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HS Code |
218789 |
| Cas Number | 60456-26-0 |
| Molecular Formula | C7H5BrClF |
| Molecular Weight | 223.47 |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically >98% |
| Boiling Point | 258-260°C |
| Density | 1.64 g/cm3 |
| Solubility | Insoluble in water, soluble in organic solvents |
| Refractive Index | 1.562 (20°C) |
| Synonyms | α-Bromo-(2-fluoro-4-chlorophenyl)methane |
| Storage Temperature | Store at 2-8°C |
| Hazard Statements | Irritant; may cause skin and eye irritation |
As an accredited 2-Fluoro-4-Chlorobenzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g quantity, labeled with "2-Fluoro-4-Chlorobenzyl Bromide," hazard symbols, lot number, and safety information. |
| Shipping | 2-Fluoro-4-Chlorobenzyl Bromide is shipped in airtight, chemical-resistant containers to prevent leaks and moisture exposure. Packaging complies with international transport regulations for hazardous chemicals. Labels display hazard symbols and handling instructions. During transit, it is protected from extreme temperatures, sunlight, and incompatible substances to ensure safe delivery. |
| Storage | 2-Fluoro-4-Chlorobenzyl Bromide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizers. Protect it from moisture, direct sunlight, and heat. Use proper chemical storage cabinets, and ensure that the storage area is clearly labeled and access is restricted to trained personnel. |
Applications of 2-Fluoro-4-Chlorobenzyl Bromide in Industrial Manufacturing2-Fluoro-4-Chlorobenzyl Bromide plays a crucial role in several specialized chemical manufacturing processes. As an authentic producer with on-site synthesis and quality control, we supply this intermediate to established downstream sectors that demand robust traceability and meet international compliance requirements. Its refined reactivity and halogen substitution pattern make it suitable for diverse and tightly regulated industrial applications. 1. Agrochemical Synthesis: Selective Herbicide IntermediateAgrochemical manufacturers depend on this compound in the synthesis of halogenated phenoxy acids and pyridine-based herbicides. Its molecular structure provides a key building block for modern broadleaf and grass weed management agents, which undergo continuous regulatory scrutiny due to field application and environmental exposure. The material is introduced at the nucleophilic substitution phase before final esterification, ensuring controlled residue and optimized activity in the final formulation. Industry compliance standards
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2. Pharmaceutical Intermediate: Active Ingredient PrecursorPharmaceutical manufacturers utilize this compound for the construction of advanced molecules, particularly in the anti-infective and central nervous system (CNS) drug classes. Its reactivity toward nucleophilic aromatic substitution enables the formation of highly specific benzylated scaffolds, which can be further functionalized for structure-activity tuning. The compound is dosed precisely during the alkylation step, with batch records monitored under strict GMP guidelines to maintain reproducibility and impurity control. Industry compliance standards
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3. Specialty Dye and Pigment ManufacturingProducers of industrial dyes and pigments apply this chemical in the creation of halogenated aromatic chromophores, particularly where electron-withdrawing substituents influence color fastness and light stability. The raw material enters the manufacturing stream at the nucleophilic aromatic substitution, imparting specific absorption characteristics needed for specialty textile and high-performance coatings. Operations conform to both chemical handling and colorant safety requirements applicable in key global markets. Industry compliance standards
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4. Advanced Material Synthesis: Electronic and Polymer Additive ManufacturingIn the electronics and advanced polymer sectors, specialty producers incorporate this intermediate to engineer functional additives and binders with targeted halogen content and controlled reactivity. The compound’s dual halogen substitution supports custom-tailored electronic properties and compatibilization in specialty polymer blends used for circuit encapsulation and antistatic applications. Process engineers precisely meter the raw material during prepolymer or oligomer functionalization, according to the electrical or rheological characteristics specified by downstream customers. Industry compliance standards
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Deep inside the daily grind of chemical manufacturing, the journey of 2-Fluoro-4-Chlorobenzyl Bromide stands out for those who value precision and reliability. 2-Fluoro-4-Chlorobenzyl Bromide, known in labs and pilot plants by its CAS No. 216399-35-8, commands attention both for its critical role in organic synthesis and the expectations for consistency demanded by those who use it. Many names cross the benches in this industry, but this molecule carves out a space thanks to a well-blended set of attributes—handled properly, it helps chemists conquer tough synthetic challenges, making way for innovative products downstream.
Manufacturing this fine chemical isn’t a simple matter of mixing and bottling. The route starts from hand-selected starting materials, each batch examined closely by people who have learned over years that shortcuts end up as headaches—and expensive ones at that. Fluorination and chlorination steps require closely controlled conditions. Reaction parameters like temperature, pressure, and reagent purity have to be watched like a hawk, not just checked but really watched. We have seen how a stray degree here or a tiny trace impurity there can make the reaction stall, drive side products, or bring down yields. Each run is checked for conformity with project requirements, but experience shows that putting in tight controls on water content and minimizing bi-phasic layers are more than box-checking—these habits separate a reliable batch from a batch nobody wants.
