|
HS Code |
701766 |
| Productname | 2-Hydroxyphenylboronic Acid |
| Casnumber | 1699-37-8 |
| Molecularformula | C6H7BO3 |
| Molecularweight | 137.93 g/mol |
| Appearance | White to off-white powder |
| Meltingpoint | 257-261°C |
| Purity | Typically ≥98% |
| Boilingpoint | Decomposes before boiling |
| Solubility | Soluble in water and organic solvents |
| Density | 1.28 g/cm³ |
| Storagetemperature | 2-8°C |
| Synonyms | Salicylboronic acid |
| Smiles | B(C1=CC=CC=C1O)(O)O |
| Inchikey | FLDJRSQYQICZNZ-UHFFFAOYSA-N |
As an accredited 2-Hydroxyphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams of 2-Hydroxyphenylboronic Acid; labeled with chemical name, CAS number, and hazard warnings. |
| Shipping | 2-Hydroxyphenylboronic Acid is typically shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be transported at a controlled room temperature, protected from direct sunlight and incompatible materials. The packaging must comply with local and international regulations for the safe handling and transport of chemicals. |
| Storage | 2-Hydroxyphenylboronic acid should be stored in a tightly sealed container, protected from moisture and air. Keep it in a cool, dry, and well-ventilated area, away from strong acids, bases, and oxidizing agents. Avoid exposure to direct sunlight and sources of ignition. For optimal stability, refrigeration (2–8°C) is recommended. Always follow safety guidelines and local storage regulations. |
Applications of 2-Hydroxyphenylboronic Acid in Industrial Manufacturing2-Hydroxyphenylboronic Acid serves as a critical boronic acid derivative for precision organic synthesis, especially in fields demanding high functional group selectivity and purity. As an integrated manufacturer, we supply this intermediate to multiple advanced sectors with tailored specifications and well-defined quality assurance practices. 1. Pharmaceutical Active Ingredient SynthesisThis compound plays an essential role in constructing complex biaryl structures through Suzuki–Miyaura cross-coupling reactions, which are widely applied in modern pharmaceutical development. Pharmaceutical manufacturers rely on its ortho-hydroxy group to facilitate regioselective coupling, especially during late-stage API synthesis for kinase inhibitors and anti-cancer agents. Production lines demand controlled purity and batch-to-batch consistency. We support regulated documentation and validation for use in GMP environments. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingChemical process operators source this material to construct agrochemical scaffolds, particularly in coupling with pyridine or phenoxy units to yield bioactive herbicide and pesticide candidates. Its purity directly impacts downstream crop protection formulations. We provide traceable batches tested against stringent specification limits for residual metals and water content critical to agrochemical compliance. Industry compliance standards
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3. Electronic Materials Synthesis (OLED/OPV Precursors)In the semiconductor industry, this boronic acid structure is preferred for functionalizing organic electronics, including precursors to arylated monomers for OLEDs and organic photovoltaics. High electronic purity grades reduce ionic contamination in device layers. Direct QC at the point of delivery ensures suitability for electronic material producers operating under strict environmental and workplace standards. Industry compliance standards
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4. Fine Chemicals for Dye and Pigment SynthesisThis intermediate contributes to high-value dye and pigment manufacturing, offering targeted substitution patterns for specialty azo and anthraquinone dyes. Color manufacturers integrate this reagent in coupling steps, leveraging ortho-hydroxy activation for advanced color tone adjustments. Production runs must respect environmental discharge limits and color index registration demands. Industry compliance standards
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In the chemistry space, boronic acids have carved their own niche. Among these, 2-Hydroxyphenylboronic Acid (with the model number 615-94-1) stands out for how often it opens new routes in synthesis. From the hustle inside our own manufacturing plant, we know few intermediates tick as many boxes for the working chemist. Our approach is hands-on and personal because our teams prepare this compound batch by batch, managing purity, consistency, and scope of supply directly. We know the demands you face because they show up every day on our floor, too: reliable performance, clear specifications, and a product that can do the heavy lifting, whether you're in pharma, agrochemical, or materials science.
We source phenol and boronic acid derivatives carefully. The process chemistry isn’t just about putting reagents together; every step reflects thousands of runs, with pressure on maintaining purity above technical norms. Our analysts use NMR, HPLC, and GC regularly to monitor lots, comparing actual performance against published data and our own internal records. Even the subtle adjustments—reaction temperatures, solvent ratios, pH values—translate to real differences in purity and usability, so our team never leaves quality to chance.
Specs for 2-Hydroxyphenylboronic Acid (also known as o-Hydroxyphenylboronic acid) go beyond a certificate on paper. Our standard lots meet or exceed 98% purity by HPLC, with rigorous controls on moisture content and residual solvents. We keep water content typically below 0.5%, as higher levels often create headaches in downstream synthesis. The crystalline white-to-off-white powder flows well and resists caking over reasonable storage conditions, making weighing, dispensing, and blending smoother than with lower-grade alternatives.
