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HS Code |
499901 |
| Chemical Name | 4-Phenylphenacyl Chloride |
| Cas Number | 3456-45-7 |
| Molecular Formula | C14H11ClO |
| Molecular Weight | 230.69 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 81-83°C |
| Boiling Point | 375.6°C at 760 mmHg |
| Density | 1.19 g/cm³ |
| Purity | Typically ≥ 98% |
| Solubility | Insoluble in water, soluble in organic solvents |
| Flash Point | 163.5°C |
| Synonyms | p-Phenylphenacyl chloride |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
As an accredited 4-Phenylphenacyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 4-Phenylphenacyl Chloride is packaged in a sealed amber glass bottle with a chemical-resistant screw cap and hazard labeling. |
| Shipping | 4-Phenylphenacyl Chloride is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. Packages are labeled according to hazardous material regulations and transported under controlled temperatures. Appropriate documentation and handling procedures are observed to ensure safe transit and compliance with international shipping standards for dangerous chemicals. |
| Storage | 4-Phenylphenacyl chloride should be stored in a cool, dry, well-ventilated area, away from heat, sparks, and open flames. Keep the container tightly closed and protected from moisture and direct sunlight. Store separately from strong oxidizing agents, bases, and water-sensitive materials. Use only chemical-resistant containers and ensure proper labeling to avoid accidental contact or mixing. |
Applications of 4-Phenylphenacyl Chloride in Industrial Manufacturing4-Phenylphenacyl chloride serves as a specialized chemical intermediate in several sectors where its unique structural attributes facilitate valuable functional group transformations. Our manufacturing standards ensure consistent quality tailored for demanding downstream requirements. Below, we highlight authentic industrial applications recognized by regulatory bodies and practiced in the global chemical market. 1. Pharmaceutical API SynthesisMajor pharmaceutical manufacturers utilize 4-phenylphenacyl chloride during the synthesis of antihistamine and antipsychotic drug intermediates, owing to its efficacy as a benzylation and acylation agent. The material enters complex multi-step organic syntheses, most notably in constructing core scaffolds for benzophenone-based APIs. Compliance necessitates traceability throughout production, stringent control of residual chlorides, and alignment with international pharmacopoeia and cGMP requirements. Our grades undergo validated QC protocols for this segment. Industry compliance standards
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2. Specialty Fragrance and Aroma Compound ProductionIn the flavor and fragrance industry, this material acts as a key acylating agent to synthesize advanced intermediates essential for generating musky and woody aromatic chemicals through precise Friedel–Crafts routes. Manufacturers in this segment require regulatory-confirmed ingredient purity plus full documentation of trace residuals to satisfy end-client and audit demands. We customize our packing and analytics protocol to support these applications’ documentation standards. Industry compliance standards
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3. Advanced Liquid Crystal Intermediate ManufacturingProducers of high-performance display and optical devices use 4-phenylphenacyl chloride as a functional intermediate during the controlled synthesis of rigid core and rod-like mesogenic units. High-purity material is critical, as final liquid crystal properties depend on defect-free aromatic substitution. As a manufacturer, our controlled production scale and release specifications are configured for supply chain transparency in this advanced technology segment. Industry compliance standards
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4. Photoinitiator and UV Absorber SynthesisSpecialty chemical firms deploying advanced UV curing systems value this raw material for its role as a precursor in formulating photoinitiators and customized UV absorbers. The chemical enters condensation frameworks for benzoin and thioxanthone derivatives, where purity and reactivity marker control are vital for predictable initiator system performance. We calibrate release criteria and analytical methods for this market’s critical traceability and batch reproducibility standards. Industry compliance standards
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From years in the lab and plenty of experience with aromatic ketones, I’ve seen the pivotal role that 4-Phenylphenacyl Chloride plays in synthetic chemistry. Chemists often know it by its CAS number, 2292-18-4, but beyond the label, most look for reliability and clarity in performance. The structure—distinct, a combination of phenyl groups and a reactive chloride sidechain—sets it apart, and that difference carries real meaning in hands-on applications.
As a manufacturer, we work to supply 4-Phenylphenacyl Chloride in its pure crystalline form, meeting a minimum assay standard above 99%. White to pale yellow crystals signify high purity, and any deviation in appearance gives us an early clue for deeper analysis. Moisture and by-product content receive strict attention in every lot. Our standard sieve size, chosen after dozens of trials, guarantees easy handling in both scale-up and lab-scale syntheses.
