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HS Code |
711511 |
| Iupac Name | 3-(4-chlorophenyl)propan-1-ol |
| Molecular Formula | C9H11ClO |
| Molecular Weight | 170.64 g/mol |
| Cas Number | 34841-35-5 |
| Appearance | White to off-white solid |
| Melting Point | 53-56°C |
| Boiling Point | 290-292°C |
| Density | 1.19 g/cm³ |
| Smiles | C1=CC(=CC=C1CCC(O))Cl |
| Inchi | InChI=1S/C9H11ClO/c10-9-4-2-8(3-5-9)6-1-7-11/h2-5,11H,1,6-7H2 |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.563 |
As an accredited 3-(4-Chlorophenyl)Propan-1-ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 3-(4-Chlorophenyl)propan-1-ol, labeled with hazard symbols, chemical name, and batch number. |
| Shipping | 3-(4-Chlorophenyl)Propan-1-ol is shipped in secure, chemical-resistant containers to ensure safety and prevent contamination. The package is clearly labeled with hazard information, handled by licensed carriers, and complies with all relevant transportation regulations for chemical substances. Shipping includes documentation for identification and regulatory conformity. |
| Storage | Store **3-(4-Chlorophenyl)propan-1-ol** in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, ignition sources, and direct sunlight. Keep separate from oxidizing agents and acids. Properly label the container and ensure compatibility with storage materials. Follow all applicable safety regulations, and use personal protective equipment when handling the substance. |
Applications of 3-(4-Chlorophenyl)Propan-1-ol in Industrial ManufacturingAs the direct manufacturer of 3-(4-Chlorophenyl)Propan-1-ol, we supply this high-purity intermediate to specialized sectors supporting advanced chemical processes. Below, we present main industrial application scenarios strictly based on established downstream practices, regulatory framework, and process workflows. 1. Synthesis of Antidepressant Active Pharmaceutical Ingredients (APIs)Pharmaceutical producers rely on 3-(4-Chlorophenyl)Propan-1-ol in multi-step syntheses for selective serotonin reuptake inhibitor (SSRI) molecules, notably as an intermediate in the transformation to active drug compounds. Use spans from pilot to commercial scale, requiring batchwise addition following validated synthesis protocols. Engineers adjust charge quantities based on route optimization, with rigorous analytical methods monitoring conversion rates and impurity profiles. The material’s purity and traceability facilitate batch release for further synthetic steps under GMP environments. Industry compliance standards
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2. Fragrance Ingredient ManufacturingProducers of aromatic alcohols utilize 3-(4-Chlorophenyl)Propan-1-ol to develop specialty perfumery bases, especially in compounds where aromatic and slightly spicy notes are needed. Technicians introduce this raw material during the condensation or esterification stage, often reacting it with aromatic acids to yield esters with defined olfactory profiles. Process reliability focuses on minimizing unwanted side reactions and maintaining consistently low impurity levels for IFRA compliance. Industry compliance standards
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3. Agrochemical Intermediates in Herbicide SynthesisAgrochemical manufacturers employ 3-(4-Chlorophenyl)Propan-1-ol as a structural intermediate for the development of selective herbicide molecular scaffolds. The compound enters the process at pre-condensation stages, enabling the introduction of the 4-chlorophenyl group essential in several proprietary herbicidal actives. Operators prioritize control of moisture and by-product minimization, guided by technical specifications agreed with major crop protection customers. Industry compliance standards
Typical usage ratio
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4. Specialty Polymer Modifier ProductionSpecialty polymer processors incorporate 3-(4-Chlorophenyl)Propan-1-ol as a chain modifier in the synthesis of functionalized polyesters and epoxy resins. Its primary alcohol group participates in esterification and crosslinking reactions, influencing molecular weight distribution and imparting unique mechanical properties. Chemists select charge levels according to targeted end-use characteristics, such as toughness or chemical resistance, while maintaining strict adherence to batch reproducibility guidelines. Industry compliance standards
Typical usage ratio
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In the world of fine chemicals, every step matters. Manufacturing 3-(4-Chlorophenyl)Propan-1-ol takes more than just good raw materials and a strict batch record. Decades standing in front of reactors and analyzing product streams taught me: little things matter. Our 3-(4-Chlorophenyl)Propan-1-ol, sometimes called 4-chlorohydrocinnamyl alcohol, finds its strength in real details, not marketing gloss. That clarity comes from handling every phase of production in our own plant, keeping a constant eye on what it means for those using this molecule in practical applications.
This compound belongs to the alcohol derivatives of substituted propanols, sporting a para-chlorophenyl ring. Not all versions meet the same bar. Our typical batch offers a purity exceeding 99.5% by GC analysis. Reactions involving aldol condensation and careful hydrogenation get us there consistently. By repeatedly testing each lot against authentic references using HPLC and NMR, we confirm batch-to-batch reliability. It’s not just a number on a certificate. Our longtime chemists can spot even faint contaminants that might go undetected elsewhere.
