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HS Code |
807062 |
| Chemical Name | 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol |
| Cas Number | 571-03-1 |
| Molecular Formula | C9H12O4 |
| Molecular Weight | 184.19 g/mol |
| Appearance | White to off-white crystalline solid |
| Melting Point | 143-145°C |
| Solubility | Soluble in methanol, ethanol, and slightly soluble in water |
| Purity | Typically ≥98% |
| Synonyms | Isovanillyl alcohol |
| Smiles | COC1=CC(=CC(=C1O)OC)CO |
As an accredited 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol, sealed with a screw cap and labeled with safety information. |
| Shipping | 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol is shipped in tightly sealed containers to prevent contamination and moisture exposure. The chemical should be transported at room temperature, avoiding direct sunlight and extreme conditions. Packaging and documentation comply with safety regulations for laboratory chemicals, ensuring safe handling and delivery to the intended recipient. |
| Storage | 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Properly label the container and avoid prolonged exposure to air to prevent degradation. Store at room temperature unless otherwise specified by the manufacturer. |
Applications of 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol in Industrial ManufacturingAs a direct producer, we supply 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol to international B2B partners integrating this specialty aromatic alcohol in multiple advanced industrial sectors. Downstream manufacturers use this material in precise roles within high-value chemical production chains, where purity, process compatibility, and regulatory alignment are critical. The following application pathways highlight actual end uses in well-established markets. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers employ 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol as a key intermediate in the synthesis of advanced small-molecule APIs, particularly for neurologically active compounds and certain anti-cancer drugs. Process chemists utilize its high reactivity and selectivity during the protected benzylation or deprotection stages, allowing for precise functional group transformations that maintain pharmacopoeial compliance throughout commercial-scale synthesis batches. Industry compliance standards
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2. Agrochemical Intermediate ProductionLeading crop protection formulators select this material as a functionalized building block in the targeted synthesis of fungicidal and herbicidal agents. Its unique aromatic substitution pattern allows for tailored reactivity in acylation or etherification steps, optimizing molecular performance while supporting compliance with residue and toxicological guidelines in regulated agricultural markets. Industry compliance standards
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3. Flavors and Fragrance Fine Chemical SynthesisSpecialty fragrance and flavor houses utilize 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol for tailored etherification and esterification reactions, producing complex aromatic compounds and fixatives. It serves as a stable precursor in the creation of floral, spicy, or woody notes in perfumes and encapsulated flavors, supporting manufacturers striving for adherence to global compositional and safety standards. Industry compliance standards
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4. Specialty Polymers and Resin ModificationTechnical resin producers introduce this compound into specialty aromatic polycarbonates and crosslinked phenolic resins to impart distinct chemical stability and improve UV resistance. The additive nature of this raw material supports fine-tuning of polymer backbone architecture in high-performance coatings and molded components used in electronic, automotive, and aerospace segments, with tightly controlled batch-scale production protocols. Industry compliance standards
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5. Laboratory Chemical Reference StandardsAnalytical laboratories and certified reference material (CRM) producers employ this specific alcohol for calibration and reference standard preparation in chromatographic assay development and method validation. Batch consistency and trace documentation enable regulatory laboratories and quality control units to apply these standards across pharmaceutical, environmental, and food safety testing. Industry compliance standards
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For decades, the landscape of fine chemical production has leaned heavily on the availability and consistency of aromatic alcohols, particularly those bearing multiple functional groups. Among these, 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol holds a reputation for its utility across both research and industrial applications. As direct manufacturers, we take a practical approach, working through raw material selection, reaction conditions, and purification to ensure a batch-to-batch uniformity that specialty users often demand. Here we share a first-hand perspective on what sets this molecule apart, touching on its technical characteristics, handling experiences, and place in innovation-driven sectors.
The structure of 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol combines reactivity with selectivity. Presence of both hydroxy and methoxy groups on the aromatic ring increases polarity and facilitates further derivatization. Throughout synthesis, the biggest challenge remains precise control over substitution patterns—minor fluctuations upstream can skew distribution, affecting downstream processes. We maintain rigorous monitoring through spectroscopic analysis, checking every lot for purity, with milestones tracked by GC and HPLC. Our facility avoids excessive use of harsh chlorinated solvents, choosing production routes that target environmental compliance and minimize waste. While some laboratories prepare this compound in small flasks for bench-scale studies, our reactors produce larger batches, supporting industrial-scale processes and pilot work at once.
