|
HS Code |
537066 |
| Chemical Name | Acetylmetacresol |
| Synonyms | 4'-Hydroxy-3'-methylacetophenone |
| Molecular Formula | C9H10O2 |
| Molecular Weight | 150.18 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 115-118°C |
| Solubility In Water | Slightly soluble |
| Cas Number | 124-43-6 |
| Pharmacological Use | Antiseptic |
| Atc Code | R02AA20 |
As an accredited Acetylmetacresol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle labeled "Acetylmetacresol, 25g," with hazard symbols, lot number, and tightly sealed screw cap for safe storage. |
| Shipping | Acetylmetacresol should be shipped in tightly sealed containers, protected from light and moisture, and clearly labeled as a chemical product. It must comply with local, national, and international regulations. Transport under ambient conditions is appropriate, but avoid extreme temperatures and sources of ignition. Ensure proper documentation accompanies the shipment for safety and compliance. |
| Storage | Acetylmetacresol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from heat, light, and moisture. Ensure containers are properly labeled, and follow all safety guidelines to prevent accidental spillage or exposure. |
Competitive Acetylmetacresol prices that fit your budget—flexible terms and customized quotes for every order.
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Factories don’t stand still, and neither do the teams who keep them running. In daily production, we rely on chemicals with proven track records to support pharmaceutical and healthcare products built for tough global regulations. One compound that always returns value in performance and reliability is acetylmetacresol. Years of direct manufacturing experience have shown us how crucial stringent control over each lot becomes for this molecule—a refined phenol derivative recognized for its use in over-the-counter lozenges and antiseptic applications.
You can trace acetylmetacresol’s relevance back to its key chemical structure. By adding an acetyl group to metacresol, we get a product with consistent antimicrobial activity. This simple synthetic process, performed in controlled environments, leads to a dependable powder or crystalline product. It finds its place in throat lozenges—sometimes paired with other actives—to provide both comfort and microbial control during seasons every manufacturer dreads: colds and coughs.
Regulators never back down on expectations for pharmaceutical ingredients. Laboratories regularly inspect batches for purity, stability, and absence of contamination. From personal experience, cutting corners with raw material or process steps leads to costly remediation—and damaged trust. That is why we focus on delivering acetylmetacresol with purity above 98%, free from unreacted solvents or by-products. Testing across narrow melting point ranges and using modern chromatography methods allows us to confirm product quality batch after batch.
Product consistency benefits everyone down the supply chain. R&D groups can confidently formulate products without running new risk assessments each time. Packaging plants get hassle-free blending, with a product that integrates smoothly alongside common excipients. Quality control teams appreciate predictable analysis, helping avoid last-minute non-conformance surprises.
Over the years, customer questions have revealed what people care most about: appearance, solubility, stability, and odor profile. Acetylmetacresol presents as a white-to-hazy crystalline powder, with a mild, familiar aroma. It stays stable in ambient storage when shielded from light and excess moisture. Avoiding yellowing or caking—both clear signs of degradation—demands proper sealing and standard warehouse discipline.
Solubility remains a top concern, especially for formulators in the food, beverage, or health sectors. Acetylmetacresol dissolves in alcohol and slightly in water, easing mixing for liquefied syrups or mouthwashes. Compared to less refined metacresol derivatives, acetylmetacresol’s lower water solubility reduces foaming and separation issues. This pays off for automated processing lines, where downtime from unplanned filter changes is a real headache.
We have tracked real-world shelf life with varying packaging materials over long production cycles. Desiccant-lined, opaque containers extend the active life of acetylmetacresol, giving suppliers over two years of reliable storage. Standard drums, if sealed well, deliver comparable results. Lower-grade polymers or badly sealed liners, on the other hand, accelerate clumping and color changes. From the production floor to the storage rack, nobody benefits from avoidable quality loss.
End-users, from multinational brands to specialized compounders, count on batches that behave in the reactor, dissolve predictably, and never spike impurity readings. Each season brings new pressure to verify incoming materials—certificates of analysis have their place, but hands-on testing in the customer’s own lab decides reorder schedules. In our plant, close communication between synthesis, quality, and logistics teams keeps feedback cycles short when changing regulatory expectations or new purity guidelines appear.
Smaller operators, fighting for market space against bigger brands, benefit from acetylmetacresol in standard form. No special customization, no extra filtering—just a product that backs up their own QA standards. It levels the playing field, so technical expertise, not procurement power, decides the winner.
Many pharmaceutical and personal care companies look at the ever-growing range of phenolic antiseptics on the market—menthol, phenol, thymol, and metacresol among them. The differences often seem subtle but can determine success or failure for a product line. Through hands-on synthesis and in-process monitoring, we see clear separation in purity achievements, particle consistency, and reactivity with common excipients.
Compared with thymol, acetylmetacresol offers a softer odor profile and avoids the lingering taste sometimes noted in menthol-based formulations. Phenol delivers strong antibacterial impact but brings higher toxicity and stricter handling requirements. Metacresol, without modification, can introduce off-notes and unwanted side reactions in finished goods. Acetylation stably modifies the base molecule, holding the desired antiseptic function while giving a gentler sensory impact and better compatibility with delicate flavor systems.
