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HS Code |
422606 |
| Chemical Name | 4-Bromomandelic Acid |
| Cas Number | 7164-98-9 |
| Molecular Formula | C8H7BrO3 |
| Molecular Weight | 231.05 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 145-150°C |
| Solubility | Soluble in water, alcohols, and acetone |
| Boiling Point | Decomposes before boiling |
| Density | 1.70 g/cm³ (approximate) |
| Purity | Typically ≥98% |
| Iupac Name | 2-(4-Bromophenyl)-2-hydroxyacetic acid |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 4-Bromomandelic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-Bromomandelic Acid, 25g: Supplied in a white, tightly sealed HDPE bottle with a clear hazard label, tamper-evident cap. |
| Shipping | 4-Bromomandelic Acid is shipped in tightly sealed containers to prevent moisture and contamination. The chemical is classified as a hazardous material and must be handled with care, following all regulatory guidelines. Shipping is typically via ground or air, with appropriate labeling and documentation to ensure safe and compliant transport. |
| Storage | 4-Bromomandelic acid should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Store it away from sources of heat, oxidizing agents, and incompatible substances. Properly label the storage area and ensure easy access for authorized personnel only. Follow all relevant safety and regulatory guidelines for chemical storage. |
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Purity 98%: 4-Bromomandelic Acid with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation. Melting point 133°C: 4-Bromomandelic Acid with a melting point of 133°C is utilized in fine chemical manufacturing, where thermal stability during processing is required. Particle size <40 μm: 4-Bromomandelic Acid with particle size below 40 micrometers is applied in catalyst preparation, where enhanced dispersion and reactivity are achieved. Stability up to 120°C: 4-Bromomandelic Acid stable up to 120°C is used in organic reaction scaling, where it maintains integrity under moderate heating conditions. Molecular weight 229.03 g/mol: 4-Bromomandelic Acid with molecular weight of 229.03 g/mol is employed in biochemical research, where precise stoichiometric calculations are necessary. HPLC grade: 4-Bromomandelic Acid of HPLC grade is used in analytical method development, where high detection sensitivity and reproducibility are critical. Water solubility 25 mg/mL: 4-Bromomandelic Acid with water solubility of 25 mg/mL is utilized in aqueous formulation studies, where rapid dissolution and uniform distribution are crucial. Assay ≥99%: 4-Bromomandelic Acid with assay ≥99% is applied in chiral resolution processes, where exceptional enantiomeric purity is required for downstream applications. |
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4-Bromomandelic Acid isn't the type of chemical you see headlining pharmaceutical ads or cropping up in flashy tech blogs. But talk to anyone who's spent time in a research laboratory, especially in the world of organic synthesis, and the name resonates. This compound, known by its model C8H7BrO3 and featuring a CAS number of 24125-79-1, quietly supports a wide span of complex reactions. People tend to focus on big, finished drugs or final product innovations, but the real backbone sits with the building blocks. As a benzenoid carboxylic acid with a bromine tag, 4-Bromomandelic Acid earns its value by providing unique chemical reactivity and selectivity in a lot of practical settings.
Over the years, I’ve seen compounds like 4-Bromomandelic Acid drift from one role to another. In academic labs, graduate students chat about how to control substitutions on aromatic rings, and this acid makes those pathways possible. Small changes in a molecule can open new routes in synthesis. With this acid, that bromine atom lets researchers fine-tune the reactivity, especially when there’s a need for optical or regioselectivity. The capacity to switch functional groups makes it a quiet powerhouse in research benches.
Scaling up is a different beast. Small-scale reactions in school or research don’t always translate to industrial processes. Yet the demand for intermediates with high purity and consistent behavior means products like 4-Bromomandelic Acid get close attention. You don’t want impurities interrupting an expensive pharmaceutical synthesis—small hitches can mean a lost batch worth thousands. For me, the most valuable trait in specialty chemicals remains simple: reliability of supply and consistency in every container. I’ve watched companies prefer acids like this one simply because each shipment matches their reaction expectations.
A lot of suppliers can claim they stock 4-Bromomandelic Acid, but just having the right label doesn’t count for much. Purity levels usually run upwards of 98%, and every fraction of a percent can matter in downstream reactions. Ask any synthetic chemist, and they'll say a solid melting point—usually around 147-150°C—demonstrates the compound is clean. Hygroscopicity matters, too; 4-Bromomandelic Acid’s stability under normal conditions gives peace of mind. Stable powders reduce storage headaches and make accurate weighing easier, saving hours in the lab that would otherwise be wasted worrying about compound degradation or weight drift.