Highly functionalized benzyl alcohols often show sensitivity to light and air. Over the years, we have optimized our packaging and storage by introducing amber glass and inert gas blankets, assuring stability for extended periods. Each output batch undergoes detailed quality checks for color, odor, melting range, and moisture content. Typical specifications show purity upwards of 99% by HPLC, with low residual solvents and trace metals. We have observed that off-grade material, with lower purity or yellowing, can present issues during synthesis, so we take extra precautions to eliminate these outliers before release. Storage in cool, dry, and well-ventilated areas remains critical, as with most phenolic compounds.
Our main customers consist of research scientists and industrial chemists who value this intermediate for the role it plays in fine chemical synthesis. In medicinal chemistry, the molecule has become a favorite scaffold for pharmacophore development. Synthetic routes that introduce this building block into trial molecules can often improve receptor binding properties, as observed in a range of CNS-active and cardioprotective agents. Other groups explore its utility as a precursor in fragrance and flavor synthesis, where the presence of both hydroxy and methoxy substituents contribute to specific olfactory profiles.
During project consultations, we hear feedback regarding reactivity and selectivity from teams building libraries of substituted aromatic ethers or esters. Subtle changes in the hydroxyl group’s reactivity—owing to the electron-donating nature of adjacent methoxy groups—lead to higher yields in typical alkylation, acylation, or etherification reactions. By offering product documentation and batch samples, we help process engineers avoid the pitfalls of by-product formation. Our collaborations have shown that the compound’s performance in transition metal-catalyzed coupling reactions makes it a core substrate for the cross-coupling community.
Successful implementation in downstream synthesis rests on several factors: the absence of common aromatic contaminants, consistent physical characteristics, and reliable solubility parameters. Our technical support team regularly assists partners with solubility challenges in both polar and non-polar solvents. Whether developing early-stage bioactive compound candidates, or designing specialty resins, knowing the exact performance characteristics of this benzyl alcohol helps researchers scale up with confidence.
Many research articles have pointed to the significance of the 4-hydroxy-3,5-dimethoxy arrangement in modulating biological activity—especially through interactions with oxidoreductase enzymes or as precursors in antioxidant library synthesis. Clients developing advanced adhesives and specialty coatings have noted the importance of methoxy group orientation for both thermal and UV stability during formulation. By sourcing directly from our own line, customers gain access to tailored support, from technical documentation to practical handling tips.
Every time we discuss this compound in context—say, along with standard benzyl alcohol or its mono- and tri-methoxy analogs—real differences in reactivity and selectivity appear. For example, mono-methoxy variants like 4-hydroxy-3-methoxybenzyl alcohol lack the electron-rich aromatic ring seen in the dimethoxy series, often resulting in lower rates of nucleophilic substitution in coupling reactions. Tri-methoxy substitutions can introduce excessive steric hindrance, sometimes complicating purification and reducing overall yield. Our 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol balances electronic activation and steric accessibility, so process chemists see fewer by-products and improved reproducibility batch after batch.
This specific substitution pattern contributes to distinctly different melting points and solubility behavior. Decades of field experience confirm that for resin incorporation or small-molecule pharmaceutical research, predictable melting and crystallization help chemists streamline their workflows. Such physical property consistency sets our material apart from lesser-refined imports. For academic labs, sourcing from a manufacturer with robust traceability and production logs matters when research reproducibility becomes a top concern.
Meeting the needs of both regulated industries and innovative startups has prompted us to expand our document support. Each consignment includes full analytic reports, COAs, and tracking of relevant regulatory guidelines. Our in-house team updates compliance references to align with the latest EPA and REACH requirements. Routine audits and external testing further reinforce our commitment to traceability.
On more than one occasion, a customer will contact us regarding impurity profiles—particularly in relation to potential genotoxic by-products or persistent organic pollutants. We maintain supply chain transparency for all raw material vendors and share Supply Chain Security documentation as needed. Staff training emphasizes the prevention of cross-contamination and the importance of closed-system handling, reflecting industry best practices.
We often contribute to technical roundtables and webinars, helping educate research teams on safe handling, optimal storage conditions, and best practices for waste minimization during use. Having seen evolving requirements firsthand, we invest in continual improvement, such as batch traceability, comprehensive product coding, and enhanced MSDS coverage. The increased demand for full supply chain disclosure—driven by global brands and consumer-facing firms—keeps us focused on the details that matter to end users.
