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1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione

    • Product Name 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione
    • Einecs 225-080-4
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    852248

    Chemicalname 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione
    Molecularformula C15H12O3
    Molecularweight 240.26 g/mol
    Casnumber 621-54-5
    Appearance Yellow crystalline solid
    Meltingpoint 123-126 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.21 g/cm3 (estimated)
    Smiles C1=CC=C(C=C1)C(=O)CC(=O)C2=CC=CC=C2O

    As an accredited 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle labeled "1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione, 25g" with hazard pictograms, batch number, and safety instructions.
    Shipping **1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione** is shipped in tightly sealed containers, protected from moisture and light. It should be transported in accordance with local and international regulations, classified as a laboratory chemical. Avoid extreme temperatures and handle with proper safety equipment to prevent accidental exposure or spillage during transit.
    Storage Store 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers. Label the container clearly, avoid prolonged exposure to air, and follow standard laboratory safety procedures when handling this compound.
    Application of 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione

    Applications of 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione in Industrial Manufacturing

    As a direct manufacturer of 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione, we supply this specialized diketone for core downstream sectors where it plays a critical role in advanced formulation design, chemical synthesis, and industrial production workflows. Below, we detail the principal industrial application scenarios, addressing compliance, dosage, integration points, and target finished goods.

    1. Photo Stabilizers for Polymer Additives

    This diketone serves as a high-performance UV absorber and photo stabilizer in engineering plastics and specialty polymers. It is favored in formulations where long-term exposure to ultraviolet light poses a risk of polymer degradation and discoloration, especially in the automotive and packaging sectors. Formulators leverage its effective aromatic structure for photoprotection during melt processing and compounding. Integration occurs at the compounding stage, supporting downstream extrusion, injection molding, and blow molding.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • RoHS Directive 2011/65/EU
    • ISO 9001:2015 Quality Systems
    • UL Yellow Card (applicable for final polymer resins)

    Typical usage ratio

    • 0.1%–1.0% by weight, adjusted per polymer type, outdoor lifespan requirements, and geographic UV index data

    Downstream process integration

    • Addition via masterbatch or direct dosing during hot melt compounding with core resin, stabilizers, and processing aids, before extrusion or molding cycles

    Final product types

    • Automotive exterior plastic parts
    • Food/beverage packaging films and containers
    • Architectural window films
    • Protective greenhouse sheets

    2. Pharmaceutical Intermediate for Anticoagulant Synthesis

    In the pharmaceutical field, this diketone acts as an intermediate in the multi-step synthesis of certain oral anticoagulant drugs, notably those with coumarin or benzopyrone structures. It participates in condensation reactions and ring-closure steps under controlled conditions. APIs manufactured downstream rely on precise input quality and traceability, strictly governed by pharmacopeial and GMP frameworks.

    Industry compliance standards

    • Good Manufacturing Practice (ICH Q7 & EU GMP)
    • United States Pharmacopeia (USP), European Pharmacopoeia (Ph. Eur.) monographs (for APIs)
    • FDA 21 CFR Part 210/211 for APIs
    • ISO 13485 (for drug-device combination facilities where applicable)

    Typical usage ratio

    • 100% basis for specific synthesis steps; consumed or converted entirely during condensation and cyclization in the API production sequence

    Downstream process integration

    • Charged at the initial or intermediate cyclization stage with compatible solvents and catalysts during active ingredient production

    Final product types

    • Oral anticoagulant intermediates
    • API grade benzopyrone compounds
    • Pharmaceutical tablets or capsules (following further downstream synthesis and formulation)

    3. Chelating Agent in Analytical Reagents

    Chemical and analytical laboratories use this diketone as a selective chelating ligand in spectrophotometric and chromatographic metal ion determination. Its high affinity for certain transition metals, notably Fe, Co, and Ni, allows precise quantification and calibration in standardized test kits and reference solutions. Analytical processes require controlled formulation and trace impurity monitoring.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • ASTM E200 (Preparation of Standard Solutions for Chemical Analysis)
    • Analytical Reagent (AR) Grade Specifications per ACS
    • GLP (Good Laboratory Practice) standards

