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4'-Chloro-3'-(Trifluoromethyl)Acetophenone

    • Product Name 4'-Chloro-3'-(Trifluoromethyl)Acetophenone
    • Einecs 249-346-5
    • 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
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    Specifications

    HS Code

    903329

    Productname 4'-Chloro-3'-(Trifluoromethyl)Acetophenone
    Casnumber 19095-87-1
    Molecularformula C9H6ClF3O
    Molecularweight 222.59
    Appearance White to off-white solid
    Meltingpoint 57-59°C
    Boilingpoint 254-256°C
    Density 1.39 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol
    Purity Typically ≥ 98%
    Synonyms 1-(4-chloro-3-(trifluoromethyl)phenyl)ethan-1-one
    Smiles CC(=O)C1=CC(=C(C=C1)Cl)C(F)(F)F
    Inchikey HIHRXNJRMRDMJH-UHFFFAOYSA-N

    As an accredited 4'-Chloro-3'-(Trifluoromethyl)Acetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25g; white printed label showing chemical name, CAS number, hazard warnings, supplier logo, batch number, and barcode.
    Shipping 4'-Chloro-3'-(Trifluoromethyl)acetophenone is shipped in tightly sealed containers under ambient conditions. It should be packed to prevent leaks and protected from excessive heat, moisture, and direct sunlight. Compliance with local, national, and international transport regulations for hazardous chemicals must be ensured. Proper labeling and documentation are required for safe and legal shipping.
    Storage Store 4'-Chloro-3'-(Trifluoromethyl)acetophenone in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep separate from incompatible substances such as strong oxidizers. Use secondary containment if available. Avoid prolonged exposure to air and moisture, and label the container clearly with appropriate hazard warnings.
    Application of 4'-Chloro-3'-(Trifluoromethyl)Acetophenone

    Applications of 4'-Chloro-3'-(Trifluoromethyl)Acetophenone in Industrial Manufacturing

    4'-Chloro-3'-(Trifluoromethyl)Acetophenone serves as a specialized intermediate in advanced chemical production, driving critical reactions across select industrial sectors. As a direct manufacturer, we support downstream partners in regulated synthesis environments, ensuring traceable quality and tightly controlled specifications for each application outlined below.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    This compound acts as a building block in the synthesis of select pharmaceutical active ingredients, particularly in the development of specialty anti-inflammatory and central nervous system (CNS) agents. Its chlorinated and trifluoromethyl substitutions facilitate site-selective reactions within multi-step organic syntheses under cGMP conditions, supporting the introduction of pharmacophoric groups. Our quality system ensures batch-to-batch reproducibility, enabling integration into compliance-driven flows for drug precursor manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals, U.S. FDA)
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for chemical substance purity
    • SFDA China Drug Master File (DMF) registration protocols

    Typical usage ratio

    • Usage typically ranges from 0.5% to 5% by mass in stepwise API syntheses, adjusted according to target molecule stoichiometry and route efficiency.

    Downstream process integration

    • Enters as an acylation substrate after halogen exchange step, followed by condensation or cyclization toward the desired API core structure.
    • Subject to purification prior to final pharmaceutical step.

    Final product types

    • API intermediates for anti-inflammatory drugs
    • Precursors for CNS modulator compounds
    • Specialty fine chemicals under investigational new drug (IND) applications

    2. Agrochemical Active Ingredient Synthesis

    This ingredient supports synthesis of selective herbicide and fungicide actives, especially for crop protection products requiring high environmental persistence and specific aromatic substitution. The molecular structure enables downstream functionalization via Friedel-Crafts or nucleophilic substitution, allowing developers to customize bioactivity profiles in regulated agrochemical APIs.

    Industry compliance standards

    • FAO/WHO Guidelines for the Registration of Pesticides
    • OECD Principles of Good Laboratory Practice (GLP)
    • National Agrochemical Registration Regulations (US EPA 40 CFR Part 152, EU Regulation 1107/2009)
    • Chinese GB/T 16631 Safety and Quality Management for Pesticide Production

    Typical usage ratio

    • Added at 1%–8% molar equivalent relative to target pesticide skeleton, fine-tuned for desired substitution efficiency and formulation scalability.

    Downstream process integration

    • Used during the first synthetic block for haloaromatic introduction, ahead of alkylation or esterification stages.
    • Controlled temperature, solvent, and catalyst adjustments according to target active.

