|
HS Code |
515619 |
| Chemicalname | m-Hydroxyphenylacetic Acid |
| Casnumber | 621-37-4 |
| Molecularformula | C8H8O3 |
| Molecularweight | 152.15 |
| Synonyms | 3-Hydroxyphenylacetic acid |
| Appearance | White to off-white powder |
| Meltingpoint | 143-146°C |
| Boilingpoint | 360.6°C at 760 mmHg |
| Solubility | Soluble in water, ethanol, and ether |
| Density | 1.346 g/cm3 |
| Pka | 4.14 |
| Smiles | OC(=O)CC1=CC(=CC=C1)O |
| Inchi | InChI=1S/C8H8O3/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11) |
As an accredited m-Hydroxyphenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, opaque plastic bottle containing 100 grams of m-Hydroxyphenylacetic Acid, sealed with a screw cap and labeled with hazard warnings. |
| Shipping | **m-Hydroxyphenylacetic Acid** should be shipped in tightly sealed containers, protected from moisture and light. It must be clearly labeled, packaged according to applicable chemical transport regulations, and handled as a non-hazardous organic acid. Appropriate documentation should accompany the shipment, and temperature extremes should be avoided during transit to maintain product integrity. |
| Storage | m-Hydroxyphenylacetic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect it from moisture and direct sunlight. Clearly label the storage container. Keep it in a designated chemical storage cabinet, ideally under controlled temperature and humidity conditions. Use proper safety practices during handling. |
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Purity 99%: m-Hydroxyphenylacetic Acid with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures consistent product quality and yield. Melting Point 109°C: m-Hydroxyphenylacetic Acid with a melting point of 109°C is applied in chemical research, where stable handling and accurate recrystallization are required. Particle Size <100 µm: m-Hydroxyphenylacetic Acid with particle size less than 100 µm is used in fine chemical production, where high surface area improves reactivity and dissolution rates. Stability Temperature up to 120°C: m-Hydroxyphenylacetic Acid with stability up to 120°C is utilized in high-temperature syntheses, where thermal integrity is critical for process reliability. Water Content <0.5%: m-Hydroxyphenylacetic Acid with water content below 0.5% is employed in moisture-sensitive applications, where low hygroscopicity maintains reagent performance. HPLC Assay ≥99%: m-Hydroxyphenylacetic Acid with HPLC assay greater than or equal to 99% is used in analytical standards production, where high analytical accuracy is necessary. |
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My career in the chemical industry has taught me that every compound lining the shelves of a laboratory comes with distinct possibilities and challenges. m-Hydroxyphenylacetic acid, or 3-hydroxyphenylacetic acid, grabs attention not because of hype, but because its clear-cut advantages fill real scientific and manufacturing needs. Scientists and process engineers often seek compounds that punch above their molecular weight, and this acid deserves space in that conversation.
Many phenylacetic acid derivatives get used in labs, from pharmaceuticals to polymers. m-Hydroxyphenylacetic steps out with a unique twist: that meta-positioned hydroxyl group. Anyone spending time synthesizing molecules quickly finds that position on the ring changes reactivity and solubility in ways textbooks can’t always predict. In batches I’ve worked with, this particular structure sometimes allows for smoother reactions, especially when coupling or derivatizing for active pharmaceutical ingredients or specialty monomers.
Beyond structure, actual physical characteristics matter hugely in practical settings. The crystalline white powder melts at a point convenient for most benchtop reactions and dissolves with less coaxing in polar solvents. This means less energy—and less frustration—when it comes to cleanup or downstream processing. Time and again, users report that this compound doesn’t introduce unpredictability into their process streams. It becomes a reliable cog in complex project workflows.
I’ve handled enough batches to see that not every supplier achieves reproducible quality. m-Hydroxyphenylacetic acid tends to arrive with a purity level meeting or exceeding 98 percent by HPLC, a solid standard for organic synthesis. Color and odor give clear hints if impurities sneak in, and this acid holds its clean appearance and faint aromatic signal, indicating fewer side products or decomposition. Shelf stability also stands out, so returns on investment come not just from the first project, but from staying ready between sprint uses. Reaction runs with this compound, whether for research or semi-scale-up, show consistent conversion rates and predictable product profiles, smoothing the road for scale-up efforts.
Every chemist has a drawer of related acids and esters. In the context of m-Hydroxyphenylacetic acid, certain points come up in bench conversations, especially when compared to para-substituted analogs or unsubstituted phenylacetic acid. Solubility differences in water and organic solvents count for a lot—with the meta-substitution, blending solvents for analytical or preparative work becomes less of a trial-and-error slog. If you’re troubleshooting late-stage reactions, the lower tendency to form unwanted by-products supports easier purification, whether by recrystallization or chromatography.
For those wondering if this molecule reshapes outcomes in formulation or synthesis, the answer lies in context. Some pharmaceuticals need that specific meta-hydroxy group for activity or metabolic profile. In materials science, the group lends different hydrogen bonding possibilities, which subtly changes polymer backbones or small molecule additives. I’ve watched scientists discover that changing from para to meta placement alters final product qualities enough to make or break a commercial process or patent application.
