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HS Code |
898003 |
| Product Name | 3,5-Difluorobenzyl Bromide |
| Cas Number | 85118-59-6 |
| Molecular Formula | C7H5BrF2 |
| Molecular Weight | 207.02 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 75-77°C at 12 mmHg |
| Density | 1.615 g/mL at 25°C |
| Refractive Index | n20/D 1.528 |
| Purity | Typically ≥98% |
| Smiles | C1=C(C=C(C=C1F)F)CBr |
| Solubility | Insoluble in water; soluble in organic solvents |
| Storage Temperature | Store at 2-8°C |
| Synonyms | α-Bromo-3,5-difluorotoluene |
| Hazard Class | Irritant |
As an accredited 3,5-Difluorobenzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 10g amber glass bottle with a tightly sealed cap, labeled "3,5-Difluorobenzyl Bromide" and hazard information printed. |
| Shipping | 3,5-Difluorobenzyl Bromide is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transportation complies with regulations for hazardous organic chemicals, typically via ground or air freight with appropriate hazard labeling. Ensure container integrity during transit and handle according to material safety data sheet (MSDS) precautions. |
| Storage | 3,5-Difluorobenzyl Bromide should be stored in a cool, dry, and well-ventilated area, tightly sealed in a corrosion-resistant container. Protect it from moisture, direct sunlight, heat, and incompatible materials such as strong acids or bases. Store under inert atmosphere if possible. Clearly label the container and keep it away from sources of ignition and substances that could cause decomposition. |
Applications of 3,5-Difluorobenzyl Bromide in Industrial ManufacturingWe manufacture 3,5-Difluorobenzyl Bromide (DFBB) to supply key intermediate needs in the pharmaceutical, agrochemical, specialty polymer, and performance coatings sectors. The following sections detail actual industrial use cases, addressing applicable regulations, integration methods, usage ranges, and reference end products for each specific application track. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient SynthesisOur customers commonly use DFBB as an alkylating agent to introduce the 3,5-difluorobenzyl moiety in the synthesis of several small molecule drug candidates and commercial APIs such as selective serotonin reuptake inhibitors (SSRIs) and antifungal agents. The bromide group enables efficient nucleophilic substitution reactions with piperazine, triazole, or imidazole derivatives in multi-step API routes. This intermediate enters downstream GMP production facilities under stringent quality management, with rigorous impurity and residual solvent testing at every batch. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis—Herbicide and Fungicide IntermediatesAgrochemical producers frequently use DFBB to build fluorinated aromatic scaffolds required for next-generation fungicides and herbicides. The presence of two fluorine atoms at the meta positions modifies metabolic stability and activity spectra. DFBB acts as the key benzylation reagent in heterocycle alkylation, especially for triazole and pyrazole based agrochemicals. The integration point depends on the downstream target but always follows industry traceability and environmental standards for hazardous intermediates. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Polymeric Materials—Crosslinkers and ModifiersProducers of specialty polymers use DFBB to introduce difluorobenzyl motifs into epoxy, polyurethane, and high-performance polyamide resins. It functions as a structural modifier that imparts enhanced hydrophobicity, chemical resistance, and thermal properties. The reaction typically involves nucleophilic substitution onto pre-formed polymer backbones or as a comonomer during polymerization. All handling and formulation comply with industrial chemical substance regulations relevant to advanced materials sectors. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Performance Coatings—Specialized Surface ModifiersManufacturers of industrial and architectural coatings apply DFBB as a surface-active additive, especially in fluoropolymer topcoats. The difluorobenzyl fragment introduces low surface energy and hydrocarbon/fluorocarbon compatibility, improving weather resistance and anti-soil properties in specialty coatings. The intermediate is dosed at well-defined stages, and stringent procurement documentation ensures traceability under regulatory and customer QC demand within the coatings supply chain. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Standing on the production line, the unmistakable aromatic notes of fluorinated benzyl compounds announce that we are running a batch of 3,5-Difluorobenzyl Bromide. We’ve been operating reactors with this molecule for years and worked through plenty of practical challenges that material scientists, pharmaceutical teams, and specialty chemical developers send our way. In the business of halogenated building blocks, reliability and clear differences make the job interesting, especially when customers bring projects where selectivity, reactivity, and purity determine success or failure.
Through hundreds of scale-ups, we have locked our model on clarity: 3,5-Difluorobenzyl Bromide with CAS number 85118-00-9, molecular formula C7H5BrF2. We keep our own standards above industry averages, not from a marketing push, but because experienced researchers and process engineers on both sides have told us where material inconsistencies threaten downstream reactions. Purity is not a theoretical number out of a catalog. You can feel it in how our product dissolves, distills, and reacts. Typical GC purity reads over 98% by area, and we guard against common side products like difluorotoluene or dibrominated residues that have no role in planned syntheses but make trouble in real reactors. Every batch rolls out after thorough GC-MS, NMR, and moisture checks.
