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HS Code |
849057 |
| Chemical Name | 1-(4-Chlorophenyl)ethanol |
| Molecular Formula | C8H9ClO |
| Molecular Weight | 156.61 g/mol |
| Cas Number | 873-56-1 |
| Appearance | White to off-white solid |
| Melting Point | 50-54 °C |
| Boiling Point | 239-241 °C |
| Density | 1.19 g/cm³ |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.561 |
| Flash Point | 106 °C |
| Smiles | CC(O)C1=CC=C(C=C1)Cl |
| Iupac Name | 1-(4-chlorophenyl)ethanol |
As an accredited 1-(4-Chlorophenyl)Ethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle labeled "1-(4-Chlorophenyl)Ethanol," tightly sealed, featuring hazard warnings and lot number for traceability. |
| Shipping | 1-(4-Chlorophenyl)Ethanol is shipped in tightly sealed containers to prevent leaks and contamination. The packaging meets regulatory requirements for safe handling and transportation. It is clearly labeled with hazard information, stored upright, and protected from moisture and extreme temperatures. Standard ground or air freight is used, following all relevant chemical shipping regulations. |
| Storage | 1-(4-Chlorophenyl)ethanol should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from light and moisture. Ensure all storage containers are properly labeled and keep away from direct sunlight. Follow all relevant safety guidelines for handling and storage of chemicals. |
Applications of 1-(4-Chlorophenyl)Ethanol in Industrial ManufacturingAs a dedicated chemical raw material manufacturer, we supply 1-(4-Chlorophenyl)Ethanol for advanced applications within specialty industrial chains. Our product supports precise processes across high-value downstream segments where strict quality, traceability, and technical control are paramount, serving customers from intermediate synthesis to formulated end-products. 1. Pharmaceutical Intermediate Production – Nonsteroidal Anti-inflammatory Drug (NSAID) SynthesisOriginating as a key alcohol-based intermediate, 1-(4-Chlorophenyl)Ethanol features prominently in the synthesis of select NSAIDs by condensing with carboxylic acids for aryl alkylation reactions. Direct input occurs at the early stage of active pharmaceutical ingredient (API) assembly, especially in synthetic routes for diclofenac and related analogues, where precise control of byproducts and product purity is essential for regulatory acceptance. Operations demand strict batch records, validated reaction steps, and unambiguous content assay. Industry compliance standards
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2. Agrochemical Synthesis – Herbicide and Insecticide Active IntermediateChemical formulators employ our product as a coupling and transformation unit in the creation of aryl-ethanol derivatives for distinctly chlorinated agrochemical molecules. Its introduction into aromatic amine and phosphonate synthesis steps ensures stable halogen incorporation, enabling downstream production of high-purity active ingredients for field-grade crop protection products. Agricultural industry buyers require COA-backed traceability and NOAEL conformance to facilitate product registrations worldwide. Industry compliance standards
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3. Fine Chemical Manufacturing – Precursors for Fragrance and Flavor IntermediatesIn the specialty fragrance and flavor industry, our compound operates as a high-purity starter unit in the construction of chlorinated benzyl alcohol structures. It enters acylation and etherification steps to create aromatic derivatives tailored for sophisticated perfumery bases and food-grade aroma chemicals. Producers demand authenticated raw material lot numbers and analytical certifications aligned with ISO QC and allergen-free production environments. Industry compliance standards
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4. Polymer Additive and Modifier Industry – Reactive Monomer and IntermediateResin and engineered plastics processors utilize our material as a functional monomer or reactive chain modifier in the synthesis of specialty polyarylether and thermoset resins. Its aromatic and halogenated structure delivers requisite reactivity in step-growth polymerizations, providing enhanced glass transition temperature and fire retardancy characteristics in final plastics. Reliable DSC/IR lot characterization and supply consistency support stringent industrial quality needs. Industry compliance standards
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5. Specialty Coating and Adhesive Formulation – Performance Enhancing IntermediateAdvanced coatings engineers select our intermediate for constructing chlorinated aryl alcohol-modified resins used in high-adhesion binder platforms. It enters polyurethane and polyester systems to increase chemical resistance and surface durability. Strict documentation and upstream supply verification ensure traceability, while process integration focuses on reaction homogeneity and color stability in finished materials. Industry compliance standards
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Over the years, the specialty chemical landscape has shifted, but one constant through evolving regulations and customer needs has been reliability in core building blocks. Our plant has produced 1-(4-Chlorophenyl)Ethanol for decades, supporting industries from pharmaceuticals to flavors. This material—known in some communities as p-chlorophenylethanol—serves as a quiet foundation behind processes and products people rarely see, yet rely on every day.
