Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride

    • Product Name N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride
    • Alias NBAH
    • Einecs 619-745-5
    • 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

    244748

    Product Name N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride
    Synonym W-7 hydrochloride
    Molecular Formula C14H19ClN2O2S
    Molecular Weight 314.83
    Cas Number 118980-40-6
    Appearance White to off-white powder
    Solubility Soluble in water and DMSO
    Storage Temperature 2-8°C
    Purity ≥98% (HPLC)
    Iupac Name N-(4-aminobutyl)naphthalene-2-sulfonamide hydrochloride
    Usage Calmodulin antagonist in biochemical research
    Ph Of Solution 5.0-7.0 (10 mg/mL in water)
    Hazard Class Irritant

    As an accredited N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed, amber glass bottle containing 5 grams, clearly labeled with product name, quantity, and safety symbols.
    Shipping N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride is shipped in tightly sealed containers, protected from light and moisture. It is handled as a chemical reagent, typically under ambient temperature, in compliance with relevant safety and transportation regulations. Proper labeling and necessary documentation accompany the shipment to ensure safe and traceable delivery.
    Storage N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride should be stored in a tightly sealed container, protected from light and moisture. Keep at room temperature (20–25°C), away from incompatible substances such as strong oxidizers. Store in a well-ventilated area designated for chemicals. Ensure proper labeling, and keep out of reach of unauthorized personnel, following standard laboratory safety protocols.
    Application of N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride

    Applications of N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride in Industrial Manufacturing

    N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride functions as a critical intermediate in various specialized industrial sectors requiring precise synthetic performance, regulated safety, and established quality systems. As a direct producer, we tailor particle size, purity, and stability for targeted downstream integration, supporting advanced manufacturing through consistent supply.

    1. Fluorescent Probe and Label Synthesis

    N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride acts as a primary amine-containing linker in the synthesis of select naphthalenesulfonamide-based fluorescent probes. Researchers apply it for covalent conjugation with biomolecules, creating sensitive fluorophores for cell imaging, protein tracking, or diagnostic assay development. Its defined reactivity profile ensures predictable coupling efficiency in labeling protocols, which pharmaceutical and biotechnology companies have standardized for high-throughput screening platforms.

    Industry compliance standards

    • ISO 13485: Medical Device Quality Management Systems
    • USP <825>: Radiopharmaceutical Preparation (if applied in life science research)
    • REACH Regulation (EC) No 1907/2006
    • RoHS Directive 2011/65/EU (for use in diagnostic devices)

    Typical usage ratio

    • Applied at 0.1–5.0 wt% in fluorophore synthesis reactions; ratio adjusted per labeling molar excess and target molecular size.

    Downstream process integration

    • Introduced in the amide coupling or sulfonamide formation step.
    • Directly conjugated to scaffolds bearing NHS ester or activated carbonate groups.
    • Integrated before chromatographic purification.

    Final product types

    • Fluorescent imaging reagents
    • Protein/peptide labeling kits
    • Cellular diagnostic probes
    • Sensor platforms for high-throughput analysis

    2. Oncological Active Pharmaceutical Ingredient (API) Intermediate

    Several researchers and advanced pharmaceutical producers utilize N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride as a building block for small-molecule kinase inhibitors in oncology pipelines. The compound’s amine and sulfonyl functional groups permit selective modification, enabling downstream formation of proprietary anticancer agents. Its consistent lot-to-lot purity is necessary for validation in GMP-compliant process development.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210, 211 (Drug Product GMP)
    • European Pharmacopoeia (Ph. Eur.) monograph reference for intermediates
    • Certificate of Suitability (CEP) submission rules for EU API supply

    Typical usage ratio

    • 0.2–2 molar equivalents in the final step of sulfonamide-based kinase inhibitor synthesis; adjusted based on route of synthesis and intermediate yield.

    Downstream process integration

    • Charged as a nucleophile or amine reactant in the condensation or substitution step of the API core structure.
    • Monitored by HPLC and LC-MS for impurity profiling after reaction completion.
    • Purification via crystallization or silica gel chromatography follows integration.

    Final product types

    • Chemically defined kinase inhibitor APIs (oncology pipeline)
    • Phase I–III clinical trial active substances
    • Reference standards for pharmaceutical development
    • Solid dosage form pre-mixes

    3. Specialty Polymer Modification for Bioengineering

    Specialty polymer manufacturers incorporate N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride as a pendant-group modifier to introduce amine-functional crosslinking in biocompatible hydrogels and membrane matrices. Utilized for tailored permeability, bioadhesion, and fluorescence in tissue engineering, its integration supports compatibility with living cells and regulatory requirements for advanced biomedical devices.

