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HS Code |
504970 |
| Name | 3-Benzyloxybenzyl Alcohol |
| Cas Number | 885-77-8 |
| Molecular Formula | C14H14O2 |
| Molecular Weight | 214.26 g/mol |
| Appearance | White to off-white solid |
| Boiling Point | 424.1 °C at 760 mmHg |
| Melting Point | 74-78 °C |
| Density | 1.17 g/cm3 |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CC(=CC(=C1)CO)OCC2=CC=CC=C2 |
| Purity | Typically ≥98% |
| Storage Temperature | Store at 2-8 °C |
| Synonyms | 3-(Benzyloxy)benzyl alcohol |
As an accredited 3-Benzyloxybenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3-Benzyloxybenzyl Alcohol supplied in a tightly sealed amber glass bottle with tamper-evident cap, labeled for laboratory use. |
| Shipping | 3-Benzyloxybenzyl Alcohol is shipped in tightly sealed containers, protected from light and moisture. It is handled as a non-hazardous chemical under normal transport regulations, but appropriate labeling and documentation are ensured. Packages are cushioned to prevent breakage and shipped via regulated carriers to maintain product integrity during transit. |
| Storage | 3-Benzyloxybenzyl 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, ideally at temperatures between 2–8°C (refrigerated). Protect from moisture and incompatible substances such as strong oxidizers. Clearly label the container, and follow standard laboratory safety and chemical storage protocols. |
Applications of 3-Benzyloxybenzyl Alcohol in Industrial Manufacturing3-Benzyloxybenzyl Alcohol serves as a vital intermediate in numerous downstream applications across the pharmaceutical, fine chemical, and specialty chemical sectors. As a dedicated manufacturer, we supply this compound to partners with advanced integration needs focused on value-added synthesis routes. Below, we outline verified industrial application scenarios, with details for compliance, formulation, process, and product output. 1. Pharmaceutical Intermediate Synthesis for Antihistamine APIsSeveral second-generation antihistamine API producers utilize this compound for constructing complex aromatic structures, applying it as a protected benzyl alcohol in multi-step synthetic pathways. API manufacturers often choose this intermediate to achieve regioselective functional group transformation, crucial during active moiety assembly and deprotection stages that precede final purification and formulation. Industry compliance standards
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2. Specialty UV Absorber Manufacturing for High-Performance PolymersThis material functions as a precursor in the synthesis of high-value ultraviolet (UV) absorbers engineered into engineering plastics and advanced coatings. Chemical plants incorporate it to build diaryl ketone or benzophenone UV-absorbing units, which protect polymers against light-induced degradation in demanding automotive, electronics, and outdoor environments. Industry compliance standards
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3. Fragrance Ingredient Intermediate in Fine Aroma ChemicalsLeading aroma manufacturers employ the compound in targeted O-alkylation processes, generating key intermediates for luxury perfumery, personal care odorants, and flavor-modifying agents. Due to its defined aromatic profile, formulators value it for building complex benzyloxy compounds that influence volatility and overall fragrance performance in finished blends. Industry compliance standards
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4. Liquid Crystal Intermediate for Electronic Display MaterialsManufacturers specializing in advanced liquid crystal (LC) mixtures deploy this material as a scaffold for core aromatic structures. Its controlled reactivity and high-purity synthetic profile make it suitable for the precise assembly of LC esters and ethers, instrumental in achieving desired birefringence and dielectric properties for modern TFT-LCD and OLED panels. Industry compliance standards
Typical usage ratio
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5. Advanced Epoxy and Monomer Synthesis for Specialty ResinsIn the specialty resin sector, this compound's benzyloxy modification enables the synthesis of high-performance monomers and epoxy intermediates. Manufacturers employ it to increase aromatic density and fine-tune molecular weight distribution, leading to customized curing profiles and superior mechanical properties in finished epoxies for electronics, high-strength adhesives, and specialty coatings. Industry compliance standards
Typical usage ratio
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Producing 3-Benzyloxybenzyl Alcohol isn’t just about following a recipe or tuning processes to meet a checklist. Working in this business, we've seen how important it is to dig into the details—right down to each batch’s appearance, the purity levels we hit, and how the product behaves further down the line for those who use it. Every reaction and every adjustment in our tanks reflects years of know-how and commitment from our plant operators, QC teams, and engineers. Each bottle or drum that leaves our site represents this teamwork.