    Typical usage ratio

    • 0.01–0.1 mmol/L final analytical solution; adjusted based on target ion detection thresholds

    Downstream process integration

    • Dissolved to precise concentrations when preparing analytical standards or chromogenic reagent solutions for use in UV-Vis or HPLC methods

    Final product types

    • Spectrophotometric reagent kits
    • Trace metal determination kits
    • HPLC calibration solutions for laboratory and environmental monitoring

    4. Component in High-Performance Organic Pigments

    This diketone acts as a precursor in the synthesis of certain high-stability organic pigments, particularly for inks, coatings, and plastics. Its role involves condensation with aromatic amines or aldehydes, yielding pigment molecules with superior colorfastness and light stability. Pigment manufacturers integrate the diketone early in their synthetic sequence to control hue and batch reproducibility.

    Industry compliance standards

    • EN 71-3 (Safety of Toys: Migration of Certain Elements)
    • ISO 787 (General Methods for Pigment Testing)
    • REACH Annex XVII for pigment substances
    • ASTM D4236 (Labeling Art Materials for Chronic Health Hazards)

    Typical usage ratio

    • Stoichiometric amount based on coupling partner; frequently 0.8–1.2 molar equivalents per pigment synthetic batch

    Downstream process integration

    • Combined via monitored reaction under reflux or condensation, followed by isolation, milling, and purification for pigment dispersion

    Final product types

    • High-opacity printing inks
    • Color concentrates for plastics compounding
    • Industrial and decorative coatings
    • Specialty artist’s pigments

    5. Aldol Condensation Catalyst in Fine Chemical Production

    Within fine chemical industries, this diketone operates as a catalyst or activator in aldol condensation processes for tailor-made specialty molecules, especially those requiring selective enolate formation. Its aromatic structure influences reaction specificity and yield, and process engineers select dosing schemes based on both substrate compatibility and reaction temperature profiles.

    Industry compliance standards

    • ISO 9001:2015 for process control
    • Responsible Care® chemical management
    • GHS (Globally Harmonized System) for labeling and safety
    • REACH/CLP compliance for catalyst substances

    Typical usage ratio

    • 0.05–0.5 mol% relative to limiting substrate, subject to substrate reactivity and target conversion

    Downstream process integration

    • Total charge at the reaction setup with other catalyst components; removed or neutralized during downstream purification and isolation

    Final product types

    • Custom aryl alkenes and fine chemicals
    • Specialty intermediates for agrochemicals
    • Functionalized aromatics for further derivatization
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione: From a Manufacturer’s Perspective

    Our Experience Shaping the Chemistry of 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione

    Working with 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione reveals fascinating chemistry, practical realities, and real competitive advantages. Over decades, our production teams have seen this compound shift from an academic talking point to a reliable workhorse in certain specialty applications. Our labs have refined the process, starting with selection of raw materials, through multi-stage synthesis and careful purification. Behind every kilogram stands a string of choices made for purity and stability, not just technical specs on a sales sheet.

    The molecule itself, with a hydroxy group ortho to a diketone bridge and a terminal phenyl ring, packs a sophisticated punch in both coordination chemistry and specialized organic synthesis. Those using it in catalysis, ligand design, or as a building block for advanced materials understand the need for consistent structural integrity. Every batch produced must deliver the same tight melting range, low water content, and very fine control over impurity profiles to avoid headaches in downstream processing.

    Manufacturing Insights: Purity, Scale, and Batch Consistency

    From a manufacturer’s point of view, achieving high-purity 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione is not trivial. We don’t just hit a target by following a recipe. Natural variability in starting phenols, benzaldehyde, or base quality all influence yield and impurity load. Trace byproducts from side reactions can shadow the main product and impact its downstream reactivity. Our purification process hinges on repeated crystallization and vacuum drying, with bit-by-bit improvements coming from years spent tracking minor contaminants via advanced chromatography and NMR.

    Scaling up from the lab bench to industrial reactors presents new puzzles. Exotherms in the aldol condensation stage can run out of control if not tamed. Solvent choice and recovery become cost drivers as much as environment concerns. Our engineers invest huge time in thermal mapping and agitation control to extract crystal-clear batches, minimizing both colored and volatile residuals that sometimes sneak through lesser setups. Random sticky residues found in less controlled syntheses never make it onto our product lines—every compromise avoided means fewer headaches for our partners.

