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HS Code |
766098 |
| Chemical Name | 4,4'-Dichlorochalcone |
| Cas Number | 2251-42-7 |
| Molecular Formula | C15H10Cl2O |
| Molecular Weight | 277.15 |
| Appearance | Yellow solid |
| Melting Point | 135-137°C |
| Solubility | Slightly soluble in organic solvents (e.g., ethanol, DMSO) |
| Purity | Typically ≥98% |
| Structural Formula | ClC6H4CH=CHCOC6H4Cl |
| Smiles | ClC1=CC=C(C=C1)C=CC(=O)C2=CC=C(Cl)C=C2 |
As an accredited 4,4'-Dichlorochalcone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g 4,4'-Dichlorochalcone comes in a sealed amber glass bottle, labeled with hazard warnings, lot number, and purity details. |
| Shipping | 4,4'-Dichlorochalcone is shipped in tightly sealed containers to prevent moisture, light, and air exposure. It is handled as a potentially hazardous material, transported according to chemical safety regulations, with appropriate labeling and documentation, and usually shipped at ambient temperature unless otherwise specified by safety data guidelines. |
| Storage | 4,4'-Dichlorochalcone should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Handle under inert atmosphere if possible to minimize degradation. Label storage container clearly and keep away from food and drink. |
Applications of 4,4'-Dichlorochalcone in Industrial ManufacturingAs a dedicated manufacturer of 4,4'-Dichlorochalcone, we supply this specialized compound directly to formulators and producers in established chemical sectors. Leveraging our in-house synthesis capabilities, we address the requirements of industries where this raw material plays a defined and proven downstream role. Below, we outline real-world application scenarios, formulation details, processing stages, and associated industry compliance relevant to major segments utilizing 4,4'-Dichlorochalcone. 1. Pharmaceutical Intermediate for API SynthesisPharmaceutical manufacturers employ 4,4'-Dichlorochalcone as a building block during the synthesis of several active pharmaceutical ingredients, particularly within the family of flavonoid and chalcone-derived drugs. The compound’s dichloro substitution enables selective reactivity during key cyclization and modification steps in multi-stage API production, supporting consistent yield and traceability required for regulated drug manufacture. The exact proportion in the process depends on targeted moieties and downstream purification route, requiring robust formulation control and compliance with pharmaceutical impurity and solvent residue limits. Industry compliance standards
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2. Fine Chemical Synthesis for Specialty Dye PrecursorsProducers in the dye and colorant sector add 4,4'-Dichlorochalcone as a precursor during the synthesis of specialty dyes, especially for organic pigment manufacturing targeting plastic, textile, and ink applications. Its dichloro-functional groups direct coupling and azo condensation reactions, enabling controlled chromophore modification. Proper handling during reaction charging and post-reaction purification ensures the resulting dye intermediates adhere to imposed purity thresholds and batch color reproducibility demanded by high-value colorant production. Industry compliance standards
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3. Agrochemical Synthesis (Precursor for Crop Protection Formulations)In agrochemical manufacturing, 4,4'-Dichlorochalcone enters synthesis routes as a controlled intermediate during the production of certain fungicidal and pesticidal active substances. The compound’s electron-withdrawing properties support the generation of targeted bioactive ring systems, critical in crop protection actives. Downstream integration demands precise control of residual levels and process effluents as per environmental standards. Batch traceability and compliance with permissible impurity limits remain central for agrochemical application safety. Industry compliance standards
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4. Specialty Polymer Synthesis for Functional MaterialsIn the field of advanced materials, select specialty polymer producers utilize 4,4'-Dichlorochalcone to introduce pendant aromatic and halogenated groups, imparting specific UV-absorbing and barrier properties to end polymers. The compound becomes part of functional monomer blends during controlled polycondensation or copolymerization. These processes demand exacting charge weight calculations and high-purity monomer streams to secure downstream product performance relevant to UV filtering films and specialty coatings. Industry compliance standards
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5. Laboratory Reagent for Organic Synthesis ResearchAcademic and industrial R&D labs employ 4,4'-Dichlorochalcone as a research-grade reagent for the development of novel molecular frameworks and testing new methodologies. Its well-defined halogenation pattern allows for targeted exploration of electrophilic aromatic substitution, cross-coupling reactions, and structure-activity relationship studies. Preparative scale is adjusted according to research protocol and does not require direct regulatory approval, but high-purity grades and batch documentation support reliable results and data integrity. Industry compliance standards
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We manufacture 4,4'-Dichlorochalcone from scratch in our plant, using a controlled process that begins with purified p-chlorobenzaldehyde and p-chloroacetophenone. This compound stands apart from many standard chalcones for a few reasons. Our team blends thorough process control with deep chemistry know-how: the result is a crystalline solid, yellow in color, with both para positions occupied by chlorine atoms. If you’re comparing it to mono-chloro or unsubstituted chalcones, the double chlorination brings unique stability and reactivity to the structure. We keep a close eye on purity, routinely checking melting point and high-pressure liquid chromatography profiles to ensure batch-to-batch consistency, because impurities can have a real impact in downstream reactions.
