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3',4'-Dichloroacetophenone

    • Product Name 3',4'-Dichloroacetophenone
    • Einecs 214-241-2
    • 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
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    VTB
    Specifications

    HS Code

    903773

    Chemicalname 3',4'-Dichloroacetophenone
    Molecularformula C8H6Cl2O
    Molecularweight 189.04 g/mol
    Casnumber 2142-63-4
    Appearance White to off-white crystalline powder
    Meltingpoint 46-49°C
    Boilingpoint 284°C
    Density 1.37 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >= 98%
    Synonyms 1-(3,4-Dichlorophenyl)ethanone
    Refractiveindex 1.587 (predicted)
    Flashpoint 122°C
    Storagecondition Store in a cool, dry place, tightly closed

    As an accredited 3',4'-Dichloroacetophenone 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, sealed with a screw cap, labeled with chemical name, structure, purity, and hazard warnings.
    Shipping 3',4'-Dichloroacetophenone is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous chemical and must be transported according to relevant regulations, such as DOT, IATA, or IMDG guidelines. Proper labeling and documentation are required to ensure safe handling during transit and delivery.
    Storage 3',4'-Dichloroacetophenone 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 it from moisture and direct sunlight. Ensure the storage area is clearly labeled and access is limited to trained personnel familiar with its hazards.
    Application of 3',4'-Dichloroacetophenone

    Applications of 3',4'-Dichloroacetophenone in Industrial Manufacturing

    3′,4′-Dichloroacetophenone serves as a key intermediate in several industrial chemical syntheses. Its properties support targeted downstream processing in the pharmaceutical, agrochemical, dye, and fragrance industries. We describe verified application routes below based on technical practice and regulatory requirements.

    1. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical manufacturers use 3′,4′-dichloroacetophenone in the synthesis of specialty Active Pharmaceutical Ingredients (APIs), especially where dichlorinated aromatic ketones form a core structure. The compound enters at early-stage condensation reactions such as nucleophilic aromatic substitution or Friedel–Crafts alkylation, providing a building block for anti-infective, anti-inflammatory, and nervous system-related APIs. Plants ensure all residual solvent and intermediate traces stay within ICH Q3C and ICH Q3A impurity limits. Material handling must comply with controlled area protocols during batch preparations. Final APIs proceed through downstream crystallization, solvent exchange, and purification before tableting, encapsulation, or sterile compounding.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • FDA 21 CFR Part 211
    • European Pharmacopeia (Ph. Eur.) monographs
    • REACH chemical registration

    Typical usage ratio

    • Batch input 0.2–1.5 molar equivalents per API target; exact ratio depends on substitution pattern and API yield optimization studies.

    Downstream process integration

    • Introduced at initial condensation during core ring assembly.
    • Maintained in jacketed glass-lined reactors with controlled temperature and inert atmosphere.
    • Intermediate purified by column or crystallization before follow-up transformations.
    • Isolated API further processed into finished dosage forms.

    Final product types

    • Oral prescription drugs (tablets, capsules)
    • Injectables
    • Bulk API for contract manufacturing
    • Pharmaceutical intermediates for outsourcing

    2. Agrochemical Synthesis for Herbicide and Pesticide Production

    Manufacturers utilize 3′,4′-dichloroacetophenone for producing key intermediates in selective herbicide and pesticide formulations. The dichloro functionality enables synthesis of novel chloro-aryl derivatives, critical for targeted soil application and foliage protection products. Reactivity control remains vital due to environmental safety regulations on residual aromatic chlorides and intermediates in the end product. Industrial protocols monitor traceability from raw input through final concentrate blending and packaging. Plant QC teams assess purity and homogeneity post-coupling and chlorination reactions before final product tank-filling.

    Industry compliance standards

    • FAO/WHO specification for pesticide products
    • ISO 9001:2015 for agrochemical manufacturing
    • US EPA 40 CFR, Part 180 (tolerances for residues of pesticides)
    • REACH Annex II (product safety and SDS management)

    Typical usage ratio

    • 0.5–1.2 equivalents per formulation intermediate based on targeted chlorine content and downstream blend requirements; adjusted for specific herbicidal compound synthesis.

    Downstream process integration

    • Charged to primary aromatic substitution or condensation reactors.
    • Subjected to alkylation, esterification, or chlorination steps as precursor to the final agrochemical active ingredient.
    • Solution filtration and in-process HPLC analysis before blending with carriers or surfactants.
    • Finished actives then integrated into EC, WG, or SC formulations.

