producers of specialty dyes integrate this component for the synthesis of high-performance pigments and optical brighteners used in textile and polymer coloration. The unique halogen-fluoro-methyl substitution on the aromatic ring enhances fastness properties and stability in finished colorants. Manufacturers impose batch-level analytical controls to monitor trace impurities which can impact final pigment hue and stability under UV or chemical exposure.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for textile applications)
    • EN 71-3 Safety of Toys (colorants used in toys)
    • ISO 9001:2015 certified pigment production
    • Restricted Substances List (RSL) compliance per end-user requirement

    Typical usage ratio

    • Applied at 0.3 to 0.9 molar equivalents in condensation or nucleophilic aromatic substitution reactions. Ratio tailored to specific pigment backbone and desired chromatic intensity.

    Downstream process integration

    • Charged into the synthesis of pigment backbones during azo condensation, Suzuki coupling, or Stille reactions. Purity impacts crystallinity and OPV (optical property value) of the pigment granules.

    Final product types

    • Sublimation dyes for polyester fibers
    • Special effect pigments for coatings
    • High-performance acid and direct textile dyes
    • UV-stable fluorescent colorants

    4. Fine Chemical Synthesis for Electronic Materials

    Manufacturers in the electronics sector rely on this compound for production of functionalized benzaldehyde precursors used in organic semiconductors, liquid crystal materials, and photoresist additives. The halogenated structure improves electronic properties and supports strict traceability for lot-to-lot reproducibility in high-purity manufacturing. Final product consistency is validated through targeted chromatographic assays and trace metal analysis.

    Industry compliance standards

    • IEC 62474 Material Declaration for electrical and electronic products
    • RoHS Directive 2011/65/EU (for components used in electronics)
    • JEITA standards for organic electronic materials
    • ISO 14001 for Environmental Management Systems

    Typical usage ratio

    • Used at 0.75 to 1.25 molar equivalents, defined by the electronic host matrix and target molecular orbital characteristics. Adjusted per device type and functional group incorporation.

    Downstream process integration

    • Introduced at the aryl aldehyde introduction stage in the synthesis of small molecule OLED materials or as a functional end group in LC host structures. Requires high purity for defect-free deposition and film uniformity.

    Final product types

    • OLED emitter or host small molecules
    • Specialty liquid crystal additives
    • Advanced photoresist formulations
    • Organic electronic coating materials

    5. Custom Fragrance Ingredient Intermediate

    Specialty fragrance compound formulators employ this benzaldehyde derivative to produce fluorinated aromatic intermediates known for delivering persistent, modern aldehydic notes in fine and functional fragrance blends. Production sites operate under IFRA guidelines and monitor side-product profiles to ensure olfactory purity. Tailored synthetic routes allow for precise control of final note intensity and residual reactant levels.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • REACH (EC) No 1907/2006 for raw and formulated fragrances
    • ISO 9235:2013 for aromatic raw materials
    • California Proposition 65, if exported to U.S.

    Typical usage ratio

    • Added at 0.2 to 0.7 molar equivalents to the core fragrance intermediate scaffold. Ratio optimized for trace aldehyde impact and shelf-life requirements.

    Downstream process integration

    • Added during the aldehyde-functionalization stage of fragrance intermediate production by direct formylation or Grignard-type reaction. Process controls track unreacted aldehyde to below 0.05% wt/wt in the final component.

    Final product types

    • Consumer perfumery bases
    • Functional fragrance intermediates for home care
    • Fine fragrance core aldehyde ingredients
    • Odorant modifiers used in air fresheners
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    More Introduction

    4-Bromo-2-Fluoro-5-Methylbenzaldehyde: A Trusted Choice for Innovative Chemistry

    Understanding the Value Behind 4-Bromo-2-Fluoro-5-Methylbenzaldehyde

    There’s something to be said for a compound that delivers reliable performance in the lab, especially when exploring the frontiers of synthetic chemistry. 4-Bromo-2-Fluoro-5-Methylbenzaldehyde stands out as one of those dependable building blocks. The CAS registration for this compound places it among the widely recognized benzaldehyde derivatives, and its distinct molecular setup brings a lot to the table for researchers and development chemists alike.

