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HS Code |
574565 |
| Chemical Name | Acetanilide |
| Molecular Formula | C8H9NO |
| Molar Mass | 135.16 g/mol |
| Cas Number | 103-84-4 |
| Appearance | White to slightly gray crystalline solid |
| Melting Point | 113-116 °C |
| Boiling Point | 304 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.22 g/cm³ |
| Odor | Odorless, or faint aromatic odor |
| Iupac Name | N-phenylacetamide |
| Pubchem Cid | 6115 |
| Flash Point | 195 °C |
| Pka | NA (neutral compound) |
| Refractive Index | 1.571 |
As an accredited Acetanilide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Acetanilide, 500g: Supplied in a sealed, amber glass bottle with a secure screw cap; labeled with hazard, safety, and product information. |
| Shipping | Acetanilide should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transport in accordance with local, national, and international regulations for non-hazardous chemicals. Ensure containers are clearly labeled. Handle with care to avoid spills, and store in a cool, dry, well-ventilated area away from strong oxidizers and acids. |
| Storage | Acetanilide should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated place away from sources of ignition and heat. Protect it from moisture and incompatible substances, such as strong oxidizers. Store at room temperature and avoid direct sunlight. Clearly label the container and restrict storage to authorized and trained personnel for safe chemical management. |
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Purity 99%: Acetanilide 99% purity is used in pharmaceutical intermediate synthesis, where high purity ensures minimal impurities in final drug products. Melting Point 114°C: Acetanilide with a melting point of 114°C is used in solid-state reference calibration, where consistent melting behavior guarantees accurate thermal analysis. Particle Size 200 mesh: Acetanilide 200 mesh is used in fine chemical formulation, where uniform particle dispersion provides enhanced reaction efficiency. Molecular Weight 135.16 g/mol: Acetanilide of molecular weight 135.16 g/mol is used in dye manufacturing, where precise molar calculations enable consistent batch production. Stability Temperature 200°C: Acetanilide stable up to 200°C is used in high-temperature organic synthesis, where excellent thermal stability prevents decomposition. Low Moisture Content: Acetanilide with low moisture content is used in analytical reagent preparation, where minimal water content reduces unwanted side reactions. Odorless Grade: Acetanilide odorless grade is used in perfumery blends, where absence of interfering aroma preserves fragrance integrity. High Assay: Acetanilide high assay is used in laboratory standardization, where precise concentration ensures reliable analytical measurements. |
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Acetanilide has spent decades in the toolkit of both researchers and manufacturers, valued for its straightforward structure and clear utility. Push together a simple benzene ring with an acetyl group, and what you get is a classic—one of the earliest modern organic synthetic compounds. The journey of acetanilide from labs to large-scale use tells a story of chemistry with practical roots. Most chemists bump into it early in their careers, either in a beaker during organic synthesis class or as an ingredient in a precise reaction. Direct handling in its solid, white, powdery form gives it a kind of tangible reality missing from many chemicals found only on paper.
The technical details—those numbers and measurements—start with its purity, usually reaching around 99 percent. The melting point lands between 113 and 115 degrees Celsius, which reliably distinguishes high-quality product from its less-refined cousins. This range matters when quality control comes around, since even a few stray impurities can throw off a reaction or feed unwanted side products. Its density hovers near 1.21g/cm³, and solubility breaks down to slight in cold water and much better in hot water or organic solvents. These numbers aren’t just trivia; they guide how chemists and manufacturers pick, store, and use this compound day-to-day.
Comparison with other similar compounds makes a big difference for professionals who care about process safety or end-product consistency. Acetanilide shares family ties to aniline and paracetamol but claims its own spot based on stability and behavior. Aniline, for instance, raises red flags due to toxicity and volatility. Handled poorly, it becomes less of a candidate for careful chemistry and more of a safety headache. Paracetamol, by contrast, owes its origin story to acetanilide’s discovery but steps into a different role entirely as a widely-used painkiller. Acetanilide sets itself apart by offering fewer risks—less prone to dangerous vapors or unexpected breakdown under heat. It stays solid, stays shelf-stable, and behaves reliably whether in large solid chunks or finer forms.
One big lesson here comes from direct experience in lab settings. In one summer spent working in formulation labs, fussing over reaction yields with a range of aromatic compounds, acetanilide consistently behaved predictably. Few surprises means fewer wasted hours. When I needed a reagent that wouldn’t throw off every variable, acetanilide did its job without fuss. Other materials in the same family gave more drama, quirks, or hazards per gram. With acetanilide, the numbers printed on the bottle matched what happened when it hit the hotplate—a rare treat.
