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3-Bromo-4-Fluorobenzaldehyde

    • Product Name 3-Bromo-4-Fluorobenzaldehyde
    • Alias 3-Bromo-4-fluoro-1-formylbenzene
    • Einecs 872-319-3
    • 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

    262983

    Cas Number 22259-44-1
    Molecular Formula C7H4BrFO
    Molecular Weight 203.01 g/mol
    Appearance White to off-white solid
    Melting Point 61-65°C
    Density 1.69 g/cm³ (estimated)
    Purity Typically >98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=C(C=C1Br)F)C=O
    Inchi InChI=1S/C7H4BrFO/c8-6-2-1-5(4-10)3-7(6)9

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, sealed with a screw cap; labeled with chemical name, hazard warnings, and supplier details.
    Shipping 3-Bromo-4-Fluorobenzaldehyde is shipped in tightly sealed, chemically resistant containers to prevent leakage and contamination. It is transported as a hazardous material, following relevant regulations for toxic and corrosive substances. Appropriate labeling and documentation are included, and handling is performed by trained personnel to ensure safety during transit.
    Storage 3-Bromo-4-Fluorobenzaldehyde should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible materials such as strong oxidizers. Avoid exposure to direct sunlight. Always ensure appropriate chemical labeling and store in a designated chemical storage cabinet, ideally under inert atmosphere if possible to minimize degradation.
    Application of 3-Bromo-4-Fluorobenzaldehyde

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

    3-Bromo-4-Fluorobenzaldehyde is a precision intermediate manufactured for integration into complex organic synthesis across multiple industrial sectors. As a direct manufacturer, we supply this material to specialized downstream partners requiring rigorous quality, traceability, and consistent physical specifications for controlled processes and registrations. Below, we describe key application scenarios, each with designated standards, blend ratios, integration points, and resulting product types.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical companies use this material primarily as a building block in the synthesis of advanced intermediates for non-steroidal anti-inflammatory drugs (NSAIDs) and certain oncological small molecule APIs. Precision in impurity profile and residual solvent control is critical, with batch traceability aligning with regulatory criteria. Material enters multi-step synthesis before condensation or reductive amination, linking directly to protected phenolic scaffolds.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • 21 CFR Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals
    • USP General Chapters pertaining to organic intermediates
    • European Pharmacopoeia monographs for related substances

    Typical usage ratio

    • 1.0 to 1.2 molar equivalents relative to coupling partners; precise adjustment based on final API yield and side-product risk

    Downstream process integration

    • Introduced after initial aryl substitution, pre-selective reduction or acylation step; batch addition under nitrogen under 10–25 °C with in-process sampling

    Final product types

    • Advanced pharmaceutical intermediates
    • Non-steroidal anti-inflammatory agents
    • Fluorinated benzene-based APIs
    • Targeted therapy reference standards

    2. Agrochemical Active Intermediate Manufacturing

    Crop protection manufacturers employ this compound as a key intermediate in synthesis routes for herbicides containing halogenated benzaldehyde frameworks. The reactivity of the bromo and fluoro positions supports downstream selective derivatization with heterocyclic fragments, assisting developers in meeting regulatory requirements for product safety. Tight control over trace halides and aldehyde purity is required for registration in regulated markets.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP)
    • FAO/WHO specifications for pesticide active ingredients
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 for quality management in chemical manufacturing

    Typical usage ratio

    • 0.9 to 1.15 molar equivalents per main heterocycle, adjusted for crop specificity and cost optimization

    Downstream process integration

    • Stepwise coupling within the aromatic core formation; added following initial diazotization, maintained under pH 4.5–6.5 for oxidative controls

    Final product types

    • Halogenated herbicide actives
    • Benzaldehyde-based insecticidal ingredients
    • Intermediates for fungicide synthesis
    • Seed treatment chemical precursors

    3. Liquid Crystal Material Synthesis for Electronic Displays

    Producers of specialty liquid crystal compounds utilize this material during the synthesis of dichroic core fragments. The compound’s specific fluorine and bromine substituents facilitate the design of high-anisotropy molecules, lending improved dielectric and birefringence properties to subsequent display materials. Stringent impurity limitations are adhered to, with deep purification before further processing for commercial display supply chains.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substance restrictions
    • IEC 62321 methods for halogen screening
    • JEITA EIAJ standards for chemical purity in electronics
    • JIS K 0050 for chemical analysis in industrial materials

    Typical usage ratio

    • 0.8 to 1.1 molar equivalents, tuned per mesogen design to control molecular polarity and viscosity in final liquid crystal mixture

