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2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid

    • Product Name 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid
    • Alias DMAPA
    • Einecs 629-475-2
    • 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
    VTB
    Specifications

    HS Code

    905644

    Productname 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid
    Casnumber 851386-76-8
    Molecularformula C8H12BNO4S
    Molecularweight 229.06
    Appearance White to off-white solid
    Meltingpoint 175-178°C
    Purity Typically ≥98%
    Solubility Soluble in DMSO, methanol
    Storagetemperature 2-8°C
    Smiles B(C1=CC=CC=C1N(S)(=O)=O)(O)O
    Inchikey FRCAOWQXCLVEKC-UHFFFAOYSA-N
    Synonyms 2-(Dimethylsulfamoyl)phenylboronic acid
    Hazardstatements May cause respiratory tract irritation
    Usage Organic synthesis, pharmaceutical intermediate

    As an accredited 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 5 grams of 2-(N,N-Dimethylsulphamoyl)phenylboronic acid, clearly labeled with hazard and handling information.
    Shipping **Shipping Description:** 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid is securely packaged in sealed, chemical-resistant containers. The shipment complies with relevant chemical transport regulations, avoiding exposure to moisture and light. Material Safety Data Sheets (MSDS) and labeling are provided. Shipment is via certified carriers, ensuring safe and prompt delivery to the required destination.
    Storage **Storage for 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid:** Store this chemical in a tightly sealed container, protected from moisture and light, at 2-8°C (refrigerator). Keep away from heat, oxidizers, and strong acids. Use in a well-ventilated area and handle with appropriate protective equipment. Ensure storage area is clearly labeled and complies with all local chemical safety regulations.
    Application of 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid

    Applications of 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid in Industrial Manufacturing

    As a specialist manufacturer, we supply 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid to advanced industries where its boronic acid functionality is vital for high-selectivity and process efficiency. Below we present its confirmed roles in major downstream sectors, specifically focusing on genuine industrial implementations, each with relevant regulations, process context, and real finished goods.

    1. Pharmaceutical API Synthesis: Suzuki-Miyaura Coupling Intermediates

    2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid serves as a boron-based building block in modern medicinal chemistry, frequently used in Suzuki-Miyaura cross-coupling for the assembly of complex biaryl structures required in active pharmaceutical ingredients (APIs). The boronic acid moiety enables precise carbon-carbon bond formation, essential to manufacturing small-molecule drugs, notably kinase inhibitors and certain antineoplastic agents. Careful control of purity and residual reagents is mandatory, with process development tailored to each target molecule’s structure and regulatory route.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • EU GMP Annex 2 for API Synthesis
    • Relevant pharmacopoeias (USP, EP) impurity limits for synthetic intermediates

    Typical usage ratio

    • Used at 1.0–1.3 molar equivalents relative to aryl halide substrates; adjusted to minimize excess and avoid boron residue exceeding pharmacopoeial standards

    Downstream process integration

    • Added to the reaction vessel during the Suzuki-Miyaura coupling step, typically in the presence of a Pd(0) or Pd(II) catalyst and a base, under controlled atmosphere and temperature (often 60–100°C)

    Final product types

    • API biaryl intermediates (e.g., for anti-cancer agents, kinase inhibitor scaffolds, select CNS compounds)
    • Patent-protected API molecules incorporating the dimethylsulphonamide motif

    2. Custom Fine Chemical Synthesis: Fluorophore and Probe Development

    Research chemical manufacturers exploit this boronic acid for the synthesis of functionalized aromatic scaffolds, facilitating the design of fluorescent or colorimetric sensor molecules. The dimethylsulphamoyl group modulates polarity and stability, allowing for the generation of diagnostic probes and biological tags used in advanced analytical and bioimaging applications. QA systems focus on batch traceability and endpoint purity, particularly where material feeds into regulated diagnostics.

