|
HS Code |
296895 |
| Chemical Name | Phenol, 2-Bromo-4-(Trifluoromethyl)- |
| Molecular Formula | C7H4BrF3O |
| Molecular Weight | 241.01 g/mol |
| Cas Number | 327-65-3 |
| Appearance | White to off-white solid |
| Melting Point | 41-44 °C |
| Boiling Point | 208-209 °C at 760 mmHg |
| Density | 1.77 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC(=C(C=C1O)Br)C(F)(F)F |
| Inchi | InChI=1S/C7H4BrF3O/c8-5-3-4(7(9,10)11)1-2-6(5)12/h1-3,12H |
| Refractive Index | 1.557 (predicted at 20 °C) |
As an accredited Phenol, 2-Bromo-4-(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure screw cap, containing 25 grams of Phenol, 2-Bromo-4-(Trifluoromethyl)-; labeled with hazard warnings. |
| Shipping | Phenol, 2-Bromo-4-(Trifluoromethyl)- should be shipped in tightly sealed containers, protected from light and moisture, and labeled according to hazardous materials regulations. Transport must comply with local, national, and international shipping guidelines for hazardous chemicals, ensuring safety for handlers and the environment. Proper documentation and hazard communication are essential during shipping. |
| Storage | Phenol, 2-Bromo-4-(Trifluoromethyl)- should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers, acids, and bases. Store it away from direct sunlight and sources of ignition. Ensure the storage area is equipped with spill containment and clearly labeled for hazardous chemicals. |
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Every step of our manufacturing process shapes how we approach each product, including Phenol, 2-Bromo-4-(Trifluoromethyl)-. Our chemists and production engineers pay close attention to technical performance, user needs, and reliability. We do not operate as traders or intermediaries. The batches leaving our production line have withstood practical scrutiny and internal discussion long before reaching any customer. Our experience stretches across tonnage scales, from small laboratory development to synthetic campaigns supporting demanding pharmaceutical and material science projects.
Manufacturing Phenol, 2-Bromo-4-(Trifluoromethyl)- offers insights not always shared in datasheets. This compound earned its reputation within custom synthesis routes and in broader agrochemical and life sciences applications. Typically referenced under the CAS number 327-10-2, the molecular arrangement combines a bromine at the ortho position and a trifluoromethyl at the para position relative to the hydroxyl group. This specific configuration influences both reactivity and downstream product stability.
We manufacture this phenolic derivative at consistent purity levels above 98%, confirmed by GC and NMR, meeting stringent criteria for sensitive coupling reactions and heterocycle construction. During pilot batches, our team repeatedly saw that trace impurities, not always detectable by less precise methods, drive major issues in selectivity and yield loss, especially in pharmaceutical R&D. Early purification process changes offset those risks for our long-term partners.
Our material presents as an off-white solid, with a melting range typically between 50°C to 54°C. The presence of both bromine and trifluoromethyl shifts the compound’s behavior away from standard phenols. In synthesis, this means altered nucleophilicity and greater compatibility with transition metal catalysts, a feature that cannot be overlooked if a process demands tight control over substitution or cross-coupling steps.
We carefully control water and residual solvents content, as persistent trace methanol and dichloromethane often interfere with subsequent steps. For applications in process chemistry, our batches consistently stay at <0.2% total solvents, avoiding interruptions in sensitive transformations. The team occasionally gets called to consult on outgoing material, assisting chemists in troubleshooting side products that arise when using less rigorously purified alternatives sourced elsewhere.
Our primary partners use Phenol, 2-Bromo-4-(Trifluoromethyl)- as a building block for introducing electron-withdrawing effects in aromatic scaffolds. The dual presence of the bromine and trifluoromethyl group increases both versatility and downstream value, whether in the design of bioactive molecules or performance materials. Compared to standard phenol derivatives, this product unlocks coupling with unique reactivity windows; it supports Suzuki, Buchwald-Hartwig, and Ullmann reactions, expanding what chemists can achieve in one-pot strategies.
In medicinal chemistry campaigns, our collaborators choose this compound to reach targets that demand both lipophilicity and enhanced metabolic stability—two features often dictated by the trifluoromethyl group. A straightforward bromination cannot recreate the performance observed with this substitution pattern. Our role has included advising on purification steps and minimizing bench time losses that snowball with lesser material grades.