Over the years, we’ve had requests for different grades of this product. Some clients want trace metals below a specific threshold; others care most about moisture content. That feedback gets discussed at weekly production meetings, not just filed away. If a client needs to avoid residual solvents, we adjust purging protocols using rotary evaporation under reduced pressure. We’ve even received raw feedback from end-users when a subtle impurity affected a downstream reaction. Working through those issues gave us the experience that no textbook can replace.
The structure of 3-(4-Chlorophenyl)Propan-1-ol turns it into a valuable building block. The chlorinated aromatic ring provides a versatile handle for coupling reactions, and the terminal alcohol group adds flexibility for further transformations. Chemists in pharmaceutical development, agrochemical trials, and specialty materials research use this combination when they need selectivity and reactivity without sacrificing stability.
We’ve participated in projects where this compound played a key role as a precursor to β-adrenergic agents and other small molecules in drug pipelines. Strong relationships with R&D teams taught us that reaction by-products or unanticipated side-reactions complicate scale-up. That is why our in-house analytical group routinely monitors isomer content, focusing on para/ortho-impurity ratios to avoid downstream headaches during process optimization.
There is nothing generic about chemical manufacturing. Our 3-(4-Chlorophenyl)Propan-1-ol typically ships under the production model QP317B. This designation reflects its route of synthesis: selective reduction of 3-(4-chlorophenyl)propiophenone, followed by controlled workup. Analytical specs have grown over the years through constant customer dialog. We set the minimum assay above 99.5%, water content below 0.1%, halide traces under 25 ppm, and color index by APHA method below 20.
As production volume climbed, we saw different customers cared about different traits. One group flagged concerns over benzyl alcohol contamination; since then, our GC protocol covers this specific peak. Another needed larger volume packaging due to intensive pilot-plant trials, so we switched to bulk HDPE carboys with inert gas padding. The specs became a living document as varied users shared real feedback about reactivity, long-term storage, and compatibility with scale-up synthesis demands.
We ship most of our product into pharmaceutical intermediates. Medicinal chemists often select 3-(4-Chlorophenyl)Propan-1-ol at the scaffold design stage, since the para-chlorine supports further derivatization, such as etherification or amide formation. They tell us that our alcohol’s low impurity profile reduces time wasted in purification and column workup. For these clients, unexpected color, odor, or residue means delays and increased cost—concerns we share, since our own plant has lived through frustrated callbacks.
In the crop science sector, this compound often acts as a nucleus for creating fungicide candidates. Our customers working on combinatorial synthesis value the high consistency in halogen substitution, since even small shifts in substitution patterns can mean a project’s success or failure. We once worked closely with a team developing an anti-mildew prototype; controlling side-product formation at our end made their SAR studies less ambiguous and kept their timeline on track.
Some clients in materials chemistry use 3-(4-Chlorophenyl)Propan-1-ol as a linker in polymer synthesis. They rely on our tight specs around trace metals, since even minor elements like iron or nickel can instigate unplanned crosslinking during catalysis. Several years ago, after alerts from a polymer engineering group, we installed new stainless-steel lines and applied stricter metal leaching controls. Direct feedback loop between user and manufacturer, ultimately benefiting finished product properties.
Labs and plants face a choice: many producers offer compounds that look similar on paper, but our clients soon notice the differences that matter during routine production. Multiple rounds of recrystallization, meticulous pH correction, and vacuum drying distinguish our batch from a bulk trader’s resold lot. There’s a real difference in how a reaction unfolds when the minor unknowns are under control.
High-concentration solutions in DMF or DMSO remain clear, with no insoluble specks at 20°C, a sign of good purification and careful solvent management during production. Customers running synthesis at scale frequently send us updates on reaction yields; they see consistent results over dozens of lots, not just the first few shipments. The drum you get in January boasts the same purity profile as one arriving in October. Our team thinks through how temperature cycling, drum headspace, and local humidity affect product stability.
We once audited a client’s pilot plant after unanticipated yield drops. Their tech team flagged differences tied to very fine particulate contamination, and we traced it back to an outdated filter module in one section of our downstream process. After switching to a sintered metal design and starting inline particle monitoring, those issues disappeared, and so did client complaints about column blockages. That episode sharpened our focus on details others might overlook in a fast-paced market.
Many alcohols offer some aromatic substitution. Few combine the para-chloro ring and propanol chain, giving this molecule a unique combination of lipophilicity, modest polarity, and reactive points. Simple benzyl alcohols can oxidize or discolor over time in storage. Straight-chain propanols, without the aryl group, lack the ability for π-π stacking and don’t serve as effective structural platforms in drug design.