    Final product types

    • Pre-emergent herbicide technical concentrates
    • Triazole-based fungicide actives
    • Custom arylation intermediates for patented agrochemical lines

    3. Photoinitiator Intermediate in UV-Curable Coatings

    Manufacturers of UV-cure coatings and inks employ this raw material as a synthetic precursor, leveraging its trifluoromethyl group to improve photolytic efficiency in final photoinitiator packages. The unique structure alters photoreactivity and stabilization, supporting downstream oligomer and monomer design for enhanced curing speed and film durability in energy-curable systems for electronics, packaging, or automotive surfaces.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Process Industries
    • European Printing Ink Association (EuPIA) Exclusion Policy and Good Manufacturing Guidelines
    • REACH Regulation (EC No 1907/2006) for chemical import and use in the EU
    • ANSI/UL 2591 Standard for Component Photoinitiators

    Typical usage ratio

    • Utilized in the range of 2%–6% by weight in photoinitiator synthesis batches, according to desired absorption and performance attributes in downstream polymer networks.

    Downstream process integration

    • Feeds as an input in the aromatic acylation stage for photoinitiator backbone construction.
    • Further processed for substitution or crosslinking as per UV formulation requirements.

    Final product types

    • UV-curable ink and varnish photoinitiators
    • Electronics-grade conformal coating additives
    • Polyacrylate-based curing accelerators

    4. Intermediate for Liquid Crystal Monomer Synthesis

    Producers of specialty monomers for liquid crystal displays (LCD) and advanced optical films apply this material for precise molecular tailoring. Its halogen and trifluoromethyl moieties support the synthesis of monomers with strict polarity, melting point, and viscosity control. Batch production features careful impurity profiling, meeting downstream quality requirements in optoelectronic component materials.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management (for specialty chemical synthesis)
    • RoHS Directive 2011/65/EU for Restriction of Hazardous Substances
    • JIS K 5600-1-7 Optical Properties Testing (Japan)
    • IEC 61249-2-21 (Halogen-Free Base Substances for Electronic Applications)

    Typical usage ratio

    • Batch formulation varies from 0.5% to 3% by mass depending on monomer backbone length and target optical properties in finished LC mixtures.

    Downstream process integration

    • Implemented as a core aromatic feedstock in the initial coupling and chain-building stages.
    • Reacted with alkyl or ether substituents for custom LC host design, prior to downstream purification and blending.

    Final product types

    • LCD-grade liquid crystal monomers
    • High-transmittance optical films
    • Reactive mesogen for electronic display matrices

    5. Fine Chemical Intermediate for Specialty Dyes and Pigments

    Colorant manufacturers use this molecule as a functionalized aromatic intermediate, capitalizing on the electron-withdrawing trifluoromethyl and chloro substituents to drive high-yield synthesis of high-performance dyes. It enables precise tuning of absorption spectra and color fastness characteristics essential in specialty pigment products for polymer and fiber coloration under industry-regulated scenarios.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Systems in Dye Manufacturing
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Code of Practice
    • REACH Regulation (EC) compliance for dye compound registration
    • ZDHC MRSL Conformance for restricted chemical use in textile dyeing

    Typical usage ratio

    • Introduced at 0.3%–2% molar basis, dependent on target chromophore structure and batch scale in pigment or dyestuff synthesis.

    Downstream process integration

    • Employed in the initial aromatic acylation as part of chromophore core construction, followed by azo coupling or sulfonation as required for color shade engineering.

    Final product types

    • Polymer colorants for high-heat plastics
    • Reactive dyes for technical textiles
    • Specialist high-stability pigments for automotive applications
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    Certification & Compliance
    More Introduction

    4'-Chloro-3'-(Trifluoromethyl)Acetophenone: Driving Advancements in Chemical Synthesis

    Practical Experience Shapes Product Quality

    After decades in specialty chemical manufacturing, I’ve witnessed firsthand how precise control during synthesis defines the value of 4'-Chloro-3'-(Trifluoromethyl)Acetophenone. Our laboratory’s standards grew tighter as we understood how even slight variances in raw material purity or process temperature could throw off yields and impact downstream reactions. Our product, model HJ324, remains consistent because we’ve leaned into process monitoring. We document every temperature spike, solvent swap, or pressure deviation, knowing every detail matters once customers scale up their processes. Real feedback from our partners—ranging from fine pharmaceutical labs to dye and pigment developers—pushes us every year to refine our technique and maintain high purity.

    Specifications Built for Application Needs

    We produce 4'-Chloro-3'-(Trifluoromethyl)Acetophenone as a pale yellow crystalline solid, leveraging high-vacuum distillation and repeated recrystallization to nail a purity above 99%. Impurities, which can clog reactors or spoil subsequent steps, are kept in check by both HPLC and GC assessment—not just by certificate, but checked lot by lot. Our experience shows that those who cut corners here pay for it later on. The melting point falls reliably between 67°C and 70°C, allowing for straightforward handling in both pilot and production reactors. Moisture content sits below 0.1%, limiting side reactions and enabling stable storage even in humid environments.

