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HS Code |
276100 |
| Productname | Cyclohexylboronic Acid |
| Casnumber | 411235-57-9 |
| Molecularformula | C6H13BO2 |
| Molecularweight | 127.98 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥ 97% |
| Meltingpoint | 85-89°C |
| Solubility | Slightly soluble in water |
| Storagetemperature | 2-8°C |
| Density | 1.04 g/cm³ (approximate) |
| Smiles | B(C1CCCCC1)(O)O |
| Inchi | InChI=1S/C6H13BO2/c8-7(9)6-4-2-1-3-5-6/h6,8-9H,1-5H2 |
As an accredited Cyclohexylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Cyclohexylboronic Acid, 25g, packaged in a sealed amber glass bottle with a screw cap, labeled with hazard and product details. |
| Shipping | Cyclohexylboronic Acid is shipped in tightly sealed containers, typically under inert atmosphere to prevent moisture contamination. Packages comply with relevant safety regulations for chemical transport. Proper labeling indicates handling precautions. Shipping is usually via ground or air as per customer requirements, with temperature control if necessary to maintain product stability during transit. |
| Storage | Cyclohexylboronic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect it from moisture, direct sunlight, and incompatible materials such as strong oxidizers. Store at room temperature or lower, preferably under inert atmosphere if available, to prevent degradation. Always follow specific manufacturer guidelines and local regulations for safe handling and storage. |
Applications of Cyclohexylboronic Acid in Industrial ManufacturingCyclohexylboronic acid is a specialty organoboron compound used in a range of value-added production processes. Our in-house synthesis and quality controls support leading industries integrating this intermediate for high-purity demands, precise catalytic function, and stringent regulatory environments. Below, we detail key downstream sectors where our material delivers performance outcomes and meets current compliance expectations. 1. Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers employ cyclohexylboronic acid as a building block in Suzuki–Miyaura cross-coupling reactions to construct complex, bioactive aromatic and cycloalkyl drug intermediates. This step introduces selective cyclohexyl groups for improved molecular properties and patent-unique profiles in targeted therapies, notably in oncology and CNS drugs. Handling and usage require rigorous control under cleanroom production with high analytical verification for impurity levels, trace metals, and residual solvents as per ICH Q3D and relevant pharmacopoeial specifications. Product batch traceability and records are strictly maintained from raw material to API release for global market compliance. Industry compliance standards
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2. Custom Agrochemical Intermediate ProductionMajor agrochemical R&D facilities utilize cyclohexylboronic acid to introduce cyclohexylphenyl moieties in the synthesis of crop protection actives, including selective herbicides and fungicides. The addition occurs via catalytic cross-coupling reactions, ensuring high positional specificity within regulated structure-activity relationship frameworks. Full process validation and control documentation address safe handling and potential residual boron in finished actives, adhering to industry stewardship principles and local regulatory frameworks for environmental safety. Industry compliance standards
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3. Advanced Material Synthesis for OLED and Electronic ApplicationsElectronic materials manufacturers leverage cyclohexylboronic acid in the production of high-performance, rigid-rod conjugated polymers and small molecule resins. This boronic acid enables tailored substitution patterns in polyarylenes, influencing charge transport, solubility, and film-forming properties for next-generation OLED emitters, organic semiconductors, and specialty coatings. Processing under inert atmosphere with stringent metal impurity controls prevents device degradation and assures consistent batch-to-batch optoelectronic properties, as required by device OEM specifications and international electronics standards. Industry compliance standards
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4. Fine Chemical Synthesis for Fragrance IntermediatesManufacturers in the aroma chemical sector use cyclohexylboronic acid for custom creation of cyclohexyl-aromatic derivatives with distinct scent profiles, incorporated into perfume bases, luxury detergents, and cosmetic formulations. The material enters catalytic arylation routes where precision is needed to achieve direct, high-yield transformations without unwanted side products. Production occurs in accordance with food-grade and cosmetic safety standards, with trace impurity profiles validated for compliance with IFRA and regional chemical inventories to support multi-national product launches. Industry compliance standards
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Years of hands-on synthesis work with cyclohexylboronic acid have shaped our outlook on its practical value and challenges. This boronic acid, with the cyclohexyl ring, stands out during the preparation of key intermediates used in API manufacture and specialty material development. In the daily run of reactions, we have encountered the visible differences this acid delivers compared to its phenyl or substituted aryl counterparts. Teams frequently refer to the solid, white crystalline appearance as a mark of purity and successful batch completion. This clarity in physical form helps us quickly assess batch consistency during production.
Cyclohexylboronic acid most often arrives from our reactors as a pure, non-hygroscopic crystalline powder. In laboratory settings and at scale, this reliable texture facilitates easy weighing, reduced moisture pick-up, and consistent transfer during automated feeding in continuous reactors. Handling characteristics directly influence how efficiently operators can run coupling steps in Suzuki–Miyaura reactions. Attempts with lower purity lots or older batches have taught us that poorly handled or aged cyclohexylboronic acid can show slight discolouration or dampness, which reduces product recovery rates and complicates solvent dissolution. So, our team adheres to regular batch revisions and short storage periods whenever possible.