    Industry compliance standards

    • ISO 9001:2015 certified QC and batch traceability
    • ISO 13485:2016 for diagnostics precursor manufacturing
    • REACH Registration (as applicable for EU manufactured probes)

    Typical usage ratio

    • Incorporated at 0.8–1.1 molar equivalents in conjugation reactions, with actual loadings adjusted to match the reactivity of halogenated partners and desired labelling density

    Downstream process integration

    • Dosed during aromatic biaryl assembly, prior to post-functionalization and dye or probe conjugation; sequence timing affects probe purity and quantum yield

    Final product types

    • Fluorescent probes for cell imaging
    • Biochemical sensor molecules
    • Labelled peptide and small molecule diagnostics (research use only and select CE-IVD categories)

    3. Agrochemical Intermediate Synthesis

    The compound finds targeted usage in the development of advanced herbicide and fungicide intermediates, particularly for the synthesis of diaryl or heteroaryl-containing active ingredients. Its tailored reactivity profile enables cost-effective and high-selectivity coupling, which is critical for agrochemical manufacturers complying with process safety and environmental protection standards. Integration of this intermediate supports the scale-up efficiency and product differentiation necessary in modern crop protection pipelines.

    Industry compliance standards

    • FAO/WHO Good Laboratory Practice (GLP) for Industrial Synthesis
    • OECD Guidelines for Testing of Chemicals
    • ISO 9001:2015 Quality Management for agrochemical production
    • EU Regulation (EC) No 1107/2009 for plant protection product synthesis

    Typical usage ratio

    • Applied at 1.0–1.5 molar equivalents per aryl halide coupling partner; surplus usage limited to control boronic acid residues in downstream technical material

    Downstream process integration

    • Introduced into the core coupling stage, after base hydrolysis of precursor aryl halide, allowing high-yield conversion ahead of subsequent ring modifications or protective group manipulations

    Final product types

    • Diarylamine-based pre-herbicide intermediates
    • Fungicide technical concentrate intermediates for final formulation and toxicological assessment

    4. Material Science: Specialty Polymer Synthesis

    In advanced materials manufacturing, 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid enables the synthesis of functionalized monomers and engineered block copolymers, useful for specialty coatings, adhesive systems, and sophisticated membrane materials. Its integration imparts selectivity in cross-linking reactions and enables the introduction of boron or sulphamoyl functional groups for targeted material characteristics, such as enhanced hydrophilicity or chemical resistance. Material specifications and polymer purity are closely linked to downstream device compliance and application area.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for polymer manufacturing
    • REACH and TSCA compliance for polymer precursors
    • ISO 10993 for biomaterials if intended for medical device applications
    • ASTM D638 (mechanical properties for thermoplastics, if applicable)

    Typical usage ratio

    • 0.5–2.0 wt% of total monomer feed, proportional to target polymer functionalization level; fine-tuned depending on required physical and chemical properties of the end polymer

    Downstream process integration

    • Monomer functionalization step prior to chain growth polymerization; may also be incorporated in post-polymerization modification cycles

    Final product types

    • Adhesive polymers with boronic functionality
    • Membrane materials for analytical filtration
    • Surface-modified specialty coatings for electronics or biocompatible devices

    5. Electronic Chemicals: Organic Semiconductors and Sensor Film Development

    This boronic acid compound is selected for building semiconducting organic molecules and tuning the optoelectronic properties of advanced sensor films. Its ability to create clean, high-yield C–C coupling allows for the reliable production of aromatic-rich systems necessary for organic light-emitting diodes, thin-film transistor elements, or selective chemical sensor substrates. Electronic manufacturing standards and contamination controls guide process and end-use suitability.

