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2',4'-Dihydroxypropiophenone

    • Product Name 2',4'-Dihydroxypropiophenone
    • Einecs 211-722-0
    • 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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    VTB
    Specifications

    HS Code

    150013

    Cas Number 2114-55-2
    Molecular Formula C9H10O3
    Molecular Weight 166.18 g/mol
    Iupac Name 1-(2,4-dihydroxyphenyl)propan-1-one
    Appearance White to beige crystalline powder
    Melting Point 85-89°C
    Solubility In Water Slightly soluble
    Synonyms 2',4'-Dihydroxypropiophenone; 2',4'-Dihydroxy-1-propiophenone
    Pubchem Cid 81596
    Smiles CCC(=O)C1=C(C=C(C=C1)O)O
    Inchi InChI=1S/C9H10O3/c1-2-9(12)7-4-3-6(10)5-8(7)11/h3-5,10-11H,2H2,1H3

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

    Packing & Storage
    Packing The 25g 2',4'-Dihydroxypropiophenone is supplied in an amber glass bottle with a tightly sealed screw cap for protection.
    Shipping 2',4'-Dihydroxypropiophenone is shipped in tightly sealed containers to prevent contamination and degradation. Store and transport it at room temperature, away from light, moisture, and incompatible substances. Follow all regulatory guidelines, including correct labeling and documentation, and comply with local, national, and international shipping regulations for chemical substances.
    Storage 2',4'-Dihydroxypropiophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from light, moisture, and excessive heat. Ensure it is clearly labeled and kept away from food or drink to avoid contamination and accidental ingestion.
    Application of 2',4'-Dihydroxypropiophenone

    Applications of 2',4'-Dihydroxypropiophenone in Industrial Manufacturing

    Our production of 2',4'-Dihydroxypropiophenone supports specialized manufacturers as a reliable intermediate for downstream chemical synthesis. The following application scenarios highlight authentic uses across focused industry sectors, with details on compliance, formulation, integration points, and finished end products.

    1. Pharmaceutical Intermediate for Non-Steroidal Anti-Inflammatory Drug Synthesis

    Manufacturers of specialty active pharmaceutical ingredients integrate this material as a key intermediate in multistage syntheses for certain non-steroidal anti-inflammatory drugs (NSAIDs). It helps construct the core skeleton of API molecules, with process controls in place for purity and byproduct removal during reactions such as acylation or condensation, prior to subsequent functionalization. The downstream process consistently monitors the intermediate’s identity and content under GMP protocols, essential for consistent bulk production of regulated APIs.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA cGMP regulations)
    • European Pharmacopoeia General Monograph 2034
    • Chinese Pharmacopoeia, Part II – Intermediate specifications

    Typical usage ratio

    • Used in stoichiometric amount based on target API structure; typically 0.9–1.2 mole equivalents relative to the next coupling partner in the synthesis

    Downstream process integration

    • Introduced after initial condensation or acylation step during API scaffold assembly
    • Purified by crystallization or column chromatography prior to conversion to active ingredient

    Final product types

    • Bulk non-steroidal anti-inflammatory drug APIs (e.g., propionyl-derivative NSAIDs)
    • Final formulated tablets, capsules, and injectables

    2. Fine Chemical Intermediate for UV-Absorber Additive Production

    The compound functions as a building block in manufacturing certain benzophenone-based UV-absorbers, essential in coatings, plastics, and personal care formulations. Downstream plants react it in multi-step synthesis with substituents to generate highly specific stabilizers, controlling batch yields and impurity profiles for light-shielding agents in commercial products. Analytical tracing ensures every lot meets quality benchmarks for downstream melt compounding or blending processes.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System (for chemical intermediates)
    • REACH (EC 1907/2006) compliance for substances used in consumer goods in the EU
    • RoHS Directive (EU 2011/65/EU) for UV-absorbers in electronic and electrical products
    • GB/T 23986—2009 (China, fine chemicals for plastics industry)

    Typical usage ratio

    • Commonly dosed at 0.8–1.5 mole equivalents, according to the specific UV-absorber synthetic route endpoints

