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3,5-Dimethoxybenzyl Alcohol

    • Product Name 3,5-Dimethoxybenzyl Alcohol
    • Alias m-Anisyl alcohol
    • Einecs 209-997-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    838841

    Chemical Name 3,5-Dimethoxybenzyl Alcohol
    Cas Number 1163-37-7
    Molecular Formula C9H12O3
    Molecular Weight 168.19
    Appearance White to off-white solid
    Melting Point 52-56°C
    Boiling Point 133-135°C at 13 mmHg
    Density 1.136 g/cm3
    Solubility Soluble in organic solvents such as ethanol and chloroform
    Smiles COC1=CC(=CC(=C1)CO)OC
    Inchi InChI=1S/C9H12O3/c1-11-8-3-7(6-10)4-9(5-8)12-2/h3-5,10H,6H2,1-2H3
    Refractive Index 1.542

    As an accredited 3,5-Dimethoxybenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g quantity of 3,5-Dimethoxybenzyl Alcohol is packaged in a sealed amber glass bottle with a secure screw cap.
    Shipping 3,5-Dimethoxybenzyl Alcohol is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It should be transported according to local and international regulations for non-hazardous laboratory chemicals, protected from moisture, direct sunlight, and extreme temperatures. Proper labeling and documentation accompany every shipment to ensure safe and compliant delivery.
    Storage 3,5-Dimethoxybenzyl alcohol should be stored in a tightly sealed container, away from direct sunlight and sources of ignition. Keep it in a cool, dry, and well-ventilated area, separate from strong oxidizing agents and acids. Proper chemical labeling and adherence to local safety regulations are essential. Store at room temperature or as recommended by the manufacturer’s safety data sheet (SDS).
    Application of 3,5-Dimethoxybenzyl Alcohol

    Applications of 3,5-Dimethoxybenzyl Alcohol in Industrial Manufacturing

    3,5-Dimethoxybenzyl Alcohol serves as a critical intermediate for multiple industrial synthesis processes. Our production process ensures high purity, consistency, and traceability, enabling efficient integration into diverse downstream applications. Below are precise industry scenarios where this material directly supports advanced manufacturing needs.

    1. Active Pharmaceutical Ingredient (API) Synthesis for CNS Drugs

    Many pharmaceutical manufacturers use 3,5-dimethoxybenzyl alcohol as a protected benzyl intermediate for the synthesis of central nervous system (CNS) drugs, including key antipsychotic and antidepressant actives. It facilitates selective alkylation and subsequent deprotection in multi-step syntheses when producing molecules with methoxy-phenyl moieties, such as tricyclic and atypical antipsychotics. Our material meets stringent requirements for residual solvents and trace impurities mandated for regulated drug manufacturing environments.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP–NF, EP, JP monographs where applicable in multi-stage synthesis
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • Pharmacopoeia impurity profiling and trace solvent regulations

    Typical usage ratio

    • 5–15% molar ratio as benzylation agent during key intermediate formation; final amount adjusted based on target molecule core and scale-up yield requirements.

    Downstream process integration

    • Used in early to mid-stage alkylation and protection steps within the API route
    • Introduced prior to critical ring closure reactions
    • Subsequent catalytic hydrogenolysis or acid hydrolysis removes protecting groups
    • Followed by purification steps specific to pharmaceutical GMP

    Final product types

    • Atypical antipsychotics (e.g., olanzapine, clozapine intermediates)
    • Tricyclic antidepressant intermediates
    • CNS-active phenylalkylamine derivatives

    2. Agrochemical Intermediate for Selective Herbicide Formulation

    The agrochemical sector employs this compound to build aromatic ether scaffolds in the synthesis of selective herbicides and plant growth regulators. It acts as a phenolic precursor for complex heterocyclic assembly, enabling the manufacture of innovative crop protection molecules with reduced phytotoxicity profiles. Quality control emphasizes traceability, conforming to global pesticide ingredient regulations and multistage synthesis documentation.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation for Plant Protection Products
    • US EPA 40 CFR Parts 152–180 (pesticide ingredients)
    • China GB 2763 Maximum Residue Limits for Pesticides
    • ISO 9001:2015 for agrochemical raw material supply

    Typical usage ratio

    • 3–10% relative to total mass in primary condensation steps; precise ratio optimised based on active ingredient structure and formulation route.

