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2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide

    • Product Name 2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide
    • Alias BDDMA
    • Einecs 695-813-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    277884

    Chemical Name 2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide
    Molecular Formula C12H22B2N2O6
    Molecular Weight 324.85 g/mol
    Appearance White to off-white solid
    Cas Number 1201909-30-7
    Solubility Soluble in common organic solvents
    Storage Temperature Store at 2-8°C
    Purity Typically ≥98%
    Smiles CCCCC1OB(OC1(C(=O)N(C)C)C(=O)N(C)C)
    Application Organic synthesis intermediate
    Synonyms Bis(dimethylcarbamoyl)-2-butyl-1,3,2-dioxaborolane-4,5-dicarboxylate
    Stability Stable under recommended storage conditions

    As an accredited 2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed in a 5g amber glass vial with a tamper-evident cap, labeled with chemical name, purity, and hazard information.
    Shipping 2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide is shipped in tightly sealed containers, clearly labeled, and protected from moisture and heat. It is transported according to applicable chemical safety regulations, typically as a non-hazardous material, with documentation and handling instructions included to ensure safety and compliance during transit.
    Storage Store 2-Butyl-[1,3,2]dioxaborolane-4,5-dicarboxylic acid bis-dimethylamide in a tightly sealed container under an inert atmosphere, such as nitrogen or argon. Keep it in a cool, dry place, away from moisture, heat sources, and incompatible materials like strong oxidizers. Protect from light and handle in a well-ventilated area or fume hood to minimize exposure.
    Application of 2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide

    Applications of 2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide in Industrial Manufacturing

    2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide is a precision-designed boron-containing intermediate adopted by leading industries for its specific reactivity in advanced synthesis. We supply this specialty raw material to manufacturers powering segmented markets with rigorous quality control and compliance imperatives. Below, we outline established downstream application fields backed by verified integration in production environments.

    1. OLED Material Synthesis for Electronic Display Panels

    Electronics manufacturers incorporate this boron-based compound as a core reactant in high-purity organic light-emitting diode (OLED) emitter and host material synthesis. Its unique boron-ligand framework ensures desirable charge transport and photonic properties during molecule engineering, making it a preferred intermediate for next-generation display components. The compound enters synthesis at the advanced coupling stage, impacting end stability and efficiency of OLED layers.

    Industry compliance standards

    • IEC 62341 (Display Devices – OLED panels)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001:2015 (Quality Management System in electronics manufacturing)
    • QC080000 (IECQ HSPM for hazardous substance process management)

    Typical usage ratio

    • Applied at 0.2–1.5 mol% of main reactant in organic synthesis, tuned per specific OLED host or guest molecule design

    Downstream process integration

    • Introduced as a boron source during Suzuki–Miyaura cross-coupling for advanced organic semiconductors
    • Integrated at the controlled purification and condensation steps prior to layer deposition in OLED pre-material lines

    Final product types

    • OLED blue/green/red emitter layers
    • Host materials for thin-film display backplanes
    • Organic conductive films for mobile and TV panels

    2. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies employ this compound as a coupling agent in specialty boron-containing small molecule API development. Its precise amino-boronate structure enables selective cross-coupling in medicinal chemistry projects, facilitating the introduction of bioactive boron units in clinical candidates. The compound’s purity and well-defined reactivity provide high reproducibility in GMP-compliant QC laboratories.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP/NF and EP monograph guidelines for organic reagents
    • 21 CFR Part 211 (cGMP regulations for finished pharmaceuticals)
    • ISO 17025 (Testing and calibration laboratories)

    Typical usage ratio

    • Employed at 0.3–3.0% w/w relative to key intermediates, set according to the individual synthesis route and target API structure

    Downstream process integration

    • Fed during late-stage Suzuki-type or analogous C–C bond-forming steps under inert conditions
    • Participates in purification by crystallization post-reaction to minimize organic residues

    Final product types

    • Novel boron-containing kinase inhibitors
    • Boron-based anticancer agents
    • Pre-clinical screening molecules

    3. Fine Chemical Catalyst Ligand Preparation

    Producers of specialized catalysts and ligands for fine chemical and agrochemical industries leverage this material as a sophisticated boron precursor. The compound’s chelation ability and steric profile support the assembly of high-performance ligand structures, instrumental for enhanced selectivity in homogeneous catalytic transformations. Proper handling and controlled feeding during complexation dramatically improve catalytic activity and yield consistency.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for chemical synthesis plants)
    • REACH Regulation (EC) No 1907/2006 (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • Responsible Care® Global Charter guidelines
    • EU CLP Regulation (EC No 1272/2008) for labelling/classification