    Downstream process integration

    • Serves as initial core for alkylation, halogenation, or etherification during UV-absorber manufacturing
    • Purification and QC by HPLC or GC after main condensation steps

    Final product types

    • UV-protective additives for polycarbonate, PVC, and PET resin
    • Photostabilizer blends in industrial coatings
    • UV-blocking ingredients in cosmetic sunscreen formulations

    3. Intermediate for Veterinary Drug Synthesis

    This compound enters the synthesis chain for several niche veterinary APIs, addressing the need for anti-inflammatory and analgesic products in the animal health sector. Regulatory compliance requires dedicated production lines and full traceability, as requests from veterinary pharmaceutical manufacturers demand batch-specific documentation to align with national veterinary pharmacopeias and animal-use GMP procedures. Process engineers scale up controlled reactions to match target output, monitoring for carry-over and specification drift.

    Industry compliance standards

    • VICH GL 3: Stability Testing for New Veterinary Drug Substances and Products
    • EU GMP Volume 4, Annex 1 – Veterinary Medicinal Products
    • US FDA 21 CFR 514 (New Animal Drug Applications)
    • Ph. Eur. monographs for veterinary intermediates

    Typical usage ratio

    • Typically 1.0 mole equivalent relative to secondary building block in veterinary API synthesis; adjusted in multi-gram to multi-kilogram scale-up based on target dosage strength

    Downstream process integration

    • Charged as a primary intermediate during heterocycle or side-chain introduction
    • Subjected to liquid–liquid extraction and vacuum drying ahead of successive steps

    Final product types

    • Veterinary oral suspension active ingredients
    • Topical anti-inflammatory veterinary formulations

    4. Chemical Intermediate for Synthesis of Flavor and Fragrance Ketones

    Flavors and fragrance formulators utilize this compound as a customizable ketone precursor, particularly for routes leading to aromatic-substituted acetophenone derivatives in the flavor and perfumery field. Downstream factories employ it in controlled Friedel–Crafts alkylation or acylation, adjusting molar ratios to steer reaction outcomes, followed by distillation and GC-MS analysis to ensure olfactory consistency. Compliant manufacturing must reference food additive directives and maintain alignment with international standards for trace-level impurities.

    Industry compliance standards

    • FCC (Food Chemicals Codex) monographs for flavor ingredients
    • IFRA (International Fragrance Association) Standards
    • US FDA 21 CFR Part 172 – Food Additives Permitted for Direct Addition to Food
    • GB 2760—2024 (China National Food Safety Standard for the Use of Food Additives)

    Typical usage ratio

    • Usually introduced at 0.5–1.2 mole equivalents based on desired ketone end compound; adjusted for selectivity and yield per target aromatic group

    Downstream process integration

    • Feeds into the initial ketone synthesis, followed by distillation, phase separation, and molecular filtration
    • Subjected to sensory panel and GC confirmation in final product qualification

    Final product types

    • Ketone-type flavor additives for confectionery, beverages, and baked goods
    • Fragrance raw materials for perfumery concentrate blending
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    Competitive 2',4'-Dihydroxypropiophenone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2',4'-Dihydroxypropiophenone: Quality and Consistency from Our Production Floor

    Real Chemical Manufacturing Experience Poured into Every Batch

    Our production line for 2',4'-Dihydroxypropiophenone comes out of years standing next to reactors, solving technical problems through firsthand trials rather than theory. This molecule, with CAS number 577-60-4, draws interest from researchers and factories alike for its role as an intermediate in pharmaceutical synthesis. Often chosen for projects involving anti-inflammatory drugs and other bio-actives, its structure enables reactions that simpler phenols cannot deliver.

    Specifications that Reflect Direct Manufacturing

    Before reaching drums and drums of final product, every kilogram of our 2',4'-Dihydroxypropiophenone faces our team’s scrutiny. Purity routinely tests above 99%, and our analytical chemists work every shift to nail down melting points and spectral signatures. You see only product that hits target appearance—fine white to pale yellow powder, free of grit, nothing sticky or off-odor. Moisture content and heavy metals stay well below pharmaceutical thresholds, not out of regulatory obligation but because process control matters to us.