Many in the market ask about impurity profiles. Our in-house analytics, using HPLC and GC methods, help us control contaminants. For 4-Phenylphenacyl Chloride, the focus centers on ensuring no excessive presence of unreacted starting materials or related phenacyl derivatives. Loss on drying tests consistently fall below 0.2%. Chloride content analysis, crucial for those using it in nucleophilic substitution, comes in within strict limits because too much residual chloride can skew subsequent chemistry.
The compound’s reputation comes from its performance in organic synthesis. Chemists in pharmaceuticals and material science reach for 4-Phenylphenacyl Chloride as a key intermediate, especially where selectivity matters. The structure’s activated methylene group, flanked by aromatic rings, lends itself well to condensation reactions, ether formation, and preparation of new heterocycles.
In one of our client’s processes, this compound speeds up benzoin condensation derivatives, delivering yields that other acylating agents struggled to approach. In another case, downstream pharma teams began favoring it for its clean conversion to substituted benzofurans, noting fewer by-products and smoother purification compared to 2-chloroacetophenone or simple benzyl chlorides. The customer feedback, paired with our own bench results, underscores the reliability that comes from purity and stereochemistry control.
I’ve fielded calls from academic researchers who value quick, predictable reactions when screening new catalysts. In their postsynthesis analytics, they point out the lower baseline interference with 4-Phenylphenacyl Chloride compared to similar halogenated acetophenones. This advantage means less time tracking down spurious peaks, more time exploring novel transformations.
A lot of chemists ask how this reagent differs from 2-chloropropiophenone or basic benzyl chloride. Practical use tells me the story here. While benzyl chloride reacts rapidly, it brings more risk of unwanted side alkylation, especially in the presence of strong nucleophiles. 2-Chloropropiophenone offers reactivity but lacks the dual aromatic stabilization, making it less effective in reactions needing high product stability or color purity.
The phenyl substituents in 4-Phenylphenacyl Chloride not only slow down unwanted reactions but also enhance selectivity in cross-coupling and cyclization protocols. Some teams still rely on 4-chlorophenacyl chloride, but they often report a higher rate of hydrolysis when stored or handled in environments with variable humidity. Over the years, we have noticed that properly packaged 4-Phenylphenacyl Chloride maintains its reactivity and appearance longer than the standard analogs, and the feedback from pilot customers confirms this observation.
Our own process team handles multi-kilogram batches, so safety and practical storage needs guide our production. In the plant, we prioritize closed-system transfers, since the lachrymatory nature comes out especially during charging and sampling. To minimize exposure, every lot is packed with desiccant under inert atmosphere, and our operators rotate handling duties for comfort and skill.
Many downstream partners want reassurance that batch-to-batch consistency stays tight. Our internal records show deviations in melting range below 0.5 degrees over the past five years, thanks to careful purification and standardized crystallization controls. Onset of decomposition, as detected with DSC, typically happens well above normal process temperatures; this safety margin remains a selling point for process chemistry managers in API development.
For every lot, we retain representative samples for two years. Several long-term customers often call for reference standards, especially during method validation or scale-up transfers. We find that traceability—being able to link back each drum number to individual synthesis steps—occasionally prevents costly troubleshooting down the line.
Our technical team shares experience not just in supplying but in using this molecule across related chemistries. For instance, if a client seeks to replace 4-Phenylphenacyl Chloride with a close analog, we can forecast the effect on end-product crystallinity, color, or downstream conversion yield. By logging these observations, we contribute insight not just as producers, but as participants in the innovation cycle of fine chemicals.
Few topics shape our efforts more than honest feedback from formulators and R&D teams. Over the years, some reported batch heterogeneity from other suppliers, often traceable to variable moisture or residual solvents. Our decision to invest in vacuum drying systems and closed-grinding technology came straight from these dialogues.
We often hear that upstream impurities in other halogenated ketones have triggered unexpected side reactions, raising costs for downstream purification. This issue pushed us to heighten our in-process analytics, matching each batch against historical impurity fingerprints. By tightening these controls and transparently reporting them in delivery documentation, we help our customers avoid unnecessary surprises mid-campaign.
