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2-(4-Fluorobenzylsulfonyl)Acetamidoxime

    • Product Name 2-(4-Fluorobenzylsulfonyl)Acetamidoxime
    • Alias NSC136469
    • Einecs 694-529-5
    • 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

    224021

    Chemicalname 2-(4-Fluorobenzylsulfonyl)Acetamidoxime
    Molecularformula C9H11FN2O2S
    Molecularweight 230.26 g/mol
    Casnumber 103877-63-4
    Appearance White to off-white solid
    Solubility Soluble in DMSO, slightly soluble in water
    Meltingpoint 117-121°C
    Purity Typically ≥98%
    Storagetemperature 2-8°C
    Synonyms 4-Fluorobenzylsulfonylacetamidoxime
    Iupacname N'-[2-[(4-fluorophenyl)methylsulfonyl]ethylidene]hydroxylamine
    Smiles C1=CC(=CC=C1CS(=O)2CC(=NO)N)F
    Inchikey YGWQLEFOZSGKQI-UHFFFAOYSA-N

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

    Packing & Storage
    Packing White, sealed glass bottle containing 5 grams of 2-(4-Fluorobenzylsulfonyl)Acetamidoxime; labeled with product name, CAS number, and hazard information.
    Shipping Shipping of 2-(4-Fluorobenzylsulfonyl)acetamidoxime requires secure packaging in compliance with chemical transport regulations. The container must be clearly labeled, sealed, and protected from moisture and heat. Documentation includes safety data and handling instructions. Only certified carriers should be used, ensuring prompt and traceable delivery to minimize risks during transit.
    Storage 2-(4-Fluorobenzylsulfonyl)acetamidoxime should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2-8°C (refrigerator temperature). Avoid exposure to incompatible substances such as strong oxidizing agents. Proper labeling and handling protocols should be followed to ensure safety and chemical stability during storage.
    Application of 2-(4-Fluorobenzylsulfonyl)Acetamidoxime

    Applications of 2-(4-Fluorobenzylsulfonyl)Acetamidoxime in Industrial Manufacturing

    2-(4-Fluorobenzylsulfonyl)Acetamidoxime serves as a key specialty intermediate in the synthesis and formulation of advanced fine chemicals. Our facility manufactures this material under rigorous quality controls for integration into a range of defined downstream industrial processes.

    1. Pharmaceutical API Synthesis – Anticancer Compounds

    This chemical is routinely used as a critical intermediate in API synthesis for select anticancer agents. It provides a sulfonylamidoxime motif essential for constructing pharmacophores found in specialty therapeutics. Process chemists integrate it during the late stage of multi-step organic synthesis, where the purity and substitution pattern directly impact the activity profile of the resultant API.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters
    • European Pharmacopoeia (Ph. Eur.) monograph requirements where applicable
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 0.08–0.22 molar equivalents per API batch, optimized according to target molecule and reaction intermediates

    Downstream process integration

    • Introduced at the penultimate synthesis step in a controlled environment, followed by purification and conversion to the final API

    Final product types

    • Small molecule oncology medication APIs (e.g., tyrosine kinase inhibitors, sulfonylurea derivatives)
    • Intermediate stages for new molecular entities under development

    2. Agrochemical Active Ingredient Development

    This compound functions as a building block for synthesizing active ingredients in modern crop protection products. Its sulfonyl fluoride structure supports the fabrication of herbicidal and fungicidal entities that demonstrate selectivity and systemic efficacy. Downstream manufacturers implement this raw material in custom synthesis pathways using automated batch reactors for precise control and traceability.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO Specifications for Agricultural Pesticides
    • EPA 40 CFR Part 158 Data Requirements for Pesticides
    • ISO 9001:2015 Quality Management Systems (relevant to processing and release)

    Typical usage ratio

    • 5–12% w/w in active ingredient synthesis lots, adjusted for reaction scale and target residue levels

    Downstream process integration

    • Charged during the heterocycle formation step, immediately before sulfonylation or amidoxime coupling; followed by solvent extraction and crystallization

    Final product types

    • Pre-mixed technical grade herbicide actives
    • Fungicide technical concentrates for further formulation

    3. Specialty Polymer Modifier Synthesis

    In the performance materials industry, this intermediate delivers controlled functionalization in the backbone and side-chains of high-performance polymers. Its unique structure enables manufacturers to impart specific chemical resistance, fluorinated surface activity, or cross-linking sites within engineered resins or thermoplastics. Formulators handle dosing via continuous feeding protocols, maintaining accurate flow rates to ensure reproducible product performance in downstream compounding operations.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical processing
    • REACH Regulation (EC 1907/2006) for polymer and monomer safety
    • ASTM D256 and D638 for polymer material properties

    Typical usage ratio

    • 0.2–1.5% by weight of total monomer feed; precise percentage determined by polymer structure and target mechanical performance

