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HS Code |
246199 |
| Chemical Name | 3,5-Dibenzyloxyacetophenone |
| Molecular Formula | C23H20O3 |
| Molecular Weight | 344.41 g/mol |
| Cas Number | 5363-36-2 |
| Appearance | White to off-white solid |
| Melting Point | 93-97 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents (e.g., ethanol, DMSO) |
| Purity | Typically ≥98% |
| Smiles | CC(=O)C1=CC(OCc2ccccc2)=CC(OCc3ccccc3)=C1 |
| Synonyms | 3,5-Bis(benzyloxy)acetophenone |
| Storage Conditions | Store at 2-8 °C, keep container tightly closed |
As an accredited 3,5-Dibenzyloxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g 3,5-Dibenzyloxyacetophenone is packaged in a sealed amber glass bottle, clearly labeled with product details and safety information. |
| Shipping | 3,5-Dibenzyloxyacetophenone is shipped in tightly sealed containers to protect it from moisture, light, and contamination. The chemical is handled according to standard laboratory safety guidelines and transported in compliance with hazardous materials regulations. Ensure proper labeling and documentation for safe shipping and handling during transit. Store in a cool, dry place upon arrival. |
| Storage | 3,5-Dibenzyloxyacetophenone should be stored in a tightly sealed container, protected from light and moisture, and kept in a cool, dry, well-ventilated area. Avoid exposure to heat, sparks, and open flames. Store separately from incompatible substances such as strong oxidizing agents. Ensure proper labeling and keep out of reach of unauthorized personnel. Follow all safety guidelines for chemical storage. |
Applications of 3,5-Dibenzyloxyacetophenone in Industrial ManufacturingAs the direct manufacturer of 3,5-Dibenzyloxyacetophenone, we supply this intermediate for highly specific industrial value chains requiring controlled purity, precise addition points, and process reliability. Below, we detail key downstream applications that benefit from its molecular structure and functional properties, with a focus on end-use impact, regulatory frameworks, exact formulation ranges, process placement, and resulting products. 1. Active Pharmaceutical Ingredient (API) Synthesis for Central Nervous System DrugsSeveral pharmaceutical manufacturers use 3,5-Dibenzyloxyacetophenone as a core building block during the multistep synthesis of certain psychotropic API classes, including tailor-made benzylated acetophenone derivatives that underpin various CNS medications. This intermediate enters complex reaction sequences, supporting both halogenation and selective deprotection as required by API process development, with rigorous controls for GMP and impurity profiles to meet international regulatory standards. Industry compliance standards
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2. Advanced Fragrance Ingredient SynthesisThe fine chemicals sector incorporates 3,5-Dibenzyloxyacetophenone to create custom aromatic compounds, especially where stable, benzyl-protected intermediates permit longer shelf-life and process flexibility in high-value fragrance molecules. Carefully monitored additions guarantee compliance with IFRA and other safety requirements in the creation of non-hazardous, complex scents for the luxury perfumery segment. Industry compliance standards
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3. Photoinitiator Intermediate for UV-Curable CoatingsCoatings manufacturers utilize 3,5-Dibenzyloxyacetophenone as a protected intermediate in photoinitiator production, especially for advanced UV coating technologies demanding high purity and reproducible destabilization kinetics. Its molecular framework ensures controlled reactivity during final functionalization steps, producing tailored photoinitiators that comply with technical and toxicological standards in industrial surface protection applications. Industry compliance standards
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4. Specialty Polymer Monomer SynthesisIn the specialty polymers industry, chemists employ 3,5-Dibenzyloxyacetophenone as an intermediate for custom monomer development, particularly for high-purity copolymers requiring precise acetophenone-derived building blocks. Its protected functional groups allow for specific substitution patterns, crucial during the controlled radical or step-growth polymerization process, with addition levels governed by desired molecular weight distribution and end-use mechanical properties. Industry compliance standards
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The story of any chemical relies as much on the production line as it does on laboratory breakthroughs. Our experience manufacturing 3,5-Dibenzyloxyacetophenone (CAS No. 5471-24-9) has shown that even small improvements in handling or purification will filter through every stage, from research to industrial use. Our process for producing this aromatic ketone has grown over years of direct development. Small tweaks in solvent choice, temperature control, and reaction time have kept both quality and output steady. The consistency in color, purity, and melting point matters to everyone downstream—something you can’t take for granted if you only trade in finished chemicals or distribute what someone else makes.
With 3,5-Dibenzyloxyacetophenone, the synthesis route often starts with phenolic compounds. By using controlled benzylation reactions, we gained reliable selectivity for the 3,5-dibenzyloxy pattern without scrambling the aromatic ring. Monitoring every stage prevents unwanted side products, such as mono-benzylated or over-alkylated intermediates. Our purification relies on batch crystallization, which gives a crystalline powder that meets the needs of chemists in synthesis labs and production technicians in pharmaceutical facilities.
