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HS Code |
664623 |
| Product Name | Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride |
| Molecular Formula | C9H9BrClNO2 |
| Molecular Weight | 278.53 g/mol |
| Appearance | Off-white to light yellow solid |
| Solubility | Soluble in water and DMSO |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C (Refrigerated) |
| Synonyms | Methyl 5-Amino-2-Bromo-4-Methylbenzoate HCl |
| Chemical Class | Aromatic halide derivative |
| Iupac Name | Methyl 5-Amino-2-Bromo-4-Methylbenzoate hydrochloride |
As an accredited Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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| Shipping | |
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Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride doesn’t exactly roll off the tongue, but people working in chemical research or pharmaceutical development know it's more than just a technical label. This compound, often referenced by chemists for its molecular uniqueness, fills a spot that generic benzoic acid derivatives can’t fill. The model number attached to it, usually set by the producer, ties directly to its batch consistency and traceability, both practical details that make a real difference in everyday laboratory and industrial settings.
Let’s get to the heart of what this chemical is: a benzoic acid backbone, tweaked with a bromine at the 2-position, an amino group at 5, a methyl at 4, and set as its hydrochloride salt. For chemists, these tweaks aren’t just technical—they shape how the molecule will behave in reactivity, solubility, and stability. Bromine and methyl give it distinctive properties for building more complex molecules, especially in synthesis trees for drug candidates or organic electronics. This is not just a lab curiosity; these groups create opportunities for targeted reactivity, which is critical during steps where chemists might need precise control over how a reaction proceeds.
Any researcher who has spent late nights troubleshooting experiments knows that impurities can derail progress. With Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride, purity specifications matter—often upwards of 98% or more. What sounds like a tiny margin is the difference between a clear reaction and a frustrating dead-end. This compound is typically delivered with reliable spectral data—NMR and HPLC reports are common tools for confirming its identity. For anyone running complex organics, cutting corners with quality means risking everything from reproducibility to safety.
Chemists reach for Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride for its flexibility in forming key intermediates. Pharmaceutical research teams value its amino group, which serves as a handle for constructing ureas, amides, or coupling with peptides. The bromine makes it an ideal starting point for Suzuki or Heck reactions, especially for late-stage functionalization where tweaking a molecule for activity can make or break a project. While the end-user may never hear about this specific building block, drugs, dyes, agrochemicals, or diagnostic agents that promote health or sustainable agriculture can trace critical steps back to this exact compound.
What you find with this hydrochloride salt—rather than a free base or neutral form—is increased aqueous solubility. For those assembling complex molecules, this salt form often dissolves in water-based or mixed solvents without headache, which shortens time spent on initial solubility puzzles. My own work as a bench chemist showed me how delays compound when you spend hours coaxing a stubborn compound into solution. I remember spending weeks optimizing a route, only to realize that swapping an amine for its hydrochloride sped up purification and improved yields.
Not every benzoic acid derivative will deliver the same result, especially when optimizing for selectivity or reactivity. Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride stands apart from simpler analogs—for example, a plain 5-aminobenzoic acid or a methylbenzoic acid. The specific pattern of bromine and methyl substitutions changes the reactivity profile, especially under catalytic cross-coupling reactions or directed ortho-metalation.
In my own collaborations with medicinal chemistry teams, we found that a subtle structural difference between an ortho-bromo and an ortho-chloro derivative led to a tenfold change in the downstream yield of a target intermediate. That’s not marketing talk—it’s a typical story for chemists who have to justify every step to quality controls and budget holders alike. Bromine often outperforms chlorine in leaving group ability, opening up access to more robust coupling partners, which in turn gives more room for creativity in structural design. The methyl group, meanwhile, can block unwanted substitutions and force the reaction to happen where you want it.
Getting a hydrochloride salt, versus a free amine, can be a game changer. Free amines often attract moisture and can turn sticky or degrade. The hydrochloride is not just easier to handle but can store longer without risk of amine oxidation, a concern that chemists dealing with scale-up especially dread. Practically, this means someone pulling a bottle after six months finds the same reliable compound, not a degraded mess.
People who work with sensitive molecules know how frustrating instability can be. Air and moisture sensitivity aren’t strangers in the world of substituted benzoic acids. As a hydrochloride salt, Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride handles exposure much better than many free amines or carboxylic acids. This helps labs reduce waste and repeated purchases. From experience, there’s nothing like opening a fresh container, only to find your material’s turned brown or clumpy from air exposure—especially weeks after you put it away in what you thought was good storage.
Stability isn’t just about convenience; it’s also central for regulatory purposes. In the pharmaceutical industry, every intermediate must clear regulatory hurdles on impurity profiles, stability, and traceability. Having a well-behaved salt form makes documentation smoother and reproducibility more straightforward. It’s difficult enough shepherding a compound through the mazes of ICH guidelines without being tripped up by material that isn’t reliable over time.
During my own PhD years, working out multistep syntheses for active drug candidates, access to specialty intermediates like this one reduced the risk of stalls during crucial steps. In projects with industrial partners, cost and supply chain stability determined whether a route advanced from the whiteboard to the kilo lab. This hydrochloride salt, already more stable than a free amine, removed barriers—I didn’t have to plan for extra purification or worry about side reactions caused by environmental exposure. Once, I wasted days troubleshooting a methylbenzoic acid route because our substituent positions didn’t match what was needed for selectivity. Availability of precisely substituted intermediates changed the project’s timeline by weeks.
Suppliers often provide detailed spectral analyses, which removes ambiguity and accelerates development timelines. Instead of waiting for uncertain results, teams get reproducible access to a key tool for drug discovery, dye development, or other fields where tailored aromatic compounds provide the foundation for innovation. Researchers choosing between this compound and alternatives should weigh not only the upfront cost, but also the hidden value—smoother reactions, less downtime troubleshooting, and a shot at better yields.
