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HS Code |
358018 |
| Name | 3,5-Dimethoxyphenol |
| Cas Number | 500-11-8 |
| Molecular Formula | C8H10O3 |
| Molecular Weight | 154.17 |
| Appearance | White to off-white solid |
| Melting Point | 123-125 °C |
| Boiling Point | 281 °C |
| Density | 1.19 g/cm³ |
| Solubility In Water | Slightly soluble |
| Inchi | InChI=1S/C8H10O3/c1-10-6-3-5(9)4-7(8(6)11-2)12-3/h3-4,9H,1-2H3 |
As an accredited 3,5-Dimethoxyphenol 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 3,5-Dimethoxyphenol; tightly sealed with a screw cap and labeled with hazard information. |
| Shipping | 3,5-Dimethoxyphenol is shipped securely in sealed, chemical-resistant containers to prevent exposure and contamination. Packaging complies with safety regulations for chemical transport, ensuring stability during shipping. Appropriate hazard labeling and documentation accompany the shipment, and temperature control is maintained if required. Always follow local and international guidelines for chemical shipping. |
| Storage | 3,5-Dimethoxyphenol should be stored in a cool, dry, and well-ventilated area, away from heat sources, sparks, and open flames. Keep the container tightly closed and protected from light and moisture. Store separately from oxidizing agents and strong acids. Use appropriate chemical-resistant containers and ensure clearly labeled storage. Follow standard laboratory chemical safety protocols. |
Applications of 3,5-Dimethoxyphenol in Industrial Manufacturing3,5-Dimethoxyphenol serves as an important synthetic intermediate across several sectors. Its chemical structure supports selective substitution, enabling advanced molecular design for producing specialty ingredients in pharmaceuticals, advanced polymers, and high-performance coatings. As a direct manufacturer, we support downstream formulations with technical documentation and consistent batch quality. 1. Pharmaceutical Intermediates for Antifungal Agents3,5-Dimethoxyphenol is widely used to synthesize key intermediates in the production of azole-based antifungal pharmaceuticals. Its dual methoxy groups allow for targeted functionalization in the benzimidazole core construction. Manufacturers obtain reliable purity to support efficient conversion in Grignard reactions and subsequent ring-closure processes. During process optimization, strict impurity controls help minimize byproducts in active ingredient isolation, supporting high yields in regulated API manufacturing. Industry compliance standards
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2. UV Absorber and Stabilizer Precursor for Polymer ManufacturingPolymer producers leverage 3,5-Dimethoxyphenol to develop UV-stabilizing agents via etherification and condensation reactions. The material enters as a base phenolic precursor in the synthesis of substituted benzotriazoles or diaryl ethers, which are embedded into polyolefin, polyurethane, and engineering plastic matrices. The controlled purity supports minimal discoloration and consistent stabilizing effects, especially in applications requiring long-term light resistance. Industry compliance standards
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3. Intermediate for Agrochemical SynthesisIn the agrochemical sector, 3,5-Dimethoxyphenol enables the construction of phenoxy- or phenyl-substituted active molecules through etherification and nucleophilic substitution. Downstream users apply it as a phenolic nucleophile in creating herbicide or fungicide scaffolds, where the methoxy groups modulate reactivity and environmental stability. Careful handling ensures compliance with residue limits in the final active ingredient lots, particularly for export markets. Industry compliance standards
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4. Building Block in Fragrance and Flavors Ingredient ManufacturingIn the fragrance and flavors industry, 3,5-Dimethoxyphenol is processed to create alkylated and acetylated aromatics with high olfactory impact. The material appears early in the multi-step synthesis of specialty musks or floral aldehydes, where its methoxy substitutions steer the aromatic substitution pattern. Manufacturers prioritize consistent chromatic and impurity profiles, given the low odor threshold requirements for end products. Industry compliance standards
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Producing 3,5-Dimethoxyphenol in a chemical plant requires an understanding of phenolic chemistry and years of handling aromatic compounds. The compound, with its molecular structure based on a phenol ring substituted with two methoxy groups at the 3 and 5 positions, draws attention through its unique combination of chemical behavior and broad application range.
At our own facility, we have found the synthesis of 3,5-Dimethoxyphenol involves careful methylation of a phenolic substrate under controlled conditions to prevent over-methylation or side formation of unwanted isomers. Precise control over temperatures, pH, and reagent addition rate makes all the difference between a clean batch and hours spent removing contaminants. This challenge produces a material known for reliability, consistent melting range, and high purity.
