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4-Bromo-3-Fluorobenzaldehyde

    • Product Name 4-Bromo-3-Fluorobenzaldehyde
    • Alias 4-Bromo-3-fluorobenzaldehyde
    • Einecs 436-740-0
    • 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

    756411

    Productname 4-Bromo-3-Fluorobenzaldehyde
    Casnumber 161793-18-6
    Molecularformula C7H4BrFO
    Molecularweight 203.01 g/mol
    Appearance White to off-white solid
    Meltingpoint 98-102 °C
    Boilingpoint No data available (decomposes)
    Purity Typically ≥ 97%
    Smiles C1=CC(=C(C=C1Br)F)C=O
    Inchikey ZCCYYMVNAZLIMU-UHFFFAOYSA-N
    Solubility Slightly soluble in organic solvents
    Storagetemperature Store at 2-8°C
    Refractiveindex No data available
    Density No data available
    Hazardclass Irritant

    As an accredited 4-Bromo-3-Fluorobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Clear glass bottle with a white screw cap, labeled "4-Bromo-3-Fluorobenzaldehyde, 25g," hazard symbols and handling instructions displayed.
    Shipping 4-Bromo-3-Fluorobenzaldehyde is shipped in tightly sealed, chemical-resistant containers under ambient conditions. The package is clearly labeled with hazard warnings and complies with all relevant regulations for the transport of potentially hazardous chemicals. It is handled by trained personnel to ensure safety and prevent contamination or accidental release during transit.
    Storage 4-Bromo-3-Fluorobenzaldehyde should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep separate from incompatible substances such as strong oxidizers. Avoid moisture exposure. Store at room temperature, and ensure appropriate chemical labeling and secure shelving to prevent accidental spillage or breakage.
    Application of 4-Bromo-3-Fluorobenzaldehyde

    Applications of 4-Bromo-3-Fluorobenzaldehyde in Industrial Manufacturing

    4-Bromo-3-Fluorobenzaldehyde supports advanced synthesis in multiple specialty chemical production pipelines. As a direct manufacturer, we supply this key intermediate to downstream partners focused on fine chemicals, pharmaceuticals, agrochemical synthesis, dye intermediates, and advanced material sectors, enabling precise functionalization for demanding industry needs.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies use this compound as a building block to introduce both bromo and fluoro groups into target molecules for active pharmaceutical ingredient (API) development. In complex synthesis, it often serves in the key step of aromatic substitution or coupling for critical anti-infective and central nervous system (CNS) agents. Customers adjust concentration depending on desired molecule complexity, working under controlled environments to assure integrity of sensitive functional groups throughout the sequence. In-house analytical labs verify purity before subsequent transformations such as reductive amination or Grignard reactions.

    Industry compliance standards

    • ICH Q7 GMP guidelines for API intermediates
    • USP-NF monographs when relevant for downstream target APIs
    • EU GMP Part II requirements for intermediates
    • FDA 21 CFR 211 for traceability and documentation

    Typical usage ratio

    • Used at 0.8–1.2 molar equivalents relative to the target core structure; adjusted based on route optimization, reaction yield, and impurity profile requirements

    Downstream process integration

    • Introduced during early-stage aromatic scaffold assembly or as a late-stage functionalization agent by Suzuki, Heck, or Sonogashira coupling
    • Tightly controlled addition to avoid decomposition of aldehyde group

    Final product types

    • Anti-infective API intermediates
    • CNS agent development blocks
    • Trifluoromethyl-substituted aromatics
    • New chemical entity (NCE) reference standards

    2. Agrochemical Active Ingredient Manufacturing

    Crop protection manufacturers select this raw material for the synthesis of halogenated benzene cores in herbicide and fungicide pipelines. The electron-withdrawing substituents support design of bioactive molecules with improved field persistence and target specificity. Synthesis protocols commonly involve nucleophilic aromatic substitution or cross-coupling, followed by introduction of alkyl or heterocyclic side chains.