The legacy of acetanilide started in medicine, serving as one of the earliest fever reducers before health concerns shifted attention elsewhere. As knowledge about its side-effects grew, its job description transformed. Chemists started leaning into its strong amide group, turning it into a core building block for diverse syntheses. Ask anyone in organic chemistry about classic acetylation—acetanilide likely makes the cut as a recommended starting material. It acts as a heat map for identifying acetyl groups during student experiments, forming bright, clean crystalline solids visible to the naked eye. The presence or absence of clean needle-like crystals can reveal much about whether a reaction has succeeded or veered off course.
Outside of classrooms, the real-world utility continues. In industry, acetanilide fills a range of jobs. It shows up in dyes, stabilizers, and even as a plasticizer. Many manufacturers seeking a smooth workflow in dye production grab acetanilide to anchor color stability and control reaction speed. Its backbone latches onto colorants and intermediates, so it’s hard to understate its value in this role. In plastics, small doses of acetanilide can shift how materials harden, helping engineers dial in the strength and flexibility they need in a finished product. Crafts like rubber manufacture and photographic chemicals also benefit from its stable, low-reactivity base. Adjusting recipes on the industrial floor becomes less stressful with such a cooperative molecule in play.
Some print shops and manufacturers keep acetanilide on hand for its effect as a stabilizer for hydrogen peroxide. This trick helps keep several household disinfectants and cleaning supplies from losing punch on the shelf or in transit. Even after its prime in pharmaceuticals had passed, acetanilide’s features—ease of handling, strong performance at modest concentrations, solid reliability—gave it staying power.
Sticking with a chemical that delivers repeatable results saves time and prevents unwanted outcomes. In one process development project, I needed a consistent melting point to confirm the presence of a specific reaction product. The compound of choice? Acetanilide. The temp readings matched, and the resulting crystals looked just right through the lens of a basic compound microscope. Run after run, acetanilide left less room for error. Try swapping in a substitute and the purity would swing, melting points might drift, and results would start raising questions during quality control. Many chemists and process engineers swap notes about surprises from reagents, but acetanilide rarely makes the list of culprits.
This quality doesn’t just help on a small scale. Big batch production in a manufacturing plant runs best with reliable, predictable inputs. Problems with inputs spiral fast—contamination, subtle purity drops, or unexpected interactions can shut down a day’s work. Sticking to acetanilide where it fits best means fewer shutdowns, simpler troubleshooting, and clear documentation for regulatory requirements.
Every chemical has risks, and acetanilide sits in the middle of the spectrum. Its toxicity, while not as acute as aniline’s, still crops up if handled carelessly. Inhalation, skin exposure, or ingestion can tip a safe workspace into danger. Yet, compare it to aniline—acetanilide’s big cousin in basic dye production—and it’s easy to appreciate the step-down in volatility and acute hazard. Practical lab habits—protective gear, good ventilation, thorough clean-up—make it possible to work with acetanilide for years without problems. Experienced workers keep a keen eye on powder dust, wash hands before breaks, and use gloves for extended exposure. In education settings, acetanilide shows up often precisely because risk remains manageable with basic controls.
The changing regulatory landscape also shapes how companies and institutions use acetanilide. Some regions enforce stricter handling guidelines or restrict its use in direct consumer goods. This tracks with broader trends on workplace safety and chemical transparency. While I’ve never run into a total ban in facilities I’ve worked in, regular checks, training, and documentation keep everyone on the same page. Factoring in all these pieces, acetanilide strikes a workable balance between utility, cost, and safety.
Plenty of choices exist for chemical building blocks or dye precursors. Paracetamol, for example, stands out for its mainstream role in medicine and extremely low impurity requirements. It’s a tightly regulated, pharmaceutical-grade product, and manufacturers pump investment into purity and quality control. Paracetamol’s focus on health makes it less practical for non-pharma industries, given the extra cost and hoops required for compliance.
Aniline, even though chemically similar, introduces extra risk and complexity. It vaporizes easily and can trigger headaches or worse after brief exposure. Plants handling it face high insurance and more regulatory paperwork. Shifting to acetanilide, the odds of acute exposure issues drop and handling becomes less fraught. In practical terms, staff turnover and training needs fall, supporting smoother operations, especially in places where robust safety infrastructure still develops. Skipping unnecessary drama with a lower-risk material pays off across the board.
Other aromatic amides circle close, too, but many lack the same ease of melting, dissolving, or reacting with predictable speed. Newcomer chemicals promoted as “innovative” often drop into the market at higher price points, chasing niche markets but missing broader appeal. Acetanilide’s combination of value and practicality delivers a rare sweet spot that continues to attract buyers who care about both performance and risk management.
