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4-(Trifluoromethyl)Benzamidoxime

    • Product Name 4-(Trifluoromethyl)Benzamidoxime
    • Alias 4-(Trifluoromethyl)benzamidoxime
    • Einecs 694-460-0
    • 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
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    Specifications

    HS Code

    174841

    Product Name 4-(Trifluoromethyl)Benzamidoxime
    Cas Number 86170-13-4
    Molecular Formula C8H7F3N2O
    Molecular Weight 204.15 g/mol
    Appearance White to off-white solid
    Melting Point 148-152°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥ 98%
    Smiles C1=CC(=CC=C1C(F)(F)F)C(=NO)N
    Inchi InChI=1S/C8H7F3N2O/c9-8(10,11)6-2-1-3-7(4-6)5(13)12-14/h1-4,14H,(H2,12,13)
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Synonyms 4-(Trifluoromethyl)benzamidine oxime

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

    Packing & Storage
    Packing Amber glass bottle containing 10 grams of 4-(Trifluoromethyl)Benzamidoxime, tightly sealed with tamper-evident cap and labeled accordingly.
    Shipping 4-(Trifluoromethyl)Benzamidoxime is shipped in tightly sealed containers under dry, cool, and well-ventilated conditions. Packaging complies with chemical safety regulations to prevent leaks or contamination. The shipment is labeled with appropriate hazard warnings, handled by trained personnel, and accompanied by a Safety Data Sheet (SDS) to ensure safe transport and handling.
    Storage 4-(Trifluoromethyl)Benzamidoxime should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed when not in use, and protect it from moisture and direct sunlight. Store at room temperature, ensuring proper chemical labeling and safety protocols are followed.
    Application of 4-(Trifluoromethyl)Benzamidoxime

    Applications of 4-(Trifluoromethyl)Benzamidoxime in Industrial Manufacturing

    4-(Trifluoromethyl)Benzamidoxime serves as a specialized intermediate in several industrial sectors where strict standards, precise formulation requirements, and dedicated process integration are critical. We supply this material exclusively to industries with proven end-use consumption and fully established downstream processing lines, ensuring our clients achieve repeatable performance and reliable compliance in their production environments.

    1. Pharmaceutical Active Ingredient Synthesis

    As a key building block in the synthesis of specific active pharmaceutical ingredients (APIs), 4-(Trifluoromethyl)Benzamidoxime enables targeted molecular modifications in the manufacture of heterocyclic drugs and advanced intermediates, such as those used in antitumor or antimicrobial therapies. Its characteristics allow chemists to introduce the trifluoromethyl group into core structures under mild to moderate conditions, which helps meet strict regulatory demands on purity, traceability, and process reproducibility at scale.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) as per ICH Q7
    • EU REACH compliant sourcing for raw materials
    • USP/NF and Ph. Eur. specifications for intermediate purity
    • ICH Q3A/B impurity guidelines

    Typical usage ratio

    • 5–18 mol% relative to total reaction substrate; adjusted based on the target API route, impurity profile control, and desired yield optimization

    Downstream process integration

    • Charged at the late intermediate synthesis stage in multi-step batch reactors, following initial condensation reactions, and prior to final heterocycle closure/hydrogenation under temperature-controlled environments

    Final product types

    • Class-specific non-steroidal anti-inflammatory drugs (NSAIDs)
    • Heterocyclic antibacterial intermediates
    • Pyrimidine- and pyridine-based cancer therapeutic lead compounds
    • Custom fine chemicals for clinical research APIs

    2. Agrochemical Crop Protection Intermediate

    The material acts as a crucial moiety for the functionalization of core structures in high-potency herbicide and fungicide synthesis. Its integration allows downstream manufacturers to impart increased metabolic stability and rainfastness in field-use formulations. Specialized production lines require precise dosing to ensure repeatable bioactivity while staying within established safety margins for environmental and worker exposure.

