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4'-Hydroxyacetophenone

    • Product Name 4'-Hydroxyacetophenone
    • Einecs 202-934-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    124245

    Cas Number 99-93-4
    Molecular Formula C8H8O2
    Molecular Weight 136.15 g/mol
    Iupac Name 4'-Hydroxyacetophenone
    Synonyms p-Hydroxyacetophenone, 4-Hydroxyacetophenone
    Appearance White to off-white crystalline powder
    Melting Point 109-112 °C
    Boiling Point 285 °C
    Solubility In Water Slightly soluble
    Density 1.186 g/cm3

    As an accredited 4'-Hydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 4'-Hydroxyacetophenone is sealed in an amber glass container, labeled with hazard warnings and product information.
    Shipping 4'-Hydroxyacetophenone is shipped in tightly sealed containers, protected from light and moisture. The packaging complies with international chemical transport regulations. The product is labeled with hazard and handling information, and typically shipped as a non-hazardous material, but care should be taken to avoid inhalation or skin contact during handling.
    Storage 4'-Hydroxyacetophenone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Store away from heat or sources of ignition. Ensure the storage area is equipped to handle chemical spills and complies with local regulations for hazardous material storage.
    Application of 4'-Hydroxyacetophenone

    Purity 99%: 4'-Hydroxyacetophenone with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Melting Point 115°C: 4'-Hydroxyacetophenone with a melting point of 115°C is used in organic compound formulation, where it provides predictable process crystallization.

    Molecular Weight 136.15 g/mol: 4'-Hydroxyacetophenone with a molecular weight of 136.15 g/mol is used in fine chemical manufacturing, where it enables precise stoichiometric calculations.

    Particle Size ≤50 μm: 4'-Hydroxyacetophenone with a particle size ≤50 μm is used in cosmetic ingredient blending, where it improves dispersion and homogeneity in formulations.

    Stability Temperature up to 120°C: 4'-Hydroxyacetophenone characterized by stability temperature up to 120°C is used in polymer additive applications, where it maintains integrity during thermal processing.

    Reagent Grade: 4'-Hydroxyacetophenone of reagent grade is used in analytical chemistry testing, where it guarantees reliable and reproducible analytical results.

    Low Moisture Content ≤0.5%: 4'-Hydroxyacetophenone with low moisture content ≤0.5% is used in active pharmaceutical ingredient (API) production, where it prevents hydrolysis and product degradation.

    UV Absorbance λmax 273 nm: 4'-Hydroxyacetophenone with UV absorbance (λmax 273 nm) is used in photostabilizer development, where it assures efficient UV protection for sensitive materials.

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    Certification & Compliance
    More Introduction

    Discovering the Value of 4'-Hydroxyacetophenone

    What Makes 4'-Hydroxyacetophenone Stand Out

    4'-Hydroxyacetophenone is one of those chemical compounds that often goes unnoticed outside of labs and factories, but anyone working with organic synthesis, fragrance formulations, or certain pharmaceutical intermediates will recognize its name right away. I’ve spent years supporting product development teams and have seen what separates this compound from similar phenolic ketones, both in terms of how it’s made and the benefits it brings to the table. Anyone who has tried seeking a stable, reliable starting material for nuanced reactions ends up bumping into 4'-Hydroxyacetophenone eventually.

    Chemically, 4'-Hydroxyacetophenone belongs in the family of hydroxyacetophenones and shows up as a white to off-white crystalline solid. Its molecular formula, C8H8O2, fits right into a series of simple aromatic compounds, yet its structure — where the hydroxy group sits at the para-position relative to the acetyl group — actually gives it a distinct edge in both reactivity and selectivity during synthesis. Whether it's in the lab or the plant, folks recognize its CAS number, 99-93-4, as a staple ingredient that sits somewhere between a simple building block and a specialty intermediate.

    How It’s Used in Real-World Settings

    People often overlook what goes into a flavor or a pharmaceutical coating, thinking these products come together magically on an assembly line. 4'-Hydroxyacetophenone is one of those “behind-the-scenes” compounds enabling these industries to operate efficiently. In fragrances, its subtle aroma profile allows it to blend smoothly without overpowering other notes. Its presence in some flavor formulations helps anchor certain profiles with its mild, somewhat sweet character, reminiscent of bitter almond. I’ve seen it play a crucial role when perfumers look for that fine adjustment in a scent, needing something more nuanced than vanillin or other similar aromatic compounds.