Producing phenyl-substituted reagents brings responsibilities beyond the plant. We follow best practices to keep releases of halogenated by-products to a minimum, maintaining scrubber and filtration systems that exceed regional compliance standards. Waste minimization starts in synthesis planning. We aim for maximum conversion and prioritize recycling solvents within the operation.
Regulatory scrutiny has only increased, especially for substances with a potential for environmental persistence. We welcome audits from responsible customers, confident in the traceability and pedigree of each shipment. Several longstanding clients have asked for detailed lifecycle data, and we now routinely provide them with breakdowns of process inputs, effluent handling, and emissions records per lot. This transparency provides mutual peace of mind, and constructive feedback helps shape continuous improvements in our facility.
From years of packing and storing hundreds of drums, we’ve learned that 4-Phenylphenacyl Chloride needs stable, dry conditions for long shelf life. Standard HDPE or amber glass keeps the crystals free-flowing for extended periods. If exposed to ambient humidity, we notice surface caking within weeks, even inside sealed steel containers. Our advice comes from these direct observations—store it cool, dry, and away from light.
The right packaging also makes a difference in process safety. Operators prefer double-bagging for bulk shipments, and our smallest pack sizes in glass come pre-packed with desiccant to prevent agglomeration. These steps bring fewer customer complaints about handling losses or caked product, especially in regions with high humidity swings.
Shipping during warmer months led us to develop temperature-controlled logistics routes. After a few documented cases of product sticking and loss of flowability in summer deliveries, we set up a redundant supply chain for temperature-sensitive orders. These operational tweaks grew straight out of regular communication with our largest users, whose schedules depend on avoiding any material delays.
No batch tells the whole story of a product’s quality. By aggregating years of quality records, complaint tickets, and positive feedback, we view each delivery as the next opportunity for improvement. Some of our customers in reagent distribution noticed that off-specification shipments from other sources often happen in the final stages: repackaging and storage. We tackle this weak link by integrating QC checks even at dispatch, not only at production finish.
In the early days, we relied more heavily on visual checks for color and flow, but this missed low-level contamination events that only showed up weeks after delivery. Now, on top of physical checks, we run rapid micro-impurity screening on each lot. This systematic focus led to a drop in customer complaints and gave us a solid repository of reference spectra and chromatograms, which customers draw upon for their own method development.
We engage with university and industrial partners regularly, trading results on new derivatization and coupling protocols. Through shared experience, 4-Phenylphenacyl Chloride stands out as a robust building block for advanced materials and pharma intermediates. When new methodologies emerge for transition-metal-catalyzed cross-coupling or photoredox activation, our team tracks these developments closely.
For those working in discovery synthesis, rapid access to clean, reliable reagents speeds up the path from bench to breakthrough. By following each new trend—such as greener activating conditions or solvent reduction—our production team refines its own methodologies. This agile response keeps our product competitive not only on price, but on its reputation for reliability and minimal side reactivity.
One issue with many fine chemicals is maintaining supply stability when feedstock markets swing. We learned early that securing multiple qualified suppliers for critical inputs like benzil and chlorinating reagents guarantees consistency. By carrying safety stock and forward contracting, we buffer our customers from sudden shortages. This approach paid off during recent disruptions across global shipping networks, where we continued to fulfill standing orders without delay.
Quality control hasn’t reached its endpoint; every new LC-MS method or trace impurity we track feeds another cycle of process improvement. Some of our most insightful updates came from fielding detailed customer audits and implementing real-time monitoring in critical purification steps. Today, many in the industry see these transparency practices as non-negotiable.
In the future, we aim to sharpen our sustainability profile further by switching to less hazardous chlorinating systems and working with collaborative waste processors to reclaim more by-products. And with the pace of regulatory change, readiness to adapt documentation and testing protocols helps us both safeguard customers and contribute to industry best practices.
Making 4-Phenylphenacyl Chloride isn’t just about meeting technical specifications. Each lot reflects accumulated knowledge from years of production, troubleshooting, and open exchange with scientists at every stage. Chemists—whether at the bench, in scale-up, or developing the next blockbuster molecule—need more than a generic reagent; they benefit from reliability, transparency, and shared purpose between user and producer. Every time a customer shares the results of a high-yielding new reaction or flags a subtle impurity, we respond not as passive suppliers, but as invested partners in their progress.