    Downstream process integration

    • Incorporated as a starting alcohol during phenolic etherification
    • Subjected to alkylation with haloalkanes for aromatic substitution
    • Feeds into sequential cyclization and side-chain modifications
    • Finishes with purification before active loading into formulation

    Final product types

    • Selective post-emergence herbicide actives (e.g., 2,4-dichlorophenoxyacetic acid esters)
    • Growth regulation intermediates
    • Crop protection agents for cereals and row crops

    3. Fragrance and Aroma Ingredient Manufacturing

    Fragrance chemical producers use 3,5-dimethoxybenzyl alcohol as a fundamental building block in the creation of aromatic ether bases. It supports the manufacture of muguet (lily-of-the-valley) notes and other powdery aldehyde scents. Typical processes require high purity to eliminate potential off-notes in delicate formulations for both fine and functional fragrances. Our controlled crystallization and solvent-free processing are verified for compliance with international fragrance safety standards.

    Industry compliance standards

    • IFRA (International Fragrance Association) Guidelines
    • ISO 9001:2015 quality management for aroma chemicals
    • REACH Registration, Evaluation, Authorization, and Restriction of Chemicals
    • Cosmetics Regulation (EC) No 1223/2009

    Typical usage ratio

    • 0.5–3% by weight in precursor mixtures for specialty aroma ingredient manufacture; varies with target molecule volatility and olfactory strength.

    Downstream process integration

    • Added in etherification stages with formaldehyde or aldehyde reactants
    • Participates in step-growth to create complex aromatic cores
    • Isolated by fractional distillation or preparative crystallization
    • Converted into fragrance bases or modifiers for compounded perfumes

    Final product types

    • Muguet-type fragrance bases
    • Powdery and floral aroma chemicals
    • Functional fragrances for home and personal care

    4. Fine Chemical Synthesis for Photoinitiators and Specialty Polymers

    In the fine chemical sector, our material functions as a key intermediate for photoinitiator precursors, especially those based on benzyl ether derivatives for UV-curable coatings and inks. Specialty polymer manufacturers use this alcohol to produce functionalized aromatic intermediates that enable precise molecular weight control and custom light absorption profiles. Quality assurance addresses both organic impurity control and batch-to-batch analytical reproducibility, supporting strict customer formulation validations.

    Industry compliance standards

    • ISO 14001 Environmental Management for Chemical Synthesis
    • US EPA TSCA requirements for new polymer intermediates
    • EN 71-3 Safety of Toys (for photoinitiators in toy coatings)
    • RoHS 2015/863/EU for coatings and electronics

    Typical usage ratio

    • 2–6% by mass in intermediate synthesis batches; adjusted with reference to target photoinitiator efficiency and polymerization kinetics.

    Downstream process integration

    • Introduced at aromatic ether construction stage for photoinitiator backbone formation
    • Followed by side-chain functionalization, typically via acylation or esterification
    • Blended into oligomerization or polymerization feeds for end-use testing
    • Subjected to HPLC and spectroscopic purity checks before shipment

    Final product types

    • UV-curing photoinitiator blends
    • High-purity prepolymers and specialty resins
    • Coating and adhesive additives for electronics and packaging
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    Certification & Compliance
    More Introduction

    Introducing 3,5-Dimethoxybenzyl Alcohol: Manufacturer’s Perspective

    An Expert’s Relationship with 3,5-Dimethoxybenzyl Alcohol

    Years of handling specialty aromatic alcohols create a certain kind of familiarity. The smell, the look, the quirks in each production batch—they become second nature. Among the dozens of compounds routinely processed, 3,5-Dimethoxybenzyl Alcohol carries its own importance, both on the stainless-steel equipment and in the hands of chemists who rely on dependable starting materials. Our facility produces 3,5-Dimethoxybenzyl Alcohol to meet the specific demands of organic synthesis and fine chemistry sectors. Quality and repeatability in its manufacture mean fewer headaches downstream for fellow chemists and formulators.