    Downstream process integration

    • Reacted with phenyl acetylene or alkoxy derivatives via Suzuki or Wittig-type cross-coupling; incorporated during early synthetic stages under solvent-free or minimal-solvent conditions

    Final product types

    • Nematic and smectic liquid crystal mixtures
    • Display-grade intermediate compounds
    • Indium tin oxide-compatible functional films
    • High-temperature liquid crystal electronic displays

    4. Synthesis of Specialty Dyes and Pigment Intermediates

    The material is integrated by dye manufacturers for construction of high-performance colorants, where the substitution pattern enables high electron-withdrawing capability and tailored absorption wavelengths. Strict control over trace metals and color purity allows downstream users to meet fastness and non-migration requirements for textile and industrial coatings markets. Multi-stage reactions utilize it both as an electrophilic partner and as a functionalized aromatic precursor in aromatic azo dye synthesis.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • REACH Annex XVII restrictions on dye additives
    • ISO 105-X12:2016 for color fastness testing
    • ZDHC MRSL guidance for pigment and dye manufacturing

    Typical usage ratio

    • 1.05 to 1.25 molar equivalents relative to dye coupler or diazonium salt; ratio optimized according to desired tinctorial strength and hue adjustment

    Downstream process integration

    • Introduced at initial coupling stage in the synthesis sequence; carried through further chlorination or reduction, followed by purification through high-performance liquid chromatography

    Final product types

    • Halogenated azo dyes
    • Specialty pigment intermediates
    • Textile disperse dyes
    • Industrial coating colorants
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    Certification & Compliance
    More Introduction

    3-Bromo-4-Fluorobenzaldehyde: Practical Experience and Real-World Value

    Introduction to 3-Bromo-4-Fluorobenzaldehyde

    Manufacturing specialty aromatic compounds brings its share of lessons. 3-Bromo-4-Fluorobenzaldehyde has proven itself in our line-up because of how it bridges the properties of halogen substitution with distinctive reactivity. This compound, with the formula C7H4BrFO, began drawing our attention early, especially once the demand for tailored aromatic building blocks took off. Its structure—a benzaldehyde core, bromine at the 3 position, and fluorine at the 4 position—lets synthetic chemists harness both electronegativity and size effects in ways that more standard benzaldehydes cannot.

    Most requests we handle come from pharma development labs or fine chemical producers building active molecules destined for screening or even lead optimization. In our own work, we've watched teams shift from tried-and-true benzaldehydes to this bromo-fluoro variant once they need more complex intermediates. Its appearance—a pale yellow crystalline solid—marks it clearly apart from unmodified analogs, and we see this change mirrored in its melting point, solubility, and reactivity.

    Why Specification Details Matter in Synthesis

    Reflecting on our manufacturing runs, the quality of 3-Bromo-4-Fluorobenzaldehyde hinges on strict raw material control and monitoring each step. We use HPLC and NMR to guarantee purity not as a talking point, but because chemists working downstream need confidence that contamination will not torpedo their yield or introduce untraceable byproducts. The product we ship consistently achieves >98% purity, with the balance essentially all accounted for by related isomers or very limited water content from the recrystallization protocol.

    From batch to batch, subtle shifts in reaction conditions (temperature, stirring, solvent proportions) alter the outcome. Over time, what has paid off most has been recording every parameter, not as a paperwork exercise but to learn which adjustments matter when scaling from kilogram to multi-ton outputs. Take crystallization: longer cooling phases coupled with staged solvent removal drops impurity levels by as much as 1%, a margin that protects both our clients and our credibility.

    The Role of Substituents and Their Impact

    Bromine and fluorine stand right at the heart of what makes this compound intriguing to medicinal and materials chemists. From our shop floor, handling brominated intermediates always demands respect: they’re denser, show higher reactivity in subsequent functionalization, and typically command controlled handling and storage. The presence of bromine lets chemists easily leverage cross-coupling reactions (think Suzuki or Heck), while fluorine’s influence emerges in how it tunes electron density on the aromatic ring.

    Adding fluorine matters for more than narrow tweaking. Labs using this compound often report that the fluorine at the 4-position shifts the lability of the aldehyde group, encouraging reactivity under milder or more selective conditions. This means researchers can run reactions at lower temperatures, avoid harsher reagents, or realize higher chemo-selectivity. In situations where sensitive functional groups or chiral centers exist elsewhere in the molecule, these factors are not just academic—they make workflows safer, cleaner, and more productive.