    Industry compliance standards

    • IEC 61340-5-1 (electrostatic discharge protection in electronics manufacturing)
    • IPC-A-610 (Acceptability of Electronic Assemblies)
    • RoHS Directive for hazardous material control in electronics
    • SEMATECH Generic Requirements for organic electronic materials

    Typical usage ratio

    • Used within 0.6–1.2 molar equivalents in semiconductor precursor coupling reactions; variation optimized by target molecular weight and electronic band gap specifications

    Downstream process integration

    • Introduced in the key aromatic coupling step prior to film casting or device fabrication; purity and side-product controls are implemented to meet performance requirements

    Final product types

    • Organic semiconductor intermediates for OLED displays
    • Sensor films for gas/vapor detection in industrial monitoring equipment
    • Precursor molecules for flexible electronic circuit coatings
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    Certification & Compliance
    More Introduction

    Introducing 2-(N,N-Dimethylsulphamoyl)phenylboronic Acid: Precision and Reliability From the Source

    Real-World Manufacturing Experience Matters

    At our chemical plant, we've spent years developing and refining specialized boron-containing reagents to meet the demands of evolving synthetic chemistry. Among our growing portfolio, 2-(N,N-Dimethylsulphamoyl)phenylboronic acid stands out due to its reliability, high purity, and demonstrated success in research and production. Across countless batches and client requests, we have learned what chemists value most: actual batch-to-batch consistency, clear traceability, and honest communication about what goes into every kilogram we deliver.

    Understanding the Unique Chemical Profile

    2-(N,N-Dimethylsulphamoyl)phenylboronic acid brings a lot to the bench. Its formula, C8H12BNO4S, reflects a fusion of a phenylboronic acid backbone with a dimethylsulphamoyl substitution—an arrangement that chemists recognize from SAR campaigns and late-stage functionalizations. The presence of both boronic acid and sulphamoyl groups allows for diverse cross-coupling pathways, particularly in Suzuki-Miyaura reactions and fragment-based construction.

    Processors and process chemists have described its solid-state stability as a key advantage over certain unstable boronic acids. The product carries a typical melting point range above 210°C (variations may occur with specific hydration levels), with minimal air-sensitivity compared to other boronic esters we routinely handle. In terms of appearance, customers regularly receive a fine, off-white or almost colorless crystalline powder—an indicator of our effective purification steps and rigorous crystallization protocols.

    Specification Through Real Practice

    We test each batch by validated HPLC to ensure purity exceeding 98%, with boron content checked by ICP-MS. Too many times, we've seen inconsistent grades from brokers lacking insight into onsite controls. That leads to tailing peaks and unpredictable conversion rates. We came up through hands-on synthesis, so every step—sulphamoylation, boronation, and crystallization—happens directly within our shop, with records going back a decade. Moisture control forms a core part of final packaging; the compound is packaged under nitrogen where feasible, in sealed HDPE containers, and we employ regular Karl Fischer titration to monitor water content, ensuring downstream reproducibility for your applications.

    Where Performance Meets Practicality

    Clients often ask us why they should specify 2-(N,N-Dimethylsulphamoyl)phenylboronic acid over more familiar phenylboronic derivatives. The answer comes from hands-on experience. Coupling chemists report cleaner conversions and fewer side-products when using our material, especially during scale-up or challenging substrate scope explorations. We routinely support pharmaceutical discovery teams, academic collaborators, and small specialty manufacturers working in medicinal chemistry. Our compound’s robust stability under inert atmosphere storage lets sites maintain active stocks for longer periods without repeated re-testing—a point our partners appreciate when planning multistep routes or library campaigns.

    Applications: Insights Gained From Direct Client Feedback

    Medicinal chemists who seek to introduce boronic acid signatures into complex scaffolds trust the unique profile of 2-(N,N-dimethylsulphamoyl)phenylboronic acid. The dimethylsulphamoyl motif offers opportunities for further derivatization, especially when selective transformation is needed downstream. In Suzuki couplings, it stands up to a variety of base and ligand conditions—Palladium(0) catalysis, various aryl halides, and combinatorial conditions have all been reported successful based on our follow-up case studies with clients. We have witnessed a noticeable reduction in problematic protodeboronation or hydrolytic decomposition, which often undermines less robust boronic acids, especially on scale.