    Industry compliance standards

    • ISO 9001:2015-certified agrochemical production guidelines
    • Global Crop Protection Product Registration (EU Directive 91/414/EEC, US EPA 40 CFR, China Pesticide Registration Regulation)
    • OECD Good Laboratory Practice (GLP)
    • FAO Specification for Pesticide Technical Materials

    Typical usage ratio

    • 0.7–2.5 wt% in concentrated technical formulations; modified per required field application rate and bioefficacy trials

    Downstream process integration

    • Applied during the ring functionalization step in the technical synthesis block prior to granule or suspension concentrate (SC) post-treatment

    Final product types

    • Broad-spectrum triazole fungicides
    • Post-emergence sulfonylurea herbicides
    • Advanced seed treatment technical concentrates
    • Chemical hybridizing agents for field crops

    3. Specialty Polymer Modification

    Used as a molecular modifier in the engineering of specialty fluorinated polymers, this raw material enables the creation of copolymers with enhanced hydrophobic and dielectric properties. Industrial polymer producers incorporate it to tailor surface energy and electronic insulation in resins and films, with process parameters tightly controlled to ensure consistent material properties and functional group incorporation for downstream electronics or coating applications.

    Industry compliance standards

    • RoHS/REACH compliance for polymer additives
    • ISO 14001 for environmental management in chemical synthesis
    • UL 94 (flammability rating) for plastic materials
    • IEC 61249-2-21 for halogen-free laminate standards

    Typical usage ratio

    • 0.2–1.5 mol% of total polymer precursor content; tailored for target dielectric and mechanical property profiles

    Downstream process integration

    • Direct copolymerization through solution or emulsion polymerization, introduced during oligomerization with comonomers under inert atmosphere, with subsequent extrusion molding

    Final product types

    • Low dielectric polyimide films for flexible circuitry
    • Anti-graffiti fluoropolymer coatings
    • Flame-retardant printed circuit board (PCB) laminates
    • High-barrier flexible packaging substrates

    4. Advanced Analytical Reagent Preparation

    Analytical reagent manufacturers use this amidoxime derivative to design tailored ligand systems for metal chelation and sample preparation in trace analytics, particularly for environmental and clinical laboratories. Accurate dosing and impurity control are essential to prevent interference, while material integration occurs under analytically clean conditions to prevent cross-contamination and guarantee consistent performance in finished kits.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory reagent qualification
    • USP Reagent specifications
    • CEN/TS 16516 for laboratory plasticware and chemical compatibility
    • GLP certification for analytical reagent preparation

    Typical usage ratio

    • 0.03–0.15 wt% in analytical kit formulations, adapted to the sensitivity and matrix type of the end-user detection method

    Downstream process integration

    • Blended during aqueous or organic phase reagent preparation under cleanroom conditions, followed by lyophilization or liquid kit assembly for analytical use

    Final product types

    • Metal extraction columns for ICP-MS
    • Colorimetric heavy metal test kits
    • Trace halogen detector reagent packs
    • Clinical laboratory chelation standards
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    Certification & Compliance
    More Introduction

    4-(Trifluoromethyl)Benzamidoxime: Designed and Produced by Chemical Manufacturers Who Know the Work

    Understanding What We Make and Why It Matters

    Each day, from reactors to drums, we see how innovation in molecular design changes the way industries solve challenges in pharmaceuticals, agrochemicals, and materials science. 4-(Trifluoromethyl)Benzamidoxime is not just another compound to tick off a catalog; it comes from years of process refinement, end-use feedback, and genuine curiosity about improving synthesis and downstream applications.

    Breaking Down the Details: Model, Form, and Purity

    In the factory, we prepare 4-(Trifluoromethyl)Benzamidoxime most often as a crystalline powder, favoring a white-to-off-white appearance. Every batch undergoes specific gravity and melting point tests to verify molecular consistency. Our experience with purification drives our decision to target high-purity grades—typically above 98%—aimed at supporting sensitive reactions in R&D and advanced manufacturing. This is important, because even small impurities can cause serious delays or unpredictable results in scale-ups or high-throughput screening.

    What Sets 4-(Trifluoromethyl)Benzamidoxime Apart?

    From a manufacturer’s perspective, one of the greatest challenges comes from controlling the influence of the trifluoromethyl group on reactivity and stability. The unique interplay between the electron-withdrawing CF3 group and the amidoxime moiety gives this molecule a profile that is harder to replicate using standard benzamidoximes or simple benzamides.