Internally, we refer to our standard grade as model CPHE-1045. The white crystalline or off-white powder that leaves our reactors must meet criteria underpinned by years of both analytical work and lived experience with batch-to-batch consistency. Purity isn’t just a number from a machine; it’s the result of thousands of hours invested in refining our process, troubleshooting unexpected variances, and listening to customers confronted by problems in their own manufacturing lines. Our QC team uses validated HPLC and GC protocols, drawing on methods we’ve tuned for this compound’s unique character—its modest solubility, its sensitivity to pH, its precise melting range.
We adjust process parameters repeatedly, because small details make large differences downstream. We use only raw materials tested in-house rather than accept vendor assurances. Each drum and bag gets an internal traceable code. There’s a practical reason: many pharmaceutical syntheses depend on our 1-(4-Chlorophenyl)Ethanol’s consistently low impurity profile, with no odd peaks in the chromatography, so the final intermediates meet the strictest regulatory needs.
Our regular clients include developers of antihistamines, agricultural substances, and performance materials. In these industries, chemists use 1-(4-Chlorophenyl)Ethanol as a synthesis intermediate. For example, a customer troubleshooting their process for a new active ingredient once traced the source of an uncontrollable impurity to their alcohol component. By switching to our tightly specified product, they cut purification steps and stabilized their process yield.
Many flavor and fragrance companies look for ingredients that impart a balance of aromatic strength and stability. Here, 1-(4-Chlorophenyl)Ethanol finds a niche—its benzene ring, altered by chlorine’s electron-withdrawing effect, gives a more controlled reactivity in acylation and etherification reactions than unsubstituted phenylethanol. Over the years, we have seen novel applications emerge. From new surfactant R&D to the creation of specialty resins, this product stands out for the reproducibility that our process provides.
There are many commercial sources—what distinguishes material made by us? The answer comes from years spent listening to real-world requirements, not just designing on paper. Labs and factory buyers usually mention how our material dissolves cleanly without unexpected haze. They report fewer process interruptions due to unpredictable side reactions. One client credits low oxidation byproducts for helping them register a key intermediate with regulatory authorities in the EU.
We focus on minimizing trace moisture, halide ions, and aromatic impurities—real impurities that can catalyze degradation or reduce selectivity in pharmaceutical campaigns. We achieve this through a specialized crystallization and washing regime, refined with feedback from partners facing GMP audits and scale-up setbacks.
Every time we get an inquiry about quality spec deviations, we find the root often lies in overlooked variables: tiny solvent residues, micro shifts in pH, or subtle changes in crystal habit. As manufacturers, we learned the hard way that any shortcut—be it skipping a purification stage or loosening raw material specs—will reveal itself in customer complaints or, worse, failed product batches. Our commitment isn’t driven by marketing; it is a daily response to the real risks inherent in chemical production.
Many replacement or off-brand products seem attractive because of lower price points, but they rarely withstand scrutiny over months or years. We have observed clients lose thousands on reprocessing or waste as a result of “off” batches with subtly different reactivity. More than one customer with ‘urgent’ last-minute requests came back to our product after pilot trials with competitors failed to scale or generated unmanageable byproduct profiles.
Our product enables not just routine runs but innovation at the bench. In custom synthesis, small variations in reagent behavior can waste labor or overturn a development project. The consistency of our 1-(4-Chlorophenyl)Ethanol—measured by running dozens of pilot reactions across multiple lots—has supported startups developing new therapy classes and new crop protection agents. In-house technical service, staffed by chemists who worked in synthesis before moving to quality, has supported clients as they troubleshoot unexpected kinetics or isolation issues.
One biotech startup, sweating delays on a tight timeline, received not just drums but comprehensive lot data and our recommendations on storage and solvent compatibility, based on our experience handling the compound in bulk. Their process worked as modeled, helping them move from bench to pilot plant in less than eight weeks.
We shipped custom particle size batches, ground under controlled temperature to support a drug company formulating a new salt form, because in formulation, flowability or dissolution rate can matter almost as much as purity. Through such collaborations, we gain direct feedback that refines our understanding of real-world challenges.
In actual production, safety and sustainability are non-negotiable. Handling chlorinated aromatics brings risks we address with exhaustive training and monitoring. As managers and operators, we pay special attention to atmospheric emissions and controlled waste handling. Local and global regulations drive us to design our processes for closed-loop solvent recycling, thermal destruction of residues, and regular effluent testing.
Besides following legal standards, we invest in equipment for better containment and personal protection, because nothing slows a plant more than an unexpected release or regulatory visit uncovering gaps. Our employees review safety protocols regularly; improvements in chemical addition or reactor design have come straight from shop floor suggestions. Inspection agencies have found our documentation clean and reflective of actual practice because hands-on operators and supervisors actively shape our procedures.
