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2,4-Dihydroxyacetophenone

    • Product Name 2,4-Dihydroxyacetophenone
    • Einecs 202-994-2
    • 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

    692370

    Chemical Name 2,4-Dihydroxyacetophenone
    Cas Number 89-86-1
    Molecular Formula C8H8O3
    Molecular Weight 152.15 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 146-148 °C
    Boiling Point 287 °C
    Solubility In Water Slightly soluble
    Density 1.28 g/cm3
    Smiles CC(=O)C1=CC(=C(C=C1)O)O
    Iupac Name 1-(2,4-dihydroxyphenyl)ethanone
    Pubchem Cid 6998
    Storage Conditions Store at room temperature, away from light and moisture

    As an accredited 2,4-Dihydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,4-Dihydroxyacetophenone is packaged in a 100-gram amber glass bottle, clearly labeled with hazard information and product details.
    Shipping 2,4-Dihydroxyacetophenone is shipped in tightly sealed containers, protected from moisture and light. It is classified as a non-hazardous chemical, but should be handled with care. Ensure the package is clearly labeled and complies with local transport regulations. Store and transport at room temperature, away from incompatible substances and ignition sources.
    Storage 2,4-Dihydroxyacetophenone should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect the chemical from light and moisture to maintain stability. Use appropriate personal protective equipment when handling and ensure proper labeling to prevent accidental misuse.
    Application of 2,4-Dihydroxyacetophenone

    Applications of 2,4-Dihydroxyacetophenone in Industrial Manufacturing

    2,4-Dihydroxyacetophenone is a specialized organic intermediate widely adopted in several high-value industrial production chains. Drawing on our manufacturing expertise, we support global producers in sectors including pharmaceuticals, cosmetics, polymer additives, agrochemicals, photographic chemicals, and dyes. The following sections detail real-world downstream uses, supported by compliance, formulation, process, and end-product considerations.

    1. Pharmaceutical Intermediate for Antipyretic and Analgesic Synthesis

    Pharmaceutical manufacturers depend on 2,4-dihydroxyacetophenone as a building block during synthesis of non-steroidal antipyretic and analgesic compounds. Its reactive phenolic structure suits condensation and alkylation steps, forming core intermediates for active pharmaceutical ingredients (APIs) such as phenacetin analogues. Our high-purity material ensures batch-to-batch consistency, supporting regulatory documentation and traceability throughout the API development pipeline from process R&D to commercial supply.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practices for Active Pharmaceutical Ingredients)
    • EU GMP Part II
    • 21 CFR Part 211 (US FDA cGMPs)
    • EP, USP monograph checks (where applicable on finished APIs)

    Typical usage ratio

    • 30–60% (molar basis relative to main condensation partner); precise ratio adjusted depending on the target API core structure and desired impurity profile.

    Downstream process integration

    • Introduced at initial coupling or condensation stage in multi-step API synthesis, after solvent charging and prior to addition of alkylating agents or acylating reagents; commonly monitored by in-process HPLC.

    Final product types

    • Paracetamol derivatives
    • Phenacetin and related antipyretic bulk drugs
    • Analgesic API intermediates

    2. Cosmetic Ingredient for Skin Whitening and Anti-Aging Formulations

    Skincare brands incorporate this compound as a depigmenting agent and free radical scavenger in creams and serums. The compound’s chelating activity interrupts melanogenesis, while its antioxidant action stabilizes sensitive ingredients in the formulation. Our material complies with national cosmetics regulations, allowing formulators to achieve reproducible results through controlled dosage and validated stability testing.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • US FDA Cosmetic Ingredient Review (CIR); INCI registry
    • Chinese GB 7916-2013 (Hygienic Standard for Cosmetics)
    • ISO 22716 (Cosmetic GMP)

    Typical usage ratio

    • 0.1–1.0% in emulsions and gels; technical assessment recommends maximum 0.5% for daily use leave-on products, subject to safety evaluation.

    Downstream process integration

    • Dosed during the cool-down phase of emulsification, post-homogenization, or solubilized into aqueous phase for gel systems; storage stability and compatibility checks advised.

