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HS Code |
708796 |
| Iupac Name | (Z)-3-chloro-1-(2-chlorophenyl)-2-(4-fluorophenyl)prop-1-ene |
| Molecular Formula | C15H11Cl2F |
| Cas Number | 145979-29-5 |
| Appearance | Solid or crystalline powder |
| Solubility | Low solubility in water; soluble in organic solvents |
| Smiles | C1=CC=C(C(=C1)Cl)C=C(C2=CC=C(C=C2)F)CCl |
| Inchi | InChI=1S/C15H11Cl2F/c16-13-6-2-1-5-12(13)10-15(11-17)14-7-3-9-18-8-4-14/h1-9,15H/b10-15- |
| Purity | Typically >98% (for laboratory-grade material) |
| Storage Conditions | Store at 2-8°C, in a dry and ventilated area, protected from light |
As an accredited Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 5 grams of Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene, labeled for laboratory use. |
| Shipping | The chemical Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-propene is shipped in sealed, chemical-resistant containers, clearly labeled with hazard and handling instructions. Packages comply with international transport regulations for hazardous materials, ensuring protection from moisture, light, and temperature extremes during transit. Safety Data Sheets (SDS) are included with every shipment. |
| Storage | Store **Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene** in a cool, dry, well-ventilated area away from direct sunlight, heat, and incompatible substances such as strong oxidizers. Keep the container tightly closed and properly labeled. Use appropriate chemical-resistant containers, and ensure secondary containment to prevent leaks or spills. Store away from food and drink. Access should be restricted to trained personnel. |
Applications of Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene in Industrial ManufacturingZ-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene delivers specific functional groups required in several chemical synthesis pathways. Our facility supports downstream industries by offering this compound for processes requiring high selectivity, controlled substitution, and batch-to-batch consistency. Below, we outline key sectors that integrate this material within manufacturing operations, including application-specific compliance, dosage, processing, and the ultimate products obtained. 1. Pharmaceutical Intermediates SynthesisThis compound serves as a targeted intermediate for the development of advanced pharmaceutical molecules, particularly in non-steroidal anti-inflammatory drug (NSAID) and selective central nervous system (CNS) agent synthesis. Clients use it for introducing specific chloro and fluoro-substituted moieties critical in structure-activity relationship studies. In this setting, the product must meet stringent trace impurity thresholds before it enters route-specific coupling or ring-forming reactions under temperature- and solvent-defined conditions. Industry compliance standards
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2. Agrochemical SynthesisIconic crop protection agents and selective herbicide actives benefit from the use of elaborated, halogen-substituted propenes. Agricultural chemistry manufacturers select this raw material for constructing base skeletons in pre-emergence herbicidal products through established alkylation and substitution pathways. Exact structure and site-selectivity of the chlorophenyl and fluorophenyl groups help develop molecules with reliable field bioactivity and desirable decomposition profiles in the environment. Industry compliance standards
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3. Advanced Material Monomer PreparationResearch and manufacturing groups in polymer science incorporate special fluoro-chloro substituted propenes for next-generation polymer backbones with controlled polar functionality. This intermediate provides tailored electronic and physical properties in high-performance coatings and specialty plastic resins—especially where chemical resistance and UV stability drive formulation design. The use of this ingredient ensures specific placement of aromatic and halogen atoms, influencing mechanical strength and degradation rates. Industry compliance standards
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4. Specialty Organic Synthesis for Fine ChemicalsManufacturers producing halogenated aromatic fine chemicals integrate this raw material into multi-step syntheses where the unique chloro and fluoro placements enable access to molecules with custom properties for UV absorbers, stable pigments, or specialty dyes. It enables precise installation of reactive units in aryl systems not accessible via simpler building blocks, supporting complex chemical transformations in fine and performance chemical sectors. Industry compliance standards
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At our chemical plant, Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene has become one of the products we produce season after season because reliable consistency matters in the specialty chemicals market. Our direct experience over years of hands-on synthesis and scale-up enables us to discuss this compound more deeply than surface-level brochures and sales talk. Each step, from raw material sourcing to purification, takes place in-house so that we have direct oversight and responsibility for every batch that leaves our tanks.
