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HS Code |
928547 |
| Cas Number | 941-98-0 |
| Iupac Name | 1-(1-Naphthyl)ethan-1-one |
| Molecular Formula | C12H10O |
| Molecular Weight | 170.21 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 31-33°C |
| Boiling Point | 304°C |
| Density | 1.14 g/cm3 |
| Solubility In Water | Insoluble |
| Flash Point | 149°C |
| Smiles | CC(=O)C1=CC=CC2=CC=CC=C21 |
| Pubchem Id | 7449 |
As an accredited 1-Acetonaphthone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Acetonaphthone is packaged in a 100g amber glass bottle, featuring a secure screw cap and hazard label for safe handling. |
| Shipping | 1-Acetonaphthone is shipped in tightly sealed containers, protected from light and moisture. It should be stored in a cool, dry place, away from incompatible substances. During transit, the chemical is classified and labeled according to safety regulations, ensuring proper handling to minimize the risk of leaks, spills, or exposure. |
| Storage | 1-Acetonaphthone should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. It should be kept away from direct sunlight, heat sources, and moisture. Proper chemical safety labeling, spill containment, and access restriction to authorized personnel are recommended to ensure safe storage and handling. |
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Purity 99%: 1-Acetonaphthone with purity 99% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal by-product formation. Molecular Weight 170.21 g/mol: 1-Acetonaphthone at molecular weight 170.21 g/mol is used in organic synthesis, where precise molar ratios support consistent product yields. Melting Point 35°C: 1-Acetonaphthone with melting point 35°C is used in fragrance formulation, where controlled fusion enables homogenous blending. Stability Temperature 80°C: 1-Acetonaphthone with stability temperature 80°C is used in polymer manufacturing, where thermal stability prevents decomposition during processing. Particle Size <10 μm: 1-Acetonaphthone with particle size less than 10 μm is used in coatings applications, where fine dispersion leads to improved surface smoothness. Viscosity Grade Low: 1-Acetonaphthone of low viscosity grade is used in ink formulation, where ease of flow enhances print quality and consistency. Solubility in Ethanol: 1-Acetonaphthone with high solubility in ethanol is used in dye manufacturing, where complete dissolution facilitates uniform coloration. |
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In the world of specialty chemicals, 1-Acetonaphthone stands out for the ways it drives progress across different industries. This pale yellow crystalline powder, also known as 1-(1-Naphthyl)ethanone, carries the formula C12H10O and boasts a molecular weight around 170.21 g/mol. Its chemical structure features a naphthalene ring with an acetyl group at the one-position, and this small tweak builds a foundation for a wide range of synthetic possibilities. As a writer with a scientific background and hands-on laboratory experience, I see why chemists keep this molecule close at hand—it’s reliable, easy to handle when proper safety measures are followed, and opens up reaction routes for both creative research and established industrial work.
Let’s talk about the shape and character of this compound. 1-Acetonaphthone appears as solid crystals at room temperature, melting between 58 and 62°C. It dissolves well in common organic solvents like ethanol, ether, and chloroform, creating clear yellowish solutions that lend themselves to precise manipulations. With a boiling point above 310°C, 1-Acetonaphthone serves people who work with high-temperature processes and need reliable performance. It comes to market in several purities, and those looking for analytical work often demand at least 98%. Industrial users, especially in fragrance or pharmaceutical manufacturing, look for reproducibility and a product free from water and low-volatile debris—details that only seem minor until a batch fails.
1-Acetonaphthone doesn’t attract the same attention as chemical heavyweights like acetone or benzene, but its effect ripples throughout many modern products. The biggest stage for this molecule rests in the field of organic synthesis. Chemists use 1-Acetonaphthone as a building block to make larger, more complex molecules. If you study organic synthesis for long, you’ll see it paired up in Friedel-Crafts acylation reactions or in carbo- and heterocycle construction. Medications, dyes, agri-chemicals, and certain flavors can all trace their family tree back to this humble ketone.
