|
HS Code |
255199 |
| Chemicalname | 2-Chloro-4-Methoxyphenol |
| Molecularformula | C7H7ClO2 |
| Molecularweight | 158.58 g/mol |
| Casnumber | 3964-52-1 |
| Appearance | White to light beige solid |
| Meltingpoint | 64-67 °C |
| Boilingpoint | 283 °C |
| Density | 1.33 g/cm³ |
| Solubilityinwater | Slightly soluble |
| Refractiveindex | 1.576 |
| Smiles | COC1=CC(=C(C=C1)Cl)O |
| Inchi | InChI=1S/C7H7ClO2/c1-10-6-3-2-5(8)7(9)4-6/h2-4,9H,1H3 |
| Synonyms | 2-Chloro-p-Guaiacol |
As an accredited 2-Chloro-4-Methoxyphenol 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 2-Chloro-4-Methoxyphenol; features a secure screw cap and hazard labeling. |
| Shipping | 2-Chloro-4-Methoxyphenol is shipped in tightly sealed, clearly labeled containers to prevent leaks and contamination. It should be handled as hazardous material and transported according to local, national, and international regulations. Avoid exposure to moisture, sunlight, and incompatible substances during transit. Appropriate documentation and safety data sheets accompany each shipment. |
| Storage | 2-Chloro-4-Methoxyphenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from light and moisture. Avoid sources of ignition and heat. Proper chemical labeling is essential, and containers should be stored at room temperature, away from direct sunlight and any conditions that could compromise integrity. |
Competitive 2-Chloro-4-Methoxyphenol prices that fit your budget—flexible terms and customized quotes for every order.
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From a manufacturer’s bench, watching a molecule develop from raw feedstock into a refined chemical is an exercise in commitment. Over the years, 2-Chloro-4-Methoxyphenol has become a regular presence in our reactors. We’ve seen the chemical world shift toward specialty phenolic compounds for their structural versatility, and this compound’s unique blend of chlorine and methoxy substitutions sets it apart. Producing it in volume, then purifying it past rigorous benchmarks, takes more than catalogue chemistry. Each batch starts with fresh supplies of starting materials that must pass our incoming quality inspection—if a drum of chlorinated precursor gives even slightly off readings, that’s a candidate for return, not reaction. Reliability depends as much on those checks as on the final testing.
Day-to-day, our work stretches across process optimization and real-time analytics. The compound’s chemical makeup, featuring a chloro group at the ortho position and a methoxy group at the para position on the phenolic ring, tends to attract technical buyers facing demands for purity and consistency. Making a 99%-plus pure product is a point of pride for our team, in part because even minor side products can interfere with downstream uses in pharmaceuticals or fine chemical synthesis. Maintaining that purity through crystallization, washing, and drying requires attention to the residue, temperature profiles, and solvent control at every stage.
Our experience underlines an important reality: if a batch leaves the line at 98%, yields a byproduct peak in the HPLC that we cannot explain, it gets pulled from external shipment schedules. We stem shipping until we clarify the anomaly. This level of traceability is neither a market buzzword nor a spreadsheet checkbox. After years of feedback from downstream partners, labs, and formulators, this hard line means fewer recalls, less troubleshooting, and improved production cycles at their plants. These details matter more than simply hitting a stated assay on a certificate.
Each time we field a technical inquiry, we recall the years spent fine-tuning the properties of our 2-Chloro-4-Methoxyphenol. Its combined electron-withdrawing and electron-donating groups on a single aromatic scaffold make it a favored starting material for several synthesis routes. Whether destined for an active pharmaceutical ingredient or crafted into an agrochemical, the molecule can tolerate functionalization steps that challenge other phenols. Through every kilogram we scale up, the melting point and moisture sensitivity guide our drying protocols, so our product doesn’t clump or degrade when it meets blending equipment or pilot reactors.
Some of the most robust projects we’ve participated in have come from teams looking for custom functionality not found in 4-methoxyphenol or 2-chlorophenol alone. Development chemists require a phenolic intermediate that doesn’t feed unintended side reactions or degrade in slightly harsher reaction conditions. The presence of the methoxy group at the para position means improved stability during O-alkylation or halogenation, compared to unsubstituted or meta-substituted variants. The chloro group, by contrast, opens up direct routes to cross-coupling or nucleophilic aromatic substitution, reducing the need for further protective-group strategies.
