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N-[2-[[[3-(4-Chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide (KN-93)

    • Product Name N-[2-[[[3-(4-Chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide (KN-93)
    • Alias KN-93
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    800898

    Chemical Name N-[2-[[[3-(4-Chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide
    Common Name KN-93
    Molecular Formula C28H31ClN2O4S
    Molecular Weight 527.08 g/mol
    Cas Number 139298-40-1
    Appearance Off-white solid
    Solubility Soluble in DMSO, ethanol
    Storage Temperature -20°C (Dry, Dark)
    Target Calcium/calmodulin-dependent protein kinase II (CaMKII)
    Usage Inhibitor of CaMKII signaling
    Purity Typically >98% (HPLC)
    Iupac Name N-[2-[[[3-(4-chlorophenyl)prop-2-en-1-yl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide
    Pubchem Cid 107848
    Smiles COc1ccc(cc1)S(=O)(=O)N(CCO)C2=CC=CC=C2CN(C)CC=CC3=CC=C(C=C3)Cl
    Application Research tool for kinase signal transduction studies

    As an accredited N-[2-[[[3-(4-Chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide (KN-93) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing KN-93 is packaged in a 10 mg amber glass vial with a screw cap, labeled with chemical name, quantity, and handling instructions.
    Shipping KN-93 is shipped in compliance with chemical safety regulations. The product is securely packaged in airtight containers, clearly labeled, and typically dispatched at ambient temperature unless otherwise specified. Shipping documentation includes safety data sheets. Specialized courier services may be used to ensure safe and prompt delivery of laboratory-grade chemicals.
    Storage KN-93 should be stored at -20°C, protected from light and moisture. Store the compound in a tightly sealed container, ideally under inert gas, to prevent degradation. Avoid repeated freeze-thaw cycles. If handling solutions, store aliquots at -20°C and use sterile, dry solvents. Proper labeling and compliance with local regulations for hazardous chemicals are recommended for safety.
    Application of N-[2-[[[3-(4-Chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide (KN-93)

    Applications of N-[2-[[[3-(4-Chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide (KN-93) in Industrial Manufacturing

    KN-93, a selective CaMKII inhibitor, supports pharmaceutical and biomedical manufacturing as a critical intermediate and research ingredient. Through strict adherence to quality and regulatory standards, our production ensures high batch consistency and traceability, helping downstream partners integrate KN-93 into formulations for targeted applications. Below, we highlight core industrial scenarios for KN-93, each segment underpinned by recognized standards, validated usage ratios, aligned process integration, and specific finished product outputs.

    1. Pharmaceutical API Secondary Synthesis – Cardiovascular Drug Development

    Pharmaceutical API manufacturers leverage KN-93 as a research intermediate in the synthesis of CaMKII-targeted compounds for cardiovascular drug development, particularly those investigating ischemia-reperfusion injury and heart failure. Its function as a lead structure or tool compound mandates exceptional purity and traceability throughout batch production, particularly for development-stage clinical candidates and pre-clinical research use.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <797> and <823> for compounding and investigational drugs
    • 21 CFR Part 211: US FDA cGMP for Finished Pharmaceuticals (development stage)
    • European Pharmacopoeia Monograph 5.2.12 (Biological Quality)

    Typical usage ratio

    • Research and lead optimization: 0.01–0.2% w/w relative to the final target compound batch; specific ratios depend on assay scale and synthetic methodology optimization

    Downstream process integration

    • Introduced at the intermediate or late-stage synthetic step in multi-step API synthesis; quality control sampling for impurity profiling and mass balance is conducted at each stage; purification by chromatography follows structural incorporation

    Final product types

    • Pre-clinical CaMKII inhibitor compounds
    • Clinical trial-grade cardiovascular drug candidates
    • Reference standards for pharmacological assays
    • Analytical research reference APIs

    2. Preclinical Biomedical Research Reagent Manufacturing

    Producers of preclinical research reagents utilize KN-93 for preparation of cell-permeable CaMKII inhibitors, formulated in sterile aqueous or DMSO-based solutions for in vitro and in vivo applications. The material’s biotrace chemical purity and structure validation underpins assay reproducibility, a critical factor for pharmacodynamic and signal transduction studies in university, contract research, and biotech labs.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical manufacturing
    • ISO 13485:2016 for medical research supply
    • US NIH reagent quality recommendations
    • REACH Annex XVII for laboratory chemical substances

    Typical usage ratio

    • Formulation as concentrated stock: 1–10 mM in DMSO; diluted 1:100 to 1:1000 for final working solutions in assays, typically yielding a final concentration of 0.5–50 μM depending on cell type and model requirements

