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4-Amino-3-(Trifluoromethoxy)Benzonitrile

    • Product Name 4-Amino-3-(Trifluoromethoxy)Benzonitrile
    • Alias 4-Amino-3-(trifluoromethoxy)benzonitrile
    • Einecs 699-669-3
    • 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

    226659

    Chemicalname 4-Amino-3-(Trifluoromethoxy)Benzonitrile
    Casnumber 885276-00-4
    Molecularformula C8H5F3N2O
    Molecularweight 202.13 g/mol
    Appearance White to off-white solid
    Meltingpoint 108-112 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles NC1=CC(OC(F)(F)F)=CC#N
    Inchi InChI=1S/C8H5F3N2O/c9-8(10,11)15-7-2-5(12)1-6(3-7)4-13/h1-3H,12H2

    As an accredited 4-Amino-3-(Trifluoromethoxy)Benzonitrile 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 25g amber glass bottle with a tamper-evident cap, labeled with product details and hazard warnings.
    Shipping 4-Amino-3-(Trifluoromethoxy)Benzonitrile is shipped securely in tightly sealed containers to prevent moisture and contamination. Packages are clearly labeled, handled as a chemical substance, and transported in compliance with relevant regulations. Appropriate cushioning and secondary containment are used to ensure safe transit and prevent leaks or spills during shipping.
    Storage 4-Amino-3-(Trifluoromethoxy)benzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep away from sources of ignition, strong oxidizing agents, and incompatible substances. Store at room temperature, and avoid moisture exposure. Properly label the container, and ensure access is restricted to trained personnel using appropriate personal protective equipment.
    Application of 4-Amino-3-(Trifluoromethoxy)Benzonitrile

    Applications of 4-Amino-3-(Trifluoromethoxy)Benzonitrile in Industrial Manufacturing

    4-Amino-3-(Trifluoromethoxy)Benzonitrile (ATFBN) is a specialized intermediate widely manufactured for select downstream sectors where its unique fluoroaromatic and cyano functionalities serve targeted molecular design needs. Our technical expertise and quality management ensure consistent material performance in high-value synthesis applications. Below, we detail the principal scenarios where this intermediate plays an irreplaceable role, focusing on tangible industrial usage, regulatory expectations, specific process considerations, and end product categories.

    1. Pharmaceutical API Synthesis: Selective Kinase Inhibitors

    Major pharmaceutical manufacturers incorporate ATFBN as a core building block during the multi-step synthesis of active pharmaceutical ingredients (APIs), particularly in the development pipelines of selective kinase inhibitors. This compound introduces a trifluoromethoxy group that improves binding affinity and metabolic stability in target molecules. Manufacturing validation and process control focus on precise input of this intermediate at the heterocyclization or amide formation stage, often under CGMP protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • U.S. Food and Drug Administration (FDA) cGMP 21 CFR Parts 210/211
    • European Pharmacopoeia (Ph. Eur.) API Purity & Impurity Requirements
    • Japanese Pharmacopoeia (JP) for applicable clinical candidates

    Typical usage ratio

    • Stoichiometric quantity: 0.8–1.2 equivalents, adjusted per batch size and synthesis stage; balance of unreacted excess minimized during stagewise addition to control impurity profile.

    Downstream process integration

    • Introduced during palladium-catalyzed coupling or amidation; functionally serves as the nucleophilic aromatic amine subunit before further derivatization and purification via preparative chromatography.

    Final product types

    • Small molecule kinase inhibitors for oncology and immunology indications
    • Lead compounds in custom library synthesis for early-stage clinical studies
    • Reference standards for validated pharmacological assays

    2. Agrochemical Intermediate: Herbicide and Fungicide Discovery

    Agricultural research firms leverage ATFBN in the synthesis of fluorinated aromatic scaffolds for next-generation herbicides and fungicides. Its introduction in key intermediate stages enables the modification of lead compounds to enhance environmental persistence or active site selectivity. Manufacturing applies tightly governed formulation practices to control batch variability and ensure traceability from laboratory scale up to pilot and production campaigns.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals (esp. Section 1 & Section 5 for substance identification and analytical methods)
    • FAO/WHO Specification Requirements (JMPR)
    • ECHA REACH Regulation (EC) No 1907/2006 for registration, evaluation, authorization
    • ISO 9001:2015 Quality Management System for raw material qualification

    Typical usage ratio

    • 0.5–1.5% by weight in the advanced intermediate or target molecule composition, adjusted in response to structure-activity relationship (SAR) screening results and downstream crop application spectrum.