We’ve processed orders for clients who started projects using plain cinnamyl alcohol, only to switch after solubility or reactivity mismatches surfaced. The 4-chloro version resists aerial oxidation during bench storage, keeping color and performance stable over extended testing runs. Some teams build up combinatorial libraries of substituted alcohols, looking for patterns in biological response; those projects thrive on analytical consistency. The para-chlorine substitution also creates a site for directed ortholithiation, which isn’t possible with simple propanols or unsubstituted aryl alcohols.
Producing 3-(4-Chlorophenyl)Propan-1-ol at ton scale forces us to confront process challenges that don’t pop up in the lab. Heat transfer, exotherm control, and cleaning validation between lots—those headaches push us every month to tweak our SOPs. Even the way we add hydrogen source, or the phase separation between organic and aqueous layers, changes when you scale to 2,000 liter reactors.
Stability during storage came up early on. The alcohol group invites moisture pickup, especially in humid summers. We invested in nitrogen blanketing for our bulk tanks after repeated customer reports of slight water uptake during international shipping. Desiccant packs, HDPE liners, and dual-seal drums became standard in response to real-world complaints, not marketing slogans. It is this sort of attentiveness, paired with willingness to open up our operation to client audits, that built our reputation as a reliable partner, not just a supplier.
Every year brings new regulatory pressures. REACH compliance, changes in allowable residual solvent levels, and shifts in customer corporate responsibility requirements—none of these stays static. We saw an uptick in calls for green chemistry approaches. Real-time feedback from environmental managers motivated us to overhaul our waste neutralization process, switching from legacy organomineral treatments to a catalyzed, zero-waste evaporation method.
We’ve spent days working through confusion over regulatory equivalency. Some regions accept slightly different analytical methods for impurities or isomeric ratios. We often get live questions from client QA teams on how we prove absence of aryl chlorides or control for potentially mutagenic impurities. For us, it’s normal to share our batch protocols, let customers run their own independent analyses, and track deviations across lots all the way back to individual operators and shifts.
In process development, chemists learn quickly that small differences upstream multiply when running large-scale reactions. With 3-(4-Chlorophenyl)Propan-1-ol, they typically report improved crystallization and a drop in tar formation during oxidation steps if they use material from our plant versus commodity grades. One partner in API synthesis told us their yield variance decreased from 10% to just 3% after switching over several pilot-scale runs—this after repeated GC-MS analysis showed clear differences in tailing peaks for the competitor’s lots.
Teams working in continuous flow setups frequently run test charges of several vendors’ material. We send not just a certificate, but a sample and an invitation to send feedback—good, bad, or perplexing. Over the years, we’ve moved from single-batch supply to multi-year framework contracts, with frequent on-site visits that deepen mutual experience and foster true process understanding.
We don’t take quality claims on faith. Every production run includes split samples that go to both our internal QA and to at least one external accredited lab. This redundancy caught two minor mis-labeling incidents in past years, allowing us to intercept affected material before shipment. There’s a policy here: if something seems off—color hint, slight off-odor, drift in chromatography—production pauses until we dig in, not just wave it through because the numbers look fine on average.
Customers ask about storage and handling even after years of doing business with us. We don’t pretend that any organic alcohol can just sit in any warehouse under any conditions. Light, humidity, drum headspace, and seal integrity all shape product shelf-life. So we train staff constantly on correct filling, sample withdrawal, and sealing. It saves us headaches later, and keeps conversations honest when troubleshooting.
International customers notice differences in transport resilience. Months spent sitting in port or under customs inspection can change more than just delivery timelines. Temperature spikes, long vibration periods, and local environmental controls all play a role in ensuring the alcohol arrives as clean as it left us. We’ve transitioned to improved thermal insulation and double-sealed drum closures, along with shock-absorbing pallets for main routes passing through rough transport infrastructure.
Sometimes we’ve lost sleep over off-label repackaging by intermediaries, which can introduce unforeseen contamination. That’s one reason we encourage customers to order in drum sizes that fit straight into their plant protocols, not repack staff. Vigilance at every node of the supply chain protects integrity, and where possible, direct-to-user shipments limit transfer risks.
Chemistry doesn’t stand still. Every year, teams across different industries push our molecules into new applications. Our first batches shipped to university labs exploring radical addition chemistry; today, much of our output feeds global generics producers and agrochemical factories. We have learned to expect change, to track feedback closely, and to approach each new request as a chance to further refine our offering. No product spec remains static, and no process runs on autopilot.
Better analytics, stricter regulations, and new synthesis approaches all shape the future of 3-(4-Chlorophenyl)Propan-1-ol production. By focusing on concrete process improvements, listening hard to what real users report from their benches and reactors, and benchmarking our output relentlessly against real situations—not only our own but those of others—we keep this product competitive, reliable, and responsive. Experience, not just machinery or certificates, defines the difference our compound makes in practical chemistry worldwide.