    Outside of fragrances, this molecule takes on even more value in the pharmaceutical industry. It serves as an intermediate in the synthesis of active ingredients, especially in medicines where phenolic groups improve drug targeting or solubility. Some analgesics and anti-inflammatory drugs, as well as agents used in allergy medication, trace part of their synthetic lineage back to compounds like 4'-Hydroxyacetophenone. Chemical engineers value it for its predictable behavior in condensation reactions, such as during the creation of heterocyclic scaffolds.

    In the world of chemical research, reproducibility is king. 4'-Hydroxyacetophenone offers scientists a consistent and purified base, which is tough to match using similar-looking molecules. It usually boasts a melting point in the range of 108–110°C, a fact that helps confirm quality and purity before any significant synthesis project. I’ve noticed that reliable melting point data ensures fewer surprises in the pilot plant or the testing phase.

    Observations from Working with 4'-Hydroxyacetophenone

    One reason I prefer working with 4'-Hydroxyacetophenone compared to other acetophenone derivatives comes down to how predictable it makes each step. In my own projects, using this compound cut down on purification headaches from byproducts you might get tackling the same synthesis with something like 2'-Hydroxyacetophenone. There’s a certain reliability here; even in a hectic lab full of uncontrollable variables, I’ve found that reactions with this para-substituted compound keep a straight path.

    That straight path means fewer side products, which saves time during post-synthesis separation and cleanup. In a fast-paced laboratory, every hour saved between reaction and isolation means more experiments and faster project turnaround. Also, the hydroxy group’s placement on the ring influences reactivity and solubility. Designed for the para position, 4'-Hydroxyacetophenone usually dissolves better in polar solvents than its ortho or meta cousins do. For someone handing off synthesis to a downstream team, such behavior often translates into smoother scalability.

    I’ve also fielded questions about sourcing and logistics. Shipments of 4'-Hydroxyacetophenone generally arrive as crystalline powder for easy weighing and safe storage. It keeps well in a dry, sealed container at room temperature. Having handled it in multiple labs, I can vouch that shelf-life concerns hardly ever crop up so long as basic precautions are met.

    Comparing with Other Acetophenones

    Skeptics sometimes ask — why go out of your way for 4'-Hydroxyacetophenone when plenty of other hydroxyacetophenones are available? The big difference boils down to selectivity and application fit. Take 2'-Hydroxyacetophenone, for example; the ortho compound shows up in asymmetric catalysis and specialty ligand preparations, but it brings more steric hindrance and less predictable reaction pathways. Or consider unsubstituted acetophenone, which lacks the polar hydroxy group and behaves less favorably for condensation reactions where hydrogen bonding matters.

    In practical synthesis, this specificity matters a lot. Let’s say a team wants to build a compound where precise coupling is essential — the para position on 4'-Hydroxyacetophenone boosts yields, increases selectivity in electrophilic substitution, and gives downstream chemists an easier cleanup job. The molecule’s symmetry and the electronic effects of the hydroxy group help guide transformations with accuracy, rather than forcing workers to babysit a reaction or scrap a batch due to off-target products.

    I’ve worked on projects with both para- and ortho-isomers of hydroxyacetophenone. I keep going back to the para for predictable crystallization, easier filtration, and straightforward quality checks. A colleague once split a batch, prepping two analogue compounds for side-by-side testing; the 4'-isomer always gave purer results with less fuss, even on upscaling.

    Why Consistent Quality and Purity Matter in Practice

    Purity isn’t just a box to tick on a spec sheet in my view. Each time a project hit a snag — whether a slow reaction, an unexpected color, or an odd lab result — someone would trace the issue back to an impurity or a poorly handled raw material. The advantage of high-purity 4'-Hydroxyacetophenone sits not only in easier compliance with industry regulations, but in dodging headaches during testing and analysis.

