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Dimethylaminoborane

    • Product Name Dimethylaminoborane
    • Alias Borane, dimethylamino-
    • Einecs 214-658-0
    • 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

    976393

    Chemical Name Dimethylaminoborane
    Chemical Formula C2H8BN
    Molar Mass 58.91 g/mol
    Appearance Colorless liquid
    Melting Point -60 °C
    Boiling Point 39-40 °C
    Density 0.713 g/cm³
    Solubility In Water Reacts with water
    Cas Number 74-94-2
    Ec Number 200-652-9
    Structure H3B-N(CH3)2
    Flammability Highly flammable
    Odor Fishy, ammoniacal

    As an accredited Dimethylaminoborane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, moisture-proof glass bottle with a blue screw cap, labeled "Dimethylaminoborane, 25g," featuring hazard warnings and chemical details.
    Shipping Dimethylaminoborane should be shipped in tightly sealed containers under inert gas, such as nitrogen or argon, to prevent moisture and air contact. It must be packed with appropriate hazard labeling in accordance with local and international regulations, and transported as a flammable solid in a cool, dry, and well-ventilated area.
    Storage Dimethylaminoborane should be stored in tightly sealed containers under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Store in a cool, dry, and well-ventilated area away from heat, oxidizers, and acids. Keep the container tightly closed when not in use, and protect from sources of ignition, as the compound may be flammable or reactive.
    Application of Dimethylaminoborane

    Applications of Dimethylaminoborane in Industrial Manufacturing

    Dimethylaminoborane serves as a specialized chemical intermediate in several precision technology sectors, where its controlled reactivity and reducing properties play a pivotal role in advanced materials production and fine chemical synthesis. Below are real-world industrial application scenarios where our manufacturing-grade material adds direct value through reliable process integration.

    1. Electroless Nickel Plating Additives for Electronic Connectors

    In the electronics industry, dimethylaminoborane functions as a boron source and reducing agent in electroless nickel plating baths, critically improving deposit uniformity and enhancing the solderability and wear resistance of electronic connectors. This compound enables the production of high-boron nickel alloys required for advanced printed circuit board connectors and microelectronic components, where precise boron content and low surface porosity are essential parameters during continuous reel-to-reel or batch plating operations.

    Industry compliance standards

    • IPC-4552A (Performance specification for electroless nickel/immersion gold plating)
    • IEC 60068-2-2 (Environmental testing for electronic components - Test methods)
    • RoHS Directive 2011/65/EU (Restriction of hazardous substances in electronics)
    • ISO 4527 (Nickel-Boron alloy coatings requirements)

    Typical usage ratio

    • Bath concentration typically ranges from 0.5 g/L to 1.5 g/L, adjusted according to required boron content (2-7 wt%) in the deposited alloy and line speed.

    Downstream process integration

    • Added directly into the plating solution after electrolyte component mixing; maintained via titration and automated dosing systems during operation cycles.

    Final product types

    • Press-fit connectors for PCBs
    • Miniaturized terminals in mobile electronics
    • Lead frame components for semiconductor packages
    • Corrosion-resistant relay contacts

    2. Advanced Magnetic Material Synthesis

    Dimethylaminoborane is applied as a reducing agent and boron precursor in the manufacture of rare earth and transition metal boride powders, which form the basis of soft magnetic cores and permanent magnetic materials. This application necessitates strict control of boron incorporation to ensure high magnetic permeability, electrical resistivity, and thermal stability of specialty alloys and ferrites produced for transformers and high-frequency inductors.

    Industry compliance standards

    • ASTM B783 (Specification for fine boron-containing metallic powders)
    • IEC 60404 (Requirements for magnetic and magnetostrictive materials)
    • REACH Regulation (EC) No 1907/2006
    • JIS H 5402 (Magnetic materials - Iron and iron alloy powders)

    Typical usage ratio

    • 0.2:1 to 0.6:1 molar ratio to target metal precursor, adjusted to control resultant boron content (1-5 wt%) in synthesized powder.

    Downstream process integration

    • Introduced in controlled-atmosphere reduction reactors during the co-precipitation step, followed by thermal treatment at 600-1200℃ to achieve desired microstructure.

    Final product types

    • Soft magnetic alloy cores for transformers
    • Nanocrystalline inductor cores
    • Permanent magnets for electric motors
    • Boron-doped ferrites for EMI shielding

    3. Pharmaceutical Intermediate in Custom Boron Compound Synthesis

    Within the pharmaceutical sector, dimethylaminoborane is a preferred specialty reagent for synthesizing organoboron intermediates used in active pharmaceutical ingredient (API) manufacturing. In particular, it supports the formation of boronic esters and acids essential for Suzuki-Miyaura coupling reactions, common in the assembly of complex, highly targeted small-molecule APIs. Process chemists benefit from improved selectivity and mild reaction conditions enabled by this borane compound, ensuring efficient downstream GMP synthesis.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) guidelines for APIs
    • US FDA 21 CFR Part 211 (CGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (ChP) production standards
    • EU GMP Annex 8 (Sampling of Starting and Packaging Materials)

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents relative to boronate reactants; optimized by process chemists during development for maximum conversion and selectivity.