Model specifications matter more than many realize, especially for those carrying out multi-step syntheses where every functional group must perform as expected. This compound supports chiral resolution, helping distinguish and separate enantiomers. That’s a game-changer in pharmaceutical research, where the difference between molecular “right hand” and “left hand” can mean the difference between a breakthrough therapy and an unacceptable side effect. The aromatic ring with a para-bromine, coupled with a carboxylic acid and adjacent hydroxyl group, creates a versatile anchor point. It connects easily with a host of other proteins, ligands, or industrial reagents.
Most publications discuss this acid within the framework of its synthetic flexibility. Med chem folks often bring it into play for making β-adrenergic antagonists and other cardiovascular agents. It’s not hard to see why. The presence of both a reactive carboxyl group and an electron-withdrawing bromine allows for further substitution, protection, and derivatization. You rarely find shortcuts to complex molecules without building blocks that set functional groups in just the right places, and this compound provides that precision.
In my own work, I’ve seen researchers use it to create chiral auxiliaries—those helper molecules that drive a synthetic reaction toward certain three-dimensional outcomes. Producing key pharmaceutical intermediates, it supports not only bulk manufacturing but also discovery-stage research, where flexibility counts for everything. Outside pharma, custom synthesis outfits lean on this acid for modifications in advanced materials research, agrochemical explorations, and even certain flavors and fragrances, as the aromatic structure opens doors for creative and controlled modifications.
Chemical manufacturers invest in it for a reason. They count on clean, reproducible reactions. Nobody wants a key intermediate that varies from batch to batch; those using 4-Bromomandelic Acid consistently report tight analytical profiles using NMR, IR, and HPLC testing. Lab notebooks fill with reaction runs, and the ones using this acid tend to avoid the columns of crossed-out mistakes tied to unpredictable reactivity.
Other mandelic acid derivatives litter the market. Many teams gravitate toward plain mandelic acid for simpler pathways or push for other halogen substitutions (chlorine, fluorine) to influence reactivity. I’ve compared these in parallel experiments, and the difference boils down to control. That para-bromine atom imparts noticeable changes in how the molecule fits and locks onto reaction partners. For example, fluorinated versions provide extreme electronegativity but lack the same bulk and hydrophobicity, so they push reactions in a different direction.
Trying to swap out 4-Bromomandelic Acid for similar compounds means accepting some trade-offs. The bromine atom not only alters electron density within the molecule; it also subtly shifts how readily that core carboxyl group can engage partners. In many synthesis plans, only the bromo version provides the right balance of reactivity and downstream modification steps. I’ve watched process engineers try to substitute with para-chloromandelic acid, thinking the chemical costs slightly less, only to see lower yields and unexpected impurities.
Another interesting element: the bromo group’s size. It adds steric bulk around the benzene ring, which means certain enzyme-catalyzed reactions proceed more selectively. In experimental projects where selectivity and yield go hand-in-hand, the difference becomes obvious. No one wants to waste time purifying side products when a single functional group can steer the reaction from the outset.
The market for specialty chemicals shifts with the seasons, but trends in personalized medicine, complex generics, and green chemistry keep 4-Bromomandelic Acid in steady demand. Pharmaceutical projects increasingly lean towards molecules with chiral centers, and this acid fits those requirements well. Researchers need starting points that can accommodate new routes—more often, you spot this compound showing up in supporting information sections of major publications.
Stories from procurement managers echo across the industry. “Keep it consistent” and “don’t change the source” might sound trivial, but any shake in quality stifles development and triggers headaches up and down the value chain. It’s easy to underestimate the challenge until a single contaminant in a kilo lot halts an entire clinical batch, costing weeks and burning resources. Suppliers who deliver 4-Bromomandelic Acid with trusted, traceable documentation help labs steer clear of those costly setbacks.
There’s another driver: sustainability. The chemical sector feels heavy pressure to reduce environmental burdens and improve synthesis routes. 4-Bromomandelic Acid plays a small but genuine role here. Its stability and ease of handle can cut waste. Fewer purification steps mean fewer solvents and less hazardous byproduct, especially when reactions run cleanly and predictably.
Not all stories are positive; the chemical supply chain can get tricky. 4-Bromomandelic Acid might look like a standard crystalline powder, but anyone who’s had to order a large batch knows shipping timelines and regulatory hoops create stress. Local regulations sometimes shift, and suppliers who handled the product last year might back away if the paperwork grows too onerous. It falls to end-users to stay updated on compliance, particularly around transportation and waste disposal.