Years of collaborating with formulation chemists reveal clear feedback: 2-Chloro-4-Methoxyphenol often trims a step or two from their sequence. Instead of dealing with reactive phenols that oxidize in storage, our product gives a comfortable window of stability. Our storage and transportation protocols reflect this practical demand. Drums leave our site in climate-controlled trucks, with tamper-evident seals and moisture barrier liners. We verify these practices with every shipment, not as a selling feature, but as a safeguard for everyone’s process.
Technical literature can supply the basics: CAS number, melting point, solubility in common solvents. The backstory unfolds in the production halls. As a plant team, we’ve spent enough seasons bringing on new reactors and updating QA routines to realize that producing 2-Chloro-4-Methoxyphenol isn’t a plug-and-play operation. Batch consistency hangs on vigilance. The exothermic chlorination stage, for instance, requires cooling circuits that react in real time to pressure spikes. In the earliest runs, we saw that overaggressive cooling would crash out intermediates prematurely. Too little, and the process drifted out of proportion. Each lesson landed on our logs, and each tweak led to sharper yields and cleaner product.
It’s tempting in this industry to chase yields at the expense of post-production purity. We invest more in fractionating columns and isolated crystallization vessels than some competitors. This means longer cycle times but also fewer headaches downstream. In customer audits, our process maps draw attention for their granularity: each process parameter gets logged and archived from raw input to finished lot, so any deviation stands out and gets corrected.
End users—many of whom call up directly to our lab—have reported success with applications ranging across pharmaceuticals, photography chemicals, and specialty polymers. Its reactivity profile fits neatly into Suzuki and Buchwald-Hartwig coupling schemes as a precursor, delivering flexibility when introducing further substitutions. The product's phenolic hydroxyl can anchor in esterification or etherification reactions without losing selectivity. Medicinal chemistry groups value the chloro group as a potential leaving group, or as a seed for constructing more complex ring systems.
Over the years, our partners have pointed out savings in their waste management protocols by using our material in place of similar halogenated phenols that yield heavier byproducts or generate problematic tar during work-up. The methoxy group’s electron-donating effect means milder oxidation steps when advancing toward more functionalized targets. These downstream efficiencies don’t show up on a spec sheet, but they save operators time and raw materials—worth real dollars on an annual balance sheet.
Seeing the material in context matters. Chemists presented with a catalogue of aromatic phenols quickly see the distinction between 2-Chloro-4-Methoxyphenol and its relatives. Take 4-methoxyphenol, for example—a widely used antioxidant stabilizer. Lacking the ortho-chloro, it participates differently in cross-coupling and does not withstand elevated temperatures with the same resilience. It tends to oxidize quicker in air, shortening shelf life. Conversely, 2-chlorophenol lacks the methoxy stabilizer, introducing harsher reactivity that doesn’t always suit multi-step syntheses, where selectivity and control bring down costs and unpredictability.
Our experience demonstrates that customers shifting from simple chlorophenols to our compound immediately notice less tar in their columns and fewer impurities in their downstream analytics. It’s not theoretical chemistry; after process swaps, technical teams call to report sharper final product HPLC profiles. Even in photography chemicals, the combination enhances image stability compared to more basic phenols, reducing the frequency of spot tests and maintenance cycles on commercial-scale processors.
As manufacturers, quality means more than keeping the item on a shelf or promising a minimum assay. Over dozens of production campaigns, we have seen small changes in solvent selection or reaction sequence impact final color, flow, and reactivity. Nitrobenzene traces or byproduct esters, if not caught, can catalyze spoilage. Our in-house team meticulously tailors every purification step—including careful recrystallization—and applies a full array of in-process controls. We favor GC-MS and UV-Vis analytics for detecting minor impurities over less precise tests, based on back-and-forth discussions with downstream users on what ultimately matters during formulation.
Feedback loops with end users have driven several improvements over the years. A recurring concern from pharmaceutical partners involved trace residual solvents detectable at the parts-per-million level. In response, we invested in longer vacuum cycles, phase-transfer catalyst screening, and solventless wash protocols, reducing average residues per batch. These changes weren’t speculative—they arose from repeatedly failed API synthesis attempts in our customer’s labs until we identified the critical root-causes with them, then retrofitted our own line.
