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HS Code |
810361 |
| Productname | 4-Bromo-2-Fluorobenzyl Chloride |
| Casnumber | 1209198-79-3 |
| Molecularformula | C7H5BrClF |
| Molecularweight | 223.47 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically >97% |
| Density | Approx. 1.6 g/cm³ |
| Solubility | Soluble in organic solvents such as dichloromethane and ether |
| Synonyms | α-Chloromethyl-4-bromo-2-fluorobenzene |
| Storagetemperature | Store at 2-8°C, in a tightly closed container |
| Smiles | ClCc1cc(Br)ccc1F |
| Hazardclass | Corrosive, irritant |
As an accredited 4-Bromo-2-Fluorobenzyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 grams of 4-Bromo-2-Fluorobenzyl Chloride is supplied in a sealed amber glass bottle with tamper-evident screw cap. |
| Shipping | 4-Bromo-2-Fluorobenzyl Chloride is shipped in tightly sealed, corrosion-resistant containers under cool, dry conditions. It is classified as a hazardous material and should be handled according to regulatory guidelines. All packages are clearly labeled, and transport follows safety protocols to prevent leaks, breakage, or exposure during transit. |
| Storage | 4-Bromo-2-Fluorobenzyl Chloride should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong bases and oxidizing agents. Keep the container tightly closed and protected from light and moisture. Store in a tightly sealed glass or compatible container, and label properly to prevent accidental misuse or contamination. |
Applications of 4-Bromo-2-Fluorobenzyl Chloride in Industrial ManufacturingAs a direct manufacturer, we supply 4-Bromo-2-Fluorobenzyl Chloride to multiple downstream sectors where high-purity substituted benzyl chlorides are required in advanced synthesis. The following sections detail verified end-user applications, real-world regulatory compliance, standard blending ratios, downstream production stages, and marketable finished goods produced with this material. Each application scenario reflects genuine industrial practices based on cooperative process feedback from leading customers. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis4-Bromo-2-Fluorobenzyl Chloride commonly enters multi-stage pharmaceutical syntheses as an electrophilic building block for the preparation of fluorinated aromatic APIs, especially in the synthesis of central nervous system (CNS) drug candidates. Manufacturers react it with protected amines or heterocyclic systems under controlled, validated conditions to form structurally advanced intermediates. Production occurs in GMP-compliant facilities using validated cleaning and changeover protocols to prevent cross-contamination and ensure traceability for regulatory audit readiness. Industry compliance standards
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2. Agrochemical Synthesis for Pre-Emergence HerbicidesThe unique reactivity of 4-Bromo-2-Fluorobenzyl Chloride enables agrochemical formulators to prepare high-value fluorinated herbicide actives that demand precise aromatic substitution patterns for crop selectivity and environmental stability. The compound participates in alkylation steps during multi-stage syntheses of agrochemical intermediates, with stringent limits on impurities and batch-to-batch reproducibility documented for global registrations. Industry compliance standards
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3. Specialty Monomer for High-Performance Polymer MaterialsIn advanced polymer chemistry, 4-Bromo-2-Fluorobenzyl Chloride serves as a specialty comonomer for producing fluorinated aromatic resins and network polymers used in electronics, aerospace, and defense. The controlled introduction of bromo- and fluoro-substituted benzyl units allows manufacturers to fine-tune polymer properties, including dielectric strength and moisture uptake, while maintaining strict control over polymerization kinetics and batch homogeneity. Industry compliance standards
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4. Fine Chemical Synthesis for Custom Intermediates and LigandsContract fine chemical producers rely on 4-Bromo-2-Fluorobenzyl Chloride for synthesizing tailored aromatic intermediates and ligands that require rigorous customization for catalysis research, dye chemistry, and chemical probe development. The compound reacts under controlled conditions with organometallic nucleophiles or metal-catalyzed systems, with detailed records maintained for traceability and audit support. Industry compliance standards
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In our daily work, we handle a wide range of fine chemicals, and 4-Bromo-2-Fluorobenzyl Chloride stands out among substituted benzyl chlorides for its versatile reactivity and value in downstream synthesis. Manufacturing this compound requires careful selection of raw materials and tight control over every reaction step, not just for regulatory compliance, but to eliminate unwanted byproducts. Each batch runs through a multistep operation where purity demands constant attention, particularly at the stages involving halogen exchange and chloromethylation. We monitor reaction kinetics in real time. From choosing batch sizes to adjusting solvent ratios, we know from direct experience that slight shifts in process parameters can influence overall product yield and impurity profiles.