Material scientists approach us because of the predictable behavior this phenol grants during polymer modification and specialty coatings research. Its electron-withdrawing signature influences local charge distribution, affecting adhesion, optics, or resistance. Here, purity directly correlates to consistent function, something we have seen during stability studies and long-term project support. Those insights drive our ongoing process optimization efforts.
We see the difference controlled manufacturing can make. Phenol, 2-Bromo-4-(Trifluoromethyl)- purchased from generic sources often comes with contaminants that react under mild conditions: halides, isomeric byproducts, even basic salts. These impurities compromise yields and lead to false positives during structural analyses, leading to extended purification cycles or even late-stage batch failures. Our team monitors by-products tightly—from intermediate stages to finished goods—to prevent these issues. Regular returns from leading pharmaceutical and crop protection teams have shown that batch-to-batch reproducibility allows them to streamline both lab and plant-scale operations.
Many other phenol derivatives lack the fine balance of reactivity that this compound offers. Electron-donating substitutions cannot match the activation energy changes required in halogenated, fluorinated targets. Conversely, using less reactive halophenols often results in sluggish cross-coupling or an explosion in side reactions. Our technical reports show that our approach avoids those pitfalls, keeping operational windows open whether working with gram- or kilo-scale transformations.
Every year brings us new requests for applications outside the expected. Our process team continuously runs root-cause analyses to track yield shifts and impurity profiles, feeding lessons learned back into both quality control and synthesis protocols. We’ve seen phenol derivatives fail due to unnoticed source variation: from reagent drift to subtle temperature irregularities during halogenation or trifluoromethyl introduction.
Analytical support comes built-in on our line. Material passes through vendor-calibrated instrumentation: GC-FID for volatility and residual solvents, NMR for isomeric purity, MS for mass confirmation. Batch records include photographs of each process stage, supporting traceability for teams working in regulated environments. While some companies cut corners here, our long-term relationships with innovators stem from eliminating guesswork—something that comes only from open reporting and process discipline.
Feedback loops matter. Our production chemists log every minor deviation, from ambient humidity changes to mechanical vibrations in grinding equipment. That level of detail might sound excessive, but it’s exactly where we’ve spotted sources of microcontamination in past years. Eliminating those has directly improved yield reproducibility for complex downstream transformations, reinforcing our belief in the practical value of internal communication and attentiveness.
Due respect for process safety sets apart high-integrity manufacturers from those who simply package and ship. In our experience, handling Phenol, 2-Bromo-4-(Trifluoromethyl)- requires protective protocols comparable to those for most halogenated phenols. We outfit our production spaces with proper air handling and fire control, and train staff in the direct effects of inhalation, prolonged dermal contact, or accidental spills. We set aside space for teams to review safety data and train on real-life simulation of containment and cleanup.
Across thousands of kilograms produced, there have been zero cases of operator injury or environmental contamination thanks to well-rehearsed, documented methods. We routinely invite third-party audits to verify actual on-ground compliance. A strong documented safety record has prompted several multinational development partners to audit our site—sometimes unannounced. Each time, direct observation matters more than what can be captured on paper.
Each package of Phenol, 2-Bromo-4-(Trifluoromethyl)- starts with source-tracked raw materials, with all steps logged by human operators and checked for consistency. We maintain manufacturing lot records and material samples for years beyond standard requirements, ensuring forensic accountability. Once, a customer traced an unexpected side reaction to a highly specific trace impurity that escaped the detection thresholds of their own incoming QC. Our historical sample library let us quickly provide matching reference material, expediting their project’s return to schedule. Traceability protects both our partners and our own brand.
Our team stands ready with rapid-response documentation—from full analytical reports to single-point pathway clarifications—because we understand that every material shipment can change the outcome of an in-lab or in-plant campaign. Manufacturing is not just about supplying product, but about supporting every transition from one synthetic stage to the next.
Research development cycles shrink dramatically with the introduction of reliable starting materials. This compound accelerates screening campaigns and intermediate construction for sulfonamides, ethers, and advanced heterocycles. Our internal R&D team applies it in our own method development projects, providing insight into both the upstream and downstream challenges our customers face.