    Downstream process integration

    • Metered into controlled polymerization reactors ahead of initiator charge, or combined as a modifying agent during reactive extrusion or pre-polymer compounding

    Final product types

    • Advanced engineering plastics with tailored fluorinated moieties
    • Chemical and solvent-resistant coatings
    • Specialty adhesives for electronics or automotive assembly

    4. Fine Chemical Intermediates for Analytical Reagents

    This material finds application within fine chemical synthesis for the preparation of selective analytical reagents. Laboratories rely on its performance in producing derivatization agents used in complex sample preparation, or in stabilizers designed to be highly sensitive for chromatographic analysis of pharmaceuticals and environmental contaminants. Precision during synthesis assures downstream batch homogeneity and reactivity, supporting regulatory submissions and accreditation.

    Industry compliance standards

    • ISO/IEC 17025:2017 Testing and Calibration Laboratories
    • USP Reagent Specifications
    • GMP Guidelines for Analytical Standards manufacturing (where applicable)

    Typical usage ratio

    • 0.5–4.0 mol% relative to core substrates, subject to application and method sensitivity requirements

    Downstream process integration

    • Applied post-purification as a core intermediate, then functionalized through acylation or alkylation to yield final analytical grade reagents

    Final product types

    • Certified derivatization agents for chromatographic assay kits
    • Trace analysis stabilizers for regulatory laboratories
    • Custom reagents for pharmaceutical method development

    5. Custom Synthesis for Fluorinated Organic Building Blocks

    Advanced research and contract manufacturing organizations utilize this molecule as a scaffold for fluorinated compound libraries. The fluorobenzyl group provides a unique synthetic handle for further functionalization, supporting structure-activity relationship studies and lead optimization. R&D chemists dose the compound using controlled addition protocols in inert environments, ensuring purity for downstream modification or functionalization, especially where trace impurity profiles must meet project-specific thresholds.

    Industry compliance standards

    • ISO 9001:2015 Quality Management in chemical synthesis
    • Chemical safety guidelines per local regulation (e.g., OSHA, Chinese GB/T safety standards)
    • Project-specific TID (Technical Information Documents) including analytical method validation

    Typical usage ratio

    • Variable, typically 1–10 mmol per custom batch, adjusted for target molecule structure and downstream derivatization demand

    Downstream process integration

    • Introduced as a core building block at early to mid-stage of multi-step solution-phase synthesis or during library pool generation

    Final product types

    • Reference standards for pharmaceutical research
    • Novel fluorinated intermediates for medicinal chemistry discovery
    • Patentable specialty chemicals for diagnostics or imaging agent synthesis
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    Certification & Compliance
    More Introduction

    Introducing 2-(4-Fluorobenzylsulfonyl)Acetamidoxime: A Core Building Block for Targeted Synthesis

    Understanding the Compound

    In the chemical manufacturing field, the search for reliable intermediates defines our day-to-day work. 2-(4-Fluorobenzylsulfonyl)acetamidoxime represents a steady performer among functionalized amidoximes. Its structure brings together a fluorinated aromatic ring and a sulfonyl-bridged acetamidoxime group. In our own large-batch synthesis lines, the process control and reliability of this compound always impress. The distinctive nature of the 4-fluorobenzylsulfonyl fragment changes reactivity and physical performance compared to other benzylsulfonyl amidoximes, shaping its downstream value.

    Our direct experience as the manufacturer, not a middleman, gives an inside view of quality factors during preparation. Purity and moisture sensitivity affect reactivity, so routine attention to solvent choice, crystallization protocols, and vacuum-drying prove critical here. We have found the right process window for this compound, consistently reaching high purity levels as confirmed by NMR and HPLC in our QC labs. Novel amidoxime intermediates draw regular interest, but this one holds particular appeal among medicinal and process chemists.

    Specifications Rooted in Actual Manufacturing

    Most requests we see concern lots ranging from several hundred grams to multiple kilograms. Consistent color, crystallinity, and a sharp melting range characterize our batches. Acetamidoximes tend to hydrate easily if exposed too long to the atmosphere, so we pack and store our product with desiccant under nitrogen. In our packing area, every drum undergoes a final dry-box inspection, avoiding problems downstream during the user’s weighting or dissolution steps.

    The typical batch finishes as a pale solid, with NMR peaks confirming clean formation, especially around the aromatic and amidoxime proton region. We ship material with direct spectroscopic traceability, matching the reference spectrum of every production run. Moisture content stays low, checked by Karl Fischer titration, avoiding issues when used in sensitive condensation or nucleophilic substitution steps. Residual solvent levels remain tightly controlled—never drifting from expected spec, since even a small margin off-target risks downstream catalysis or safety.