The perfume industry values 1-Acetonaphthone for the slightly woody, narcissus-like aroma it imparts when modified just right. Not every batch ends up in a famous fragrance, but derivatives stemming from this compound find their way into everyday soaps, air fresheners, and sometimes even the flavoring of tobacco products. Those working in pigment manufacturing use ketones like this to help shape stable, colorfast dyes for industrial plastics and textiles. Having tested such colorants under sunlight myself, I can vouch for the difference a well-designed precursor like 1-Acetonaphthone makes in making colors stay true.
Ask a chemist who needs a naphthyl ketone about their options, and the conversation soon covers both 1- and 2-Acetonaphthone. The difference may look small—a switch in position around the aromatic ring—but it matters deeply in outcomes. The 1-position unlocks reaction pathways that the 2-position can’t match. This matters most in fine chemical synthesis, where even a slight impurity or isomer variance changes the whole game. Researchers looking for high selectivity or unique patterns in their products choose 1-Acetonaphthone because it often delivers cleaner, more predictable reactions. Several peer-reviewed studies back this up—yields track higher and side-products stay minimal in carefully controlled reactions involving the 1-isomer.
Digging into practical lab work reveals other differences. 1-Acetonaphthone offers consistent melting and boiling points, important for purification steps and large-scale production. Any time I’ve moved from the gram-scale flask to a pilot batch, the predictability of crystallization and the ease with which this compound purifies via recrystallization or chromatography have saved long days in the lab. The 2-isomer isn’t quite as forgiving, with broader melting curves and more stubborn impurities, making 1-Acetonaphthone look all the more tempting for those aiming at precision.
There’s no way around handling chemicals safely, especially aromatic ketones which deserve respect in the workplace. 1-Acetonaphthone isn’t as volatile or flammable as something like acetone, but exposure to dust or vapor shouldn’t be taken lightly. People who work with it regularly use gloves, goggles, and well-ventilated hoods. Material Safety Data Sheets suggest avoiding skin or eye contact and storing the product away from light, air, and sources of ignition. Over the years I’ve found that diligent housekeeping—good labeling, proper secondary containment for liquids, and prompt cleanup of any spills—turns what could be a big risk into nothing more than a routine day’s work.
Some folks wonder about the footprint left behind by widespread manufacturing. Industrial-scale synthesis of 1-Acetonaphthone most often involves acylation of naphthalene using acetic anhydride and an acid catalyst such as aluminum chloride. This process can create environmentally challenging byproducts, including acidic waste streams and chlorinated residues. Companies have begun shifting toward green chemistry by using alternative catalysts or recycling reagents, improving yields and cutting down on hazardous waste. The pace of innovation depends in part on regulatory pressure but also on the incentive to save costs on waste disposal. My own observation shows a steady trend toward more sustainable practices, especially wherever end-users demand products that meet international environmental standards.
Purity matters a lot in any operation involving fine or bulk chemicals. In my experience, pharmaceutical and fragrance firms go to great lengths to confirm every incoming batch meets tight specifications—so much so that producers of 1-Acetonaphthone invest continually in better analytical testing like HPLC, NMR, and gas chromatography. Even a trace contaminant makes a big difference in high-value synthesis. Buyers know to check certificates of analysis carefully and often keep trusted suppliers on speed dial. A single source of failure in the supply chain can lead to lost months of work.
When people discuss differences between 1-Acetonaphthone suppliers, they look beyond purity alone. Particle size, ease of dissolving in various solvents, packaging that prevents clumping or moisture uptake—all these details shape the daily experience of working with the chemical. There’s a big difference between a drum of clean, consistent crystals and a poorly sealed bag where material wants to cake or degrade. Over time, I’ve learned the value of open communication with suppliers, clear technical data, and prompt response when something deviates from the norm.
Change is routine in the world of specialty chemicals. Sometimes a regulatory change tightens the purity allowances on ingredients that go into cosmetics or fragrances. Other times, big manufacturers make small tweaks to save pennies, yet those tweaks ripple out to researchers, smaller manufacturers, and all downstream users. The best defense is building flexibility into your sourcing and process management. From what I’ve seen, researchers and technical buyers who invest in relationships with a variety of suppliers weather disruptions best. They can compare side-by-side, switch streams, or mix batches if a problem arises.
