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2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone

    • Product Name 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone
    • Alias BDCTFA
    • Einecs 813-002-2
    • 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

    502557

    Chemicalname 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone
    Molecularformula C9H4BrCl2F3O
    Molecularweight 353.93 g/mol
    Casnumber 690632-78-1
    Appearance White to off-white solid
    Solubility Soluble in common organic solvents
    Purity Typically ≥98%
    Storagetemperature 2-8°C
    Smiles CC(=O)c1ccc(Cl)c(C(F)(F)F)c1ClBr
    Inchikey OHOFKHNMQPSAKZ-UHFFFAOYSA-N

    As an accredited 2-Bromo-2',6'-Dichloro-4'-(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 with secure cap, white label displaying chemical name, hazard warnings, and quantity: 10 grams, stored in secondary containment.
    Shipping This chemical is shipped in tightly sealed, chemically resistant containers to prevent leaks and protect from light and moisture. Shipping complies with all local and international hazardous materials regulations, including correct labeling and documentation. Only certified carriers are used, ensuring safe, secure transit and compliance with all applicable chemical shipping standards.
    Storage 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-acetophenone should be stored in a tightly sealed container, protected from light, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizers and bases. Store at room temperature or as recommended on the product’s safety data sheet (SDS). Ensure proper chemical labeling and access to spill containment materials.
    Application of 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone

    Applications of 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone in Industrial Manufacturing

    As a specialized manufacturer, we supply 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone to precisely defined markets where its molecular structure delivers critical performance in advanced synthesis. Below, we detail real application scenarios supported by validated industrial practice and regulatory compliance.

    1. Synthesis of Pharmaceutical Intermediates (Aryl Ketone Core)

    Pharmaceutical companies utilize this compound as an advanced intermediate during the multi-step synthesis of high-value active pharmaceutical ingredients, particularly those based on aryl ketone cores for oncology or CNS therapies. Its distinctive brominated, chlorinated, and trifluoromethylated substituents enable specific regioselective couplings and further nucleophilic or reductive elaboration in API route development. Formulators adjust ratios according to targeted molecule yield and downstream conversion kinetics; typical application involves multigram to kilogram scales within tightly controlled batch reactors under GMP guidelines to avoid molecular decomposition.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4, Part II (API production)
    • US FDA 21 CFR Part 211 (CGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (where applicable for regional supply chains)

    Typical usage ratio

    • 0.9–1.2 molar equivalents based on final API yield requirements; the exact charge depends on route optimization and impurity profile targets

    Downstream process integration

    • Charged at the intermediate coupling or halogenation step—typically following base-catalyzed alkylation or during late-stage derivatization stages prior to final crystallization and purification

    Final product types

    • Active pharmaceutical ingredients for anti-cancer, CNS-active, or anti-inflammatory drugs (e.g., halogenated arylketone APIs)

    2. Agrochemical Intermediate for Advanced Herbicide Synthesis

    Major crop protection manufacturers require this specialty acetophenone as a customized building block for next-generation herbicide actives where electron-deficient aromatic systems modify bioactivity profiles. The precise halogenation pattern supports stability and targeted reactivity during condensation reactions, particularly for triazine or heterocyclic ring-forming steps. Formulation chemists optimize usage based on batch size and required conversion rates in pilot and commercial lines, factoring in efficiency of downstream purification to meet stringent residue limits.

    Industry compliance standards

    • FAO/WHO JMPR Pesticide Specifications
    • ISO 9001:2015 (agrochemical quality system)
    • Chinese GB/T 1600-2016 Pesticide Manufacturing Standards
    • EPA 40 CFR Part 174 (if entering the USA market)

    Typical usage ratio

    • 0.8–1.1 equivalents per downstream synthetic batch, fine-tuned to the specific cyclization or condensation yield and mandated by impurity control strategies

    Downstream process integration

    • Introduced during the first-stage condensation phase or subsequent electrophilic aromatic substitution in continuous or batch reactors, followed by solvent exchange and solid–liquid extraction

    Final product types

    • Selective pre-emergent or post-emergent herbicide actives incorporating halogenated aromatic frameworks

    3. Specialty Dye and Pigment Intermediate

    High-value colorant producers incorporate this acetophenone derivative to achieve precise structural control in the synthesis of complex, halogen-rich dyes and pigments demanded by electronics, plastics, or specialty printing industries. The compound’s substitution pattern boosts stability and chromophore resonance, resulting in colorfast products with tailored hue and brightness. Final usage levels reflect both the target color strength and the performance criteria dictated by the end application—especially important in non-fading industrial pigments.