    Molecular Purity: Keeping It Consistent

    3,5-Dimethoxybenzyl Alcohol comes with the CAS number 705-76-0, a simple identifier on paper but a complex challenge in practice. Reliable production must always pay attention to the starting 3,5-dimethoxybenzaldehyde, controlling moisture and reaction conditions. The product's molecular formula, C9H12O3, means it offers not just a methylated benzyl alcohol, but one with symmetrical substitution on the aromatic ring. This structural feature sets it apart in terms of physical properties and reactivity.

    Chemists depend on purity—impurities in this kind of substrate translate into complications during downstream reactions. Typical specification targets include purity of at least 98 percent, low chloride and sulfate residues, verified by GC and HPLC. Customers running multi-step syntheses rely on this assurance. We keep the water content below 0.2 percent by Karl Fischer titration because hydrous alcohol can sabotage moisture-sensitive transformations, including any involving Grignard reagents or acid chlorides.

    Process Insights on Large-Scale Synthesis

    Producing 3,5-Dimethoxybenzyl Alcohol isn’t about simply reacting one compound with another. The reduction step, frequently performed with sodium borohydride or catalytic hydrogenation, requires precise control to avoid over-reduction or formation of homolog contaminants. In each batch, process engineers balance conversion versus selectivity, tune pH, monitor temperature, and test for side products such as 3,5-dimethoxyphenol or unreacted aldehyde through chromatographic analysis. Any deviations leave telltale peaks on chromatograms.

    Continuous monitoring during work-up and crystallization makes sure the product doesn’t carry through any color or insoluble matter, both of which could point to incomplete purification or equipment residue. We insist on a clear, colorless to slightly pale yellow liquid—hints of haze or darkening can signal degradation or the need for further filtration.

    End Uses: Why Quality Affects Downstream Value

    Pharmaceutical laboratories, agrochemical developers, and research institutes use 3,5-Dimethoxybenzyl Alcohol chiefly as a synthetic intermediate. It acts as a building block for a cluster of substituted aromatic compounds, including molecules of biological relevance. During etherification, alkylation, or esterification, its two methoxy groups protect the ring and guide reactivity. Some novel polyether or phenolic drugs depend on a precisely manufactured batch, as tiny contaminants or isomeric impurities trigger difficulties during final compound isolation.

    Researchers investigating new catalysts often select 3,5-Dimethoxybenzyl Alcohol because the electron-donating methoxy groups modulate reactivity. The alcohol group serves as a handle for attachment, as in the creation of benzyl-protected intermediates. In contrast, related alcohols such as 4-methoxybenzyl alcohol or unsubstituted benzyl alcohol display different steric and electronic behaviors, affecting yields and product profiles in synthetic steps.

    Comparing 3,5-Dimethoxybenzyl Alcohol to Related Compounds

    Experience with a variety of benzyl alcohol derivatives highlights several distinctions. The 3,5-dimethoxy variant is less volatile than benzyl alcohol, offering higher boiling points for certain reaction setups. Compared to 4-methoxybenzyl alcohol, which provides only one site of electron-donation, the dual methoxy groups of the 3,5-derivative allow for more pronounced resonance effects. This property surfaces during reactions such as nitration or bromination, where regioselectivity and by-product formation come into play.

    Users in academic labs as well as industry report greater stability for 3,5-Dimethoxybenzyl Alcohol under storage compared to 3,4-dimethoxy variants. Oxidation to the corresponding aldehyde occurs less readily, provided storage containers exclude air and light. Our plant takes this experience to heart, focusing on airtight bottles or drums, and strict light shielding during bulk handling. The bottom line: every benzyl alcohol brings unique performance, but the 3,5-dimethoxy structure offers a careful balance between reactivity, protection, and process reliability.

