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HS Code |
446987 |
| Chemical Name | 2-Chloro-5-Fluorobenzyl Bromide |
| Cas Number | 57381-25-4 |
| Molecular Formula | C7H5BrClF |
| Molecular Weight | 223.47 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Boiling Point | 250-252°C (estimated) |
| Density | 1.62 g/cm³ (approximate) |
| Solubility | Soluble in organic solvents such as acetone, dichloromethane |
As an accredited 2-Chloro-5-Fluorobenzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, tightly sealed with tamper-evident cap and hazard labeling, shipped inside secondary protective packaging. |
| Shipping | 2-Chloro-5-Fluorobenzyl Bromide is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as hazardous and should be transported according to local, national, and international regulations. Shipping requires appropriate labeling, documentation, and handling by trained personnel to ensure safety and regulatory compliance. |
| Storage | Store 2-Chloro-5-Fluorobenzyl Bromide in a tightly sealed container, in a cool, dry, and well-ventilated place, away from direct sunlight and sources of heat or ignition. Keep separated from incompatible substances such as strong bases and oxidizers. Handle under an inert atmosphere if possible. Ensure proper labeling and restrict access to trained personnel. Use appropriate personal protective equipment when handling. |
Applications of 2-Chloro-5-Fluorobenzyl Bromide in Industrial ManufacturingAs an established manufacturer of 2-Chloro-5-Fluorobenzyl Bromide, we serve downstream industrial partners who demand material consistency, regulatory alignment, and well-documented integration into active chemical synthesis. Below, we detail actual applications supported by global clients, structured by specific sector demands, formulation practices, and compliance expectations. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers employ this intermediate in the synthesis of targeted APIs, particularly within fluorinated benzyl derivatives for central nervous system and oncology drug development. The material enters multi-step organohalide coupling processes, serving as a controlled reactant where halide selectivity and purity directly affect batch consistency. Chemical engineers maintain defined stoichiometry relative to substrate structure, especially when working under cGMP conditions for regulated entities. Industry compliance standards
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2. Agrochemical Active Ingredient PrecursorAgrochemical formulators utilize this compound in the creation of selective herbicide and fungicide intermediates, leveraging the electron-withdrawing profile for targeted biocidal activity. Its introduction supports scalable synthesis, where batch consistency and regulatory traceability remain critical under global agricultural standards. Industry compliance standards
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3. Specialty Chemicals for Electronic Materials SynthesisManufacturers of electronic and liquid crystal materials leverage this compound as a functional benzyl source for OLED intermediates and advanced display technologies. The precise halogen positioning enables integration into complex aromatic frameworks, essential for electronic performance—requiring high purity and batch-to-batch trace records to satisfy supply-chain audits. Industry compliance standards
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4. Fine Chemicals for Dye and Pigment SynthesisProducers formulate high-performance dyes and pigments by incorporating this aromatic halide in key substitution reactions, which impart lightfastness or specialized optical properties. The molecular design supports downstream application in automotive coatings, plastics coloration, and high-stability ink production where consistency in hue and dispersion must be validated by QC analysis per batch. Industry compliance standards
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5. Intermediate for Synthesis of Advanced PolymersPolymer research and manufacturing sectors incorporate this fluorinated benzyl halide while creating specialty copolymers, particularly where thermal and chemical resistance profiles are required, such as in membranes and engineering plastics. Formulation specialists employ rigorous mass-balance checks to ensure monomer conversion rates align with end-use performance targets and safety documentation under local market regulations. Industry compliance standards
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Working in chemical manufacturing, I’ve spent my share of hours fine-tuning intermediates like 2-Chloro-5-Fluorobenzyl Bromide for use on the production floor and in the lab. This compound’s structure—a benzene ring carrying both chloro and fluoro substitutions and capped with a reactive bromomethyl group—may look simple in a line formula, but each batch has a story built from raw materials, reaction tracking, and hands-on quality evaluation. Reliability matters, and for 2-Chloro-5-Fluorobenzyl Bromide, there’s no shortcut when purity and solid consistency drive the work downstream.
Chemists in pharmaceutical R&D often rely on halogenated benzyl building blocks. The pairing of chlorine and fluorine on the benzene ring impacts how the molecule binds and survives in synthetic steps. The extra electron-withdrawing fluorine at position five shifts the ring’s reactivity in ways you can only appreciate at the bench. One can switch between different halogen patterns, but the (2-chloro, 5-fluoro) setup has gained favor because it tunes both steric and electronic influences perfectly for selective transformations.
In our plant, we often see requests for derivatives featuring only fluorine or chlorine, but the dual substitution of 2-Chloro-5-Fluorobenzyl Bromide brings fresh options to experienced medicinal chemists. By introducing both halogens, the benzyl bromide reacts cleaner in certain nucleophilic substitutions and forms carbon-carbon or carbon-heteroatom bonds more predictably. It also makes installing subsequent groups onto the aromatic ring more straightforward, saving hours on purification and rework.