    Packing avoids unnecessary handling—favoring double-sealed polyethylene bags inside UN-rated drums for sites requiring larger volumes. For clients requesting custom particle sizing, we provide controlled milling, but we always guide buyers on whether extra steps are truly necessary to match their reactor requirements. Over the years, we’ve seen some buyers insist on fine powder only to find that dusting or static in their process created more cleanup headaches than benefit.

    Real Use Cases: Beyond the Data Sheet

    Our acetophenone derivative stands on the front line for building complex molecular architectures. Pharmaceutical innovators use it as a key intermediate in synthesizing fluorinated heterocycles and functionalized aromatics. The presence of both the chloro and trifluoromethyl substituents offers orthogonal reactivity: the chloro group opens up nucleophilic aromatic substitution, while the trifluoromethyl group provides heightened metabolic stability and receptor affinity in medicinal targets.

    Dye and pigment chemists approach us for this molecule because the electron-withdrawing groups shift chromophore absorption peaks, leading to desirable hues and reliable product stability under harsh light or solvent exposure. Agrochemical field studies point to this intermediate’s ability to improve the performance profile of active crop protection compounds, helping them remain effective after application and resist environmental breakdown.

    R&D teams in electronics materials have come to appreciate how our product’s structural features improve polymer backbone properties when built into specialty resins. Adhesion testing and weathering studies show that the combined influence of the chlorine and CF3 groups make the end polymers more robust against moisture ingress and thermal degradation—an advantage in microelectronics encapsulation and display applications.

    Direct Manufacturer Knowledge: Problems and Solutions

    A repeating issue in industry discussions comes from clients running multi-step syntheses who find themselves fighting low yields or troublesome by-products. Most of these headaches trace back to inconsistent input material. Several years ago, one client working on a new CNS-active compound contacted us after noticing unexpected peaks in their final HPLC. It became clear the acetophenone they sourced elsewhere contained higher levels of related halogenated impurities. Our manufacturing employs fractional distillation and tailored crystallization conditions specifically to winnow these out. With us providing material meeting tighter impurity specs, their chromatograms cleaned up and process throughput recovered. We never treat such process deviations as mere noise—each informs our next round of improvements.

    During scale-up, the difference between a slightly yellow and a nearly white solid might look trivial on a bench, but in a production environment it can indicate serious downstream issues. Color intensity often hints at minor oligomers or side products. We don’t just log this with a spectrophotometer, but actively discuss color and odor changes with customer R&D teams, as they often flag subtle shifts that statistical quality checks can miss. A solvent swap technique that worked in our plant but failed at customer scale taught us to always check solvent compatibility beyond the lab environment. That’s why we welcome technical site visits, so our own engineers can walk the floor and see how our material performs under real industrial conditions.

    How This Product Differs from Other Acetophenones

    Chemical functionality is not just a matter of degrees—it’s a matter of hard-won performance. 4'-Chloro-3'-(Trifluoromethyl)Acetophenone stands apart from standard acetophenones by virtue of its twin electron-withdrawing groups: the para-chloro and the meta-trifluoromethyl. These adjust both the reactivity and the physicochemical properties beyond simple additive effects. With classic acetophenone, you get base reactivity suited for simple condensations and acylations. Once you add a chloro at the para position, substitution selectivity sharpens, helpful in stepwise building of more elaborate aromatic systems.

    Incorporating a CF3 group at the meta site does more. It drops electron density, making electrophilic aromatic substitution reactions more selective, and lends downstream molecules improved resistance to oxidation and biological degradation. For pharmaceutical and agrochemical developers, these features can mean better lead compound pharmacokinetics or shelf-stable formulations. Over the years, we’ve seen our clients, particularly those in drug development, emphasize how switching from a methyl or plain acetophenone to this derivative advanced their projects—reducing off-target effects or increasing blood-brain barrier penetration in test molecules.

    Compared to acetophenones with only halogen substitution or only trifluoromethyl groups, this product strikes a balance between chemical reactivity and handled volatility. A mono-substituted trifluoromethyl acetophenone might go further in electron withdrawal, but becomes harder to process and control in standard reactors. On the other hand, relying solely on chloro-substitution often doesn’t provide enough shift in reactivity or solvent compatibility. That’s where the pairing here solves problems that neither substituent alone can address—offering predictable melting behavior without needing high-pressure or exotic solvents for most applications.