    Final product types

    • Liquid herbicide concentrates (ECs)
    • Water-dispersible granules (WDGs)
    • Technical pesticide actives
    • Custom pre-mixtures for OEM packing

    3. Intermediate in Industrial Dye and Pigment Manufacturing

    Specialty dye and pigment producers source 3′,4′-dichloroacetophenone as a starting material for synthesizing high-performance azo and anthraquinone dyes. The controlled dichloro substitution fosters selective coupling with aromatic or amino intermediates, strengthening color fastness and light stability in industrial-grade dyes. Processing involves careful pH and agitation control to maintain consistent particle size, ensuring end-use compatibility in textile, leather, and printing industries. Factories rely on automated dosing and temperature monitoring to minimize byproducts and environmental impact during diazotization, coupling, or acylation stages.

    Industry compliance standards

    • OEKO-TEX® Standard 100 dye component restrictions
    • EU REACH Regulation (1907/2006) – SVHC screening
    • ZDHC MRSL Version 3.0 (textile chemical compliance)
    • ISO 9001:2015 for pigment manufacture

    Typical usage ratio

    • 10–40% by weight in dye intermediate synthesis; adjusted according to final chromophore requirement and color strength.

    Downstream process integration

    • Charged in closed reactors during initial coupling reaction.
    • Integrated before diazotization to maximize dichloro group transfer to dye backbone.
    • Downstream sulfonation or metallization as per end-use fastness criteria.
    • Wet cake or dry pigment milled and blended for distribution.

    Final product types

    • Sulfonated anthraquinone dyes
    • Direct and acid dyes for textiles
    • Color fast printing inks
    • Polymer-compatible pigments

    4. Intermediate for Fragrance and Aroma Chemical Synthesis

    Our clients in the fragrance and fine chemical sector utilize 3′,4′-dichloroacetophenone as a precursor for synthesizing aromatic ketones and alcohols used in perfumery and flavoring applications. The compound supports stepwise transformations such as reductions, Grignard additions, and selective halogenation to produce stable, aromatic-rich ketones. Manufacturing lines run multiple purification sequences, ensuring product meets IFRA and flavor regulation purity requirements. Strict odor threshold testing accompanies every batch to validate aroma profile consistency across applications.

    Industry compliance standards

    • IFRA Standards for fragrance material content
    • Food Chemicals Codex (FCC) for flavor ingredients
    • EU Regulation (EC) No 1223/2009 for cosmetic safety
    • ISO 22716 GMP for cosmetics

    Typical usage ratio

    • Initial batch input 5–25% by weight per target aroma chemical during synthesis; refined by pilot runs based on yield and GC-MS purity testing.

    Downstream process integration

    • Fed into primary reduction or Grignard reaction lines as carbonyl source.
    • Processed under controlled temperature with inert blanket to suppress unwanted chlorination.
    • Multiple vacuum distillations employed to isolate key aroma intermediates.
    • Final aroma chemical compounded into fragrance or food additive base.

    Final product types

    • Aromatic ketones for perfume bases
    • Flavoring agents for beverages or confectionery
    • Intermediate alcohols for fine fragrance compositions
    • Cosmetic fragrance ingredients
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    Certification & Compliance
    More Introduction

    3',4'-Dichloroacetophenone: A Practical View from the Plant Floor

    What 3',4'-Dichloroacetophenone Really Means for Chemical Production

    Daily operation in the plant involves more than formulas or catalogues. Each chemical produced reflects decisions, process discipline, and a relationship with long-standing industry needs. Among the compounds we focus on, 3',4'-Dichloroacetophenone stands out for both its reliability and demand in organic synthesis. Years of practice have demonstrated its practical uses, especially for those developing intermediates for pharmaceuticals or specialty materials.

    3',4'-Dichloroacetophenone, with the model designation 3,4'-DCA, takes its place in our in-house lineup thanks to clear performance in lab trials and scaled production. Chemists working with the compound recognize the versatility of the acetophenone structure, particularly with two chlorines positioned at the 3' and 4' locations on the phenyl ring. This particular arrangement is not just a textbook matter. On the production line, the difference in reactivity compared to other dichloro isomers becomes obvious. Consistent batch-to-batch quality here saves time in purification and downstream synthesis—something our clients tell us matters much more than slight differences in theoretical yields.