For process chemists, minimizing crosstalk between steps is crucial. Our regularly scheduled shipment cycles and strict packaging standards—double-bagging, nitrogen blanket, moisture barrier containers—have prevented cross-contamination even during lengthy transport. This attention to logistical detail reflects our belief that performance excellence doesn't end at the reactor; it extends to every phase of the product’s journey toward the customer’s bench or reactor.
We have supported teams engineering new herbicides and fungicides by supplying multi-kilo lots, with project timelines fluctuating year by year depending on market needs. We understand the demands of milestone-driven research, where delays from unreliable material sourcing lead to exponential costs. Our team fields calls and emails directly to the scientists who design and operate the processes; we trade insight for insight, and improve our own process as a feedback result.
Comparing this compound with other phenol derivatives informs every decision, from synthetic route planning to end-use value. Unsubstituted phenol or bromophenols without the trifluoromethyl group lack the same potency for tuning lipophilicity or metabolic stability in medicinal chemistry programs. The unique feature of this material lies in its ability to facilitate challenging cross-couplings without introducing the instability seen in some higher halogenated or heavily fluorinated species.
Some research teams attempt to synthesize this compound from simpler phenol cores with post-hoc substitution. Our data logs indicate such approaches often yield lower purity and introduce process variation. Direct manufacturing from clean, verified starting materials—and continuous oversight—produces more sustainable, scalable, and reproducible outcomes. That result lowers the overall cost of failure.
Not all laboratories can support the quality assurance routines needed to achieve single-digit ppm impurity levels. We take the burden off research and manufacturing clients by assuming responsibility for that aspect. This dynamic increases throughput and reduces the need for in-house material remediation.
We pack Phenol, 2-Bromo-4-(Trifluoromethyl)- in liners with full lot traceability, using containers proven in temperature and humidity stress tests. Material sits in dry, ventilated storage, with batch-by-batch review to prevent exposure risks from accidental container puncture or extended shelf time. Over many years, standard warehouse conditions have produced no detectable product shift or degradation.
We advise on refrigerated or dark storage when material must be held longer than six months. This extends the product’s shelf life for customers running seasonal or irregularly paced projects. We have recovered and retested multimodal shipments delayed for months, each time finding batch quality fully preserved.
Global supply chains throw many unpredictable problems at chemical manufacturers: shipping backlogs, raw material shortages, tightening regulatory oversight in major jurisdictions, sudden customer forecast changes. Our approach—proactive communication and quick production adjustments—has minimized disruption. For example, in several recent quarters marked by international shipping delays and customs backlogs, our in-house inventory planning let us fulfill standing orders with less than a day’s lag despite unplanned outages upstream.
We regularly share best practices in packaging and logistics with clients, helping them mitigate on-site storage challenges or ensure safe, regulatory-compliant internal transfers. In situations involving hazardous material reclassification or new paperwork requirements, our regulatory and documentation team provides detailed, real-time compliance guidance. Collective problem-solving, not just transactional interaction, defines our ongoing relationships in the research and production communities.
On several occasions, we have partnered directly with client teams to troubleshoot difficult or novel reactions involving this product. Our chemists share protocol insights based on years spent scaling up and optimizing the synthesis, offering suggestions for improved reagent selection, work-up, or purification. We have helped customers adapt to new environmental or occupational standards, from green chemistry push initiatives to stricter local and international transport regulations. These real-world deliverables matter far more than a technical brochure or faceless online invoice ever could.
User experience shapes every production run. Direct feedback—positive and negative—drives us to continually innovate, raise standards, and support our partners beyond simply selling them chemical compounds. Our investment in analytical infrastructure, safety, and talent reflects our belief that consistently producing high-quality Phenol, 2-Bromo-4-(Trifluoromethyl)- means building long-term value and trust, not chasing short-term margins.
Daily practice in the factory and the laboratory transforms the abstract into the reliable. We invite our partners and collaborators to visit, observe, and participate in process reviews. Only through face-to-face interaction and technical transparency can either party truly trust the quality and integrity of the material they receive or supply. The compound’s complex balance of performance, processability, and safety comes into clear focus through shared real-world experience—not just numbers on an assay sheet, but tangible, repeatable success across applications.