    Downstream process integration

    • Metered into synthesis reactors at low temperature under inert gas, prior to catalyst introduction in boron-functional group formation step.

    Final product types

    • Boronic acid esters for anticancer drug APIs
    • Boron-containing antifungal intermediates
    • Chiral organoboron building blocks
    • Intermediates for targeted molecular therapeutics

    4. Fine Chemical Reducing Agent for Photoinitiator Synthesis

    Dimethylaminoborane functions as a selective reductant in the preparation of complex photoinitiators and specialty resins for the UV-curable coatings and inks industry. Process control during reduction steps affects the purity level and absorption profile of the photoinitiator batches, which determine final product color stability and reactivity critical for high-speed inkjet, 3D printing, or high-gloss lacquer applications.

    Industry compliance standards

    • SOCMA Responsible Care® Product Safety Code
    • ISO 9001:2015 (Quality Management Systems for chemical production)
    • TSCA (Toxic Substances Control Act) regulation
    • China GB/T 37515-2019 (UV curing materials industry standard)

    Typical usage ratio

    • Stoichiometry typically set at 1.0-1.5 molar equivalents per reducible group in precursor, adjusted for batch scale and desired end-point purity.

    Downstream process integration

    • Added during reactor charging, with continuous in-process monitoring of reductive conversion and quenching before downstream isolation of photoinitiator.

    Final product types

    • Benzoin ether-based photoinitiators
    • Acylphosphine oxide initiators
    • Boron-modified oligomeric resins
    • UV-cured coatings and inkjet inks

    5. Hydrogenation Catalyst Precursor for Asymmetric Synthesis

    Dimethylaminoborane serves as a key boron and nitrogen donor in the preparation of organometallic catalysts specialized for asymmetric hydrogenation in the fine chemical and agrochemical industry. These catalyst systems enable stereoselective reductions that underpin high-value intermediate manufacture for crop protection agents and chiral pharmaceutical building blocks, under tightly controlled reaction conditions to achieve regulatory-grade optical purity.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • ISO 14001:2015 (Environmental management systems for chemical processes)
    • Responsible Care® Process Safety Code
    • European Pharmacopoeia (Ph. Eur.) for chiral intermediates

    Typical usage ratio

    • Precursor mol ratio typically 0.5-2.0 equivalents relative to metal complex, tailored per target catalyst’s activity and loading strategy.

    Downstream process integration

    • Reacted with transition metal salts under inert atmosphere during catalyst precursor complexation, followed by purification and application to hydrogenation reactors.

    Final product types

    • Asymmetric hydrogenation catalyst powders
    • Enantioselective chiral intermediates
    • Crop protection active ingredient intermediates
    • Chiral pharmaceutical building block intermediates
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    Certification & Compliance
    More Introduction

    Dimethylaminoborane in Modern Chemical Production: Manufacturer’s Insights

    Our Journey with Dimethylaminoborane

    Working over the years with a host of organoboron compounds, one product that repeatedly stands out for us as a manufacturer is Dimethylaminoborane. We synthesize this compound under strict temperature and atmospheric controls in our production line. Each batch must adhere to tight purity demands, with a focus on sensitive handling from raw material storage to finish packaging. Out in the field, chemists rely on our ability to keep impurities at bay and strict moisture exclusion throughout the cycle from synthesis to shipment. We have built up these systems after seeing, repeatedly, how any compromise here will quickly impact both reactivity and performance, especially in catalytic and reduction applications.

    Defining Dimethylaminoborane: What It Brings To The Table

    Dimethylaminoborane, chemically named as (CH3)2N–BH3, offers a unique blend of boron and nitrogen chemistry in a single, highly reactive package. Unlike other borane complexes, this molecule carries a dimethylamino substituent, shifting both its electron density and stability profile. The presence of that dimethylamino group sets it apart from simple borane and many alkylboranes, both in terms of reactivity and selectivity. Over years of working with different boron sources, this variant consistently brings a pronounced edge in fine chemical synthesis, specialty reductions, and certain types of polymer chemistry, due to its ability to donate hydride under milder conditions.