    Downstream process integration

    • Dissolved in high-purity solvent under inert conditions, sterile-filtered, and aliquoted for research kit assembly; analytical QC validates compound identity and absence of microbial contamination before vial filling and cold chain packaging

    Final product types

    • Cell culture pharmacology assay kits
    • Signal transduction reagent sets
    • Protein kinase inhibitor libraries
    • Ready-to-use DMSO stock solutions for biomedical laboratories

    3. Diagnostic Kit Components for Laboratory Assays

    KN-93 forms a component in custom diagnostic and research assay kits where CaMKII inhibition is necessary for mechanistic studies of cardiac, neuronal, or immune cell signaling. Kit and reagents manufacturers focus on microdosing and buffer compatibility, emphasizing stringent documentation for lot composition and traceability to facilitate regulatory or peer-reviewed research requirements.

    Industry compliance standards

    • ISO 13485:2016 Medical device and IVD kit production
    • EN 13612:2002 for performance evaluation of in vitro diagnostic medical devices
    • CFR 820 Quality System Regulation for IVD reagents (US)
    • US Pharmacopeia General Chapter <1043> Ancillary Materials

    Typical usage ratio

    • Final kit solution concentration: 1–10 μM in proprietary buffers; aliquot volumes based on single or multi-well protocols, with ratio adjusted for specific assay target and protocol

    Downstream process integration

    • Compound incorporated post-batch buffer sterilization; combined with other assay reagents during kit assembly; formulations undergo freeze-thaw stability and protein-binding compatibility validation prior to final fill and QC release

    Final product types

    • In vitro diagnostic kinase activity kits
    • Calcium signaling assay reagent kits
    • Signal pathway inhibitor panels for academic and clinical labs
    • Biochemical screening plates

    4. Custom Chemical Synthesis for Reference Standard Supply

    Contract research organizations and reference material suppliers request KN-93 as a synthetic intermediate or as a purified standard to support analytical method development for pharmaceutical, academic, and clinical laboratories. This sector requires comprehensive analytical data, including NMR, HPLC, and mass spec, with documented batch records to satisfy customer and accreditation body audits.

    Industry compliance standards

    • ISO/IEC 17025:2017 for reference material producers
    • USP <1225> Validation of Compendial Procedures
    • Good Laboratory Practice (GLP) for Analytical Chemistry
    • COA and trace impure profile reporting to ICH Q3A/B

    Typical usage ratio

    • Preparation as neat solid or ≥98% pure analytical standard; delivered in vialized quantities of 5–100 mg per customer specification, with dilution protocols provided for end-user solution preparation

    Downstream process integration

    • Final purification by preparative chromatography post-synthesis, lyophilization, and validation through full suite of analytical techniques; product packaged under low-humidity, inert conditions, labeled with full traceability and storage guidance

    Final product types

    • Analytical calibration reference standards
    • HPLC or LC-MS/MS assay validation controls
    • Pharmacopoeial monograph establishment samples
    • Internal QC system reference items for pharmaceutical labs
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    More Introduction

    KN-93 (N-[2-[[[3-(4-Chlorophenyl)-2-propenyl]methylamino]methyl]phenyl]-N-(2-hydroxyethyl)-4-methoxybenzenesulfonamide): A Closer Look from the Manufacturer’s Perspective

    Understanding KN-93 from the Ground Up

    Producing KN-93 isn't just about chemical synthesis, it's about careful control from the earliest intermediates to the final material handling. Anyone reading about KN-93 in scientific papers or product lists often sees a long name, a catalog number, a few brief notes about purity or storage condition, and assumes every batch from any supplier works the same. Experience tells a different story. For over a decade of hands-on production experience, we have learned that researchers and formulation teams rely deeply on rigorous consistency in their signaling modulators, and KN-93 demands a higher level of vigilance than many of the standard laboratory reagents.

    Getting KN-93 Right: The Real Work is in the Details

    KN-93 first grabbed the attention of researchers for its ability to inhibit calmodulin-dependent protein kinase II (CaMKII) with excellent selectivity. Early investigations opened up new possibilities in neurobiology, cardiac research, and cell signaling pathways. At the production level, synthesizing this molecule isn't a single reaction, but a series of steps where temperature, solvent ratios, and purification choices guide the yield and the quality. From making the 4-chlorocinnamyl starting material to the sulfonamide coupling, each stage builds on the reliability of the previous. Any lapse or rush soon shows itself in reduced purity, poor crystallinity, or batch-to-batch drift.