In our plant, 3-Benzyloxybenzyl Alcohol stands out among benzyloxy-substituted benzyl compounds due to its consistent performance in fine chemical synthesis. Its molecular structure is C14H14O2, and our output comes out as a colorless to pale yellow, oily liquid. Purity targets are not just a number to us—they drive our daily routines. We routinely achieve a purity above 98.0%, with water and related-substance levels tested by GC and HPLC in-house, so what leaves here aligns with rigorous standards of specialty chemical applications.
We've worked out reliable routes to synthesize 3-Benzyloxybenzyl Alcohol over the years. Most commercial processes use a selective reduction approach after careful etherification of precursor aromatics. Real-world production means managing issues like byproduct removal, resin fouling, and residue disposal. Clean isolation and drying allow us to keep lots off-spec incidents to a minimum without cutting corners. Every kilogram tells a story of raw materials chosen for reactivity and easy handling, solvents selected for their impact on both yield and environmental control, and a technician’s know-how with temperature and agitation.
This product mainly serves as a building block in pharmaceutical research, functional polymer production, and fragrance chemistry. Our conversations with formulation chemists or downstream blenders confirm that the downstream utility of 3-Benzyloxybenzyl Alcohol is determined by low levels of metal ions, minimal peroxide formation during storage, and a neutral odor profile. Some batches go out to R&D labs where trace metals might wreck a catalyst run; other shipments end up as intermediates for patent-protected APIs or specialty resins.
Many chemists ask why this material works where similar benzyl alcohols might not perform as needed. The answer comes back to molecular substitution and the benzyloxy group’s unique positioning. Compared to 4-benzyloxybenzyl alcohol, the 3-position brings different reactivity for controlled ether cleavage, cross-linking, and mild oxidation. Customers have shared stories where small changes in the starting material—like shifting a benzyloxy group from para to meta—led to entire process redesigns due to changes in solubility, melting point, or even regulatory approval for trace impurities.
In our lab, we routinely run comparison tests: 3-Benzyloxybenzyl Alcohol exhibits stronger resistance to para-directed side reactions. Its stability in basic and acidic media means fewer headaches when handling, storing, or shipping—even at higher temperatures or after long-haul transport. This translates straight to less batch-to-batch variability, which many R&D teams appreciate when they scale up from gram-level experiments to multi-kilo runs.
Sitting across the table from formulation chemists, we’ve heard time and again how 3-Benzyloxybenzyl Alcohol factors into active ingredient synthesis. Last year, a major agricultural client approached us to troubleshoot a persistent side-reaction issue—a byproduct that kept popping up while using unsubstituted benzyl alcohols as starting points. Swapping in our 3-benzyloxy derivative dramatically cut byproducts and improved selectivity after two test campaigns. They shifted the protocol; yields climbed, and unnecessary purification steps dropped out.
Another client working on functionalized polymers for electronics described difficulties incorporating 4-benzyloxybenzyl alcohol: their cross-linking efficiency was erratic. We supplied small pilot lots of our 3-substituted grade. They immediately noticed a smoother reaction curve during polymerization, with fewer unreacted monomers at the endpoint. The product’s better solubility profile allowed them to bump up active concentrations, trimming energy input and waste across the board. These operational wins don’t grab headlines, but in the factory, they mean cost savings and less downtime.
Too often, buyers looking for high-purity specialty chemicals assume everything rests on a certificate of analysis. Our experience challenges this idea. The analysis document is a snapshot, not the full picture. What matters is the story behind the data—how our crews cleaned the reactors to minimize contamination, or how we validated each analytical step from melting point checks through spectral confirmation. Every day starts with a walk-through of the plant floor. Unplanned noise, leaks, or batch delays don’t hide long in our shop, because everyone’s got skin in the game.
