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HS Code |
615625 |
| Productname | 4-Bromo-3-Fluoro-2-Methylaniline |
| Casnumber | 105271-86-1 |
| Molecularformula | C7H7BrFN |
| Molecularweight | 204.04 g/mol |
| Appearance | Light yellow to brown crystalline solid |
| Meltingpoint | 58-62°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥97% |
| Synonyms | 2-Methyl-4-bromo-3-fluoroaniline |
| Smiles | CC1=CC(=C(C=C1Br)F)N |
| Inchikey | HWGOXSDQLUKGBY-UHFFFAOYSA-N |
As an accredited 4-Bromo-3-Fluoro-2-Methylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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4-Bromo-3-fluoro-2-methylaniline stands out in the world of specialty chemicals. With the molecular structure C7H7BrFN, this compound takes its place among aniline derivatives, but adds nuance by bridging bromine, fluorine, and a methyl group to the aromatic ring. Chemists often reference this molecule by its CAS number 129554-87-4. Even without a catchy trade name, its structure sparks interest because of its selective substitutions—something not every chemical sibling can claim. Models for this product often emphasize high purity, with material reaching 97% or greater, based on batch and source.
I’ve spent time working in analytical labs where shelves brimmed with plain anilines. The moment compounds like 4-bromo-3-fluoro-2-methylaniline arrived, demand quickly followed. A simple methyl group at the ortho position throws off electron density, switching up reactivity. Pair that with the electronegativity from fluorine and the bulkiness of bromine, you get a molecule that behaves quite differently from plain aniline or even single-substituted variants. This precise combination isn’t just for show. When it comes to planning organic syntheses, such as those involved in pharmaceutical research or material development, the choice of starting block matters. Muting or bumping reactivity in key areas often cuts down side products and improves yields. It’s here—between the lines of substitution patterns—that 4-bromo-3-fluoro-2-methylaniline steps forward and offers something new.
Other similar-sounding chemicals sometimes focus on a single halogen or methyl addition. Those products can be easier to obtain or more familiar, but they can’t always match the specificity or behavior that this trifecta brings. For researchers chasing after new kinase inhibitors or bioactive fragments, changing a single atom can mean the difference between a promising lead and a failed candidate. That experience is humbling, and why structure–activity relationships are more than just buzzwords.
This compound often ships as a solid, typically a crystalline powder, pale beige or tan by eye. Reliable sources provide melting points around 40–45°C, with chemical purity verified by NMR, HPLC, or GC. Moisture can cause headaches, so most labs keep it sealed and out of direct light. With the molecular weight close to 220 g/mol, it’s manageable for reaction scale-ups or small-batch screening.
From personal experience, measuring reactivity in aromatic substitution needs more than a casual glance at the reagent. Full characterization—including spectra and purity scans—builds trust, especially when a single impurity can trash downstream results. Users expect batch-to-batch consistency, not just in percentage points but in the feel of the product—granularity, solubility, and how quickly it dissolves in reaction solvents like dichloromethane or DMF. Failure to meet these benchmarks wastes resources and time that no research group can spare.
Over years in the lab, I’ve seen 4-bromo-3-fluoro-2-methylaniline open doors for med-chem teams. The molecule captures a niche for Suzuki-Miyaura couplings, Buchwald-Hartwig aminations, and other palladium-catalyzed cross-couplings. Its dual halogenation—the electron-pulling fluoro and the heavier bromo—provide two axes for selective transformations, making it a favorite for creating complex heteroaromatics.
Medicinal chemists appreciate the subtlety. The methyl group brings lipophilic character, often increasing membrane permeability when the derivative becomes part of a drug scaffold. The combination of bromine and fluorine serves not only as a handle for further chemistry but sometimes boosts pharmacological activity or metabolic stability. These are not idle considerations; they often show up in pre-clinical screening when a series of analogs gets tested side by side for selectivity, toxicity, or bioavailability.