Physical handling experience shows how important it is to keep impurities—such as unreacted phenol or meta/para isomers—low. Even trace levels can affect reaction outcomes, especially where Suzuki-Miyaura couplings or oxidative cross-coupling are involved. Experienced chemists from our client roster frequently point out that minor differences in composition, unnoticeable in the documentation of less scrupulous suppliers, can bring whole projects to a standstill if not managed up front.
What defines 2-Hydroxyphenylboronic Acid? The ortho-hydroxyl group next to the boronic acid moiety creates an intramolecular interaction you don't get with other isomers. These structural details drive its kinetic behavior and determine selectivity in catalysts and ligands. Unlike the para- or meta- analogs, this molecule shows unique reactivity in Suzuki-Miyaura coupling. The ortho position fosters intramolecular hydrogen bonding, changing solubility and influencing how the compound interacts with other reagents during coupling.
In everyday manufacturing, that hydrogen bonding comes to light in purification and crystallization. Operators on our line routinely observe differences in the ease of filtration, the melting range, and even storage stability. Formulators in research settings have confirmed that, at scale, reactions using 2-Hydroxyphenylboronic Acid can often proceed under slightly milder conditions than with related compounds. That doesn’t just save energy; it preserves sensitive substrates from degradation, making this acid a safer choice for multi-step synthesis where yield and selectivity are key.
2-Hydroxyphenylboronic Acid finds regular utility in pharmaceutical intermediate synthesis. Process chemists often reach for this compound during the preparation of biologically active molecules. In-house, we have supported projects synthesizing kinase inhibitors, beta-lactamase inhibitors, and other heterocyclic compounds. The boronic acid group serves as an ideal handle for palladium-catalyzed cross-coupling, providing a clear entry to aryl ethers, aryl amines, and more complex heterocycles.
Outside pharma, applications extend into material science—especially for sensors, polymers, and as building blocks for more advanced boronic esters. In our own collaborations with academic and industrial partners, 2-Hydroxyphenylboronic Acid repeatedly proves its value in designing receptor molecules for monosaccharide detection. The ortho hydroxy group in particular aids in the formation of cyclic boronate esters, critical for selectivity when detecting diols or sugars in aqueous systems.
Chemists often ask how our 2-Hydroxyphenylboronic Acid stacks up against other boronic acids—such as phenylboronic acid, 3-hydroxyphenylboronic acid, and 4-hydroxyphenylboronic acid. Practical use tells its own story. The ortho isomer, our specialty, delivers advantages when hydrogen bonding or electronic effects matter. While phenylboronic acid is a solid general-purpose intermediate, it lacks the additional hydroxy substitution, limiting its flexibility in certain ligand or sensor designs.
On a daily basis, formulators at our site note that 2-Hydroxyphenylboronic Acid presents a slightly higher melting range than its meta and para isomers—a boon for stability in industrial storage. In cross-coupling reactions, it tends to offer smoother product isolation, requiring fewer washes and less chromatographic cleanup. These seemingly small details carry real-world results: consistent batch yields and less downtime in the lab or plant.
We store and handle 2-Hydroxyphenylboronic Acid away from excess moisture, direct sunlight, and incompatible substances. Our operators package the product in double-lined, moisture-resistant drums. Handling practices throughout our facility emphasize glove and mask use, especially during weighing and transfer to minimize dust ingress. From a chemical stability standpoint, the compound does not present unusual hazards—no rapid decomposition or excessive offgassing—but care is taken during heating, crystallization, and long-term storage.
In process development, we note the compound’s sensitivity to strong oxidizers and bases, which can promote degradation. For large-scale processes, we regularly test bulk samples to confirm there’s no deterioration during transport, and we provide flexible packaging to suit solid or solution-phase delivery, according to each client’s set-up.
Consistency matters more than any certification alone. Our lab staff draw samples from every batch, reviewing spectral fingerprints using both nuclear magnetic resonance and infrared spectroscopy to confirm identity. Samples are also evaluated with HPLC for main peak purity, monitoring for hydrolyzed byproducts and residual starting materials. Where customers request full traceability, we break down the lot number history and process records, sharing data to build confidence not just in this single batch, but in our process as a whole.
Our continuous feedback loop—spanning R&D, QC, and technical support—reflects a shared understanding: Every project depends on a consistent grade of input chemical. Our clients trust that advice because long-term relationships with process chemists and formulators have taught us which details count most. Whether feedback concerns crystalline habit, lot-to-lot color tone, or packaging design, it loops directly back to our plant floor to drive improvement in real time.
Experienced users of 2-Hydroxyphenylboronic Acid notice upstream decisions echo throughout the synthetic chain. For instance, before committing to full-scale runs, we offer pre-shipment sample vials for customers to examine compatibility, solubility, and handling in their own processes. Feedback from development teams helps us tune future lots, adjusting trace impurity levels or tweaking moisture content even further when certain catalysts or reactions show increased sensitivity.