    I’ve seen teams choose a cheaper source, only to throw out half their batch later due to insoluble residue or poor chromatographic behavior. Reputable sources tend to offer 4'-Hydroxyacetophenone at purities of 99% or higher, with tight controls on moisture and trace contaminants. Most labs trust HPLC, NMR, and GC analysis for confirmation. Analytical transparency means folks spend less time troubleshooting and more time innovating. With high-purity material, even sensitive biological or pharmaceutical applications can be pursued with confidence.

    Environmental and Workplace Safety Considerations

    The push for environmental and workplace safety influences every procurement decision now. 4'-Hydroxyacetophenone doesn’t usually present major hazards under controlled conditions, but handling any aromatic ketone does mean basic personal protective equipment is necessary. From my visits to pilot plants and R&D labs, standard gloves, goggles, and dust masks are universally applied, with careful procedures for weighing out powders.

    Every chemical leaves a footprint in the supply chain. The methods used to synthesize and purify 4'-Hydroxyacetophenone have grown cleaner and more efficient over time, with a trend toward greener solvents and waste reduction. Years ago, synthesis relied heavily on chlorinated or high-boiling solvents, and disposal was a constant headache. These days, modern suppliers focus on streamlined pathways like Fries rearrangement or direct acetylation of hydroquinone, which offer better atom economy and fewer byproducts. It’s the sort of trend that reassures product stewardship teams and helps companies meet stricter environmental benchmarks.

    Where 4'-Hydroxyacetophenone Really Shines

    I meet folks from many sectors who come to this compound with different needs. For perfumers and flavorists, it provides a gentle nuanced note that fills a gap between almond, vanilla, and floral. In both fragrance and flavor work, the ability to dose it precisely and avoid overpowering subtle blends makes it essential for consistent production.

    Synergistic effects matter too. Blending 4'-Hydroxyacetophenone with other aromatic aldehydes and ketones amplifies its stability and reduces volatility. This makes it particularly valuable in long-lasting fragrance compositions and specialty foods. Fermentation scientists and microbial engineers, working to biotransform simple substrates into complex molecules, sometimes use 4'-Hydroxyacetophenone as a probe or precursor for testing new enzyme systems.

    For anyone scaling up, the compound’s stability throughout storage and processing — paired with reliable analytical fingerprints — leads to smoother regulatory submissions, fewer recalls, and faster time to market. Over the years, regulatory scrutiny has grown more intense, especially in industries touching consumer health, so each batch’s chain of custody and analytical data goes under more scrutiny than ever.

    Building Trust Across the Industry

    Google’s E-E-A-T principle — Experience, Expertise, Authoritativeness, Trustworthiness — rings true in the specialty chemical world. I’ve watched senior team members check shipment documentation for each raw material before releasing it for production. Sourcing high-quality 4'-Hydroxyacetophenone doesn’t just keep auditors happy; it builds trust among chemists, QA managers, procurement officers, and the end clients, too.

    Instead of treating this product as a commodity, leading companies in fragrance, flavors, and pharma have started looking beyond the lowest price. They pay attention to the analytical support, supply chain transparency, and certified batch-to-batch consistency. Teams expect suppliers to show detailed impurity profiles, sustainability certifications, and up-to-date research supporting each application.

    Some of the most important lessons I’ve learned as a chemist and consultant stemmed from watching what happens when corners are cut. Plants forced to reprocess off-spec material rack up costs and lost hours. Downstream partners lose confidence, and client relationships grow tense. A few dollars saved upfront on raw materials will never offset the cost of missed shipments or spoiled batches in the end. Trust is built slowly, and smart teams preserve it by sticking with reliable suppliers and demanding thorough documentation at every stage.

    Who Benefits Most from Using 4'-Hydroxyacetophenone

    Formulators and application scientists in the perfume, flavor, and pharma industries find the biggest advantages here, but the reach spreads out even farther. R&D teams working in academic institutions rely on predictable building blocks during organic synthesis and natural product isolation. Polymer chemists value the hydroxy functional group for its reactivity and potential in cross-linking, making new functional materials for coatings or adhesives.

    Anyone working on combinatorial chemistry libraries will appreciate how easily 4'-Hydroxyacetophenone can be adapted to fit various scaffolds. Researchers focusing on medicinal chemistry projects use it to introduce both hydrophilicity and aromaticity in a single synthetic step, which can address solubility challenges for drug candidates.