We keep extensive batch histories to track how process tweaks affect final specs. For 3-Benzyloxybenzyl Alcohol, we monitor not only purity and residual solvents, but also shelf-life stability. Past runs have shown that adjusting crystallization speed during work-up prevents oily residues, and tiny changes in distillation pressure yield marked improvements in the product’s handling properties. Each lesson comes written in the logs, and we teach newcomers not to overlook small operational details, because one slip can snowball into a quality incident.
Sourcing raw materials for specialty aromatic alcohols can trigger surprises. Sometimes, a global spike in benzyl chloride pushes us to qualify alternative suppliers. Other times, solvent markets tighten after regulatory shifts. These supply chain realities directly hit the bottom line and challenge how we commit to customers on delivery timelines and lot uniformity. Through it all, we rely on long-standing vendor relationships and a robust QA process to lock in material specs and minimize disruptions.
There have been years when an upstream issue forced us to tweak our process mid-campaign—like having to pre-treat incoming phenol batches to remove trace inhibitors, or extending purification cycles to counteract subtle impurities showing up in test chromatograms. Each course-correction means additional reporting, more stress tests, and long hours for our technical teams. In the end, real-world manufacturing means embracing these variables, not wishing them away. We adapt on the fly, because our customers have delivery schedules to meet and formulation pipelines to keep moving forward.
Talk to a process chemist who actually uses 3-Benzyloxybenzyl Alcohol, and the conversation quickly shifts from purity certificates to practical details—how fast it reacts, what byproducts show up, and how robust it is in standard reactions. The electron-donating benzyloxy group at the 3-position paves the way for selective oxidation, ether cleavage, and condensation. Compared to ortho- or para-analogues, we see fewer ortho-quinone byproducts and more streamlined purification steps.
We’re often asked to share reactivity data. Oxidation with manganese dioxide runs clean at lab and pilot scales, while catalytic hydrogenation yields the parent alcohol with minimal residue. In peptide and pharmaceutical synthesis, clients have reported that our product’s improved solubility profile in polar aprotic solvents simplifies work-up steps—a small detail, but one that shaves hours off downstream processing time. Even changes in minor byproduct distribution have ripple effects, especially where tighter impurity profiles make the difference between a successful drug approval and a missed opportunity.
Handling specialty chemicals like 3-Benzyloxybenzyl Alcohol means spending time on the ground—refining procedures, optimizing ventilation, and supporting robust emergency drills. Over the years, our plant operators have helped refine spill and exposure responses, based on hard-earned experience. Our facilities incorporate closed-system charging and advanced scrubber units, addressing both local regulatory standards and our own commitment to team safety.
We’ve seen how poor ventilation or inadequate PPE can undermine plant safety during large tank transfers or decanting. We’ve also learned to manage waste streams tightly—with on-site treatment for wash solvents, and high-integrity storage to avoid leaks. Producing this material responsibly means more than meeting a checklist: it’s about building muscle memory in the crew, designing better batch records, and reinforcing culture so that a deviation doesn’t spiral into a real incident.
Direct conversations with users shape how we scale. Unexpected questions in a lab or pilot trial get back to our process engineers within hours, not weeks. Last quarter, a customer flagged subtle changes in GC trace profiles; after digging through our process logs, we traced a new trace impurity to a vendor’s resin switch and adjusted our purification steps. For us, follow-up communication always mirrors factory reality—complete with the usual challenges and lessons learned.
We see the long-term value in sharing practical handling tips. Over the last few years, feedback on storage stability led us to invest in improved drum linings to cut peroxide formation and boost shelf life. This reduces surprises at the customer’s site and avoids costly investigations or returns. The line between our batch records and your laboratory notebook stays clear thanks to transparent technical support, close coordination, and shared success metrics.
Developing 3-Benzyloxybenzyl Alcohol in response to real industry needs gives our team a sense of pride. One pharma partner kicked off a series of pilot trials, aiming to shorten a multi-step synthesis for a new CNS-active compound. They wanted reliable supply and lots matching regulatory expectations on trace residues. We worked side by side with their scientists—providing batch samples, running parallel impurity profiles, and pivoting our purification protocols as their route matured from the benchtop to full scale. Thanks to this close collaboration, they cut production wash cycles and reached process validation ahead of schedule.