From an industry view, purity in fine chemicals isn’t negotiable. Any researcher who has ruined a week’s work chasing a ghost impurity knows this all too well. Consistency in product quality lets synthetic chemists predict reaction conditions, avoid purification nightmares, and build on results with confidence. For 4-bromo-3-fluoro-2-methylaniline, trace amounts of closely related isomers or leftover reagents can spell disaster for peptide conjugation, biaryl synthesis, or specialty dye production.
Working with this chemical, every batch is handled with the same care as a rare resource. That means full transparency on certificates of analysis and clear communication on actual content—not marketing speak, but tabs on everything from moisture to trace metals. In sectors like pharmaceuticals or advanced materials, even a hint of inconsistency can cause whole projects to be rerun. That’s as real as it gets for companies or academics operating on tight budgets and tight deadlines.
The impact of 4-bromo-3-fluoro-2-methylaniline isn’t limited to a single sector. In pharmaceuticals, it helps synthesize new candidates for cancer therapy, central nervous system drugs, or anti-inflammatories. The fluorine atom offers more than just fun chemistry trivia. It changes how a molecule interacts with enzymes or fits into biological receptors, which can matter for potency, selectivity, and metabolic half-life.
Material chemists also find valuable uses. With electronics growing ever smaller, fine-tuned aromatic compounds help design specialty polymers and liquid crystals. A carefully placed methyl or halogen substitution can provide the thermal stability and solubility required for OLED displays or conductive films. If you ask people working in small-molecule LEDs or organic electronics labs, they’ll highlight just how much a single substitution can influence real-world performance.
Agrochemical researchers don’t ignore it either. Fine-tuning the substituents on aromatic rings can lead to herbicides or fungicides with improved activity and less environmental persistence. Some of the world’s most persistent crop protection agents began with an inspired tweak to an aniline core. This product gives those scientists one more arrow in the quiver as they search for safer, more targeted solutions.
Selecting 4-bromo-3-fluoro-2-methylaniline over more familiar compounds reflects a willingness to push boundaries. My years helping to troubleshoot stubborn reactions showed me that creative chemists look for leverage points. Sometimes, using a more elaborate building block reduces the need for tricky protecting group strategies. Stronger—and sometimes more delicate—reactivity profiles can make reaction planning easier, especially if time or money is tight.
Cost factors in, too. Specialty chemicals never come cheap, but the cost-to-benefit ratio shifts if the product saves significant hours at the synthesis bench, avoids redundant purification steps, or drives better outcomes in biological testing. Every project lead I’ve worked with weighs up-front price against the chance for more reproducible, higher-yielding chemistry downstream.
Buying chemicals, especially ones destined for next-generation drugs or electronics, calls for more than a blind purchase order. The strongest suppliers provide up-to-date batch records and let users trace back quality issues quickly. As a customer, I’ve found that the best relationships grow when companies listen to feedback on solubility quirks, packaging problems, or concerns about shelf stability.
Quality management systems matter. Labs that can show ISO-certified processes and regular internal audits inspire trust. That level of care stops bad batches in their tracks and lets end users focus on the science, not damage control. Even small-scale operations can keep meticulous records, giving researchers peace of mind when questions about trace impurities or bioactivity in context come up. Without trust between supplier and scientist, innovation stalls. My own projects have been delayed more than once by silence or a lack of data. For a compound as specialized as 4-bromo-3-fluoro-2-methylaniline, that kind of openness isn’t just nice to have—it’s a must.
If there’s one lesson from years at the bench, it’s that feedback makes products better. Early on, a lot of specialty chemical suppliers worked in isolated pockets, used to dealing mainly with bulk buyers or academic groups. Since then, it’s become clear that tighter collaboration between supplier and end-user can smooth over growing pains.
Sharing reaction outcomes and purification tips (without crossing into trade secrets) lets chemists sidestep obstacles that might have seemed unique but turn out to be common experience. That could look like technical data sheets with more than the basics—real-world example reactions, reports on solubility, or notes on common side reactions. Supply companies that reach out for regular user input and actually follow up set themselves apart. The lifeblood of modern chemistry, especially in competitive pharmaceutical or materials markets, is a willingness to adapt and problem-solve together.