    Key Specifications: Beyond the Numbers

    We don’t think of our product mainly in terms of catalog numbers or certificates of analysis, but as a tightly defined chemical entity that makes or breaks results in synthesis. Most batches run above 99% purity by HPLC, with water content usually under 0.2% as measured by Karl Fischer titration. Our team has seen even tiny deviations—say, a 0.2% rise in minor isomer—lead to failed crystallizations or odd spectral signatures in customers’ applications. This molecule’s pale color, consistent melting point, and particular odor have become familiar markers of a job well done. Every time we fine-tune particle size, moisture content, or storage conditions, it’s because one of our longtime customers pointed out a reactivity or handling quirk that only shows up in-the-field, not a spreadsheet.

    We’ve ended up optimizing our process to allow for both bulk orders and custom runs with altered particle size distributions or tighter impurity specifications. Some partners want powdery, highly dispersible product for rapid dissolution, while others need crystals for precise metering. We routinely provide microanalysis down to trace ions, because traces of alkali or iron picked up from process equipment can catalyze degradation in sensitive systems.

    Typical Applications: Real-World Usage and Feedback

    This diketone compound proves its worth in university labs and R&D departments focused on chelation, catalyst design, and advanced polymer development. Academic groups lean on its unique binding motifs in the creation of metal complexes for photochemistry, analytical methods, and catalysis. We routinely help them troubleshoot reaction outcomes, not just supply product. Over the years, we’ve fielded questions about residual solvent effects, or why one synthetic derivative refuses to crystallize. More often than not, the answer lies in the tiny impurity profile—recognizing which lingering moiety or trace cation needs removal comes from real hands-on experience, not generic guidelines.

    Many of our industrial colleagues use this compound as an intermediate in the synthesis of more complex molecules. Since purity problems propagate through each synthetic step, the upfront investment in quality always comes back saved down the track when yields increase and clean-up work decreases. The repeatability of our lots means less time spent on analytical troubleshooting and more time focused on new product development.

    In pigment and resin chemistry, the presence of the ortho-hydroxy group opens doors to additive manufacturing, UV absorption, and enhanced crosslinking performance. Choosing the right polymorph and achieving near-perfect isomeric purity allows for predictable batch-to-batch reactivity. Users in these industries have given us feedback that small process tweaks—cooling rates, filtration methods, or drying techniques—noticeably impact brightness, transparency, and compatibility.

    Handling, Storage, and Shelf Life: Practical Learning

    Handling this molecule in bulk presents unique challenges. Despite seeming robust, it proves sensitive to light and humidity over storage cycles. Early on, we noticed that product left in standard bins lost its punch over several weeks, with hydrolysis or small-scale oxidative changes creeping into sensitive batches. Now, we seal every lot under inert atmosphere and use blacked-out packaging, limiting air and UV exposure. Customers who skip these steps usually pay the price later with diminished activity.

    Shipping conditions also can’t be an afterthought. We customize our logistics for seasons and shipping transit time—heat or damp during summer freight can push batches out of spec before they even reach the user. Experience taught us to double-pack materials and insert humidity indicators to reassure both shippers and end-users about current lot quality. It’s a small cost up front but saves unplanned headaches and lost time due to spot re-testing or urgent replacements.

    How 1-(2-Hydroxyphenyl)-3-Phenyl-1,3-Propanedione Stands Apart

    From a manufacturing viewpoint, there’s no shortage of analogs and alternate diketones on the market. What sets this molecule apart is its unique balance between reactivity and selectivity, coupled with manageable toxicity and user-friendly handling compared to others in the same class. Compounds lacking the ortho-hydroxy group often miss out on stable chelate formation, a feature our customers depend on for experimental repeatability and high-yield synthesis. Others with additional substitutions can behave unpredictably under standard lab conditions, complicating purification and scaling.

    We regularly review side-by-side comparisons of use cases. Take, for example, the trend in exploring higher substituted diketones for bandgap tuning in photonic applications—those efforts often run into issues with solubility or excessive degradation, challenges we regularly troubleshoot for research groups. Meanwhile, straightforward 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione keeps delivering stable, crystalline batches that hold up under moderate heat and a broad pH range, offering practical reliability where it counts.

