|
HS Code |
311622 |
| Chemical Name | 3-Chloro-2-Methoxyphenol |
| Molecular Formula | C7H7ClO2 |
| Molecular Weight | 158.58 g/mol |
| Cas Number | 7780-94-3 |
| Appearance | White to light beige solid |
| Melting Point | 59-62°C |
| Boiling Point | 281°C (estimate) |
| Density | 1.34 g/cm³ (approximate) |
| Solubility In Water | Slightly soluble |
| Smiles | COC1=CC(=CC=C1O)Cl |
| Inchi | InChI=1S/C7H7ClO2/c1-10-7-4-5(8)2-3-6(7)9/h2-4,9H,1H3 |
| Flash Point | 151.8°C |
| Refractive Index | 1.567 (estimate) |
As an accredited 3-Chloro-2-Methoxyphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle labeled "3-Chloro-2-Methoxyphenol, 100g." Features chemical structure, hazard symbols, batch number, and safety instructions. |
| Shipping | 3-Chloro-2-Methoxyphenol is shipped in tightly sealed containers, protected from moisture and light. It should comply with relevant chemical safety regulations, including labeling and documentation. The shipment must avoid extreme temperatures and be handled as a potentially hazardous substance, following all applicable transport guidelines for chemicals to ensure safe delivery. |
| Storage | 3-Chloro-2-Methoxyphenol should be stored in a tightly closed container in a cool, dry, and well-ventilated area. Protect it from direct sunlight, heat, and incompatible substances such as strong oxidizing agents. Keep the storage area secure and clearly labeled. Ensure appropriate chemical spill containment and have suitable safety equipment, such as gloves and eyewash stations, available nearby. |
Competitive 3-Chloro-2-Methoxyphenol prices that fit your budget—flexible terms and customized quotes for every order.
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3-Chloro-2-Methoxyphenol stands out as a key intermediate for many chemical processes. From my years on the production floor, minor tweaks in molecular structure can make a pronounced difference, both in reactivity and application. This compound — also referred to in the lab as 6-chloro-o-vanillin or 3-chloro-guaiacol — offers a unique combination of chloro and methoxy groups on a phenol base. These contribute to its versatility in fine chemical synthesis, especially in the pharma, agrochemical, and fragrance sectors.
Handling barrels and kilo-packs of 3-Chloro-2-Methoxyphenol, I’ve seen its fine crystalline or powder form, which gives easy access to precise dosing and mixing. The melting point and bulk density usually remain stable over long periods. Purity rarely dips below 98 percent in our output, even with industrial-scale throughput. This consistency reduces downstream troubleshooting for clients. Chlorination and methoxylation steps during our synthesis route ensure a low residual content of starting phenols and minimum byproduct, translating to cleaner product flows.
Most of our testers run product quality checks via HPLC and NMR, finding predictable peaks without traces of heavy impurities or abnormal byproducts. Water solubility stays limited, restricting its use to mostly organic-phase reactions or solvent-based systems. In the plant, we clearly separate each production batch and maintain color-monitoring procedures — this compound, if pure, doesn’t drift into the yellow-brown hues that commonly signal phenol oxidation.
Our customers most frequently purchase 3-Chloro-2-Methoxyphenol as an intermediate for active ingredient synthesis. Pharmaceutical labs use it as a direct precursor in the synthesis of antibacterial agents, anti-inflammatory compounds, and some niche central nervous system drugs. With the chloro and methoxy pairing, medicinal chemists find greater selectivity during aromatic substitution or amination reactions. These subtle differences foster higher yields and fewer side-products compared to unsubstituted phenols or those carrying just one functional group.
Agrochemical formulators value this molecule for selective crop-protection products. Halogenated phenols typically serve as core scaffolds for fungicide or herbicide development, and our clients feed it forward into a variety of aromatic ring transformations. The purity and tight control of trace contaminants have allowed manufacturing partners to minimize downstream impurities — a decisive factor where regulatory filings need to reference product precursors.
Fragrance chemists also explore derivatives of 3-Chloro-2-Methoxyphenol. The ortho-methoxy and para-chloro groups introduce stability and subtle olfactory notes once further functionalized, meaning they serve as a building block for prized aromatic molecules. Some derivatives slip into blends for their woody, slightly spicy base notes, providing professional perfumers more control in complex formulas.
