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HS Code |
965660 |
| Name | Phenacetin |
| Chemical Formula | C10H13NO2 |
| Molecular Weight | 179.22 g/mol |
| Appearance | White crystalline solid |
| Melting Point | 134-136°C |
| Solubility In Water | Slightly soluble |
| Cas Number | 62-44-2 |
| Atc Code | N02BE03 |
| Mechanism Of Action | Analgesic and antipyretic |
| Original Uses | Pain relief and fever reduction |
| Route Of Administration | Oral |
| Odor | Odorless |
| Storage Conditions | Store at room temperature, away from light and moisture |
As an accredited Phenacetin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The Phenacetin is packaged in a sealed, opaque plastic bottle, labeled clearly, containing 100 grams of fine white crystalline powder. |
| Shipping | **Phenacetin** should be shipped in tightly sealed containers, clearly labeled, and kept away from heat, moisture, and incompatible substances. During transport, it must comply with local, national, and international regulations for hazardous chemicals. Use appropriate packaging to prevent spills and damage, and provide applicable documentation, including safety data sheets (SDS). |
| Storage | Phenacetin should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and direct sunlight. It should be kept away from strong oxidizing agents and incompatible substances. The storage area should be secure and clearly labeled, with access limited to authorized personnel to prevent accidental exposure or ingestion. |
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Purity 99%: Phenacetin with 99% purity is used in pharmaceutical synthesis, where enhanced yield and reduced by-product formation are achieved. Melting Point 134°C: Phenacetin with a melting point of 134°C is used in analytical chemistry calibration, where it ensures accurate melting point determination. Particle Size 50 microns: Phenacetin with a particle size of 50 microns is used in tableting processes, where uniform compression and consistent tablet dissolution are obtained. Stability Temperature 25°C: Phenacetin with stability at 25°C is used in storage of reference standards, where long-term material integrity is maintained. Moisture Content <0.5%: Phenacetin with moisture content below 0.5% is used in dry-blend pharmaceutical formulations, where it prevents caking and extends shelf-life. Solubility in Ethanol 10 mg/mL: Phenacetin with solubility of 10 mg/mL in ethanol is used in solution preparation for spectroscopic analysis, where it enables homogenous sample distribution. Molecular Weight 179.22 g/mol: Phenacetin with a molecular weight of 179.22 g/mol is used in chemical research, where precise stoichiometric calculations are facilitated. HPLC Assay ≥99%: Phenacetin with HPLC assay of 99% minimum is used in quality control laboratories, where product authenticity is assured. Bulk Density 0.7 g/cm³: Phenacetin with bulk density of 0.7 g/cm³ is used in powder blending, where optimal flow and mixing efficiency are supported. Residue on Ignition <0.1%: Phenacetin with residue on ignition below 0.1% is used in high-purity reagent production, where contamination risk is minimized. |
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The name Phenacetin still rings out among chemists and historians. Back in the late 1800s, Phenacetin made a splash as a go-to over-the-counter pain reliever, giving people a new way to tackle fevers and aches without turning to stronger, riskier solutions. Its chemical formula, C10H13NO2, sets it apart from the more common acetaminophen you find on pharmacy shelves today. For decades, it helped people everywhere deal with headaches, muscle pain, chronic neuralgia, and the discomfort that comes with fever. But the real story of Phenacetin isn't just about what it did, but why it drifted out of use, what people learned along the way, and why it still matters to researchers and collectors.
Those who worked in pharmacies some time ago will remember Phenacetin’s once-standard white, odorless crystals. Standard-grade Phenacetin landed in bottles labeled with 99% purity or higher, but many formulas on the market edged up beyond that. Its melting point hovers just above 134°C, a baseline that—paired with a bitter taste—made it easy to spot when people switched brands or batches. In labs and among chemical suppliers, pure and well-characterized samples matter because anything less can throw off research results and lead to confusion when comparing properties. In lots of older research, Phenacetin often set the benchmark in pain relief testing, letting scientists see how newer compounds stacked up.
Beyond personal experience, books and medical records track the spread of Phenacetin-based blends throughout much of the twentieth century. Aspirin and Phenacetin mixes hit the shelves by the thousands, sometimes with caffeine to jack up effectiveness. The reason for the blend comes straight from practical experience: Phenacetin worked best on mild-to-moderate pain and low fevers, but combining it with other ingredients offered more lasting relief. The goal was pretty simple—let folks get through the day without feeling wiped out by headaches or low-level illnesses.