    Industry compliance standards

    • ISO 10993-1: Biological Evaluation of Medical Devices
    • FDA 21 CFR 177.2600: Indirect Food Additive Regulation (if used in food-contact materials)
    • GMP for Medical Devices (EN ISO 13485)
    • REACH & SVHC guidelines for polymer raw materials

    Typical usage ratio

    • Introduced at 0.5–3.0 wt% relative to base polymer (e.g., polyacrylamide, PEGDA); ratio determined by targeted crosslink density and desired mechanical property set.

    Downstream process integration

    • Dissolved in aqueous or mixed solvent prior to polymer network formation.
    • Participates in free-radical or Michael addition during hydrogel synthesis.
    • Polymer blend processed into sheets, beads, or injectable matrices.

    Final product types

    • Biofunctional hydrogels for tissue scaffolds
    • Fluorescent-labeled polymer membranes
    • Implantable medical coatings
    • Chemical sensor substrates

    4. Chemical Reagent for Analytical Research

    Global laboratory reagent producers and reference material suppliers include this compound as a selective amine donor or sulfonamide reference in high-sensitivity analytical kits. Applied for calibration, derivatization, and as a performance standard in chromatographic and spectrophotometric assay systems, its batch-certified purity is critical for controlled laboratory environments and accredited quality systems.

    Industry compliance standards

    • ISO/IEC 17025: Testing and Calibration Laboratory Accreditation
    • USP <621>: Chromatography
    • CNAS-CL01: General Requirements for the Competence of Testing and Calibration Laboratories (China)
    • OECD Good Laboratory Practice (GLP)

    Typical usage ratio

    • Stock solutions prepared at 0.01–1.0 mg/mL for HPLC/LC-MS; quantity adjusted according to instrument detection limits and calibration curves.

    Downstream process integration

    • Dissolved in analytical-grade solvents to generate calibration standards.
    • Added during derivatization steps prior to quantitative detection of sulfonamides or amines.
    • Integrated into multi-component reference material panels.

    Final product types

    • Calibration and reference standards for HPLC/LC-MS
    • Analytical reagent kits for quality control labs
    • Standard solution sets for regulatory laboratories
    • Performance validation spiking materials
    Free Quote

    Competitive N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing N-(4-Aminobutyl)-2-Naphthalenesulfonamide Hydrochloride: A Chemist’s Look at a Versatile Intermediate

    Why This Molecule Matters in Synthesis

    Working in the fine chemical manufacturing industry over the last twenty years, I have seen firsthand how molecules—often long-named and little-known outside specialized circles—can quietly power the progress in biological, pharmaceutical, and material science labs around the globe. Among those, N-(4-Aminobutyl)-2-naphthalenesulfonamide hydrochloride stands out for its utility as a synthetic intermediate and biological modulator. Our team has been producing this compound at scale to meet the demanding needs of both research and commercial laboratories. Every batch reflects not just synthetic complexity, but a commitment to quality, traceability, and application-oriented thinking.

    Unique Structure, Real-World Applications

    This compound combines the rigidity and aromaticity of the naphthalene ring with the flexibility of an aminobutyl chain. The sulfonamide moiety weeds out many unwanted side reactions and adds a dimension of stability that draws the interest of medicinal and materials chemists alike. The hydrochloride salt enhances solubility in aqueous and polar solvents, a practical consideration during purification and downstream processing. People who handle scale-up and batch manufacturing know that minimizing losses and avoiding clumping or inhomogeneous mixtures matters far more than small price differences between materials. The refined salt form of N-(4-Aminobutyl)-2-naphthalenesulfonamide reflects that pragmatic wisdom.

    Labs working on calcium signaling pathways have valued this compound for its role as a calmodulin antagonist. Unlike many peptide-based inhibitors, the molecular structure here offers robust resistance to enzymatic degradation, which extends its window of usefulness in in vitro and preclinical settings. Because of the naphthalene core, researchers have also explored its fluorescent properties for labeling and detection studies. It’s clear that this single molecule draws attention from multiple disciplines, from basic biochemistry to the early steps of small-molecule drug discovery.

    Differentiating Our Product

    We do not outsource the synthesis or purification stages. Full in-house oversight means tighter control over impurity profiles, trace residues, and byproducts. Years ago, we learned that third-party batches could introduce unpredictable coloring, odor, or mislabeling—a risk no scientist wants in their workflow. Our method starts from quality-vetted naphthalenesulfonic acid derivatives and employs meticulous column purification under conditions tailored to the needs of this unique salt. Each kilogram undergoes comprehensive identity and purity assessments using methods like HPLC, NMR, and FT-IR. A stable shelf life and crystalline form translate to less time spent redissolving or recrystallizing, allowing customers to proceed directly to target applications.

