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HS Code |
277577 |
| Chemical Name | 5-Bromo-2-hydroxyphenylacetic acid |
| Molecular Formula | C8H7BrO3 |
| Molecular Weight | 231.05 g/mol |
| Cas Number | 37289-50-8 |
| Appearance | White to off-white powder |
| Melting Point | 150-154°C |
| Solubility | Soluble in DMSO and ethanol |
| Purity | Typically ≥98% |
| Synonyms | 5-Bromo-2-hydroxybenzeneacetic acid |
| Storage Conditions | Store at 2-8°C, protected from light |
| Smiles | C1=CC(=C(C=C1Br)O)CC(=O)O |
As an accredited 5-Bromo-2-Hydroxyphenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Anyone who’s spent time in a chemistry lab knows the importance of reliable reagents. 5-Bromo-2-hydroxyphenylacetic acid has gained a strong following among researchers for good reason. As an organic molecule with a bromine atom at the 5-position, a hydroxy group on the 2-position, and acetic acid as a side arm, this compound fits neatly into both academic and industrial research settings. Its chemical formula, C8H7BrO3, might seem simple on paper, but that specific structure unlocks a surprising amount of utility on the bench and beyond.
What people value about this acid comes from its reactivity and versatility. The presence of both bromine and hydroxy functional groups opens pathways for further modifications—something organic chemists don’t take for granted. Whether building more complex molecules or testing specific reactions, this compound acts as both a useful intermediate and a stepping stone to bigger projects. With purity frequently exceeding 98%, researchers don’t worry about excess impurities muddying their results. Recent quality control advances also mean that reproducibility from one batch to the next rarely becomes a concern.
Let’s cut through the usual technical jargon for a moment. Everyone wants a compound that does its job and doesn’t get in the way of progress. For years, inconsistent sourcing led to setbacks—one lab’s version of 5-Bromo-2-hydroxyphenylacetic acid could differ from the next in purity, physical properties, and unwanted side products. Today’s reputable suppliers have turned this around. Melting points tend to hover around 136-139°C, and products arrive in a stable, free-flowing powder—manageable and easy to measure. Solubility in polar aprotic solvents like DMF and DMSO means broader options for direct use in syntheses, decreasing the time spent laboring over stock solution prep.
If you’ve ever had to troubleshoot a stalled or messy synthesis, you know where poor characterization leads. High-purity 5-Bromo-2-hydroxyphenylacetic acid now comes with spectra verified by NMR, IR, and HPLC reports. There’s nothing like running a reaction with the confidence that your starting material matches the literature. It beats the uncertainty that older, less rigorous production standards sometimes brought. Reliable specifications might not make headlines, but they let complex research keep moving forward without avoidable delays.
This compound doesn’t just sit on the shelf. Ask professionals in medicinal chemistry, and many can point to instances where small changes made a world of difference in their drug development efforts. 5-Bromo-2-hydroxyphenylacetic acid often serves as an intermediate for synthesizing bioactive molecules—think pharmaceutical candidates, antimicrobial agents, or inhibitors tested in the earliest stages of discovery. That extra bromine provides a handle for Suzuki or Buchwald couplings, which expands the pool of possible analogues. Modestly adjusting the structure, then running through SAR (structure-activity relationship) cycles, lets chemists map how minute tweaks affect biological function.
Chemical biology and material science also benefit from this compound’s profile. In one project, a collaborative team set out to modify hydroxyphenylacetic acid derivatives to probe enzyme selectivity. Swapping out other substituents for bromine changed binding affinity in ways models didn’t fully predict. This ability to tune the molecule—thanks to selective reactivity—provided critical info for follow-up studies. Similarly, the carboxylic acid group acts as an anchor for attaching the molecule to resins or surfaces, creating tools for affinity purification or sensor platforms. These ideas take shape in academic settings, but real-world advances in diagnostics and industrial biotechnology often build from these early studies.
Not every lab uses chemistry for new product development. Environmental researchers sometimes need marker compounds for tracking reactions in water or soil, while analytical chemists run reference standards to validate their methods or calibrate instruments. Stable and well-defined materials like 5-Bromo-2-hydroxyphenylacetic acid enable both these activities. Trace analysis requires predictable response factors, and labs working on method validation gain peace of mind when relying on thoroughly characterized batches.
