|
HS Code |
816679 |
| Chemical Name | 3-Trifluoromethyl-4-Bromophenol |
| Cas Number | 137485-91-5 |
| Molecular Formula | C7H4BrF3O |
| Molecular Weight | 241.01 |
| Appearance | White to off-white solid |
| Melting Point | 84-89°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1O)Br)C(F)(F)F |
| Inchi | InChI=1S/C7H4BrF3O/c8-5-2-3-6(12)4-7(5)1-10-11-9/h2-4,12H |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Synonyms | 4-Bromo-3-(trifluoromethyl)phenol |
As an accredited 3-Trifluoromethyl-4-Bromophenol 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 3-Trifluoromethyl-4-Bromophenol, tightly sealed with a screw cap and labeled hazard warnings. |
| Shipping | **Shipping Description for 3-Trifluoromethyl-4-Bromophenol:** Shipped in tightly sealed containers to prevent moisture and air exposure. Transported under ambient conditions, away from incompatible substances. Compliant with applicable regulations for hazardous chemicals. Packaging ensures protection from physical damage, with clear labeling of chemical and hazard information. Standard shipping methods apply unless otherwise specified by the customer. |
| Storage | 3-Trifluoromethyl-4-Bromophenol should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong bases and oxidizing agents. Keep the container tightly closed and clearly labeled. Store at room temperature or as recommended by the manufacturer. Protect from moisture and sources of ignition. Use in accordance with proper chemical hygiene practices. |
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Working in chemical manufacturing offers a front-row seat to the ongoing evolution of specialty intermediates. With every new compound comes the promise of improvement—greater selectivity in synthesis, cleaner downstream reactions, solutions to bottlenecks that slow product development. In this environment, 3-Trifluoromethyl-4-Bromophenol, known across the industry by CAS number 1522-92-5, has earned a steady place on our production line for good reason.
This compound’s molecular signature balances the demanding needs of pharmaceutical, agrochemical, and advanced material research. Starting with the heart of the molecule—a phenolic ring—the presence of both a trifluoromethyl and bromine substituent opens up diverse reactivity options that few other phenols can match. From our daily work, the backbone of this product feels less like a simple raw material and more like a toolkit for chemists needing reliability and flexibility.
Our batches of 3-Trifluoromethyl-4-Bromophenol come optimized for the users who have requests ranging from next-step coupling to final assembly in drug and crop protection agent synthesis. We have learned from repeated pilot runs and scale-ups where the real problems tend to emerge—impurities at low levels, unpredictable melting points, color changes during storage, or drops in titer after a few months. Through careful process design, like close monitoring of halogenation and reminding ourselves not to overlook the effect of slightest acid traces, our team has managed to lock in a consistent quality standard: minimum purity 98%, white to off-white crystalline powder, melt point typically around 70°C, almost always under 72°C when lab-tested within six months of batch production. Most of our requests ask for gram-to-multikilo lots, and these are table stakes rather than optional details.
Each batch carries the signature odor that comes with phenolic compounds combined with a sharp edge—nothing unexpected for those who have spent time with similar fluorinated aromatics. Dissolution properties matter a lot: in-house, we see ready solubility in common organic solvents like dichloromethane, ethyl acetate, and a mix in polar aprotic media. Water solubility runs low, but that characteristic adds to its selective behavior in certain isolation steps.
The substitution pattern—trifluoromethyl at the third position, bromine at the fourth—does more than just differentiate this substance on paper. The electron-withdrawing trifluoromethyl group makes the phenolic hydrogen less prone to unwanted oxidation, while the para-bromine adds a true handle for Suzuki and other cross-coupling strategies. Over years of hands-on process feedback, our team has seen this combination lower the odds of side-product formation during key bond-forming steps, compared to ordinary 4-bromophenol or even most trifluoromethyl phenols without the halogen. Lab notebook entries from scale-up trials often come back with the same note: yields improve, and workup is cleaner.
Chemical manufacturer's worth gets decided in process reliability as much as in sheer technical data. 3-Trifluoromethyl-4-Bromophenol routinely makes a difference for research chemists needing high-purity aryl intermediates that behave the same from batch to batch. In manufacturing, any failure or even a hitch can cause hours of lost productivity. So, progress means eliminating sources of error before the product leaves the warehouse.