Batch consistency matters in our line of work. The material comes off our reactors as solid white crystals, with odor faintly reminiscent of other methoxyphenol analogs. Chemically, 3,5-Dimethoxyphenol (C8H10O3) melts in the narrow range of about 90–93°C, and purity checks by HPLC and GC regularly give us values above 99%. As manufacturing chemists, we look for easy dissolution in organic solvents, minimal presence of colored trace impurities, and ideal particle size for downstream processing. These factors determine how well the product performs for our customers, from research labs to industrial plants.
Every stage in the synthesis and isolation matters. Simple operations like filtration or crystallization gain new meaning when scaling from grams to metric tons, exposing bottlenecks or inefficiencies that are invisible at lab scale. We have learned that trace metals used as catalysts, or certain acids for neutralization, can introduce impurities impacting later applications. Small differences in washing protocols leave behind unwanted inorganic residues, clouding the product’s future use in sensitive formulations.
Drawing from experience, we maintain rigorous in-process monitoring. Spectrophotometric analysis, dry weight tracking, and solvent recovery checks promote both quality and environmental safety. As many phenolic compounds show sensitivity to light and air, we opt for inert gas blanketing and moisture-free storage in our warehouse. These approaches came about through years of real-world troubleshooting, not from any academic playbook.
Clients order 3,5-Dimethoxyphenol for several reasons, of which the largest share belongs to fine chemical synthesis and pharmaceutical intermediates. The methoxy groups on the aromatic ring alter reactivity, opening doors to downstream derivatives through ether cleavage, Friedel–Crafts acylation, or halogenation reactions. Our plant frequently supplies this compound to customers formulating advanced agrochemicals, certain types of APIs, and custom polymer additives.
Scientists working in organic synthesis value our material’s consistent purity and controlled moisture content. A very minor amount of water or unknown side products can throw off later steps, especially in multi-step pharmaceutical projects. In agricultural chemistry, the compound serves as a precursor for certain herbicide and fungicide candidates. Some research teams exploit its electron-donating methoxy groups, studying substrate specificity in biochemical assays or using the phenol ring as a scaffold for ligand design.
Some customers in the dye and pigment industries also draw on the color-modifying capacity of 3,5-Dimethoxyphenol’s aromatic core. It helps tune absorption spectra and stability in specialty colorants, especially when used alongside other substituted phenols. Years of supplying this sector taught us the importance of removing rusty or yellowish byproducts, which indicate incomplete methylation or old stock.
From a chemical manufacturer's perspective, differentiation means understanding subtle and not-so-subtle differences among similar-looking molecules. In the family of dimethoxyphenols and related compounds, placement of the methoxy groups governs every property that later impacts a user’s project. 3,5-Dimethoxyphenol stands out compared to 2,4-dimethoxyphenol, 2,5-dimethoxyphenol, or the more famous guaiacol and syringol derivatives.
Methylation at the 3 and 5 positions, rather than at neighboring sites, results in cleaner NMR signals, distinct reactivity patterns, and altered solubility compared to ortho-methoxy isomers. We noticed that some customers initially order the wrong isomer, only to find different melting points, reactivity in cross-coupling reactions, and biological response. Our technical team guides these clients, running comparison tests and providing reference spectra on request.
Other materials in our catalog sometimes overlap in use but differ in performance. For example, guaiacol (2-methoxyphenol) offers higher water solubility but can introduce greater instability in some formulations. Syringol (2,6-dimethoxyphenol) brings three electron-donating groups, tipping the aromatic ring’s electron balance and affecting subsequent reaction routes. Among these, 3,5-Dimethoxyphenol preserves an ideal balance of reactivity and manageability, which explains its ongoing popularity among medicinal chemists and advanced materials researchers.
The realities inside our plant echo concerns throughout the chemical industry. Handling reagents like methyl iodide or dimethyl sulfate requires constant vigilance and well-practiced safety drills. We maintain strict access controls, air monitoring, and personal protective equipment protocols, born out of respect for these materials and the lessons of past incidents.
Solvent recovery and waste reduction receive regular investment. We engineered our process lines to minimize chlorinated solvent usage and favor recyclable aromatics such as toluene and ethyl acetate. Our staff collects spent catalyst batches for responsible disposal or, whenever feasible, for metal recycling. Emissions abatement systems—once an afterthought—now form a core part of our operation.