    Industry compliance standards

    • ISO 9001:2015 for documented quality control
    • REACH registration for raw materials within Europe
    • FAO/WHO specification for technical raw input (when applicable)
    • Occupational health and safety compliance, e.g., GBZ/T 240.49-2011 (China)

    Typical usage ratio

    • Employed at 0.9–1.5 molar equivalents relative to the next coupling or cyclization partner; adjusted based on targeted bioactivity and yield efficiency

    Downstream process integration

    • Used as a halogenated aromatic precursor in early core scaffold construction or as a side chain modulator following main ring assembly
    • Frequently subjected to subsequent oxidation or condensation steps

    Final product types

    • Halogenated phenyl herbicide intermediates
    • Triazole-based fungicide components
    • Pyridine/pyrazole derivative seed treatment actives
    • Strobilurin analog synthesis blocks

    3. Dye and Pigment Intermediate Fabrication

    The dye and pigment industry incorporates this compound into synthetic routes for specialty azo, anthraquinone, and heterocyclic colorants that demand electron-rich substituents for improved bathochromic shift. Process engineers utilize its reactivity in condensation reactions and as an aldehyde source for chromophore modification during the pre-final stages of dye synthesis.

    Industry compliance standards

    • ISO 14001:2015 for environmental impact control
    • EN 71-3 (Safety of toys – migration of certain elements) for colorant applications in toys
    • EU REACH regulation for dye intermediates registration
    • Standard test methods for trace metal and halogen content (e.g., DIN EN ISO 14362-1)

    Typical usage ratio

    • Added at 1–2 molar equivalents based on the nucleophile used and the desired dye structure; fine-tuned for color strength and hue consistency

    Downstream process integration

    • Employed during intermediate condensation, particularly with hydrazine or aromatic amines, before final diazotization or coupling
    • Careful control of solvent polarity and temperature to suppress side-product formation

    Final product types

    • Specialty azo pigment intermediates
    • High-performance vat and disperse dyes
    • Organic colorants for engineering plastics
    • Fluorinated dye markers for security printing

    4. Advanced Material Monomer Production

    Producers of high-performance monomers and specialty polymers integrate this compound to engineer halogen-, fluoro-, or formyl-functionalized polymers. These are crucial for liquid crystal displays, specialty adhesive formulations, or electronic resins. Polymer chemists use it for precision modification through step-growth or chain-growth polymerizations where controlled side group introduction significantly enhances thermal and chemical resistance.

    Industry compliance standards

    • RoHS 3 Directive (EU 2015/863) for electronics materials
    • ISO 9001 for production traceability
    • Restriction of Halogen Content Standards for plastics (IEC 61249-2-21)
    • SDS and hazardous material handling based on GHS labeling

    Typical usage ratio

    • Introduced at 0.5–1.0 molar equivalents per monomer feed; tuning dependent on target molecular weight and desired polymer backbone structure

    Downstream process integration

    • Incorporated by direct polymerization, often after aldehyde group protection or conversion to imine or oxime prior to bulk processing
    • Post-polymerization functionalization for end-group modification

    Final product types

    • Liquid crystal monomers for display technologies
    • Halogen-functional epoxy resins
    • Specialty fluorinated engineering polymers
    • Electronic encapsulant formulations
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-3-Fluorobenzaldehyde: Value in Detail-Oriented Synthesis

    Looking Closer at the Molecule

    We manufacture 4-Bromo-3-Fluorobenzaldehyde as an intermediate for pharmaceutical and specialty chemical synthesis. This compound—produced under strict batch control—offers a bromine at the para position and a fluorine at the meta position relative to the aldehyde group, fitting advanced multi-step production needs. Years of experience in our reactors have shown us the importance of molecular purity and precision when handling such halogenated aromatics. Our product, with the model number 3FBAL-4050, regularly meets a minimum assay of 99.0%, and GC results show very narrow impurity profiles, helping chemists achieve reliable coupling and downstream transformations.

