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

2-(Trifluoromethyl)Acetanilide

    • Product Name 2-(Trifluoromethyl)Acetanilide
    • Alias o-(Trifluoromethyl)acetanilide
    • Einecs 242-011-5
    • 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

    149953

    Chemicalname 2-(Trifluoromethyl)Acetanilide
    Molecularformula C9H8F3NO
    Molecularweight 203.16 g/mol
    Casnumber 350-91-2
    Appearance White to off-white solid
    Meltingpoint 89-91°C
    Boilingpoint 317°C at 760 mmHg
    Density 1.31 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles CC(=O)NC1=CC=CC=C1C(F)(F)F
    Refractiveindex 1.500 (estimate)
    Synonyms 2-(Trifluoromethyl)phenylacetamide
    Flashpoint 145°C

    As an accredited 2-(Trifluoromethyl)Acetanilide 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 25 grams of 2-(Trifluoromethyl)acetanilide, sealed with a screw cap, labeled with hazard warnings.
    Shipping 2-(Trifluoromethyl)Acetanilide is shipped in a tightly sealed container, compliant with chemical transport regulations. It is typically packed with protective materials to prevent breakage or leaks. Standard shipping is via ground or air freight, labeled as a laboratory chemical, and accompanied by a Safety Data Sheet for safe handling and transport.
    Storage **2-(Trifluoromethyl)Acetanilide** 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. Protect the chemical from light and moisture. Clearly label the storage container, and follow all relevant safety procedures, including using suitable personal protective equipment when handling.
    Application of 2-(Trifluoromethyl)Acetanilide

    Applications of 2-(Trifluoromethyl)Acetanilide in Industrial Manufacturing

    As a dedicated manufacturer specializing in high-purity 2-(Trifluoromethyl)Acetanilide, we supply global industrial clients operating in agrochemicals, pharmaceuticals, specialty dyes, and polymer additives. Our raw material supports advanced synthesis routes in these sectors, functioning as a critical intermediate or enabler in well-established, regulation-driven markets. Below, we detail real downstream applications and technical integration for our clients.

    1. Agrochemical Synthesis: Herbicide Intermediate

    Many agrotech firms utilize 2-(Trifluoromethyl)Acetanilide as a key intermediate in the synthesis of selective herbicides, notably in the construction of aryl-based acetanilide formulations. Its inclusion into the synthesis stage enhances target molecule reactivity and final product stability due to the trifluoromethyl group, which alters the electron density. The compound features predominantly in the stepwise buildout of pre-emergent herbicides for cereal and broadleaf crop protection.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • REACH (EC) No 1907/2006
    • ISO 9001:2015 for quality management in synthesis
    • US EPA Registration Guidelines

    Typical usage ratio

    • 10–25% by molar ratio in active ingredient intermediates; formulators adjust based on desired selectivity and synthesis yield benchmarked against target herbicidal compounds.

    Downstream process integration

    • Introduced at the coupling or acylation stage for precursor construction, commonly after halogenation or nitration steps within in-house flow or batch reactors at client sites.

    Final product types

    • Post-emergent herbicide active ingredients (e.g., acetanilide subclasses such as metolachlor analogues)
    • Commercial crop protection formulations
    • Custom-blend pre-mixtures for seed treatment manufacturers

    2. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Our clients in pharmaceutical manufacturing integrate this material during the construction of fluorinated aromatic scaffolds, mainly for non-steroidal anti-inflammatory drugs and certain antipsychotics. Its trifluoromethyl-bearing structure facilitates regioselective reactions and improves overall pharmacokinetics in the finished molecule, directly contributing to the bioactive core present in final drug APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF Monograph alignment (where applicable)
    • EU GMP Part II for API intermediates
    • Drug Master File (DMF) registration for key intermediates

    Typical usage ratio

    • 0.8–1.2 molar equivalents per target molecule; precise ratio calculated in process development to minimize byproducts and maximize API yield based on batch synthesis optimization.

    Downstream process integration

    • Inserted at controlled nitration or amidation stages during the multi-step route for API precursor synthesis, followed by reduction and coupling with tailored aromatic units in compliance-enforced plants.

    Final product types

    • Non-steroidal anti-inflammatory drug APIs
    • Psychotropic drug core intermediates
    • GMP-compliant pharmaceutical intermediates for further synthesis

    3. Dye and Pigment Synthesis for High-Performance Coatings

    Chemical companies specializing in functional dyes incorporate this raw material during the manufacture of fluorinated azo and anthraquinone pigments, particularly those targeting weather and solvent resistance. The trifluoromethyl acetanilide fragment increases pigment fastness and chemical durability, making the compound a fixture in the synthesis of specialty dyes for military, automotive, and electronic applications.