    Switching Gears: Use Cases in Real Labs

    Pharma chemists search for “privileged scaffolds” all the time. Working with 3-Bromo-4-Fluorobenzaldehyde, we’ve seen it fill this role because it integrates into many heterocyclic synthesis strategies. For instance, several clients in lead discovery programs pull this aldehyde in for base-mediated reactions, forming key intermediates for benzoxazoles, benzothiazoles, and other fused ring systems. Its electron distribution pattern (thanks to the strategic halogenation) often sets up clean, high-yield formations of these compounds.

    Beyond pharmaceuticals, clients in the agrochemical and dye sectors have incorporated this building block to induce specific activity profiles. Some dye manufacturers turn to bromo-fluoro substituted aromatics to fine-tune color fastness and affinity on textiles or plastics. Agrochemical researchers, always seeking pest selectivity and controlled degradation rates, exploit the subtle interplay of bromine and fluorine to introduce metabolic stability or modify environmental mobility. Over the last two years, we’ve also fielded increased demand from contract research organizations in Asia, confirming a broader trend toward complex, multi-halogenated building blocks.

    Comparing with Other Benzaldehydes

    Our catalog holds various benzaldehydes—plain, mono-halogenated, di-halogenated, and more. What separates 3-Bromo-4-Fluorobenzaldehyde from its cousins centers on the balance between reactivity and selectivity. A plain benzaldehyde (or even 4-fluorobenzaldehyde) cannot deliver the same level of orthogonal functionalization. If a project calls for cross-coupling and later electrophilic substitution, the bromo-fluoro combination unlocks more pathways, especially with today’s focus on late-stage diversification.

    Working with mono-bromo or mono-fluoro analogs sometimes leads to excessive one-sided reactivity—either too much nucleophilic attack or insufficient selectivity for oxidative transformations. The dialed-in properties of this aldehyde offer greater latitude for multi-step synthesis: once the bromo group installs a new function, the fluorine’s electron-withdrawing effect helps with subsequent steps, tempering unwanted side reactions and stabilizing sensitive intermediates.

    Analytical comparisons have shown differences not just in yields but also in the types of by-products formed during condensation or coupling reactions. Our QC group mapped out impurity profiles under various conditions, and the 3-Bromo-4-Fluorobenzaldehyde runs deliver tighter control, translating into higher downstream product purity (especially relevant for pharmaceutical regulations).

    Handling and Storage: Lessons from Practice

    Every specialty chemical comes with a unique set of storage hazards and best handling practices. Our warehouse and quality assurance team constantly review shelf-life and packaging strategies for 3-Bromo-4-Fluorobenzaldehyde. Experience has shown that trace moisture or exposure to excess heat slowly encourages degradation, so we package with high-barrier liners and reinforce climate control. The aldehyde functional group attracts moisture and can self-condense under less-than-ideal conditions—nothing theoretical here, just the facts of long-term storage trials. Double-bagging and regular rotation of stock remain critical for keeping batches within spec and minimizing waste.

    Our dispatch team keeps close tabs on temperature and humidity during transit, as repeated cycles of warming and cooling open the door for minor decomposition. Labs worldwide continually ask for shipment in smaller increments to cut down on storage risk, and our fulfillment procedures keep up with those evolving requirements. Proper labeling, clear shelf-life indicators, and rapid batch turnover undergird our shipments.

    Environmental and Safety Impact

    Safety considerations guide every part of our operation, from custom reactor design to shipping protocol. Working hands-on with 3-Bromo-4-Fluorobenzaldehyde gives you a perspective broader than regulatory minimums. Brominated organics always raise flags for possible persistence or bioaccumulation; at our site, effluent streams receive active monitoring to ensure no bromo-organics end up in water discharge. Standard PPE—nitrile gloves, goggles, and fitted lab coats—already form the baseline, but targeted training with the hazard communication standard cements safe operation.

    Our research and pilot teams regularly evaluate process enhancements to reduce energy use, minimize by-product formation, and recover solvents. Rather than wait for mandates, we’ve built closed-loop systems that scrub volatile halides and reclaim process water. Waste minimization always pays off in the long-term—not just as a compliance metric but as an economic imperative, too. Every kilo of lost product or extra work-up means lost hours and higher costs for everyone.

    Supply Challenges and Market Evolution

    The past few years have tested the resilience of every chemical supply chain. In producing intermediates like 3-Bromo-4-Fluorobenzaldehyde, upstream shortages of brominating or fluorinating agents sometimes derail production schedules. Rather than chase spot markets, we’ve built long-term supplier partnerships, combining fixed allocation contracts with strategic inventories to weather disruptions.