Years in the research trenches shape a certain skepticism, but m-Hydroxyphenylacetic acid’s real-world uses put much of that skepticism to rest. Drug discovery often leans heavily on benzene derivatives, and this acid features in synthetic pipelines for multiple therapeutic candidates. Its structure makes it a good intermediate for the synthesis of non-steroidal anti-inflammatory drugs and various central nervous system agents.
I’ve also seen m-Hydroxyphenylacetic acid used on the formulation side, where it acts as a building block for more complex molecules, especially those targeting chiral centers or specific steric configurations. Microbial biotransformation studies use this compound as a substrate—researchers track how different species metabolize modified acetic acids, potentially leading to new enzyme discovery or more efficient production strains.
Polymer chemists have picked up this acid for specialty resins and adhesives. Its meta-hydroxyl group encourages hydrogen bonding and influences cross-link density, giving the resulting polymers a different set of mechanical and thermal properties than their para- or ortho-analog counterparts. An industry technician once told me they picked m-Hydroxyphenylacetic over the para form simply because product shelf-life at their customer’s facilities improved, shrinking waste and keeping blends in spec longer.
Easy access to high-quality reagents can’t be taken for granted. I’ve navigated more than a few markets where reliable supply changes work dynamics overnight. Customers today want to know that each batch of m-Hydroxyphenylacetic acid carries traceability, conforms to analytical standards, and ships without hidden environmental hazards. Labs running regulated processes demand documentation and testing data that survives regulatory scrutiny. Any misstep—impurity peaks, inconsistent particle size, odd odors—can push a process out of spec, resulting in costly downtime or failed runs.
I often recommend seeking trusted sources who’ve invested in both human expertise and automated quality control. Labs reporting high batch-to-batch consistency and minimal recalls for this acid tend to rely on suppliers with deep roots in fine chemical manufacturing and clear ties to raw material audits. It’s not about choosing the cheapest catalog entry—you need the one that won’t surprise you with out-of-spec results in unforgiving final steps.
Today, every chemical comes with scrutiny about its footprint and lifecycle. m-Hydroxyphenylacetic acid fits well within established regulatory frameworks. Though not classified as hazardous under many global schemes, best practice means checking local requirements and aligning with REACH or TSCA regulations before integrating any new molecule into production. Labs moving toward greener practices appreciate that the molecule’s straightforward physical handling reduces the temptation to overuse solvents or face complex waste disposal.
Discussions with environmental safety officers often highlight the importance of clean synthesis routes. Suppliers who’ve moved toward lower-emission and energy-efficient manufacturing for m-Hydroxyphenylacetic production usually share emissions data, which suits procurement teams working toward annual sustainability goals. Simple packaging—resealable, non-reactive, and appropriately labeled—makes compliance with both transport and storage regulations less of a chore. Teams assembling environmental statements for audits often mention this acid’s predictable risk profile as an asset, not a liability.
Process integration sometimes brings unexpected turns. During pilot facility setups, engineering teams sometimes underestimate particle size or wetting challenges. This compound, if prepared to tight pharmaceutical standards, usually enters solution consistently, sparing engineers the headache of dealing with clumping or filter blockages. Automated dosing and weighing procedures benefit from its stability against humidity and mild temperature variations.
Another under-appreciated bonus comes during process scale-up. While some related compounds show unpredictable behavior in large reactors, m-Hydroxyphenylacetic acid behaves the same whether in beaker or kilo-batch. This reliability cuts wasted time recalibrating equipment or chasing down new operating parameters mid-run. For continuous processing, where fouling or clogging sinks margins, I’ve noticed this acid doesn’t build up on surfaces easily, saving maintenance staff both time and frustration.
I’ve watched m-Hydroxyphenylacetic acid go from a curiosity in academic literature to a real-world staple across a range of sectors. Collaboration between research universities and commercial labs keeps pulling new applications for this compound out of traditional routes. Medicinal chemistry teams value the compound, leveraging its flexibility to anchor different drug structures, either through direct coupling or by functionalizing the hydroxyl group for unique pharmacophores. Intellectual property officers sometimes revisit synthesis plans, realizing that shifting to m-Hydroxyphenylacetic acid opens up paths closed by prior art involving other benzylic acids.
In analytical chemistry, the molecule’s well-defined structure makes it a popular choice as an internal standard, particularly in HPLC or capillary electrophoresis studies. Metabolite profiling relies on clear, sharp signals, and this acid meets that mark. Protein engineers digging into enzyme-substrate interactions use the molecule as a test probe for hydroxylation or decarboxylation kinetic studies.
Inefficiencies in distribution or supply chain break trust quickly, especially for fast-moving labs. One proven strategy involves diversifying suppliers based on track record, not brochure promises. Chain-of-custody documentation reduces the risk of hidden substitutions or tainted batches—critical when regulations require full traceability for every milligram used. Another approach gathers feedback from lab teams about handling issues at the point of receipt, rather than months down the line, so packaging and documentation can flex to real-world needs.