    Industry compliance standards

    • EN 71-3:2019 (for restricted substances in pigments/dyes)
    • OEKO-TEX Standard 100
    • ISO 9001:2015 for pigment manufacturing
    • ASTM D4303 for lightfastness testing in coatings

    Typical usage ratio

    • 5–15% by weight in coupling or acylation steps; manufacturers tune this proportion based on pigment grade requirements and required stability profiles for final coating systems.

    Downstream process integration

    • Unveiled during condensation or diazotization units in batch reactors, where it chemically binds with aromatic amines or diketones to form color-stable pigment frameworks.

    Final product types

    • UV-resistant automotive coatings
    • Weatherproof industrial paints
    • Electronic substrate dyes with high chemical resistance
    • Textile pigment dispersions for specialty fibers

    4. Polymer Additive for Fluorinated Resin Modification

    Manufacturers in the engineered plastics sector employ 2-(Trifluoromethyl)Acetanilide as a modifier and intermediate for specialty polymers. It plays a role as a fluorinated building block in the production of modified polyimides and aramid fibers, resulting in improved thermal and chemical stability for demanding end uses, including aerospace wire insulation and microelectronics encapsulants.

    Industry compliance standards

    • UL 94 (Flammability of Plastic Materials)
    • ISO 1043-4 (for fluorinated plastics and copolymers)
    • RoHS Directive 2011/65/EU (for restricted substances in electronics)
    • ASTM D638 for mechanical testing of plastics

    Typical usage ratio

    • 0.2–1.5% by weight, applied as a monomer or chain-terminating agent; dosage controlled with respect to targeted molecular weight and end-use performance attributes in final polymer formulations.

    Downstream process integration

    • Introduced during polycondensation or grafting reactions, co-reacted with dianhydrides or diamines to impart trifluoromethyl functionality into backbone structures in custom compounding or extrusion lines.

    Final product types

    • High-temperature polyimide films
    • Fluorinated aramid fibers for protective garments
    • PCB insulating layers in electronics
    • Microelectronic device encapsulation resins
    Free Quote

    Competitive 2-(Trifluoromethyl)Acetanilide 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

    2-(Trifluoromethyl)Acetanilide: A Closer Look from Our Production Floor

    What Makes 2-(Trifluoromethyl)Acetanilide Unique in Practice

    We’ve been working with 2-(Trifluoromethyl)Acetanilide, also known to many development chemists as N-(2-Trifluoromethylphenyl)acetamide, for years. The journey begins at our reactors, where fluoroaromatic building blocks combine with acetanilide structures to produce this unique molecule. Unlike some other substituted acetanilides, the trifluoromethyl group at the ortho position changes more than just the structure: it introduces a strong electron-withdrawing effect, impacting how the molecule behaves in downstream processes.

    You don’t see this compound featured in mainstream catalogs as much as standard acetanilide or para-substituted alternatives, largely due to its more technical synthesis route. Our team tackles these steps at scale, starting from rigorously purified raw materials. Control of moisture, temperature, and timing during substitution and acetylation remains crucial, because stray conditions often lead to unwanted byproducts or reduced yields. The experience we’ve collected refining every batch means we know what works—and what doesn’t—far beyond what’s written up in literature.

    Physical and Chemical Properties That Matter in Real Usage

    2-(Trifluoromethyl)Acetanilide carries over its crystalline, slightly off-white appearance to finished product forms. The structure packs an ortho-positioned -CF3 right on the phenyl of the classic acetanilide backbone. That’s a direct effect on solubility, handling, and compatibility. The melting point sits comfortably higher than most other acetanilides, which matters for those running reactions under elevated temperatures or recrystallizations.

    In practical use, the trifluoromethyl group doesn’t just sit idle. The increased hydrophobicity and lower nucleophilicity of the anilide nitrogen compared to unsubstituted or para-substituted versions changes everything—how it dissolves, how it interacts with organic solvents, and how downstream transformations run. That feature stands out in the lab, since some intermediates or target molecules demand these effects to perform as anticipated.

    Purity is a topic that never gets old here. Our batches routinely clear HPLC and NMR checks, and a typical specification keeps the purity above 99%, so what arrives is what reacts on your bench. Working through any fine separation of regioisomers or minor impurities during production means familiarity with both classic and modern chromatography—not all labs have the luxury of this attention to detail, and impurities can upset research or scale-up efforts.

    Real Applications: Not Just a Catalog Item

    People in chemical R&D pay attention to detail, which means 2-(Trifluoromethyl)Acetanilide draws interest not as a commodity, but as an enabling building block. In pharma research, the compound’s electron-deficient ring attracts those aiming for selective arylation, amination, or cross-coupling reactions. The -CF3 group blocks certain metabolic sites, bringing higher metabolic stability to candidate molecules—a highly prized trait when the early discovery team needs compounds that resist facile oxidation in biological tests.

