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3,5-Dibenzyloxybenzyl Alcohol

    • Product Name 3,5-Dibenzyloxybenzyl Alcohol
    • Alias 3,5-Bis(benzyloxy)benzyl alcohol
    • Einecs 629-042-2
    • 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

    131335

    Name 3,5-Dibenzyloxybenzyl Alcohol
    Cas Number 67518-11-2
    Molecular Formula C21H20O3
    Molecular Weight 320.38
    Appearance White to off-white solid
    Melting Point 90-94°C
    Solubility Slightly soluble in organic solvents
    Density 1.17 g/cm³ (estimated)
    Purity Typically ≥98.0%
    Storage Temperature Store at 2-8°C
    Smiles OCC1=CC(OCc2ccccc2)=CC(OCc3ccccc3)=C1
    Synonyms 3,5-Bis(benzyloxy)benzyl alcohol

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

    Packing & Storage
    Packing 3,5-Dibenzyloxybenzyl Alcohol, 25g, is packaged in a sealed amber glass bottle with a secure screw cap for protection against light.
    Shipping 3,5-Dibenzyloxybenzyl Alcohol is shipped in secure, airtight containers to prevent contamination and moisture exposure. It is packed following chemical safety guidelines, typically labeled with hazard information. During transit, the chemical must be protected from heat, direct sunlight, and incompatible substances, ensuring compliance with local and international shipping regulations.
    Storage 3,5-Dibenzyloxybenzyl alcohol should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents. Properly label the container, and store at room temperature unless otherwise specified by the manufacturer’s guidelines. Always follow standard chemical storage protocols for laboratory safety.
    Application of 3,5-Dibenzyloxybenzyl Alcohol

    Applications of 3,5-Dibenzyloxybenzyl Alcohol in Industrial Manufacturing

    3,5-Dibenzyloxybenzyl Alcohol, manufactured under stringent quality systems, serves as a vital intermediate or functional additive in several advanced chemical industry sectors. Below, we describe practical industrial settings that regularly incorporate this compound in processes adhering to the regulatory and operational norms of their respective value chains.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical companies employ 3,5-Dibenzyloxybenzyl Alcohol as a key structural building block in the multi-step synthesis of specialty APIs, especially in the development of complex heterocyclic drugs. Chemists integrate the compound in the alkylation or protection phases within proprietary synthetic routes. Its high purity ensures consistent product yields and contamination control from laboratory to pilot and commercial manufacturing, supporting regulatory documentation and downstream formulation objectives.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia / National Formulary) for intermediates
    • EDQM (European Directorate for the Quality of Medicines) guidance
    • WHO Technical Report Series for pharmaceutical manufacturing

    Typical usage ratio

    • In API synthesis, introduced typically at 0.08–0.15 molar equivalents relative to core pharmaceutical scaffolds; precise ratio determined by reaction stoichiometry and stage of synthetic route.

    Downstream process integration

    • Alkylation or benzyl protection stage in intermediate formation, added after initial condensation reactions. Purified by crystallization or chromatography before proceeding to deprotection or further transformation steps.

    Final product types

    • Antineoplastics with benzyl-protected intermediates
    • Atypical antipsychotic drug active ingredients
    • Small-molecule oncology compounds
    • API intermediates for patent-protected medicines

    2. Fine Chemical Synthesis for Agrochemicals

    Producers of high-value selective herbicides and fungicides employ this alcohol as a protecting group agent and as a nucleophilic precursor during the structural modification of active molecules. Its contribution enables the assembly of active compounds with improved resistance to environmental degradation and optimized field performance, crucial for downstream formulation plants certified under pesticide quality standards.

    Industry compliance standards

    • FAO/WHO Specification Guidelines for Pesticides
    • ISO 9001:2015 for agrochemical manufacturing
    • REACH Regulation (EC) No 1907/2006 compliance for European market
    • China GB/T 1604 for chemical synthesis in agrosciences

    Typical usage ratio

    • Added at 2–7% w/w as an intermediate in synthetic batch processes, with exact concentration based on desired precursor conversion and downstream yield requirements.

    Downstream process integration

    • Feeds into selective benzyl protection and subsequent functionalization prior to final active ingredient assembly. Recovered intermediates undergo selective hydrogenation or deprotection before formulation.