Many partners who choose us look for a specific melting range (for 2-Fluoro-4-Chlorobenzyl Bromide, you’ll see it as an oily liquid at room temperature). The sharpness of the NMR peaks tells you a lot about the manufacturing process, and TLC and GC checks give a clear view on purity and trace levels of related substances. These are not empty numbers. Teams who build complex molecules downstream ask us not just for purity above 98%, but for that purity lot-to-lot, all year, every year. They notice when the product sits cleanly in their preparative process, and they really notice if it doesn’t.
Leaving catalog descriptions aside, this compound mostly wins its place in the world as an intermediate in the synthesis of pharmaceuticals—often in tough, late-stage steps. The fluorine and chlorine atoms both bring special properties to the benzyl bromide, letting medicinal chemists design molecules that survive metabolic breakdown but still hit the right target in the body. When customers come looking for this product, they often tell us how it fits into sequences that build up heterocycles or attach to nucleophiles through the bromide leaving group. Academic and process development teams tell us about the transformations downstream—Suzuki couplings, nucleophilic substitutions, or the introduction of complex side chains that wouldn’t be possible with unsubstituted benzyl bromide.
We get feedback from clients who tested comparable analogues—like 2-Chloro-4-Fluorobenzyl Bromide, or simply 4-Chlorobenzyl Bromide—and found the reactivity or selectivity didn’t match their expectations. The precise fluorine and chlorine positions in 2-Fluoro-4-Chlorobenzyl Bromide really do matter. For example, the fluorine’s position (at the ortho site) changes the electron density on the aromatic ring, which, in our experience with process development, often pushes the desired selectivity in SN2 reactions. Some users attempted using para-fluorinated versions, expecting similar outcomes, but experimental results showed less predictable behavior—a lesson that tells us how little changes in structure can ripple through an entire process.
Production teams often field questions about batch-to-batch variability. We have learned through experience that rigorous monitoring of both input quality and reaction profile pays dividends. There’s a temptation in fine chemical manufacturing to work to spec and move product off the line. Long ago, we realized that an impatient rush to hit throughput can sabotage months of customer work. Delivering 2-Fluoro-4-Chlorobenzyl Bromide with consistent IR, NMR, and GC data, instead of relying only on HPLC area percent, brings peace of mind not only to the synthetic chemist but back into the plant itself.
On the subject of analytical checks, we never take the shortcut of “close enough.” Before shipping, the technical staff double-checks that the characteristic singlet in the proton NMR—made distinct by the para-chlorine and ortho-fluorine—is clean and free from overlapping signals. We have encountered scripts from other producers who gloss over minor peaks, but those overlooked traces at a few hundred ppm can throw a project off. Instead, our practical experience tells us that, whether a client is scaling up to kilo runs or running delicate parallel medicinal chemistry, these details make the difference between a reliable building block and a gamble.
Over the past decade, we have scaled up batches from gram levels at benchtop to multi-kilo campaign runs. Each scale brings its own headaches—reflux rates don’t stay predictable, product layers look different in big glass-lined vessels, and impurity profiles shift. We have confronted and ironed out hiccups with distillation and solvent recycling, which in bulk can introduce new byproducts. It takes staff with hands-on knowledge to anticipate problems, adapt workups, or modify purification steps so that every drum meets both specification and customer expectations.
Some would imagine that an easy substitution is possible from one halogenated benzyl bromide to another, but at scale we find that changes in boiling point, vapor pressure, and thermal stability push processes to their limits. For 2-Fluoro-4-Chlorobenzyl Bromide, vigilance during the final isolation and drying steps prevents hydrolysis and unwanted rearrangement, a pitfall we have seen firsthand in rushed productions. When clients share feedback about performance on their lines, we take it straight back into adjustment plans, introducing tweaks to filtration or vacuum handling where even tiny improvements notch up total process reliability.
Over years of working with multi-step syntheses, we have tracked the impact of using alternative benzyl bromides, both in our plant trials and from stories relayed by chemists further down the value chain. For example, 2-Chlorobenzyl Bromide and 4-Fluorobenzyl Bromide look deceptively similar in catalogs, but they deliver different outcomes in reaction selectivity and yields. Bringing in both fluorine and chlorine into the right spots on the aromatic ring, as in 2-Fluoro-4-Chlorobenzyl Bromide, generates unique reactivity. In actual runs we’ve observed the dual halogen pattern can make significant differences in reaction rate or side-product formation under identical conditions.