    Some available products on the market cut corners on drying or storage. Moisture leads to aggregation as well as slow hydrolysis, especially troublesome in high-throughput settings where stability saves time and resources. During pilot-scale development, we saw that control over environmental exposure and residual solvents is the difference between a working reagent and a lab headache. So we optimized storage protocols and packaging to maintain quality over months of ambient and refrigerated storage. Real experiment results consistently trounce theoretical purity figures in determining material quality.

    Why Consistency Matters

    We get regular feedback from laboratory customers about repeatability and the headaches caused by lot-to-lot variation. In biological experiments—especially where low micromolar concentrations matter—any trace residue or batch impurity can skew whole datasets. That puts pressure on the manufacturer to think like an end user. By running repeated small-scale simulations during scale-up, we flagged critical parameters: pH, stoichiometry, and partner reagent addition rates. Minor deviations can affect both the physical quality and the reactivity of the final salt. It comes down to the manufacturing chemist being in sync with the scientist at the end bench. That gap narrows when every run records not only product yield but also physical appearance, melting point, and trace side product patterns. It’s part of building trust over multiple orders.

    If you’ve ever struggled with inconsistent product quality, you know how much work is lost to troubleshooting, not to mention wasted resources. We take a practical approach—preferring to rerun purification or update drying protocols rather than release something we would not use ourselves. Our aim is to be dependable, not just compliant. It’s impossible to overstate the disruption that comes from unexpected batch-to-batch differences, especially for labs moving toward GMP or GLP pipelines.

    The Technical Details That Matter

    In research pipelines, application specificity can make or break a project. N-(4-Aminobutyl)-2-naphthalenesulfonamide hydrochloride often finds use as a tool compound for probing signal transduction pathways, modulating protein targets, and studying molecular interactions. The hydrochloride form is easier to dissolve in physiological buffer solutions. Some users prefer this over the free base, which tends to have lower solubility and may precipitate under neutral to slightly acidic lab conditions. We have found that by minimizing the water content and controlling for microcrystalline polymorphism, each lot dissolves cleanly without residual clumping.

    Routinely, people ask about purity thresholds. We provide technical support that goes beyond the printout, offering guidance on solvent compatibility, recommended concentrations, and handling tips—drawn from our own day-to-day work with the compound. Researchers who want to use it as a labeling reagent can expect stable fluorescence signatures, given the aromatic naphthalene backbone. For those deploying the molecule as a calmodulin inhibitor, we can share insight into concentrations that balance specificity and cellular toxicity, since we’ve tested these settings in our own laboratories.

    Product Model and Specifications

    Our standard offering features product code NABN-HCl-98, reflecting a commitment to a minimum purity of 98%, with most lots registering above 99% by HPLC analysis. The actual chemical formula reads C14H19N2O2S·HCl, with careful verification of molecular weight for accurate experimental planning. Each bottle is weighed under low-humidity conditions to reduce mass fluctuations. Appearance is a white to off-white crystalline powder, packaged in tamper-evident bottles and always labeled with full synthesis and testing date. We listened to feedback about lot traceability, so each label carries not just a lot number, but QR-coded links to batch-specific data sheets.

    Packing sizes run from small-scale research vials (100 mg, 1 g) to multi-kilogram drums for production-scale labs. We know that materials for cell culture assays and biochemical tests can’t carry the contamination risks found in commodity chemicals, so each batch is further tested for metals and organic contaminants on request. Spectroscopic data accompanies every order so users can cross-reference their own quality control. For specialty needs, such as anhydrous material or alternate salt forms, we coordinate with partners in formulation R&D to ensure methods translate smoothly from benchtop to pilot plant.

    Comparisons With Other Calmodulin Antagonists and Sulfonamide Intermediates

    Calmodulin antagonists span quite a spectrum, from peptide fragments to naphthalenes and substituted phenothiazines. Peptide-based inhibitors often degrade fast under in vitro and in vivo conditions. Their synthesis and handling require cumbersome steps and expensive analytical verification. N-(4-Aminobutyl)-2-naphthalenesulfonamide hydrochloride, by contrast, offers higher stability and easier handling in buffer systems. Its aromatic core maintains function without the rapid oxidative breakdown seen in more labile molecules.