    Rapid changes in regulatory environments, especially around halogenated aromatics, have led us to closely track international guidance from REACH and other frameworks. Some countries call for more granular documentation for trace quantities; our compliance division maintains exhaustive records and responds quickly to documentation requests from clients. This level of transparency does not happen by accident; it kills two birds—bridging regulatory diligence and reinforcing the trust required in custom manufacturing.

    On the global market front, we notice rising demand for distinct scaffolds as green chemistry principles take hold. Scientists now favor molecules that build complexity with fewer steps—a trend that bodes well for 3-Bromo-4-Fluorobenzaldehyde, given its potential to streamline synthesis. Practical needs push us to stay nimble: expand reactor capacity, digitize quality control, and strengthen supply links to keep up with the research pace.

    Analytical Testing and Supporting Data

    Every liter of solvent, every kilogram of raw material, and every degree on the temperature gauge influences the final product. We lean hard on routine analytical data. Our in-house QC runs HPLC, GC-MS, and NMR on every lot, not just for regulatory checkboxes but to ensure clients skip troubleshooting and hit their yields out of the gate.

    Clients often ask for spectral data sets to verify identity and chase down even trace impurities. Instead of generic response, our technical team regularly assembles tailored analysis summaries with COAs backed by full chromatogram files. This way, every user—pharma chemist, academic group, dye formulator—sees not only the numbers but also the performance background underpinning those numbers. Internal consistency builds external trust, which cycles back into long-term project partnerships.

    Beyond compliance, this analytical depth pays forward. Recently, a client needed a fingerprint impurity profile run against a new process—our archived data set from past lots detected the subtle by-product emerging under revised conditions, shortening their troubleshooting time.

    Process Development and Continuous Improvement

    No run stays the same for long. Our engineers and chemists thrive on process signals—color changes, gas evolution, even subtle changes in viscosity. Over the years, iteration has sharpened both chemical yield and operational safety. Early pilot runs showed that with slow reagent addition and staged cooling, the formation of polycondensation products drops sharply.

    We use real-time monitoring to learn directly which points in the workflow offer the most leverage for consistency. In one example, a small tweak to the base washing protocol changed downstream impurity carryover, stabilizing product color and reducing end-user complaints about tints in their own reactions. Every improvement at our level rolls up into the easier handling, quicker analytic confirmation, and smoother reaction runs for the labs we support.

    Collaboration with End Users and Customization

    Contract manufacturing means real conversations with people doing discovery work. Many groups building combinatorial libraries or investigating SAR series come to us with specific requirements. Some need a particular crystal habit, others want strict water content, and a few demand tighter exclusions of related byproducts. Our variability control grew directly from iterating alongside these groups—modifying drying protocols, filtering to sub-micron specs, or even redesigning packaging to fit glove box feeds.

    Open dialogue reveals unseen hurdles and new applications. Recently, a team working on solid-phase synthesis needed a packaging solution for milligram-scale access that minimized waste and cut exposure risk. The collaborative approach—a combination of precision dosing, pre-weighed vials, and tamper-evident packaging—evolved out of these direct conversations, not from generic product brochures.

    The Value of Experience in Predicting Project Outcomes

    After years making and delivering 3-Bromo-4-Fluorobenzaldehyde, we rely not just on specs but also on what history has taught. Projects that start with the clearest communication about needs, batch size, and schedule always succeed. We encourage customers to share intended applications as early as possible—are they testing stability at pH extremes, scaling up cross-couplings, or running downstream reduction and oxime formation? Each scenario sometimes triggers additional cycles of drying, refining, or sieving on our end.

    Understanding these project parameters early lets us catch potential pitfalls and deliver batches shaped for real-world needs. Our most successful partnerships never treat specialty chemicals like commodities. Instead, each run becomes a learning cycle—whether that means adjusting particle size for a high-throughput flow system, or hitting purity ranges needed to satisfy ICH Q3A guidelines for trace impurities.

    Conclusion: Ownership, Accountability, and Continuous Growth

    Manufacturing 3-Bromo-4-Fluorobenzaldehyde shapes not only products but also mindset—one of ownership and deep-rooted accountability. Every gram we produce stands as a record of many hours spent on protocol development, customer collaboration, and process troubleshooting. Direct engagement with the end-users sharpens our ability to spot trends and drive continual improvements.

    Where others see just another chemical, we see the practical advantages, built on daily experience and proven relationships. For every application—pharma, materials, agro, or dyes—the right properties, reliable data, and sustainable process matter. As the market keeps evolving and demands grow more sophisticated, so does the work behind every batch we ship.