Having worked with a range of chalcones, we see 4,4'-Dichlorochalcone perform especially well in advanced synthesis settings. The presence of two para-chloro groups not only adjusts solubility in polar and non-polar solvents but also increases electron-withdrawing capacity. This gives chemists tighter control over subsequent additions to the double bond, whether in heterocycle synthesis or targeted pharmaceutical intermediates. While some chalcones seem to oxidize too easily or invite byproduct formation, the dichloro version holds its structure well under a variety of reaction conditions. Our customers running long multi-step syntheses count on that reliability.
Refining process conditions over dozens of batches, our optimum method yields a product with a typical purity of 99% or greater as measured by HPLC. The melting point lands between 130–133°C. Particle sizing takes attention during final crystallization; our standard process produces a fine free-flowing powder that handles and dissolves well. Chlorine substitution in both aromatic rings puts some restraints on crystal packing, yet that works to prevent caking and keeps it shelf-stable. Some labs request micronized product for faster dissolution, so we extend grinding services as needed.
Unlike generic chalcones from other producers, we filter every batch with a focus on residual solvent content and controlling for common byproducts such as unreacted aldehydes or acetophenones. Trace analysis tells us if the batch meets our criteria; we’ve found that keeping these side-impurities low reduces headaches in customers’ later synthetic steps. Shelf life stands strong—properly sealed drums of our dichloro derivative keep their properties for years when protected from light and moisture.
Decisions to use 4,4'-Dichlorochalcone usually rest on reactivity and reliability. For anyone synthesizing bioactive heterocycles—particularly in exploratory medicinal chemistry—this molecule’s double chlorine substitution opens up routes that simple chalcones can’t access. The para-chloro pattern acts as a good leaving group in cross-coupling or nucleophilic substitution reactions. We have seen teams build both small benzo-fused systems and larger polyaromatic structures off this backbone.
Academic researchers and pharma labs often highlight selectivity: mono-chlorinated and unsubstituted chalcones might generate more side products, especially during cyclization steps or oxidation. Not as much with our dichloro version. It withstands both acidic and basic conditions better, and even in strong oxidizing environments, the core structure resists breakdown. When projects depend on yield and reproducibility, there’s little room for roulette with precursor consistency, and that’s a gap our product fills.
We make a range of chalcones in our plant—plain, mono-chloro, and other substituted types. Each has its role, but there are clear differences in handling and application. For instance, simple chalcones without substitution often show better solubility in ethanol or methanol, but their electron density makes them too reactive in many couplings. They can form dimers or unwanted byproducts if you’re not watching conditions carefully. Mono-chloro chalcones do raise selectivity, yet the difference is measurable on both the bench and in the flask; sometimes a single chlorine atom doesn’t hold back side paths enough, especially in cases demanding heavy duty.
We’ve compared side-by-side yields in cross-coupling reactions and electrophilic addition; consistently, 4,4'-Dichlorochalcone demonstrates tighter conversion rates, less waste, and better crystallization after isolation. The full dichloro substitution works like armor. It doesn’t just impact yields and stability—storage, ease of filtration, and even color during processing all show measurable advantages.
Not every lab has the same needs. Some teams want high batch turnover for pilot runs. Others need meticulous documentation for regulatory submission or industrial upscaling. Over the years, we found that smaller-scale traders sometimes cut corners: they blend off-grade lots or skip analytical testing. That kind of unpredictability stacks up against the big pharma timelines we support. We invest in validated procedures, not just during process creation, but from raw material screening onward. QC reports for each batch include all the numbers we rely on ourselves—purity, melting point, and comprehensive impurity scans. Often, we help troubleshoot processing issues for customers right down to the specific solvent or pH buffer.
Waste reduction in manufacturing drives a big part of our R&D. Producing 4,4'-Dichlorochalcone has taught us a lot about process efficiency. Our team optimized the condensation to use less solvent and incorporated inline filtration, lowering both raw material costs and disposal fees. Ensuring low residual solvents isn’t just regulatory box-checking; it stops batch carryover and supports green chemistry goals.
Running a plant that has produced 4,4'-Dichlorochalcone for years sharpens the view of its value—and its quirks. New staff learn early on to watch for early precipitation, to monitor pH close as the reaction nears completion, and to check every filter cake for full removal of byproducts. Some batches want to foam near the end of the condensation; adding antifoaming agents is one lesson we wish we’d known sooner. We keep the recrystallization process efficient by timing temperature drops carefully. Reacting too quickly or cooling off too fast traps impurities, while waiting too long wastes time and energy—details that only emerge from practical production cycles.
Some customers send questions about scale-up. We share not just specs or certificates but our stories—about how too rapid a solvent addition can run a batch out of spec, or how controlling exotherms prevents runaway reactions. We walk them through the best ways to introduce the crystalline powder to various solvent systems. Even with thousands of kilograms delivered to date, we keep learning: sometimes a simple step like pre-heating the receiving vessel improves yield by several points.