    Industry compliance standards

    • REACH Regulation (EC No 1907/2006) for pigment intermediates
    • ISO 9001:2015 (pigment manufacturing)
    • EN 71-3 Safety of Toys (where required for end-use)
    • RoHS Directive 2011/65/EU for electronic applications

    Typical usage ratio

    • 1.0–2.5% w/w in the initial dye/pigment formulation batch; the amount increases with requirements for deep-toned or UV-resistant product grades

    Downstream process integration

    • Added at the primary synthesis stage—typically during azo coupling or subsequent ring closure in melt-phase or solvent-based reactors, followed by controlled crystallization and filtration

    Final product types

    • Halogenated dyes, electronic pigments, and colorants for high-performance plastics and specialty coatings

    4. Building Block for Chemical Research and Development

    Contract research organizations and fine chemical developers select this raw material as a starting scaffold for the development of new heterocyclic compounds and structure–activity relationship libraries. The trifluoromethyl group and dual halogen pattern serve as essential moieties for tuning physicochemical and biological properties, which is critical in early-stage discovery. Research chemists determine input ratios by stoichiometry of desired molecular analogues; precise feeding is essential to limit by-product formation and maximize screening library diversity.

    Industry compliance standards

    • ISO 9001:2015 (R&D chemical quality management)
    • Responsible Care® Management Practice
    • Internal institutional research lab standards (as regulated for chemical procurement and safety)
    • OECD Good Laboratory Practice (GLP) where substances enter regulatory screening

    Typical usage ratio

    • 0.5–1.5 molar equivalents per reaction, depending on desired compound complexity and scale (mg/g/lab batch to multi-kilogram pilot runs)

    Downstream process integration

    • Entered at the initial synthetic step for construction of functionalized aromatic or heterocyclic scaffolds; subsequent modifications include cross-coupling, nucleophilic substitution, or metal-catalyzed elaboration

    Final product types

    • Research reference compounds, screening libraries for pharma/agro, and new heterocyclic entities for patent filings
    Free Quote

    Competitive 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone: Our Experience with Manufacturing, Application, and Product Distinction

    Understanding the Product

    We work with 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone every day on our production floor. This compound, structurally complex and tailored for demanding synthetic needs in pharmaceutical and specialty chemical industries, stands out due to its unique arrangement of bromo, chloro, and trifluoromethyl moieties on the acetophenone backbone. Chemical researchers often recognize this molecule by its structural formula, but in our facilities, it is characterized by its high purity, consistent physical traits, and reliability in downstream synthesis.

    We have observed that this compound carries a deep yellow crystalline appearance when properly produced and purified. The trifluoromethyl and halogenated groups define more than the name—they directly influence the reactivity profile and its performance as an intermediate, particularly for advanced pharmaceuticals, agrochemicals, and custom organic syntheses.

    Our Approach to Manufacturing

    Making this compound isn't just about mixing starting materials and waiting for a reaction. We control reaction exotherms, manage molar ratios, and monitor for side products at every step. Each batch runs through column chromatography and HPLC purity checks—QC doesn’t just sample the batch, we draw from multiple collection points. Crystallization controls the polymorph produced, especially with complex aromatic ketones like this one. NMR and GC-MS often catch trace impurities other less thorough processes might miss.

    Small changes during bromination or improper temperature ramps can throw off product quality. Our chemists watch reaction kinetics in real time. We have reaped the benefits of investing in in-process analytical technology—issues with incomplete halogenation or unwanted byproducts drop when you can catch them before isolation. Production scale brings its share of headaches, like odor control for halogenated intermediates and proper venting of HBr. Our years of experience have shown that rigorous ventilation and automated charging reduce both risk and downtime.