    Downstream process integration

    • Engaged in nucleophilic substitution and subsequent aromatic functionalization; introduced prior to cyclization or amide linkage steps, followed by solvent-extraction and crystallization.

    Final product types

    • Pre-emergence and post-emergence herbicides with enhanced metabolic profiles
    • Broad-spectrum fungicides targeting resistant crop pathogens
    • Patentable lead candidates and analog libraries for agrochemical discovery

    3. Specialty Dye and Pigment Manufacturing: Electronic Display Materials

    Manufacturers in the specialty dye and pigment segment utilize ATFBN in the preparation of advanced fluorinated chromophores for electronic display and imaging applications. Its incorporation enables the fine-tuning of chromatic properties and solvent compatibilities essential for OLED and organic photovoltaic device performance. Downstream processes demand meticulous control of input ratios and impurity management to comply with strict device material standards.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances for electronic components)
    • IEC 62474 Material Declaration for Electrical & Electronic Products
    • REACH SVHC Screening (for raw material eligibility in EEE applications)
    • ISO 14001:2015 for Environmental Management Systems in specialty chemical processing

    Typical usage ratio

    • Typically 3–8 mol% relative to total monomer input in the target chromophore synthesis; the precise ratio is established based on quantum yield optimization and device application protocol.

    Downstream process integration

    • Added at the Suzuki coupling or condensation phase; facilitates the installation of electron-withdrawing trifluoromethoxy and cyano functionalities onto the aromatic core prior to final pigment isolation and device formulation.

    Final product types

    • High-purity OLED display dyes for mobile and television screens
    • Fluorescent markers for photolithography and imaging reagents
    • Specialized photoresists and organic photodetector bulk materials

    4. Advanced Polymer Additives: Fluorinated Functional Materials

    Materials science companies integrate ATFBN into fluorinated polymer architectures to impart chemical resistance, dielectric stability, and unique surface properties required in demanding electronic and protective coating industries. The molecule’s cyano and trifluoromethoxy functionalities facilitate improved compatibilization and chain extension efficiency within controlled radical or polycondensation polymerizations.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics Materials
    • IEC 60216 (Thermal Endurance Properties of Polymer Insulation Materials)
    • ASTM D638 for Tensile Properties of Plastics
    • ISO 9001:2015 for manufacture and supply chain traceability

    Typical usage ratio

    • Loaded at 0.2–2.0 wt% in homopolymer or copolymer formulations; ratio determined by targeted dielectric needs and cross-linking efficiency in performance testing.

    Downstream process integration

    • Fed during initial polymerization (solution or melt phase); reacts with co-monomers or acts as an end-group modifier, followed by extrusion or molding under controlled thermal and shear conditions.

    Final product types

    • High-dielectric fluoropolymer films for flexible printed circuits
    • Protective conformal coatings for electronic assemblies
    • Durable industrial membranes and advanced engineering plastics

    5. Chemical Research and Analytical Reference Standards

    Research institutes and analytical laboratories employ ATFBN to prepare structure-confirmed analytical standards and reaction mechanism probes. In this context, purity and trace element specification demand highly controlled synthesis, analytical validation, and packaging protocols to support reliable method development and cross-laboratory reproducibility.

    Industry compliance standards

    • ISO/IEC 17025:2017 (Testing and Calibration Laboratories Accreditation)
    • IUPAC Standard for Chemical Reference Materials
    • GLP (Good Laboratory Practice) as defined by OECD Principles
    • REACH Annex XIII Purity/Impurity Profile Reporting for Research Chemicals

    Typical usage ratio

    • Concentration is precisely determined and certified; typical stock standards are supplied at 100–1000 mg/L, with adjustment by gravimetric or volumetric dilution for specific test methods.

    Downstream process integration

    • Material is purified to >99.5% and aliquoted into vials under inert atmosphere; supplied with full certificate of analysis (CoA) for direct use in calibration and method validation.