Uncontrolled byproducts, such as unreacted starting material or trace hydrolyzed derivatives, have been common problems in this product’s historical production outside of rigorous in-process checks. By adapting purification steps—careful solvent washes, well-controlled crystallization conditions, frequent checks for color impurities—we cut out most sources of interference. The outcome: our product works smoothly for custom syntheses where every percent of yield translates to budget savings and faster time-to-market for new compounds. Large pharma clients have been vocal about needing this level of consistency, so we’ve made it a point of pride: ambient-stable, reliable purity, flexible lot sizes, fast turnaround from warehouse to bench or plant.
Another key performance factor is carryover risk during scale transitions. Many chemicals lose quality when moving from pilot to bulk, with scale-dependent issues like local overheating or incomplete mixing leading to breakdown. In our facility, batch-to-batch reviews center on identifying and managing these hurdles before scaling. Our investment in analytical chemistry—regular HPLC, GC-MS analysis, attention to even minor shifts in impurity profile—raises the bar for what customers come to expect.
Placing 3-Trifluoromethyl-4-Bromophenol alongside related molecules shows the nuance of small structural changes in real synthetic chemistry. Regular 4-bromophenol, for example, cannot match the same resistance to oxidation and tends to degrade more quickly in air or in storage. Substituted trifluoromethyl phenols, especially those lacking a good cross-coupling handle, require extra steps to install side groups and create functionalized intermediates. With both substituents in place, our product speeds up those downstream steps.
Chemists tell us that starting from our compound reduces the amount of catalyst or special ligands required for key reactions, like Suzuki or Buchwald-Hartwig couplings. The para-bromine is sufficiently activated by the trifluoromethyl group that reactions proceed efficiently, but not so overreactive that stability suffers. In practical terms, fewer unwanted side-products mean less time spent on purification columns, less solvent used, and a smaller environmental footprint in the lab. Compared to 2,4-dibromophenol or other multiply halogenated phenols, this product avoids introducing unnecessary toxicity or airflow issues on scale—lower halogen load translates to less concern over persistent pollutants during large volume synthesis.
From the customer side, we hear regularly about bottlenecks trying to scale up specialty intermediates only to hit regulatory friction traced to impurities—sulfonated byproducts, mono- or di-halogenated offcuts—slipping through less rigorous supply chains. Our team answers these challenges with both production controls and transparent documentation. Alongside each dispatch, full trace analysis and certificate of analysis goes out; our staff remains accessible for technical support and troubleshooting, because so many of our buyers come back to us not for price, but for process assurance.
Pharmaceutical development sets the highest standard for any fine chemical intermediate, and 3-Trifluoromethyl-4-Bromophenol stands out for its versatility in building blocks for clinical candidates. Medicinal chemists benefit from quick modification options— attaching various heterocycles or bioactive moieties—using the bromine as a launchpad for carbon-carbon or carbon-nitrogen coupling. The trifluoromethyl group isn’t just a decorative add-on: it modulates metabolic stability, increases membrane permeability, and often encourages better pharmacokinetics in final drug candidates.
Every year, more research pipelines specify this particular phenol variant as a go-to substrate. It allows for simplified routes to several classes of kinase inhibitors, anti-inflammatories, and small-molecule probes. Moving to agrochemical development, the same electron pattern underpins qualities that matter—improved uptake in plant systems, slower environmental breakdown, and ease of conversion into selective herbicides or fungicides. Industrial material scientists also find that this molecule brings useful features to specialty coatings and fluorinated polymers, where performance under heat or corrosive conditions calls for a blend of stability and reactivity.
We see creative uses emerging too: surface modification treatments, advanced battery testing, and even niche applications in dye synthesis depend on this building block. Direct feedback from technical teams in these sectors points to lower defect rates in finished materials and a measurable reduction in screen failures for new compounds built on this phenol template. Such information doesn’t come from datasheets—it arrives through relationships and candid reporting from researchers who put time and trust into every gram of new intermediate they test.
Working with halogen- and fluorine-substituted phenols demands commitment to plant safety and responsible logistics. Every container carries a risk profile based on long laboratory experience: inhalation risk from fine powder, skin and eye irritation potential, sensitivity to strong oxidizers. Our facilities implement rigorous controls at every stage—closed transfer systems, routine respiratory protection, and rapid spill management procedures. Our goal: zero lost-time safety incidents, every batch, every year.