    Typical usage ratio

    • Added at 0.4–2.0 equivalents relative to metal center during coordination complex synthesis, modulated for binding efficiency

    Downstream process integration

    • Charged into the ligand formation reactor after initial solvent and metal precursor charging
    • Purified through vacuum distillation or crystallization prior to catalyst assembly

    Final product types

    • Boron-ligated palladium and nickel catalysts
    • Fine chemical-grade chiral ligands for asymmetric synthesis
    • Agrochemical synthesis catalysts

    4. Advanced Functional Polymer Production

    Polymer laboratories and manufacturing plants use this compound as a functionalization agent to introduce boron moieties into specialty polymer backbones. This unique modification enables fine-tuning of optical, conductivity, and mechanical properties required for niche applications such as membrane fabrication and sensor components. Adoption of tightly controlled feed processes maintains product uniformity batch-to-batch.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for polymer production)
    • EN 71-3 (Safety of materials for polymer applications in sensor devices)
    • REACH-compliant supply chain certifications
    • RoHS Directive 2011/65/EU for additive use in electronics polymers

    Typical usage ratio

    • Incorporated at 0.5–2.0 wt% of total monomer content, adjusted for target degree of functionalization

    Downstream process integration

    • Metered addition during copolymerization or post-polymerization grafting steps
    • Undergoes controlled curing and washing before film extrusion or molding

    Final product types

    • Boron-functional polymer membranes
    • Conductive sensor sheets
    • Specialty films for laser and optical applications
    Free Quote

    Competitive 2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide

    Meeting Modern Synthetic Challenges Head-On

    Every year brings new targets and heightened demands from researchers and industrial chemists. As a manufacturer steeped in the daily grind of reaction development, we see the reality: there’s constant pressure to deliver building blocks that reliably produce complex, high-purity products. 2-Butyl-[1,3,2]Dioxaborolane-4,5-dicarboxylic acid bis-dimethylamide has quietly become one of those reliable molecular workhorses. Our experienced staff have guided this compound from the earliest kilo-lab batches into robust commercial runs, and it keeps pulling its weight where consistency and smart molecular design matter most.

    What Sets This Boron Compound Apart

    We work directly with scientists who keep pushing the envelope, and many turn to this material for a good reason: the structure unlocks unique reactivity in borylation sequences, cross-couplings, and ligand development. Unlike common boronic acids or pinacol boronate esters, this bis-dimethylamide variant delivers elevated stability against hydrolysis, allowing for extended bench time and safer handling during scale-ups. This extra margin greatly reduces the frustration from batch rejections caused by small atmospheric slipups or delays in downstream processes. Our reaction crews rarely see issues with unwanted transesterification or acid-catalyzed decomposition during storage or in process holding, which cuts down on waste and lets researchers focus on chemistry, not logistics.

    Engineered Specifications for Reliable Results

    After several years of real-world campaigns, we can say: tight process control pays off. Many boron intermediates are notoriously finicky. From the very first kilo batch we optimized, we focused on consistent particle size and bulk density to avoid dust generation and clumping during transfer. Our QA teams regularly document melting points and color standards to flag cross-lot variances. Chemists value that the dimethylamide ligands promote selective transformations; they can achieve cleaner reactions compared to less selective boronate complexes—especially in iterative coupling protocols without worrying about crosstalk or side-product overload.

    Downstream users report that this compound dissolves predictably in both polar aprotic and nonpolar solvents, opening the door to diverse reaction conditions. We worked through multiple process trials to minimize metal contamination from reactors and transfer lines, staying under low ppm for iron, copper, and zinc—critical for researchers running ligand screens or palladium-catalyzed couplings where metal poisoners would choke off yields. In one scale-up campaign, a process engineer pointed out the reliable filtration rate of our material compared with an imported alternative, which reduced his campaign runtime by thirteen percent. Tweaks in crystallization conditions and solvent swaps made the difference, and nothing beats hands-on experience in the plant for driving those improvements.

    Supporting Both Innovation and Routine Production

    Over years of close work with the pharmaceutical and agrochemical synthesis teams, we have seen the anticipation for every expensive gram of new boron fragments destined for lead optimization. This molecule bridges that gap between R&D and routine production. Early screening runs showed that the dimethylamide-protected boronate group resists premature hydrolysis, allowing for more rugged and predictable handling. Chemists running iterative Suzuki–Miyaura couplings found fewer headaches from random byproduct peaks; the dioxaborolane ring offers solid protection against hydrolytic and oxidative stress, even at higher temperatures, keeping yields where they should be.

