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N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline

    • Product Name N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline
    • Alias N-(chloroacetyl)-m-(trifluoromethyl)aniline
    • Einecs 633-383-3
    • 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

    742031

    Product Name N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline
    Cas Number 72607-25-1
    Molecular Formula C9H7ClF3NO
    Molecular Weight 237.61 g/mol
    Appearance White to off-white solid
    Melting Point 46-50°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥97%
    Density 1.43 g/cm³
    Storage Store in a cool, dry place, tightly closed
    Synonyms 3-(Trifluoromethyl)-N-(chloroacetyl)aniline
    Smiles FC(F)(F)c1cccc(c1)NC(=O)CCl
    Inchi InChI=1S/C9H7ClF3NO/c10-6-9(15)14-7-3-1-2-8(4-7)5-12(11)13/h1-4,14H,5-6H2

    As an accredited N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Clear, sealed glass bottle with a white screw cap, labeled "N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline, 25g," including safety and hazard information.
    Shipping **Shipping Description:** N-(Chloroacetyl)-3-(Trifluoromethyl)aniline is shipped in tightly sealed, chemically resistant containers, clearly labeled according to hazardous material regulations. It should be transported under ambient conditions, protected from moisture and incompatible substances. Compliance with local, national, and international chemical shipping and safety regulations is mandatory to prevent leaks, spills, or exposure.
    Storage **N-(Chloroacetyl)-3-(Trifluoromethyl)aniline** should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizers and acids. Properly label the container, and handle it using appropriate personal protective equipment to avoid skin and respiratory exposure.
    Application of N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline

    Applications of N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline in Industrial Manufacturing

    N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline is a specialty intermediate widely adopted in selected fine chemical sectors requiring precise molecular profiles. Its application remains focused within high-value downstream production, delivering controlled reactivity for critical synthesis. Below are distinct industrial scenarios illustrating how leading manufacturers integrate this compound to achieve consistent output aligned with regulatory and quality expectations.

    1. Agrochemical Active Ingredient Synthesis

    Crop protection manufacturers utilize N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline during the preparation of select herbicidal and fungicidal actives which demand an electron-rich aromatic system with halogen substitutions. Its functional groups participate in N-acylation and subsequent nucleophilic substitution reactions, essential for constructing advanced ring systems within regulated pesticidal molecules. Synthesis routes incorporating this material are optimized to maintain high assay yields and minimize unintended by-products, thereby supporting compliance and formulation consistency.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • US EPA Pesticide Registration Requirements
    • GB 2763 National Food Safety Standard: Maximum Residue Limits for Pesticides (China)

    Typical usage ratio

    • 3–7% by weight relative to final API target, with ratio fine-tuned based on target synthetic pathway, desired selectivity, and activity profiling data.

    Downstream process integration

    • Initial charge in multi-step organic synthesis, particularly in acylation or halogenation steps before cyclization or coupling; typically introduced after the stage 1 intermediate purification.

    Final product types

    • Selective herbicides for cereal crops
    • Systemic fungicides for fruit and vegetable applications
    • Pre-mix technical concentrates
    • Stabilized formulated agricultural sprays

    2. Pharmaceutical Intermediate in Heterocyclic Drug Synthesis

    Producers of specialty active pharmaceutical ingredients source N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline for its unique ability to introduce both chloroacetyl and trifluoromethyl moieties into heterocyclic ring structures, especially in second-generation small-molecule drug candidates. The compound’s consistent physical properties support reliable scale-up from kilo-lab scale to commercial production, meeting stringent GMP tracking, analytical documentation, and impurity control standards throughout the route.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP and EP Monographs for relevant APIs
    • 21 CFR Part 210/211 (cGMP for Finished Pharmaceuticals)
    • EDQM Certificate of Suitability (CEP) processes for starting materials

    Typical usage ratio

    • 0.8–1.5 equivalents by mole within key cyclization or aromatic substitution steps, with optimization based on impurity profiles required by DMF submissions.