Production runs yield a product with a melting point in line with published benchmarks. Carefully monitored processes give reproducible purity levels, often exceeding 98%, which is not a bonus but a necessity for people downstream. We know slight drops in purity can disrupt steps in fine chemical synthesis and force researchers to reclean or discard batches—problems that manufacturers see firsthand. Every failed reaction, cloudy solution, or off-color intermediate traces its cause back to raw materials. This drives our commitment to consistent quality, not just hitting an average figure.
What does this mean concretely? The product comes as a white or near-white solid. We keep impurity levels tight. Any inconsistency in our upstream solvents, starting phenols, or benzyl chloride can show up as faint yellowing or unexpected melting range drift. Through in-house testing by HPLC and NMR, we track even minor byproducts. We dodged several pitfall batches before we tuned the workup to minimize solvent residues and leftover benzyl ethers.
We manufacture the chemical in batches large enough to supply multiple partners but small enough that issues in one lot won't domino into later runs. Strict environmental and workplace safety controls are integrated into every production step. The chemical does not produce hazardous off-gassing under normal conditions, though proper ventilation is used whenever possible. Our preference for closed-system benzylation and rotary evaporation reduces exposure and waste, keeping the focus on yield and cleanliness.
Strict adherence to specifications protects end-users from wasted effort and expense. Melting point, appearance, and chemical purity exist for good reason: a little deviation might not appear in early screening steps but can undermine later product quality or regulatory compliance. We see this in customers who might stem from pharmaceutical, agrochemical, or specialty intermediates backgrounds. If a project depends on the ketone’s reactivity, minor contaminants from incomplete benzylation will interfere with subsequent condensation or reduction reactions. The difference between a well-behaved crystal and a sticky, oily product runs deeper than appearance—it impacts every further transformation.
We receive requests occasionally to tailor aspects such as solubility or particle size. Other sectors demand pellets or micronized powders; here, solid uniformity and minimal dusting matter most. By working in small batches, we can tune crystallization conditions to give a specific range if needed. Choice of drying method also changes physical properties: vacuum drying minimizes thermal decomposition and gives a fluffier texture, while ambient methods work for scales where speed is not critical.
Researchers using 3,5-Dibenzyloxyacetophenone look mainly to its role in multi-step organic synthesis. The twin benzyl ether groups protect the phenolic positions during tricky cross-coupling or chain extension reactions. Both medicinal and materials chemists reach for this ketone when they want to build fused aromatic scaffolds or introduce complex side chains. Protecting groups like benzyl ether mean subsequent transformations can run under broader conditions, without unmasking the underlying phenol until the right stage. The robust protection and ease of removal in final deprotection steps are well established—bench scientists like to avoid repeat rounds of purification as much as possible.
Scale also matters. In university or biotech research, users might need only grams at a time. In larger pharmaceutical or technical production, kilo quantities come into play. Our product specification reflects that: smaller packs are sealed with minimal headspace, while bulk drums include desiccant and are batch-tested on arrival and after transport. Based on feedback, repackaging and storage matter just as much as in-lab handling—moisture pickup or surface yellowing can change user perceptions even if the core chemical remains unchanged.
We’ve compared 3,5-Dibenzyloxyacetophenone with other substituted acetophenone derivatives. The substitution pattern matters for functional group compatibility. For labs where only mono-protected versions are needed, cost and complexity drop, but so do reaction flexibility or compatibility with strong reagents. Benzyl ethers are robust but can be cleaved without harsh conditions. Alternative protecting groups like methyl or silyl offer easier installation, but they often lack the stability under oxidative or acidic conditions.
Some end-users consider starting from 3,5-dihydroxyacetophenone and doing in situ protection right before further reaction. We tried this route as a direct comparison and found that yields and purity dip every time on larger scale; purification headaches increase, and process throughput drops. At the manufacturing level, buying a reliably finished, pre-protected intermediate like 3,5-Dibenzyloxyacetophenone removes these issues, even if the up-front cost appears higher. In manufacturing, overall value isn’t just price per kilo but hours of saved troubleshooting and downstream improvements.
Generic or mass-market substitutes can look attractive, but we have watched projects turn on the details. A downstream Suzuki coupling or Friedel–Crafts acylation might work fine with a lower-purity intermediate, but the product profile shifts at scale. Some suppliers blend high-purity and recycled streams; we found that reactions with reclaimed batches can take longer, stall, or give unknown impurities at trace levels. We have always chosen single-origin batches to keep this risk as low as possible.
We recognize that specs on paper don’t guarantee lab performance. We regularly sample from every batch prior to release for reactivity and processability, not just for basic chemical identity. A batch might pass HPLC but fail to give expected conversion in standard condensation with aromatic amines or in selective hydrogenolysis. This method gives us direct evidence of suitability—lessons learned that go missing when all you see are distributor catalog numbers. Our repetition and batch retention system lets us revisit any outlier lot, usually by running side-by-side comparison testing with past batches and fresh control samples.