A product like 2-Chloro-4-Methoxyphenol doesn’t thrive in long chain-of-custody arrangements. We pack and document all logistics in-house rather than leaving it to generic contract warehouse partners. Tightly sealed drums, silica gel inserts, and opaque lining shield the chemical from moisture and UV. Our on-site team inspects humidity around product storage weekly. Shipments move on a just-in-time basis straight to customer docks, limiting time spent outside controlled settings.
We believe safety grows with familiarity. Over years of handling, we have learned that 2-Chloro-4-Methoxyphenol delivers a mild phenolic odor, but vapor exposure remains manageable with typical PPE standards. Written procedures, eyewash stations near bottling lines, and routine staff training help prevent mishaps. Our plant manager reviews all incident reports monthly for patterns. We work directly with partners to customize batch sizes, so operators don’t handle excess volumes or rush through weigh-outs.
The chemical marketplace often favors large volumes and generic intermediates. Specialties like 2-Chloro-4-Methoxyphenol carve out a niche built on reliability and performance feedback. We monitor regulatory updates and revise our quality management protocols to trace every lot number, linking data across synthesis, shipping, and user feedback.
This experience creates trust. Our QC manager stands behind each test result, and our technical support doesn’t defer questions to another time zone or turn over repeated queries to sales desks. Long-term relationships emerge from decades of shared troubleshooting, not from digital paperwork or branding exercises.
Chemicals aren’t commodities for the end user faced with a critical batch or late-stage development hurdle. Instead of swapping one phenol for another, most process engineers prefer getting consistent, predictable reactions every time a drum is opened. Repeat order data and long tenures in the business tell us this lesson over and over. Efficiency in scale-up and device compatibility sometimes depends on minor tweaks in purity and impurity profiles that only a manufacturer sees and can address.
Often, users face challenges ranging from minor inconsistencies during formulation trials to regulatory hurdles around residuals or labeling. Years of industry experience have guided us toward practical, technology-driven solutions. Working alongside equipment suppliers, process engineers, and application specialists, we regularly reassess our SOPs, updating everything from in-line drying systems to segregated processing tanks for different aromatic phenols. Each challenge leads to measurable improvements—not documented in procedural manuals but in reliability out on the line.
Modern applications increasingly demand near-zero impurity contents or tailored reactivity. Continuous dialogue with our partners produces joint trials: supporting development teams with samples for analytical benchmarks or running split-batch tests to validate process yield improvements. Iterative improvements, informed by real-world use cases, sharpen our understanding of exactly how 2-Chloro-4-Methoxyphenol performs—insights that extended well beyond academic journals or safety data sheets.
Working with phenolics in today’s regulatory climate means aligning every process with both regional and international standards. Auditors and compliance monitors demand documented traceability. Experience confirms that real compliance emerges from disciplined internal reviews, not merely ticking off a checklist. Every scale-up, every line cleaning, every raw material swap gets cross-checked against our risk assessment protocols.
Where issues emerge—say, a new overseas client flags a need for revised labeling in another language or increased documentation for substance traceability—our regulatory team collaborates quickly across departments to deliver what’s needed. This level of responsiveness has allowed us to serve global markets without service interruptions or compliance problems.
The field won’t stay static. Research and end-user expectations shape the future of compounds like 2-Chloro-4-Methoxyphenol. Common feedback signals a growing preference for greener, more sustainable chemistry. We’re moving forward with targeted studies for lower-emission processes and solvent recycling. Interest in circular chemical manufacturing leads us to analyze lifecycle impacts and explore ways to cut energy use and reduce byproduct generation.
New applications fuel deeper innovation. We receive regular inquiries from biotech labs and electronics manufacturers probing whether the product fits in next-generation materials. Each request drives us to test hypotheses, establish new benchmarks, and stretch our process controls to meet emerging purity and functionality requirements.
Producing 2-Chloro-4-Methoxyphenol is more than chemistry. The expertise, engineering, and collaborative touchpoints woven into each shipment showcase the difference manufacturing experience makes. Traceable data, lot-by-lot transparency, and process improvements come from decades of close work with real users across industries.
Through these efforts, every customer project builds on a foundation of discipline and flexibility—including tailored specs, detailed analytics, and responsive troubleshooting. Unlike generic alternatives or off-the-shelf phenols, each drum produced here represents a deeper understanding of what customers need and how downstream processes can benefit. Offering more than just a molecule, our approach carries forward the knowledge, care, and innovation needed to help partners achieve better outcomes in their fields.