Cyclohexylboronic acid plays a pivotal role in Boron cross-coupling chemistry. Our manufacturing logs show main demand coming from medicinal chemistry and agrochemical sectors. The preference for the cyclohexyl ring often ties back to its ability to tweak molecular scaffold bulk and basicity. Compared to phenylboronic acid, cyclohexylboronic acid introduces more steric bulk and pushes up aliphatic character. Customers in pharma often describe this as an essential factor for tuning metabolic stability and enhancing receptor binding diversity in candidate molecules.
Production teams quickly learned that standard Suzuki coupling with cyclohexylboronic acid rarely matches the yield profiles observed with arylboronic analogs. Extra optimization in base choice and temperature often become necessary. Our chemists sacrifice some throughput for improved selectivity against beta-hydride elimination—an issue less pronounced with aryl boronates. We have shared our solution with multiple partners: maintain lower temperatures, extend reaction time, and avoid polar aprotic solvents that might accelerate side pathways with the cyclohexyl group.
Operator experience taught us that customer results directly reflect small changes in specification standards. We focus attention on boron content, water content, and residual metal (especially iron and palladium, after coupling steps). Reflecting on a batch prepared a few years ago, we found that traces of chloride and iron led to color drift and compromised isolation of pure product. Now, our synthesis protocol incorporates extra water washes and filtration stages. Sulfate and nitrate testing now forms a routine part of the certificate of analysis.
Granule size also has a subtle, yet meaningful effect. Course powder sometimes causes bridging in automated feeders, particularly in winter when the air dries and static builds. Finer powder delivers better homogeneity but is easier to spill or lose in the air, as operators noticed during shift handover. Direct feedback from packaging teams led us to introduce tamper-resistant, double-sealed line packaging, which sharply reduced spills and moisture uptake.
Experience shows striking contrasts when our teams substitute cyclohexylboronic acid with other boronic acids. For example, phenylboronic acid, its close cousin, handles more forgivingly during purification—often yielding higher output per reaction and requiring less post-processing. Despite this, the bulkiness of the cyclohexyl group gives our customers a strategic advantage in synthetic versatility. Agrochemical firms say that using cyclohexylboronic acid allows for syntheses of crop protection agents with specific activity, which are otherwise tough to achieve using more planar arylboronic acids.
On the other hand, cyclohexylboronic acid resists hydrolysis better under standard lab humidity. Customers who previously handled vinyl or alkyl boronic acids remarked that cyclohexylboronic acid stores more reliably and shows reduced risk of slow decomposition in ambient air. This stability reduces waste losses, especially when inventory turnover slows in the off-seasons.
Lean manufacturing depends on responsible solvent choices and energy savings. Cyclohexylboronic acid, due to its moderate melting point and manageable reactivity, allows us to avoid extreme heating and strong oxidants. Our switch from batch to continuous flow production cut solvent volumes by more than a third. Less solvent handling reduced operator exposure to hazardous fumes and lowered plant-wide emissions by a measurable margin.
Residual boron waste always deserves care in every facility. We developed a set of borate scavenging measures that lower the environmental burden from neutralization tanks. Weekly monitoring of emissions and water runoffs keeps us aligned with local best practices. In some cases, boron content from spent reaction mixtures is successfully recovered and reused within the plant, thanks to our solvent extraction and distillation units. Technicians all agree that, although these changes required upfront investment and retraining, they paid off in both compliance and cost savings.
Plant staff receive regular training on cyclohexylboronic acid. Compared to some organometallic reagents we use, cyclohexylboronic acid presents fewer volatile or acute hazards. Eyes and skin remain the main risk areas; gloves, goggles, and local exhaust hoods do most of the work. On two known occasions, operators suffered mild eye irritation due to improper goggle use. Our shift leaders responded by increasing eyewash availability and checking protective gear every morning.
The acid’s low vapor pressure means spills are less threatening, but powders require care to avoid inhalation. We switched to closed transfer systems after our old open-drum filling area led to avoidable dust incidents. Now, exposure levels during powder transfer stay below regulatory limits, but we still keep a strict incident reporting policy. Our safety record continues to prove the value of straightforward, regular training.
Production rarely proceeds without hurdles. Trace impurities, batch-to-batch color differences, and variable solubility have challenged us over the years. Most issues trace back to upstream cyclohexyl precursor purity or to inconsistent mineral acid sources. Operators have reported that batches prepared from local acids often introduce more chloride and nitrate impurities than imported ones, and this difference impacts the downstream coupling step. To resolve this, our procurement team audits and pre-qualifies only trusted acid sources.