We often get feedback from process chemists who push the boundaries at pilot scale. What works in flasks may break in continuous reactors or larger vessels, with unexpected fouling or filter blockages. We track these issues closely. Adjusting particle size during crystallization, improving pre-drying steps, or switching filtration aids has decreased user complaints about filter clogging or extended dissolution times. Every insight that returns to the production floor shapes how we run future orders. Manufacturing is iterative—direct user experience tightens each quality loop.
As a chemical manufacturer, our perspective includes the fine details of cleaning, storing, and packaging. Direct observation shows how even sturdy crystals of 3,5-Dibenzyloxyacetophenone can pick up strong odors from local solvents if not sealed properly. This seemingly minor inconvenience can lead to unnecessary investigations or batch rejections at the client end. For large orders, we now use double-lined drums, and for sensitive pharmaceutical partners, we offer optional low-permeation liners.
Across all sectors using 3,5-Dibenzyloxyacetophenone, regulatory questions shape both supply and use. Batch traceability and quality documentation form the backbone of every shipment we deliver. Each lot receives a unique reference number with a certificate showing analytical data, crystallization date, and test methods. Should any issue arise, we can map back to the day, time, and equipment involved. We build these processes in-house because regulatory failings can haunt all downstream users, with recalls and audits disrupting entire supply chains.
Some applications, notably in pharma synthesis, require that starting materials and key intermediates meet both internal and external standards. Our facilities maintain documentation for every process change, raw material update, and validation round. Once, an unexpected impurity led to a full product recall for a partner; through our tracking systems, we pinpointed the root cause to a change in upstream solvent quality. That traceability prevented a more extensive issue and reinforced our procedures for routine and ongoing stability testing.
Challenges always arise with select intermediates in practical use. We have seen moisture-sensitive reactions derailed by undetected hygroscopic impurity; our drying and storage adjustments now pre-emptively address this, aided by batch-by-batch Karl Fischer analysis. We support users facing unexpected color changes by offering expedited technical troubleshooting, reviewing shipping conditions and internal storage practices with them.
Production scale-up brings process risks, not covered in small-scale academic publications. We’ve encountered slow crystallization in humid summer months, which led to stuck filters or off-form product. After investigating, we modified both solvent systems and workup temperatures. Manufacturer feedback cycles speed improvements that would be invisible to end-users, yet they shape product quality for everyone down the line.
On occasion, we field application questions outside vanilla organic synthesis. Researchers in advanced materials and functional coatings sometimes challenge us with requests for exceptionally low ionic contamination or specific thermal behavior. We have expanded our on-site analytical capacity to offer trace ion chromatography and simultaneous TGA-DSC analysis. These additions reflect the real-world complexity of modern R&D, borne out of repeated demand and careful listening to our client base.
As the manufacturer, our motivation blends technical curiosity, responsibility to downstream users, and pride in tangible output. Anyone can read a specification sheet; fewer can explain why a slight shift in pH control or choice of benzylating agent matters for long-term reliability. We revalidate every new raw material supplier, running small batch trials with full analytics before scaling up, rather than chasing marginal cost savings at the expense of predictability. This decision occasionally increases cost per unit but avoids long-term surprises in downstream reactions or user complaints.
We have seen the trust that grows from consistent product performance and the mess that results from shortcuts. Every year, we review process improvements and recalibrate methods, balancing customer needs, market shifts, and evolving technical standards. Listening to laboratory and production partners helps us anticipate and solve issues before a build-up triggers major problems. Repeat partnerships often develop because we address hurdles directly—if a batch didn’t perform right, we replace and investigate, not hide behind paperwork or excuses.
Future challenges and improvements will always waiting. We invest in process control upgrades, improving accuracy in batch monitoring and scaling up green chemistry approaches. Supply chain volatility—unstable access to key reagents, shifting transport costs, evolving regulatory thresholds—means we must keep both agility and quality at the forefront. Flexibility in logistics supports our clients’ rapid development or production changes. Clear, frequent communication with users helps us pre-empt many common pitfalls.
We remain committed to understanding, making, and improving 3,5-Dibenzyloxyacetophenone from the perspective those who live with it every day. Unlike resellers or distributors, our experience runs from raw materials to finished product, with oversight along every step. This hands-on knowledge lets us support research and production partners with more than technical sheets. For any project demanding reliability and flexibility in aromatic synthesis, we see no substitute for experience born directly from the production floor.
In direct production, subtle differences define success. Our 3,5-Dibenzyloxyacetophenone arose from ongoing process adjustment, in partnership with chemists who value both detail and stability. Direct manufacturing oversight lets us offer not only the chemical itself but robust technical support, adaptable solutions, and a sense of shared progress with those integrating the product into new discoveries. Every feedback loop and quality improvement traces back to the simple fact: we make what we know, and we keep learning from every batch.