We handle several grades for research and industrial users. High-purity lots come out of glass-lined reactors using rigorously dried solvents. Chlorination and fluorination steps depend on careful control of temperature and pressure. Each run is monitored with in-process GC and HPLC, and final content is analyzed by NMR and mass spectrometry because small changes can affect downstream reactions. Moisture and trace metal content never escape our analysis. Users demand dependable profiles, so we focus on batch reproducibility rather than merely chasing high assay numbers. Whether the demand comes from a pilot plant manager or a kilo-lab, we recognize purity, isomer percentage, and color all carry weight.
This compound offers unique substitution patterns, thanks to its 3-chloro backbone, 2-chlorophenyl, and 4-fluorophenyl rings. Synthesis chemists and discovery teams favor it because the combination unlocks reactivity not found in simpler alkenes or halogenated benzenes. We have seen it chosen for its suitability in various pharmaceutical syntheses. Medicinal chemistry labs run coupling reactions or explore it as an intermediate for building complex molecules. Its molecular scaffold adds diversity to libraries, particularly where halogenated aromatic units play a role in binding or metabolic profiling.
Production at scale introduces its own challenges. We optimize yield and minimize impurities that could hinder purification in later stages. Diligent attention to reaction exotherms, workup conditions, and solvent recovery serves not only our internal goals but also addresses the downstream needs of customers formulating under tight specs. Customers come to us with feedback—sometimes about color drift or unanticipated byproducts—so we treat every lot as a learning opportunity.
Working hands-on with Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene provides a clear look at the reality of large-scale chemical production. There is no magic to quality—just patient adaptation to process feedback, sometimes machine by machine, batch by batch. If the exotherm spikes during chlorination, holding temperature for a few extra minutes prevents decomposition. These adjustments live in our lab books and inform every shift.
Physical properties such as melting range, stability under light and air, and solvent compatibility become the focus here. Our experience tells us that this compound has a low-to-moderate volatility and remains stable below 40°C for typical storage durations, but we keep it in amber glass or lined drums anyway. Keeping moisture low extends shelf life, and minimizing agitation during transfers prevents foaming and air oxidation. Not every halogenated styrene behaves the same; this one reacts briskly in organometallic couplings but can linger unchanged in nucleophilic aromatic substitutions unless a catalyst triggers movement.
Third-party handlers may repack or relabel, but our value comes from direct manufacturing control. Each step—chlorination, fluorination, alkene formation—takes place under our roof with oversight from chemists who designed and scaled the process. There’s no gap between design and execution. This approach eliminates the surprises that often occur when a warehouse operator discovers contamination or high water content. We receive real-time feedback from engineering and logistics, learning directly from the people running the pumps and cleaning the reactors.
Our commitment to full disclosure about ingredients, processes, and trace contaminants builds trust. The researchers purchasing our compound sometimes reach out for details about possible byproducts after they run their own analytics. We don’t send out generic brochures in response; instead, we pull out our own QC records, retention samples, and method validations and share directly what our analysis found.
Most users purchase this compound for research, but we also supply early-stage pilot plants and process chemistry teams testing new medicines, agrochemicals, and even specialty materials. Medicinal chemistry teams praise its structure because the blend of chloro and fluoro groups can trigger unique electronic effects in target molecules. For some, it functions as a building block, a handle for Suzuki or Heck couplings, or a test subject for metabolic stability studies. Its electron-rich and electron-deficient aromatic rings create opportunities for regioselective substitutions most simple styrenes or alkene derivatives can’t match.
We have supplied batches for solid-phase synthesis, library generation, and even as seed compounds for combinatorial programs. The range of reactivity within one structure lends it to use in programs investigating SAR and exploring diversity. Not all batches go to large pharmaceutical labs; some reach academic groups eager to walk the boundary between known and new chemistry.
We often get questions about why Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene produces different outcomes compared to the corresponding non-fluorinated or non-chlorinated analogs. Our side-by-side experiments confirm that the 4-fluoro substitution increases stability under certain conditions and also impacts electron distribution within the aromatic ring system. This can alter coupling rates, regioselectivity, or even product purity in cross-coupling chemistry.