    Why Fluorination Makes a Practical Difference

    Over years of manufacturing functionalized sulfonyl intermediates, we have witnessed increased demand for fluorinated building blocks. The 4-fluorobenzylsulfonyl group in this amidoxime does more than add novelty. Fluorination modifies the electron density of the entire molecule. In practical synthesis, such adjustment directly influences nucleophilic attack and final yield in later steps. We've gained steady feedback from multidisciplinary clients—process chemists, agricultural development teams, and early-stage pharmaceutical project leads—each noting that this variant helps them control selectivity and stability, especially in conditions that can strip or defluorinate less robust molecules.

    In our hands, the presence of fluorine slightly sharpens crystallinity, reduces oiling during isolation, and improves long-term shelf-life versus non-fluorinated analogs. Incoming requests often focus on these distinctive handling and performance features, not just because of unique reactivity but also improved storage and reproducibility. Process improvements trickle down to user efficiency at scale, a factor easily missed by third-party sellers.

    Applications Guided by Real-World Use

    Our plant team frequently receives follow-up reports from R&D division partners using 2-(4-fluorobenzylsulfonyl)acetamidoxime as a key intermediate in API (active pharmaceutical ingredient) research campaigns. This molecule enters staged reactions, most often for synthesizing advanced heterocyclic scaffolds or novel nitrogen-containing ligands. Researchers gravitate to this fragment for its tuning effect on target binding, metabolic stability, and early lead compound bioavailability, not just as a simple chemical handle.

    Beyond the pharmaceutical space, this amidoxime variant surfaces in requests for crop protection research. In the agri-chemical section of our client base, it functions as a versatile starting point for sulfonamide or isoxazole formulations. Some polymer chemists look to attach the fluorobenzylsulfonyl group onto backbones, seeking improvements in chemical resistance and UV durability. From the supply side, these downstream sectors place high value on batch-to-batch reproducibility and the traceability we maintain, attributes stemming directly from our on-site custom synthesis capability.

    Consistent Experience: Reactivity and Handling

    Through direct plant operations, our technicians watch for common pitfalls during final workup. Amidoximes with electron-poor sulfonyl groups may show sluggish behavior in condensation partners, yet the para-fluorine in our product reliably activates the molecule during palladium-catalyzed couplings and other amide formation steps. Having produced multi-kilo runs for pilot programs, we see smoother filtrations, better solubility in common polar-aprotic solvents, and easier purification outcomes, compared with alkyl or unsubstituted benzylsulfonyl analogs.

    Hands-on experience has shown the importance of temperature control and agitation rates. Too much local heat introduces minor byproduct formation that derails downstream routes. Our operators understand this balancing act, making controlled upgrades in reactor design and automation within our facility. These practical details do not appear in most data-driven catalogs but make the distinction between a seamlessly integrated building block and one that costs hours of troubleshooting.

    How Our Direct Manufacturing Shapes the Offer

    Sourcing 2-(4-fluorobenzylsulfonyl)acetamidoxime from the originating manufacturer provides a series of quality and traceability benefits. Unlike bulk trade resellers or repackagers, our facility sets analytical checkpoints at every stage, responding directly if customer labs report off-spec behavior during early route scouting. We retain reference samples and digital production histories on file, so repeated requests for the same grade—or tailored modifications in particle size or salt form—come from informed adjustments, not guesswork.

    Batch manufacturing keeps this compound available in short lead times, thanks to local raw material partnerships and in-house intermediate inventory. Having encountered numerous complex synthesis trends over the years, we witness how subtle batch-to-batch variation can create issues in scale-up. We tackle this with full in-process control and robust crystallization routines, so customers receive what our technical team uses for their own synthesis without unexplained deviations.

    Reliable Support for Custom Synthetic Needs

    Every research chemist and production manager working with sulfonyl amidoximes knows purely catalog-based sourcing runs dry when project needs shift midstream. Our team frequently gets involved in helping troubleshoot routes encountering problems with byproduct formation or isolated impurity peaks. Having handled hundreds of production runs, we can offer guidance drawn directly from prior campaign experience—knowing which solvent swaps help, what order of addition keeps color low, and how careful seeding improves product isolation. This technical feedback comes from real trial and error, not just literature citations.

    We remain in regular dialogue with customers scaling up for toxicology studies, stability testing, and pilot plant output. Process modifications—alternate salt forms, specialized drying, or solvent swap recommendations—result from our direct tests, not hypothetical calculations. The relationship with every batch runs deeper than shipment and invoice; fielding process-specific questions and providing authentic, data-backed advice matters to both sides.