    Final product types

    • Benzyl-protected herbicide actives
    • Fungicidal core intermediates for post-emergent applications
    • Precursors for specialty insecticide scaffolds
    • Complex agrochemical intermediates

    3. Monomer Synthesis for Specialty Polymer Manufacturing

    Manufacturers in the specialty plastics and advanced polymer sector include 3,5-Dibenzyloxybenzyl Alcohol in the creation of custom monomers for resins targeted at electronics, coatings, and heat-resistant polymers. Its aromatic benzyl groups contribute to achieving high glass transition temperatures and controlled cross-link densities. Quality control throughout integration ensures downstream batch-to-batch reproducibility and safety in compliance with regulatory oversight for polymer applications.

    Industry compliance standards

    • ISO 9001 certified QMS for polymer raw material suppliers
    • RoHS (Restriction of Hazardous Substances Directive) for electronic materials
    • REACH Regulation (EC) No 1907/2006 for monomer registration
    • UL 94 standards for polymer flame retardancy if used in electronic parts

    Typical usage ratio

    • Incorporated at ratios between 1–4% by mol in co-monomer blends, with final percentage determined by required polymer characteristics and tested in laboratory screening prior to scale-up.

    Downstream process integration

    • Charged during pre-polymerization phase as a functional monomer component, followed by step-growth or chain-growth reactions such as A-B stepwise addition for high-performance thermosets and specialty copolymers.

    Final product types

    • Thermosetting resins for printed circuit boards
    • Specialty coatings and varnishes for industrial use
    • High-temperature-resistant engineering plastics
    • Optically clear polymer sheets for electronic applications

    4. Organic Synthesis of Liquid Crystal Precursors

    Producers for the liquid crystal display (LCD) industry rely on this alcohol as a precursor in constructing rigid-core liquid crystal molecules. The unique arrangement of aromatic benzyl ethers assists in tuning mesogenic properties essential for high-clarity display performance. Precise documentation and traceability of raw input support QC benchmarks required by international display panel manufacturers and component suppliers.

    Industry compliance standards

    • ISO 14001 for environmental management in chemical handling (for display panel supply chains)
    • RoHS for electronic material application
    • IEC 61249-2-21 standards for base materials used in displays
    • JEITA standards (Japan Electronics and Information Technology Industries Association)

    Typical usage ratio

    • Integrated at 0.5–2% molar proportion in the core-forming steps for most nematic and smectic liquid crystal precursor syntheses. Ratio depends on desired phase transition temperature and mesophase stability.

    Downstream process integration

    • Introduced during aromatic coupling or etherification steps, forming rigid biphenyl or terphenyl cores. Reaction monitored by HPLC and mass spectrometry to ensure consistent precursor profile for downstream blending.

    Final product types

    • Nemato-stable liquid crystal molecules
    • Precursor compounds for TFT-LCD materials
    • Advanced mixtures for display component manufacturing
    • High-purity mesogenic intermediates

    5. Reference Material and Analytical Standards Production

    Companies manufacturing certified reference materials for pharmaceutical and fine chemical analysis exploit the precise molecular purity of 3,5-Dibenzyloxybenzyl Alcohol to calibrate and validate analytical systems. Used for system suitability and calibration of HPLC, GC-MS, and LC-MS instruments, it ensures quantitation accuracy in corporate and independent laboratory networks, contributing to method validation and regulatory dossier submissions worldwide.

    Industry compliance standards

    • ISO/IEC 17025 for testing and calibration laboratories
    • ISO Guide 34 for reference material producers
    • USP Chapter <1058> for analytical instrument qualification
    • Ph. Eur. General Chapter 2.2.46 for chromatographic purity

    Typical usage ratio

    • Prepared as analytical standards at concentrations of 0.5–20 µg/mL for calibration curves, and as internal standards at 0.01–0.1% w/w relative to sample mass as dictated by standard operating procedures.

    Downstream process integration

    • Precisely weighed and dissolved during certified reference material formulation and bottled under nitrogen. Used in QC departments for validating method performance before sample series analysis.

    Final product types

    • Certified calibration standards for HPLC and GC-MS
    • System suitability solutions
    • Pharmacopoeial reference substances
    • Analytical method validation kits
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    Certification & Compliance
    More Introduction

    3,5-Dibenzyloxybenzyl Alcohol: Reliability Through Experience

    Digging Deeper: The Product Inside Our Reactors

    Producing 3,5-Dibenzyloxybenzyl Alcohol isn’t a simple routine. Over decades on the plant floor and in pilot labs, we’ve learned every step has a direct impact on purity and reproducibility. At its core, this molecule features a benzyl alcohol group attached to a benzene ring shielded by two benzyloxy groups at the 3 and 5 positions. Why does that distinct structure matter? The two benzyloxy groups determine how it interacts in downstream syntheses, governing pathways that depend on shielding reactive sites.