    We see customers arrive looking for alternatives to less stable or less selective intermediates—especially for projects demanding resistance to metabolic degradation or improved target binding in pharmaceutical leads. The trifluoromethyl substituent introduces both lipophilicity and electronic tuning that standard benzamidoximes cannot provide. It resists hydrolysis better in most synthetic environments and offers tighter control over regioselective transformations. This means that in the hands of a skilled chemist, the compound delivers superior reliability with handling and fewer surprises under various reaction conditions.

    Practical Usage: Views From the Production Floor and the Lab

    We manufacture to serve real workflows, not hypothetical ones. This compound often finds its way into the early-stage screening for drug candidates. Groups working in medicinal chemistry lean on its combination of chemical stability and electron distribution to modify lead compounds or introduce new analogues with stronger pharmacological potential. We’ve noticed repeated purchases from teams optimizing inhibitors or seeking to block pathological enzymes, since the CF3 group can enhance binding affinity while reducing unwanted side reactions that plague more reactive analogues.

    Agricultural chemistry uses run along similar logic. The introduction of the trifluoromethyl element affects bioavailability and environmental persistence—attributes highly valued in new pesticides, herbicides, or fungicides. By building on the backbone of benzamidoxime but shifting toward the CF3-modified version, formulators can tune both reactivity and stability to meet shifting regulatory environments and pest resistance trends.

    Our technical team hears often from formulations labs about the need for reliable solubility data under real-world processing conditions. Our direct production access means we can tailor certain particle sizes or deliver precise impurity profiles as needed by scale-up teams, avoiding the problems that come with blended or cut material from third-party sources. Users benefit from tight batch-to-batch consistency, helping avoid costly surprises in times of tight production schedules or regulatory scrutiny.

    Comparisons With Similar Compounds: Why Go With the Trifluoromethyl Version?

    Chemically, standard benzamidoximes offer baseline performance and affordability, making them a fair choice for bulk intermediates or non-critical reactions. Still, feedback from advanced labs tells a different story once the requirements sharpen, especially for lead optimization or regulatory tolerance. The inclusion of the trifluoromethyl group imparts noticeably increased metabolic stability—a trait increasingly demanded in modern drug synthesis where enzymatic degradation can break development pipelines.

    The modification also enables access to analogues that regular benzamidoximes simply cannot reach. This mattered recently when one customer switched from a non-fluorinated amidoxime, plagued by variable assay results and storage instability. Swapping to the trifluoromethyl variant brought their variability down to within statistical control, saving months in a time-critical project.

    Other competing chemistries, including halogenated or alkoxy-substituted benzamidoximes, may bring certain desirable properties, but none consistently deliver the same set of features found in the trifluoromethyl variant: better lipophilicity, tighter spectra, and greater predictive power in finished product performance.

    Production Under Manufacturer’s Control: What Makes Reliable Supply Work

    We oversee each synthesis from start to finish. At scale, minor variations in temperature, reaction times, or solvent choice can ripple into big downstream headaches or recall risk. Our reactors operate under carefully tuned kinetics; we run NMR, HPLC, and GC-MS checks at every key step, not just at final quality control. By doing this, we catch issues early.

    Direct manufacturing access means we control raw material sources, solvent grades, and even storage conditions before and after crystallization. This vertical integration helps avoid batch-to-batch drift and ensures that what leaves our drum matches exactly what went through verification.

    Customers usually want to discuss how a compound like this transitions from lab idea to full-scale production. Questions about scalability, exotherm management, and trace residuals come up often. Because we synthesize and ship ourselves—rather than reselling from bulk—we provide live technical data based on real production, including how isolation or purification steps were modified to deliver top-quality material for both pilot and kilo scales.

    Addressing Challenges with Purity and Stability

    Every manufacturer faces hurdles with reactive intermediates and storage. 4-(Trifluoromethyl)Benzamidoxime stands up to various ambient conditions, and we confirm this through stability studies as part of our release procedures. By controlling water content and minimizing exposure to strong acids or bases, we lengthen product shelf life, which is vital for clients managing multi-month development timelines.