    Unlike some intermediates where plant engineers have to tweak post-processing to work around byproducts or color, ours remains clean because we control our raw material supply tight. On days when crude material starts showing hints of residue, our operators adjust the purification sequence so the customer doesn’t face problems in subsequent steps. We owned the learning curve on this one—high-throughput HPLC on every batch, not just one-in-a-dozen spot checks.

    Using 2',4'-Dihydroxypropiophenone for Pharmaceutical Development and Beyond

    Researchers see this compound’s two hydroxyl groups and picture flexibility. In the laboratory, it often serves as a building block for more advanced molecules. Scientists use it to introduce specific ortho and para substitutions, launching a cascade of further functionalizations. In practice, our product finds its role in syntheses targeting corticosteroid side chains, as well as certain analgesic and anti-tumor agents. Formulators appreciate the well-defined melting point—between 112 and 116 degrees Celsius—which keeps reactions predictable and reduces side product formation.

    Several multinational pharma companies come back to us because they’ve tried dozens of sources for this precursor. Many of those sources just buy and resell material with uncertain history. Some batches on the open market come with inconsistent crystal quality or stubborn contamination. Our clients don’t need to chase after technical support because they get us, the original manufacturer, to help with troubleshooting. Sometimes that’s adjusting solvent systems for better dissolution, and other times it means walking through analytical data together.

    How Our Product Differs: Beyond Brochures and Certificates

    Plenty of chemical suppliers list 2',4'-Dihydroxypropiophenone—very few put the muscle into controlling batch consistency and traceability. Our operation runs with raw notes taken at every stage. Process history gets logged: operator names, batch temperatures, reaction times, solvent rotations, filtration throughput. Years ago, poor reproducibility sparked headaches for process chemists, especially in kilo-lab scale-ups. So we re-designed the isolation protocol, balancing crystallization temperature and solvent proportion, then kept records open to technical clients.

    Our product's particulate profile sets it apart. Some competitors move material with uneven particle size; that’s not trivial if you scale up or work under GMP. We reduced fines and oversized granules by optimizing stirring and filtration—less caking, better dispersibility in downstream reactors.

    Trace impurities often sabotage assay yields. Market surveys show that imported batches sometimes harbor persistent organochlorides or sulfur-trace residues. We went deep on testing input reagents and forced extra purification rounds when our TLC or GC flagged trace outliers. Instead of keeping fingers crossed, we invite buyers to walk through technical details: Karl Fischer moisture checks, UV-Vis analysis for chromophores, and even unknown peak tracking on our LC-MS systems.

    Meeting New Demand in Research and Industry

    The regulatory landscape changes from year to year. Several countries raised scrutiny over upstream transparency for chemical intermediates, especially those likely to end up in human health products. Our in-house compliance team reads each directive and works with plant staff directly. It isn’t about cutting corners or racing shipments—reliable product documentation stays with each batch, signed off by everyone on that night’s shift.

    As synthesis projects evolve, researchers need different grades or particle sizes. We ship pharmaceutical, fine chemical, and even research-grade lots. For contract scale-ups or tech transfers, the same process engineers responsible for day-to-day plant work consult with buyers. If a customer chooses to purify further, we offer the original reaction logs so that their troubleshooting starts from real data, not assumptions.

    We don’t chase every request for “just-in-time” micro-batches. Instead, we plan capacity based on actual demand signals from ongoing collaborations—chasing last-minute orders too often leads to mistakes. Our approach: keep quality stable, then scale production predictably, holding back some material as pipeline buffer to handle surprises.

    Sustainability and Worker Safety: Not Just Buzzwords to Us

    Manufacturing fine chemicals and pharmaceutical intermediates involves risk every day—corrosive reagents, flammable solvents, and complex machinery never sleep. Our process safety record marks more than just zero incidents. We keep teams running regular leak checks on reactor seals, fit PPE that actually fits, and rotate tasks so no one burns out. Waste streams get pretreated before entering the main effluent lines. For this compound, we retooled one entire purification sequence to reduce solvent usage by half, even if it meant a longer process window.

