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5-Bromo-2-Hydroxyphenylacetic Acid

    • Product Name 5-Bromo-2-Hydroxyphenylacetic Acid
    • Alias Bromosalicylacetic acid
    • Einecs 618-912-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    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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    Application of 5-Bromo-2-Hydroxyphenylacetic Acid

    Applications of 5-Bromo-2-Hydroxyphenylacetic Acid in Industrial Manufacturing

    5-Bromo-2-hydroxyphenylacetic acid is a specialty intermediate valued throughout several industrial chemical production chains. Our integrated manufacturing process ensures strict material traceability and meets stringent quality controls at each production stage. The following sections detail practical industrial applications substantiated by regulatory standards and real-world usage requirements.

    1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug (NSAID) Synthesis

    Our 5-bromo-2-hydroxyphenylacetic acid supports the scale manufacturing of key NSAID active pharmaceutical ingredients. It reacts in aromatic substitution and coupling steps, forming functionalized intermediates such as phenylacetic acid derivatives. Chemical process engineers implement our material in multi-step API syntheses, maintaining careful control of impurity profiles and consistent particle size distribution for API crystallization. Production lines adjust batch parameters based on real-time chromatographic purity monitoring, ensuring efficiency while meeting regulatory quality milestones.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <1078> Good Manufacturing Practices for Bulk Pharmaceutical Excipients
    • EDQM Certificate of Suitability (CEP) relating to starting materials
    • FDA 21 CFR Part 210, 211 (Subpart B, Subpart F)

    Typical usage ratio

    • 1.0–2.5 molar equivalents per API batch, as determined by target substitution degree and downstream impurity control

    Downstream process integration

    • Direct charge into the aromatic functionalization reactor after solvent exchange and in-line filtration
    • Integration before carboxyl protection or activation steps in multi-stage synthesis
    • Purification monitored via HPLC before coupling to later-stage intermediates

    Final product types

    • Ketoprofen and related anti-inflammatory APIs
    • Custom non-steroidal anti-inflammatory intermediates (CMO/CDMO projects)
    • Co-crystal form pharmaceutical actives

    2. Agrochemical Synthesis: Herbicide and Fungicide Intermediate

    Specialty agrochemical manufacturers use 5-bromo-2-hydroxyphenylacetic acid as a controlled precursor for the selective synthesis of new-generation herbicides and fungicides. By introducing both bromo and hydroxy substituents, this material supports molecular modifications that improve target spectrum, environmental persistence, and crop safety. Custom process lines specify strictly defined input ratios, since deviations influence purity and field performance. Trace metal analysis and batch homogeneity testing regularly accompany each consignment for regulatory records.

    Industry compliance standards

    • FAO/WHO Guidelines on Pesticide Specification & Quality Control
    • ISO 9001:2015 Quality Management Systems for Fine Chemicals
    • REACH Regulation (EC) No 1907/2006 as a registered chemical intermediate
    • National agrochemical registries (EPA, EU, China ICAMA)

    Typical usage ratio

    • 7–15% w/w in active ingredient conversion batches, with adjustment based on target molecule and field application profile

    Downstream process integration

    • Introducted in-phase for bromination or esterification reactors ahead of bioactivity group addition
    • Pre-treated to remove phenolic impurities for selected active ingredient lines

    Final product types

    • Herbicidal active agents containing bromo-phenylacetic acid substructures
    • Fungicidal seed treatment compounds
    • Intermediate concentrates for liquid formulation packaging

    3. Specialty Dye and Pigment Manufacturing

    Colorant producers incorporate our 5-bromo-2-hydroxyphenylacetic acid to achieve specific chromophore modifications in specialty dyes and organic pigments. The unique substitution pattern enables the creation of color-stable, light-fast molecules suitable for high-performance textile and ink applications. Formulators optimize the input of this intermediate depending on desired absorbance profiles and target hue. Laboratory-qualified lots supply pilot and commercial production, maintained under rigid contaminant controls to avoid adverse color shifts.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemical inputs
    • EN 71-3 Safety of Toys – Migration of Certain Elements, for pigment use
    • ISO 105-A05 Textiles – Tests for Colour Fastness
    • European Printing Ink Association (EuPIA) guidelines for ink raw materials

    Typical usage ratio

    • 2–8% by mass, determined by target pigment molecule and solvent matrix used

    Downstream process integration

    • Charged to primary synthesis vessel for controlled coupling reactions
    • Used in late-stage diazonium chemistry to set color depth and shade

    Final product types

    • Reactive and direct textile dyes
    • Organic pigments for specialty inks and coatings
    • High-stability printing ink concentrates

    4. Laboratory Reagent and Analytical Standards Production

    Accredited laboratories and standards producers select our 5-bromo-2-hydroxyphenylacetic acid for the manufacture of analytical reference materials and certified calibration standards. The traceable high-purity lots undergo validated quality control protocols, including NMR, HPLC, and GC analysis. Material purity and batch consistency are documented in Certificates of Analysis supplied with each shipment for auditing and laboratory accreditation needs.

    Industry compliance standards

    • ISO 17034:2016 General Requirements for Reference Material Producers
    • ISO/IEC 17025:2017 for testing and calibration laboratory chemicals
    • Traceability requirements of NIST guidelines
    • National pharmacopoeia reference standards handling (e.g., USP-NF, EP)

    Typical usage ratio

    • Variable, typically 0.5–5 mg per analytical preparation; determined by calibration batch size and method sensitivity

    Downstream process integration

    • Precision weighing and dissolution prior to gravimetric or solution calibration standard formulation
    • Final solution or solid reference material formatting, sealed for analytical lab distribution

    Final product types

    • Chemical analytical standards for QC and research
    • Certified reference materials for method calibration
    • Trace impurity checks in food, environmental, or pharmaceutical laboratories
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    Certification & Compliance
    More Introduction

    Introducing 5-Bromo-2-Hydroxyphenylacetic Acid: Practical Applications and Why It Matters

    Understanding the Compound

    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.

    Why Specifications Matter to Chemists

    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.

    Practical Applications and Real-World Use

    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.

    Differences from Other Phenylacetic Acids

    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.

    Quality, Transparency, and Laboratory Experience

    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.

    Environmental Health and Sustainable Sourcing

    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.

    Addressing Supply Chain Challenges

    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.

    Solutions and Future Directions

    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.

    Looking Beyond the Lab

    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.

    Personal Reflections and the Value of Experience

    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.

    Conclusion: Moving Science Forward, One Molecule at a Time

    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.