    Looking at its structure, with a bromine at the fourth position, a fluorine at the second, and a methyl group at the fifth, it becomes clear why this aldehyde stirs interest. That particular arrangement provides a balance between reactivity and selectivity. It doesn’t just float through the reaction sequence unchanged; it offers sites for targeted transformation, which can help streamline multistep syntheses. This is especially important for pharmaceutical routes, agrochemical prototypes, and specialty applications within fine chemical development.

    The presence of both the bromine and fluorine leaves room for cross-coupling innovations. Take the Suzuki–Miyaura reaction, for instance, an approach I’ve seen save time and reduce byproducts when adding complexity to aromatic scaffolds. Thanks to that bromine, coupling reactions using palladium catalysis can proceed gently, even with sensitive substrates. Now factor in the fluorine—its electron-withdrawing punch supports site-specific modifications that wouldn’t be possible with simple benzaldehydes.

    Specifications that Matter in the Lab

    Accuracy in ingredients shoulders a lot of responsibility in chemical research. With 4-Bromo-2-Fluoro-5-Methylbenzaldehyde, purity levels typically clock in at 98% or higher, as validated by HPLC and NMR. A lot of my colleagues check for impurities using these tools, and most appreciate the reliability these tests bring for reproducibility. The compound usually comes as an off-white to light yellow crystalline powder. That physical form makes it easy to handle, measure, and store; it avoids the dustiness and clumping that can slow a day’s work at the bench.

    The chemical formula C8H6BrFO bears out its moderate molecular weight and elemental composition. At atmospheric pressure and room temperatures, it keeps stable, resisting degradation for extended periods with proper storage—sealed container, cool environment, away from direct sunlight. Moisture doesn’t readily trigger hydrolysis, which helps prevent frustrating spoilage between uses. That’s not just a comfort, it’s a cost-saving detail that many overlook until they’re tossing out an expensive reagent due to careless handling.

    Where Innovation Begins: Applications in Modern Chemistry

    Wave after wave of modern organic synthesis leans hard on custom benzaldehyde intermediates. In my time supporting medicinal chemists and process scale-up, I’ve watched 4-Bromo-2-Fluoro-5-Methylbenzaldehyde enable steps that would take far longer—or stall out—using less adaptable aldehydes. It’s a key stepping stone for synthesis of heterocyclic cores, including bioactive motifs found in oncology pipelines and antimalarial projects. The aldehyde group invites nucleophilic addition and condensation reactions, while the halogenated ring supports complex cross-coupling.

    In practice, the compound’s bromine allows for installation of aryl, vinyl, or alkynyl groups by trusted protocols. That supports library synthesis, where I’ve seen medicinal teams create hundreds of analogs quickly—sometimes uncovering unexpected leads. The presence of fluorine adds a twist: not only does it push electron density around the ring, but the C–F bond’s strength lends pharmacokinetic value for drug candidates. Metabolic stability and improved bioavailability aren’t just buzzwords; they can make or break a promising molecule’s progress to the next stage of development.

    Researchers involved with electronic materials aren’t left out, either. The structure finds its way into studies on organic light-emitting diodes and thin-film transistors. The unique arrangement of substituents provides useful tuning of optical and electronic properties. I’ve seen more than one group report altered band gaps by introducing this compound into their polymeric systems, suggesting that demand won’t wane anytime soon.

    Comparing to Other Benzaldehyde Derivatives

    Any seasoned chemist will agree—not all benzaldehydes are created equal. Unsubstituted benzaldehyde gives little control when designing a new pathway. Once substituents enter the picture, the differences become obvious. Take 4-Bromo-5-Methylbenzaldehyde, just lacking that fluorine. Without it, the electron distribution in the ring shifts, and so do reaction outcomes. There’s often less control over regiochemistry, and yields can lag in reactions that benefit from the electron-withdrawing zing of a fluoro substituent.

