|
HS Code |
712867 |
| Chemical Name | 4-Bromo-3-fluorophenol |
| Cas Number | 138488-93-6 |
| Molecular Formula | C6H4BrFO |
| Molecular Weight | 191.00 |
| Appearance | White to off-white solid |
| Melting Point | 73-77°C |
| Boiling Point | 238.6°C at 760 mmHg |
| Density | 1.77 g/cm3 |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1O)Br)F |
| Inchi | InChI=1S/C6H4BrFO/c7-4-1-2-5(9)6(8)3-4/h1-3,9H |
| Refractive Index | 1.597 (predicted) |
| Storage Conditions | Store in a cool, dry place, away from incompatible substances |
As an accredited 4-Bromo-3-Fluorophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 4-Bromo-3-Fluorophenol; sealed with a red screw cap and hazard labeling. |
| Shipping | 4-Bromo-3-Fluorophenol is shipped in sealed, chemical-resistant containers to protect against moisture and contamination. It is handled and transported as a hazardous material under applicable regulations, with appropriate hazard labels and documentation. Packaging ensures secure containment, and the shipment is tracked during transit to guarantee safe and compliant delivery. |
| Storage | **4-Bromo-3-Fluorophenol** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect it from moisture and direct sunlight. Ensure appropriate labeling, and restrict access to trained personnel. Follow all relevant regulations and safety guidelines for chemical storage. |
Competitive 4-Bromo-3-Fluorophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Every day on the production floor, we’re reminded how small changes in a molecule can drive big results upstream in synthesis labs. 4-Bromo-3-Fluorophenol, which we also refer to by its chemical structure 3-fluoro-4-bromophenol, often goes unnoticed in the world of aromatic intermediates. But anyone who’s run a reaction with highly substituted phenol derivatives knows the challenges behind that simplicity—especially when targeting high purity and consistently reliable performance batch after batch.
Developing quality 4-Bromo-3-Fluorophenol took us years of reworking purification steps, comparing different bromination and fluorination reagents, and working alongside downstream chemists who needed a dependable starting point. Slight shifts in impurity profiles can gum up expensive multi-step reactions, adding hours of troubleshooting that nobody wants on their calendar. We’ve seen the headaches caused by off-spec batches: wider melting ranges, unexpected retention times, and, sometimes, unworkable crude products in subsequent couplings. It is for these reasons that our attention to detail didn’t stop once we dialed in the basic synthesis; it’s ongoing, with every batch run.
We produce 4-Bromo-3-Fluorophenol in white to pale beige solid form, engineered to flow and dissolve readily under standard industrial bench conditions. The CAS number—34052-35-2—identifies its precise fingerprint in regulatory and scientific registries, but our focus lies in purity, consistency, and the needs that come up during real-world application. We manufacture this compound to contain less than 0.5% related aromatic impurities thanks to high-efficiency distillation and crystallization steps that we’ve refined through hundreds of reaction cycles. A typical melting point for our material sits between 50 and 54°C—a range we monitor closely, since drift here often signals a deviation before HPLC or GC even tells us.
Each batch we produce receives analysis using multiple analytical techniques: GC, HPLC, and in some cases, NMR for clients asking for additional documentation. This way, we provide more than just a purity number; we share chromatograms and spectra that matter to technical teams planning the next steps in their workflows.
For those less familiar, 4-Bromo-3-Fluorophenol incorporates bromine and fluorine substituents onto a phenolic ring. This seemingly modest adjustment from simple phenol not only tweaks polarity and reactivity, but also opens up options for stepwise modifications that plain phenol or single-halogenated counterparts cannot accommodate. In practice, this difference can streamline multi-step syntheses or allow for selective cross-coupling at one halogen while retaining the other for later functionalization. Medicinal chemists, in particular, have leveraged this strategy to build libraries of candidate molecules—especially when exploring fluorinated scaffolds mimicking biologically active analogues.
The phenol group’s hydrogen-bond forming potential means that, even with bulky halogen substituents, reactivity towards etherification, esterification, or coupling remains excellent. We’ve heard from process chemists that rapid, predictable behavior with boronic esters and organozinc partners is increasingly valued as many research groups venture toward more complex fragment-based strategies.