    Practical Uses Beyond the Textbook

    In our own process, 3',4'-Dichloroacetophenone serves mostly as an intermediate. Colleagues in the field often use it to make advanced intermediates for pharmaceutical actives or for finer chemical syntheses where selective chlorination delivers value. We have observed a steady pull from the agrochemical industry as well, mostly driven by the ability of this compound to act as a building block for tailored herbicides and fungicides.

    Our organic chemists point out how its physical profile—typically a pale solid with good stability at ambient temperatures—lets us avoid extensive refrigeration during storage and transport. Melting point sits within a moderate range, which is practical both for bulk packaging and in-process handling. These things seem small until a tanker sits waiting just because a batch refuses to solidify or melts too easily.

    Comparisons with standard acetophenone or even the 2',4'- or 2,3'-dichloro variants often come up. For a reaction that needs predictable electrophilic substitution, having chlorines at the 3' and 4' positions brings a specific reactivity not found in other isomers. Years ago, switching from a commercial batch of the 3,4'- isomer to a mixed dichloroacetophenone from another supplier created noticeably more byproducts—a lesson for process scale-ups. This subtlety affects purification, cost, and final product profile. We tend to run GC/MS and NMR analyses on production lots, both for in-house control and to give customers a complete view of the final product.

    Consistent Specifications Mean Efficient Operations

    Product specifications extend beyond purity numbers on a certificate. From our end, the focus remains on key points: purity by HPLC, low moisture, and confirmed isomer identity using in-house NMR spectrometry. Typical lots show purity levels above 98 percent by HPLC, but we maintain an open approach; any deviation, even by half a percent, goes through an internal root-cause check. Most issues stem from trace impurities during chlorination or side reactions during work-up. Addressing this early, long before any packaging happens, prevents future surprises.

    Those in synthesis know small impurities can spike costs when they appear later in downstream reactions. This feedback shapes our production controls. We routinely test moisture content with Karl Fischer titration to guard against hydrolysis—especially important when the compound sees long transits or faces storage cycles in humid climates.

    Physical specification—appearance, melting point, bulk density—gets treated as more than a routine box-ticking exercise. One batch with unusual bulk density can gum up an automated transfer or slow a reactor feed; everyone on our line knows this from hard-won experience. By standardizing our recrystallization process and monitoring grinding methods, we target repeatable particle size wherever possible.

    Safety and Handling: Learned from Real-World Challenges

    Although 3',4'-Dichloroacetophenone does not require unique PPE beyond standard chemical plant protocols, its handling reminds us every day about the importance of correct containment and ventilation. Volatility is lower than lighter acetophenones, but thermal degradation at elevated temperatures remains a risk. Over the years, process changes—such as switching from batch to semicontinuous—reduced operator exposure considerably during transfer and blending. Room airflow and robust local exhaust made a tangible difference in worker comfort and downstream cleaning effort.

    Given its low water solubility, incidents involving spills or leaks usually stay confined to solid floors. We found that rapid response with standard absorbents and follow-up with solvent wipe-down works best; residue from slow cleanup sometimes reacts with aggressive solvents used in other plant areas. Emergency drills once seemed redundant, but after one unplanned spill during a weeklong shipment delay, they proved their worth.

    Consistency from Source to Application

    Reliable shipment and storage add as much value as lab purity. Over the years, feedback from partners brought subtle improvements to our packaging methods. Standard plastic-lined fiber drums balance protection and cost for us; for long-haul shipments, triple-layer polyethylene liners offer an extra margin of moisture resistance. This strategy came about when a shipment to a coastal city experienced a customs delay—when it arrived, material integrity matched start-of-journey records.

    Our customers push for year-round consistency. Beyond purity, they often ask about how the compound will behave under various temperatures and in different storage rooms. Plant operators, particularly in regions with wide humidity swings, count on a product that doesn’t clump or degrade after sitting for several weeks post-arrival. Drawing from previous product iterations, we tuned our process controls to reduce potential for hydrolysis and clumping, especially during the final drying stage—changes that came directly from customer case studies, not assumptions.

    Differences from Other Isomers: Practical Value for Process Chemists

    Small position changes in chlorinated acetophenones bring disproportionate effects downstream. Chemists who tried switching from a 3',4'- to a 2',4'- isomer often report changes in their reaction yields, isolation procedures, and even the safety profile of their process. Colleagues in both lab and scaled environments confirm that the unique substitution pattern on our 3',4'-Dichloroacetophenone enables more selective reactions, with cleaner downstream intermediate profiles. What might seem like small details in an academic setting show up in hours saved at purification, lower solvent costs, and better throughput at scale.