    Specifications That Matter in the Real World

    We manufacture Dimethylaminoborane to a minimum purity of 97% by weight, based on NMR and titrimetric analysis. Trace water content is always kept under 100 ppm, using in-line Karl Fischer titration. The product typically presents as a colorless to slightly yellow liquid, and every tank batch falls within an expected 0.82–0.84 g/cm3 density window at 20°C. From a manufacturer’s perspective, these metrics only tell half the story. In our experience, maintaining a rigorous exclusion of oxygen and water throughout storage and transfer impacts the shelf-life and reactivity far more than published parameters suggest. We use only stainless lines and specialized seals along our filling stations, because conventional rubber or plastic gaskets lead to trace decomposition and fouling problems.

    How We See Usage in Industry

    Many of our customers in pharmaceutical R&D favor Dimethylaminoborane for reductive amination processes, as it gives clean conversion to secondary and tertiary amines without over-reduction. In contrast to sodium borohydride and other traditional reducers, this compound can offer greater selectivity toward nitrogen-containing substrates. That selectivity rises partly from the electron-donating influence of the dimethylamino ligation, which tones down the boron’s reactivity. We have seen it open up several direct routes to intermediates that would be tricky or less-efficient using classical boranes or hydrides. Enterprises involved in specialty polymer synthesis use this compound to introduce boron-nitrogen bonds into precision frameworks and block copolymers, a feat less reliably achieved using more volatile borane adducts.

    On the pilot plant scale, Dimethylaminoborane delivers consistent reduction results, with fewer by-products than we typically see using diborane or other trialkylboranes. Handling is still a hands-on task: our operation stores it in pressure-rated, nitrogen-flushed vessels due to its air and moisture sensitivity. We've established close feedback loops with partner labs on both sides of the value chain, as real-world performance and ease of work-up matters just as much as textbook reactivity. This open, technical dialogue with chemists and engineers in active service—rather than relying wholly on theoretical models or old literature—guides our ongoing improvements in quality.

    How Dimethylaminoborane Differs From Other Boron Compounds We Have Made

    Across multiple campaigns with trialkylboranes, borane-THF, borane-dimethylsulfide, and sodium borohydride, we consistently note Dimethylaminoborane’s unique balance of reactivity and selectivity. Unlike borane-THF, which volatilizes easily and poses storage complications, Dimethylaminoborane remains relatively manageable in liquid handling systems under dry nitrogen. Unlike sodium borohydride, which provides high reactivity but sometimes poor selectivity—especially in the presence of complex organic frameworks—our Dimethylaminoborane delivers a more nuanced reduction profile.

    When synthesizing sensitive intermediates such as α-amino boranes, using more traditional boranes or hydrides often yields broad distributions of products or, worse, rapid decomposition of valuable starting materials. Dimethylaminoborane, by contrast, permits more fine-tuned control under milder conditions, lowering by-product formation and improving yields in the hands of an attentive operator. Its intermediate volatility and ability to be applied neat or in common solvents like toluene or tetrahydrofuran increases flexibility for scale-up or continuous processing. Direct comparisons with trimethylborane reveal that our product grants a steadier, more predictable reduction effect, especially for amine and imine substrates.

    Why Handling and Packaging Make All The Difference

    Dimethylaminoborane requires respect and proper technique through every step: from finishing reactors to the point it leaves our loading docks. Because this compound reacts with atmospheric moisture and oxygen, we developed all-stainless, sealed transfer rigs with in-line desiccant columns. Our packaging team packs every shipment under high-purity nitrogen, and we recommend end-users draw off only with syphoning or pumping under positive nitrogen pressure. Small lapses here invite unwanted hydrolysis, so we regularly check the seals and atmospheres even on storage containers left idle for a few days. Anyone new to this chemistry quickly learns that borane-related waste from poor packaging costs far more in lost activity, cleanup, and safety measures than any upfront investment in correct containers or protocols.

    Customers running continuous or multi-batch reductions especially benefit from bulk supply delivered in lined drums or pressure cylinders, kept cold and inert until point-of-use. For those running bench-scale reactions, we offer aliquoted glass ampoules that open only immediately before use. Our manufacturing team crosses every ‘t’ on logistics because a single breach in packaging, even in transit, can spoil a full lot. We have learned the hard way that packaging integrity is as crucial as chemical purity.

    Operational Experience: Learning From Scale-Up and Real Conditions

    Direct feedback from larger plant trials gave us sharp insight into practical limitations and strengths. Unlike the relatively simple behavior of solvents or stable acidic catalysts, Dimethylaminoborane can lose potency quickly under sub-optimal storage or if exposed to ambient humidity. We reserve product for distribution only after full in-plant aging and stress testing, including exposure to critical storage and transfer steps. Customers running multi-tonne campaigns often share their working-up protocols and observed by-product ratios, pushing us to tweak purification and stabilization steps on our end for greater consistency.

    We found in practice that mixing regimes and temperature ramps during addition matter more for getting smooth, controlled reactions than most published procedures suggest. Operators in our plant—trained to spot subtle viscosity changes and suspect exotherms—know to halt addition or adjust nitrogen blanket flow in response to what they see, not just a recipe. Such points of operator vigilance feed directly into process documents and training programs we offer to new clients, because in the field there is no substitute for sharp, skilled attention.