    We handle this compound as the starting point for more advanced molecules used in fields like pharmaceuticals, liquid crystal research, and certain polymers. For chemists looking to build more complex aromatic structures or seeking a pinpoint-selective protecting group that stands up to basic and acidic conditions, this alcohol offers a reactivity profile distinct from less-protected counterparts. It steps up in targeted O-alkylation, cross-coupling reactions, and stepwise assembly of substituted benzene derivatives when both electron-donating effects and steric hindrance are needed.

    In our own experience scaling up from flask to batch reactors, the biggest stumbling blocks haven’t come from the chemistry, but rather from the mounting of purification. Benzylation, if not controlled carefully, can yield a product riddled with mono-benzylated or over-benzylated byproducts – neither of which matches your needs downstream. We monitor not only by standard HPLC, but also run controls for trace residual solvents and metal catalysts, since these can derail catalytic steps in pharma synthesis or photophysical measurements in material science.

    The finished product emerges as a white to off-white crystalline solid, typically packed in moisture-tight HDPE bottles or drums depending on scale. We aim for a purity—checked by GC-MS and NMR—that routinely falls above 99%, with water content kept ultra-low for applications like pharmaceutical intermediates. Customers have shown us time and again that even slight upticks in moisture or unseen impurities show up as retention issues in their columns or as soft signals in their NMR runs. Consistency comes not just from validated prep steps, but from a crew trained to notice when a batch crystallizes with even the slightest off-shade or crystal habit.

    Why Structure and Process Details Matter

    Chemists sometimes ask us what actually sets apart our 3,5-Dibenzyloxybenzyl Alcohol from more basic benzyl alcohol derivatives or even similar 2,4-substituted homologues. From repeated feedback, the dual substitution at the meta positions enhances both chemical stability and selectivity during further modification. In research labs and production, positional isomers can introduce separation headaches. A non-meta-symmetric molecule like 2,4-dibenzyloxybenzyl alcohol may seem interchangeable, but in our experience, downstream yield and isomeric purity can nose-dive if the wrong starting skeleton sneaks in.

    The presence of the extra benzyloxy groups at 3 and 5 positions doesn’t just influence synthesis; it noticeably affects solubility, resistance to oxidative degradation, and even shelf profile. This is not a compound you toss in with generic solvents and expect no surprises. Through years of trial and error—especially dealing with purification after large-scale reactions—we’ve seen how improper handling or storage can introduce benzyl alcohol oxidation products, darkening the appearance or producing faint but sharp odors. A research chemist told us how a trace of oxidized impurity derailed their peptide coupling strategy, something we take to heart in how we package and store.

    Many newcomers assume that differences in benzyl alcohol derivatives are minor, with only subtle changes in melting points or solubility. Our plant trials showed otherwise: batches produced with generic benzylating agents often ran into issues with persistent oiling-out or crystallization defects. Scaling dozens of batches, we’ve learned to adjust temperature ramps, order of addition, and even cooling rates, since these make or break crystallinity and purity. With each run, production and QC teams meet to compare crystal scans, speak up on odd lots, and tighten controls. Every kilogram of 3,5-Dibenzyloxybenzyl Alcohol reflects both a controlled manufacturing system and an experienced set of hands.

    Where 3,5-Dibenzyloxybenzyl Alcohol Shows Its Strengths

    Most of our product finds its way into the hands of medicinal chemists and process developers building core scaffolds for APIs, particularly those exploring ether protections that stay inert during hydrogenolysis or acidolysis. The dual benzyloxy pattern doesn’t fall off easily, so it lets chemists build up and deprotect in sequential steps without risking side reactions. Traditional benzyl or mono-benzyloxy alcohols can dislodge too soon, unraveling a multi-step synthesis.

    A trend among some of our clients includes using the alcohol group for further diversifications: Suzuki couplings, Mitsunobu reactions, and formation of specialized carbamate or ester derivatives. Applications in the specialty chemicals sector include advanced materials for optoelectronics. Techs working at pilot plants have relayed that using less purified starting alcohol makes downstream photochemical steps unpredictable, causing slowdowns and increased quality control interventions. Many times, a well-characterized starting material cuts out hours of troubleshooting and unnecessary repurification.