Proper storage matters. The compound doesn’t react wildly with air or moist conditions, but keeping containers well-sealed and labeled prevents mistakes. Once a container sits unmarked on a crowded shelf, someone will misuse it sooner or later. Every lab manager has met the chaos of poorly tracked chemical inventories. In regulated industries, unexpected contamination or misuse can cost more than just the price of the product—it can undermine audit trails and damage reputations.
In my time working around the analytical bench, I’ve seen just how seriously quality control teams approach compounds like this one. HPLC purity, mass spectrometry data, and NMR spectra form the backbone of purchase decisions. Experienced chemists want confidence from every supplier: their acid dissolves as expected, their spectra align with reference standards, their reactions fire reliably without trace contaminants hijacking the synthesis. This obsession with detail isn’t just academic posturing—it bears out in every finished drug lot.
Labs working under good manufacturing practices keep these reference standards close at hand. Internal testing of every new batch becomes second nature. Even if a supplier claims 99% purity, nobody trusts a label without a matching spectral fingerprint. That’s a tradition built from hard experience. A handful of botched reactions can cost a month’s worth of labor, and time lost in research means competitors edge closer to patent filings or regulatory submission.
Pressure builds across the industry to drive more reliable sourcing. One answer comes from building longer-term partnerships between buyers and reputable producers. Open communication means fewer surprises, especially during shortages or regulatory overhauls. Forward-looking organizations invest in dual sourcing and maintain a backup set of analytical data, so they’re ready if supply interruptions hit.
Some manufacturers step up by publishing transparent certificates of analysis and extending technical support to users. They train customers on proper handling, reduce left-field errors, and cement trust in a crowded landscape full of “almost good enough” chemicals. Digital inventory tools have made it much easier to track lot numbers, cycle expiration dates, and generate audit logs automatically. That approach trims down panic buying and last-minute emergencies.
Traction is also growing for “greener” manufacturing approaches. Chemical development teams now refine syntheses to minimize hazardous byproducts and select more benign reagents. Switching solvent systems or updating process steps adds upfront work, but payback arrives in the form of safer work environments and easier waste handling. Down the road, these efforts benefit from compounds like 4-Bromomandelic Acid, which often tolerate less harsh conditions and generate fewer unwanted byproducts.
On the research side, several collaborative networks have emerged, sharing best practices for use and documentation. These networks allow newcomers—graduate students, start-up lab techs, specialist chemists—to step into projects without losing weeks retraining on protocols or sorting through outdated filing cabinets full of specifications. As newcomers pick up insights from experienced hands, best handling and sourcing practices spread throughout the field.
Safe handling and responsible sourcing go hand in hand. Many firms have added explicit training programs tailored to specialty chemicals. Companies set policies for PPE, waste containers, and even spill protocols directly tied to compounds like this one. Those safeguards grew from lab managers confronting real accidents—the industry doesn’t wait for the next incident before fixing holes in safety nets.
A lot of this work happens quietly. Many chemists learn from their mentors, moving from textbook theory to hands-on application. Used properly, 4-Bromomandelic Acid becomes a valued member of the bench, not a hazard lurking in the back corner. Its crystalline appearance almost belies the necessary respect it commands. Treating each bottle with the same seriousness, day after day, sets a standard for lab discipline.
There’s plenty of chemistry ahead, and the road will keep winding. As demand rises for bespoke pharmaceuticals and advanced material innovations, intermediates like 4-Bromomandelic Acid can keep providing those small, precise changes that bigger breakthroughs demand. The ability to modulate and adapt synthetic routes using specialized building blocks remains a crucial advantage.
It’s not a glamorous compound, but it doesn’t need a spotlight. Instead, it delivers consistency, flexibility, and adaptability across projects large and small. Through years in different organizations, I’ve watched lab teams celebrate a clean reaction—not because the chemistry was simple, but because each ingredient worked the way it should. 4-Bromomandelic Acid fits that story well. Consistent batches help scientists waste less time troubleshooting, focus on discovery, and move promising molecules closer to real-world use.
With specialty chemicals, the devil always lives in the details. 4-Bromomandelic Acid keeps showing its worth by delivering on both purity and performance. As the scientific community asks more from each synthesis, the role of reliable intermediates only grows. Factoring in the importance of transparent sourcing, responsible use, and continuing education turns a simple chemical into a far more valuable resource. It’s never just about one bottle or one shipment. Reputations, research programs, and the health of future patients ride on every gram used.
Every chemist who’s relied on a clean, predictable intermediate knows the peace of mind that comes with top-tier quality. 4-Bromomandelic Acid doesn’t solve every problem on its own, but it does let researchers and process engineers breathe a little easier with each finished batch. For anyone looking to build tomorrow’s breakthroughs, compounds like this play a far larger role than most realize—quiet, steady, and always ready to support the next big step forward.