    Production Practices and Operator Know-How

    Routine bulk operations for this alcohol begin long before actual synthesis. Sourcing of precursors involves strict relationships with trusted primary producers, as the purity of starting aldehyde becomes critical. Plant operators, with years behind the helm, adapt to the nuances of each batch. Slight shifts in hue or odor receive immediate attention. Aging equipment can introduce trace iron or nickel, so regular cleaning and passivation of reactors and piping remain part of daily protocol.

    During distillation, careful fraction collection ensures minimal carryover of higher-boiling by-products. For especially demanding customers, a second distillation step can reduce phenolic traces to undetectable levels. Our focus never stops at clear liquids—smell, solubility tests in typical solvents, and checks for polymorphic changes all play a role before any batch leaves the facility.

    Sustainability and Regulatory Considerations

    As regulatory scrutiny increases for aromatic intermediates, responsible manufacturing sits high on the agenda. Waste minimization ranks equal to product purity in importance. Our process recovers and re-purifies solvents whenever practical; mother liquors from crystallization undergo treatment to recover unreacted starting materials, reducing overall environmental load.

    Newer generations of process engineers focus on catalytic hydrogenation over metal hydride reductions to decrease waste streams containing boron or metal residues. Operators document the absence of controlled substances and check compliance with EU REACH and US TSCA regulations—not just during audits, but in every batch shipped. Periodic external audits and in-house GC-MS checks confirm that the material matches regulatory requirements, and also matches customer documentation needs.

    Challenges in Maintaining Batch-to-Batch Consistency

    Chemists frustrated by inconsistent raw materials know how small variations compound into lost yield or even failed projects. The biggest technical hurdle for 3,5-Dimethoxybenzyl Alcohol always lies in reproducibility— both analytical and performance-wise. Operators compare infrared spectra and HPLC retention times from new batches to archived reference material. This discipline prevents subtle contamination or shifts in impurity profiles from sneaking through.

    Equipment maintenance and operator training prove just as vital as analytical vigilance. Clean-in-place validation targets all transfer lines and reactors, since even micro-scale cross-contamination from previously handled materials proves disastrous for high-purity requirements. We maintain production logs and digitized batch records dating back over a decade, which not only fulfill traceability requirements but offer real-world peace of mind during process troubleshooting.

    What Users Expect from High-Purity 3,5-Dimethoxybenzyl Alcohol

    Pharmaceutical process chemists communicate exactly what they want—consistency above all else. Any deviation in melting point, GC purity, or even solvent solubility means longer purification protocols and diminished process efficiency. We provide characterization sheets per lot, including not just purity, but also heavy metal and residue on ignition data, since downstream biological tests demand minimal interference from trace contaminants.

    For academic researchers, accessibility and reliability top the list. If a doctoral candidate or postdoc orders a shipment expecting a certain reactivity, the real-world performance cannot disappoint—research budgets are tight and experiment failure means weeks lost. Over many years, we’ve come to recognize direct calls from recurring customers who value not just product, but manufacturer support regarding shelf-life, handling, and compatibility with specific reaction types.

    Supporting Innovation and Customization

    Demand for 3,5-Dimethoxybenzyl Alcohol sometimes arrives with requests for tailored features—deuterated variants for NMR studies, or customized grades for particularly sensitive reaction steps. Our experience with scale-up, batch segregation, and impurity tracking allows for accommodation of such requests within current technology limitations. Some R&D chemists look to alternative solvents or stabilizing agents, and our development team directly supports troubleshooting of these process changes.

    Recent years have also shown more users exploring continuous flow synthesis, both for efficiency and green chemistry goals. We work with these teams to supply material in reactor-compatible packaging and to discuss any issues with in-line impurity accumulations. Some novel catalyst development projects request in-depth impurity breakdowns and performance guarantees. Our analytical labs deliver full chromatographic profiles for every batch, supporting the design and validation work further downstream.