    Final product types

    • Certified analytical reference standards for LC/MS and NMR
    • Mechanistic probes for kinetic and reactivity studies
    • Calibration solutions for trace-level method development in pharmaceutical and environmental labs
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    Certification & Compliance
    More Introduction

    4-Amino-3-(Trifluoromethoxy)Benzonitrile: A Practical Look from the Manufacturer

    Understanding the Compound in a Working Chemical Plant

    We make 4-Amino-3-(trifluoromethoxy)benzonitrile every day in our facility, so we come to know it in ways the paperwork never really covers. The compound, usually labeled as ATFMBCN in our technical logs, carries a structure that blends the reactive amino group with a powerful trifluoromethoxy function and a sturdy nitrile anchor. Each of those parts brings something essential to synthetic chemistry, but together, they make a building block that stands out in pharmaceutical and agrochemical projects.

    Our crew engages with this compound not as a number on a safety sheet, but as a product that anchors development efforts in very real labs around the world. Any chemist who has struggled to introduce trifluoromethoxy into a benzene ring knows the headaches—high temperatures, lousy yields, touchy reagents. By supplying ATFMBCN, we deliver a shortcut that saves time, energy, and resources. The molecule’s chemical fingerprint means that it acts as a ready intermediate, streamlining the construction of many specialty molecules, especially where the presence of fluorine confers metabolic stability or unique physical behavior.

    What Sets Our ATFMBCN Apart in the Market

    In our plant, the model most customers use falls under the 98% pure, off-white crystalline form. That level of purity grew out of countless process improvements. Impurities that stick around in lower grades raise issues downstream—catalyst poisoning, unpredictable side-reactions, and waste. Nobody wants that. We run careful chromatography, tight controls on temperature, and double filtration so what leaves our warehouse shows a sharp melting point and consistent HPLC trace. It took us years to settle on the ideal solvent mix when working up batches, and even now, our engineers tweak reactor and crystallization conditions to squeeze every bit of unwanted byproduct out of the system.

    We believe in transparency because our team tracks impurities batch by batch. Several customers have called us mid-project with questions about possible residual solvents or unknown specks. We collect those questions in our internal logbooks, feed them back into the process, and some of our engineers have made careers out of troubleshooting what seems like a minor impurity problem. For us, quality doesn’t just mean numbers on a certificate but the confidence the chemist at the bench can have when starting a complex synthetic sequence.

    A Chemist’s Tool, Not Just a Catalogue Entry

    Most people ordering this compound care less about buzzwords and more about actual results in their reactions. In our own test labs, the chemists use the same lot that goes to customers. We use it in palladium-catalyzed aminations, heterocycle construction, and coupling reactions that demand reliable reactivity at the amino position. The trifluoromethoxy group impacts both the molecule’s electronic and steric profile, so it requires consistent handling. It’s not a generic benzene derivative, nor a commodity chemical you toss into a drum.

    Fluorinated compounds have a reputation for being less forgiving in synthesis. Incorporating the OCF3 group can block routes that otherwise work with plain methoxy or methyl. So, having the group ready-attached to a stable, isolable benzonitrile core solves a real bottleneck. The extra nitrogen on the ring opens doors for further derivatization—acylation, sulfonation, or even exploration of more exotic heterocycle scaffolds.

    Why Not Use Standard Aminobenzonitrile?

    Customers sometimes ask why they shouldn’t use 4-aminobenzonitrile or a standard aromatic amine. The answer is the trifluoromethoxy's effect. Adding those three fluorines fundamentally shifts lipophilicity and reactivity. Our process plants handle fluorinated gases and have ventilation systems to contain the risk, because waste disposal and operator safety with these compounds call for more than standard procedure. If you’re after a molecule that needs metabolic resistance or specialized activity in a biological system, the OCF3 can make a difference that shows up in the data—and in late-stage development costs.

    We have watched agrochemical companies shorten their synthetic route timelines because our product bypasses the need for in-house trifluoromethoxylation steps. They’ve shown us that skipping three extra synthetic steps matters more than shaving a few cents per kilo on the initial compound. That drives us to keep production tight and reliable.