Supporting R&D labs and production plants involves more than producing a technical grade product. Production chemists let us know early on how variations in melting point or color alert them to potential side reactions. For advanced intermediates with high value, even minor impurity levels matter. We started offering custom solutions, whether it’s adjusting particle size, adapting packaging to fit glovebox protocols, or providing detailed impurity maps to inform downstream processing.
Catalog suppliers sometimes offer a “one-size-fits-all” approach. That often leaves process development teams with cleanup steps or extra purification. Running our own reactors gives us tighter control and fast turnaround for custom requests. When a global customer wanted ultra-low water content, for example, our team developed a specialized drying protocol and analytical verification. The result: reduction of trace water by half and improved solubility in their non-aqueous system.
Some projects call for repeat orders with tight spec windows. Inconsistent supply and shifting impurity profiles can create delays, loss of expensive reagents, or failed campaigns. By managing raw materials at the source and building relationships with analytical labs, we reduce those headaches. Shipping modules designed for chemical compatibility and regular in-house stability studies keep inventory ready and usable for long-term customers. We mark and store each batch under tracked conditions, and we frequently support customer audits—opening our SOPs and showing the actual reactors, not just certificates.
Safety also takes priority. The dichloro groups do create some handling cautions; dust control during grinding and transfer stays top of mind in our plant. Our production floor is equipped with extraction hoods and all staff train on proper PPE protocols. While the product remains stable, the fine powder can cause irritation on direct contact, so we work to limit dust and package securely. Transportation uses UN-approved drums or double-bagged liners as required by the intended application or customer protocols.
Pharmaceutical teams regularly share their results with us, highlighting 4,4'-Dichlorochalcone’s performance as a core scaffold in kinase inhibitors, anti-inflammatory projects, and emerging anti-infectives. The electron-withdrawing chlorine atoms set up the aromatic rings for coupling chemistry that less-substituted chalcones struggle to handle. This selectivity matters in lead generation and library development, powering faster knockout of unwanted candidate molecules.
Beyond pharma, chemical engineers exploring polymer additives or specialty pigments have found value in the compound's stability. The chlorinated aromatic rings resist breakdown under UV exposure, giving coatings and processing intermediates longer shelf life and more predictable color retention. Some agrochemical research teams utilize 4,4'-Dichlorochalcone as a bridge to produce advanced fungicides and crop protection compounds where unmodified chalcones would fall short due to instability or over-reactivity under field conditions.
Growth in advanced materials and pharmaceuticals keeps tightening standards for purity, trace analysis, and waste reduction. Regulatory pressure on solvent use and environmental exposure makes it vital to have full process transparency. In our own plant, cutting waste per batch and ensuring recyclable packaging both support broader sustainability goals, while also controlling costs. The need for lower impurity profiles continues to rise, driven by both health authorities and performance expectations.
We continue to refine our analytics: investing in newer spectrometry can shorten detection timeframes, while better impurity mapping reduces risk for downstream customers. Close collaboration with end users brings both challenges and innovations—sometimes a bottleneck in their lab becomes the starting point for new process improvements. For example, solvent swaps and filtering techniques designed for one customer’s project now streamline our general batch production and lower risks of contamination.
One area with growing attention is the adaptation of 4,4'-Dichlorochalcone in complex, automated synthesis workflows. Robotics and automated platforms demand solid feeding, rapid dissolution, and minimal foaming—a set of characteristics not always present in the raw chalcone market. Through adjusting grind, optimizing density, and testing batch flow in simulated setups, we are moving closer to providing “plug-and-play” form factors to suit emerging automation.
Being a manufacturer opens a unique channel to share not just specifications but working wisdom. Visitors to our site often connect with engineers or chemists who oversee actual reactors, not just sales teams or distribution partners. We see our product run through different hands and processes—from small synthetic labs up to full-scale manufacturing lines. That two-way flow of feedback shapes both our daily operations and the way we share solutions.
Whether advising on scale-up solvents, discussing solvent blends, or warning about how trace water impacts yield, we get to pass along fixes earned through real-world experience. This kind of manufacturer-to-user connection builds a culture of continuous improvement that third-party brokers simply can’t match.
Greater demand for reliable, pure, and consistent chemical building blocks will only climb. As automation, green chemistry, and stricter regulatory climates move forward, details such as trace impurity levels, safe packaging, and process documentation mean the difference between success and delay in R&D cycles. We invest in production because cutting corners shows up quickly on the customer’s bench—wasted resources, failed syntheses, lost time.
Our experience with 4,4'-Dichlorochalcone teaches plenty: thorough control during manufacture yields not just a better product, but a smoother, more predictable experience for every downstream scientist or technician. Over years, continuous tweaks and production trials built a chemistry that stands up—even under tough synthesis or demanding storage conditions. This kind of reliability doesn’t happen by chance; it grows from daily discipline and an open channel to those putting molecules like 4,4'-Dichlorochalcone to work in the real world.