Over the past decade, our facility has fine-tuned the synthesis process. We start with high-grade resorcinol or substituted guaiacols, making careful choices between direct chlorination or sequence-controlled methoxylation. Factors like temperature, solvent selection, feed rate, and drying process play a role in achieving the right molecular profile. Our in-house team monitors these features, tweaking equipment settings for the season, humidity, and even aging of reagent stocks.
In any batch, real-world setbacks can surface due to moisture intrusion or inconsistent catalyst efficiency. We tackle these issues head-on, not by masking irregularities, but with accountability to each customer. Samples pulled during runs are tracked for any color shift, trace acidity, or off-odors, with problems intercepted long before shipment leaves the gate. Frequent dialogue with our buyers brings feedback on application performance, guiding us to refine filtration methods or tweak purification stages.
Not all phenolic intermediates manage the balance between reactivity and selectivity like 3-Chloro-2-Methoxyphenol. Standard guaiacol (2-methoxyphenol), without the chloro, behaves differently in halogenation or alkylation. I’ve watched pharmaceutical partners struggle with side-product formation or poor yields using basic guaiacol under the same conditions; adding the chloro group lowers electron density in targeted positions, steering reactions toward cleaner outputs and specific substitution profiles.
Compare it to 3-chlorophenol or 2-methoxyphenol alone, and the dual substituent structure means more options for building complex molecules. Where simple chlorinated phenol might generate reactive intermediates too early, incorporating both groups helps modulate activation energy and stepwise reaction control. These real-world benefits translate to savings in raw material waste, less solvent usage, and fewer purification headaches during scale-up.
Some customers experiment with 3-bromo-2-methoxyphenol or even 3-iodo-2-methoxyphenol thinking the halogen swap will boost performance, but in our experience production risks jump and the costs skyrocket. The chloro variant balances performance, safety, and supply stability — issues that genuinely matter in a modern chemical business. We've tracked the downstream analytics ourselves: lower halogen toxicity, easier handling, and comparable reactivity, all factored into day-to-day plant management decisions.
Years in the industry have shown the best chemical is only as good as its reproducibility. Plant teams follow a batch-oriented model with continuous monitoring, not just a pass-fail final QC check. Operators rotate between blending, reaction staging, and product isolation — giving everyone hands-on familiarity with the product characteristics. We’ve reduced cross-contamination risks by using dedicated equipment and strict clean-out protocols between different runs.
Batch logs tie every output drum to its precise production campaign, recording variables down to hourly test results and ambient temperature at each phase. Warehouse crews store finished material away from sources of heat and direct sunlight to protect against degradation. Our plant retains retain samples for years after shipment, and any customer can reference their batch history for performance questions.
Routine HPLC, GC, and spectroscopic analyses catch any outliers before the product leaves our facility. Operators perform visual inspections and odor checks alongside analytic techniques, giving an added safety net. Customer return rates have dropped below one percent year-over-year after introducing more thorough mid-process checkpoints and data logging at each critical control point.
Trace solvent residues, heavy metals, or cross-process byproducts fall well under published thresholds. We partner with independent third-party labs not just for compliance — our team views outside validation as a chance to push for further process improvement, not just a regulatory box to tick. Internal chemists compare analytical data against standard reference charts, ensuring batch-to-batch performance reproducibility.
Manufacturers can’t ignore the environmental footprint of specialty chemicals. We treat chlorinated compounds and solvent washings with multiple step filtration, in-process capture, and secondary treatment measures. Effluent monitoring teams supervise all waste streams, and engineering crews regularly upgrade process containment in the main synthesis halls. By anchoring the process design on green chemistry principles, we’ve slashed water and energy use per kilo output compared to a decade ago.
Although chlorinated aromatics draw concern, we’ve cut fugitive emissions with packed-bed scrubbers and solvent-recycling loops. Each year, we send samples of air and water byproducts to certified external labs, backing up internal reports with data fit for customer and regulator scrutiny. These investments aren’t short-term marketing — they’re responses to community input and team feedback from operators who want safer working conditions and less plant downtime.