    How We Managed Consistent Supply and Quality

    Our production volumes started small, only moving kilogram batches out the door. Pharmaceutical and materials science projects don’t always need bulk orders, but that’s changed lately. Global research into new therapeutic targets, custom polymers, and advanced coatings turned this into a product we make on multi-ton scale each year.

    Scaling up involved reworking almost every step. Our early reactors leaked heat, and we ran into inconsistent mixing that showed up as batches with wide melting point ranges. We learned a lot from those first failures. Now our batch records show near-identical material from month to month. Many of the process improvements came not from the top but from technicians on the floor watching for subtle shifts in product appearance and solvent residue.

    Reliability extends beyond the molecule itself. We’ve refined packaging based on feedback from companies who needed sample-sized bottles for method development and multi-kilo drums for pilot runs. We use HDPE and fluoropolymer liners to guard against moisture uptake, which can affect the nitrile’s chemical stability if left unchecked.

    Physical and Chemical Behavior

    The product typically presents as an off-white to pale yellow solid, depending on trace impurities and subtle lot-to-lot variations. The melting point hovers close to 90°C in our standard production batches, confirmed by DSC runs. We store samples alongside production, checking for decomposition or discoloration under routine warehouse lighting over extended periods.

    It dissolves readily in typical organic solvents—DMF, DMSO, acetonitrile, and even in slightly more polar protic mixtures. We get calls each year from formulation teams troubleshooting solubility problems, only to find their issue lies elsewhere, because ATFMBCN stays true to form batch after batch.

    Reactive groups on the molecule make it useful in both small-scale discovery and scale-up campaigns. The -NH2 group offers a clean entry point for diazotization, coupling, or protection strategies. The nitrile provides an avenue for exploitation via reduction or hydrolysis, depending on the target product. The OCF3 group doesn’t fall off under standard synthetic stress—it endures both acid and base treatment in our process runs. This resilience carries through to customer formulations, saving unnecessary failures at the worst possible time in a project.

    Sustainability and Safety in Production

    As a direct manufacturer, we face different challenges than repackagers or resellers. The handling of potent fluorine-based reagents requires a steady investment in safety, not just regulatory paperwork. Our team maintains negative pressure vent hoods, local environmental monitoring, and periodic audits of our solvent recovery units. Strict protocols spare us the headaches of emergency shutdowns, and our partnership with local authorities strengthens trust for everyone working in the plant.

    We have reduced our process waste streams by incorporating solvent recycling. Customers often ask about sustainability, and our experience shows fluorinated product manufacturing requires constant vigilance. Any slip-up with these materials spreads downstream and can close off export markets or add hidden costs. By recycling over 60% of process solvent, and rigorously tracking waste, we keep those concerns manageable and demonstrate our commitment to safe, responsible chemical manufacturing.

    Supporting Our Customers’ Projects—Real-World Impact

    Most of our customers are innovative research chemists, process engineers, and project leads who count on regular delivery, consistent product, and honest communication. We don’t believe in hiding behind sales speak. A researcher working on a new drug scaffold wants to know impurities lot by lot, and trusts our team for support during scale-up. Our technical staff remain available during their working hours, responding with spectra, batch details, or necessary background so projects can move ahead smoothly.

    We’ve assisted in trouble-shooting more than a few failed reactions by digging into our own process data to spot batch-specific quirks, something a surface-level reseller couldn’t offer. Once, one of our customers hit problems with amine reactivity in a late-stage process. Our in-house chemists cycled through reaction runs with archived batches and tracked the issue to a rare trace metal impurity. Data from our plant solved their problem, because our familiarity with the compound’s complete production history gave clarity.

    Pharmaceutical scale-ups live and die by the predictability of their intermediates. The nuances—slight variances in color, melting point, amorphous versus crystalline content—matter far more than catch-all catalog descriptions. Customers expect straight answers and real technical support. We pass on what we’ve learned, update batch packaging as requests come in from the field, and document every response in our records to support future improvements.

    Why Consistency Beats Low Cost

    Some might wonder if other amine-bearing benzonitriles could substitute to bring down cost. In our experience, the answer is rarely yes. Attempts to swap in less pure or non-fluorinated analogs lead to extra purification steps, diminished yields, or outright project failure. We see the effects not just in wasted time, but in the additional regulatory headaches that surface if a product profile shifts down the line.