    On the other hand, compare 4-Bromo-2-Fluorobenzaldehyde, which lacks the methyl group. The methyl brings bulk and a tiny electron push, nudging selectivity in certain reactions. In my experience, the extra methyl has helped avoid unwanted side products more than once. It also tweaks solubility; subtle differences in partition coefficient can change how well a compound dissolves in various organic solvents, speeding up purification steps and improving overall workflow.

    Some turn to 2-Fluoro-5-Methylbenzaldehyde, dropping the bromine for other leaving groups. While this works in specific cases, it stalls any hope of palladium-catalyzed coupling, unless another site is halogenated. For synthetic teams trying to keep flexible pathways open, this can limit options downstream, especially as they adapt routes for new analogs or try to scale up a promising reaction sequence.

    Quality Considerations: Purity Isn’t Just a Number

    As scientists, we talk a lot about purity, but the conversation doesn’t end with a percentage. Analytical data plays a heavy role in daily decisions. Lot-to-lot consistency helps avoid the headaches of revalidating processes each time a new shipment arrives. Besides NMR and HPLC, teams often run GC-MS and IR tests to double-check composition. In one collaborative project, our team flagged a minor impurity by GC-MS that steered downstream reactions off course, nearly costing a week of effort. A supplier committed to honest batch records helped us track the source and solve the issue quickly, a reminder that transparency isn’t just polite, it’s vital.

    Packing matters, too. A well-sealed amber bottle isn’t just an extra precaution—it helps extend shelf life. Even the best aldehydes suffer from oxidation if exposed to prolonged air and light. I’ve had to toss more than a few bottles of degraded material in my time; the sight of yellow-brown goo where pristine crystals should be is all too familiar for many in this field. That kind of loss is frustrating but avoidable with the right care and handling from both suppliers and internal logistics.

    Building for Safety and Sustainability

    Chemistry has seen a surge in safety focus. 4-Bromo-2-Fluoro-5-Methylbenzaldehyde brings a safe handling profile typical for halogenated aldehydes, but standard lab precautions apply. Nitrile gloves, eye protection, use of chemical fume hoods, and proper waste disposal are day-to-day practices. One lesson I’ve learned: keeping clear, updated protocols for new personnel ​prevents mishaps, and regular training reinforces good habits.

    Environmental stewardship calls for more than just ticking boxes. Minimizing waste and considering greener reaction media for transformations involving this compound can make a difference. For example, switching from chlorinated solvents to less hazardous options has steadily gained traction. Reducing overall use of harmful reagents not only cuts disposal costs but also shows respect for both the team and the broader community. Suppliers that openly share environmental, health, and safety data show they value these principles.

    Challenges and Progress in Sourcing

    Everyone knows interruptions in the supply chain can derail even the best research plans. 4-Bromo-2-Fluoro-5-Methylbenzaldehyde, while widely available from specialized suppliers, sometimes faces delays, especially if custom synthesis is required or global shipping hits a snag. Recently, increased scrutiny around import permits for brominated organics has introduced hiccups for some labs. I've watched teams double up on inventory planning or set up backup agreements with alternates to ride out these uncertainties.

    For small-scale operations, buying in reasonable lots without incurring excess cost remains a balancing act. Sometimes forming cooperative purchasing groups among local institutions helps meet minimum order requirements and lowers per-gram costs. Transparent pricing remains a concern, so seeking out partners who value open communication often results in smoother transactions and more reliable supply.