Sustainability in chemicals matters more each year. Acetanilide isn’t without its environmental footprint, but compared to many alternatives, its story offers reasons for cautious optimism. Sourced from aniline, the pathway features modest waste compared to some longer, more convoluted syntheses. Disposal after use brings its own challenges, since acetanilide should never go straight down the drain or into landfill. Responsible facilities set aside dedicated containers for disposal, contract with waste management companies, and monitor for environmental compliance.
Yet in terms of legacy waste, acetanilide fares reasonably well against relatives like chlorinated hydrocarbons, which linger for decades and migrate through soil. The shift toward greener chemistry in universities and manufacturing plants nudges users toward materials that offer high yields, fewer byproducts, and low acute toxicity. For those prioritizing environmental stewardship, acetanilide stands out as a case where good habits—reducing waste, reusing solvents, filtering before disposal—deliver real results with manageable effort.
Looking forward, better outcomes come from combining classic compounds with smarter workflow and technology. Improved ventilation systems, safer packaging, and regular safety refreshers support both new and seasoned users. Easy-to-read labeling and online documentation help demystify proper handling. Over time, the expansion of digital monitoring tools can reduce the number of hands-on interventions needed, shrinking risk without giving up performance.
Researchers invested in green chemistry continue to tinker with new synthetic pathways that might lower emissions or waste products linked to acetanilide. Some labs experiment with biobased reactants or energy-saving reaction conditions. The results, though uneven so far, point to a trend of steady refinement—using what works while shedding what no longer fits with modern priorities.
Industry-wide, suppliers who offer batch-level traceability, upfront details on residuals, and clear environmental disclosures will likely gain the trust of better-informed buyers. My own experience finding the right chemical supplier involved asking direct questions about residual solvents, trace impurities, and disposal support. Firms willing to go deeper on details, rather than hide behind standard data sheets, often supplied not just a better product but peace of mind.
Many compounds pass through the hands of scientists, engineers, and technicians without leaving much of a mark. Acetanilide stands apart because of its reliability, its role as a learning tool, and its spot at the intersection of tradition and progress. Each time a reaction kicks off with a few grams of acetanilide, it builds on decades of trial, error, and refinement. Recipes for making dyes sharper, plastics stronger, or processes simpler link back to the quiet dependability of this white powder.
Modern chemistry often demands more—not just of materials, but of the people who choose them. Picking acetanilide means betting on experience, documented results, and—let’s be honest—a chance to save on cleanup and emergency costs. For all its unassuming appearance, few compounds offer the same blend of familiarity, safety, utility, and value. Dig into the stories behind the products lining a factory shelf or lab drawer and acetanilide’s fingerprints are hard to miss, shaping safer workspaces and better outcomes for years to come.
Science doesn’t stop moving. As innovation brings smarter monitoring, tougher regulations, and greater demands for clean, efficient reactions, even an old standby like acetanilide will face new challenges. Process engineers may push for cleaner production methods, industry may mandate lower impurity thresholds, and government oversight could continue tightening. While these shifts mean short-term adjustment for labs, the end result often means better products and safer conditions.
One forward-thinking approach involves looking upstream in the supply chain. Assessing where and how raw materials come together affects everything downstream. Responsible sourcing, supplier audits, and third-party testing layer on protections for both workers and end-users. Many companies already request batch records and impurity profiles for each delivery. In my own projects, more transparency often led to higher costs per unit but delivered big savings on waste reduction and fewer compliance headaches.
Education continues to play a role. With clearer guidelines on risk, better technology in hands-on training, and fast access to up-to-date safety information, acetanilide stays usable as safely as possible. For years, student chemists have learned the value of discipline, observation, and respect for material integrity through their first experiments with acetanilide. Modern tools—from digital thermometers to personal protective equipment—make these lessons safer to teach and learn.
Across classrooms, factories, and research labs, acetanilide sticks around for reasons that matter. It’s approachable, it performs, and its story weaves together a rare balance of old-school chemistry and modern best practice. Differences from close relatives help labs and companies fine-tune for safety and efficiency. That persistent ability to match textbook promise with real-world results makes it a fixture even as new alternatives come and go.
Anyone who has spent serious time in a lab knows there’s no silver bullet—every choice means balancing convenience, cost, and consequence. Acetanilide hasn’t faded from use because it keeps meeting the needs of the day, standing up to scrutiny and getting work done with less fuss than many of its peers. As safety standards rise and sustainability moves to the front of more conversations, its role may shift, but value comes from materials that let people do more, worry less, and build confidently for the future. For as long as reliability, manageability, and cost matter, don’t be surprised to find acetanilide in the mix, making modern chemistry just a little bit easier to manage.