    Working hand-in-hand with pilot and commercial plants, we watched synthetic throughput rise as analysts flagged fewer reprocessing events. Each campaign brings fresh insights, but the ease of scale-up for this compound stands out. Large-batch crystallizations prove clean and filterable, batch-to-batch reproducibility stays strong, and packaging remains simple without the need for special atmosphere controls or fiddly inert containers. These might sound like small logistics details, but ask anyone running a 500-liter reactor what a caked-up transfer valve does to a night shift and you’ll know why we take handling seriously.

    Where 2-Butyl-[1,3,2]Dioxaborolane-4,5-Dicarboxylic Acid Bis-Dimethylamide Topples the Status Quo

    Standard boronic acids can let you down—hygroscopicity leads to steadily climbing water content, then the lot slumps, performance drops, and a replacement batch is needed. Our product, shielded by dimethylamide functionalities, retains free-flowing characteristics even after weeks outside a dry box. This means less re-testing, fewer dry-room interventions, and a smoother workflow for both custom synthesis houses and internal process teams. Analytical QC teams confirm that after stress testing in humid environments, the molecular integrity barely drifts, and the main peak remains clean by both LC and NMR, simplifying release protocols.

    For some, the chemical’s butyl substituent raises eyebrows—one client questioned the value of moving away from more mainstream methyl or ethyl analogues. In practice, that extra alkyl length tunes both hydrophobicity and solubility profiles. Those running PGM-catalyzed cross-couplings saw measurable improvements in the organic layer partition behavior, washing away frustrations tied to emulsion formation. The dioxaborolane ring, fused with those two carboxylic acid positions, locks in the geometry needed for site-selective functionalization; iterative arylations or alkynylations run cleaner and produce less material loss in purification. Technicians report less gumming in lines and minimal foam during dosing, which adds up to fewer headaches per batch.

    Backing Our Words with Data and Experience

    Experience in real-world production doesn’t lie. We’ve tracked this compound across dozens of lots, from 10-gram new product intro runs to multi-ton commercial campaigns. At each stage, feedback from downstream users prompted process tweaks—extra drying steps for some applications, finer sieving for automated dispenser feeds, or anti-caking agents for long-distance shipments. Every suggestion gets a trial, because process chemists and formulation teams live and die by batch variability, especially when schedules are tight and no one can afford a do-over. Analysts regularly comment on the tight GC purity, which habitually lands above 98% as required by many advanced synthesis protocols.

    Regular in-process controls help maintain this standard. NMR and mass spectrometry are standard for verifying structure and purity; for those scaling up for regulated markets, our team documents trace metals, residual solvents, and byproduct exclusion. After executing numerous pilot abort-and-restart drills forced by unexpected contaminant spikes—mostly avoidable with less robust boron reagents—our crew doubled down on line flush protocols and dedicated filtration trains. These investments save time and money for users down the line, no need to chase micro-impurities downstream in final synthesis steps.

    Comparisons That Matter to Working Chemists

    Of all the alternatives on the market—boronic acids, mono- or tri-dentate boronates, or single amide-substituted boron complexes—ours uniquely balances stability and reactivity. Methyl and ethyl analogues decompose faster on the bench, generating yields that drift down over time and drive extra labor chasing purity. Pinacol boronate esters, though cheap, offer little defense against water; even quick exposure during weighing sees those lots shift color and pick up volatility byproducts, causing headaches both in QC and in the plant.

    Customers with experience in automated dispensing consistently note the lack of “bridging” and clumping in feedstock bins—attributes traceable directly to improved crystallization and drying right at production, not during post-processing. Large projects in medicinal chemistry—teams working night and day screening hundreds of building blocks—benefit from our material’s forgiving shelf-life and bench stability. One group, working at a European pharma giant, slashed their monthly rejects by half after moving to this bis-dimethylamide variant, a change that rippled from the lab to purchasing as inventory stayed usable longer.

    The two dimethylamide groups help in selective cross-coupling reactions where group transfer selectivity often hampers scale-up from microgram to kilogram. We see less byproduct formation, more consistent catalyst turnover, and shorter reaction times. This isn’t just theory—daily lot results back it up, and supervising process engineers mention it in routine campaign debriefs. We’ve watched dozens of scale-ups move seamlessly from glassware to glass-lined steel without the usual hiccups, especially in iterative functionalization campaigns.