    Final product types

    • Skin whitening creams
    • Anti-aging serums
    • Spot treatment lotions
    • Sunscreen adjuncts

    3. Precursor for Agrochemical Synthesis

    Agrochemical manufacturers utilize this material in the synthesis of hydroxy-substituted benzene derivatives used in crop protection. Its dihydroxy arrangement supports functionalization into ether, ester, and carbamate groups required for herbicide and insecticide actives. Precise metering and compound quality play a pivotal role in achieving regulatory-compliant residues in treated crops.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides
    • China GB 2763 (MRL for Pesticide Residues in Food)
    • US EPA 40 CFR Part 180 (Tolerances and Exemptions for Pesticide Chemicals)
    • ISO 9001:2015 for quality management in agrochemical plants

    Typical usage ratio

    • 15–25% per batch synthesis of target active ingredient, variable according to desired substitution and downstream coupling partners.

    Downstream process integration

    • Added during initial aromatic substitution or protected as an intermediate during multi-stage synthesis; monitored by GC or LC-MS for impurity control.

    Final product types

    • Herbicidal active intermediates
    • Pre- and post-emergent pesticide compounds
    • Insecticidal synthetic building blocks

    4. Polymer Additive for UV Absorber Synthesis

    The specialty plastics sector uses 2,4-dihydroxyacetophenone in the synthesis of advanced UV absorbers and stabilizers. These block damaging radiation in engineering plastics, coatings, and films. High-purity inputs are essential for high molecular weight absorber performance, with full traceability across batch, ensuring reproducible light fastness and base resin compatibility in downstream extrusion or compounding operations.

    Industry compliance standards

    • EU Regulation (EC) No 10/2011 (Food Contact Plastics)
    • US FDA 21 CFR 177 (Indirect Food Additives: Polymers)
    • RoHS/REACH compliance for electronics and automotive plastics
    • ISO 9001:2015 for additive and masterbatch manufacturers

    Typical usage ratio

    • 20–40% as precursor in UV absorber chemical synthesis; 0.2–0.8% in final masterbatch or compound, adjusted for polymer matrix and stability requirements.

    Downstream process integration

    • Reacted in the synthesis of benzotriazole- or benzophenone-type UV absorbers; the purified absorber is metered into compounding or extrusion phase with thermoplastics.

    Final product types

    • UV-stabilized PE, PP, and PC films
    • Automotive coatings
    • UV absorber masterbatches
    • Outdoor-grade furniture plastics

    5. Intermediate in the Manufacture of Azo and Anthraquinone Dyes

    Dye and pigment manufacturers use this dihydroxy ketone as a coupling component or as a reductive substrate in the synthesis of azo- and anthraquinone-based dyes. Its unique substitution pattern lends specific hue and fastness properties required for high-performance textile and paper colorants. The quality of this intermediate influences the purity and robustness of the final dye batches, particularly in high-shade consistency applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 (Textile Dye Safety)
    • ZDHC MRSL v3.1 (Global Chemicals Management for Textiles)
    • REACH Annex XVII Substances of Very High Concern (SVHC) restrictions
    • ISO 105 Series (Color Fastness Tests)

    Typical usage ratio

    • 10–25% in coupling reactions; ratio adjusted to tone depth and yield requirements for different dye classes.

    Downstream process integration

    • Charged into diazotization or coupling step in dye synthesis reactors, with reaction endpoint and product profile monitored by TLC or spectroscopy; by-product control critical for shade consistency.

    Final product types

    • Textile azo dyes
    • Anthraquinone dyes for paper
    • High-fastness pigment dispersions
    • Synthetic fiber colorants

    6. Photographic Chemical Intermediate

    Producers of specialty photographic chemicals employ this compound as a chemical intermediate in the formulation of developers and photographic couplers. It modulates redox properties and stabilizes other phenolic agents in developing baths, contributing to fine image reproduction. As photographic formulations demand purity and batch homogeneity, our QC controls guarantee minimal interference with silver halide processes.