    Why Chemists Seek Specific Building Blocks

    Process chemists choose 4-Bromo-3-Fluorobenzaldehyde for its reactivity and selectivity in cross-coupling, condensation, and substitution reactions. We’ve worked hand-in-hand with research teams designing active pharmaceutical ingredients or advanced materials, and have seen demand grow for well-defined building blocks. Our technical crews have refined the synthesis route to tightly control isomer content and minimize contaminants such as unreacted precursors or side products that could complicate purification in the client’s process. Product arrives as a pale yellow to light brown crystalline solid, with a melting range of 46-51°C and characteristic aromatic-aldehyde odor for easy identification in process lines.

    Key Differences from Conventional Benzaldehydes

    Handling halogenated benzaldehydes demands extra vigilance, and over time we’ve seen users place special value on the dual substitution pattern. Compared to mono-halogenated or unsubstituted benzaldehydes, 4-Bromo-3-Fluorobenzaldehyde introduces both steric and electronic effects that can steer reaction regioselectivity or modulate biological activity in lead compounds. We have collaborated with clients optimizing SAR (structure-activity relationships) studies who routinely share how the ortho-fluorine helps boost metabolic stability, and the para-bromo enables efficient Suzuki or Buchwald-Hartwig couplings.

    Many labs still start with parent benzaldehyde or simple 4-bromobenzaldehyde, only to face extra synthetic steps and yield losses trying to introduce fluorine. Our route avoids hazardous reagents like elemental fluorine or harsh oxidants and delivers precise substitution, helping users focus their attention on downstream innovations rather than upstream troubleshooting.

    Traceability in Manufacturing Practice

    Experience on the shop floor has taught us that keeping a reliable chain of custody from raw material selection through finished packaging makes a difference in customer confidence. We maintain traceable records on every production lot, from purchasing high-purity resorcinol or fluorobenzaldehyde precursors to logging all stages in our ERP system. Internal and third-party audits validate that our material maintains consistent halogen ratio and low water content, critical for sensitive palladium-catalyzed reactions.

    Our QA staff closely examines every lot by NMR, GC-MS, and titration, verifying the absence of residual solvents beyond regulatory cut-offs. Even as environmental and safety standards become stricter, our facility continues to invest in emission capture and improved waste neutralization methods, reducing impact not only for those working at the bench but also for the communities where we operate.

    Respecting Detail in Research and Process Development

    Over the years collaborating with both academic and industrial chemists, we’ve noticed a common frustration: inconsistent intermediate quality holds back method development or causes batch variability. Through real project feedback, we shifted our process from generic to dedicated lines with glass-lining and halogen-compatible pumps to address corrosion and cross-contamination. No shortcut takes the place of regular monitoring. We encourage our customers to use the accompanying certificate of analysis for each drum and reach out to troubleshoot reaction issues, not only to resolve quality concerns but to keep all parties progressing in tandem.

    Our tech support has heard feedback about ease-of-use—chemists want a clean melting profile, minimal static charge during weighing, and reliable solubility in common organic solvents. Samples undergo microanalysis for carbon, hydrogen, and nitrogen, even though this compound only has trace N from certain synthesis variants. Any deviation gets tracked, and corrective steps feed back into process refinement, not just for certification compliance, but to heighten reproducibility in end-use settings.

    Facility Upgrades and Process Safety Investment

    Shifting from gram-scale bench practice to kilo and metric-ton runs comes with substantial challenges. For 4-Bromo-3-Fluorobenzaldehyde, the dual halogen content means monitoring hydrogen halide evolution during chlorination or bromination steps, and making sure all process streams stay contained. We select autoclave-grade reactors with venting and active scrubbers to capture any fume bursts. Our operators carry out reactions under inert nitrogen with real-time monitoring of temperature, pressure, and pH, learning from pilot-scale studies to avoid runaway reactions.

    The aldehyde group’s sensitivity to oxidation also calls for careful temperature control, especially at isolation stages. Our plant’s workflow includes staged crystallization and controlled solvent removal. Even moisture pickup from the environment can degrade yield or color, so storage and handling shifts take place under desiccant and low humidity. Each new safety study leads our team to fine-tune PPE protocols and infrastructure, balancing operator protection with process efficiency.