    Downstream process integration

    • Charged into the synthetic stage prior to ring closure, during N-acylation or direct functionalization, ensuring regioselectivity within multi-component reactions for drug substance build-up.

    Final product types

    • API intermediates for anti-inflammatory agents
    • Precursors for anticancer pharmaceuticals
    • Intermediates for CNS-active molecules
    • Pilot and commercial-scale GMP drug substances

    3. Specialty Dye and Pigment Precursor Manufacturing

    Fine dye and pigment producers integrate N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline in advanced organic pigment synthesis where thermal stability and solvent fastness are critical. The material provides a highly reactive chloroacetyl functionality combined with an electron-withdrawing trifluoromethyl group, facilitating cross-coupling reactions without excessive side-product formation. Colorfastness, regulatory compliance with heavy-metal limits, and batch-to-batch consistency define integration requirements.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile dyes
    • EN 71-3: Safety of Toys (Migration of certain elements in pigments)
    • REACH Regulation (EC 1907/2006) Annex XVII for restricted substances
    • ISO 105-E04: Color Fastness to Perspiration

    Typical usage ratio

    • 0.5–2% by mass in pigment backbone synthesis, adjusted for target chromophore intensity and process yield optimization at bench and plant scale.

    Downstream process integration

    • Introduced during azo coupling or condensation synthesis, immediately prior to pigment formation and salt formation steps, often in continuous stirred-tank reactors under inert conditions.

    Final product types

    • High-performance azo dyes
    • Organic pigments for plastics and coatings
    • Textile and printing ink formulations
    • Stain-resistant and UV-stable colorants

    4. Fluorinated Fine Chemical Synthesis for Electronics Industry

    Electronics chemical suppliers employ N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline in the custom synthesis of building blocks for high-performance liquid crystal and dielectric materials. The rigid aromatic framework and trifluoromethyl substitution enhance molecular alignment and tunability of dielectric constants, which is vital for producing consistent thin films and photoresist components. Integration in this field requires close alignment with purity and metal impurity restrictions as demanded by semiconductor-grade standards.

    Industry compliance standards

    • SEMI C3 Standard for High Purity Chemicals
    • IEC 61249-2-21: Electronic materials (halogen content limits)
    • RoHS Directive 2011/65/EU for electronic substances
    • JEITA ET-7304: Quality standards for electronic chemical materials

    Typical usage ratio

    • 0.2–1 mol% in batch input, precisely controlled depending on downstream LC or dielectric target specifications and process throughput.

    Downstream process integration

    • Added during the monomer pre-polymerization phase for specialty resins or incorporated as aryl intermediate within the custom synthesis of electronic chemical blends, with quality checked by GC-MS for trace impurity content.

    Final product types

    • Advanced liquid crystals
    • High-dielectric constant resins
    • Photoresists for microfabrication
    • Electronics-grade intermediate mixtures for display panel manufacturing

    5. Synthesis of Specialty Polymer Additives

    Plastic additive makers selectively use N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline as a reactive modifier for chain-stop or branching agents in specialty polymers. The chemical structure imparts increased hydrophobicity and chemical resistance to engineering plastics, while maintaining processability during extrusion and molding. Regulatory review focuses on migration and stability in the final polymer matrix, particularly for applications in automotive and electronics components.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastic Materials
    • ISO 1043-4: Coding for additives in plastics
    • EN 13432: Packaging standards (where used in biodegradable blends)
    • RoHS substance limits for finished plastic goods

    Typical usage ratio

    • 0.1–0.5% by weight in polymer additive masterbatches, determined by resin base feedstock and expected performance tests for mechanical and thermal properties.

    Downstream process integration

    • Incorporated during compounding or twin-screw extrusion phase, pre-blended with other masterbatch ingredients before melt processing and pelletizing for downstream molding or extrusion customers.