    Industry compliance standards

    • ISO 18911:2010 (Imaging Materials—Processing Chemicals)
    • RoHS compliance (electronics-related photo applications)
    • Environmental protection norms for effluent discharge (local EC or EPA)

    Typical usage ratio

    • 2–8% in developer formulations; optimized based on sensitivity and clarity targets in end-use processes.

    Downstream process integration

    • Blended with development agents at solution preparation stage; QC routine includes photographic grade impurity screening and color formation endpoint analysis.

    Final product types

    • Photographic film developers
    • Document imaging couplers
    • Photo print stabilizers
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    Certification & Compliance
    More Introduction

    2,4-Dihydroxyacetophenone: Our Direct Perspective From the Factory Floor

    Getting Down to What 2,4-Dihydroxyacetophenone Really Means for Industry

    The chemistry world keeps turning, and for those of us rooted in production, no day comes without a challenge or a lesson. Take 2,4-Dihydroxyacetophenone, for instance, a compound that has seen a steady rise in demand across a range of applications, especially in pharmaceutical development and specialty chemical synthesis. In our work, the story behind a molecule like this isn’t only about its paper specs, but also about what it delivers once it leaves our reactors.

    Some chemicals sound technical or obscure until you see them at work inside your plant. We always recognized 2,4-Dihydroxyacetophenone by its pale yellow appearance and crystalline form during harvest. That yellow blush doesn’t come from impurities—it’s part of its chemical character, coming out strong and clean when the raw materials and purification steps have gone right. After all, the formula—C8H8O3—only tells a slice of the story. After years of hands-on manufacturing, we know its function and purpose reach far past formulae and batch records.

    Why the Standard Matters: Technical Specifications as Reflected in Practice

    Every batch begins with close attention to melting point and purity. In our plant, we typically set our internal standard for melting point at around 146-149°C. Too low or too high tells us something’s off in isolation or drying. A high-performance liquid chromatography (HPLC) assessment provides us the purity profile—usually not less than 99%. Poor isolation, shortcuts in crystallization, or pushing the washing stage too fast, and you’ll see an extra peak where you shouldn’t.

    Moisture content slips into focus as well, especially since some customers develop active pharmaceutical ingredients straight from our 2,4-Dihydroxyacetophenone. We keep water level below 0.5%, not just for the shelf life, but to avoid downstream issues for the next manufacturer using our material. Small issues snowball into major costs down the line if not caught at this stage.

    Appearance isn’t just cosmetic, either. Over time, we’ve seen that bright yellow crystalline powder forms tend to flow better, dissolve faster, and handle with less dusting compared to amorphous off-white lots that come from rushed crystallization. Handling bulk shipments over months, consistency saves everyone headaches.

    Direct Use Cases: Where 2,4-Dihydroxyacetophenone Goes And What It Delivers

    After leaving our facility, most lots wind up in intermediate synthesis for pharmaceuticals—especially in the design of certain anti-inflammatory, anti-bacterial, or neurologically active substances. The dual hydroxy groups on the aromatic ring prove handy, forming symmetrical frameworks that chemists value when designing target molecules. Our technical staff often field questions right from researchers for whom minor shifts in purity or trace impurities can define whether a reaction route works at all.

    A less obvious but no less important use extends to dye and pigment manufacture. Years back, we began working with a small lab group looking to shift old azo dye processes to more stable, environmentally conscious intermediates. They ran headlong into reproducibility problems until we supplied a tighter loss on drying and iron content limit. Technically minor, but real results followed—yield stability went up and filtration became easier. These are stories that statistics alone don’t show but matter to anyone concerned about batch-to-batch headaches.

    Cosmetics and flavors sometimes utilize derivatives or downstream products based on our own 2,4-Dihydroxyacetophenone. None of us who walked the shop floor forgets the persistent vanilla-like undertone that creeps in around certain synthesis routes. Some of this makes its way into natural or nature-identical fragrance formulations, and even though the quantities pale compared to pharma use, the demand for traceability and high purity never lets up.