    Environmental Considerations and Responsible Manufacturing

    Manufacturing this compound brings responsibility. As direct producers, we encounter the environmental and safety trade-offs firsthand, not as abstract targets but as daily operational realities. Effluents from the condensation and purification process are carefully monitored and treated onsite. We’ve invested in solvent recovery processes and are constantly pushing to minimize energy usage during drying and crystallization steps, not simply for cost but out of real concern for sustainable practices.

    Our teams implement PPE protocols and facility controls that go beyond the paper requirements. Accidental exposure to intermediates reminded us early on about the actual hazards, so operator training is built in from hiring onward. Every improvement limiting dusting, volatile emission, or accidental spillage reduces not only regulatory risk but also supports the well-being of skilled folks we count on to run each batch. Feedback from team members on workflow or ventilation directly drives our upgrades in process engineering.

    Troubleshooting and Continuous Improvement

    Any experienced producer knows process hiccups come with chemical manufacturing. In our own experience, attempts to shortcut steps—less filtration, hotter drying, swapping solvents—almost always bit us down the line. Odd color formation, changes in melting point, or slower dissolution serve as the tell-tale signs. Instead of hiding errors, we keep logs of each deviation and treat them as springboards for process improvement. Internal audits, batch recall analysis, and direct customer feedback cycles hone our process as much as any textbook.

    A fair chunk of ongoing effort goes into anticipating changes in raw materials. Crop variability, evolving supply chains, and the occasional contaminated drum all force us to adapt—often at short notice. Having a deep bench of analytical techniques and experienced eyes on the floor lets us catch problems before they cascade. Critical tweaks like adjusting base concentrations or changing the crystallization temperature often come not from the lab, but from operators who know the process at gut level. Over time, fostering this culture means fewer surprises and faster recovery from inevitable hiccups.

    Industry Collaboration and Real-World Value

    We’ve seen the greatest product improvements come from partnerships with users, not from internal brainstorming alone. Researchers at one partner site found the standard sodium form of our product left trace cations in their downstream catalyst prep, impacting yields. After months of back-and-forth, we developed a variant processed with potassium and improved our washing protocols, all initiated by field results. Another industrial customer asked for tighter sieve fractions to enhance dosing uniformity—this led to an investment in new equipment, raising quality for all clients.

    Conversations with customers uncover application trends faster than trade shows or market surveys. Demand for low-metal content, reduced solvent residues, or enhanced traceability all rose as direct responses to problems users encountered in the field. New requests often challenge us to think differently—could we deliver material pre-packed under vacuum? Could we supply extra-anhydrous grades for more sensitive syntheses? These conversations light the path for the next improvements, bridging the gap between theory and application.

    Looking Ahead: Innovation and Next Steps

    We view 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione as a platform rather than a commodity. As spectroscopy, catalysis, and material science expand, the need for sharper definition grows. Complexation chemistry, chiral ligand development, or advanced photonic materials require narrower impurity bands and highly characterized lots. Our own roadmap tilts toward integrating continuous flow synthesis, advanced in-line process controls, and deeper digital batch records. Close monitoring of spectral and microanalytical signatures promises to improve not only compliance, but also customer freedom to explore new applications with confidence.

    Every product shipped bears the fingerprints of direct engagement and continuous improvement. We expect future iterations of this molecule to find their way into even more demanding roles. Already, groups testing new doped materials or searching for greener processes push us to think outside current playbooks. By embracing new technologies, expanding dialogue with field users, and holding firm on what counts—consistent purity, reliable behavior, transparent manufacturing—manufacturers like us will continue to provide the trust and results customers deserve.

    Practical expertise, not marketing gloss or third-party handoffs, marks the true difference in this business. Making, refining, and delivering 1-(2-hydroxyphenyl)-3-phenyl-1,3-propanedione amounts to much more than filling a drum. It means close attention to both lab chemistry and industrial scale-up, a steady hand on batch-to-batch consistency, and genuine care for the chemists, analysts, and R&D teams who rely on our experience to advance their own technical frontiers.