    Specification and Quality

    The product typically leaves our plant in lots between 500 grams and 20 kilograms, packed to limit light, moisture, and contamination. A single impurity above 0.2% can ruin the downstream synthesis, so we never cut corners or relax controls. Customers in demanding industries want certificates of analysis, not just on paper but backed by the hard numbers from NMR, HPLC, IR, and GC-MS. Loss on drying, melting range, and Rf value on TLC mean something tangible to our technical team—we catch out-of-spec lots well before packing.

    Some specialty buyers seek particle size optimization or pre-grinding for better handling in automated dosing systems, and we can deliver when asked. In contrast, some partners prefer unground crystals to prevent dust hazards. We keep flexible because researchers and scale-up teams need more than just a chemical name: they ask for practical solutions based on their handling, storage, and reactivity needs.

    How It’s Used in the Field

    This compound doesn’t find its way into consumer products but operates behind the scenes as a building block for more sophisticated molecules people depend on. Process chemists value the activated acetophenone ring for selective functionalization and high-yield step growth. Halogen and trifluoromethyl substitutions reinforce the molecule’s stability and reactivity, allowing synthetic routes that might not be feasible with less robust analogues.

    Case in point: medicinal chemistry groups use it to add structural diversity to candidate compounds, often seeking increased metabolic stability or improved pharmacokinetics. The electron-withdrawing groups shift reactivity in ways that open up chemoselective transformations, sometimes leading to higher-active pharmaceutical ingredient (API) yields or shortening total synthesis routes. Agrochemical researchers appreciate how the compound’s unique halogen and trifluoromethyl pattern correlates with stronger activity in some pest-resistant molecule classes.

    Scale-up teams working in kilo labs and pilot plants notice the difference this molecule makes when optimization moves from bench to reactor. Its consistent purity and defined melting range mean fewer purification cycles, faster throughput, and less product loss. Chemical engineers regularly feed back that process performance stands or falls on input quality, and missed batches mean weeks of lost time and sunk costs. We understand how crucial this is and shape our production around these feedback loops.

    What Sets It Apart from Other Halogenated Ketones

    Having produced many halogenated acetophenone derivatives, we clearly see the differences each design brings in reactivity, physical form, and cost of production. 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone is neither the cheapest nor the easiest compound to produce. But compared to mono-halogenated or non-fluorinated analogues, it offers more defined site-selectivity in downstream transformations. The position and type of each substituent dramatically alter the chemical landscape—for example, the dual chlorine at the 2' and 6' positions work with the bromine for controlled cross-coupling reactions and better regioselectivity.

    We see this illustrated when contract research teams request small lot comparisons: analogues lacking the trifluoromethyl group may suffer from poorer solubility or decreased shelf life. Monohalogenated versions may oxidize at a higher rate or prove less stable under process conditions. Every ring substitution pattern requires different purification and isolation protocols, so we don’t just stop at the chemistry—we engineer our process for each product variant.

    Challenges in Production and Handling

    Manufacturing this compound involves more than technical skill or well-tuned reactors. Brominated and trifluoromethylated intermediates come with health, safety, and environmental responsibilities. Our team handles HBr and similar corrosive agents in PPE-regulated spaces. We invest in air quality monitors and secondary containment, recognizing that safety lapses hurt our reputation as much as our workforce. Halogenated waste gets segregated, tracked, and sent for specialized incineration rather than cheap disposal.

    Production efficiency and environmental compliance move hand-in-hand. We optimize for high-yield, low-waste reactions, minimizing byproduct streams and maximizing material recovery. Our solvent reuse system reduces costs but increases complexity—we need solvent purities that don’t compromise product standards. These trade-offs matter because customers look not only at price or quality but at responsible sourcing and manufacturing stewardship.

    Supporting Evolving Customer Needs

    Our direct partnerships with end users in research and development, scale-up production, and custom synthesis have shaped how we approach both customer service and on-site support. Technical teams ask specific questions about stability, hydrolysis risk, and shelf life under different conditions. We offer real-world storage advice, drawn from actual warehouse and shipping data—keeping the compound cool and out of sunlight matters more than theoretical guideline documents might suggest.