Real-world use rarely matches the assumptions of academic research; batch cycles, temperature swings, or even minor contamination from upstream processes can affect outcome. We do not frame 1-(4-Chlorophenyl)Ethanol as a single static product—we deliver it as part of an ongoing relationship with clients who call when batches drift, when color shifts occur, or when a new impurity is spotted.
On one occasion, our customer’s equipment change altered reaction yields; by reviewing their process with them and reviewing our own plant records, we traced the issue to solvent carryover at their site, not a shift in our own product compounding. These kinds of collaborations, where manufacturer and customer pool expertise, have built long-standing trust. The real-world understanding gained from hundreds of discussions with technical managers, QC analysts, and operators guides every adjustment we make to specifications, packaging, or technical support.
Large-scale users want assurance of continuous supply. Our experience shows raw material scarcity and logistics disruptions can interrupt critical manufacturing. We hold buffer stocks of both product and key precursors, and monitor global shipping cycles to minimize risk for customers with tight timelines. Our standard packaging—fiber drums with multilayer liners—evolved after direct feedback about clumping or contamination in older-style bags. We introduced dedicated loading bays for this compound after a near-miss shipment that almost crossed with an incompatible aromatic intermediate.
Every batch goes out with full analytical documentation, and transport logistics are coordinated to manage temperature and humidity exposure—not simply at the port but through to the customer’s facility. If a customer ever reports transit damage or shift in properties, our logistics and quality teams launch direct communication, sometimes retrieving suspect drums for root cause investigation.
What we learn on the plant floor shapes every improvement—be it in analytical method, batch record, or packaging. Listening to customer returns and complaints, we act on feedback rather than sending out canned responses. Once, after repeated comments about static generation during transfer in dry conditions, we adapted our process to include anti-static additives in liner films. In another instance, customers reported difficulties in integrating our product in high-throughput feeder systems, so we revised our granulation size.
We do not regard these changes as burdens, but as shared solutions—because someone mixing tonnage in a reactor in upstate New York, or prepping a kilo batch in a Tokyo lab, can see different challenges than those designing specs in a conference room.
1-(4-Chlorophenyl)Ethanol offers important reactivity distinctions compared to related alcohols such as 1-(2-chlorophenyl)ethanol or the unsubstituted phenylethanol. The para-chloro group changes electronic distribution, allowing more predictable behavior in reductive or coupling steps. In reactions where ortho substitution can bring sterics and side reactions, the para isomer gives cleaner transformations. Over time, formulators and synthetic chemists have noted that p-chlorinated variants avoid the excessive volatility or odor issues of unsubstituted analogs, making plant-scale handling simpler and less prone to fugitive emissions.
Comparisons with halogen-free analogs reveal further differences: the chlorine atom confers slightly higher density, changes the partitioning in certain solvent systems, and can subtly affect final product stability. These differences alter, for example, how flavor molecules behave in a beverage system, or how intermediates crystallize in APIs destined for solid-dose forms. We have worked with clients switching from meta- or ortho-substituted materials to our para compound to troubleshoot unanticipated reactivity or separation concerns.
No chemical manufacturer stands still. New applications, tighter regulations, and supply chain bumps drive continual investment in both plant and people. Over the past year, tightening environmental rules on legacy solvents have compelled us to reengineer not just waste treatment but core reaction pathways. Labs developing greener transformation methods seek more predictable raw materials, and we have responded by building alternate grades for projects testing enzymatic synthesis or continuous-flow processes.
We keep an open channel with research consortia and academic partners. Many insights originated outside our company—university work on process intensification, customer pilots looking to reduce organic residues, or global efforts to minimize persistent organic pollutants. These experiences shape how we prepare, analyze, and ship each drum.
To those using 1-(4-Chlorophenyl)Ethanol as a minor ingredient, switching suppliers can appear low-risk, but in our years as a manufacturer, true reliability emerges only after repeated cycles of scale-up, stability, and field use. Years of handling customer complaints, refining QA procedures, or dealing with unexpected plant upsets have tested our material in ways no catalog specification can cover. Whether customers use tons per month or kilos per campaign, our role is to reduce their risk and respond when something unforeseen arises.
What matters most is transparency, responsiveness, and a shared commitment to actual process success—a bond built less on marketing claims, and more on years of practical engagement between those who manufacture and those who rely on that expertise to keep their own production moving. That, for us, remains the real story behind every bag, drum, and shipment of 1-(4-Chlorophenyl)Ethanol we make.