    Downstream Uses and Business Impact

    Medicinal chemists need predictable reactivity for library synthesis. This boron source stands up to the repeated functionalization steps integral to generating analog sets for SAR studies. Each iteration runs with minimal byproduct interference, leaving less time debugging HPLC surprises. Plant-scale teams roll out bigger campaigns with fewer cleaning breaks, since pipes stay clear and batch transitions move along smoothly. For agrochemical developers, the clean, robust functional group support means fewer carryover artifacts in formulations and a lower burden on downstream separation and drying stages.

    We routinely exchange technical feedback with industrial partners. One information-rich dialogue with a mid-sized contract developer led us to revisit our drying protocol, finding that one degree less in the final stage cut static charges by a measurable amount. Following implementation, they reported smoother gravimetric metering in a semi-automated line and less downtime for hopper jams. That’s the kind of front-line, boots-on-the-ground change that never shows up on specification sheets, but those gains matter to commercial operators.

    Other boron compounds lag in recovery and purity after stressful purification sequences. Bis-dimethylamide’s stability preserves the active boryl group throughout silica or reverse-phase prep, even under moderate acid or base. If you ask synthetic chemists managing ten or fifteen analogs in parallel, fewer purification slowdowns translate into reliable timelines for drug candidate submissions, or speedier progression from hits to lead series.

    Our Real-World Approach to Risk and Supply

    Shortages and price swings rattle everyone’s nerves, from purchasing managers to research leads. We built our production around in-house raw material controls. Batch after batch, we’ve prioritized local sourcing wherever possible, dual-vetted input chemicals, and maintained relationships that ensure backup deliveries. This focus proved critical during shipping disruptions, giving our clients steady access even when competitors experienced delivery shortages or rolling backorders.

    Our logistics department mapped optimal packing formats for both regional shipments and ocean-freight dispatch to overseas tech centers. Double-lined drums, moderate-pack bulk, or small-dose high-purity containers—flexibility matters to every chemist, whether running 100 grams or scaling to several metric tons. Each packing format underwent testing to validate integrity against vibration, humidity, and temperature swings, removing surprises on receipt that could delay campaigns. Shipping validation became routine because the stakes for clean, dry, and pure deliveries are high.

    Continuous Dialogue Drives Us Forward

    Every real-world campaign teaches what no datasheet can tell. Our R&D team interacts directly with chemists facing problems, whether in high-throughput screening, pilot scale-ups, or commercial process transfers. Only by staying tuned into these needs have we kept rejection rates ultra-low and built a stable, repeatable supply chain.

    Community is built on shared knowledge, and every chemist, from junior bench hand to senior plant manager, played a role refining our process. Our technical staff frequently collaborate with teams running pressure reactors, automated feed systems, and tight-staged purification trains. When a frustration occurs—an unexpected lump, a spot on a TLC plate, a strange off-gas—we pick up the phone, run fresh samples, and adapt. Keeping those conversation lines open separates real manufacturers from those far removed from the plant floor.

    Pushing the Envelope—Safely and Sustainably

    Responsibility runs hand in hand with commercial success. We invest in closed-loop solvent recovery systems to minimize emissions, capture process off-gas for reprocessing, and document every disposal in strict adherence to environmental regulations. Safety specialists oversee everything from PPE compliance to process hazard analysis, and we conduct regular drills on site containment. Continuous improvement runs beyond just chemistry, shaping how we treat staff, manage risk, and engage with our local communities.

    We recognize pressure on global supply chains, volatility in the raw material markets, and stricter regulatory expectations every year. By designing our process for flexibility—modular reactors, redundant drying and sieving lines, and constant sampling—our factory can adapt to disruptions without sacrificing quality. Our sustainability team tracks waste reduction, reuse of packaging, and energy intensity. We transparently share these metrics with partners, knowing that real progress demands accountability along the entire value chain.

    The Road Ahead

    As customers set their sights higher and workflows grow more complex, we continue to refine what we make and how we make it. 2-Butyl-[1,3,2]Dioxaborolane-4,5-dicarboxylic acid bis-dimethylamide stands out for practical reasons. Stability under real-world conditions, consistent batch quality, and adaptability in both development and commercial campaigns keep its value high for our partners. Feedback feeds improvement. We remain hands-on in both our labs and our clients’ experiences, seeing each new campaign as another round of learning.

    In a world with tight timelines and higher expectations every season, a stable, versatile molecule like this one becomes more than a catalogue item—it’s a tool built through listening, iteration, and chemistry that works where it matters most. The path forward brings new challenges, but with the right team, committed manufacturing, and honest exchange with our customers, solutions keep coming. Every problem we’ve solved together proves that smart choices about raw materials ripple far beyond the reaction flask.