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1,3-Diphenylacetone

    • Product Name 1,3-Diphenylacetone
    • Einecs 211-032-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    915357

    Cas Number 102-04-5
    Molecular Formula C15H12O
    Molar Mass 208.26 g/mol
    Iupac Name 1,3-diphenylpropan-2-one
    Appearance White to off-white crystalline solid
    Melting Point 62-64 °C
    Boiling Point 360.5 °C at 760 mmHg
    Density 1.099 g/cm³
    Solubility In Water Insoluble
    Refractive Index 1.577

    As an accredited 1,3-Diphenylacetone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,3-Diphenylacetone is supplied in a 100g amber glass bottle, securely sealed, with hazard labeling and a tamper-evident cap.
    Shipping 1,3-Diphenylacetone is shipped in tightly sealed containers under ambient temperature and dry conditions to prevent contamination and degradation. Packaging complies with chemical safety regulations, including correct labeling and documentation. Transport follows relevant hazardous material guidelines, ensuring secure and safe handling throughout the shipping process to minimize risk.
    Storage 1,3-Diphenylacetone should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and acids. Protect from light and moisture. The storage area should be clearly labeled and access restricted to trained personnel. Always follow appropriate chemical hygiene and safety protocols.
    Application of 1,3-Diphenylacetone

    Applications of 1,3-Diphenylacetone in Industrial Manufacturing

    Our production of 1,3-Diphenylacetone supports specialized chemical manufacturing processes across several focused downstream sectors. Here, we detail the principal industrial applications, each reflecting real use cases, process routes, and compliance frameworks demanded by large-scale formulation teams and ongoing commercial practice.

    1. Pharmaceutical Intermediate Synthesis—Preparation of α,β-Unsaturated Ketones

    This material plays a significant role as a structural intermediate for synthesizing pharmacologically active compounds, especially α,β-unsaturated ketones, which are key building blocks for non-steroidal anti-inflammatory drugs (NSAIDs) and certain antihistamines. Its rigid framework and functional group accessibility streamline sequential transformations including aldol condensations and Michael additions, reducing side-product formation and facilitating GMP-compliant synthesis pipelines.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) for Active Pharmaceutical Ingredients (ICH Q7, US FDA 21 CFR Part 210/211)
    • USP/NF Monographs and EP Quality Standards
    • REACH Registration for use in pharmaceutical synthesis
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • Employed at 0.8–1.3 molar equivalents relative to target product synthesis batch size; precise ratio determined by downstream yield and impurity profile requirements.

    Downstream process integration

    • Introduced at initial stage of batch synthesis as the substrate for catalytic condensation and ring-closure reactions; integration with in-line analytical controls (HPLC, NMR) to monitor intermediate conversion.

    Final product types

    • Finished API intermediates for NSAIDs (e.g., ketoprofen synthesis chains)
    • Synthetic intermediates deployed in second-generation antihistamine manufacture
    • Specialty building blocks for custom drug discovery

    2. Fine Fragrance Ingredient Manufacturing—Scent Complex Precursors

    Our raw material forms a precursor in fine fragrance chemistry, where it serves as a scaffold for creating aromatic compounds with high olfactory impact. Major fragrance houses employ it in syntheses such as Grignard reactions or controlled oxidation to craft musky or woody note molecules, ensuring batch-to-batch reproducibility for complex scent formulations used in high-value branded perfumes and colognes.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • European Chemicals Agency (ECHA) REACH Substances of Very High Concern (SVHC) regulation
    • IFRA Certificate of Conformity for raw materials
    • ISO 22716:2007 (Cosmetics—Good Manufacturing Practices)

    Typical usage ratio

    • Applied at 0.2–0.6% weight-by-weight in the master batch concentrate, with further dilution depending on the desired intensity and stability of the final accords.

    Downstream process integration

    • Engages in controlled organic synthesis as an initial feedstock for constructing macrocyclic musk molecules; subsequent distillation and purification steps isolate specific fragrance molecules used in perfumer blends.

