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HS Code |
673468 |
| Product Name | 2-(Dimethylamino)pyridine-5-boronic acid hydrate |
| Synonym | DMAP-5-boronic acid hydrate |
| Cas Number | 1165203-49-1 |
| Molecular Formula | C7H13BN2O3 |
| Molecular Weight | 180.01 g/mol |
| Appearance | White to off-white powder |
| Solubility | Soluble in water and polar organic solvents |
| Purity | Typically ≥97% |
| Storage Conditions | Store at 2-8°C, protect from moisture |
| Smiles | B(C1=CN=C(N(C)C)C=C1)(O)O |
| Inchi | InChI=1S/C7H11BN2O2.H2O/c1-10(2)7-3-5(8(11)12)4-9-6-7;/h3-4,6,11-12H,1-2H3;1H2 |
As an accredited 2-(Dimethylamino)pyridine-5-boronic acid hydrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5g amber glass bottle with a secure screw cap, labeled “2-(Dimethylamino)pyridine-5-boronic acid hydrate,” including hazard and batch details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Typically loaded with securely packed drums or fiberboard boxes, ensuring safety and stability for 2-(Dimethylamino)pyridine-5-boronic acid hydrate. |
| Shipping | 2-(Dimethylamino)pyridine-5-boronic acid hydrate is shipped in a tightly sealed container under ambient conditions. The package is clearly labeled and cushioned to prevent damage and moisture ingress. Standard chemical shipping regulations and documentation are followed to ensure the material’s integrity and safety during transit. |
| Storage | 2-(Dimethylamino)pyridine-5-boronic acid hydrate should be stored in a cool, dry, well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Keep container tightly closed when not in use, and protect from light. Store under inert atmosphere if recommended by supplier. Ensure appropriate chemical labeling and access only to trained personnel with proper protective equipment. |
| Shelf Life | 2-(Dimethylamino)pyridine-5-boronic acid hydrate typically has a shelf life of 2 years when stored tightly sealed, cool, and dry. |
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Purity 98%: 2-(Dimethylamino)pyridine-5-boronic acid hydrate with 98% purity is used in Suzuki-Miyaura coupling reactions, where it ensures high catalytic efficiency and product selectivity. Molecular weight 181.01 g/mol: 2-(Dimethylamino)pyridine-5-boronic acid hydrate of 181.01 g/mol is used in pharmaceutical intermediate synthesis, where it allows precise stoichiometric calculations for reproducibility. Melting point 176–180°C: 2-(Dimethylamino)pyridine-5-boronic acid hydrate with a melting point of 176–180°C is used in solid-phase synthesis, where high thermal stability minimizes decomposition during heating. Hydration state monohydrate: 2-(Dimethylamino)pyridine-5-boronic acid hydrate in monohydrate form is used for organoboron compound library generation, where it offers enhanced solubility in polar solvents. Particle size <10 µm: 2-(Dimethylamino)pyridine-5-boronic acid hydrate with particle size below 10 µm is used in automated synthesis platforms, where fine particle size facilitates uniform dispersion and reaction kinetics. Stability temperature up to 80°C: 2-(Dimethylamino)pyridine-5-boronic acid hydrate with stability up to 80°C is used in elevated-temperature cross-coupling reactions, where it retains structural integrity under robust process conditions. |
Competitive 2-(Dimethylamino)pyridine-5-boronic acid hydrate prices that fit your budget—flexible terms and customized quotes for every order.
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Walking through the synthesis lines, one will notice the close attention given to boronic acids, particularly derivatives with robust, tunable performance in cross-coupling and related applications. Over the past decade, our team has scaled and refined the production of 2-(Dimethylamino)pyridine-5-boronic acid hydrate, often known by its shorthand DMAP-5-BAH, recognizing demand among laboratories and scale-up plants that need both reliability and adaptability in their synthetic routes.
Anyone who has worked with Suzuki couplings or similar transformations knows the frustration when boronic acids underperform, either due to instability under storage, troublesome purification, or sluggish reactivity. Early on, we observed that labs push the limits with substituted pyridine boronic acids but often run into challenges with yield, moisture sensitivity, or poor reproducibility batch-to-batch. DMAP-5-BAH bridges those gaps by offering a more water-tolerant, shelf-stable form while preserving the electronic tuning power provided by the dimethylamino and pyridine rings. This gives it an edge in research environments where chemists constantly shift between discovery and process optimization, relying on predictable performance.
On paper, this molecule presents itself as a boronic acid hydrate, carefully controlled for hydration content during packaging to prevent drifting material weights. Our batches run with a typical purity above 98% by HPLC, and since the hydrate form can attract ambient moisture during handling, we seal it right after drying and formulation. This level of quality control is critical for customers who often set up air- or moisture-sensitive reactions.