    A cheap but inconsistent 4-amino benzonitrile derivative won’t pass the acid test in real-world pharma or crop protection synthesis lines. The cost savings get burned up in troubleshooting, product recalls, or customer complaints. For medicinal chemistry, this can set projects back months, threatening patent windows and trial schedules.

    Meeting New Regulatory Demands

    We track new global regulations regarding fluorinated intermediates, not out of fear, but because proactive compliance builds trust. Each year, new guidelines emerge across Asia, Europe, and North America with limits on waste, expectations for impurity reporting, and legal obligations on final content. Our internal records tie each batch not just to test logs, but to full supply chain documentation, so that we support customers in regulatory inspections. That kind of traceability means our partners don’t face production delays or penalties from missing paperwork or incomplete impurity reports.

    We keep our process up to date, because many of our clients must file documentation for regulatory submissions where intermediate quality isn’t optional. If doubts emerge about our intermediate, it cascades upward, risking re-submission of dossiers or even loss of a product or market.

    Scientific Collaborations and Product Development

    We maintain open lines with both academic and commercial researchers. Our approach isn’t to push a single application or chase trends, but to listen. Material science labs in Europe sent requests for crystalline variants with specific particle size distributions—we answered by tweaking filtration and milling steps, testing samples in our own reactors before offering them at any scale. One team working on OLEDs asked us to lower trace water content to boost their device stability. Our production manager worked out a low-moisture batch protocol, shipped it for testing, and results showed up in their publications.

    This cycle of dialogue and adjustment shapes what we produce. We are not just a factory running endless drums through reactors—we are a team refining product together with every end user who shares their experiences and needs. Over time, this approach has led to more robust processes and a broader portfolio of closely related products, many based on requests that pushed us outside our comfort zone.

    Differences Compared to Other Intermediates

    Every chemical manufacturer claims their product is different. We prefer to point to details. Traditional aminobenzonitriles can’t match the stability of the trifluoromethoxy group in oxidative or harsh synthetic conditions. In our hands, the OCF3 group resists hydrolysis and oxidation better than methyl or non-fluorinated ethers. Runs that wreck classical precursors show much higher recovered yield with our ATFMBCN.

    Some competing intermediates lack the same purity benchmarks, skipping expensive process steps or blending surplus product into their lots to widen margins. We do not shortcut quality for price. If an impurity appears regularly above our internal thresholds, we won’t ship the batch—simple as that. Call it old-fashioned, but keeping a clean, consistent quality record means more repeat business and fewer tangled customer support threads.

    Looking Forward: Expanding Applications and Future Development

    We watch new application areas for ATFMBCN open up steadily. Focused research in advanced materials and next-generation molecules for electronic devices expands demand year after year. Coatings researchers working at the limits of durability and performance evaluate our lots for next-gen polymers. We consult regularly with both pharmaceutical and electronic materials chemists who seek ever-finer control over physical and chemical properties.

    Some formulations, especially in the electronics and specialty polymer industries, require tighter particle size distribution, lower moisture levels, or even surface passivation. Our plant runs pilot trials in close collaboration with customers, adjusting synthetic conditions or post-processing steps, and we share our success stories openly at technical conferences. We think the product’s future will not just be limited to being a pharmaceutical intermediate but will serve in advanced functional materials, thanks to its unique mix of functional groups.

    Commitment Built on Experience, Not Marketing

    Our relationship with this product goes much deeper than market trends or catalogue lifespans. The knowledge we’ve built about 4-amino-3-(trifluoromethoxy)benzonitrile comes not only from scientific literature but from daily production, technical firefighting, and long-term accumulation of feedback from the field. What we offer customers isn’t a simple commodity—it’s a solution shaped by real-world needs, technical detail, and years of hands-on engagement.

    We believe in a transparent production process and believe that honest evaluation and product stewardship deliver results. Our investment isn’t in short-term profit but in long-term trust, and every chemist who calls us for technical support or batch-specific questions gets answers drawn from a genuine working knowledge accumulated over years of manufacturing experience. As new applications surface and research labs seek even more precise building blocks, we’ll keep refining and adapting—to ensure every batch of ATFMBCN delivers on reliability and performance, whatever the next challenge may be.