Anhui Liwei Chemical Co., Limited
Products

Phenol, 2,3-Dimethoxy- (8Ci)(9Ci)


    • Product Name Phenol, 2,3-Dimethoxy- (8Ci)(9Ci)
    • Alias 2,3-Dimethoxyphenol
    • Einecs 202-739-6
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    701567

    Iupac Name 2,3-Dimethoxyphenol
    Molecular Formula C8H10O3
    Molar Mass 154.16 g/mol
    Cas Number 20729-55-1
    Appearance Colorless to pale yellow liquid
    Boiling Point 263 °C
    Melting Point 36-38 °C
    Density 1.138 g/cm3
    Solubility In Water Slightly soluble
    Pubchem Cid 150013
    Smiles COC1=C(C=CC(=C1)O)OC
    Inchi InChI=1S/C8H10O3/c1-10-7-4-3-6(9)8(5-7)11-2/h3-5,9H,1-2H3
    Refractive Index 1.548

    As an accredited Phenol, 2,3-Dimethoxy- (8Ci)(9Ci) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Phenol, 2,3-Dimethoxy- (8Ci)(9Ci) is packaged in a 25g amber glass bottle, sealed, with proper hazardous material labeling.
    Shipping Phenol, 2,3-Dimethoxy- (8Ci)(9Ci) is shipped in compliance with hazardous materials regulations. It is securely packaged in appropriate, leak-proof containers, clearly labeled, and accompanied by required safety documentation and material safety data sheets (MSDS). Shipping is typically via certified carriers specializing in radioactive and hazardous chemicals, ensuring safe, regulated delivery.
    Storage **Storage Description:** Store Phenol, 2,3-Dimethoxy- (8Ci)(9Ci) in a tightly closed container in a cool, dry, well-ventilated area, away from heat, ignition sources, and incompatible substances. Protect from light and moisture. Follow all safety protocols for handling radioactive materials, including proper labeling and use of shielding as required. Access should be limited to trained personnel only.
    Free Quote

    Competitive Phenol, 2,3-Dimethoxy- (8Ci)(9Ci) prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615380400285

    Email: sales2@liwei-chem.com

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    Certification & Compliance
    More Introduction

    Phenol, 2,3-Dimethoxy- (8Ci)(9Ci): A Reliable Choice from a Chemical Manufacturer's Perspective

    Understanding Phenol, 2,3-Dimethoxy- (8Ci)(9Ci) as a Raw Material

    Manufacturers rarely talk about the day-to-day realities of producing a consistent, high-purity chemical like Phenol, 2,3-Dimethoxy-. This compound, often recognized in the trade by its (8Ci)(9Ci) notation, brings value beyond its straightforward molecular formula. In our facility, we’ve watched this substance move from small-scale requests to an established position in both research and industrial verticals. Its reputation is built on reliability, purity, and reproducibility—qualities that matter to researchers and process engineers alike.

    We know Phenol, 2,3-Dimethoxy- by its systematic methods of synthesis, typically via methylation of catechol. The control required during manufacturing cannot be understated; even minor variations in conditions can skew reaction outcomes. Precision matters at every step, from solvent selection to the timing of quenching. Through years of running these reactions, we’ve refined our process to deliver a product that meets consistent purity thresholds batch after batch. There are no shortcuts. Our attention to the identity, physical form, and analytical profile of each lot remains constant.

    Most of our Phenol, 2,3-Dimethoxy- is produced to technical or reagent grades, depending on the final application. In practice, this means tailoring the production to meet the target impurity profile. Many customers choose this compound as a building block in organic synthesis, especially those exploring phenolic derivatives or testing new intermediates for pharmaceuticals and agrochemicals. We’ve observed demand spikes as some industries push for alternative phenolic ethers, looking for reliable alternatives that handle downstream chemistry or offer slight structural differences for testing new biological activity.

    Key Specifications and Manufacturing Practices

    We typically manufacture this compound in solid form, white to light beige crystals with a faint aromatic odor. Moisture control remains critical: water content can introduce side-products or complicate downstream reactions, especially for customers running sensitive substitutions. During purification, column choices and filtration sequences impact the crystalline quality. Over time, we’ve adapted our protocols to deliver a product with minimal trace metal content and low residual solvent, determined by GC and HPLC.