In practice, supporting users of 3-Chloro-2-Methoxyphenol goes beyond paperwork and certificates. Technical service chemists work alongside clients on application trials, often simulating reaction steps using specific solvents, catalysts, or temperature profiles matching customer procedures. This collaborative feedback loop identifies possible bottlenecks and preempts issues with scaling, handling, or disposing of waste associated with our product. Direct conversations with clients help us understand challenges in filtration rates, product dispersion, and interaction with other synthesis intermediates.
Returns or complaints get full traceability, tracked against retained samples and in-plant QC archives. When outliers arise, investigations don’t just address the symptom — they scan upstream and downstream variables, uncovering root causes and advising practical measures for prevention on both ends. Chemists document these findings and update user guidance, so future shipments avoid repeat issues.
Observing changes in market demand, our plant teams keep track of which downstream routes see highest success rates. Several pharmaceutical buyers have shared optimization case studies, pointing out how small changes in chloro orientation or methoxy group purity influence their final API yields. We’ve acted on this input by upgrading our main reactor automation, giving our chemists more control over temperature ramping and reagent addition — methods directly tied to feedback from partners pushing for tighter specs.
On-site technical visits let manufacturing engineers observe customer challenges in real-world production environments. This partnership doesn’t just inform future batches — it retroactively improves run plans. For example, one client flagged further purification was necessary for certain regulatory filings, which led us to recalibrate our crystallizer step and install in-line colorimetry sensors.
Warehouse staff keep shipments of 3-Chloro-2-Methoxyphenol under lock and key, away from oxidizing agents and moisture-rich areas. We ship in high-barrier drums lined with antistatic bags, giving users longer shelf life and less clumping over time. Operators avoid open handling in humid environments to keep the compound free-flowing and good for dust-free dispensing. Anyone managing bulk use will benefit from airtight transfer lines and periodic drum rotation to avoid settling and compacting, especially for larger pack sizes.
In higher-temperature regions, storage spaces get additional insulation to cut down heat exposure. Staff regularly cycle inventory using a FIFO system, paired with periodic inspections for off-odor development or color changes. If field teams spot changes on-site, we tap into our sample archives to trace any issue back to its batch run and shipping conditions.
All of our production batches follow guidelines set by leading pharmacopoeias when product goes to regulated-medicine applications. This goes well beyond basic purity — we verify compliance for residual solvents, metal content, and unwanted halogenated byproducts. For export shipments, our staff keeps up to date on region-specific documentation, giving clients a smooth customs clearance process and faster plant start-ups.
Facility engineers and quality personnel attend peer group training and supplier audits each year, staying sharp on trends in process safety and raw material traceability. These connections feed directly into adjustments at our own facility, with many improvements first tested in small-scale pilot lines before full rollout.
Through in-house R&D, we continue exploring improvements in process metrics, cost reduction, and greener process variants. Recent work has focused on mild-condition alternatives for chlorination, both to reduce risk and to lower plant emissions. Some teams evaluate next-generation catalysts, searching for ways to further lift selectivity without sacrificing throughput. Annual review of competitor outputs and international best practices fuels new ideas, keeping our product lineup evolving to fit real user needs.
Pilot research projects — some inspired by customer requests for custom purity or specific impurity profiles — sometimes transition to commercial output after validation phases. This ethos of experimentation lets us support not only the existing market for 3-Chloro-2-Methoxyphenol, but new application routes as they emerge. As green chemistry expectations grow, our engineering staff tracks advances in solvent substitution, biobased feedstock feasibility, and end-of-life treatment strategies for this compound.
The chemical industry keeps growing, and requirements for phenolic intermediates like 3-Chloro-2-Methoxyphenol change every year. Direct feedback from global clients and research alliances shows where our attention is needed. By sharing real-world process data and practical lessons, we help others adapt this compound to their own sectors — not just with standard specs but with adaption support, formulation tweaks, and transparent reporting.
Whether the demand is for scale-up of a pharma launch or tighter environmental limits on byproduct discharge, our goal stays clear: maintain an open door with end users, listen to unique process needs, and deliver a refined, reliable product batch after batch. The cumulative effect of this approach shows not just in customer satisfaction, but also in the ongoing trust that keeps our plant running year after year.
3-Chloro-2-Methoxyphenol has earned a strong reputation among technical users for its adaptability and manageable handling. Practical lessons learned — from raw material selection through to bulk batch shipment — shape how this product performs in challenging applications. Teams working with this compound can expect support, honest feedback, and a manufacturing partner invested in every step of their supply chain.