The 3-chloro-1-propene backbone sets this molecule apart from typical styrenes. Testing reveals that it offers higher selectivity than simple halostyrenes in Pd-catalyzed reactions. Not every process route accepts substitution at the ortho or para positions, so our chemists learned that these positions influence the way the compound interacts with downstream catalysts or reagents. It’s not just the molecular formula that counts—batch performance in the real world drives every formulation or scale-up. This is information we capture with every process tweak and QC run.
Ongoing production means learning from every run. Persistent impurities forced us to upgrade our filtration and extraction methods, reducing the burden on downstream crystallization. Investment in sealed, inerted vessels lowers oxygen exposure, which in turn protects from color drift and maintains stability. Our lab teams monitor retention samples over time to spot aging in real-world conditions, not just accelerated aging studies, and that data gets fed directly into our shipping guidelines.
Some customers push us with specialized requirements, asking for documentation on crystal forms, microtraces, or proof of absence of specific heavy metals. Our method development chemists tackle these requests in partnership with QC, often running multi-dimensional analyses to explain even minor anomalies. This constant conversation with end-users spurs more precise manufacturing and QA practices and has influenced us to expand GC headspace and ICP-MS testing for trace organics and inorganics. Sharing these findings advances not only our reliability but also the confidence of the researchers trusting their projects to our materials.
Producing Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene safely ties directly to our facility workflow. Halogenated intermediates can produce reactive byproducts, especially at larger volumes. Our operators train regularly in safe chemical handling, containment, and emergency response. Equipment operates fully interlocked, and ventilation is measured frequently. Solvent tanks, reactor seals, and transfer lines face routine inspection to counter leaks and prevent contamination—a practical outcome of thinking long-term as a producer, not a transient packager.
Safety doesn’t stop at plant boundaries. We provide up-to-date documentation on hazards, storage conditions, and safe disposal. A commitment to responsible supply includes ongoing dialogue with shipment handlers and end-users. We receive questions from new lab groups asking about handling or storing small quantities, and we support them by sharing those details—not just sending a data sheet but offering practical advice from our plant experience. This attitude stems from knowing the real-world impact of each shipment, not from policy compliance alone.
Every drum, bottle, or sample of this product carries a production record traceable to individual operators and date-stamped to each synthesis. We keep thorough logs—no batch is anonymous and every anomaly, if any, is documented openly. Users have asked us for historical batch data to pinpoint sources of downstream trouble, and we’ve been able to support their investigations because we do not cut corners in record-keeping. We recognize open disclosure builds partnerships rather than just completing transactions.
Sustainability shapes our decisions, not just for appearances but because the efficiency of our process influences plant economics and community impact. Investing in solvent recovery and energy use optimization pays off both in daily operations and in credibility when meeting the standards of the industries we serve. Managing halogenated waste streams and minimizing air emissions of volatile organics is not optional for us; it is core to the way we operate. Industry audits and continued certification renewals validate our approach, but employee safety and neighborhood trust motivate us even more.
Every process, from synthesis to analytics, benefits from constant feedback. Scale-up doesn't always behave like the lab—small parameters shift and real problems appear. Manufacturing chemists adjust conditions, swap out suppliers, and work directly with plant operators to root out issues. Our site teams learn on the job, updating SOPs not by committee but through direct experimentation and evidence.
Sometimes our improvements start with a customer call pointing out an outlier in their own runs. We replicate their conditions, diagnose problems hands-on, and make adjustments. Crossing that bridge between laboratory claims and manufacturing experience is where many producers fall short. We prefer transparency and problem-solving over marketing spin, and sharing those results strengthens the trust of repeat partners who rely on continuity batch after batch.
Over time, our approach to Z-3-Chloro-1-(2-Chlorophenyl)-2-(4-Fluorophenyl)-Propene manufacturing has matured thanks to feedback from real-world application, batch experience, and the hard lessons that come from production hiccups and customer requests. We view every lot as a tangible expression of our experience—not a commodity churned out by a process no one can explain.
Chemistry advances through shared knowledge and hard-won process understanding. No one knows better the quirks, performance envelope, or opportunities of this compound than our plant teams. Demand changes, synthetic techniques evolve, regulatory standards sharpen, yet direct production experience remains vital to delivering reliable, reproducible chemicals to those who build the world’s future medicines and materials.