|
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 | 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. |
Applications of 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid in Industrial ManufacturingAs 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 Intermediates2-(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
Typical usage ratio
Downstream process integration
Final product types
2. Custom Fine Chemical Synthesis: Fluorophore and Probe DevelopmentResearch 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
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Intermediate SynthesisThe 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
Typical usage ratio
Downstream process integration
Final product types
4. Material Science: Specialty Polymer SynthesisIn 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
Typical usage ratio
Downstream process integration
Final product types
5. Electronic Chemicals: Organic Semiconductors and Sensor Film DevelopmentThis 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
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-(N,N-Dimethylsulphamoyl)Phenylboronic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
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.
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.
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.
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.
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.
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).
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.
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.
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.
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.
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.
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.