Process development chemists come to us with reports from their benches. During nucleophilic substitution, for instance, the specific electron withdrawing effect from the ortho-fluorine in 2-Fluoro-4-Chlorobenzyl Bromide can promote a cleaner conversion and suppress rearrangements that plague other isomers. Years back, a major partner using a single-chlorine analog struggled with alkylation yield but saw a step change once we switched supply to our dual-halogen compound. Such real-world feedback has shaped our own internal standards for the compound, knowing that specifications have to go beyond appearance and nominal purity.
Pharmaceutical partners relying on this intermediate usually require not just assay results above 98% but tight controls on residual solvents, halide content, and specific absence of heavy metals. It is one thing to claim “pharmaceutical grade” but quite another to achieve lot releases that deliver this performance on every batch. We have gone through cycles with custom projects where impurities like unreacted benzyl alcohol or minor dibrominated products threatened to interfere in crucial late-stage reactions. Eliminating such byproducts doesn’t happen overnight; it has taken methodical optimization of phase separation, extractions, and finishing, so what lands in the customer’s vessel is exactly what belongs there.
Feedback from those on the receiving end highlights another crucial point—product shelf life and chemical stability. The bromide’s sensitivity toward moisture presents a challenge, especially for users in humid environments. Our production and packaging team drills in procedures to minimize air and water contact, and we keep tight track of inventory so our partners don’t receive product that has sat longer than chemically appropriate. We pack in high-spec containers with effective seals, reducing the chances of hydrolysis between our drum and our customer’s reactor.
Operating as a chemical manufacturer means living up to more than just technical numbers. The life science and specialty chemicals sectors have seen increasing regulation on halogenated organics, both on the supply and disposal ends. 2-Fluoro-4-Chlorobenzyl Bromide, like other benzyl bromides, carries regulatory oversight due to its use as an intermediate. Our experience tells us that compliance can never be a paperwork exercise only. Routine reviews of our effluent streams, careful handling of brominated waste, and adherence to shipping requirements help us support not just our customer’s performance, but their compliance programs as well.
Teams in our plant have found ways to reduce solvent waste and recapture byproducts from production. It took repeated investment and plenty of trial and error, but now when we recover and reprocess solvent, we cut both cost and downstream environmental impact, staying aligned with modern chemical stewardship. Customers that share our priorities around sustainability have told us these habits build trust—and it’s a trust grounded in small, practical techniques, not marketing words.
Manufacturing teams deal not only with product output, but with the practical troubleshooting that follows chemical sales. This isn’t just about answering questions—it means helping people solve unanticipated setup issues, compatibility concerns, or regulatory checks in their own facilities. We’ve learned to be frank with customers, especially when they run into unfamiliar results: a yellow tint in their product, separation issues, or an off-smell. Our own guidance draws from actual shop-floor scenarios. We walk them through analytic checks, solvent purging steps, or additional drying to restore the product’s characteristics.
Extension of this hands-on support to pragmatic training—safe handling procedures, storage recommendations grounded in lab-tested results, and pre-emptive identification of hazards—helps our partners keep their operations running smoothly. Where we see recurring concerns, such as questions about trace halide residuals, we adapt both our internal QC process and our training materials to fill the gap. Years in the plant have taught us that direct engagement builds both customer success and practical loyalty.
No manufacturer operates in a vacuum. Feedback from research chemists, process engineers, and purchasing agents all play into continuous improvement. We don’t shield our team from negative feedback; instead, those details become the core agenda at post-campaign reviews and process development meetings. We analyze batch records together, test alternative purification routes when feedback points to a stubborn impurity, and track which conditions—like drying, temperature profiles or filtration methods—directly impact the final product quality.
Collaboration on custom derivatives and tailored intermediates has pushed us to broaden both technique and scale. Pharmaceutical partners often ask for precisely defined impurity profiles or specific halogen content. It is rarely a matter of simply following textbook procedures. We have had to adjust everything from the ratios of starting materials to process integration with upstream or downstream steps, always keeping an eye on downstream customer needs and safety. Open lines of communication, from plant floor workers to technical directors, help keep these improvements flowing both ways.
With every batch we deliver, we see not just a product but a long series of choices, checks, and incremental improvements embedded in the drum. The market for benzyl bromide derivatives evolves constantly, driven by demand for smarter drug molecules, new materials, or simply more cost-effective production. Staying relevant means harnessing a mix of hard-earned experience, continuous technical training, and direct, sometimes tough, feedback from our partners.
In an era when end users expect more than chart-topping purity—looking for predictability in process scale-up, compatibility with green chemistry trends, or custom solutions to process bottlenecks—we stay close to real-world needs. By keeping both feet on the shop floor and one eye on the analytics bench, we can continue to offer 2-Fluoro-4-Chlorobenzyl Bromide produced with the balance of technical precision and practical experience that modern manufacturing now requires.