It’s easy to look at this compound and lump it in with the family of phenylacetic acids, but the substitution pattern changes a lot. Classic phenylacetic acid, the parent compound, lacks both the bromine and the hydroxy group. Those additions matter. The bromine atom makes the molecule heavier, often increases lipophilicity, and provides a unique point for further functionalization, especially in cross-coupling chemistry. On top of that, the hydroxy group can engage in hydrogen bonding or serve as a site for additional modification—either via etherification, esterification, or directed ortho metalation reactions. Let’s not forget that these features shift acidity, solubility profiles, and even melting points compared to basic phenylacetic acid.
Making direct substitutions in drug discovery pipelines also tells a story. Some analogues resist metabolism better or enter cells more readily based on these small differences. The market offers halogenated, methoxylated, or other substituted phenylacetic acids, but 5-bromo-2-hydroxy stands out for applications that demand dual reactivity on the ring—both as an electrophilic and nucleophilic site. In practice, chemists appreciate the broader selection because each derivative presents new opportunities and challenges. Still, this compound consistently appears in literature for robust reasons: it balances ease of use with transformative value in synthetic schemes.
No one wants to gamble lab time or research budgets on unreliable chemicals. Skimping on reagent grade causes more harm than any perceived savings could offset. Early in my own training, I watched projects stretch on for weeks as we puzzled through unexplained impurities—each traced back to inconsistent sourcing. Repeat that experience a few times, and you start to recognize the real value in transparency from suppliers. Today, trusted sources share comprehensive analytical data, including batch-specific NMR, mass spectrometry, and HPLC traces. This practice lowers the risk of hidden surprises and gives teams the freedom to focus on what they do best—innovating and solving real-world problems.
In my own casework, the jump to higher-grade compounds like 5-Bromo-2-hydroxyphenylacetic acid paid dividends. Synthetic sequences ran cleaner, purification steps needed less iteration, and downstream biological testing yielded results that matched expectations. These benefits weren’t magic—they came from a solid foundation where each reagent met or exceeded published standards. Every team member, from benchtop chemist to principal investigator, breathes a little easier knowing overnight reactions won’t go awry due to unexpected side products.
The modern lab also cares about more than just cost and performance. Environmental responsibility and resource management can’t feel like afterthoughts anymore. Traditional production routes for complex organics sometimes relied on harsh conditions or generated non-trivial amounts of waste. Recent regulatory shifts and green chemistry initiatives have pushed many producers to adopt cleaner synthesis strategies. Labs now expect transparent disclosure on residual solvents, waste minimization steps, and safe transport. It’s promising to see how some suppliers openly discuss their eco-friendly approaches, like using solvent recycling and adopting catalytic rather than stoichiometric halogenation methods. These shifts reduce the overall impact, align with global environmental goals, and reflect the values many scientists hold personally as well as professionally.
Eco-conscious sourcing isn’t just a matter for grant proposals either. Some funding agencies scrutinize procurement policies or require documentation that chemicals originate from responsible suppliers. Choosing high-quality 5-Bromo-2-hydroxyphenylacetic acid from ethical sources demonstrates commitment not only to research integrity but to the safety and health of both lab staff and the wider community. Responsible disposal practices matter just as much; knowing the upstream supply chain reduces headaches when it comes to waste management and compliance down the road.
No discussion about laboratory chemicals feels complete without touching on the realities of global supply chains. Scientists in both academic and industrial settings have felt the sting of delays, unpredictable lead times, and shifting regulatory requirements. Certain reagents, especially those not produced in massive quantities, faced shortages during recent years. 5-Bromo-2-hydroxyphenylacetic acid, being somewhat specialized, experienced these fluctuations. Forward-thinking suppliers responded by expanding local inventory, investing in small-scale custom synthesis, or partnering with secondary manufacturers to bridge any gaps. Lab managers now diversify their sources to hedge against future disruptions.