    When we receive a call from a process chemist frustrated by inconsistent crystallinity or unexpected byproducts, we know from direct production experience that off-spec batches often come from lax purification standards at intermediary suppliers. Our strict adherence to appropriate column, recrystallization, and micronization methods helps customers avoid these pitfalls.

    Differences Realized Through Manufacturing

    Many boronic acids look similar on paper but behave unpredictably in live reactions. Through firsthand practice, we have observed that 2-(N,N-dimethylsulphamoyl)phenylboronic acid carries extra resistance to oxidation and displays excellent retention on hydrophilic stationary phases. This is not a trivial enhancement—handling ease and storage reliability can spell the difference between a seamless kilo campaign and a troubleshooting headache.

    Other phenylboronic acids, including simple phenylboronic acid or para-substituted analogues, often suffer from higher self-condensation tendencies. We have measured lower loss on drying and less tendency to form sticky clumps compared to monofunctional or minimal-substituent derivatives. For users needing crystalline, free-flowing powders, this is more than a luxury; it often means the difference between an easy transfer into reactors or laborious scraping and inconsistent weighing.

    Some clients in chemical development groups have highlighted how our compound’s distinct sulfur and nitrogen profile opens up post-coupling modifications, such as oxidation to sulfonyl derivatives or N-dealkylation routes. These extended handles allow for analog design well beyond what a standard boronic acid can deliver. New methods exploiting orthogonal transformations often show better compatibility, thanks to this broader functional group tolerance.

    Operational Safety and Handling: Practical Insights

    We ship this material globally, so we understand the importance of genuine, hands-on knowledge about shipping stability and storage demands. Reports we receive from shipping partners confirm that our packing and rigorous QC protocols minimize issues with caking, moisture ingress, or off-gassing—a testament to the tight controls maintained across our loading docks.

    Workers handling benchtop transfers value the visible particle size uniformity that results from our in-house micronization. Agglomeration becomes rare, weighing consistency improves, and less time is lost to sieving or re-drying. We do not overpromise on hazard mitigation, but our experience shows that diligent containment, regular glove checks, and routine monitoring for airborne particulate ensure safe working conditions in both lab and pilot plant settings.

    Environmental Responsibility Rooted in Actual Production

    Our engineers assess every process step for waste minimization and responsible use of auxiliary chemicals. Sulphamoyl formation often involves volatile amines or sulfonyl chlorides; careful recovery and recycling have allowed us to cut organic emissions by over a third in the past five years. Spent borates and acid streams are neutralized and sent for downstream mineral recovery, not simply dumped in hazardous waste. We operate our reactors under best-available control measures, with scrubbers and real-time air quality monitoring in place.

    As boron is both an essential plant micronutrient and a regulated emission in some jurisdictions, we monitor trace borate content in site effluent, keeping levels well below local limits. Our plant’s environmental auditors routinely verify compliance, creating transparency for downstream users who receive our regulatory documentation (not just standard SDS paperwork but full chain-of-custody tracking).

    Cost Efficiency Informed by Experience

    While low-cost offers from third-party traders may look attractive, years of supply chain troubleshooting have demonstrated the hidden expense of off-spec product, shipment delays, and untraceable manufacture. Our pricing reflects the realities of quality raw material sourcing, skilled workforce, and direct control of every process stage. Clients balancing budget and scale tell us the up-front savings of unverified sources melts away when reaction failures or unexpected impurities threaten entire projects.

    In our own facility, we keep piloting campaigns of this compound ready in both kilogram and larger drum quantities. Flexible batch campaigns allow us to accommodate urgent needs without depending on outside intermediaries. Many clients negotiating tight production schedules report shorter cycle times and lower waste rates when using our product, as measured by fewer failures in final coupling or purification—a data-backed advantage over commodity-grade competitors.