    Every chemist in this business knows that academic citations and elegant pathways don't always survive when scaled up to industrial volumes. Small impurity peaks—so easy to ignore on a research scale—turn into stability headaches or unpredictably cloud the clarity of a cell culture assay. Over years of process refinement, we've stuck to high-performance purification—even if it costs a few more working hours—because that’s where the reliability surfaces, not just in analytical purity, but in long-term stability, handling, and consistent batch identity.

    Specifications with Purpose: What Sets Our KN-93 Apart

    Some manufacturers tout above 98% HPLC purity on paper, but leave the story of unlisted byproducts or residual solvents unspoken. Our QC teams run routine checks beyond what regulations require. Microtraces of process solvent—which seem negligible—can alter cell signaling results in high-sensitivity systems. We have learned the hard way that pushing for fully characterized profiles, not just purity percentage, saves customers hours of troubleshooting down the line. This runs deeper than an assay sheet. Every batch comes with solvent gradient traces, impurity characterization, and repeat analytical signatures.

    Stability is not merely about storage at -20°C; it’s about packaging that really seals out moisture, real-world transit that might expose vials to unpredictable temperature swings, and internal testing of samples after months of storage. Some users request custom forms—amorphous powder versus crystalline, larger packaging that fits automated handling, or extra-dry product for air-sensitive work. We have experience meeting these specifics, not because they look good on a shelf, but because research collaborators return to the source that takes custom manufacturing seriously.

    Direct Comparison: KN-93 Versus Other Inhibitors

    KN-93’s unique profile as a selective CaMKII inhibitor often draws comparison with KN-92, its structural analog. The two differ by a single methyl group, but their biological effects diverge more than expected. KN-92 acts as a negative control, lacking the inhibitory activity. Any error in manufacturing—such as incomplete methylation—can ruin selectivity and lead to misleading results during validation or screening. Direct manufacturing controls every step; residual raw material isn’t simply an inconvenience, it undermines the entire purpose of the research.

    Many signaling inhibitors on the market claim similar purity ratings, yet subtle differences—unnoticed until cell response or control experiments—highlight the importance of authentic, well-characterized batches. Researchers considering off-brand or gray-market sources might think price is the main factor. Based on our customer feedback, it’s clear that troubleshooting failures or inconsistent results is far costlier in the long run than sourcing directly from manufacturers who stand behind each gram with analysis and decades of bench-tested process refinement.

    Intended Usage and Why It Matters

    KN-93’s application space extends far beyond its first mention in kinase research. Pharmaceutical groups use our high-purity product for preclinical studies, seeking reliable CaMKII blockade in early stage compound screening. Neuroscientists demand trace-level uniformity for patch-clamp electrophysiology, where small inconsistencies manifest as experimental drifting or unexplained outliers. Cardiac researchers chase highly controlled signaling inhibition to unravel arrhythmia pathways. In all these areas, it’s not enough to send out a drum of white powder with a sticker. We’ve worked side by side with research teams to optimize form, batch size, packaging, and even documentation protocols for each unique lab’s needs.

    Over the years, we’ve received granular feedback: unexpected moisture uptake during weighing, batch-to-batch smell hints indicating volatile byproducts, or requests for more granular solubility data in specific solvents—details that rarely cross the desk of a reseller or catalog distributor. We don’t treat these as add-ons but as standard elements of product stewardship. Direct communication with manufacturing engineers leads to process improvements that benefit each subsequent batch, not just individual requests.

    Supporting Academic Integrity: Transparency and Traceability

    The field has shifted toward stringent reproducibility requirements, and as direct manufacturers, we’ve adopted detailed traceability practices well ahead of regulatory mandates. Years of collaboration with university labs and pharma startups taught us not every experiment works the first time, but every failure can help us build more robust support. Instead of just sending updated certificates, our technical teams re-examine retention times, impurity signatures, and shelf stability for each reported concern.

    We have seen competitors re-label or resell bulk KN-93 from outside sources, which can create traceability black holes—especially if reformulation or repacking introduces contamination or mislabeling. Those who work with direct manufacturers get proven chain of custody, batch documentation, and often—even input into next-generation process adjustments. It isn’t about compliance alone, but building a direct line between the bench and the production floor.

    Expert-Level Manufacturing: Technical Insights from the Floor

    Synthesis of KN-93 requires unwavering focus on raw material quality. Minor fluctuations in starting amines or chlorinated intermediates ripple through the process. Over the years, we noticed that certain glassware rinsing agents could leach into the product during late-stage synthesis. Direct, hands-on production control meant swiftly changing suppliers, re-purifying water lines, or even swapping reaction vessels for non-porous variants. No amount of specification writing replaces the value of in-lab experience. What looks trivial on a process chart can spell trouble after the hundredth kilo, as both micro and macro impurities accumulate unseen.