    Sulfonamide intermediates built from shorter chains or other aryl groups sometimes reveal unpredictable reactivity or undesired cross-linking during conjugation. Our compound’s aminobutyl tail provides workable spacing for conjugation while keeping the naphthalene’s core fluorescence intact—a desirable trait for dual-use as both biochemical modulator and labeling reagent. Where other products force a choice between stability and reactivity, this molecule balances the two with proven performance in published protocols.

    Standard calmodulin antagonists like trifluoperazine bring their own issues: potential CNS activity, problematic side effects, and regulatory headaches. N-(4-Aminobutyl)-2-naphthalenesulfonamide hydrochloride wasn’t developed as a psychiatric agent, so it doesn’t present the same downstream hurdles. For materials scientists, the robust sulfonamide and aromatic backbone also allow for easy incorporation in sensor platforms or polymer backbones, opening up roles beyond the purely biological.

    Supporting Researchers Beyond the Sale

    People sometimes overlook the value of direct communication between users and the actual chemists who made the compound. By fielding technical inquiries ourselves, we spot trends in experimental troubleshooting, whether it’s stubborn insolubility in atypical buffers or confusing background signals in spectroscopic assays. When users share feedback about unexpected results or side reactions, we run in-house batch testing to either confirm or correct the concern. Open dialogue between manufacturing chemists and active researchers prevents repeating old mistakes and leads to process changes that benefit everyone.

    Scaling chemistry from small flask to plant-level batches often exposes hidden issues not obvious in early trial runs. Unexpected side reactions, trace impurities, and environmental factors become more pronounced. We invite customer feedback, and every batch improvement comes from addressing real-world problems—not from theory or standard procedure alone. No product ever reaches a state of ‘finished’ because labs continually push the boundaries of experimental conditions and project scope.

    Lessons Learned From the Manufacturing Floor

    Sourcing and making a compound like N-(4-Aminobutyl)-2-naphthalenesulfonamide hydrochloride involves more than ticking boxes for purity or compliance. I’ve watched as well-laid synthetic plans ran aground on what looked like small technical details: a water-sensitive intermediate, a filtration bottleneck, or unexpected exotherms in scaling up. That is why we treat every new kilo as a test, not a given. Our plant operators check by eye for off-colors. Our quality analysts sniff for tell-tale amine notes. We’ve learned that relying on instruments alone misses early signs of instability or contamination.

    Real reliability grows from standardizing parameters based on practice, not only by vendor spec. Filtering through fine grades, controlling for static, and ensuring complete conversion saves end users from wasting time on repurification. Our staff continuously records small deviations and outcomes—pinpointing factors like humidity during drying, or solvent batch variations that influence final solid form. This practical data ensures that, for each run, we can anticipate issues before they surface downstream.

    A chemical manufacturer’s value lies in responsibility for what happens after the cap unscrews. Every research chemist knows the frustration of a material that doesn’t perform as expected and the headache of revisiting every upstream choice. We keep these realities in view, guiding each decision from raw material selection through to final packing.

    Customer-Centered Innovation

    As markets for biochemical intermediates expand, so do expectations. Our facility receives requests for custom modifications, alternate salt forms, or even analog synthesis for comparative testing. The most innovative applications rarely stay within neat silos—each new inquiry helps us update protocols and expand support documentation. We respond quickly to verified user challenges—if a researcher encounters unexpected degradation or requires solubility enhancement, our R&D partners step in to help. These relationships add to a knowledge base built from hundreds of customer interactions.

    We notice shifts in the field: more high-throughput screening, rapid prototyping of new drug candidates, and evolving requirements for traceability. Our practice is to anticipate—not just react—to these shifts. The result is a product that adapts to new experiments, not one frozen at a point in time. Feedback cycles run both ways: we take insights from the lab and build them into future production batches, adjusting synthesis or purification details as needed.

    The Ethical and Environmental Perspective

    As global obligations around chemical manufacturing tighten, transparency around sourcing, process safety, and waste management moves to the forefront. We chose routes and reagents designed to minimize waste and hazardous byproducts, both because regulations demand it and because our own staff handle these materials daily. We monitor for environmental release of organosulfur and amine derivatives, and recycle solvent streams wherever possible. These steps lower both the cost and the carbon footprint of each produced kilogram, aligning with broader commitments to environmentally conscious chemistry.

    The story of N-(4-Aminobutyl)-2-naphthalenesulfonamide hydrochloride is not just about molecular utility, but about a shared responsibility for safe, sustainable, and high-value chemistry. By holding ourselves to a higher standard, we earn not just repeat business, but the trust of colleagues who rely on materials that do not cause unexpected headaches. That ethos shapes every step, from the first weighing through to shipping and support.