    Years ago, a customer working on a specialty dye intermediate compared their results with several dichloroacetophenone isomers. The 3',4'- variant displayed fewer side reactions during Friedel–Crafts acylation, which cut downstream rework by half. Other customers focusing on heterocycle synthesis comment on the same pattern; while literature often treats isomers as interchangeable, reality proves otherwise.

    For customers working with 2',3'- or 3,5'- dichloroacetophenones, subtle differences in melting point and solubility complicate handling. Some isomers remain sticky or prone to caking under standard warehouse conditions, while the 3',4'- version offers a more manageable, crisp crystalline form. This aspect reflects choices we made in process drying and purification, always with the intent to avoid surprises in customer setups.

    Usage Insights: Listening to the Chemists

    Production values chemistry that “works the first time,” and we keep this in mind when formulating and testing our 3',4'-Dichloroacetophenone. Our user base stretches from pharma core labs to pilot-scale agrochemical plants. Typical applications include Grignard reactions, selective acylations, and field synthesis of advanced active intermediates.

    These users rely on batch-to-batch consistency, which goes back to repeatable chlorination methods, reliable raw materials, and vigilant process control. Flash chromatography is easier on pure, non-sticky intermediates. We know stories of researchers who lost days purifying byproducts because of subtle supply variations—issues we take seriously. A hands-on approach lets us spot potential deviations early, whether in color, odor, or handling profile.

    In the lab, bench-scale trials with our 3',4'-Dichloroacetophenone often show sharp NMR signals, a welcome sight for time-pressed chemists. On larger scales, plant engineers appreciate a predictable solid-to-melt transition for precise feed to reactors, which means less downtimes. After years of working with this product, we value direct feedback from bulk users as a key input into our process improvement cycle.

    Environmental and Regulatory Perspectives in the Real World

    Our view of compliance extends beyond regulatory paperwork. Operating with an eye on both safety and the environment means taking extra steps in managing by-products and waste from 3',4'-Dichloroacetophenone production. We built dedicated treatment for aqueous phase streams coming off chlorination, capturing both organic and inorganic residues before water leaves the plant. On the air side, scrubbing systems and well-tested venting procedures mitigate emissions.

    Years spent managing audits proved one lesson: preempting issues brings peace of mind. Full disclosure about composition, trace impurities, and process details enables easier downstream documentation for our clients. Those exporting or importing these chemicals often remark how transparent analysis reports take burden off their regulatory teams, and save costly surprises at customs.

    Discussions on lifecycle tracking of hazardous substances have grown in recent years. We contribute our field experience to improve voluntary tracking schemes, increasingly requested by multinational partners, and push for ever-tighter batch traceability. This approach reflects both regulatory demand and internal discipline, creating a more reliable supply chain.

    Continuous Product Development—Shaped by Practical Experience

    Our history with 3',4'-Dichloroacetophenone taught that continuous improvement trumps theoretical optimization. Initial challenges involved reproducibly controlling chlorine addition and minimizing side-products. Early trials often left persistent residue; gradual process refinement and tighter raw-materials selection solved this.

    One major improvement came from direct user feedback: researchers complained of erratic melting points during summer transport, which led us to rework our drying cycle and add temperature monitoring to our packing lines. A simple change—adding a buffer chamber to the drying step—stabilized final product handling significantly.

    Process engineers periodically suggest tweaks to blending protocol or in-process filtration. We find that flexible thinking and hands-on adaptation—not a rigid SOP mentality—solves most of the small issues that crop up in real-world manufacturing. Tracking and sharing these lessons, internally and with trusted customers, adds more value than any one-off process optimization.

    Looking Forward with Knowledge Built from the Production Floor

    The value of 3',4'-Dichloroacetophenone comes not just from chemistry textbooks but from every day spent refining how it’s made, packed, handled, and shipped. On the floor, employees learn to spot problems before they leave the lot, and attention to such details gives our clients quieter days and better outcomes.

    Adaptability, specification, and transparency matter as much as the molecule’s structure or its formal registry. What we make is only one part—how we deliver, support, and stand behind it reflects what we have learned by standing at the reactor and at the loading dock alike. The world of specialty chemicals constantly shifts with new regulation, evolving customer needs, and operational realities that textbooks never quite describe—each batch of 3',4'-Dichloroacetophenone reflects that living story.