    From a process engineer’s perspective, the handling of this compound compares favorably to its closest analogs. Acetophenones with higher halogenated content bring risk of corrosion in plant infrastructure and possible regulatory concerns around waste and emission control. Our product gives a solid balance—reactive enough to provide versatile options in synthesis, stable enough to avoid the maintenance headaches of more aggressively substituted aromatics.

    Supporting Compliance and Sustainability Needs

    Long-term viability depends on both safety and environmental stewardship. We support clients aiming to meet tightening regulatory standards—every batch ships with detailed impurity profiles, and users have access to our technical support to interpret these. Wherever possible, manufacturing wastes are minimized at source rather than relying solely on downstream treatment. We’ve retrofitted several mother liquor handling lines after seeing solvent recovery improvements not just save cost, but measurably reduce VOC emissions.

    Supply chain disruptions have taught us to keep reliable lines of raw materials, and to validate dual suppliers for both solvents and starting halogenated benzenes. This may sound straightforward, but as global logistics shift, we face realities that distant traders and commissioned merchant houses rarely see. If a container gets held up at port, or an upstream supplier alters their own synthesis which impacts our inputs, we spot bottlenecks early, alert partners, and switch to validated alternatives quickly. This helps our customers keep their timelines when new chemical entities move from pilot to full industrial runs.

    Safe handling practices form part of our product assurance. During loading and transloading, we provide training both for our staff and, wherever allowed, for client plant teams. Every incident, spill, or near-miss gets shared as a learning story—layered PPE, local extraction, and continuous quality checks all form part of the way we keep both material and people safe on a daily basis. This practical awareness, not just compliance for the sake of ticking a box, came about after learning from accidents in the early days of our operation. We appreciate every phone call where a client checks a minor detail before a batch run; open channels always keep everyone safer.

    Why Consistent Material Matters in Research and Industry

    No scientist or process engineer wants the frustration of reactivity swings making scale-up unpredictable. Early in our manufacturing experience, we saw how a single lot-to-lot variation in halogen or trifluoromethyl content could derail multi-million-dollar projects. Our response was to integrate continuous in-process testing and to back up every delivery with full data transparency. For customers pushing boundaries—whether in creating next-generation APIs, engineered resins, or high-performance agrochemicals—the assurance of consistent, high-purity material unlocks project success. Tech transfer from pilot plant to manufacturing scale runs smoother. Regulatory filings go faster. Synthesis yields match R&D predictions.

    Listening teaches us more than any spec sheet. Once, a client scaling up for a new OLED emitter experienced batch-to-batch color drift. Labs had assumed it was lighting or handling differences, but our closer look tracked a ppm-level impurity in one input. Working together, we found a fix and shared those learnings with others in the optoelectronics field. Being a direct manufacturer puts us close to the realities of process troubleshooting and keeps us invested in our customers’ long-term success.

    Continuous Improvement: Earning Trust Over Time

    Over the past ten years, we’ve expanded our reactor capacity not just to chase volume but to meet tighter purity demands from life sciences and high-tech sectors. Each scale-up project reveals new details to refine—from understanding impurity migration during solvent exchange, to optimizing crystal habit for easier filtration and minimal dust formation. Process optimizations aren’t kept secret; we engage in joint development with select customers who trust us as partners, not just providers. Their feedback and our willingness to adapt our production enable us to keep pace with shifting application demands.

    As chemists and engineers ourselves, we know the pressure our customers face to hit timelines or recover from unexpected process hiccups. Every production batch brings its own learning, and we fold those insights back into SOPs and staff training. Our on-site pilot reactor helps us troubleshoot client-specific synthesis routes, staying close to the realities of scale-up chemistry, not just the lab bench theory.

    Final Thoughts on Value Creation with 4'-Chloro-3'-(Trifluoromethyl)Acetophenone

    Nearly every client inquiry teaches us something. Whether they’re navigating new regulatory filings, troubleshooting a tricky reaction, or bridging lab and plant-scale results, the fine details of our manufacturing practice make a difference. Working with this acetophenone, with its unique combination of chloro and trifluoromethyl groups, we see direct advantages through every step of the supply chain. Customers depend on accurate, repeatable results, and we answer those needs with hard-earned manufacturing experience, not just certificates and datasheets.

    In our ongoing drive to refine production and add value, we balance agility with safety and predictability. Our long-standing focus on both the molecule’s chemistry and the realities of plant-scale operation make a difference for real-world users. Meeting the demands of pharmaceutical, electronic, and specialty chemical innovators means staying alert to process trends, customer feedback, and regulatory landscapes. Each batch, each improvement, and each shared lesson brings the wider field of industrial chemistry forward—one molecule at a time.