Several years ago, a research group brought us feedback after building a pilot plant route using 4-Bromo-3-Fluorophenol. They found that product sourced from different factories could swing between workable to unmanageable within a single campaign. Our own team saw that trace contaminants—often chlorinated or di-brominated byproducts—led to erratic yields and byproduct formation. This drove us to fine-tune our halogenation sequence: careful control of temperature, reagent addition, and solvent selection almost eliminated side reactions for our preferred pathway.
As a result, users now report drop-in performance without the need to repurify our product before use. We encourage technical partners to initiate incoming QC on their end—no manufacturer can guarantee perfect logistics. Still, it’s our job to minimize surprises. Joint troubleshooting sessions have sharpened how we address moisture uptake, optimal storage containers, and onboarding staff for best handling practices. You wouldn’t overlook a small impurity peak when scaling to a 100-liter batch, and neither do we.
Serving the specialty chemicals sector has taught us that users don’t care for one-size-fits-all answers. Many downstream applications test combinations: 4-Bromo-3-Fluorophenol, 4-Fluoro-3-Bromophenol, or their non-halogenated relatives are all in play, depending on synthetic targets. Our process specialists regularly compare these options, running side-by-side reactivity studies. We’ve noticed that the order of substituents on the aromatic ring affects both electron distribution and favorite reaction sites. For instance, the selectivity observed in palladium-catalyzed couplings differs between the 3-fluoro-4-bromo and 4-fluoro-3-bromo isomers due to differing electron withdrawal and localization, leading to faster or more controllable outcomes for certain bond formations.
A key learning point: comparably pure isomers deliver reproducible kinetic profiles. Still, even small positional changes in halogen placement demand adjusted process parameters, and our technical liaisons are keen to talk through those differences with R&D partners. We don’t chase trends; we take detailed notes, so whether you’re screening a series for electronic effects or targeting a property like metabolic stability in a pharmaceutical lead, knowledge of molecular behavior pays dividends down the road.
Over years of supplying 4-Bromo-3-Fluorophenol to both discovery and process chemistry teams, clear themes have emerged. The pharmaceutical sector, in particular, prefers reliably pure, low-moisture, and well-characterized intermediates. A compound like this, with its two halogen substituents, often becomes a backbone for antiviral, anti-inflammatory, or CNS-active compound synthesis. Downstream, analytical groups have highlighted that clear and clean spectra—GC/MS, NMR—translate directly into shorter project timelines and more accurate patent submissions.
As regulatory demands tighten, we have responded by generating detailed impurity profiles, stability test data, and batch-specific analytical documentation. While regulations shift, our standard remains: support customers through evolving territory with transparency and practical know-how. This approach has built longstanding partnerships and helped process chemists win internal advocacy for scaling new synthetic routes.
During scaling trials with global partners, we’ve observed unexpected hiccups due to overlooked basics like storage. 4-Bromo-3-Fluorophenol, like many low-molecular-weight aromatic compounds, responds to moisture and light. This material often undergoes subtle changes during long transit routes or when stored under suboptimal conditions. After several client-run stability studies flagged shifts in impurity content, we optimized our packaging to reduce these risks—using lined, airtight drums, minimal headspace, and desiccants in each shipment.
We recommend, based on field experience, storage in a cool, dry area, away from direct sunlight or sources of humidity, to maintain purity. Avoiding prolonged exposure to air—especially in humid climates—has helped users avoid discoloration or clumping that complicates dosing or weighing. For scale-up chemists, these preventative measures mean fewer last-minute interventions, less wasted material, and a smoother flow from receiving goods to charging the reactor.
We see ourselves as more than a raw materials plant. Feedback loops between our production teams and client R&D chemists drive how we develop, test, and release new batches of 4-Bromo-3-Fluorophenol. Some years ago, a pharmaceutical customer faced cascading batch failures during an oxazoline ring-closing step, traced back to traces of dibromophenols in a faulty input batch from another supplier. As part of the solution, we stepped in to troubleshoot their workflow, exchanged analytical reference standards, and supplied a run of ultra-high-purity material. Their issues vanished, project timelines recovered, and the partnership deepened.