Work with academic labs also shapes how we operate. Earlier this year, a university researcher requested support for a subtle isotope-labeled variant. Our team drew on past experience with hazardous intermediates and designed a safe path for small-scale synthesis—balancing practical plant safety with exacting research demands. These efforts rarely turn into mass-market sales, but they improve our skills, refine our processes, and drive us to tackle new technical obstacles with confidence.
Picking the right intermediate often means trading off yield, cost, and cleanup requirements. Against other benzyloxy-substituted benzyl alcohols, the 3-position stands out for its consistent handling, reliable reactivity under diverse conditions, and minimal formation of byproducts that could require laborious purification downstream. This helps researchers and manufacturers hit target specs more quickly, reducing unnecessary waste.
Talk with users who tried the 4- or ortho-analogs, and stories of stuck crystallizations or shifting impurity patterns surface. Our operational data, gathered over years, shows tighter control over residual solvents and side products in the 3-benzyloxy isomer, cutting off unexpected regulatory or QC headaches before they begin. By listening to these reports—not just measuring them—we adapt our plant procedures so every shipment builds on lessons learned in the field.
Switching from a different benzyl alcohol isomer isn’t always straightforward, but in many cases, direct feedback tells us the benefits stack up: lower energy input at comparable output, more predictable process cycles, and stable product supply even during market shortages. Each transition also serves as a training ground—forcing our team to revisit SOPs, refine test methods, and improve operator training.
Working as a manufacturer, we see how market swings, seasonal fluctuations, and regulatory changes affect specialty chemical supplies. There have been times when upstream disruptions forced us to draw down local inventories, recruit new raw material partners, or tweak our production schedule on short notice. Despite these twists and turns, we have developed a playbook that rests on flexibility, steady communication, and investing in supplier relationships that go beyond contracts.
Each campaign—whether a single 200-liter batch or a full multi-ton annual order—draws on the insights of every person, from shift supervisors spotting minor process deviations to analytical chemists developing rapid screening protocols for contaminants. Over time, our willingness to troubleshoot and solve production challenges—rather than just fill out paperwork—sets us apart from suppliers who never witness the process from inside the factory.
We run post-mortems after each production run, looking for small gains or process bottlenecks, aiming to cut scrap, speed up cycle times, and reduce manual handling hazards. Last year, by introducing a refined filtration step and a new temperature control sequence during synthesis, we boosted average yield by four percent and trimmed time-to-drum loading by two hours. Over a full campaign, those numbers translate to real value for customers facing tight production forecasts or sudden upticks in demand.
Paying close attention to customer returns, storage data, and in-house analytics has also helped us cut product complaints. Discovering that a specific batch absorbed more moisture during humid months prompted investments in improved warehouse climate control, slashed internal waste, and improved delivered material quality. Our learnings don’t just stay in-house—they flow back to development partners, speeding up their project timelines and reducing unwanted surprises.
Trust in specialty chemicals supply comes from a willingness to share real data, good or bad, and an openness to scrutiny. Over the years, our willingness to invite third-party auditors, improve product documentation, and respond promptly to deviation reports has set the foundation for long-term industry relationships. For 3-Benzyloxybenzyl Alcohol, this translates into an open line for feedback after every delivery and a culture of transparency from ordering through delivery.
We know that issues sometimes arise: a shift in product color, a trace impurity detected in an application, or an unexpected stability question. What separates robust manufacturers isn’t a promise of perfection; it’s a demonstrated ability to respond quickly, investigate systematically, and put in corrective actions. Our records, logs, and testing standards aren’t just regulatory checkboxes—they’re the backbone for delivering materials people can rely on, year after year.
As a chemical manufacturer, we're excited to see new research and market trends shaping demand for compounds like 3-Benzyloxybenzyl Alcohol. Improvements in green chemistry, growing demand for advanced functional materials, and new directions in API development keep pushing us to improve production, invest in cleaner routes, and fine-tune quality assurance.
Our team believes that a genuine partnership mindset underpins unique advances in specialty chemical manufacturing. By drawing on the lessons of past campaigns, learning alongside our customers, and refining both old and new routes, we've built a resilient platform for pushing process and product innovation. Every improvement we introduce reflects a shared dedication with downstream innovators who count on stable, high-quality intermediates for their next chapter of research and manufacturing.