Our operating line has matured to produce consistent purity above 98%, with residual 2-fluorobenzyl species below 0.5%. This helps customers run downstream reactions with fewer purification headaches. We sample intermediates during each batch run, analyzing with GC and NMR to confirm that only the right substitution patterns make it through. This hands-on testing roots out common impurities like multi-halogenated derivatives. It’s tempting to cut corners and skip labor-intensive steps, but customers in pharmaceutical synthesis or crop science expect material that holds up every time, batch after batch. This means devoting real time to filtration, drying, and final analysis, not just doing it once per week for the paperwork.
4-Bromo-2-Fluorobenzyl Chloride comes off our reactor as a colorless to pale yellow liquid, carrying a sharp, distinctive odor characteristic of halobenzylic compounds. This material melts below room temperature, and volatilizes easily above 100°C. Its molecular weight sits at 223.48 g/mol, with a benzyl chloride functional group that makes it a prime alkylating agent for chemists targeting fluorinated and brominated aromatic systems. We track and document every lot, so the structure and substitution pattern never leaves room for misidentification. This traceability doesn’t just tick boxes for GMP or ISO audits. Chemists in our customer’s labs rely on this data to reliably predict reaction outcomes every time they attach this benzyl fragment to a new scaffold.
Compared to standard benzyl chloride, the presence of two different halogens at the 2- and 4- positions transforms both the electronic and steric environment of the molecule. The electron-withdrawing fluorine para-orients further substitution, and the bromo group imparts unique reactivity for palladium or copper-mediated coupling, but also affects the physical handling properties. We regularly hear from customers who’ve tried sourcing similar compounds elsewhere, only to discover trace halide isomers or diminished stability after storage. Meticulous fractionation after chloromethylation preserves the single product, with minimal overlap from isomeric impurities.
Pharmaceutical research often calls for building blocks that can be rapidly diversified. 4-Bromo-2-Fluorobenzyl Chloride delivers a benzyl fragment that incorporates both bromine and fluorine, prized for introducing metabolic stability and distinct bioactivity. Our largest customers use this compound as an intermediate in synthesizing kinase inhibitors and CNS-active compounds. Medicinal chemists count on the strong C-F bond to resist biotransformation in vivo, while the para-bromo position offers a reliable handle for Suzuki, Stille, or Ullmann-type cross-coupling. The chloromethyl group reacts cleanly with a range of nucleophiles — amines, thiols, and oxygen nucleophiles — to rapidly build out analog series in drug development.
Pesticide and herbicide research benefits from the same structural motifs. The bromo and fluoro groups shift biological activity, improve leaf adherence, and delay environmental breakdown. Field researchers give us feedback on how subtle shifts in substitution can alter uptake and selectivity. Our product's reliable substitution positions — never a mix of ortho/meta isomers — help avoid wasted time screening unpredictable analogs. We work directly with both R&D chemists and those overseeing scale-up to pilot lots, making sure that from vial to bulk drum, there’s no mystery about what was delivered.
In the world of halogenated benzyl chlorides, small differences translate into significant changes for synthetic utility. Pure benzyl chloride remains widely used for quaternary ammonium surfactants, but the electron-rich ring and unadorned side chain produce different reactivity profiles compared to our 4-Bromo-2-Fluoro analog. Introducing either fluorine or bromine alone changes product outcome and metabolic resistance, yet using both together creates unique opportunities for medicinal and materials chemistry. The dual substitution modulates chemical polarity, lowers lipophilicity, and delays enzymatic breakdown; simple mono-halogenated analogs can’t match this effect.
Through head-to-head testing, we’ve noticed that many competing products, often sourced from third-party vendors or repackers, contain minor isomers, incomplete chlorination, or elevated residual solvents. Shortcuts in the chloromethylation step lead to persistent levels of 2-fluorobenzyl alcohol or over-substitution on the arene core, which disrupts downstream chemistry or contaminates final products. Our clients report improved reaction selectivity and fewer chromatographic purification cycles after switching to our direct-manufactured material. Rigorous in-process monitoring ensures no surprises in stability, crystallinity (for those who solidify at lower storage temp), or reactivity.
Producing and handling halogenated agents never comes without challenges for safety and emissions control. 4-Bromo-2-Fluorobenzyl Chloride, like its analogs, merits robust containment and engineered ventilation. We long ago invested in packed bed scrubbers and multi-stage offgas capture, converting waste halide streams to benign forms before release. Residual chlorinated waste is segregated and shipped for accredited hazardous disposal; nothing leaves the plant untreated. Our workforce trains regularly on liquid handling, splash, and inhalation risk, with emphasis on fail-safe transfer processes and routine leak detection. Routine monitoring and proactive equipment maintenance keeps occupational exposure below the most stringent allowed levels.