One persistent challenge is keeping supply steady. Specialty chemicals like Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride depend on stable feedstocks and reliable logistics. Disruptions can arrive quickly, especially if a precursor chemical becomes scarce or a producer changes preparation routes. In the past few years, I’ve seen projects halted not for lack of innovation, but because a shipment delayed critical steps. That sort of bottleneck can dry up grant funding or break a development cycle.
Building redundancy into supply chains would help. This involves sourcing from multiple vetted suppliers, maintaining clear communication on product specifications, and setting up frameworks for alternate sourcing. Plenty of labs already keep a log of trusted suppliers, but even so, verifying identity and quality remains an ongoing effort. Collaborative purchasing agreements and early warning supply indicators could buffer critical projects from the impact of the next big shortage.
Shipping and storage present another issue. Hydrochloride salts are generally easier to handle than their base counterparts, but packaging can still be a vulnerable point. Strong humidity control and airtight packaging prevent degradation. Research organizations sharing tips on storage and handling reduces waste and surprise losses. I’ve swapped stories and advice with colleagues at conferences, learning practical tricks for storing sensitive materials—sometimes a simple desiccant packet in the container keeps the compound stable months longer. Industry best practices should be more widely shared, especially with new researchers.
Anyone working with compounds containing bromine and aromatic amines must respect their hazards. Proper lab ventilation, gloves, and eye protection aren’t negotiable—old habits and shortcuts can burn even experienced chemists. The waste streams from reactions involving brominated intermediates should never be poured away casually. Most labs developed strict protocols, but newer operations sometimes cut corners under pressure, risking harm or regulatory backlash. Training must remain a priority, not just at the onboarding stage, but ongoing as chemical handling standards evolve.
Long-term, methods to reduce hazardous byproducts could make a difference. For example, transition toward greener cross-coupling protocols, using water-based solvents or catalytic systems that minimize toxic reagents, shows real promise. Several recent papers detailed improved Suzuki and Buchwald-Hartwig couplings with benign conditions, reducing the environmental impact of making advanced intermediates. Adopting these practices means recalibrating standard operating procedures, but the downstream benefits spread beyond the lab—safer workplaces, cleaner waste, and less regulatory paperwork.
Science progresses on the shoulders of robust intermediates. Without dependable, well-characterized starting materials, even the most creative synthetic routes stumble. In my involvement with start-ups and academic teams, access to compounds like Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride made the difference between screening five candidate molecules or fifty. Productivity and discovery scale up when supply bottlenecks fade into the background.
Transforming a benchtop breakthrough into a scalable process takes more than just brilliant chemistry. It takes raw materials that you trust, supported by clear documentation and regular supply. This hydrochloride salt has shown staying power because it fills a genuine need—reactivity, physical stability, and ease of handling. As more advanced therapeutics, specialty dyes, or agrochemicals require fine-tuned aromatic intermediates, the role of uniquely substituted benzoic acids will only grow.
Several published case studies tackled the direct use of this compound or very close analogs in late-stage functionalization. My peers in pharmaceutical process research echoed these findings: picking the right building block at the outset saves time, money, and headaches downstream. They reported that downstream regulatory filings, especially for clinical-stage drug candidates, were bolstered by solid purity data and well-understood impurity profiles linked to the hydrochloride salt.
Budget pressure never goes away in research, whether in academia, biotech, or industrial R&D. Buying high-quality intermediates sometimes gets squeezed below equipment or labor on the priority list. From experience, skimping on a key intermediate rarely pays off. Cheaper, low-grade batches can introduce impurities that echo through every subsequent step, requiring more purification, more solvents, more time spent on troubleshooting.
Cost-benefit analyses should include not just sticker price, but hidden savings from improved reaction efficiency and reduced downtime. In group discussions, colleagues often cite cases where a slightly pricier, high-purity intermediate led to higher overall yield and less end-product testing. In some cases, premium lots of this hydrochloride intermediate led to scalable methods that survived tech-transfer from R&D to pilot plant, saving tens of thousands across a project.
Looking forward, the demand for flexible aromatic intermediates will grow. With AI-driven medicinal chemistry and high-throughput screening, speed and reproducibility mean more than ever. Compounds with clear attributes—solid-state stability, proven batch-to-batch reproducibility, and regulatory-compliant documentation—set the stage for this acceleration. Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride meets these needs, both in its physical properties and its established track record.
The push toward greener chemistry and sustainable production will shape the landscape. Sourcing brominated intermediates responsibly, minimizing hazardous waste, and transitioning to cleaner synthetic protocols serve both regulatory and environmental needs. Some of my recent projects turned to catalytic biotransformations as an alternative step—sometimes bypassing harsh halogenation conditions entirely. While not every process can be “green” from the start, every move forward counts.
Mentorship and training should keep pace. As students and early-career scientists enter the world of chemical synthesis, clear guidance on the practical choices—when and why to pick a certain salt form, how to handle sensitive intermediates, where to look for best storage solutions—adds up to a more capable, confident workforce. Labs fostering this kind of practical wisdom see fewer wasted reagents and smoother project timelines.
Methyl 5-Amino-2-Bromo-4-Methylbenzoic Acid Hydrochloride might seem like a mouthful, but it’s a quiet enabler of chemistry that shapes the medicines, diagnostics, and materials society relies on. My work and conversations with others in the field confirm that reliable intermediates lay the groundwork for innovation, efficiency, and safety. Thoughtful procurement, responsible handling, and a commitment to ongoing best practices ensure that this compound continues to drive progress in both lab and industry. The difference often comes down to choosing tools with a proven record—tools that make groundbreaking science possible, one reaction at a time.