    We have also supplied this compound for companies working in peptide chemistry, specifically as a building block for orthogonal protection schemes. In these settings, if protecting groups come off at the wrong pH or after the wrong amount of time under hydrogenation, entire project timelines stretch out. Direct conversation with their lab teams has thrown light on maintenance of protecting groups, the risk of premature loss of the benzyloxy, and the downstream effect on project costs.

    Inside Our Manufacturing Mindset

    Ask anyone on our production team about 3,5-Dibenzyloxybenzyl Alcohol, and you’ll get an answer rooted in repetition: it’s a process honed through trial, failure, and incremental change. We source raw benzyl chloride and phenolic intermediates only from suppliers who document each lot, after seeing too many failed batches in the past from off-spec reactivity or contaminated drums. Each kilogram that leaves our gates carries not only a certificate of analysis, but the expectation that any deviation—impurity profile, melt point drop, or inconsistent color—calls for immediate review.

    Our facility works at scales ranging from 500 grams in glass reactors up to multi-hundred kilo stainless systems, depending on downstream customer demand and project pipeline. In the early days, we noticed the transition from kilo lab to plant presented solvents and pressure control challenges. By re-designing venting, swapping stirrer configurations, and fine-tuning distillation rates, we managed to lower byproduct formation rates and raise overall yields. Regular meetings bring together operators, safety engineers, and chemists to swap notes and propose further tweaks.

    The best feedback, though, comes from customers sending back analytical comparisons: overlayed chromatograms showing that our batches stack up batch-after-batch, regardless of size. We keep archiving these reports, building a data set that guides future adjustments. Keeping full traceability from packed drum back to source drum matters for regulated industries, but to us it also keeps the culture of vigilance front and center. We have seen first-hand how lapses in documentation or casual acceptance of substandard batches result in returns, wasted hours, and sometimes lost client trust.

    The Everyday Challenges and Working Solutions

    Making a pure 3,5-Dibenzyloxybenzyl Alcohol isn’t just about running a reaction to completion and writing down a number on the purity line of a certificate. Solvent removal step after filtration needs close attention, because traces of polar solvents or stabilizers used upstream will show themselves weeks later during client analysis. We switched over to an in-house multi-vacuum line system years back, giving us more control over residuals. It was not a cheap move, and brought pushback at first, but higher upfront costs paid off with a drop in client complaints and a better reputation in the field.

    Another pain point revolves around packaging and long-distance logistics. During humid seasons or airfreight delays, we saw some lots arriving with subtle color changes—usually a red flag for hydrolysis or oxidation. Working with packaging partners, we shifted away from standard drum liners to a more robust multilayer bag system with gas flush, and started quarterly audits of packouts. Each small improvement came about after someone raised their hand during a quality review, often spurred by a client’s phone call or a surprise stability fail.

    Scale brings its own set of issues. In small batch production, even a single operator’s oversight—such as rushing a crystallization or missing a filtration endpoint—shows up in downstream product performance. At multi-ton scale, process drift isn’t always obvious, so we now rely more on automated analytical checks, not just waiting on standard QC reports. Automated melting point, HRMS, and water content checks run on every batch, with side-by-side human review for crystal appearance and lot-to-lot consistency. Relying solely on machines would dull our team’s edge and let smaller visual cues slide.

    Listening and Adapting: User Experiences in the Field

    We manufacture, but our best lessons come from hands-on chemists and engineers who don’t hesitate to share pain points. A materials scientist who ordered a large shipment for OLED precursor studies reached out about out-of-spec luminescence after processing. After a joint review, we traced the culprit to subvisible particulate matter, prompting a complete overhaul of our pre-packing sieving protocol. Since then, additional cross-filtration and in-line filters all but eliminated the issue.

    On a separate project, a pharmaceutical partner required 10-times the usual batch size, but their synthetic step proved sensitive to even minor shifts in trace halide content. As a result, we retrofitted an ion-exchange purification step, adding extra cost and days to our process, but ensured the batch passed their QC with room to spare. Since then, every process scale-up review asks whether additional halide control, or other trace element checks, might prove necessary in the coming year.

    The most eye-opening feedback has come from R&D chemists at start-ups. They tend to push our product into non-traditional reactions: testing photoredox catalysis, novel cross-linking strategies, and even hyperconjugation-driven syntheses. Because our 3,5-Dibenzyloxybenzyl Alcohol resists many standard deprotection steps, these users have found ways to use it as a “stubborn” placeholder—removable only under carefully controlled reaction environments, allowing them to try novel pathways. Each time they meet complications, our support team and their bench chemists open up a dialogue, frequently improving how both sides view reactivity quirks and stability trade-offs.