    Final product types

    • High-concentration perfume bases for luxury and mainstream market fragrances
    • Signature aroma compounds for personalized perfumery lines
    • Scent components for air care and high-end personal care applications

    3. Specialty Polymer Synthesis—Chain Modifiers and Cross-Linkers

    In the advanced polymer industry, 1,3-Diphenylacetone incorporates as a chain-modifying agent or intermediate in the production of specialty resins. Its diphenyl groups enhance rigidity and alter glass transition temperatures in engineered polymer systems used for niche coatings, structural adhesives, and electronics encapsulants, where precise molecular weight control is required to meet downstream performance targets.

    Industry compliance standards

    • ISO 9001 Certified Quality Management (Polymer manufacturing scope)
    • EU REACH Registration and Notification for polymer intermediates
    • RoHS Directive (2011/65/EU) for electronics applications
    • ASTM D638/ISO 527 for mechanical properties of final resin products

    Typical usage ratio

    • Reactive loading of 0.5–2% by total polymer matrix weight, adjusted based on end-use application and compatibility with copolymer blends.

    Downstream process integration

    • Directly charged during polymerization in melt-kneading or solution batch processing; participates in cross-linking or end-capping steps, usually before stabilization and extrusion or casting operations.

    Final product types

    • Thermal-resistant resin films and injection-molded specialty plastic parts
    • High-performance epoxy adhesives for automotive and aerospace sectors
    • Encapsulation materials for micro-electronics

    4. Organic Electronic Material Development—Small Molecule Synthesis for OLEDs

    In the organic electronics sector, especially for Organic Light Emitting Diode (OLED) development, 1,3-Diphenylacetone serves as a strategic starting material for constructing conjugated small molecules. Its symmetrical structure allows efficient introduction of electron-donating and accepting motifs, enabling tunable photoluminescent properties in the final emissive layers of optoelectronic devices.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management (required for electronics chemicals)
    • IEC 60068 (Environmental testing for electronics)
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) for organic electronic materials
    • RoHS compliance for hazardous substances in electronics markets

    Typical usage ratio

    • Dosed at 0.3–1.0 molar equivalents in target molecule synthesis; the precise ratio is defined by the desired molecular architecture and quantum yield in final film formation.

    Downstream process integration

    • Undergoes condensation and cyclization reactions during organic molecule synthesis, feeding directly into purification—typically chromatography—then onward to vacuum deposition or spin-coating processes for OLED layer fabrication.

    Final product types

    • Organic emitter materials for OLED TV and smartphone display manufacturing
    • Custom small-molecule compounds for research-grade optoelectronic devices
    • Specialty additives in printable electronics formulations

    5. Agrochemical Intermediate Synthesis—Herbicide and Fungicide Precursor

    The compound is also integral to select agrochemical manufacturing chains, where it acts as a precursor for target-specific herbicides and fungicides. Its aromatic backbone enables the synthesis of bioactive agents with improved stability and spectrum of action, supporting crop protection products marketed under regulated frameworks in major agriculture economies.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • US EPA Pesticide Registration Requirements (40 CFR Part 158)
    • EU PPP Regulation (EC No 1107/2009)
    • ISO 17025 for agrochemical analysis laboratories

    Typical usage ratio

    • Introduced at 1.0–1.5 molar equivalents in intermediate step synthesis, calibrated to achieve desired purity and reaction throughput in kiloton-scale campaigns.

    Downstream process integration

    • Added as an initial reactant during the multi-step synthesis of key bioactive molecules, following with controlled halogenation or acylation steps before formulation into technical concentrates for finished plant protection products.

    Final product types

    • Technical grade herbicide and fungicide active ingredients (e.g., phenyl-based selective herbicides)
    • Intermediates for formulation into water-dispersible granules and emulsifiable concentrates
    • Active blends for integrated pest management in large-scale agriculture
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    Certification & Compliance
    More Introduction

    1,3-Diphenylacetone: A View From the Factory Floor

    How We Make 1,3-Diphenylacetone and Why It Matters to Chemists

    Inside our facility, everything starts from the practical needs of real scientists. Over the years, we've watched research projects chase tighter syntheses, cleaner reactions, and solid yields. 1,3-Diphenylacetone—model DPA-102, as our chemists call it on their production sheets—anchors more reaction pathways than most people realize. Its molecular backbone, drawn from true phenylacetone chemistry, gives it steady demand among academic groups and manufacturing labs. While most labs talk about acetophenone or benzyl derivatives, 1,3-Diphenylacetone often becomes the unsung workhorse for bench chemists aiming to step further into fine organics or specialty pharmaceuticals.