Training up younger staff on proper storage and handling pays dividends as well. For instance, teaching the difference between humidity-sensitive acids and more robust compounds like m-Hydroxyphenylacetic acid means storage decisions stay rational, avoiding over-spending on climate control without gambling with sensitive materials. Implementing staggered inventory audits—biannual checks rather than annual—keeps old stock from spoiling or going missing when demand surges during critical projects.
Current momentum toward greener synthesis makes compounds like m-Hydroxyphenylacetic acid more attractive. Its classic structure and ease of modification let researchers drop it into biocatalytic systems or other low-waste approaches with minimal fuss. Production teams trying to slim down solvent use or adopt recyclable reagents get a clearer workflow, since the acid dissolves under moderate conditions. In my own work on designing lab teaching modules, this molecule stood out as a safe, reliable “fixer” for error-prone steps, opening space for low-waste, demonstration-scale syntheses.
Genetic engineers look at this molecule as both a target and a tool: assigning students to evolve new bacterial strains that selectively transform related precursors into m-Hydroxyphenylacetic acid gave results quicker than with other ring-substituted acids. By leaning into well-studied metabolic paths, these students learned both modern enzyme technique and practical aspects of scale, cost, and process safety. The result was a significant drop in hazardous by-products compared to legacy phenylacetic derivatives.
Supply always drives market cycles, but steady, growing demand reveals where real value lies. In recent market analyses, m-Hydroxyphenylacetic acid sales have ticked upward, driven mainly by increased use in pharmaceutical research and specialty polymer blends. I’ve seen purchasing departments become more adept at forecasting, avoiding roller-coaster price swings that hit smaller users hardest. Industry consolidations, though disruptive, seem to have nudged major suppliers toward more stable pricing and increased transparency around origin and batch analytics.
Transparency on sourcing and composition matters more than ever. Regulatory authorities review processes and ingredients closely—making solid documentation and robust quality assurance routines essential. Chemical companies want reassurance about both composition and provenance, as regulatory audits increasingly sweep through every link in the supply chain.
Discussion with research chemists and plant managers paints a consistent picture. One researcher in drug development explained how, in their hands, m-Hydroxyphenylacetic acid enabled late-stage diversification, speeding up SAR (structure-activity relationship) optimization by weeks. Plant operators discussed reliable flows through feed hoppers and reduction of unplanned stoppages for cleaning and unclogging. A recurring point: switching to off-brand or substitute materials sometimes introduced headaches—and often, folks wound up switching back to the m-Hydroxyphenylacetic acid they trusted to do the job.
Every compound faces a clock—either obsolescence or re-invention through application in new science. For m-Hydroxyphenylacetic acid, momentum sits with creative chemists using it as a springboard. New bio-derived routes to the compound could lower environmental impacts. I’ve spoken with process chemists exploring catalytic routes that cut waste and energy, positioning the acid as a greener alternative in both large-scale and boutique applications.
Machine learning in chemical synthesis design may open unexpected routes or uses. Libraries of phenylacetic acids—including m-Hydroxyphenylacetic—are often used as model compounds to train AI systems to predict reactivity and process bottlenecks. If the acid helps teach machines how to find better catalysts or synthesize new drugs, its value climbs even higher—not just as a product, but as a platform for the next jump in synthetic strategy.
Nearly every seasoned professional has a wish list. For m-Hydroxyphenylacetic acid, supply chain resilience stands out—establishing backup sources, locally and internationally, would buffer risks from transport disruptions or raw material shortages. Expanded data sharing about production methods, residual solvents, and batch impurities helps both research and industry users align around process improvements and regulatory best practices.
Packaging isn’t a trivial issue either. Chemists who go through multiple kilo-lots often ask for more ergonomic, easy-open containers that prevent spillage and contamination during weighing or transfer. Thoughtful design from suppliers—down to labeling with full batch analytics—streamlines compliance and record-keeping, saving hours of back-office labor during audits.
Working with hundreds of organic acids over the years, some stick in memory for their reliability. m-Hydroxyphenylacetic acid stands out as one that rarely disappoints—and that consistency makes even high-stress projects feel just that bit more manageable. Tight deadlines, pressured timelines, and high expectations fade a little when basic materials do their job without fuss. Most colleagues—from academic researchers to process engineers—share that feeling: in the day-to-day push toward better products and new science, a reliable acid wins loyalty through performance and a clean record.
Chemical innovation often focuses on what’s new and just around the corner. Plenty of unsung hero compounds stand in the background, quietly powering breakthroughs by being solid, consistent, and understood. m-Hydroxyphenylacetic acid isn’t a celebrity among reagents, but its unique combination of easy handling, predictable performance, and real-world flexibility creates the bedrock on which successful projects, prototypes, and products get built.
Anyone considering bringing this compound into a workflow benefits from taking time to understand both its technical strengths and its proven reliability across diverse industries. As teams aim for ever-leaner, greener, and more effective processes, trusted classics like m-Hydroxyphenylacetic acid often lead the way forward—not with flash, but with precisely the qualities that matter most at the bench and on the shop floor.