    Stored in sealed, inert packaging, our product holds up beyond standard warehouse durations. But the real quality comes from eliminating trace contaminants—organics, solvents, or metal ions. Purity here is not just a number; it means an end to false positives in high-throughput screening or downstream synthesis, reducing troubleshooting for chemists and saving entire batches from rework.

    Supporting Evolving Customer Demands

    We deal directly with researchers pushing at the boundaries of what trifluoromethylated benzamidoximes can do, in drug metabolism studies, analytical method development, and bioactive compound synthesis. Requests for material can change fast. By keeping reaction precursors and process controls in-house, we answer with flexibility—such as modifying recrystallization techniques or scaling up output to match project timelines without risking supply shortfalls.

    We’ve kept careful records and maintain ongoing dialogue with industry partners. Sharing insights into how trifluoromethyl substitution patterns affect in-vivo and in-vitro outcomes helps both sides refine their approaches and avoid dead ends early. This not only improves our process efficiency but supports broader scientific progress using real-world feedback rather than speculative claims.

    Environmental and Safety Considerations from an Operational Viewpoint

    Operating chemical reactors at scale means facing ongoing scrutiny over waste, emissions, and workplace health. The synthetic routes applied to 4-(Trifluoromethyl)Benzamidoxime benefit from continuous process improvements. We use closed-loop solvent recovery, minimize by-products, and manage process effluent responsibly to meet both local and international standards. On a practical level, plant workers receive up-to-date handling guidelines and safety protocols. Our choices about reaction solvents and reagents balance both process yield and downstream environmental impact.

    Personal engagement shapes our safety culture. We make sure that everyone—from shift supervisors to shipping—knows the characteristic properties of 4-(Trifluoromethyl)Benzamidoxime: low volatility, sensitivity to oxidizing agents, and the requirements for inert storage. Modern plant design allows fast isolation from potential cross-contaminants. This has resulted in a record of safe operations with no major incidents or recalls related to this product line.

    Building Trust Through Consistent Delivery

    End-users expect honesty about what they’ll receive—down to spectral certificates, batch analyses, and shipping documentation. Because we run the full production cycle, we do not just share data sheets, but open access to technical staff with hands-on knowledge. Our team can track exactly how each lot differs, what solvents were used, and the history from reaction to drum.

    Lab teams facing tight research deadlines know they can reach out for reorder or custom prep without waiting weeks for a distributor to check stock. With our on-site warehousing and cold-chain logistics experience, timelines are shorter and less prone to error, especially for multinational projects under regulatory clock pressure.

    Where the Product Goes Next: A View Forward

    We find satisfaction in seeing our materials lead to new patents, regulatory filings, or even first-in-class clinical candidates. Industry shifts toward more complex, fluorinated frameworks show that compounds like 4-(Trifluoromethyl)Benzamidoxime mark an inflection point—balancing the promise of improved bioactivity with practical manufacturability.

    As needs evolve, we retain the ability to refine synthetic approaches and invest in greener processes. We welcome input from formulation chemists, analytical specialists, and development leads, all working toward solutions that move products to market faster and with greater certainty.

    From Factory to Lab Bench: The Manufacturer’s Unique Role

    From raw material sourcing to lab-ready delivery, we approach each lot of 4-(Trifluoromethyl)Benzamidoxime as a test of our reputation. It takes more than knowledge on paper; it requires attention to real process feedback, the patience to troubleshoot synthesis bottlenecks, and the willingness to stand behind each specification.

    Personal involvement at every stage sets apart a real manufacturer from intermediaries. Whether the molecule ends up in a university research project, a pilot production run, or as part of a major pharma’s clinical pipeline, the constant is direct communication and full transparency on how it was made. Through experience, technical rigor, and accountability, we hope to drive progress not only in specific applications but also in responsible, sustainable, and innovative chemical production.

    Final Thoughts on 4-(Trifluoromethyl)Benzamidoxime’s Role in Modern Chemistry

    Producing 4-(Trifluoromethyl)Benzamidoxime is a partnership, not just a transaction. From synthesis optimization to reliable logistics, every step reflects a manufacturer’s commitment to quality, transparency, and ongoing collaboration with those on the cutting edge. We invite technical discussions, real-world feedback, and a shared drive to explore what’s next in chemical synthesis and molecular innovation.