    Watching each batch run its course, you glimpse the reasons this molecule stands out. The symmetrical structure delivers unique reactivity for aldol and Mannich reactions, especially where a straight or branched chain won’t serve. Compound purity doesn’t just save effort down the road; it cuts both labor time and unexpected side products. Our standard lot achieves 99.5% minimum assay (GC), the endpoint most research heads crave. The color—light yellow crystals and nothing darker—isn’t just appearance. Significantly, any deviation from this color tells operators here about microcontaminants, polymerization, or over-oxidation—a lesson learned through years of keeping reactors in line and catching outliers before they move forward. This matters a lot when you’re not just moving grams, but planning to move multi-kilo projects where intermediates snowball any impurity all along the way.

    Choosing the Right Intermediate: 1,3-Diphenylacetone and Its Peers

    Chemistry outfits can draw on several aryl ketones to solve a synthetic challenge. In routine conversations with process chemists, you’ll hear phenylacetone, acetophenone, benzyl methyl ketone, and dibenzyl ketone compared swiftly. The real difference appears when a route calls for vicinal di-substitution—essentially, two phenyl groups attached at 1 and 3 positions with an acetone nucleus in between. This is exactly where our product performs.

    Unlike monofunctional ketones, 1,3-Diphenylacetone promotes strong C–C bond creation but with control over regioselectivity and electronic effect. One key difference, observable for any bench operator: the increased stability in base or acid conditions. It resists polymerization during extended heating and tolerates stronger acids than 1,5-diaryl pentane derivatives. We tune our crystallization profiles to suppress minor byproducts such as dibenzalacetone or benzyl alcohols. Over time, careful monitoring of batch records leads the team here to recognize patterns that can affect batch-to-batch consistency—insights gained only by consistently running real production-scale lines.

    Modern organic synthesis has raised the bar. Today’s medicinal chemists push for rapid molecule libraries supported by intermediates that don’t build impurities or force multiple purifications. We see 1,3-Diphenylacetone showing up again in those projects where stability, ease of isolation, and compatibility with metal catalysis all matter. Most other aryl ketones either lack the twin-point functionality or break down under the more extreme conditions common in research scale-up. These factors remain crucial for universities and process development teams that order our product to bypass dead-ends during scale-up to pilot or production runs.

    Quality Demands: From Raw Materials to Finished Product

    The production floor follows strict protocols, as any deviation undercuts not only yield but clean downstream work. Raw ingredients undergo full traceability and documentation: only high-purity benzyl derivatives and stable, certified solvents are accepted. Properties—like melting point (53–55°C), density, and chemical identity by GC-MS and IR—tell us whether a batch passes or fails. Each operator runs checks at critical control points, drawing on years of internal data and knowledge sharing. Our technical staff spends hours troubleshooting feeds, water content, and reactor parameters to keep the output within tight specification—through winter cold as much as summer heat.

    Customers—ranging from R&D divisions at major pharma to boutique fine-chemical firms—want to cut through routine issues. Product crystallinity affects filtration speed and reproducibility. Dull or off-color crystals often signal exposure to oxygen or micro-scale impurities from previous runs. We correct for this by continuous upgrades in cleaning protocols and in-house analytics. As the team meets every week, data trends trigger incremental improvements, whether it’s a new drying method or purging nitrogen lines longer before batch charging.

    There’s no hiding small problems in real-world output. Batches with even marginal moisture content above specification turn up as "sticky" product or cause lost yield in subsequent users' reactions. High-boiling point solvents occasionally drag in minor residual peaks on GC; those peaks flag for rework or complete discard, not just because of paperwork, but because long-term clients count on a reliable profile. You can’t fake these details through sales talk—operators here listen as researchers point out any glitches in trial runs.

    Focused Applications: Where 1,3-Diphenylacetone Delivers Value

    Through years of technical feedback, our clients have charted 1,3-Diphenylacetone into a few standout roles. Medicinal chemistry leverages it for new API candidates, particularly where symmetrical ketone fragments provide points for derivatization. Its use in chalcone synthesis, or as a Michael acceptor, puts it close to anti-inflammatory or anti-tumor compound development. Our records show requests spiking during research cycles focused on new CNS drugs or oncology molecules.