    Some research partners work under synthesis deadlines for grant cycles or new product launches, so we guarantee turnaround times matching their needs. Logistics teams coordinate shipment routes to limit time in transit, with dry ice or cold packs as required for extra-sensitive lots. Documentation, like regulatory registration support and declarations of REACH compliance, also keeps projects moving forward. These needs grow more complex as product development moves from lab to pilot scale. We track real feedback and adapt, not just to stay competitive, but because these real-world requirements improve our own reliability and efficiency.

    Quality and Traceability: Our Role as Manufacturer

    Each production lot has a traceable batch record—it's non-negotiable. From raw input materials to finished product delivery, our logs show every intervention, test, and corrective action. Regulatory inspectors and customer auditors can review records spanning years. Confirming purity and authenticity gives our customers confidence, especially as regulatory, pharmaceutical, and fine chemical compliance standards continue tightening.

    Our experience demonstrates regular audits catch issues upstream, limiting downstream complications. Companies unfamiliar with hands-on manufacturing often ignore subtle changes in color, odor, or crystal habit—all of which can suggest instability or uncontrolled impurities. Our technicians take pride in catching such signs before they translate into larger issues for our customers. Open communication, backed by technical expertise, creates trust—a critical resource in every competitive sector we supply.

    Development and Customization: Meeting New Challenges

    Research and industry do not stand still, so neither can we. Requests for process optimization, impurity profiling, and out-of-spec documentation arrive regularly. Our R&D chemists feed improvements from pilot studies back into continuous production: shorter cycle times, reduced waste streams, alternative greener solvents, and custom particle engineering. Product variations tailored for specific synthesis approaches often begin with a simple call or email from an end user, leading us to run small-lot customizations or adjust drying parameters.

    Where product regulation allows, we trial new purification steps on small production lines to validate impact before incorporating at full scale. Speed to change matters in a market where both regulatory and technical shifts present new demands. This responsiveness marks the difference between traditional chemical suppliers and true manufacturing partners.

    Why Consistency and Technical Support Outweigh Price Alone

    Dozens of generic suppliers promise lower prices or quick delivery. Yet we have heard time and again from process development and QC managers that inconsistent batch quality leads to failed reactions, extra purification costs, and schedule delays. Technical teams remember the compounds that work exactly as specified, month after month. We view every batch as a showcase of our expertise, and we support our product’s performance with real troubleshooting and technical sharing.

    In our market, performance failures don’t just risk a batch—they jeopardize business relationships built over years. We do not outsource critical steps or gamble with non-traceable materials, because we carry the manufacturing standard our partners recognize and expect. This approach may mean slower expansion in some cases, but it preserves the reliability and trust that define sustainable chemical production at scale.

    Trends and Future Directions with Halogenated Acetophenones

    The market for functionalized acetophenones like ours grows in step with pharmaceutical innovation and emerging agrochemical needs. Academic and corporate R&D increasingly seek more elaborate substitution patterns to pursue patentable molecules with novel properties. Trifluoromethyl and multi-halogenation are not passing trends—they have become required features in certain high-value classes of therapeutic candidates and specialty materials.

    Our technical development team keeps pace by screening new synthesis routes and purification protocols, enhancing both environmental profile and cost efficiency. We welcome collaborative research: joint studies, custom pilot runs, or scale-up challenges. This ongoing dialog results in shared progress. If a partner faces a synthetic hurdle, we welcome the chance to experiment alongside, developing and de-risking routes with their in-house staff.

    Regulatory and sustainability demands only get tougher. We continue investing in emissions mitigation, better waste management, and safer working environments—as much to safeguard our workforce as to maintain compliance. The technical capability to deliver on every one of these fronts has moved from being a competitive edge to a baseline requirement.

    Conclusion: The Value of Direct Manufacturing Experience

    Making, purifying, and supporting a specialized product like 2-Bromo-2',6'-Dichloro-4'-(Trifluoromethyl)-Acetophenone demands more than theoretical knowledge or generic claims. Our day-to-day interaction with the compound and the feedback from scientific teams shape how we approach production, application support, and continuous improvement. Markets and standards may shift, technologies may evolve, but the core value of direct, knowledgeable manufacturing will always set the benchmark for trust, performance, and sustained partnerships.