    Pushing Research Boundaries With Reliable Building Blocks

    Breakthroughs in medicinal chemistry and materials synthesis rely on reagents that perform as expected, time after time. Our own staff have worked on timelines where every delay puts a project at risk. It is easy to underestimate the value of stability, but a single malfunctioning reagent can throw off downstream analytics, purity assessments, and even regulatory filings. We have made it a top priority to ensure that researchers can trust what arrives with each drum or bottle.

    The unique combination of boronic acid and sulphamoyl functionality opens new reaction windows absent in simpler reagents. Creative teams have leveraged this to cut weeks from lead optimization cycles, exploring SAR options and enabling sophisticated structural edits late in campaigns. Feedback from collaborating universities and biotech start-ups has shown that our 2-(N,N-dimethylsulphamoyl)phenylboronic acid allowed them to expand their screening libraries rapidly, achieving high-quality hits in focused screening efforts.

    Supply Chain Strength: No Substitute for Experience

    A manufacturer’s perspective brings a reality check to lofty product claims. By controlling every step—from raw amine and boronic acid sourcing to final blend and packout—we keep lead times predictable and offer real-time updates during production and shipment. No excuses, no guesswork; customers know where their material stands, and we’re always a phone call away for troubleshooting unusual reactivity, unexpected filtration behavior, or advice on alternative coupling partners.

    Our relationships with global freight partners and customs specialists mean that delays at borders become rare and compliant, document-backed shipments arrive when promised. For clients with demand spikes or unusual regulatory requests, we can quickly adjust packaging lot sizes or documentation. This matters when project timelines are tight and change orders hit at the last minute.

    Challenges and Solutions: Hard-Learned Lessons

    Producing 2-(N,N-dimethylsulphamoyl)phenylboronic acid at scale presents obstacles, not all visible in the lab. We have refined filtering and drying systems to address clogging from fines during extended runs. Process intensification—switching mixing profiles, upgrading filter media, and optimizing slurry transfer—has paid off in minimized downtime and more consistent egress from reactors. Temperature swings during sulphamoylation once led to unwanted oligomers; our technicians tamed these with optimized jacket control and in-process GC monitoring.

    Customers benefit from these investments, as process reliability translates directly to purity and yield. In one case, a client upgrading to our material for multi-hundred gram campaigns reported reduced reactor fouling and fewer purification steps, saving them two full workdays and substantial solvent costs. Our technical support team draws from these live production scenarios, never relying on abstract theory or untested lab precedent.

    Supporting Innovation Through Direct Communication

    We view each order as part of an ongoing partnership rather than just a transaction. If manufacturing conditions or compound complexity shift, our in-house chemists remain ready to discuss custom modifications. For analytical standards or isotope-labeled needs, we take requests seriously and leverage our process know-how to design routes that respect both purity and cost targets. We prefer open conversations, not just emailed spec sheets.

    As customer projects grow—from early discovery to pilot scale—we adapt, often reshaping blend size, packaging, or labeling to match new requirements. For instance, oncology drug developers benefited from our willingness to monitor and limit residual iron from upstream boronation, as small traces can impact biological assays. Running actual process chemistry gives us this insight, letting us bridge the gap between bench and plant in ways that third parties rarely manage.

    Building Value One Batch at a Time

    Our reputation results from the hard work of chemical operators, process engineers, and quality control staff who see every batch of 2-(N,N-dimethylsulphamoyl)phenylboronic acid through from raw material intake to final shipment. Chemists trust us for that reason—they know shortcuts get caught and corrected here, not shipped out as mystery variances.

    Looking ahead, we are continuing to expand production capabilities, invest in greener chemistry, and push for tighter reproducibility. Through steady learning and listening to the real experiences of downstream partners, we keep tuning our process for both performance and sustainability. Advanced synthesis is only as strong as the foundation of its key reagents. For every bottle we ship, we commit to delivering a product worthy of its place in your most demanding reactions.