From my conversations with purchasing agents and bench scientists, many now track the origins and traceability of their orders more closely than ever before. Barcode scanning, batch serialization, and transparent returns policies all help keep research moving when the unexpected happens. Suppliers competing for loyal business now prioritize customer service, speedy tech support, and rapid document turnaround. What once seemed like distant logistical issues now land squarely on the research team’s plate. The days of assuming every bottle arrives on time, every time, have passed. Open communication and early planning play bigger roles than ever in successful project management. As labs adapt and become more resilient, the whole research landscape benefits.
Tackling the challenges that surround specialty reagents like 5-Bromo-2-hydroxyphenylacetic acid calls for a coordinated approach. Investing in supplier relationships stands tall on the list; those who build trust both ways—consistent quality, rapid resolution of concerns, and proactive logistical support—form partnerships that weather market bumps. Some research teams support ongoing education, keeping staff updated on the latest synthesis methodologies, analytical techniques, and green chemistry advances relevant to their favorite building blocks. This investment pays off through better experiment design, faster troubleshooting, and higher success rates over time.
Technology also moves the needle. Automated inventory management and forecasting software help labs predict future needs, cutting down on last-minute scrambles. Real-time access to technical documents and certificates of analysis give teams information they can rely on. A few years ago, searching for that latest spectral comparison felt like a slow crawl through digital archives; now, direct links or even QR codes speed up access to critical data. So much of this progress reflects conversations between scientists and suppliers—real feedback, user surveys, and partnerships working together. Collaboration replaces the old one-way street and results in tangible improvements for all involved.
For newcomers, the search for meaning behind each reagent sometimes feels overwhelming. In talking with friends just entering graduate programs, I often share how even seemingly small products play outsized roles in larger scientific stories. 5-Bromo-2-hydroxyphenylacetic acid, in particular, shows up far beyond the immediate reaction flask. Its modifications influence what medicines reach patients, what tools reach diagnostics labs, and even how we monitor environmental contaminants. Every high-quality molecule sent from a supplier becomes part of a chain that stretches across fields, continents, and decades of discovery. Recognizing this depth keeps research grounded and highlights just how interconnected the modern scientific enterprise remains.
Calls continue for improvements at every step—from more sustainable sourcing to robust local support. Researchers step up, too, by sharing their own findings and pitfalls, fostering stronger community standards and sharper quality expectations. Those choosing and using biochemicals shoulder a responsibility that goes beyond today’s results. The choices made in procurement ripple into tomorrow’s breakthroughs, shaping toolkits not just for one lab, but for the scientific workforce as a whole. Thoughtful selection, transparent communication, and ongoing education create the conditions for both progress and trust.
Through years at the bench, what stands out about reliable reagents isn’t just getting clean yields or matching analytical scans. It’s the way dependable supplies free teams to ask deeper questions. Each time a new graduate student pulls a clean vial, runs a textbook reaction, and gets exactly what’s promised on the label, they build the confidence needed for bolder designs and riskier pathways. Every veteran scientist who’s wrestled with contaminants or uncertain origins knows the extra value of that peace of mind. Over time, those shared stories turn into a culture of best practices—a living knowledge base guiding tomorrow’s researchers.
Conversations with university colleagues and industry friends always loop back to basics: clean starting materials, open technical dialogue, and a willingness to learn from each mistake. Whether scaling up for pilot production or troubleshooting a puzzling transformation, these foundations matter. Lab work becomes less about troubleshooting avoidable disasters and more about leaning into real innovation. 5-Bromo-2-hydroxyphenylacetic acid, with its unique functional groups and proven track record, slots neatly into this pattern. Its value lies not only in the product itself but in the trust, transparency, and shared expertise built around its use.
Research doesn’t thrive on shortcuts, and progress comes from making careful decisions at every point. 5-Bromo-2-hydroxyphenylacetic acid might never land a spot in mainstream headlines, yet its presence echoes through countless scientific advances each year. Its structure, properties, and the lessons learned from its use all reflect the best of modern laboratory practice—care, precision, and a commitment to improvement at every level. By choosing carefully, staying informed, and demanding both quality and transparency, today’s researchers can turn complex challenges into new opportunities for discovery. That’s the real story behind any great chemical reagent: reliability, backstopped by genuine expertise and a community of people who see more than just a name on a label.