Seasoned formulators appreciate the absence of residue or haze in most acetylmetacresol-dosed solutions. Cleaning times drop for mixing operations, filter longevity improves, and defective batch rates drop sharply. This difference seems small on paper but in the chaos of commercial-scale mixing, time lost to avoidable shut-downs adds up.
The broadest use for acetylmetacresol remains in cough and sore throat lozenges. This ingredient backs up label claims with tested antibacterial activity, helping end-users get through seasonal illness without prescription medicine. It fits in combination products, matching well with ingredients like amylmetacresol or mild local anesthetics. Many buyers ask about performance in oral sprays or mouthwashes—the answer always circles back to predictable solubility and flavor stability across shelf life.
Demand grows fastest in regions upgrading regulatory requirements for over-the-counter treatments. Our experience shows that meeting new analytical standards early opens up markets and creates partnerships with customers working to validate their own key processes. Acetylmetacresol’s tried-and-true regulatory background simplifies documentation and supports clean, uninterrupted product registration.
Overseeing day-to-day batch manufacturing gives a front-row seat to inspection cycles from local and international auditors. Full traceability from raw phenol sources to finished product supports audit readiness and troubleshooting. Every shipment leaves the plant with full test results covering UV absorbance, melting point, and appearance assessment. These details go back to time spent on production lines, where missing a small deviation often means the difference between an accepted batch and forced rework.
Supply chain interruptions sting—especially when customers need guaranteed lead times for retail season launches or hospital procurement cycles. Over the years, we've learned the value of maintaining buffer inventory and secondary sourcing for key intermediates. Emphasizing forward contracts and maintaining hands-on relationships with upstream partners has allowed us to deliver in tough market conditions, limiting disruptions and price spikes.
Sustainable practices keep a plant competitive in today’s regulatory arena. Our transition to closed-loop solvent recovery, on-site air scrubbing systems, and stepwise water treatment reduced discharge and improved community trust. Proper chemical handling in production—ventilated rooms, protective gear, and operator rotation schedules—reduces risk and keeps people performing at their best. Years of refining work procedures made these standards the base, not the goal.
Safe packaging and shipment round out the process. Securely-sealed containers, labeled for transport and tracked from gate to dock, lower the risk of contamination or accidental release. Real-world experience shows that the strongest packaging standards, supported by checklists and hands-on oversight, curb liabilities and demonstrate industry commitment to responsible stewardship.
Each year brings updates to GMP, pharmacopoeial monographs, or contaminant limits. By working inside the manufacturing plant, our teams see how seemingly minor regulatory language pushes real change. Transitioning to better analytical methods, validating new impurity standards, or re-training staff adds upfront cost but guards against far larger risk. On-site approach to documentation lets us adapt and pre-empt external audit findings—this proactivity builds supplier status in customer eyes.
Investment goes further than regulatory compliance; it establishes long-term supply contracts with top-tier buyers—groups that reward transparency and guarantee purchase volumes for years to come.
Standing still hurts product performance and operator morale. Yearly feedback from pharma formulators, third-party research groups, and even end consumers hones focus on use improvements. We’ve changed synthesis routes to minimize energy use and waste, streamlined purification steps, and evaluated real-world performance in test labs across the country. A recent example showed that small tweaks to crystallization reduced trace particulate content, improving dissolution times in finished lozenges. Operators contributed directly—suggesting adjustments to temperature profiles that improved both texture and speed of filtration. Collaborating on application trials, we've supported customers working with newer delivery formats. These customers needed a lower-dusting powder, a challenge that required modifying grinding protocols, improving air filtration, and delivering a product that handled better in high-speed tablet presses. Real insights from the factory floor—sometimes dismissed by outside observers—have a way of finding solutions academic resources overlook.
Market noise can distract buyers from the benefits direct-from-manufacturer supply brings. Third-party agents often create uncertainty about traceability, inventory position, or root cause analysis during quality events. Years spent in both commercial and technical service roles confirm that open lines between customer QA labs and manufacturing teams cut problem-solving time in half.
Hands-on discussions about performance outliers, storage best practices, and response to customer audits build trust while supporting process improvement both upstream and downstream. Partnering directly with users allows for real-time feedback, efficient resolution of technical issues, and proactive sharing of changes brought by new regulations or process upgrades.
In the realm of specialty chemicals, product consistency sets the leaders apart from the pack. Acetylmetacresol continues to meet real needs for performance, predictability, and clear provenance. Every batch, every test, and every shipment draws from years spent learning which processes protect quality and which shortcuts cost more in the long run.
From the design table to the blending tank, this ingredient delivers value with each use. Open communication with customers, ongoing investment in equipment, and adaptive improvement cycles anchor this reliability. Acetylmetacresol doesn’t just support today’s pharmaceutical and healthcare products; it stands ready to back innovative new solutions for seasons and challenges yet to come.