    Our production chemists run method optimization projects alongside the main process rather than as afterthoughts. Open dialogue with downstream users highlighted that some process solvents, though not technically retained past purification, still left persistent trace olfactory signatures. These observations led to process solvent modifications and tighter vacuum drying steps, eliminating the issue at its root.

    Even the smallest packaging changes, such as double-sealing with barrier bags, started with customer feedback about shipping through humid climates. Our team tested not just material compatibility but also real-world vibration and temperature cycling, ensuring product stability during the unpredictable journey from loading dock to lab freezer.

    Supporting Long-Term Research Success with KN-93

    Many customers reach out again months or years after the initial order for detailed batch histories or advice about process scale-up. We routinely provide analytical archives and method transfers, not just for regulatory compliance, but because a direct manufacturing partner preserves product history—every lot, every batch, every reanalysis. Our technical team carries institutional memory forward, able to discuss adjustments made years ago and the rationale behind each.

    Requests often arise for specialized formulations—sterile-filtered solutions, particular particle sizes, or dry-box packaging—driven by emerging lab requirements or new instrumentation. We have experience working with these evolving needs, tailoring process modifications to serve both legacy techniques and cutting-edge research trends.

    Global Reach, Local Attention: Delivering KN-93 Worldwide

    KN-93 travels from our facility to research centers in every major region. We have adapted our processes to suit not only international quality mandates, but also the specifics of local practice—temperature controls for equatorial regions, robust packaging for areas with inconsistent shipping infrastructure, documentation and translation for multilingual research teams. Ensuring each vial arrives in perfect condition takes as much determination as the synthesis itself.

    Over time, we have built shipping and support capabilities that minimize customs delays, guarantee product handling, and offer responsive troubleshooting for any issues arising in transit. Real-world logistics—unexpected customs holds, seasonal transit temperature spikes, the demands of remote rural labs—have prompted us to constantly upgrade both packaging and notification systems. These adaptations grow out of close manufacturer-client relationships, not out of blanket procedural requirements.

    Addressing Challenges with KN-93: Solutions from Practice

    Production experience makes clear the pitfalls of shortcutting on process safety, documentation, or post-manufacturing handling. Some challenges arise from raw material quality—occasional shortages or slight specification drift from upstream suppliers. Building a robust internal QMS, combined with early-warning supplier audits and alternative sourcing strategies, means our processes flex instead of failing when pressure mounts.

    Batch-to-batch variation sometimes traces back to subtle environmental shifts—humidity changes during crystallization, temperature fluctuations in long syntheses, or even micro differences in glassware. To maintain tight product specifications, production teams maintain environmental logs, monitor equipment health, and prepare parallel samples for archiving and re-testing. Leaning only on technical standards or robotic automation neglects the judgment of veteran process staff, whose experience reading subtle process changes is irreplaceable.

    Future Directions: Supporting New Science with KN-93

    Research doesn’t stand still. Emerging applications in neurodegenerative disease models, cancer signaling, and cardiac therapies constantly stretch demand for higher grade product, tighter process control, and ever-broader documentation. Collaboration with research teams around the globe pushes us to refine, adapt, and share manufacturing insights.

    Our ongoing R&D invests in alternative routes to KN-93 with greener chemistry and less resource-intensive methods, both to improve efficiency and to anticipate future regulatory requirements. Technical feedback loops with customers—regardless of whether they are academic investigators or pharmaceutical drug developers—inform every process improvement, batch scale-up, and documentation update.

    Real Connections: Building a Legacy of Reliability

    Manufacturing KN-93 isn’t a static job. It is a relay between synthetic chemistry, real-world logistics, and close partnership with end users. Proprietary know-how, constant process monitoring, and the ability to respond to field feedback drive each improvement. Over the years, the trust built with researchers stems not just from analytical numbers, but from solving real problems—be it slight pH drift on dissolution, optimizing custom packaging for unique project requirements, or swiftly troubleshooting formulation quirks in a late-night overseas lab call.

    Direct manufacturer support doesn't only assure purity or supply continuity; it means standing by to help researchers pursue the next breakthrough without hesitation, knowing their materials are reliable, documented, and backed by experience. Through continuous conversation with the scientific community and obsessive focus on the fine details of production, our commitment to KN-93 remains as strong as the first day the synthesis came off the bench.

    Closing Thoughts

    KN-93 represents more than a line item on a research supply list. Its performance in the hands of scientists across disciplines rests on deep experience, ongoing process monitoring, and a dedication to full transparency. Relying on direct manufacturer expertise brings clarity and continuity, helping push forward the boundaries of bioscience, pharmacology, and cell signaling investigation. For us, every batch is not just a product—but a promise of reliability, knowledge, and continuous evolution alongside the needs of science.