Transparency is a practical solution to many pain points. If a company can communicate clearly about actual stock, lead times, transportation challenges, or regulatory shifts, customers can plan projects better. Losing time or project funding to unexpected delays is a reality for groups at all levels. Facing those challenges head-on—honestly and promptly—keeps both supplier and user on track, even when global events shake up raw materials or transportation lanes.
Laboratories preparing, handling, or disposing of halogenated aniline derivatives cannot ignore the environmental and health implications. Here’s where experience in regulated environments pays off. In every well-run lab, storage, labeling, and fume hood usage are non-negotiable. Proper PPE—gloves, goggles, and fitted coats—should top the checklist. Waste handling also warrants attention. Halogenated organic material demands special disposal protocols, never regular trash or general chemical waste. Agendas set by environmental, health, and safety officers may feel cumbersome, but they protect people and ecosystems from unnecessary risk.
From an environmental angle, it matters how the product is manufactured. Leading companies move toward greener processes—better atom economy, less hazardous solvents, and closed reaction systems. Simple changes, such as recovery and recycling of solvents, can reduce both environmental footprint and operating costs. Forward-looking procurement teams prefer sourcing from suppliers invested in cleaner chemistry, not only because it aligns with global responsibility but also because regulatory pressure is only moving in one direction. Rising awareness among customers only strengthens this shift.
No specialty chemical reaches the market without obstacles. For all its promise, 4-bromo-3-fluoro-2-methylaniline faces some of the same issues as other advanced reagents—cost, scale, availability of precursor chemicals, and ever-present regulatory hurdles. Often, labs working on small scale find themselves leapfrogging bottlenecks, only to run into trouble when demand for a promising new molecule spikes. Planning ahead for scale-up, securing stable sources, and building redundancy into the supply chain tend to pay dividends in these moments.
Smart procurement proves invaluable in a crisis. During the global supply chain disruptions of the past few years, researchers and companies who spread their purchasing between multiple sources or kept an eye on lead times came out ahead. This isn’t just a lesson for purchasing managers. For bench-level scientists, knowing the vulnerabilities in one’s supply chain can help plan better experiments, guard against wasted effort, and stay ahead of disruptions.
Ethics aren’t just for policy documents. Scientists, suppliers, and end-users each have a role in preventing misuse or diversion of advanced intermediates. As regulatory agencies examine more closely not only what’s made but also how and where, traceability systems become critical. Laboratories are adjusting to this reality by implementing better record-keeping, adjusting security protocols, and openly discussing best practices for preventing chemical misuse. This isn’t alarmism; it’s a realistic response to new regulations and higher expectations from both the scientific community and the public.
Credibility grows from a culture of sharing—not just through published papers, but by letting emerging researchers and students get their hands dirty with real, challenging molecules. Mentorship programs and open forums for troubleshooting difficult syntheses can accelerate the start of many careers. Access to up-to-date, accurate information about reagents like 4-bromo-3-fluoro-2-methylaniline gives the next wave of chemists a running start.
Supplier-led workshops, hands-on seminars, and collaborative networks bridge gaps that used to slow progress. The pace of chemical synthesis innovation is driven as much by community as by any one breakthrough compound. After years working at the intersection of academia and industry, the value of curiosity—fueled by transparent data and real-world feedback—continues to prove its worth.
Whether you’re working on the next life-saving drug, tackling frontier electronics, or developing smarter crop protection, the difference between success and a dead-end often comes down to having the right tools. 4-bromo-3-fluoro-2-methylaniline stands as more than just another chemical. It brings new options to the table, supporting innovation from early idea to product launch. People who use it—scientists, engineers, and quality managers alike—share a common need: reliability, transparency, and true partnership with their suppliers.
From my own vantage in the lab trenches, nothing replaces the foundation laid by solid communication, consistent quality, and a shared commitment to moving science forward. As new challenges come into view, the role of advanced building blocks like 4-bromo-3-fluoro-2-methylaniline will only grow. It’s not about complexity for its own sake, but about meeting progress with the right tools—ready for whatever tomorrow brings.