|
HS Code |
401562 |
| Iupac Name | 1-Phenylethanone |
| Cas Number | 98-86-2 |
| Molecular Formula | C8H8O |
| Molar Mass | 120.15 g/mol |
| Appearance | Colorless liquid |
| Odor | Sweet, pungent, resembling almonds |
| Melting Point | 19-20 °C |
| Boiling Point | 202 °C |
| Density | 1.028 g/cm3 |
| Solubility In Water | 5.5 g/L (20 °C) |
| Vapor Pressure | 0.4 mmHg (25 °C) |
| Flash Point | 77 °C |
| Refractive Index | 1.532 (20 °C) |
| Un Number | 1992 |
| Pubchem Cid | 7410 |
As an accredited Acetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Acetophenone is packaged in a 500 mL amber glass bottle, tightly sealed, clearly labeled with hazard warnings and chemical information. |
| Shipping | Acetophenone is shipped in tightly sealed containers, typically made of glass or high-density polyethylene, to prevent leaks and evaporation. It must be labeled as a hazardous material and transported in accordance with regulations such as DOT, IATA, or IMDG. Containers should be kept away from heat, sparks, and incompatible substances during transit. |
| Storage | Acetophenone should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and open flames. Keep the container tightly closed and protected from direct sunlight. Store separately from oxidizing agents, acids, and bases. Use containers made of materials compatible with acetophenone to prevent leakage or reaction. Proper labeling and secure shelving are essential to ensure safe handling and storage. |
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Purity 99%: Acetophenone with purity 99% is used in fragrance synthesis, where it imparts a sweet and floral aroma with high olfactory intensity. Stability temperature 120°C: Acetophenone with stability temperature 120°C is used in high-temperature polymerization processes, where it maintains chemical integrity and enhances process safety. Molecular weight 120.15 g/mol: Acetophenone with molecular weight 120.15 g/mol is used in pharmaceutical intermediate production, where precise molecular consistency ensures reproducible drug formulation. Melting point 19.6°C: Acetophenone with melting point 19.6°C is used in resin modification, where it enables uniform blending and improved product homogeneity. UV Absorbance 274 nm: Acetophenone with UV absorbance 274 nm is used in photoinitiator systems, where it provides effective initiation under specific UV irradiation for optimized curing. Boiling point 202°C: Acetophenone with boiling point 202°C is used as a solvent in organic synthesis, where it allows for efficient solubilization and reaction rate enhancement. Density 1.028 g/cm³: Acetophenone with density 1.028 g/cm³ is used in analytical reagent preparation, where accurate dosing and homogeneity are critical for reproducibility. Viscosity 2.36 mPa·s: Acetophenone with viscosity 2.36 mPa·s is used in specialty ink formulation, where optimal flow characteristics ensure precise print quality. |
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Acetophenone is a chemical I’ve known from college days and it always finds its way into more conversations than expected. Most people hear “Acetophenone” and assume you’re talking about something that belongs in a chemistry lab and nowhere else. The reality turns out to be broader, blending industry, research, and daily products. In the world of organic compounds, Acetophenone carries a straightforward structure — a benzene ring attached to a carbonyl group, simple enough that even introductory chemistry textbooks use it as a stepping stone to explain more complex molecules. It comes as a colorless, sharp-scented liquid, usually bottled with care because it tends to evaporate and leave its sweet, almond-like smell behind.
Acetophenone usually shows up with the formula C8H8O. Chemistry labs rely on it for purity checks with specifications that matter for its target job, be it in flavors, synthesis, or perfumes. Most suppliers offer it at assay levels around 99% pure, keeping moisture well below 1%. Its melting point sits near 20°C, though it turns to liquid slightly above room temperature, with a boiling point close to 202°C. These details might seem minor if you don’t handle chemicals daily, but even a small shift in purity can change its behavior and applications.
Its molecular weight sits almost at 120 g/mol, which might not mean much outside laboratory settings. In reality, this gives it the kind of volatility that matters in perfume formulation and organic synthesis. The density runs just above water’s, which helps when separating layers during extractions. If you have ever watched transparent layers in a funnel, you’ve seen this play out.