    Beyond the Reaction Flask: The Importance of Community and Shared Knowledge

    Behind every successful synthesis is a network of scientists, suppliers, and industry professionals sharing data, observations, and tips. 4-Bromo-2-Fluoro-5-Methylbenzaldehyde brings together researchers facing similar synthetic puzzles. From the nuances of purification to troubleshooting failed reactions, colleagues trade notes and foster a collaborative spirit. Attending regional conferences, browsing online forums, and participating in roundtable discussions regularly pays off; the latest insights or unpublished tricks can shave weeks from a challenging route.

    Publication of robust methods, including yields, conditions, and pertinent analytical data, offers newcomers a clearer road map. In my experience, labs that make rigorous sharing a pillar of their operation see both fewer errors and more rapid progress. It also supports reproducibility, a concern that’s drawn increasing attention as research teams aim to deliver work that stands up under external review.

    Keeping an Eye Toward the Future

    The landscape is shifting, with growing demand for molecules that combine efficacy and sustainability in pharmaceutical, materials science, and beyond. 4-Bromo-2-Fluoro-5-Methylbenzaldehyde, with its versatile structure and dependable behavior, has carved a niche that seems poised for further expansion. As the synthetic toolkit evolves, so does the potential for new derivatives springing from this core. Machine-assisted synthesis, continuous flow platforms, and data-driven reaction optimization will likely rely on intermediates like this one—in part because their predictability enables rapid iteration.

    Supply chain resilience, transparency, and a re-energized commitment to environmental responsibility are goals often discussed but harder to achieve. I’ve seen promising signs as suppliers adapt more agile logistics and take feedback seriously. Ongoing discussions about reducing hazardous waste and implementing renewable feedstocks point the way forward.

    Potential Solutions for Persistent Challenges

    Bottlenecks don’t go away by wishing. Securing stable sources of 4-Bromo-2-Fluoro-5-Methylbenzaldehyde sometimes means partnering directly with manufacturers that invest in robust quality systems. Some organizations work with multiple regional suppliers to spread risk. In-house synthesis, while a chore, acts as a last line of defense in times of shortage. Researchers also benefit from openly sharing feedback, flagging impurities, and reporting packaging flaws—an industry practice that helps drive overall improvements.

    For those concerned with cost, long-term contracts and forward planning provide a hedge against market fluctuations. Funding flexibility—from both public and private sources—can make or break a project, especially in university settings where tight budgets are the norm. Joining cooperative agreements to pool orders or share technical support pays dividends down the line.

    Adopting green chemistry principles isn’t just a trend; it carves out genuine value. Tweaking reaction conditions to cut hazardous waste and favor milder, safer reagents supports long-term performance goals and aligns with rising regulatory standards. Sharing greener procedures through publications, preprints, or online repositories spreads those benefits far and wide.

    Real-World Impact: Bridging the Lab and the Marketplace

    Compounds like 4-Bromo-2-Fluoro-5-Methylbenzaldehyde offer more than laboratory curiosity. Their applications ripple outward into the products and technologies people rely on every day, from novel therapeutics to improved electronic devices and cleaner agricultural solutions. My experience watching a lead series move from benchtop success to preclinical trials underscores just how significant these intermediates become. Each batch handled with care, tracked for purity, and selected with forethought contributes to building a foundation for discoveries far beyond solitary experiments.

    Every project that benefits from this compound’s unique properties helps set the bar higher for the next generation. As teams refine techniques, demand better quality data, and push for smarter, safer chemistry, the role of reliable building blocks becomes more pronounced. The trust that comes with consistent, high-quality offerings isn’t a given; it’s earned over years of attention to detail and responsiveness to evolving needs.

    Conclusion: A Compound with Staying Power

    4-Bromo-2-Fluoro-5-Methylbenzaldehyde may not make headlines, but it’s the unsung hero behind a wealth of scientific advancements. By offering a unique blend of reactivity, selectivity, and practicality, it remains a favorite in the toolbox of both seasoned and emerging chemists. Staying vigilant about purity, safety, sustainability, and open communication ensures that this dependable intermediate will keep fueling innovation across disciplines for years to come.