These lessons shape every improvement we make on our end. Incoming raw materials now undergo stricter verification, and our batch tracking has moved to a digital ledger accessible to our tech support partners. Real-time data sharing strips out much of the friction that once slowed down scale-ups or led to finger-pointing over yield drops. Whenever challenges appear, we’re open to joint root-cause analysis sessions, refining sample prep to match downstream analytical runs or testing packing configurations that align with climate variables found along complex transit routes.
Because our staff includes several PhDs with both academic and industrial backgrounds, we’re plugged into changing synthetic strategies—bioconjugate chemistry, streamlined one-pot couplings, and green chemistry routes among them. We routinely provide bulk 4-Bromo-3-Fluorophenol for method development, where chemists try to cut steps, replace toxic reagents, or improve atom economy. These efforts often spur us to supply customized lots: adjusted particle sizes, tighter purity specifications, or custom packaging requirements.
One story stands out—a group trialed a photoinduced fluorination step that relied on our material serving as both substrate and internal standard due to its well-characterized properties. Over several months, we worked together to ensure each new method tweak could be directly correlated to the starting material, cutting time lost to uncontrolled variables. Clients tell us this hands-on approach means fewer failed experiments and broader adoption of our phenolic intermediates in next-generation pharmaceuticals and agrochemicals.
Supply disruptions have hammered chemical markets in recent years. After experiencing firsthand how delayed approvals for a critical precursor could impact not just our plant but multiple downstream customers, we revised our supply strategy: holding larger in-house stocks of sensitive starting reagents, qualifying additional backup vendors, and developing in-house analytical reference protocols.
This integrated system gives our clients peace of mind—particularly those with high-volume, multi-year contracts, who can’t afford risk at the sourcing stage. Predictably, some still prefer to stagger deliveries over quarters or invest in co-signed rolling stockpiles at regional warehouses. We’re flexible because we know reliable delivery is sometimes more important than shaving off a cent per kilogram on short-term deals.
Chemicals aren’t just poured from drums and forgotten. Process chemists, bench scientists, and QC analysts depend on us for insight as well as raw material. Regular site visits, virtual troubleshooting calls, and annual quality review meetings keep us connected—and accountable—to our users’ evolving needs. Feedback from a recent scale-up project, which encountered unexpected catalyst poisoning during a Suzuki-Miyaura coupling, led us to revisit our in-process sampling and add a post-purification wash with custom solvents. The improvement shaved several hours off customer purification time, bumping up throughput and cutting overhead—a win for everyone involved.
Our own learning curve echoes those working at the front lines of experimental research. Sometimes the biggest leaps come not from sweeping changes, but from incremental improvements: retuned crystal growth parameters, faster solid-liquid separation during workup, or subtle drying tweaks for every order dispatched in peak humidity. It’s this mindset—continuous but targeted improvement—that keeps us and our customers at the leading edge of chemical manufacturing.
Regulatory standards around halogenated organics are shifting. Environmental stewardship means doing more than checking paperwork. Over the last decade, our site has phased in greener reagents, solvent recycling streams, and investments in emissions abatement. These upgrades let us minimize unwanted byproducts and waste footprints related to 4-Bromo-3-Fluorophenol without compromising product quality. Long-term clients working under REACH or comparable standards see tangible results—a reduced carbon impact, not just compliance on paper.
Each production decision—choice of solvent, workup protocol, packaging material—takes these factors into account. Collaboration continues upstream with the manufacturers who produce our precursors, where we advocate for closed-loop systems and cleaner energy sources. Ultimately, responsible production isn’t just marketing speak; it anchors trust with customers, regulators, and local communities alike.
As a direct manufacturer, we see firsthand how investing in meticulous process control, documentation, and ongoing client support undergirds success. 4-Bromo-3-Fluorophenol isn’t a buzzword; it’s a benchmark for reliability and transparency in the specialty chemical world. Over years of partnership with leaders in pharma, agrochemicals, and advanced materials, we have learned that dialogue and operational flexibility are worth more than flashy brochures—especially to the professionals whose work depends on getting the right material, on time and without complications. It’s this dedication to delivering value, shaped by experience at the plant and at the bench, that guides how we approach both routine supply and challenging, one-off projects.
For those seeking deep technical knowledge, a willingness to adapt, and the assurance of a manufacturer who stands by each shipment with data and real-time support, our door remains open.