    Not All Acetophenones Are Built Alike—What Sets 2,4-Dihydroxyacetophenone Apart?

    Over the years, we’ve seen people confuse 2,4-Dihydroxyacetophenone with compounds like 4-Hydroxyacetophenone or 2,5-Dihydroxyacetophenone. On paper, they don’t seem that different. In production, the differences couldn’t be starker. Positioning of the hydroxyl groups on the aromatic ring doesn’t just change the name—it throws the solubility profile, reactivity, and stability onto totally different tracks.

    For example, 4-Hydroxyacetophenone comes out less polar, sometimes crystallizes much more easily, and handles larger-scale filtration without clogging. But it loses versatility in certain coupling or substitution steps. 2,4-Dihydroxyacetophenone, with both ortho and para hydroxyls, lends additional hydrogen bonding opportunities, which can be exploited for making more polar derivatives or even for direct chelation in coordination chemistry.

    That’s why in the plant, adjusting the process for one or the other isn’t just about changing the starting materials—the solvent system, crystallization conditions, and even expected impurities all need a rethink. On the safety front, too, not all handling requirements match from one acetophenone to another. Years of storage trials have shown us that some analogues weather temperature and humidity swings much better than others.

    It’s this direct experience—the technical back-and-forth between chemistry and plant operation—that gives us more than a theoretical understanding of product differentiation. The performance in actual synthetic procedures, the stability through shipping, and the reaction to minor process tweaks—these define 2,4-Dihydroxyacetophenone just as much as any chemical identifier.

    Sourcing, Consistency, and Quality: Challenges That Color the Real World

    As manufacturers, we start every campaign by putting raw material audits and process validations at the forefront. Ensuring reliable and consistent supply chains for starting phenols and acylation reagents isn’t a paperwork exercise for us—it affects cost, output, and overnight capacity. Fluctuations in raw phenol purity or availability have forced us to adjust schedules more than once. What we learned over time is that close relationships with raw material producers anchor reliability. For many years, we’ve kept most key inputs under direct contract, so we aren’t caught flat-footed when global supply chain issues flare up.

    Quality monitoring runs through our day. Our team keeps daily logs of equipment cleaning, solvent distillation, and batch statistics—not after something goes wrong, but as part of every shift. Process deviations, even minor ones, get tackled through root cause analysis, often involving different departments talking directly, sidestepping red tape.

    Analytical robustness forms another backbone. We’ve implemented regularly calibrated gas and liquid chromatographs, UV-Vis spectrometry, and sometimes even NMR for structural verification when working with new applications or custom lots. A spec sheet on paper means little if the tools reading it aren’t tuned and the standards set within the context of the customer’s actual needs.

    It’s also no small thing to say a word about clean labeling. Fewer chemical manufacturers talk directly about trace metals, residual solvents, or vessel cross-contamination, but we’ve learned the hard way how a trace amount of iron or copper can derail sensitive catalytic reactions for downstream clients. To avoid recurrence, we implemented more stringent vessel cleaning protocols—for instance, with dedicated equipment or single-use liners for certain specialty batches.

    Practical Pollution Control and Sustainability

    Chemical production today doesn’t just answer to price or specs—sustainability and environmental control run alongside every batch assignment. Years ago, manufacturing acetophenone derivatives would sometimes mean a cloud of solvent fumes, barrels of colored effluent, and headaches for local communities. Regulatory demands aside, good practice calls for solvent recovery, precise effluent treatment, and minimization of transport mileage.

    In our own facility, every process upgrade now starts with whether we can recycle wash solvents or install in-line purification instead of relying on large-batch single-use techniques. Water treatment stations close the loop on aqueous waste—activated carbon, ion exchange, pH neutralization—the works. Modern reactors with closed vapor paths and vacuum lines mean fewer fugitive emissions and better control over yield-destroying side reactions.

    The upshot is more than meeting compliance. Lower solvent loss and higher recovery mean our product remains more price-stable during spikes in raw material costs. Less waste means faster cleaning and shorter downtime between campaigns, which circles back to fewer delays for customers. These improvements are good for the bottom line, but they matter to the teams that run, maintain, and clean out the same vessels day after day.