    Final product types

    • Chemically-resistant ABS blends
    • Modified polycarbonate resins
    • Electronic connector housings
    • Automotive under-hood plastic components
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    Certification & Compliance
    More Introduction

    N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline: A Key Ingredient Shaping Modern Synthesis

    Innovation Grows from Raw Materials

    Anyone who spends time on a chemical plant floor knows that reliability and purity shape project outcomes more than anything else. At our manufacturing site, every batch of N-(Chloroacetyl)-3-(Trifluoromethyl)aniline tells the story of why sourcing directly from an experienced producer fuels both consistency and confidence. We aren’t in the distribution business, we are in the business of understanding what this compound does inside reactors, how it handles in actual use, and how minute differences in its synthesis can ripple through downstream processes.

    Details Matter at Every Step

    N-(Chloroacetyl)-3-(Trifluoromethyl)aniline, an aryl amide with a chloroacetyl group on the nitrogen and a trifluoromethyl group on the aromatic ring, appears simple on paper. In practice, controlling isomer and impurity levels across scaled batches transforms that theoretical molecule into a robust building block. We control every input, right down to the solvent type and purification sequence, because finished product quality rarely survives shortcuts. Process stability predicts safety, so every batch receives our close attention. Spot checks don’t replace thorough validation in our operation. We run analyses on-site, using GC, NMR, and HPLC, tracing impurity profiles and solvent residues well below the thresholds that could trip up a critical reaction. We have learned over years that a reliable color and odor profile signals consistency; an unexpected shade or volatility flags a deviation worth immediate investigation.

    Why N-(Chloroacetyl)-3-(Trifluoromethyl)Aniline Speaks to the Demands of Modern Chemistry

    There’s a reason research teams and production chemists keep returning to this compound. The trifluoromethyl group embedded in the aromatic ring brings a set of physical properties unmatched by conventional aniline derivatives. Polar and electron-withdrawing, this functional group tunes reactivity for downstream modifications. Add in the chloroacetyl group and the result is a compound with just the right electrophilicity to open up routes in the synthesis of fine chemicals, pharmaceuticals, and advanced materials. For API makers targeting halogenated or fluorinated intermediates, this backbone offers pathways that simple benzoyl or acetyl anilines cannot match. We’ve tracked performance in condensation reactions, nucleophilic substitutions, and even some photochemical transformations, each time noticing how the balance of steric and electronic effects cuts down on byproducts.

    Labs often demand short lead times and predictable workflows. This is where direct purchases from the manufacturer pay dividends. We can guarantee supply because we plan production capacity based on direct communication with partners, not on speculation. During scale-up, process development professionals have called on us to modify grades or adjust drying parameters — tweaks that traders and traders’ traders just don’t have the infrastructure to support. Our crew can tell you how a humidity spike in storage rooms might degrade a sample, and we have practical solutions—both in packaging and logistics—based on that accumulated, hands-on experience.

    Building for Usability: From Plant Floor to Laboratory Bench

    Every day, our people work with the compound under real conditions, seeing how it handles in drums, how it dissolves, and how it interacts with stabilizers. With N-(Chloroacetyl)-3-(Trifluoromethyl)aniline, stability and shelf life depend as much on process hygiene as on chemical structure. Some producers focus primarily on purity, but we’ve found that moisture content and micro-impurity profiles can influence not only yield but also safety in subsequent steps. For sensitive pharmaceutical syntheses, excess hydrochloride or oxidation byproducts trigger side reactions, so we remove contaminants below even strict pharmacopoeial standards. Each run of the product is built to order, using in-house-developed controls rather than “one size fits all” processes.