Beyond technical compliance, we consider the impact of our products after sale. Customers have approached us about greener alternatives to methylating agents or ways to lower the residual solvent content in shipped batches. We see growing demand from buyers who measure the environmental footprint of the chemicals in their pipeline alongside cost and performance. Our sustainability push includes developing continuous-flow synthesis methods, reducing the energy footprint per kilogram, and partnering with downstream users to collect feedback about life cycle impacts.
Supplying 3,5-Dimethoxyphenol means more than filling drums. Research teams rely on unbroken continuity of supply, and production planners need timely information about availability. Our team shares real-time stock levels with qualified buyers, drawing on detailed forecasts and raw material lead times.
Through years of collaboration, we learned that clients benefit from reliable technical support. Our chemists answer questions about analytical characterization, reactivity with specific coupling partners, and optimal storage practices. Working closely with customers, we solved problems involving caking of the product under humid conditions and optimizing the compound’s dissolution in polar aprotic solvents before use in production-scale runs.
Part of our commitment involves periodic product benchmarking. Internal quality teams authenticate each lot not just through spectroscopic and chromatographic analysis but also by running trial reactions designed to mimic end-use. These steps identify subtle shifts in performance long before a customer would see them.
3,5-Dimethoxyphenol poses technical demands not found in lower-molecular-weight phenols. Large-scale acetylation and methylation generate heat and exotherm management issues, especially when ramping up new equipment. Precise metering valves and jacketed reactors help us contain runaway reactions and control batch progress.
Crystallization and drying also present their own hurdles. Solvent choice affects yield and crystal habit, requiring iterative optimization. Some solvents deliver high-purity material but leave behind persistent traces, which later interfere with user formulations. Our solvent screening team tracks volatility and washing efficiency, settling on solvent systems that balance efficiency, cost, and residual solvent safety.
Packaging becomes its own science, especially for shipments across climates. Early attempts with standard drums or bags led to hydration in humid ports and compaction in winter climates. We now use lined fiber drums with double barriers, together with humidity indicators, giving customers easy verification and reliable downstream processing.
Analytical advances also help us stay ahead. NMR, FTIR, and mass spectrometry remain standard, but isotope dilution and trace impurity screening reveal more about each batch. We share this data with customers working on regulated products, supporting them in meeting global quality standards without interruption.
Regulatory changes affect our manufacturing cycle from raw material choice to labeling and documentation. Jurisdictions vary, so we keep up with evolving standards, particularly for compounds flagged for environmental or workplace exposure. We supply detailed safety and traceability files, supporting clients who move final products through customs or regulatory checks.
Handling export to North America, EU, and East Asia gives us perspective on batch testing needs and the repercussions of non-compliance. Documentation—openly traceable from raw material batch through finished product—protects everyone along the supply chain. Our team prepares sample documentation packs on request, aligning with local laws as well as customers’ internal audit protocols.
Environmental health and safety drive many improvements. We reduced our reliance on certain solvents thanks to public pressure and industry guidance, and we added permanent fume capture hooding above packaging lines. While not every change comes cheap or quickly, the upstream payoffs eventually show in a solid safety record and smoother customer audits.
Market signals show stable demand for 3,5-Dimethoxyphenol, particularly in Asia-Pacific and North American labs. The compound retains its status as a valued intermediate in medicinal, agricultural, and pigment chemistry. Our investment in process reliability and forward-looking sustainability opens new conversations with innovative clients.
The future direction involves more automation, online quality tracking, and shifting further toward low-impact synthesis pathways. Interest in continuous-flow reactors and further solvent recycling grows as chemical manufacturers face increasing cost and compliance demands. We expect tighter regulatory oversight and new green chemistry targets to reshape the production landscape, and our operations evolve in anticipation.
Staying in tune with changing project needs, our technical team keeps improving both product purity and user experience. Packaging, trace analysis, solvent options, and collaborative application studies all matter as much as base product purity. Our lifelong investment in plant, people, and partnerships will carry us through coming changes in regulations, raw materials, and market demand.
Our story with 3,5-Dimethoxyphenol includes the respect for chemistry’s details, patient troubleshooting, and a shared desire to see customers succeed through reliable material supply. Years spent in hands-on production have cemented our belief that the full value of a specialty chemical lies not just in specs but in practiced expertise. The journey starts with sourcing and synthesis but continues through transparency, support, and a commitment to keep pace with real-world needs. This approach, shaped through long experience, helps ensure that 3,5-Dimethoxyphenol remains not just a product number in a catalog, but a vital working tool for chemists worldwide.