The shift away from Phenacetin started with hard data. Studies from the 1950s onward dug into the risks people faced with long-term use. Scientists linked steady Phenacetin use to kidney damage, a painful bit of news for anyone relying on the old standby. Cases of analgesic nephropathy—the medical term for kidney issues from painkillers—started cropping up more often. With every report, medical experts grew uneasy about letting this chemical stay in medicine cabinets. Acetaminophen and ibuprofen took over, offering similar pain-fighting power without as much risk. Anyone who has read up on how drug regulations evolve will see how this played out in headlines and policy: agencies around the world started restricting and banning Phenacetin. Today, you rarely see it in pain relief products, and talk about its use centers on research or chemical analysis, not daily living.
The focus now falls on the differences between Phenacetin and current options. Both Phenacetin and acetaminophen come from the same chemical family, but the body breaks them down in its own way. Acetaminophen is less likely to damage kidneys, but brings its own headache: take too much, and you risk hurting your liver. By comparison, Phenacetin’s kidney risks jump out at lower doses, turning chronic use into a gamble. Ibuprofen enters the fight from a different side, working through anti-inflammatory pathways that leave both liver and kidney safer, at least in the short run and within the right dosage. The lesson from this: progress in medicine doesn't always mean picking the most powerful option. Sometimes, it's just about putting safety ahead of nostalgia.
The facts about Phenacetin’s moves off pharmacy shelves are clear. Regulatory bans crisscross Europe, North America, and much of Asia. The product now pops up mainly in analytical labs and chemical supply lists. Its clean melting point and stable crystalline structure serve chemists running calibration tests on lab equipment. In other settings, it acts as a standard in forensic work or quality control, helping teams compare unknown compounds or check for contamination in other painkillers. For someone who has spent time in analytical chemistry, Phenacetin’s sharp, reliable features often make the difference between fuzzy or exact instrument calibration. Though it's true that some have abused its resemblance to acetaminophen or used it to cut illicit drugs, the real story in reputable circles comes down to its solid performance as a lab reference material.
While Phenacetin's medical past shapes its reputation, that doesn't overshadow its continued role as a chemical benchmark or teaching tool in university courses. It stands as a touchstone in physical chemistry labs, where instructors rely on its predictable melting point for teaching recrystallization and purity analysis. I remember running my first melting point experiment with old Phenacetin samples—the clean, decisive results stick with you. In these situations, Phenacetin earns trust because it holds up across samples and batches. Compare this to some modern calibration standards, which cost more or break down quickly, and it becomes clear why experienced lab workers keep small quantities around, tucked away in chemical storerooms and reference sets.
For most, Phenacetin belongs to a world that vanished with stricter drug rules and improved patient advocacy. Still, looking at its journey reveals lessons about safety and the hidden dangers of over-the-counter medicine culture. Until the 1970s, you could find Phenacetin in all sorts of household remedies, sold by the box in corner shops with little public warning about overuse. Growing up in a pharmacy-owning family, you could see firsthand how easy it was for customers to assume “over-the-counter” meant “risk-free.” The steady stream of research and patient outcomes eventually pushed authorities to tighten up access, introduce warnings, and promote better health literacy around daily drug use. For me, these changes reinforced the value of checking ingredients and reading up on old medications before trusting tradition and hoping for the best.
Industry now shapes its approach to consumer drugs with Phenacetin’s legacy in mind. Every new over-the-counter pain reliever faces scrutiny on both short-term effectiveness and long-term organ safety. Pharmaceutical companies dig through decades of patient data, run complex modeling on how metabolites circulate, and open every report of toxicity for independent review. No one wants a repeat of the Phenacetin story, where a helpful product created a slow-moving public health problem behind the scenes. The push for real-world evidence, post-marketing surveillance, and patient reporting comes straight from hard lessons learned over old medicine bottles and court cases. Such practices aren’t just box-ticking—they keep today’s alternatives safer.
An overlooked problem comes from the black-market trade and counterfeit drugs. Since Phenacetin shares some features with acetaminophen, unscrupulous manufacturers sometimes substitute it in counterfeit pills, leading to renewed incidents of kidney harm in places where drug oversight falls short. The World Health Organization lists continued Phenacetin adulteration as a risk, especially in Asia and Africa. Poor-quality medicines hurt already vulnerable populations and chip away at trust in global pharmaceutical supplies. For people in the field, the only real fix lies with persistent inspections, rapid field tests, and public alerts that don’t mince words about the health fallout. Narcotics enforcement teams in many countries also point out that Phenacetin sometimes lands in the illegal drug world, often as a “cutting agent” for cocaine, causing downstream harm far from its original context as a painkiller. These risks only highlight the need for vigilance in drug safety, both among professionals and among ordinary buyers at the counter.