    Fragments derived from our product play roles in agrochemical lead development, too. There’s a push for molecules with tuned lipophilicity, as those properties help move actives across biological membranes in vivo. Over years of supplying this compound, we’ve seen it move from basic intermediate status to a spot in promising patent claims and development candidates.

    In process chemistry, labs often lean on fluorinated aromatics to manipulate substrates in late-stage routes or screening libraries. The traceability and batch consistency we achieve with 2-(Trifluoromethyl)Acetanilide over hundreds of kilo-scale runs give these users confidence that what they order next month will match last year’s lot. Batch-to-batch reproducibility exists as more than a buzzword for us—it’s a contract with our fellow scientists downstream.

    Distinctions from the Crowd: Comparing Structural Cousins

    Some try to swap 4-(trifluoromethyl)acetanilide or non-fluorinated acetanalides into routes designed for the ortho CF3 analog. They quickly discover that ortho substitution acts differently; steric hindrance marks out new reaction selectivities or blocks others entirely. The electron-withdrawing effect gets felt most acutely when the ring undergoes metalation, aryl halide activation, or coupling studies. Para- and meta-substituted products just don’t deliver these same effects due to the physics and chemistry built right into their structures.

    We share structure–activity data with partners on occasion, and side-by-side comparisons paint a clear picture. The ortho -CF3 shifts chemical reactivity too far for it to be a simple “drop-in” for less bulky or less electron-hungry variants. That difference makes its way to how the parent acetanilide shows up in spectra and kinetics, which cannot be faked or substituted by switching to something similar on paper.

    Development Realities: Making the Molecule Work at Scale

    Batches scale up from lab to plant, and challenges reveal themselves in new forms. We often adjust our approaches based on real-world factors: atmospheres sensitive to HF release, tricky crystallizations, even packaging choices that protect against traces of moisture or UV light. Seeing the process from grams to kilos brings up questions about cost, waste, and safety—topics that only manufacturer experience really covers.

    Each run gets tracked for performance: yield, purity, particle size, and byproduct profile. When scale-up throws surprises our way, the answer calls for grounded changes—in solvents, time, ingredient source, or temperature protocols. Solving these puzzles early means customers don’t inherit avoidable headaches in their own labs.

    We’ve invested in closed-system reactors to handle the exothermic stages, and our QC team interprets more than just data—they bring hands-on feedback from the line, shaping real improvements. No generic handling or theoretical yields; we deliver what chemists expect based on a strong record of technical output and troubleshooting.

    Quality, Consistency, and the Human Element

    Any lab can check a melting point or HPLC spectrum, but years in the field teach us that numbers only tell part of the truth. We regularly conduct stability studies, looking for changes in color, solubility, or spectral features months down the line. Humidity, container type, and even small temperature fluctuations leave their mark, so we shape protocols to keep the compound true from dispatch to your bench.

    Feedback cycles between our production and QC teams bridge the gap between analytical results and hands-on properties. Handling characteristics—how crystals pack, flow, or respond to solvents—often mean more than a one-line spec in a technical sheet. Our operators flag anything off-spec, not just analytical values but the visual or tactile cues that chemists recognize in practical use.

    Training for our staff covers not just equipment, but pattern recognition—spotting changes batch over batch, and knowing which observations point to upstream or downstream issues. This attention becomes obvious in the consistency and reliability of finished product that reaches labs focused on research, pilot, or commercial investigations.

    Meeting Today’s Needs in a Changing Research Environment

    Research priorities shift quickly—new patent claims, process changes, regulatory demands. 2-(Trifluoromethyl)Acetanilide holds value for those pushing projects towards approval or looking for molecular novelty in a crowded field. The pharmaceutical and agrochemical sectors ask more each season: not just reliable supply, but traceability, documentation, and the ability to adapt processes for custom requirements.

    Our facility keeps validated production records, full process histories, and retains samples so that any question—from regulatory authorities or customers—meets a transparent, detailed response. This is not just about compliance; experienced chemists know that process drift or unexamined batches can stall projects and waste valuable time.

    We’re also seeing more research groups prioritizing sustainability and waste reduction. Our plant recycles solvents and minimizes effluent, and we track yield improvements year-over-year to lessen raw material waste. Engaging with partners who share these goals makes a difference in how projects run from start to finish.

    Process Innovation: Reflections from the Plant

    Doing the same reaction thousands of times means familiarity with its pitfalls. From our side, process improvements don’t always come from sweeping overhauls; they often arise from small, targeted interventions. Maybe it’s a better source for trifluoromethyl precursors, a refined drying cycle that tightens the melting range, or a filtration step that clears trace colored impurities.