By keeping hydration within a tight window, unexpected performance swings and pipetting inconsistencies drop off. During our own scale-up studies, we found that keeping impurity profiles under control, especially boroxines and unreacted starting material, made downstream purification far smoother, whether using reverse-phase chromatography or crystallization.
Comparing DMAP-5-BAH to simpler boronic acids illustrates the effect of fine-tuning molecular electronics. The dimethylamino group increases electron density on the pyridine ring and modulates coupling reactivity, often speeding up room-temperature or low-base reactions. Early on, we saw the difference during ligand screening for Suzuki and Buchwald–Hartwig reactions: catalysts that gave mediocre conversions with phenylboronic acid soared with DMAP-5-BAH, particularly with less-activated aryl chlorides or deactivated electrophiles.
We hear from process chemists who push for higher-throughput screens, often with automated platforms. In these workflows, reliable solubility in aqueous or mixed polar solvents isn’t just a convenience—it’s a necessity. DMAP-5-BAH’s solubility profile translates to fewer failed plates, easier dilution into stock solutions, and less crystallization in your pipette tips. Our in-house comparisons showed this often shaves a day or more off the method development stage compared to less soluble analogs.
Our formulation team deals directly with the realities of bench and pilot plant work. Customers often ask about consistency between lots, since small differences in hydrate content or impurity profiles can sway analytical readings or impact yields in multi-step series. To address this, our hydration process and packaging are designed to minimize drift even with ambient exposure. It took several cycles to optimize drying and storage conditions so each drum spends the minimum time between final QC and sealing. As practical evidence, long-term stability studies in our own inventory and in customer hands have shown that the product performs consistently without caking or clumping, and it doesn’t convert to boroxine on the shelf over months of storage.
Many users prefer to weigh directly from our sealed bottles, moving quickly to closed reaction vessels to limit atmospheric pickup. We include trace water content as standard with each batch, allowing process chemists to adjust stoichiometry precisely. Whenever we pilot a new batch, our manufacturing and quality control units coordinate over impurity profiles—residual solvents, minor oxidized byproducts, and inorganic residues—so the research chemist never has to wonder about variability or unexpected reaction results.
Chemists moving from small-molecule discovery to process optimization want building blocks that won’t limit innovation. Early in our manufacturing experience, we collaborated with institutes working on kinase inhibitors and substituted heterocycles, where minor changes in boronic acid reactivity or stability affect both discovery and downstream scale-up. For these teams, DMAP-5-BAH delivered conversion rates that accelerated lead development, with less time spent solving QC issues or repeating reactions due to poor batch reliability.
The molecule’s compatibility with water-rich or polar solvents stands out in the context of greener chemistry. During method development, several clients attempted to drop organic solvent volumes or switch to more benign bases. In these cases, the hydrate form outperformed less hydrated competitors, especially during extended runs at ambient temperatures or when exposed to air. Even during mistakes—delays in vessel charging or instrument holdups—the product maintained stability, saving runs that would otherwise require repeat syntheses.
Conducting hundreds of bench-scale reactions annually, you notice which materials become go-to standards. DMAP-5-BAH secures that position in part because of its electronic structure. The dimethylamino group at the 2-position interacts with both the nitrogen of the pyridine and the boronic acid at the 5-position, subtly shifting electron density throughout the molecule. As a result, reactivity profiles for coupling or addition reactions show faster and more complete conversions under conditions where more basic or less electron-rich boronic acids lag.
This advantage emerges in both fundamental research and applied synthesis, especially in the preparation of functionalized heterocycles or pharmaceutical intermediates. Where a generic boronic acid might require a catalyst change, temperature increase, or longer reaction time, DMAP-5-BAH often clears these hurdles without adjustment. We have documented instances where researchers scaled up library production simply by swapping in DMAP-5-BAH, cutting reaction times significantly or reducing catalyst loadings without yield losses.
We look closely at our customers’ work: early-stage pharma, agrochemical research, new materials development, and academic studies on coupling methodologies. Many steps in their processes are sensitive to trace impurities or shifts in hydrate level. Our production lines flex around these realities with rapid feedback loops between quality, synthesis, and logistics. For example, when a bulk customer flagged minor changes in melting point during a process scale-up, we traced it back to a small shift in water content during packaging. Adjusting sealing times closed the gap, restoring consistency and process reliability.
This level of responsiveness grows from decades on the manufacturing floor, not distant paperwork. We see ourselves as partners who share in every experiment’s outcome. Our pilot batches, continuous scaling reviews, and batch-level tracking all flow from direct conversations with our customers about their own scale-up hurdles, not abstract textbook guidelines.