    Practical Differences: Dimethylaminoborane Versus Competing Borane Products

    Compared to borane-tetrahydrofuran, our product stores more robustly under inert conditions—even for periods extending past six months. Handling borane-tetrahydrofuran leads to routine venting and loss of material due to solvent volatility. Dimethylaminoborane, with its higher boiling point, brings down these headaches. In contrast to sodium borohydride, which ships safest as a solid but generates hydrogen gas during use, our Dimethylaminoborane streamlines reduction chemistry with less hydrogen evolution and more heads-up selectivity. We watched enough parallel reduction runs—both in-house and in customer labs—to vouch that dimethylaminoborane consistently minimizes over-reduction of sensitive substrates, streamlining purification and bolstering consistency for scaling up.

    Some of our pharmaceutical and electronic material manufacturing partners switched away from triethylborane or trimethylborane, citing not only the improved performance and handling but the reduced hazard potential. Dimethylaminoborane does not ignite quite so readily at room temperature and can be made to react only on command if handled by practiced hands. Even so, we drill both our people and our clients on safe, sealed operation throughout the supply chain. The benefit of a less volatile, but still powerful, hydride donor matches well with today’s needs for reliable, robust chemistry.

    Supporting Innovation with Consistent, Hands-On Supply

    Dimethylaminoborane supports a range of routes in complex molecule assembly, especially where classic borane reagents fall short. Customer case studies highlight successes in building up advanced ligands and boron-labeled pharmaceuticals, for which control over each addition matters more than flat-out maximum reducing power. Our in-process controls—NMR monitoring, regular moisture/hydrolysis testing—offer reliable feedback on each drum and shipment. We always compare the outcome from plant-scale applications against small-batch purity indexes, aiming to keep process drift in check.

    Our manufacturing line invests in analytical improvements year over year, adding bench NMR, trace metal and water testing, and regular round-robin quality trials against outside labs. We take seriously the challenge of keeping dimethylaminoborane both pure and as active as possible, because downstream results hinge on our side’s discipline. Teams on site continue to recommend incremental safety tweaks or process optimization, learning from both production snags and client-side user reports.

    Eliminating Waste and Enhancing Sustainability Concerns

    Producing and shipping an air- and moisture-sensitive chemical at scale raises environmental and safety responsibilities. We have rolled out closed-system filling and recovery operations in the plant, and we reclaim spent packaging for safe cleaning and recycling. By minimizing open transfers and batch purging, we sharply reduce both operator risk and fugitive emission. Lab operators in client plants have adopted similar measures after site visits, encouraged by the stability and reliability these enhancements provide.

    Waste minimization also factors into our upstream raw material procurement: favoring boron and amine sources with minimal by-products allows us to limit the need for intensive downstream purification. Over years of scaling up, we transitioned away from conventional batch pilot runs to continuous reaction and fill lines, using measured, small volume additions to gain the best yield for each increment of raw stock. By revealing our internal controls and testing benchmarks, we have promoted greater trust and traceability for customers aiming to certify their supply chains or meet regulatory reviews.

    Supporting Researchers, Developers, and Manufacturers

    Our long-standing partnerships with academic and commercial research groups brought invaluable direct feedback on how Dimethylaminoborane meets modern synthetic challenges. In-demand processes for assembling bioactive pharmacophores or high-performance electronic resins now depend on this reagent’s selective reduction behavior. In several joint collaborations, we explored custom purification grades of Dimethylaminoborane: ultra-dry, ultra-pure, or specifically stabilized versions tailored to certain routes.

    We maintain an open-door technical support cycle that welcomes direct questions on both assay and application. Chemists often describe unique performance issues, such as slow starts in cooled reactions or spurious byproducts in mixed-solvent systems. These user-level conversations shape our in-plant priorities. Thus, improvements in purity and application recommendations arise not from our assumptions, but from hands-on, real-world experiments. Plenty of research partners prefer to work side-by-side with our process staff, knowing they’ll get not just a drum or sample, but responsive troubleshooting and shared experience. Our entire operational model centers on these open exchanges, which in turn keeps our product at the forefront of innovation.

    Consistent Product, Reliable Chemistry

    In more than a decade of continuous production, our team has learned every shortcut and every pitfall attached to Dimethylaminoborane. This chemical’s performance depends on steady hands, exacting process discipline, and an uncompromising focus on purity right up to the customer’s bench or plant. By refining our manufacturing, packaging, and support around end-use realities, we deliver more than just a reagent: we bring informed partnership and genuine technical reliability to the table. The proof shows itself not only in the number of repeat buyers, but in the high bar our customers set for us—and we willingly work to exceed it, batch after batch.