    How 3,5-Dibenzyloxybenzyl Alcohol Differs From Other Benzyl Alcohol Derivatives

    A persistent misconception: all benzyl alcohol derivatives play the same role in multistep organic synthesis. Based on years of talking directly to process chemists, it’s plain that the position and nature of protecting groups change everything. Take mono-benzyloxybenzyl alcohol—side reactions and partial deprotection rear up, with uneven reactivity making downstream batch purification much more tedious. Customers who shift from generic mono-protected alcohols to our 3,5-disubstituted version find fewer surprises during both hydrogenation and acidic work-ups.

    Products similar in name, but different in structure, often show up in catalogs—2,4-dibenzyloxy isomers or even analogues with larger alkoxy groups. We have tested several of these in-house. Consistently, their resistance to unwanted cleavage and their predictability in multi-step sequences fall short. The precise 3,5 pattern not only steers synthetic intermediates away from byproduct formation during harsh deprotection, but its physical properties—higher melting point, greater resistance to acid-catalyzed hydrolysis—hold up even under repeated solvent-swelling and evaporation cycles in pilot plants.

    Another difference comes in the ease of purification. Some similar compounds show broad melting transitions, oil out during crystallization, and force reprocessing. Our product, due to both process refinement and careful control of seed crystals, reliably delivers sharp melting points and solid recovery every time—a bonus for those handling multistep final assemblies.

    As the original producer, we keep open lines of communication with users who spot anomalies. We see the whole spectrum—users who drive the compound into unfamiliar territory, or who scale up with new solvents and see new impurities. This feedback doesn’t just inform our technical bulletins but directly tweaks our process, benefiting each subsequent lot.

    Keeping Up with Regulations and Customer Needs

    Every year brings fresh regulatory scrutiny and shifting project requirements from our various partners. Manufacturing 3,5-Dibenzyloxybenzyl Alcohol isn’t just about getting numbers right on analytical reports. In highly regulated industries—especially pharma and food contact materials—documentation, traceability, and impurity profiling take priority. Our people keep records that don’t just meet paper standards, but offer deep transparency if any lot requires a review months or years later. QA audits cross-check raw material certificates, blending records, and shipping logs. This tangled paper trail has saved time during surprise audits or client site visits in the past.

    Globally, some regions ask for a different grade or specific analytical certification. South Korea and Switzerland, for instance, set particular standards for trace metals, solvents, and benzylating agents. This led our QC team to split production lines, offering both research and full cGMP-compliant versions. The global regulatory scene can shift yearly, so we track new directives and test proactively, not just reactively, in our analytical lab. For well-established partners, we send samples from each new batch, even if the end-use falls into research and not production.

    Clients in more regulated applications occasionally ask for full transparency: impurity breakdowns, spectral overlays, and method validation records. After many years in this business, we prefer giving more than enough detail rather than fielding hurried phone calls after-the-fact. Over time, our customer support pipeline matured from areas just covering order fulfillment to technical advice and detailed regulatory consultation—often before the order even ships.

    A big part of keeping trust lies in the availability of experienced technical staff. Chemists preparing for process qualification phases need someone on the other end who not only understands the chemistry, but has seen first-hand the batch-to-batch quirks that matter. Sustaining this accessibility remains a point of pride for us—and stands apart from generic resellers who may not even know who produces their material.

    The Road Forward: Improving the Process

    Learning and adapting is constant. As more downstream industries ramp up their quality expectations and regulatory frameworks sharpen, our team keeps pushing for trace impurity reduction, tighter moisture control, and improved reproducibility. We have expanded our in-line analytical testing suite, invested in further automation for mixing and crystallization, and encouraged a workplace culture where pointing out potential problems isn’t just accepted, but expected.

    Each batch of 3,5-Dibenzyloxybenzyl Alcohol reflects years of plant-level insight, equipment upgrades, and the experience drawn from close work with customers. It’s a collaborative effort—one rooted just as much in listening and adapting as in technical know-how and manufacturing scale. Every drum shipped carries not only our guarantee of quality, but also the lessons gathered from every preceding run, every troubleshooting call, and every user pushing the molecule in new directions.

    By listening, refining, and tracking our own performance, we aim not just to meet, but to anticipate, the challenges customers face—delivering a material that stands up in the real world, batch after batch.