People brush against acetophenone more often than they realize. Chemists first think of its use in organic synthesis—as a starting block for substances like pharmaceuticals, resins, and fragrances. The pharmaceutical role gets a lot of attention because it works as an intermediate for certain active ingredients, especially when synthesizing compounds that help treat health issues.
I once worked with a group testing flavor profiles for sweets and found acetophenone listed in essence compositions. It gives off a sweet, floral aroma that companies use to boost vanilla or cherry notes in consumer products. If you peel the label off a mainstream candy and look at the ingredients, acetophenone might be behind the “natural flavors” umbrella.
Its use in perfumes stands out even more. Some classic scents lean on acetophenone for that subtle note that makes a fragrance linger. Perfumers know the molecule as both reliable and flexible, letting them balance floral or almond notes without overpowering the rest. Chemical stability also helps, as finished products last longer on shelves, something brands ensure before shipping.
Industries leverage acetophenone for polymer manufacturing as well. I’ve spent hours watching technicians run reactions where acetophenone alters the physical properties of plastics, lending extra strength or flexibility to finished products. In industrial chemistry, the predictability of acetophenone acts as an anchor in scaling recipes from the lab bench to the reactor.
Newcomers to manufacturing look at acetophenone and see just another ingredient. Compared to other aryl ketones like benzophenone, acetophenone carries different reactivity in key applications. Benzophenone, commonly used in UV blockers or photo-initiators, stays more stable under harsh light, but acetophenone’s smaller structure tends to blend better with flavor and fragrance systems.
One key distinction from compounds such as methyl ethyl ketone comes down to scent and safety. Methyl ethyl ketone has a sharp, almost biting odor and more solvent-like behavior, so it drifts toward industrial solvent uses. Acetophenone, being aromatic, feels softer to the nose and works much better in applications meant for human senses. Synthetically, chemists choose acetophenone when a reaction calls for gentle reactivity on its aromatic ring, as it opens options for substitution or further extension.
The comparison with similar-sounding molecules can confuse buyers. For example, acetone, a thinner and much more volatile solvent, evaporates quickly, left behind as occasional nail polish remover residue. Acetophenone, with its higher boiling point and milder volatility, allows for slower evaporation and greater control in both the lab and the factory. This feature, while subtle, shapes protocol across multiple industries.
Handling acetophenone in the lab requires a combination of caution and familiarity. Working with aromatic ketones brings predictable risks—its volatility means good ventilation comes first on any checklist. The almond smell, while pleasant in small doses, can get overwhelming without proper airflow. Gloves and goggles become standard not out of paranoia but from years of watching chemical splashes ruin clothing and cause irritation.
Shipping and storing acetophenone brings its own lessons. Suppliers usually use brown glass bottles or tight plastic containers to ward off light and minimize evaporation. Those details came up during summer internships, as we boxed up sample kits for clients working in food science or fragrance research. Keeping acetophenone dry and pure makes all the difference during experimental trials, as moisture or contaminants throw off results in surprising ways.
Manufacturers appreciate acetophenone for how easily it adapts to scale, whether they produce a few liters for research or thousands of kilograms for commercial use. My visits to mid-sized chemical plants showed acetophenone’s flexibility firsthand. One facility ran acetophenone through a reactor to create more complex pharmaceuticals. Down the hall, its cousin batch transformed it into a precursor for specialty polymers. The difference often shows up in minor tweaks to temperature or concentration, not in the molecule’s core behavior.
In food science, acetophenone’s reputation comes from delivering authentic flavor notes. Scientists working in beverage development find it reliable among the mix of hundreds of possible aromatics. The simplicity in its molecular design means fewer unexpected byproducts during processing. Its flavor contribution stands out as subtle but necessary—a quality found in real cherries but hard to capture with broader aromatics.
Perfumery and personal care ride on acetophenone’s consistent aroma. Having spent time interviewing fragrance specialists, I’ve learned that subtle differences in ketone profiles can shift a scent from subtle to overpowering. Brands rely on the known quirks of acetophenone, counting on it not to compete with the higher-priced essential oils but to blend in and round out sharp notes.
Another emerging trend puts acetophenone in advanced materials research. Scientists look at it as a platform for further derivatization, a starting point for compounds with intended medical or electronic functions. Startups interested in new battery technologies have started paying attention to acetophenone derivatives, seeking stability and consistent electron flow.