    Our facility employs batch reactors suited for phenolic compounds, using jacketed glass-lined vessels for optimal temperature regulation. Reaction monitoring takes place at regular intervals, and we use both TLC and real-time spectroscopy to avoid over-alkylation. End-of-run workup includes repeated washing and vacuum drying. Analyses, both in-process and final, rely on a combination of NMR, MS, and IR. This not only secures the structure of 2,3-dimethoxyphenol but also clears out unwanted regioisomers that can result from careless process control.

    Each drum or package bears its batch ID, tied directly to an internal tracking system that lets us pinpoint raw material lots, operator logs, and in-line QC records. Such traceability ensures consistent deliveries—an aspect our long-term clients have come to expect. Several internal audits each year keep our SOPs up to date and compliant with evolving quality standards.

    Differentiating from Similar Phenolic Ethers

    Those working with phenol derivatives know that minor shifts in substitution pattern create significant differences in chemical properties. Phenol, 2,3-Dimethoxy- is not interchangeable with its positional isomers (such as the 2,4- or 3,4-dimethoxy variants). During production, controlling for regioisomers presents a challenge. Certain catalysts and solvent combinations push the methylation towards undesired positions on the aromatic ring. We routinely run long-term stability and impurity studies, comparing various dimethoxyphenols and tracking performance under different conditions.

    In our direct experience, 2,3-dimethoxy positional isomer exhibits unique reactivity in halogenation, acylation, and oxidative coupling routes. For chemists exploring regioselective transformations or who require blocking patterns for further functionalization, this subtle difference becomes crucial. Our manufacturing emphasizes this selectivity, ensuring that our product yields reliable results—whether in a benchtop organic synthesis or larger-scale chemical plant.

    Unlike more commoditized phenolic ethers, 2,3-dimethoxyphenol sits in a space where small impurity levels wreak havoc downstream. We’ve dealt firsthand with complaints about off-color by-products from casual competitors, learning that even 1-2% of an unresolved isomer can complicate chromatography or throw off analytical workups. Our batches undergo further scrutiny, especially during the final crystallization step. Some producers cut corners at this stage; we don’t, and we have the repeat business to prove it.

    Applications in Industry and Research

    Years of conversations with synthetic chemists and industrial formulators reveal clear trends in how Phenol, 2,3-Dimethoxy- performs. Most inquiries come from laboratories developing new aryl ether compounds, where the position and pattern of methoxy groups decide the biological and chemical properties of the final product. For example, pharmaceutical companies order by the kilogram, running pilot-scale batches to test fungicidal or anti-inflammatory candidates. Our experience tells us that even on this scale, reproducible performance matters—what works in the flask has to hold up in the reactor.

    Some customers tap us for gram-quantities destined for academia’s exploration of new coupling methods or as standards for analytical chemistry. Our data and batch records often become reference points for publication, reinforcing the trust placed in our quality control. The feedback we receive from these users sharpens our process; atypical impurities flagged in their spectra make their way back to our QA discussions, improving future runs.

    Industrial users depend on the reliability we guarantee. One recent run involved toll-manufactured batches for a specialty surfactant producer. In their process, side-reactions caused by impure feedstock led to unacceptable levels of off-odor in the final product—trace contaminants like benzaldehydes and catechols were the culprits. After a switch to our tightly controlled lots, complaints stopped and the customer recouped their previous yields without further purification steps. Such direct customer experience supports the view that careful upstream manufacturing saves time, labor, and cost downstream.

    Quality Assurance and Analytical Approach

    Our technical team oversees each process stage, prioritizing outcome over speed or cost savings. We source raw phenol and methylating agents with full documentation, regularly rotating vendors to hedge against supply disruptions or changes in quality. Batch-to-batch reproducibility rests on robust housekeeping; reactors, condensers, and ancillary lines undergo thorough decontamination—residual acids or previous reaction leftovers spell trouble for such sensitive synthesis.

    Lab teams employ validated methods for purity measurement. We calibrate our GC/MS and HPLC instruments before each run, verifying retention times and instrument response with certified standards. Each lot undergoes triplicate analysis for assay, water content, and trace metals. System suitability tests precede every analytical sequence, avoiding confounding variables that might mask a real impurity. The data feed our batch release process—no product ships without matching our acceptance range.

    Training and experience matter. Senior chemists often catch oddities in early QC readouts—a slight baseline drift, an unexpected split in the NMR spectrum—and pull the batch for review. No amount of automation eclipses the value of well-trained eyes interpreting real-world data. For years, this internal culture of vigilance has prevented downstream complaints, strengthened client relationships, and maintained our reputation in the industry.