Every decision, from raw material sourcing to packaging, traces back to real-world impact. We use high-density polyethylene drums with double seals, resistant to halogenated solvent creep. All labels track batch histories and QC approval. This deep attention to leak protection and regulatory readiness flows from hard lessons in plant operations, not just theory or textbook recommendations. We designed our facility to hold and decant with minimum open transfer, removing worker risk from valve failures or drum stack accidents. No product moves downstream without signed-off environmental and safety risk reviews. We know the long-term reputation of any specialty chemical manufacturer lives and dies on visible commitment to safety and transparency.
We don’t stop at meeting minimum specifications or regulatory cutoffs. Every customer conversation or technical complaint feeds back into how we operate on the shop floor. When a customer reports crystallization during shipping, we review every solvent batch and packaging routine until the root cause becomes clear. If we notice trace unstable byproducts at scale, we tweak the reactor parameters, not just batch documentation. Our chemists compare synthetic alternatives — from photochlorination conditions to alternative halogen sources — so that subtle improvements in product consistency or yield eventually show up on every delivery ticket.
Location-specific regulations for transport and handling can present hurdles, especially for international shipments. Working from the manufacturer’s side, we’ve streamlined paperwork, temperature logs, and lot-release documentation so our product moves swiftly through customs, even for air shipments or regulated exports. Volume customers and early-stage research groups alike get access to technical data, not just off-the-shelf SDS sheets. We encourage dialogue about formulation needs, alternative grades, or custom pack sizes, based on real process demands, not theoretical case studies.
Handling reactive halogenated compounds isn’t just about gloves and goggles. Over the years, we’ve adopted segmented process lines, automated dosing, and closed transfer systems after seeing the real-world spill and exposure risks from open-batch handling in small shops. High vapor pressure means even slow leaks can degrade air quality, so we use active ventilation, rapid leak detection tags, and positive pressure loading halts. These measures stem from actual incidents and on-site risk audits, not generic warnings.
Our support doesn’t end at the loading dock. Customers who request guidance on storage and shelf life receive honest data on degradation rates and compatible plastics. We confirm our liquid stays stable at standard laboratory temperatures and recommend cold storage for long-term reserves. If we notice color shift or off-odor in returned containers, we verify whether higher temperatures or improper venting caused breakdown, then adapt our recommendations. The advice we offer comes from hundreds of actual field events, not canned responses or product inserts.
Growth in complex molecule synthesis and the demand for more selective and efficient molecular fragments keeps increasing. We supply 4-Bromo-2-Fluorobenzyl Chloride in response to real requests for difficult structures. It isn’t a molecule with universal demand, yet for targeted research in fluorinated frameworks, it saves weeks of synthetic time. Researchers building novel pharmaceuticals or crop protection agents leverage the compound’s distinct profile. Our job as a manufacturer isn’t just to ensure purity, but to deliver the same structure lot after lot, without drift in isomeric content or new impurities creeping up.
Volume flexibility matters. Some customers—working in discovery chemistry—only need 20 or 50 grams per project; others run kilo-scale trials on pilot lines. We accommodate both, producing to order and holding safety stock for urgent demands. Fielding requests for alternative grades — such as ultra-low water or residue content — has pushed us to refine drying steps, improve drum sealing, or investigate custom filtration media. Demand forecasts help prevent shortages or outdated lots, ensuring the material reaches each lab still in top condition.
Our team has learned that the utility of a specialty intermediate rarely comes down to a single number on a spec sheet. Four decimal point purity won’t help if the byproduct profile isn’t known, or if the flask-to-barrel consistency sags from lot to lot. We stress-test each process stage because chemistry at the research bench doesn’t forgive shortcutting upstream steps. Feedback from clients clarifies which parameters make a difference; we document and communicate even subtle shifts, such as slight tints or odor changes, rather than pretending variability doesn’t exist.
Precision in substitution patterns underpins why fixed-halo benzyl chlorides keep outperforming more generic analogs in advanced synthesis. Chemists who’ve wasted time purifying off-target isomers or tracing unknown NMR peaks appreciate that our product answers deeper questions about structure and performance. This trust grows from years spent scaling up and refining the manufacturing process, constantly learning from outcomes as much as from initial intentions.
4-Bromo-2-Fluorobenzyl Chloride continues to unlock new synthetic routes and molecular scaffolds. As the field shifts toward more heavily substituted and polar intermediates, experience in control of multi-step halogenation and precise benzylation only grows in value. Our ongoing investment in plant safety, analytical support, and customer-driven process improvements means researchers can count on the material as a stable, transparent part of their workflow. Each delivery reflects the real work done behind the scenes—quality control, operator training, and honest communication about risks and solutions. While others may push flashy marketing or generic purity guarantees, we focus on the fundamentals: secure, consistent supply backed by people who know the molecule, the risks, and the true requirements from years in the industry.