    How 2-(4-Fluorobenzylsulfonyl)Acetamidoxime Stands Apart

    In the crowded world of nitrogen-functionalized sulfonyl intermediates, 2-(4-fluorobenzylsulfonyl)acetamidoxime holds a specific foothold due to the reliability and specialized performance it brings. Not every amidoxime in our portfolio matches the purity, stability, or functional selectivity seen with this fluorinated variant. Our chemists appreciate the greater resistance to hydrolysis under mild base or weak acid—critical in the fine-tuning of multi-step syntheses. Bulkier or multi-substituted variants may offer niche properties but often lag in solubility or purification ease, causing hurdles for researchers seeking broad, adaptable intermediates.

    On the supply chain side, this product’s long shelf-life and well-characterized handling profile encourage repeat orders from those who value consistency over “novelty” at the expense of reliability. Major differences from other benzylsulfonyl amidoximes start with more stable storage and finish with higher observed yields in key condensations and functional group exchanges, verified year over year in our own test runs.

    Supporting the Path from Lab to Pilot Scale

    Most of our end-users begin with gram-scale feasibility studies, then rapidly require kilo-quantities for validation or small pilot runs. This compound offers an accessible transition from research to early production, since we operate direct synthesis and not repackaged stocks. Early research in our labs focused on both thermal properties and safe scale-up.

    We learned that the para-fluoro substituent softens the usual exothermic reaction profile compared with non-halogenated analogs, easing hazard controls at higher throughput. Our in-house process team continually refines operating procedures to ensure dust control, consistent feed rates, and streamlined lot release—key for pharma and ag-chem partners running multiple parallel routes.

    Direct Feedback Loops Informed by Manufacturing Experience

    Our experience brings insight beyond datasheets. We have seen teams run into cracked seals, leaking containers, or “mystery” color changes sourced to poorly finished third-party products. By keeping the entire manufacturing, QC, and packing process on-site and within our direct supervision, these headaches stay rare.

    We regularly invest in staff training within our technical operations wing, running real product through every possible bottleneck: from scale-up agitation tests to long-haul stability studies. On the rare occasions operators notice a deviation— say, unexpected polymorphs during storage or a subtle shift in IR profile—they flag it for root-cause analysis, not simply batch rejection. This culture of vigilance and willingness to adapt processes on the fly is part of how we keep this particular compound above par for demanding applications.

    Responsive Adjustments for Evolving Research and Manufacturing Trends

    The world of pharmaceutical and specialty chemical development never stands still. New regulatory guidelines, changing synthetic routes, greener chemistry drivers, and even new analytical tools shape the frontier. As a direct producer, we continually monitor which downstream needs emerge. That might mean changes in preferred solvent system, adoption of lower-waste process steps, or the creation of alternate crystalline forms for easier formulation.

    Our technical and quality teams stay current with customer feedback on changing target profiles for lead compound work. Thanks to our presence at the manufacturing level, we can fine-tune the material to match those needs: less dust, faster solution times, cleaner combustion profiles. Lab-based suppliers lack this hands-on adjustment capability; operating at scale encourages real innovation, because quality improvements and process tweaks are immediately tested and validated.

    People, Not Just Process: The Human Factor at the Core

    Our factory's bench chemists, production engineers, and logistics coordinators all contribute to the reliability of 2-(4-fluorobenzylsulfonyl)acetamidoxime shipments. Whether it’s monitoring a reactor’s progress at 2 a.m., testing a drum after transit, or providing on-the-spot advice to a researcher facing a failed step, our staff know their role forms part of a wider scientific endeavor. Practical experience matters: small improvements in drying or packing can shave hours off a customer’s workflow, and being open about real-world issues, such as safe venting practices or material handling under high humidity, marks the difference between generic product and trusted supply.

    Most downstream success stories trace back to this culture of practical ownership, not only compliance. For technical clients working under strict regulatory oversight, seeing first-hand how the chemical looks, how it handles, and getting transparent records of every manufacturing step builds confidence. This material supports not just experimental research but full process validation, since each lot comes with supporting spectral and compositional evidence gathered with modern equipment and trained staff. We provide this long before shipment, acting as partners rather than faceless suppliers.

    Looking Ahead: Keeping 2-(4-Fluorobenzylsulfonyl)Acetamidoxime At the Cutting Edge

    By keeping our manufacturing entirely in-house, we exercise full control over the safety, quality, and performance of each kilogram synthesized. Scaling innovations across runs, retaining institutional memory from every successful campaign, and acting promptly on partner feedback positions this amidoxime to remain a tool of choice in high-precision chemical synthesis.

    As environmental and technical standards rise, so do our internal benchmarks—stricter emissions control, solvent recovery, and process water recycling are not just ambitions but ongoing improvements. Our regular cycle of process optimization extends to both small-scale orders for R&D and large production runs for commercial partners. Real accountability starts at the plant and moves outward, ensuring every drum shipped is not only analytically compliant, but ready for immediate, reliable integration into the buyer’s project workflow. Experience and commitment at the manufacturer's bench drive every technical and operational advantage offered by 2-(4-fluorobenzylsulfonyl)acetamidoxime now and into the future.