    Process chemistry isn’t just about moving mass; it’s about ensuring every batch stands up to scrutiny. We run pilot lots that mirror larger campaigns, gather comparative data, and make tweaks before commercial runs ship out. The feedback loop lets us spot trends—unexpected changes in yield, shifts in impurity profiles—that catch broader issues before they become headaches downstream.

    We stay away from cutting corners, since the upstream shortcut tends to show up as a downstream problem—longer purification times, lost material, or unpredictably variable reactivity. That’s not the sort of product anyone wants to encounter mid-project, especially where experimentation dollars and time are at stake.

    Looking Beyond the Molecule: The Value of Experienced Production

    What separates good 2-(Trifluoromethyl)Acetanilide from the rest isn’t just the chemical structure. It’s the open channel for support, the willingness to troubleshoot tough points, and the documentation that holds up under expert review.

    Those in scale-up or manufacturing support value facts: actual NMR data, batch records, ongoing communication, real samples for testing. We provide not just product, but a human link between production and application. People developing new routes or scaling innovation rely on honest reporting and a partner willing to problem-solve—from order to successful application at scale.

    We’ve learned that listening to user feedback—concerns on shipping, requests for alternative pack sizes, questions about long-term storage—leads to better products and stronger partnerships. The practice of incorporating real-world user experience translates to continuous improvement, not just on paper but in each finished lot, each delivery, and each follow-up.

    Challenges and Solutions Facing 2-(Trifluoromethyl)Acetanilide Producers

    Not every reaction goes to plan, and that’s true for synthesis and downstream application. The scale-up of trifluoromethyl-substituted aromatics often comes with unique hazards—high reactivity, formation of acidic byproducts, and increased sensitivity to processing conditions. Our safety protocols reflect this, keeping chemists and operators confident every step of the way.

    On the shipping side, fluorinated organics pose logistical challenges. Some carriers shy away from specialty chemicals, and regulatory paperwork must match actual container contents and labels. Our logistics team gets trained in handling these tasks, shortening delays and smoothing delivery. Every package comes with documentation for easy traceability, easing worries for regulatory compliance and internal audit requirements.

    Some customers come to us after disappointing results with commodity-grade product: solubility issues, off-color crystals, or performance failures during fine chemical or drug synthesis runs. We troubleshoot directly, pulling retained samples for comparison, reviewing process documents, and running parallel application studies. These efforts turn early-stage roadblocks into project milestones.

    As labs push for increased automation and digitization, we adapt data capture and reporting practices, linking quality results directly to final product documentation. The move towards digital compliance, whether for R&D or commercial registration, asks producers for more transparency and speed with records. Our systems grow with these expectations, letting us support more rigorous audit trails without losing hands-on responsiveness.

    Practical Advice for Users: From Bench to Pilot Plant

    Those handling 2-(Trifluoromethyl)Acetanilide at the research or pilot level should prepare for its unique traits—the lower nucleophilicity at the anilide nitrogen, the higher lipophilicity, the tougher ring activation compared to its cousins. Efficient solvent choice, accurate temperature control, and proper storage make a world of difference in performance. Over time we’ve developed guidelines for material handling and process troubleshooting based on thousands of hours working with this molecule.

    Crystallization behavior deserves attention, since subtle solvent traces or small temperature drifts change the way the product comes out of solution. For those scaling up, filtration speed and cake characteristics need adjustment in comparison with less-hindered acetanilides.

    We recommend mid-to-long-term storage in airtight containers, ideally in a cool and dry place. Larger orders ship with batches serialized for tracking and stored under conditions that minimize degradation. These aren’t just theoretical points—they come straight from watching batches held too long under harsh conditions, and seeing impact on color or purity.

    Shaping the Future of Specialty Chemicals

    2-(Trifluoromethyl)Acetanilide hasn’t always enjoyed the recognition of more well-known acetanilide derivatives, but its rising use in discovery and development pipelines proves its growing relevance. The operational lessons picked up over years of manufacturing have shaped our approach: one that centers on reliability, transparent support, and technical depth.

    Chemists across industries bank on their suppliers to deliver more than a bag of powder—they need assurance of quality, ongoing support, and a partner who understands the stakes of research deadlines, process validations, and real-world testing. Our company thrives by delivering on these needs, drawing from lived experience and a refusal to settle for average.

    Whether it’s a new route in an R&D lab or a scale-up for commercial batch registration, real-world experience brings forward the best of our processes, our team, and our product. 2-(Trifluoromethyl)Acetanilide isn’t just another entry in a database. For us, it stands as a benchmark for quality, service, and practical problem-solving at every level of production and use.