    Supporting Custom and Scalable Needs

    Years of working with innovators have shown us that scale-up needs flexibility. Small startups seek 100-gram bottles to screen for initial hits in combinatorial chemistry. Global pharma companies order 25-kilogram drums with stability data for regulatory filings. Scaling up the same quality standard, whether for research or commercial runs, means keeping supply intact through inventory planning and verified shipping partners who handle hazardous materials responsibly. Because some users request specific grades, our staff works with customers to define custom impurity thresholds or packaging formats. We have responded with amber-glass, HDPE, or lined steel containers, each batch accompanied by paperwork listing actual values from HPLC and TGA scans.

    We track emerging needs across organic electronics and agrochemical sectors as well. Some applications require IP protection, so our production lines maintain confidentiality for customer-specific modifications. Our business stays shaped by long-term relationships that grow out of routine tech support calls and transparent failure analysis. Every new project helps us learn more about the subtleties of 4-Bromo-3-Fluorobenzaldehyde in complex synthetic routes, knowledge that feeds back into better product for everyone.

    Regulatory Awareness and Environmental Performance

    Global expectations have shifted. Today’s buyers ask not just about purity, but also about compliance with REACH, TSCA, and other regulations. We attach region-specific documentation as required, and our regulatory affairs team monitors update cycles to add new substance notifications or respond to shifting substance limits. From our experience, clients value not simply a checklist, but a supplier who anticipates regulatory reviews or supports traceable lot documentation all the way from supplier to finished batch.

    On the environmental side, aromatic halogenation once depended on batch runs with difficult-to-treat waste. Our facility transitioned to closed-loop solvent recovery and stepwise hydrobromic acid neutralization, aiming for near-zero discharge. Residual process water undergoes active carbon treatment on site, and halogen content in spent solids gets monitored for safe landfill or authorized incineration. Regular energy audits and raw material efficiency checks guide periodic improvement projects. Each step helps lower the environmental footprint not only because of regulation, but from our belief that responsible chemistry sustains business and society together.

    Advancing R&D and the Path to New Molecules

    Within our own R&D labs, 4-Bromo-3-Fluorobenzaldehyde serves as a stepping stone toward more complex, value-added molecules. Our chemists investigate it as a precursor for constructing biphenyls, heterocycles, and fused aromatics targeting pharmaceutical leads or sensor materials. Joint development programs sometimes call for selective modifications—introducing groups at other aromatic positions or attaching functionalized side chains. Our teams run trials on new catalysts or flow protocols aiming to cut cost, raise space-time yield, or expand to greener solvent systems.

    For customers in drug discovery or crop protection, ready access to such intermediates means synthetic schemes can move from the planning board to the lab bench without supply chain bottlenecks. Many users report that sourcing directly from a manufacturer makes troubleshooting easier. If a coupling fails or if unexpected byproducts crop up, our chemists can recreate the reaction, consult on possible causes, and work together to solve the bottleneck, whether it traces to trace metal content, residual chloride, or just vapor-phase interaction with reactor linings.

    Future Challenges and Customer Collaboration

    As demand grows for selectively substituted aromatics, chemists keep raising the bar on what they expect from manufacturers. Commercial production of 4-Bromo-3-Fluorobenzaldehyde today requires more than just legacy processes and bulk output. Clients bring forward tough questions about ESG (environmental, social and governance), worker safety, and materials traceability. Each challenge forces our facility to adapt and improve, but also sharpens our expertise in meeting next-generation needs.

    Feedback-led process improvements now set the tone for how we invest in new synthesis lines and downstream clean up. For every challenge—managing shipments in hot and cold weather, or preventing discoloration in long-term storage—our staff learns new ways to support customers not just as suppliers, but as technical partners. By reporting on real impurities, sharing suggestions for optimized work-ups, or anticipating specialized logistical support, our crew builds more loyalty than any simple price quote or product flyer ever could. In developing 4-Bromo-3-Fluorobenzaldehyde at this scale, we keep our ears tuned to the market and our hands ready for the next production run—ensuring researchers and process chemists get what they need to keep science moving forward.