We saw that late-stage hydrogenation sometimes leaves trace cyclohexanol and over-reduced byproducts in the finished acid. Our technical managers deployed inline gas chromatography checks, letting us catch these contaminants well before final isolation. Over countless cycles, small changes in filtering agents and water temperature during washes improved removal efficiency.
Regular customer feedback shapes our ongoing improvements. An agrochemical manufacturer reported occasional trace amines in received Cyclohexylboronic acid, affecting their next synthesis step. Careful review revealed those amines came from incomplete vessel cleaning between batches. Now, plant cleaning protocols include extended detergent rinses and random cross-contamination checks. Operators also receive recognition showing how end-use quality depends on attention to minor residues.
Cyclohexylboronic acid stores best in cool, dry conditions, shielded from direct sunlight. Our warehouse logs show that even moderate summer humidity can clump powder if double-sealing fails or secondary containers are skipped. Teams found out the hard way: a single rainy week caused two entire drums to cake up, forcing manual grinding and risking loss during transfer. Since then, every container ships in moisture-barrier bags with humidity indicators visible upon arrival.
A long duration in inventory can dull the bright white color and signal a potential dip in purity, especially if opened repeatedly for sampling. Operators now rotate inventory following strict “first-in, first-out” routines to prevent extended exposure. Customers with annual ordering cycles receive updated storage recommendations to maintain color and activity.
Internal researchers rely on cyclohexylboronic acid to form new carbon-carbon bonds and create analogs unattainable with other building blocks. Having access to well-characterized lots matters not just for large-plant production, but also during early R&D. Researchers reported that lot-to-lot consistency saves weeks of troubleshooting unexpected side-reactions, especially during scale-up from milligrams to kilograms.
We maintain sample retains from every batch, catalogued and accessible on short notice. The R&D team tracks reaction reproducibility and purity retention using these archived samples. Few other acids in our catalog are monitored as closely for research support. The documentation that accompanies every lot captures physical characteristics, spectral purity, and residual metals—giving scientists the context they want for synthetic planning.
Direct communication with partners led us to adjust packaging size, labeling, and even specs for unique manufacturing lines. Some customers requested a pre-ground, fine powder form to match the needs of microfluidic coupling equipment. Our operations group responded quickly, setting up a dedicated grinder and dust capture system. Others, running larger batch reactors, required kilo-bag shipments for their continuous lines. We developed antistatic drums and improved labeling to prevent mix-ups during busy production days.
Every significant adjustment comes from shared project goals, rather than standardized, impersonal requests. A pharmaceutical manufacturer noticed their cyclohexylboronic acid required extra drying time in glovebox operations. After walking the process with their team, our site engineers adjusted drying protocols and changed drying tray mesh to limit clumping and humidity pockets.
Regulations for boron compounds shift rapidly, especially for products destined for the EU or regulated pharma segments. Our regulatory affairs department keeps all production lines in sync with key updates. Cyclohexylboronic acid, thanks to its benign reactivity and established use, remains less restricted than many halogenated or mixed-metal compounds. As of this writing, teams have not seen acute regulatory pressure, but we monitor all boron-specific regulations for preemptive process updates.
Global supply chain disruptions from energy pricing or freight delays sometimes force operators to reformulate reaction conditions using currently available base or solvents. Customer transparency means we routinely alert users to minor changes in potential impurity profiles, stemming from temporary supply substitutions. Many in the production team see these periods as benchmarks in flexibility and creative troubleshooting since risk of inconsistent output goes up during these times. It gives us more incentive to automate quality monitoring and keep a larger inventory buffer.
Research continues within our plant to streamline the synthesis of cyclohexylboronic acid and expand our capabilities for new derivatives. Chemists see opportunities in switching to more sustainable catalysts for borylation steps or adopting solvent-free microwave techniques. We currently explore enzymatic transformation routes that might reduce byproduct generation and lower energy consumption.
Digitalization allows the team to track every lot’s journey, from raw material intake through packaging and shipping. Real-time data monitoring picks up deviations faster than manual checks. Historical data analytics reveal which process tweaks led to reductions in impurity spikes or downtime. Operators increasingly rely on tablet-based process logs, which cut paper waste and reduce duplication. These hands-on changes keep the process robust—even as global conditions and customer preferences shift.
Manufacturing cyclohexylboronic acid at scale means much more than executing a reaction protocol. Each step, from raw material choice, batch monitoring, purification, packaging, shipping, and post-sale support, leaves a measurable mark on reliability and user confidence. All insights shared here stem from real production cycles, supply chain adaptations, and operator feedback—not from generic descriptions.
The lessons, tweaks, and improvements in cyclohexylboronic acid manufacturing keep our product trusted by bench chemists and plant operators alike. As demand builds in both established and emerging markets, our day-to-day hands-on stewardship continues to bridge new application needs with manufacturing stability and environmental responsibility. We look forward to more collaboration, more feedback, and more practical insight as cyclohexylboronic acid works its way through the next generation of pharmaceutical, material, and crop protection chemistry.