    Teams focused on scaling lab syntheses to small pilot runs or even to commercial production lines will find the consistent melting point, solubility, and purity profile of 4'-Hydroxyacetophenone reduce the risks associated with process scale-up. I’ve watched startups and spin-offs use the molecule for rapid prototyping and small-batch tests; its reliability saves time during both the optimization and validation steps.

    Potential Issues and Ways Forward

    No chemical compound is perfect, and 4'-Hydroxyacetophenone comes with its own set of challenges. Trace impurities sometimes show up when producers cut corners, often in the form of polymeric material or residual acids. Poor storage or exposure to moisture can lead to clumping and reduced flow, causing trouble in automated dispensing. Supervision and formalized testing protocols make a difference — companies with robust QC protocols and dedicated analytical support sidestep most logistics headaches before they escalate.

    Supply chain bottlenecks exist, especially when global markets see shifts in feedstock pricing or regulatory shifts on a key precursor. Forward-thinking teams keep backup suppliers on hand and monitor geopolitical developments closely. They also invest in long-term supplier relationships, visiting production facilities and auditing environmental compliance to guard against disruption. Increased digital tracking, sustainability certifications, and blockchain verification further reinforce trust and transparency, offering peace of mind to busy purchasing managers.

    Environmental sustainability remains top-of-mind for modern producers. Research into green chemistry, biocatalysis, and recyclable solvents has opened doors for cleaner and more energy-efficient synthesis. I’ve met teams adopting continuous-flow reactors and in-line monitoring to minimize waste and reduce risk. Some have begun incorporating renewable feedstocks, which may cut the carbon footprint and align with long-term corporate responsibility targets.

    Suggestions for Those New to Working with This Molecule

    Anyone exploring 4'-Hydroxyacetophenone for the first time stands to benefit from up-to-date product literature and clear dialogue with technical representatives. Detailed analytical data and application advice help teams match the product to their intended use case, whether that’s a new crop protection agent, a medical intermediate, or a unique scent molecule. For those in large facilities, automation in handling and dispensing can help maintain consistency in batch preparation.

    Lab-scale users often find personal experience valuable. Document your process each time you receive a new batch, including visual checks and quick purity screens. Peer-reviewed publications and technical bulletins can offer process optimization tips and reveal best practices for purification and downstream processing. Networking with other chemists, offering insight into challenges and wins alike, helps build a pool of collective experience around specialty chemicals like this one.

    Innovative Uses and Future Directions

    Innovation in chemicals typically comes from teams willing to experiment — sometimes literally. 4'-Hydroxyacetophenone continues to crop up in patent filings and exploratory grants across industrial and pharmaceutical chemistry. Emerging areas, like molecular sensors, enzyme mimics, and next-generation drug delivery, draw on the predictable reactivity this molecule brings.

    Some synthetic biologists are now testing enzyme systems tailored to selectively hydroxylate acetophenone substrates — aiming to produce 4'-Hydroxyacetophenone using engineered microbes in a low-energy, biodegradable process. Green manufacturing methods like this could one day make aromatic ketones even more accessible and eco-friendly.

    Research on advanced polymers and functional materials often features 4'-Hydroxyacetophenone as a pivotal cross-linker or precursor. By tweaking its reactivity, scientists design smart coatings, water-resistant films, and adhesive systems. Academic chemists exploring sustainable catalysis and bio-inspired synthesis have begun documenting higher yields and greater selectivity using this molecule as a model substrate.

    Final Thoughts from Experience

    In my years of chemical development and project management, I’ve seen firsthand the difference a reliable raw material makes, both in the lab and in full-scale production. 4'-Hydroxyacetophenone offers advantages across several industries, from consistency and purity to efficiency and application flexibility. Teams that put in the work — verifying quality, supporting suppliers, building analytic expertise — get the most out of it.

    Just as importantly, buyers should seek out detailed documentation and transparency from suppliers. Not only does this improve regulatory compliance, it ensures safer, more reliable production in the long run. For anyone striving to create lasting solutions in flavors, fragrances, pharmaceuticals, or materials science, 4'-Hydroxyacetophenone delivers a proven edge, shaped as much by smart sourcing and careful handling as by its own chemistry.