No conversation about chemicals is complete without looking at safety and regulation. Agencies in North America and Europe monitor acetophenone in all major applications. I’ve seen firsthand how production facilities routinely test stockpiles for purity and check limits on residue in food-related applications. NGOs occasionally raise concerns over its presence in high concentrations, especially if used without clear labeling. The push for transparency presses manufacturers to offer detailed usage documentation, from molecular source to intended product lines.
Environmental scientists raise questions about production waste and emissions. While acetophenone breaks down in natural environments far more quickly than some of its industrial cousins, disposal practices matter. Factories near waterways undergo tight scrutiny, with regulators checking downstream conditions on a regular basis. These processes don’t halt innovation; instead, they push companies to invest in more efficient reaction systems, closed-loop recovery, or greener manufacturing catalysts.
Managing risk and maintaining reliability shapes lab protocols. In teaching settings, students learn quickly that inconsistent material can wreck synthesis. On an industrial scale, quality assurance matters just as much. With acetophenone, repeatable properties anchor entire production runs. Companies that invest in greater batch-to-batch consistency see lower waste and fewer recalls, translating into actual savings and greater trust among downstream users.
Tackling waste and emissions offers the most visible opportunity for improvement. Research teams advocate for catalytic systems that use milder conditions and generate fewer byproducts. Reactors built for energy efficiency, combined with improved separation and recycling systems, drop environmental release to safer levels. I’ve visited production pilot lines that reclaim and reuse acetophenone from mixtures, reducing both cost and pollution.
Product labeling stands as another point of focus. Consumers increasingly want to know what goes into products they eat, wear, or apply. Clearer information about acetophenone, down to how and why it appears in finished goods, builds confidence and reduces rumors about safety. Some companies have started breaking out ingredient origins even in non-food sectors, seeing early rewards from more loyal buyers.
Education within the workplace matters as well. Many incidents reported in chemical labs or food plants stem from overlooked handling points—spills, improper storage, poorly ventilated mixing areas. Training sessions, even short hands-on refreshers, deflate incident rates and drive up compliance. Having observed both sides—trained employees and rushed staff—I know the difference in accident rates and long-term productivity tracks closely with attention paid to basics.
Acetophenone, over decades, keeps winding up at the pivot between classic organic chemistry and modern consumer goods. Those who underestimate its utility often end up recognizing it in unexpected roles—from the backbone of headache remedies to the hint of almond in a new perfume. Industry-wide, the ability to understand and refine acetophenone’s uses speaks to a greater trend: desire for maximum return on simple, reliable molecules.
Research and development hinge on the ability to trace molecular origins. Academics have begun working closer with industry, tracking how acetophenone can form base structures for green chemistry initiatives. By shifting old processes onto newer, less wasteful tracks, even long-familiar molecules like acetophenone earn a second look. The result: streamlined pharmaceuticals, safer flavors, and more durable plastics.
Innovation often spins off from tiny tweaks—adjusting how a chemical gets produced or how strictly purity is monitored before shipment. As acetophenone’s market evolves, those small changes open room for safer, more efficient, and more transparent chemical lives. Companies slow to adapt risk losing ground to startups or corporations willing to invest in monitoring, reporting, and cleaner technology.
Having spent years seeing acetophenone roll through labs, pilot plants, and real factories, I’ve noticed patterns. The most successful teams invest in precision—keeping records scrupulous, equipment clean, and purity uncompromised. Past shortcuts always come back to bite, sometimes as a bad batch, sometimes as a product recall that stings both wallet and reputation.
Demand for acetophenone likely won’t fade, as its building-block versatility weaves into every corner of industrial chemistry. The practical future lies in raising the standard for how it’s produced, labeled, and delivered. Large and small companies alike gain from investing in real-time monitoring, constant training, and open dialogue about risks and benefits. My experience says that culture matters as much as process; open communication lines and respect for detail bring out the best in people and product alike.
Acetophenone always finds new life as needs shift and research deepens. Every advance connects to lessons learned by those with hands-on experience—technicians, researchers, managers—who keep asking how to do better, safer, and smarter work. As industry heads toward a future defined by transparency and efficiency, acetophenone stands both as a symbol of reliability and a challenge to stay vigilant in every step of chemical design and application.