Purity counts. In my early days on the production team, I quickly learned that a contaminated intermediate can wreck the efficiency of an entire downstream synthesis. For 2-Chloro-5-Fluorobenzyl Bromide, we source starting materials with closely monitored impurity profiles. Careful fractional distillation helps us keep byproducts like dibromides, benzyl alcohols, or unreacted precursors out of the drum. I’ve seen batches checked by NMR and GC-MS after subtle changes in reaction conditions, because one overlooked spike in the chromatogram could spell a problem for a customer’s next coupling reaction.
In our process, controlling moisture is more than a matter of protocol. Even trace water speeds up hydrolysis, converting benzyl bromides to benzyl alcohols, and leaves behind a mess that strains purification efforts. We run on rigor—dried glassware, nitrogen blankets, and prompt bottling of the finished product. Each batch typically passes strict benchmarks for GC purity, and verification by an independent team ensures our published numbers aren’t just theoretical.
The main stage for this compound lies in pharmaceutical and agricultural research. Customers come to us when their synthetic strategies hit bottlenecks that other benzyl halides can’t solve. As a versatile benzylating reagent, 2-Chloro-5-Fluorobenzyl Bromide excels in alkylation steps for heterocycles and protected amines, oxygen, or sulfur nucleophiles. The choice of the (2-chloro-5-fluoro) motif often brings greater selectivity in these transformations, which keeps the workflow clean, especially when costly intermediates are on the line.
Pharmaceutical process chemists tell us they prefer this compound for late-stage functionalizations, especially when working with complex molecules sensitive to over-reactivity or decomposition. The dual halogen pattern can slow down undesired side reactions, making purification simpler. In synthesis of advanced intermediates for central nervous system drugs or agrochemicals, small details like this make large-scale runs more predictable.
Handling larger production volumes—ranging from bench-scale grams all the way to multi-kilogram batches—calls for established protocols. Over the years, we’ve optimized conditions using solvents like toluene, acetonitrile, or ether, balancing solubility and reactivity while considering safety controls. Implementing in-line monitoring with spectrophotometry or HPLC allows us to spot off-spec results before the batch reaches the bottling line.
We receive requests not just from medicinal chemistry groups but also from agrochemical researchers and specialty polymer labs. A customer once shared that switching to our 2-Chloro-5-Fluorobenzyl Bromide shortened their campaign by several weeks, after fighting with a stubbornly unreactive precursor. They discovered that the unique halogen arrangement improved their target yield, and the downstream purification ran smoother. Not every intermediate delivers such savings, but when a building block works at this level, the value becomes tangible across industries.
Some labs might reach for alternative benzyl bromides—such as 4-chlorobenzyl or 2-fluorobenzyl analogs—aiming to save on costs or because they have supplies on hand. After projects run their course, teams often circle back to us, seeking a more reliable end product without the byproducts or inconsistent reactivity that plagued their earlier runs. Subtle differences in halogen placement really do compound in scale; not every benzyl bromide fills the same synthetic role.
Making chemicals for real-world use always tests both the process and the people behind it. For 2-Chloro-5-Fluorobenzyl Bromide, standard specifications tell only half the story; the practical side shows in how smoothly a batch goes through downstream steps. Inconsistent material can choke an entire project. Our team puts experience at the center of every production run, troubleshooting reaction temperatures, mixing speeds, or isolation times not just by following a checklist but by working in tandem with the analytical team and relying on seasoned instincts to read the batch at every stage.
We have seen how small deviations—from solvent residue to trace metal contamination—can turn a seemingly routine batch into a headache. Deciding when to rerun a work-up or strip a distillation again falls to the judgment of a crew that has felt the consequences of shortcuts. Sharing technical reports with clients, talking through specific application profiles, and responding to feedback become part of the cycle in getting each lot right.
Chemistry never stands still, and neither does our process. Over several years, recurring challenges sparked incremental changes. Swapping out outdated batch reactors for new glass-lined units helped us control local hot spots and trimmed the formation of side products. Regular solvent quality checks cut down unplanned variability. Tracking batch history—including yield fluctuations and impurity levels—built up baselines that guide decisions on scaling up or troubleshooting.
Responding to environmental requirements, we’ve phased out certain reagents and found ways to limit waste from bromination steps. These changes reflect input from both the plant staff and our customers, who appreciate both greener process choices and the improved reliability this brings. We continue to share updates on these improvements with our users—even mid-project—because open communication leads to smoother collaboration and better outcomes.