    Handling and Storage—Lessons from the Floor

    Aromatic alcohols with two methoxy groups like 3,5-Dimethoxybenzyl Alcohol store well under nitrogen in sealed containers, especially when light and air are excluded. In our years operating bulk inventory, we’ve learned temperature swings catalyze polymerization and darkening—cool, dry rooms minimize decomposition. Fluctuations in warehouse humidity play a role in product longevity and ease of handling during drum fills or smaller bottle preparation.

    Disposal routines always hew to local regulation, but our plant recycles most processing solvents internally where feasible. Trace residues of 3,5-Dimethoxybenzyl Alcohol found in spent drums undergo washing and reclamation, and testing waste streams for regulatory compliance remains standard procedure for every outgoing lot. Every operator on the line respects the balance between loss prevention and environmental stewardship.

    Feedback from the Industry: Evolving Needs

    Over the last decade, demand patterns for 3,5-Dimethoxybenzyl Alcohol have shifted as pharmaceutical synthesis routes and green chemistry requirements move forward. Bulk buyers have pushed for lower residual solvent counts, reflecting heightened regulatory focus on extractables in both API and excipient manufacture. Our process engineering teams have responded by optimizing washing and vacuum stripping steps to minimize residuals to well below ICH Q3C guidelines.

    Input from R&D teams helps shape product development—organometallic researchers need further assurance on trace metal levels, organic photonics groups seek to understand long-term aging characteristics. Clear two-way dialogue with users on product limitations and handling risks has advanced not just our internal standards but the knowledge base of our industry peers. This ongoing exchange drives fine-tuning of everything from closure types to recommended storage atmospheres.

    Supply Chain Realities

    Despite advances in technology, 3,5-Dimethoxybenzyl Alcohol, like many specialty reagents, faces periodic raw material supply shocks. From sourcing benzaldehyde derivatives to maintaining production capacity during peak demand, our facility has built secondary supplier networks and maintains buffer stocks. Experience shows that preemptive production scheduling and communication with end users can forestall disruption, especially for customers who lock in quarterly or annual volume requirements.

    Global logistics challenges, like port slowdowns and customs delays, prompt a shift toward regional warehousing and direct air shipments where necessary. During peak cycles, we keep turnkey packaged stock close to major demand centers to avoid delays in project timelines for critical users. Our teams stay on top of packaging quality—often double-sealing or providing inert gas overlays—to ensure the material delivered matches the analytical profiles we certify.

    Workforce Pride and Perspective

    Many of our operators began as line workers and advanced to supervisors through years of training with specialty aromatic alcohols. On the floor, the pride in perfectly clear glassware, sharp test results, and zero deviations serves as fuel for teams during long production campaigns. Each drum or bottle sent out carries the signature not just of our brand, but of generations of chemical craftsmanship.

    The satisfaction of hearing back from a customer who saved weeks of troubleshooting or improved their yields thanks to clean, unadulterated 3,5-Dimethoxybenzyl Alcohol carries weight for every member of the team. We share best practices at industry gatherings and publish findings, recognizing that better manufacturing ultimately means higher standards across the board.

    Looking Forward—Supporting Progress and Quality

    Progress in field chemistry and manufacturing methods set new benchmarks every year. Higher standards for trace metal analysis, stricter residue thresholds, and increasing demand for greener processing drive continuous investment on our production floor. Plant upgrades and new filtration technology help us deliver better batch uniformity today than a decade ago.

    Every user counts on the difference—whether synthesizing an active pharmaceutical ingredient or developing a new sensing molecule for diagnostics. Each bottle of 3,5-Dimethoxybenzyl Alcohol stands as proof of partnership between manufacturing experience and laboratory know-how. We welcome the ongoing challenge of helping customers push the edge of chemical innovation with carefully crafted, dependable materials every step of the way.