    Environmental and Regulatory Considerations

    Several years back, we adjusted our protocols to align with shifting environmental regulations around phenolic compounds. Our waste streams include aqueous washes and organic residues, both monitored and treated to meet discharge standards. We voluntarily adopted closed-loop practices in solvent recovery, cutting down on total emissions. These steps became second nature to operators, as continuous training and investment in the plant infrastructure paid off not only with regulators, but with the broader community—neighbors notice when odors or incidents spike.

    Manufacturing Phenol, 2,3-Dimethoxy- means accepting full responsibility for safe handling and waste minimization. Our team reviews safety literature frequently, implementing fresh control steps as new data emerges. Chemical workers visit occupational clinics every year to catch any early signs of exposure. Safety hurdles—leak detectors, pressure-relief protocols, PPE audits—become ingrained habits, not afterthoughts imposed by outside mandates.

    Interactions with Our Partners and End Users

    Our long-term clients often surprise us with how they adapt our Phenol, 2,3-Dimethoxy- to new workflows. Open communication reveals recurring bottlenecks. In certain applications, customers found dustiness in standard crystalline product led to static charge buildup and material loss. After their feedback, we modified particle size distribution during milling, reducing fines and easing their downstream processing. That kind of iterative collaboration speaks louder than any marketing claim.

    Few substitutions can replace 2,3-dimethoxyphenol in processes geared towards precise aromatic substitutions. Research teams working on enzyme studies or investigating oxidative couplings rely on the placement of methoxy groups. In biochemistry, the position affects enzyme-substrate affinity, steric compatibility, and even UV-visible absorption. Our experience manufacturing this compound in ton-scale volumes confirms that demands for consistency are not limited to paperwork, but ripple directly into scientific accuracy and reproducibility.

    Supply chain interruptions test everyone’s patience. Where we see competitors cutting back inventory or outsourcing production, our team keeps a local stock, even during slower quarters. The lead times we quote come with a buffer: fluctuations in demand have a habit of cascading through the customer’s scheduling, affecting research timelines or scheduled plant maintenance. Maintaining tight lot control, repeatable release standards, and backup supply ensures our partners deliver results on schedule.

    Challenges and Solutions in Production

    Continuous improvement defines our manufacturing style. Even familiar reactions like phenol methylation present new wrinkles each year. Variability in raw material purity, fluctuations in temperature during extreme weather, and subtle differences in reactor agitation force constant troubleshooting. Process engineers and chemists work side by side, documenting outcomes and iteratively adjusting conditions to dial in the best yield and purity.

    Unforeseen complications arrive in many forms. Small impurities introduced early often magnify during scale-up, so analytical rigor at every juncture has become a norm. Several years back, we switched to higher-grade solvents after a spate of off-odor complaints from a key customer. While the expense stung initially, end users reported better downstream compatibility, fewer wasted runs, and sharper analytical spectra.

    Systems for monitoring and evaluating trending data, including batch deviations and complaints, lead to tangible process upgrades. We revise training, update process parameters, or recalibrate equipment—pragmatic responses to feedback. Not every solution comes from management. Some of the best process ideas started with an operator noticing a color change at an unexpected stage, recording details in the batch log, and mentioning it during our regular shift meetings.

    Broader Impact and Industry Role

    Producing a stable supply of high-purity Phenol, 2,3-Dimethoxy- creates a ripple effect throughout the chemical landscape. Research institutions, pilot plants, and manufacturers rely on our consistency to anchor their workflows. Using our product, labs can chase new molecular frameworks without worrying about contamination or compromised data. Industrial facilities ease their purification burdens, freeing up capacity elsewhere in the plant. Each incremental improvement compounds across the value chain.

    Market dynamics around specialty phenolic compounds ebb and flow, driven by evolving regulatory constraints, supply chain shocks, and breakthroughs in end-use application. We keep a close eye on these trends, staying ahead by investing in staff training, upgrading quality systems, and listening to how clients use our material. The best insights rarely come from top-down strategic plans. Ideas and improvements surface through honest dialogue with customers, lessons from failed batches, and the continuous drive to do better with each run.

    Direct experience informs everything we do. Each batch tells a story, reflected not in abstract metrics, but in the lived reality of plant workers, technical staff, and customers up and down the line. In making Phenol, 2,3-Dimethoxy-, our team commits to the standards our industry demands and the trust our partners have built in us over time. Reliable supply, transparent data, and continuous improvement—these traits define our role as a chemical manufacturer and ensure this product continues to serve its vital place in synthesis and innovation.