    Our leadership invests in cleaner production not to meet an external audit, but to keep local groundwater safe and our people healthy. Regular air quality checks run every few hours in the plant, not just at shift changes. Workers have the right to stop a process if something looks off and report issues without delay.

    Solving the Scaling Challenge: From Kilo to Multi-Ton with Learning Built In

    Some chemicals give you headaches when you move from lab-bench to production-scale. Emulsions break down, heat transfer goes sideways, and even stirring speeds throw surprises. The early days scaling 2',4'-Dihydroxypropiophenone showed us where most suppliers go wrong—neglecting foaming control, missing small shifts in solubility due to seasonal changes, or ignoring how subtle build-up in holding tanks can affect downstream purity. We learned by running small test campaigns before opening up to full batches, logging every glitched run, and iterating the protocols.

    Whether bulk clients order drums or want custom packaging, we fill containers only in humidity-controlled areas to keep clumping and moisture-related degradation in check. Labels don’t just carry generic information—they track batch lineage and offer links to analytical reports. For international shipments, we support direct pre-shipment sample testing wherever possible, saving headache for those about to invest in scale-up projects.

    Technical Support Grounded in Real Operations

    Many of our customer questions revolve around solubility—how will this compound behave in a specific solvent system, or what’s the recommended best practice to get it into solution without hot spots or stubborn residues? We answer these questions based on results from our own plant, not borrowed textbook answers. Each plant trial adds to our internal knowledge base.

    For buyers exploring new synthetic targets, we sometimes support method development by trialing different purification strategies on small lots. That can mean microfiltration tests, high-vacuum drying, or alternate crystallization solvents. If research indicates new contaminants or alternative uses, we tweak the cleanup steps and measure exactly what changes downstream. Above all, we treat every technical inquiry as an opportunity to learn and improve versus sticking to a formula.

    Differences You Can Measure and Rely On

    Comparing products only by COA doesn’t show the full picture. Some samples look fine yet fail in actual process conditions—poor dissolution, off-odor, inconsistent reactivity. Our approach leans on deep process knowledge and constant improvement. Instead of aiming for good-enough, we lock in quality at each production stage. Every drum comes inspected by people who know what to look for—small hints in color, crystal habit, or subtle odor shifts. Any lot not up to our standards gets sequestered, retested, and never shipped.

    Freight can sometimes go rough, especially over long summers in uncooled containers. We learned years ago to stress-test our packaging against heat and humidity spikes, backed by controlled room stability trials. If a client’s facility faces warehouse challenges, we discuss local storage conditions and suggest adjustments, based on our firsthand experience running plants through multiple climate zones.

    Supporting Innovation and Consistent Production for the Long Haul

    By staying rooted at the manufacturing site—not outsourcing or operating intermediated sales—we maintain direct technical feedback and process control with minimal lag time. This means we respond quickly to clients chasing new molecular targets or battling scale-up bottlenecks. No need to wait weeks for support; usually the plant engineer responsible for your batch can field specific process advice or share original reaction logs within hours.

    The future for 2',4'-Dihydroxypropiophenone stretches beyond pharmaceuticals—new research points to applications in agrochemicals and specialty fine chemicals. We keep an eye on these developments, running parallel plant trials even before formal demand arrives. Feedback from past collaborations directly shapes recipe tweaks and purification upgrades, so upcoming batches routinely surpass industry-standard test results.

    Your Feedback Drives Our Plant Forward

    Every suggestion from clients—whether it’s about particle size, appearance, or reactivity—gets taken seriously and often finds its way into process improvements. Our chemists walk both ends: they make the product and interface with buyers, closing the traditional loop that so often fails in larger organizations. Our technical staff gladly open plant logs to resolve any question, big or small.

    In the chemical manufacturing world, relationships matter. We build our business not around chasing quick sales, but by ensuring every shipment reflects the depth of care and practical expertise that comes from making 2',4'-Dihydroxypropiophenone with our own hands, shift after shift, year after year.