    Handling matters. The compound’s slightly hydrophobic nature makes it less prone to atmospheric hydration than less substituted anilines, but that same feature suggests different storage solutions compared to high-purity polar amides. We specify containers and liners from direct experience: poly-laminates for larger shipments, custom-sealed glass for R&D scaleouts. Over the years, our feedback loop with end-users has modified everything from granule sizing—reducing caking—to outer carton design to survive overland shipping. You can trace every improvement back to someone in a plant reporting a real-world inconvenience, prompting us to engineer it out of the process.

    We developed purification and isolation methods that keep the final product dry and free-flowing during long stretches in transit. The crystalline material remains stable in sealed drums, resisting degradation across temperature swings that would destroy less carefully produced batches. By testing these limits ourselves, the team anticipates problems before they arise. Several customers in climates with high seasonal humidity have found that switching to our desiccant-packed shipments reduced clumping and improved product metering. These aren’t dramatic breakthroughs, but they come from listening on the ground instead of living on spec sheets.

    What Sets This Compound Apart

    Anyone can buy solvents and basic chemicals in bulk. Specialty intermediates like N-(Chloroacetyl)-3-(Trifluoromethyl)aniline demand a different approach. For years, research and process teams have wanted a cleaner, more reactive amide than traditional N-acetylanilines. What they got from early suppliers often fell short: variable melting points, inconsistent particle sizes, or unexplained reactivity. By refining our process—starting from fluoroaromatic intermediates with controlled halogenation steps—our product consistently beats market equivalents for purity and reactivity. Our proprietary route, using in-house catalyst blends, produces higher yields with fewer side impurities, simplifying downstream purifications for our clients.

    Physical appearance, although not the most important aspect, remains an everyday clue to batch-to-batch reliability. Dusty or yellowed product signals something wrong, possibly from oxidation or improper storage. Ours arrives as off-white to pale-yellow crystals, always within a tight range defined by in-house colorimetric checks. It dissolves consistently in typical organic solvents, supporting hassle-free integration into ongoing syntheses. Our experience shows that even seemingly minor differences—from trace hydrolysate to off-ratio residual solvents—cause headaches for scientists trying to troubleshoot unexpected results.

    Comparing our compound with other suppliers’ offerings, the differences show up not only in purity but also in the spread of side species visible by NMR or mass spectrometry. We sample competitors’ products through technical exchanges and external testing and observe recurring byproducts from incomplete halogenation or side-chain cleavage, sometimes as high as 2-3% in material bought by volume distributors. These numbers matter when every side reaction risks a lost batch or a failed regulatory submission.

    Meeting the Needs of Medicinal, Agrochemical, and Material Chemistry

    N-(Chloroacetyl)-3-(Trifluoromethyl)aniline serves as a lynchpin in both drug and chemical development cycles. Medicinal chemists appreciate its readily available handle for nucleophilic substitution, opening pathways to new heterocycles and ring-closed systems. The trifluoromethyl feature tunes lipophilicity and metabolic stability, offering medicinal chemistry teams a direct line from synthetic intermediate to candidate molecule. In the agrochemicals sector, the compound’s robust stability allows its use in weather-tolerant formulations, helping crop scientists extend pest control and disease resistance over longer growing seasons. Material chemists developing liquid crystals, coatings, or polymer additives also take advantage of the trifluoromethyl group’s influence on electronic properties, crafting specialty resins and performance polymers.

    We worked with research labs pioneering new kinase inhibitors, where our product’s exceptional batch purity enabled selective functionalization. In one case, a client scaled up a route relying on high-reactivity amide bonds for cyclization; our attention to residual water content made the difference between a successful pilot run and repeated purification failures. These case studies surface often, validating the efforts invested at our site to root out unwanted isomerization and minimize organic halide carryover. No one calls a supplier back for a second order if unexpected side reactions derail scale-up. In our industry, repeat business speaks louder than advertising.