Those who order halogenated benzyl compounds often ask about differences between isomers, such as how 2,4-difluorobenzyl bromide behaves, or whether a simple monofluoro version does the job. Sitting in a manufacturing plant, learning from both plant engineers and benches at customers’ sites, reveals why 3,5-difluorobenzyl bromide deserves its own focus. The 3,5-positions on the ring produce a product less prone to side substitutions on adjacent carbons, which proves essential when building up pharmaceutical intermediates or specialty polymers. Some routes depend on this selectivity to control downstream halogenation or introduce other functional groups. Isomeric variants often push yields down or create tangled purification routines. Some newer chemistries in crop sciences and electronics flourish only because of the unique substitution pattern and reactivity this molecule offers.
Having dealt directly with feedback loops from organic synthesis teams, I’ve come to appreciate why cost-per-gram numbers miss the mark if purity swings or isomer content isn’t right. A minor impurity in a halide may seem harmless at first but becomes a headache as it sneaks through costly purification columns or slows catalyst cycles. Over months, the cumulative effect eats up hours, solvents, and budget. Over the years, I’ve watched buyers return to our material after chasing price around the world and coming up short when it comes time to scale up.
I’ve seen requests from pharmaceutical developers who rely on this compound as an intermediate for layered synthesis steps. In R&D discussions, chemists explain that substituent location and bromine activation serve as pivotal control points for ring-opening and nucleophilic substitution. Some use our compound to create difluorinated phenethylamines or ring systems that later form anticancer candidates or CNS-active molecules. If monofluorinated analogs are used, their side reactions complicate process validation, not to mention impurity concerns at regulatory submission time.
Polymers researchers have brought up unique traits enabled only through 3,5-difluorination, including improved thermal and chemical resistance, and lower dielectric constants in final materials. In electronic films or coatings, a balance between halogen content and reactivity influences stability and performance at nanoscale thickness. There’s no single shortcut — skipping to a less substituted benzyl bromide won’t sustain the desired profile. Other customers, especially those in fine chemistry or agrochemical areas, favor this material’s ability to introduce dual fluorines cleanly before further derivatization, which helps with selective downstream activation and increases yields with less aggressive conditions.
Producing 3,5-difluorobenzyl bromide isn't just a matter of having the right reactors and chillers. We started in small lots, refining bromination conditions and solvent selections to limit unwanted isomers and side reactions. Colleagues learned early that even minor variations in temperature or bromine addition rates would flip the selectivity, generating more waste and lowering yields. Process analytical technology now lets us steer the reaction in real time, ensuring tight impurity profiles. Every operator here carries the legacy of these experiments — today’s smooth batches only happen because earlier ones flagged which parameters control quality.
Product consistency does not only depend on what comes out of the reactor. Drying and packaging pose their own risks, enough that we overhauled our post-reaction treatment. Moisture or traces of mineral acid leftover from workup alter long-term storage stability. Handling crystalline solids and viscous residues requires discipline and documentation: one incorrect valve setting can introduce contamination, so operators check and cross-check at every hand-off. After seeing how a rushed bulk transfer compromised product stability in a customer’s pilot, we tripled our packaging inspection steps. This attention isn’t about box-ticking; it’s about respecting how much a single batch means to end-users with complex synthesis plans.
Comparing 3,5-difluorobenzyl bromide to more common benzyl bromide variants delivers ample lessons. Basic benzyl bromide lacks the electron-withdrawing effect that fluorines bring, so it won’t match the same reactivity or stability. Isomers like 2,4-difluorobenzyl bromide behave differently in coupling reactions, sometimes pushing unwanted rearrangements due to altered electron density or steric effects. We’ve fielded requests to swap in less fluorinated versions to save cost, and most trials result in repeat business with our 3,5-substituted material once chemists see diminished yields or unexpected color and odor in their target molecules.
Another angle comes from the environmental and safety side. Adding fluorines at the right positions can enhance product shelf life and process efficiency, which means less waste generated on both ends. In contrast, using versions with less selectivity often increases purification steps, solvent volumes, and energy needs. Over time, factories and labs recognize the value in predictability — nobody wants a surprise by-product in a critical medicinal chemistry campaign or specialty monomer production. Having walked plant floors with R&D visitors, I’ve seen firsthand how our 3,5-difluorobenzyl bromide cuts troubleshooting and lets professionals focus on bigger questions instead of cleaning up after a tricky reagent.
Most purchase orders give little insight into the real battle chemists and engineers face downstream. We invite researchers and process development scientists into our plant to talk about their actual problems. Some request custom packaging to better match glovebox acceptance or reduce product loss. Others seek insight on how our drying protocols affect moisture-sensitive downstream reactions. We’ve adjusted our production schedule to meet peaks in demand — particularly before regulatory windows or new patent filings.