Packaging practices respond to both chemical stability and user convenience. We seal and fill product directly from cooled reactor vessels into airtight, chemically resistant containers—usually HDPE-lined drum or bottle for larger quantities, amber glass for research lots. These formats keep out light and moisture, both of which have been shown to alter the product over time, especially during prolonged shipment or in humid conditions.
Logistics teams at our company know how backing up the supply chain can cause real problems downstream. Delays are not just a headache; they can halt an entire project or leave a team idle while they wait for critical inputs. Our inventory systems use digital, batch-tracked storage. Orders ship with clear chain-of-custody, both to support our customers' needs for traceability and to make sure no corners get cut in process or documentation. Having watched more than one competitor lose out because of missed deadlines, we have worked hard to build a reputation for delivering the actual product—on time, as promised, and without supply gaps or last-minute quality questions slowing a team’s work.
Production routines for compounds like 3-Trifluoromethyl-4-Bromophenol pull hard on resources—from specialty starting materials to hazardous reagents and utilities. By tightening yield optimization and solvent recovery, we limit raw material and energy waste. Our in-house approach cuts emissions by favoring greener oxidants and controlling halogenated waste, sending residues for responsible high-temperature incineration rather than relying on simple landfill. Process engineers revisit each work-up step regularly, seeking opportunities where a new piece of equipment or a slightly more efficient quench can cut tens of kilograms of waste per ton of product shipped.
The same principle applies to packaging: customers increasingly challenge us with requests for safer, lower-mass, and recyclable options, and progress has come from trial and error. Early glass-only shipments proved too fragile for bulk; HDPE-only lost out to multi-layer barrier linings that last longer even in warm climates. When a better format surfaces, such as solvent return programs or closed-loop container exchange, we offer it directly to our regular clients. Each improvement signals a real commitment to reducing environmental burden, not just on our shop floor, but throughout the life cycle of the product from synthesis to end-use and disposal.
Years in bulk and custom synthesis has shown our staff that successful fine chemical supply requires more than just chemical know-how—it calls for hands-on understanding of what clients expect from every drum shipped. Whether the application is in high-throughput screening or multi-ton drug development, the risks and stakes rise with every extra step needed to purify or troubleshoot a batch. Consistent crystallinity, reproducible melting point, no residues that creep into next-stage reactions: this level of assurance is the benchmark.
Our history with 3-Trifluoromethyl-4-Bromophenol began with small-batch requests and quick turnover to address urgent gaps in medicinal chemistry programs. Today, we work directly with some of the world’s largest R&D teams, fielding technical questions about possible byproducts, shelf life, or reaction compatibility. Having walked the manufacturing floor personally, our team knows that a stray trace impurity in a kilo lot can spell headaches for someone purifying a late-stage intermediate. So, our routine goes beyond standard QC—each outgoing lot gets a second round of spot checks, with spectra and physical property tests twice before shipment. Feedback from process chemists and material scientists comes back regularly, and drives each process adjustment forward.
When we hear from customers about real wins—like being able to avoid an entire chromatography step, or discovering a more robust synthetic pathway because of the selectivity our phenol brings—it means more than just a ticked box in a technical review. It means trust gained through repeated performance. As a chemical manufacturer, this reputation sustains relationships far longer than price points or novelty products ever could.
The future of 3-Trifluoromethyl-4-Bromophenol, and specialty intermediates like it, depends as much on what happens inside manufacturing facilities as in research labs. Feedback cycles between bench and plant matter. Teams that invest in analytical controls, invest as well in customer success. With every batch, we ask not just whether the specification has been met, but whether the chemists at the far end of the supply chain can move faster, with fewer surprises and more confidence in their results.
Our house approach grounds itself in daily practice: prioritizing technical transparency, welcoming open discussion about product performance, responding to changing client needs, and running iterated risk assessment at each step of production. This process has led to steady innovations—a tweak to a crystallization, an updated filtration, a new package format—each one aimed at eliminating friction and adding reliability where it counts.
With every gram of 3-Trifluoromethyl-4-Bromophenol produced, we measure success in repeat orders, positive process feedback, and few (if any) customer complaints about lot-to-lot variability. The world of advanced research demands it; our commitment to this class of products is built on knowing, from the inside out, how every variable can affect the next reaction or application. This inside-out perspective on manufacturing is what guides ongoing change—and what keeps specialty chemistry moving forward for everyone who decides to work with our product at any scale.