    Responsibility Born out of Experience

    Trust grows in this trade from transparency and expertise, not from broad claims. Every drum that leaves our plant carries both a commitment to analytical traceability and a deeper understanding of how it should perform once in our customers’ hands. Our QC archive holds batch records for years, including trend analyses and full spectra—tools that our technical support draws upon if a partner requests deeper insight or runs into an unexpected hiccup. Many of our regular clients tap into that resources pool, using our spectral archive to fine-tune their own analytical protocols, especially important in regulated industries.

    Handling specialty amides also means taking environmental impact seriously from the outset. We continuously review routes for process intensification—cutting waste, recycling solvents, and reducing halide-containing effluent. We have retrofitted parts of our plant to reduce fugitive emissions and have adopted solvent recapture wherever possible to minimize environmental footprint, not because it has become a compliance issue, but because years in this industry teach that unchecked waste creates costs and credibility risks down the line. Our solutions draw not only from regulation books, but from on-the-job experience with older process designs where small leaks and waste streams quietly escalated maintenance costs.

    From R&D Scale to Industrial Production

    Research teams sometimes require only grams, while pilot and production teams may need kilos or tons. Direct conversation with the plant team enables users to secure the form and pack size that fits their laboratory or process, minimizing repacking and contamination risks through unnecessary transfers. In our experience, direct shipment from site to facility (with coordinated logistics) slashes not only costs, but also scheduling headaches. Engineers and chemists working late shifts find it easier to trace back to the source when any troubleshooting becomes necessary.

    Regulatory compliance forms a part of every story, whether the compound flows into an API or a specialty polymer. We maintain records supporting major regulatory and GMP requirements, and our QA/QC team frequently interacts with customer regulatory affairs experts to facilitate submission packages. By maintaining control of upstream and downstream traceability at our site, we streamline these interactions, saving everyone time and reducing frustration over misaligned paperwork or batch history gaps. We have seen that clients appreciate the comfort of knowing where every kilogram came from, how it was made, and which processes kept it pure.

    Continuous Dialogue, Continuous Improvement

    Experience has taught our team that product quality always benefits from conversation. Our plant’s technical support line and email channels are staffed by people who know the reactors and can answer questions without delay. Specific feedback, even as simple as an observation about a sticky residue during sampling, feeds into our continuous improvement cycle. Operational changes result, and repeated site returns for audits from strict clients encourage us to keep no secrets. The trust developed with long-term research partners and scale-up teams is less about promises of “best in class” quality, and more about an unbroken record of solving problems that we have the tools to address.

    Our history as the makers of N-(Chloroacetyl)-3-(Trifluoromethyl)aniline keeps us embedded in the challenges that real users face. This comes through in how we respond to spikes in demand, through downturns when inventory needs careful management, and in quick-turn R&D support for customers stuck at a synthetic roadblock. We keep our catalog wide enough to accommodate new requests but focused enough that expertise doesn’t get diluted across hundreds of unrelated products.

    The Path Forward: Hands-On Manufacturing for Real-World Chemistry

    In today’s climate of supply chain disruption and rising quality expectations, the value of dealing directly with a true manufacturer grows clearer. N-(Chloroacetyl)-3-(Trifluoromethyl)aniline stands out not as a generic intermediate but as a specialty molecule crafted through experience. Our responsibility extends beyond keeping the tanks and lines clean. Every tweak in process, every QC data point, reflects a collective effort among operators, chemists, and logistics staff sharing both the pain and the pride of making a challenging product right, every time. Delivering on those efforts means listening to real problems, adapting processes, and standing behind quality in a way only a manufacturer, boots on the ground, can promise.

    Day by day, N-(Chloroacetyl)-3-(Trifluoromethyl)aniline keeps finding new uses. Its story, from raw materials to finished product, keeps unfolding with each batch. We bring our accumulated knowledge, practical improvements, and dedication to supplying a compound that doesn’t just meet the standard—it raises the standard for everyone, ourselves included. We encourage partners, new and old, to reach out and put our expertise to the test. Every batch, every inquiry, becomes part of a bigger conversation about what it means to produce chemicals the right way.