A manufacturer’s role doesn't end at shipment. Feedback from analytical labs or pilot plant chemists has brought important changes, from improved drum liners that shield the compound from air and humidity to better inner packing that prevents caking over months in storage. Pharmacists in scale-up trials taught us the limits of bulk handling—how our product behaves across different climates and over various timeframes. We watched a customer adjust their quenching chemistry to incorporate lower water activity, after a batch showed minor hydrolysis due to unexpected shipping delays in the humid season. That feedback triggered updates in our packaging and notification process for shipping windows subject to weather swings.
Sometimes the difference between materials from a trader and those from a true manufacturer comes down to details invisible on a certificate of analysis. Consistency, transparency, and accountability underpin not just the chemical profile, but how users experience the intermediate in their workflows. We stand by the batches we make because we see our product perform in the field, not just through our own analytics but through the tangible successes—and the challenges—reported by those who put their trust, and money, on the line.
The past several years have reminded us that strong partnerships between the makers and users of specialty intermediates improve not only individual projects, but also industry standards overall. 2-Chloro-5-Fluorobenzyl Bromide has made its mark by showing that carefully optimized halogen substitution on the benzene ring can transform a difficult synthetic step into a routine operation. That requires disciplined manufacturing and honest, continuous dialogue between chemists, engineers, and the people executing R&D across markets.
We often field calls not just for product orders but for technical guidance: advice on optimal solvents and reaction conditions, tips for minimizing hydrolysis during work-up, and troubleshooting unexpected reaction behavior. Our technical team shares lessons learned from thousands of kilograms of production experience—sometimes resolving issues before a pilot run ever initiates. Years of firsthand engagement shape our risk assessments for handling, storage, and shipping. We match our production procedures to the range of customers’ needs, always focusing on predictable quality for demanding applications.
Where 2-Chloro-5-Fluorobenzyl Bromide really delivers value is in tough synthetic campaigns that depend on clean, consistent material. Colleagues running batch or flow processes need benzylating reagents that don’t introduce unwanted surprises—no unpredictable reactivity or decomposition issues. A medicinal chemistry team scaling a promising lead series wants to avoid headaches with byproducts or batch-to-batch drift. Our plant team knows that hits a company’s project timeline and bottom line just as much as the purchase price per kilo.
Consistent quality not only helps avoid costly rework, but also ensures strict documentation and traceability requirements in regulated industries are met. Our quality systems and detailed batch records support audits by pharmaceutical partners, and feedback from on-site inspections continues to refine our operational protocols. Customers report fewer failed runs and smoother analytical checks when they rely on a controlled supply chain, where anything out of spec can be traced and addressed directly and quickly.
There’s a reason specialist labs keep returning to the well-established 2-Chloro-5-Fluorobenzyl Bromide structure. Other benzyl halides—such as 3-fluorobenzyl or 4-chlorobenzyl analogs—fill certain roles, but just don’t deliver the same nuanced electronic profile. The presence of both electron-withdrawing groups at key positions shifts reactivity, promoting controlled substitutions in complex substrates and cutting back on side reactions. The difference often turns up in higher yields, cleaner product profiles, and easier purifications—outcomes that matter after months of project investment.
We have tested many analogs side by side in our analytical labs and in pilot partners' hands. While some compounds might seem interchangeable on paper, in demanding runs—such as multi-step API syntheses—only the (2-chloro, 5-fluoro) motif delivers the selectivity and yield profile process teams need. Whether that means a sharper endpoint in the alkylation of heterocycles or reducing product loss when isolating late-stage intermediates, attention to the specific structure pays dividends.
As a team with decades of combined experience, we know why reliability in intermediate production matters. Each batch of 2-Chloro-5-Fluorobenzyl Bromide reflects lessons drawn from countless campaigns: every successful kilogram testifies to careful sourcing, deliberate process control, and honest feedback from users. We keep improving—incorporating updated safety and sustainability protocols, refining reactions and extraction techniques, even redesigning packing in response to what our partners tell us.
Our technical support connects with small research groups and major pharmaceutical teams alike, sharing practical insights for both routine and challenging transformations. Beyond transactional supply, we see our work as part of a broader commitment to innovation and trust—because in chemical manufacturing, the details that don’t show up on a spec sheet are the ones that sustain real progress in the lab and marketplace.
From early-morning reaction setups to late-night troubleshooting sessions, our experience with 2-Chloro-5-Fluorobenzyl Bromide underscores what matters most in the fine chemicals business: trusted relationships, unyielding standards, and adaptive problem-solving. Whether supporting a pharmaceutical launch, an agrochemical breakthrough, or a polymer innovation, our commitment means the compound you receive supports your process, rather than complicates it. With each bottle shipped, we’re building more than supply chains—we’re extending a partnership based on experience, earned trust, and proven outcomes.