I recall several occasions where purity swings of just one percent forced us to adjust reaction conditions and purification steps in pharmaceutical labs. Having in-house testing, careful documentation, and contingency plans saved weeks of lost time. As regulatory regimes tighten—especially in the EU, North America, and growing Asian markets—those who preempt changes in labeling, documentation, and tracking keep their edge in a crowded marketplace.
There’s a quiet evolution taking place with 1-Acetonaphthone. Academic and industry researchers are finding ways to make its synthesis greener, less energy-intensive, and more cost-effective. Enzyme-catalyzed reactions, solid acid catalysts, and continuous flow processing all offer ways to trim waste and boost efficiency. I’ve worked on scale-ups where a reliable continuous reactor made a world of difference—saving time in both energy input and downstream purification. More efficient catalysis and in-line analytics mean faster turnaround for new product development and faster response to changing market needs.
End uses are also evolving. With the rising demand for specialty chemicals in electronics, smart polymers, and advanced coatings, the search is on for new derivatives that build on the framework provided by 1-Acetonaphthone. Aromatic ketones have long been valued for their stability and ability to shape the electronic properties of larger molecular structures. Research into organic semiconductors and dye-sensitized solar cells continues to draw on the building blocks offered by this compound. As demand for functional molecules rises, sourcing and quality control must keep pace. From the bench to the pilot plant, the standards that have made 1-Acetonaphthone popular now serve as the baseline for new, even more finely tuned intermediates.
My years working hands-on with specialty chemicals taught me that unsung intermediates like 1-Acetonaphthone make the difference between a successful synthesis and a failed project. Attention to purity, understanding quirks in reaction behavior, and building strong lines of communication with everyone who touches your supply—these steps reduce surprises and keep production on track. In research, no one forgets a reagent that performs as expected, time after time.
1-Acetonaphthone stands out among naphthyl ketones for more than just its chemistry—the way it ties into the supply chains of pharmaceuticals, dyes, fragrances, and even advanced materials gives it staying power. When innovation calls for new molecular architectures, this compound remains one of the trusty tools that chemists turn to. As manufacturing pressures push for greener chemistry and stricter quality controls, those producers and users who adapt smartly will keep meeting demand.
Moving forward, sustainability and transparency will shape the way the world looks at 1-Acetonaphthone. Stakeholders want to see producers disclosing more about process safety, waste management, and the lifecycle impacts of every product. Much of this comes from consumer and regulatory demand alike: increasingly, customers ask not just about performance, but the story behind the molecule. In my lab days, I watched scrutiny grow as large buyers began sending auditors right into suppliers’ factories to look over waste streams and energy footprints.
Solutions don’t come overnight. Still, smart firms have begun closing process loops, using less toxic catalysts, and reclaiming solvents to reduce the overall load. Knowledge gained from advanced analytics feeds back into process tweaks—cutting scrap, trimming downtime, and keeping quality high. Performance testing now often runs side by side with environmental impact measurements. The most reliable vendors don’t just offer a product—they offer a record of stewardship, transparency, and flexibility.
Education also matters. Those entering the chemical industry—whether on the science side or in procurement—benefit from a deep understanding of how seemingly small intermediates like 1-Acetonaphthone ripple through countless products. Real-world learning builds sharper technical teams and closer partnerships across the supply chain. This shared experience drives both efficiency and innovation.
From the synthesis bench to the warehouse, from lab notebook to finished consumer product, 1-Acetonaphthone proves what a well-chosen molecule can do. The growing field of chemical intermediates doesn’t rest on big names alone—it depends on reliably crafted building blocks that let innovation happen. Through attention to purity, commitment to safety, and a growing focus on sustainability, this compound earns its place in the toolkit of countless research teams and manufacturers.
For those just meeting 1-Acetonaphthone, the opportunities are wide open. Whether used as a testing ground for new syntheses, a bridge to more complex pharmaceuticals, or a dependable precursor in the world of dyes and fragrances, this substance keeps science moving forward. It brings together consistency, versatility, and the promise of new discoveries to come.
In the real world, the care shown at every step—not just in how a chemical looks on data sheets but in how it performs under pressure—makes the lasting difference. As the industry looks for ever higher standards, better stewardship, and deeper understanding, 1-Acetonaphthone stands as both example and opportunity—a solid building block ready for whatever comes next.