    Talking to Researchers—Tailoring What We Make to What They Need

    Not every facility gets calls directly from academic chemists or formulation leads in R&D centers, but we do. Once, a university group working on novel antioxidants hit a wall with off-the-shelf stocks, so we worked with them to design a purification route that lowered trace metals and raised the alpha-phase content of the product. Another time, a pharmaceutical client needed their batch reformulated to minimize a specific aldehyde impurity that kept showing in their final assay. Getting this right took some lateral thinking—a tweak to recrystallization solvent, a longer drying stage, and more attention to protected storage.

    These direct conversations feed back into the plant in a way marketing sheets never capture. Yes, we use formal QA reports, but it’s the collaborative trial-and-error—something that develops only after repeated mutual trust—that really lets us tune process and product beyond what regulators or even our own routine process could dictate.

    Looking Forward: Innovation, Compliance, and Market Direction

    Market shifts shape our priorities. Regulatory frameworks have grown more far-reaching, whether it’s REACH in the EU, TSCA in the US, or growing scrutiny in Asia-Pacific markets. It would be easier to see compliance as a burden, but often these rules push us to improve. In the case of 2,4-Dihydroxyacetophenone, new customer requirements for documentation, batch traceability, and Green Chemistry metrics led us to digitize all plant data and introduce advanced lot tracking.

    Along the way, we started reviewing catalyst systems to cut down on waste, assessing biodegradable solvent options, and routinely collaborating with downstream users to validate that our input strengthens—not weakens—the final molecule’s properties. The feedback cycle—produce, ship, collect feedback, improve—may not be glamorous, but it’s honest work. Every new regulation ticks up our costs in the short term, but the product in the drum ends up more predictable, safer, and more widely accepted in regulated supply chains.

    Troubleshooting Challenges—Lessons Learned the Hard Way

    Every manufacturer accumulates stories of troubleshooting gone both right and wrong. Once, we suffered a spike in batch rejection rates that linked back to a seemingly minor change in the water treatment cycle upstream from our crystallizers. Water sourced from a different well, even though all routine parameters matched, threw subtle minerals into the mix, which led to altered crystal habit and lower drying efficiency. Only after bringing together plant engineers, QC techs, and third-party auditors did we put the pieces together and change the source back. Weeks of lost production and customer complaints underscored that even indirect inputs demand scrutiny.

    We’ve seen the effect of ambient air quality too. Pollen season, lasting two weeks each spring, once led to contamination through filtration equipment vents not fully sealed. Microscopic particles snuck into a batch, eventually showing up as downstream haze complaints—again leading us to rethink HEPA filtration set points and ramp up training for anyone working with open drums during periods of higher environmental particulates.

    Tales like these fill the background at every post-mortem review meeting. Solutions often prove homespun and direct—better filter changes, more staff briefings, and tight attention to every stage from receiving raw inputs through releasing a shipment.

    The Value of Real-World Experience

    We’ve stood at the confluence where theoretical specifications meet the messiness of real production. Experience teaches that no chemical product exists on paper alone—the day-to-day realities of temperature swings, variable feedstock, and shifting market needs sharpen the difference between products, even within one class of chemicals like substituted acetophenones.

    At the heart of 2,4-Dihydroxyacetophenone production is steadfast attention to every variable—raw material sourcing, reaction kinetics, purification method, and logistics. It’s not the name of the molecule that makes for a trusted relationship with buyers, but a consistent response to issues, a willingness to talk specifics, and a shared desire for improvement over time.

    Chemical manufacturing remains a work of balance: pressure for greater compliance stands alongside pushes for lower costs, cleaner processes, and tighter specs. The story of every batch includes the fingerprints of the people who make, test, and ship it—not just the data points in a digital record. For those in the field, 2,4-Dihydroxyacetophenone means more than an entry in a catalog. It’s an intersection point of chemistry, business, and the lived reality of making materials that matter across the world.