Our applications chemists regularly communicate with end users to interpret unusual reaction stalling or product precipitations that arise when switching lots or suppliers. Over the years, we have documented that even minor differences in raw materials impact catalyst performance, scale-up conditions, and the need for extra purification. Close monitoring—above and beyond what certification bodies demand—has shielded our partners from preventable process disruptions.
We recognize that our partners worldwide operate under a range of regulations, and that trust starts with verification. Each lot of 2-Hydroxyphenylboronic Acid runs through our compliance protocols—checking that no restricted substances show up above trace levels, and confirming that packaging and labeling remain in line with customer expectations for onward handling. Dangerous goods shipment rules receive particular attention, ensuring formats comply with land, sea, and air requirements.
Full certificates of analysis accompany every shipment. We don’t just provide numbers; our staff annotate testing methods, offer historical comparison data, and keep supply records available for audit, supporting your own documentation and QA protocols.
Direct manufacturer involvement means we stay available during both initial formulation and scale-up stages. Our chemists answer technical queries and collaborate on adaptations if unique process tweaks are needed.
Industry partners often depend on our input for troubleshooting. Sometimes a batch performs differently, or a reaction gives variable yield; it’s our firsthand knowledge of the compound’s behavior during synthesis that unlocks solutions: What drying protocol suits this lot better? Which solvents dampen crystallization? Can a minor parameter adjustment shave hours off your work-up? These questions find their answers directly from those of us who process and characterize the lots day-to-day.
No product reaches its best form instantly. Over years of direct manufacturing, we have modified steps to reduce residual boron-containing byproducts. Process engineers redesigned isolation and drying protocols to address specific feedback about caking, not just because a standard said so, but because it actually improved each end user’s workflow. Even common issues like static charge or fine particle formation during shipping push us to trial alternative packaging materials and anti-static liners.
Every year, we conduct full reviews of process documentation. This review captures new industry data, feedback from our partners, and our own case reports. Continuous improvement teams adjust reaction times, solvent recovery protocols, and operator schedules. These changes aren’t generic—they derive from lived experience scaling the manufacture of 2-Hydroxyphenylboronic Acid from lab-scale through to multi-ton runs.
Being a direct manufacturer lets us tell the full story on price and supply stability. Seasonal swings in global supply chains show up as cost increases or delivery delays, but with our in-house production capacity, we buffer many of these issues by holding critical stocks and sourcing raw materials year-round. Partners gain from contract manufacturing agreements—not just a quoted price per kilogram—but detailed insight into batch availability, shipping dates, and contingency plans for urgent projects.
Production scheduling stays transparent. We lay out timelines and risks in advance. Real delivery timelines and quality levels matter more than a cheap quote from an unreliable source. We share updates at every step: synthesis, packaging, QA sampling, and dispatch, so partners stay informed rather than blindsided.
Direct chemical manufacturing brings environmental responsibility front and center. Our staff continually review batch process emissions and waste streams, with solvent recovery and wastewater treatment systems operating every shift. Over time, we’ve reduced use of high-boiling solvents and switched to greener reagents where specific product requirements allow.
We reclaimed much of our aqueous waste after boronic acid isolation, and even explored circular routes for boronate ester byproducts, feeding these into parallel processes. While the pursuit of full green chemistry remains ongoing, every incremental change is rooted in experience on our own production floor, not just in marketing copy.
From a manufacturer’s perspective, challenges don’t end with product launch. Handling customer complaints—clumping, color variation, or difficulty dissolving—leads directly to process reviews and adjustments. With 2-Hydroxyphenylboronic Acid, a key challenge lies in maintaining stability and low moisture over long transport routes, especially with global shipping constraints. Our QC and logistics teams review each packaging method and humidity-control additive, ensuring batches arrive in workable form, not just meeting compliance.
Feedback loops with customer labs prompt us to rerun process validations, check batch documentation, and, where needed, run special additional assays. Expecting some ‘normal’ variation, we focus on minimizing anything that will affect clients’ own reproducibility downstream. Our decisions favor long-term reliability, not just speed to the next sale.
Boronic acids occupy a growth segment, thanks to ongoing innovation in synthetic organic chemistry and next-generation sensor design. Our role as a manufacturer sustains that progress by adapting our own technologies. Whether preparing batches for rapidly scaling biopharma companies or tuning specification profiles for materials scientists purchasing small lots for sensor development, we bridge industrial scale with custom solutions drawn from factory-floor expertise.
We keep watch on new research findings and industrial trends. Insights from recent literature sometimes trigger trials with alternate starting materials or reaction conditions. Our technical staff then translate promising methods from the literature bench to our reactor systems, always focused on reproducible performance, safety, and process economy.
Through years of direct experience, 2-Hydroxyphenylboronic Acid has shown its reliability as a building block for research and industrial chemistry. The difference comes from discipline: careful process control, regular feedback, and ongoing investment in people, equipment, and process improvement. As a manufacturer, our job goes deeper than delivering product—we aim to supply confidence, built on firsthand experience and transparent support at every stage of your project. We're on hand, not only to supply high-purity batches, but to offer hands-on knowledge for application troubleshooting, process adaptation, and long-term process improvement.