Handling boronic acids in high-throughput research suites or contract manufacturing organizations brings practical safety and regulatory needs. Our QC team checks for residual solvents and inorganics, with clear lot data so customers can keep compliance reports accurate. Observing upstream suppliers, we source raw materials only from audited suppliers, running small-scale impurity screens before full-scale production proceeds. Each batch passes through multiple drying and sealing stages, as our experience shows that even small lapses in storage conditions ripple out to inconsistent downstream chemistry.
From synthesis vessels to final drumming, every technician and QC analyst works with documentation built up from iterative improvements and shared lessons. By tracking small deviations and responding immediately—say, a spike in boroxine formation during a humid spell, or a batch taking up trace acetic acid on drying—we catch issues before they affect our customers’ research runs.
Placing DMAP-5-BAH next to other boronic acid hydrates, several details separate it from more generic compounds. Chemists often compare it directly to phenylboronic acid or even other heterocyclic boronic acids, seeking more than just another substituent. The hydrate form shields against uncontrolled dehydration (and boroxine formation) while maintaining easy solubility. In head-to-head testing during library synthesis runs, we found more consistent conversion rates, narrower melting ranges, and fewer processing interruptions due to crystallization on vessels or in lines.
Other boronic acids may demand stricter anhydrous handling or produce higher rates of oligomerization during storage, leading to irregular dosing and unpredictable outcomes. With DMAP-5-BAH, our feedback from customers—both at bench scale and in early pilot plant runs—highlights smoother charging, lower risk of bottle-to-bottle variation, and less troubleshooting during upstream and downstream steps.
Our role doesn’t stop at batch release. Feedback from scale-up partners prompts ongoing tweaks in the hydration and packaging process. We share lessons between production, QC, shipping, and technical teams, often revising our SOPs based on small details spotted on the shop floor—dust ingress during open transfers, seal weaknesses, or observed changes in particle morphology under different drying cycles. This iterative approach, rooted firmly in production experience, maintains high lot consistency and reliability.
As researchers push chemistry faster or into new solvent systems, we watch how minor composition shifts affect performance. Sudden changes in atmospheric humidity, for example, exposed weaknesses in early packaging approaches, so we re-engineered both container materials and sealing processes. Empirical shelf-life studies pushed by client requests now back up our claims with real-world stability numbers, not just manufacturer’s assurances.
An often-overlooked aspect in choosing fine chemicals sits beyond the initial purchase price. Total cost hinges on yield, failed batch rates, extra method development time, and unplanned repeats due to material inconsistency. In our internal tracking, most failed runs result from supplier variability—batch-to-batch swings in hydrate, unlisted impurities, or inconsistent packaging—rather than user errors. With DMAP-5-BAH, our intention has always been to narrow those variables so research and process teams spend more time on innovation, not troubleshooting.
By integrating feedback from each batch into our next cycle, we reduce rework and scrap both for ourselves and our customers. This focus distinguishes a producer’s mindset: we succeed only when the chemistry in a customer’s hands is as robust as it was in our own labs. Clients repeatedly comment that our products give them the confidence to shift more reactions onto automated or multi-parallel platforms—a level of trust built batch by batch.
Boronic acids, like DMAP-5-BAH, contribute to safer, cleaner, and more efficient chemical processes when handled and transported with care. Drawing lessons from years of bulk shipping and custom packaging, we stress clear communication and transparent lot information over marketing buzz. If a batch ever fails to meet published specs due to shipping mishaps or rare quality dips, we act directly—dispatching replacements from retained splits, sharing real-time stability data, and looping clients back into our internal review so every lesson strengthens our next production run.
Regulatory and environmental scrutiny rises with every year. We register and update all required documentation for global shipment and maintain tracebacks for every raw material lot. Working with contract manufacturers and regulated labs, we share impurity and water content data as part of the delivery documentation to keep compliance smooth for the end user. Our stewardship is measured daily by how well our clients’ experiments and scale-ups succeed with our material.
Producing 2-(Dimethylamino)pyridine-5-boronic acid hydrate isn’t just a matter of preparing another catalogue product—it’s a daily exercise in process refinement, attention to detail, and direct feedback between manufacturing and global users. From choosing raw materials to finessing the final drum seal, every stage reflects lessons learned from customer experience and our own scaling.
This focus on reproducibility and usability, built from the manufacturing floor upward, means that when a researcher reaches for this product, they trust that every synthesis, whether a tiny screening run or full kilogram scale-up, starts on solid footing. We understand these pressures because we live them, every day, batch by batch.