Facing real-world setbacks together bridges the gap from manufacturer to partner. There was an occasion when a pharma scale-up ran into trouble — not because our product failed spec, but because their process wasn’t dialed for this level of fluorination. It took a few rounds of phone calls, tech exchanges, and careful logistics to get everyone past the setback, and since then collaboration has only grown. Stories like this remind me that we’re not just delivering molecules; we’re helping professionals bring next-generation medicines and materials to market.
3,5-Difluorobenzyl bromide’s value isn’t just in its reaction profile. Handling halogenated organics demands proper safety training and responsible stewardship — which we take seriously on the ground. Management backs regular hazmat drills and expects engineers in lab coats as much as they expect operators at the controls. We log every material transfer, monitor for fugitive emissions, and run exhaust treatment as standard practice, not just as regulatory compliance. We’ve also developed container systems to minimize exposure and enable safe opening in both dockside and cleanroom settings, based on customer feedback.
Regulatory teams inspecting our site dig into batch records, storage logs, and shipment trails. We keep these records complete and ready for all key jurisdictions, including US, EU, and major Asian standards. On more than one occasion, we’ve worked alongside a customer to create collaborative traceability files for complete chain-of-custody evidence — a practical service for those aiming their finished products at FDA, EMA, or REACH submissions. Customers ask specific questions about fluorine sourcing and bromination route: we provide origin documents for raw materials and guarantee non-conflict sourcing for key reagents.
Every conversation with end users, every audit from a multinational, every technical mishap, strengthens our plant’s understanding and ability to improve. We don’t just tinker with batch size and equipment; we also invest in the people who commit to running reactors through the night or catching typos in QC sheets. Staff who started in the packing area have moved into R&D — they bring practical experience about why packaging failures occur, which helps us make better decisions during scale-up.
Long before a brochure exists, our engineers run real trials, answer technical requests with specifics, and stand accountable in case of a recall or product change. When a customer says their synthesis line halted mid-campaign because of unexpected byproducts, we put in overtime until their line moves again, not because a contract demands it, but because both our names travel together on reports up the chain. I've seen operators bring solution samples to my desk when something “looks off,” well before data says so, and catching a near-miss in time. That care ripples through every shipment we send.
Supply chain resilience became more than a buzzword these last few years. Shipments delayed by port backups or raw material shortages test both our patience and our planning skills. One thing our teams have learned: customers buy from us not for speculative price swings or clever marketing, but for the promise that their production will run on time. We keep extra inventory in validated conditions, not to drive up costs, but to back up projects that can’t afford gaps in supply.
Partners have called late at night seeking rush orders when a process runs longer than expected. Fulfilling those orders comes down to the reliability of our own upstream partners, careful documentation, and respect for the urgency of others’ work. Sometimes, that means pivoting equipment schedules at odd hours, or chartering dedicated shipments. We treat every shipment — from hundred-gram research lots to multi-tonne commercial quantities — with the attention we expect from the vendors we trust ourselves.
Halogenated intermediates have drawn plenty of attention for environmental persistence, both in waste streams and in end-use. We have adapted our own procedures to address these realities, recycling solvents where feasible, and capturing halide-containing off-gases in approved, monitored treatment systems. Our waste-handling partners undergo frequent audits; we carry insurance and government registrations as required, but more importantly, seek ways to minimize offsite risk. R&D investments have targeted byproduct reduction and closed-cycle processes so less raw material goes past the intended transformation. We share practical waste minimization strategies with customers who ask — real world advice, drawn from actual plant experience, not just corporate policy.
Every drum, bottle, or can leaves our dock with the silent effort of dozens of people who checked, filled, and documented each container along the way. We respect the knowledge of our operators, engineers, and support staff — they know how small differences in procedure ripple outward toward the finished molecule. Our team doesn’t approach 3,5-difluorobenzyl bromide as a faceless commodity. Instead, we see each order’s path through the plant, from the first quotation to the final seal on the shipping carton. The pride stems not from grand gestures, but from realizing that a customer’s next big breakthrough may depend on what we loaded onto a truck this morning.
Chemical manufacturing, especially in specialty organics, cannot run on autopilot. Customer challenges evolve as new synthesis routes, regulations, and market expectations roll out. As partners introduce next-generation intermediates at clinical and commercial scales, our factory stays ready for tweaks and upgrades. We treat every new inquiry as a practical challenge, whether it asks for an odd container size, tighter impurity levels, or alternate documentation. More often than not, we find technical obstacles also point the way to broader improvements for all our customers.
Our story with 3,5-difluorobenzyl bromide draws from thousands of hours spent on actual plant floors, tracking batch logs, fixing pumps, and adjusting parameters based on feedback from scientists at the bench. As long as innovation demands reliable, high-purity halogenated intermediates, we will keep showing up with both molecules and practical solutions to make progress possible.