After Phenacetin fell out of favor, researchers chased new drug designs that could offer relief with less risk. Acetaminophen stands as the closest relative, sharing similar pain-relieving strength but breaking down in the body without creating the same toxic intermediates that trouble kidneys. Even here, the lesson carried forward—every hospital toxicology handbook stresses that too much acetaminophen wrecks livers. Recent years brought further innovation with COX-2 inhibitors and nonsteroidal anti-inflammatory drugs (NSAIDs), which target pain pathways while reducing long-term risk for internal organs. For instance, ibuprofen and naproxen now anchor most home medicine cabinets because their patterns of side effects are better understood and easier to manage in practice. These advances set a bar for combining relief, affordability, and long-term safety based on clear, trackable evidence.
Developers and researchers now keep Phenacetin’s historical record close at hand when proposing any new molecule for consumer use. Across published studies and clinical guidance, examples pile up where a promising painkiller fizzled out on real-world safety or caused subtle harm in chronic users. The hurdles set by modern regulators—long-term kidney panels, population risk breakdowns, thorough post-marketing checks—all stem from the push to never let a well-intentioned compound like Phenacetin quietly chip away at public health again. Compared to the more “open” era when Phenacetin appeared, the current culture of pharmaceutical safety puts every new product on trial before approval and keeps a watchful eye during its years on store shelves.
Among chemical suppliers, Phenacetin now sells mostly to research labs, specialty educational settings, and analytical teams needing a crystallization reference. No modern supplier of repute markets it as a consumer-grade painkiller. This matters because transparency forms the backbone of both ethical chemistry and public health. Packaging always stresses that Phenacetin isn’t intended for human consumption and should be handled with care. In honest discussions, the risks and history come front and center. As a chemical, it performs admirably in controlled conditions, but its past as a household painkiller serves as a warning not to take purity or safety for granted.
Focusing on the specifics, Phenacetin works as a white crystalline powder, melting at roughly 134–135°C, and dissolves in hot water and ethanol, but only sparingly in cold water. These properties make it easy to spot and handle in small-scale lab use. For undergraduates or beginning chemistry students, Phenacetin proves especially effective for demonstrating classic purification protocols and solid-liquid separation techniques. It offers a sharp melting point—something every first-year student learns to measure and interpret. In that sense, Phenacetin puts knowledge in students’ hands, not capsules.
To those who spend years in public health or pharmaceutical engineering, Phenacetin means more than just an entry on safety data sheets. Its journey tells how popular remedies can outstay their welcome if safety signals get missed or ignored. For lab managers, keeping a sample bottle of Phenacetin on the reference shelf often sparks discussion with new hires about why older drugs vanished and how patient outcomes force change. In this way, chemical standards take on a historical dimension and anchor ethical standards for current research and development.
When journalists and consumer advocates ask about “legacy drugs,” Phenacetin sits high on the list of cautionary tales. The World Health Organization and national regulatory bodies point back to the wave of kidney injuries in the 1960s and 1970s as proof of why constant surveillance and patient education matter. Graduate programs in pharmacology run case studies on how easily public trust can get stretched by incomplete warnings, missed reports, or industry inertia. For those building future medicines, Phenacetin’s record leaves no illusions—a good painkiller must balance potency against risk, and honest reporting trumps any nostalgia for “what used to work.”
Schools and universities, along with professional boards, now encourage students in chemistry and medicine to explore the story of Phenacetin not just for technical details, but for its broader social impact. Case studies include details of how a popular medicine left behind a trail of unexpected health issues. Putting theory into practice, chemistry labs use Phenacetin to train students in careful technique and meticulous measurement, reinforcing the need for attention to detail in every step. In talks with pharmacy colleagues, many recall the shift away from Phenacetin as a defining moment for modern drug safety policy—a pivot away from “harmless until proved otherwise” to “only trusted if proved safe.”
The lesson that emerges is plain: all effective drugs carry some cost, and letting old favorites stick around out of habit risks more than inconvenience. Major health bodies now urge regular auditing and continuing education for all pharmacists and health professionals—a standard shaped by experience with compounds like Phenacetin. In community settings, increased public access to drug safety databases means that anyone curious about a product’s track record can dig up real-world alerts, recall notices, and safety studies anytime. Open science and transparent labeling mark progress that simply wasn’t possible during Phenacetin’s heyday. These changes empower patients to make choices based on clear evidence, not hearsay or habit.
Phenacetin’s story isn't just about one chemical or one era. It serves as a reminder that popular solutions can hide risks, and keeps the goal of evidence-driven, patient-centric practices front and center. Every lab worker who calibrates a melting point or every student measuring crystal samples learns the lesson: reliability goes hand in hand with responsibility. In my own time as a researcher and teacher, I have seen how studying Phenacetin opens rich discussion, from the technical to the ethical. These conversations keep everyone honest—no matter if they’re designing new drugs, working in the field, or just helping neighbors pick safe medicine from crowded shelves. Phenacetin’s legacy endures, not as a cure, but as a compass for making better, wiser choices in science and health.