Designing syntheses at gram, kilogram, and multi-ton scale uncovers inevitable bottlenecks. Our plant engineers work with pilot and commercial partners to adjust formulations, reactivity, or even offer technical blends tailored for specific downstream reactions. Feedback gathered over multiple campaigns reveals value in open communication—be it for reactor loading, filtration practices, or custom packaging. We have supported scale-ups from initial benchtop tests through validation, with equipment that can adapt to both continuous and batch modes. It’s not uncommon to help customers optimize for both cost and quality, by reviewing impurity tolerances and analytical batch controls.
Our experience supplying 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol for regulatory submissions in both the US and European markets has informed the evolution of our documentation and process transparency. Early-stage substances that move toward clinical or production phases demand not only chemical purity but also robust data packages addressing every stage of production. As projects move from R&D into full-scale manufacturing, we guide customers through changing requirements for analytical validation and GMP-readiness.
Throughout decades in chemical production, we've encountered questions about the best practices for handling sensitive phenolic alcohols. The tendency for some batches to darken with prolonged exposure to sunlight led us to overhaul our filling and shipping lines, moving to UV-blocking containers and rigid fulfillment timelines. Our on-site storage units maintain tight temperature control, stemming loss of potency or appearance shifts. Feedback from field users has nudged us towards creating detailed storage instructions and application notes, distributed with each delivery and updated regularly after each technical review.
Handling inquiries from academic labs, we’ve seen demand spike as research turns to the synthesis of analogs for disease study and organic electronics. We have also provided technical support in troubleshooting scale-up issues, particularly with controlling side reactions due to the compound’s electron-rich nature. In several collaborations, process chemists noted a reduction in impurity formation when employing our recommended slow addition techniques or using specialty glassware. In high-throughput settings, stable and easily weighed crystalline products deliver faster batch process times than sticky resins or poorly crystallized analogs.
Longstanding environmental standards shape our choices in raw materials and process solvents. Where possible, we select greener synthetic routes to reduce both hazardous by-products and downstream waste. Instead of relying on high-temperature, acid-catalyzed protocols that bring excess by-products, we use milder conditions and recyclable catalysts. Finished product solutions must adhere to strict local discharge requirements before any on-site waste leaves our facility, as routine monitoring for phenolic runoff meets all regulatory levels.
On the safety front, our team takes a hands-on approach to risk reduction, both for staff and users. We host internal safety audits and coordinate with local agencies for compliance checks, keeping process improvements current. Detailed guidance for personal protective equipment (PPE), emergency response, spill control, and fire risk accompanies product shipments. With frequent turnover in research labs, especially universities and contract research facilities, we supply comprehensive user training and technical bulletins to ensure end-users integrate safe practices from day one.
Following up with our long-term customers provides a steady stream of insight into how our chemicals perform at the bench and in real-world settings. Sectors ranging from life sciences and materials research to fragrance formulation report that consistent purity and physical state markedly improve efficiency and reproducibility in their processes. In organic electronics, our compound aids in constructing unique charge-transport materials, with companies appreciating consistent batch-to-batch photostability. Pharmaceutical labs find that non-interfering impurities ensure clearer results during candidate screening, reducing hours wasted on chromatography or troubleshooting.
Engaging with university consortia has been a learning process. We regularly attend feedback sessions, hearing firsthand about the impact of reagent purity on failed syntheses or project deadlines. Realizing the critical role that reliable supply plays, we have invested in building inventories that satisfy both rush orders and long-term projects. As a manufacturer, we remain nimble—responding quickly to unique requests for alternative lot sizes, documentation needs, or shipping arrangements suited to teaching labs and multinational labs alike.
Our reputation rests on a combination of technical experience, responsible sourcing, and a commitment to customer dialogue. As global standards and research frontiers evolve, we remain focused on transparency and process optimization. Technical support, custom documentation, and traceable supply lines have all come from listening to the working chemists, engineers, and quality teams that use our 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol every day. For us, no shipment heads out the door without a thorough review from production to packaging.
Looking back, refinements in process efficiency and impurity control trace directly to practical feedback from project managers and bench chemists. This material’s unique mix of physical stability and chemical functionality has carved a niche in the toolbox of researchers and industrial innovators. As new routes in drug discovery, polymer chemistry, and biosciences emerge, we stand ready, drawing from decades of practical manufacturing experience to supply 4-Hydroxy-3,5-Dimethoxybenzyl Alcohol that consistently meets the demands of each new challenge.