    For polymer chemists and material science teams, 1,3-Diphenylacetone acts as a building block in multi-step preparations. The stability through mid-stage oxidations and reductions, plus resistance to overreaction from strong base, makes it a core intermediate. A handful of customer projects focused on OLED materials tap this property for cleaner transitions between aryl and alkyl substitutions.

    Academic labs, on their end, push the product to teach advanced synthesis methods. Lab instructors choose it because the clear melting range and sturdy handling make glassware work safer and more predictable. Our test samples have found their way into hundreds of graduate projects, from small-scale organic methodology to the start of route scouting for patentable lead compounds.

    Each year, data collected from our post-sales support helps us log new synthetic pathways enabled by our product. These user stories help refine both the technical profile and our Q&A documentation, giving newer researchers a foundation built off genuine industrial practice.

    Handling and Storage: Lessons From the Shop Floor

    Anyone on the production team can share stories about careless storage creating more headaches than actual manufacturing. 1,3-Diphenylacetone prefers cool, dry conditions. Crystals stored above 25°C for weeks usually clump or lose flow; moisture seeps in and can yellow the otherwise clear crystals. Our team double-packs every shipment and spots-checks cartons before sealing. Efforts go into making sure no trace of basic material touches soft packaging, which can leach trace impurities on long export routes.

    Years in this business have taught us direct shipment in thick HDPE drums cuts contamination risk, especially for multi-kilo clients. For research-scale volumes, certified amber glass jars block UV degradation, a lesson drawn after one unfortunate shipment in clear containers years ago. Keeping full chain of custody with barcodes ensures the product hitting a user’s bench matches the batch certificate sent ahead of arrival. This may sound routine, but direct feedback loops surfaced more than one bug over the years, allowing us to patch practices before they could escalate.

    All this comes down to anticipating the hazards chemical users face—not just the published ones in generic datasheets, but the practical surprises any seasoned chemist recognizes. We keep the whole team briefed on changing shipping regulations and update handling protocols each season. Requests for alternate packaging arise every year, and our plant works jointly with clients to tune specs around their real workflow, not just our production averages.

    Product Differentiation Through Real Experiences

    While 1,3-Diphenylacetone sits among a set of complex organic intermediates, our long production history creates sharp differences. One area is the lot-to-lot consistency. In repeated engagements, longtime clients confirm that getting a new drum that performs identically to last year’s delivery saves weeks in validation steps. Many alternative suppliers can match batch size, but few produce lots that react identically in demanding NMR or chiral HPLC setups. Variability at the micro-impurity level, missed by casual suppliers, creates real risk for users scaling up beyond pilot.

    Another point is technical assistance. Our onsite chemists have spent years tweaking the synthetic process, so when client-side process teams hit a snag, our staff answers directly. Case notes documenting past troubleshooting runs serve as live references, not generic lines from a script. When regional regulatory agencies or audit teams question a shipping batch, our compliance staff responds with full access to original records—sometimes even inviting client technical teams to our site for firsthand review.

    Many of our clients learned the hard way about “invisible” variables that upend sensitive operations. For instance, a leading specialty pharma group once flagged a failed step caused by an insoluble byproduct traced back to low-level initiators in materials from another source. Our tracking and in-house reactivity tests exposed the mistake, ultimately ensuring the follow-up batch ran smoothly. That event led to tightening internal controls across all intermediates in this structural class, not just 1,3-Diphenylacetone.

    A good product isn’t just the molecule itself—it’s also the judgment, history, and expertise it’s built on. Such trust means a flat supply chain, where clients spoke directly with us, problem-solved in real time, and received shipment patterns that matched their evolving research or production calendars.

    Continuous Improvement: Keeping Pace With Modern Science

    Chemistry keeps evolving, and production never stays static. Our technical leaders embrace both new analytical tools and incremental process tweaks. Upgrades to in-line FTIR and expanded GC-MS libraries help us track process impurities previously missed by older protocols. We rolled out custom SOPs as client projects flagged new byproduct spectra last year, funneling knowledge back to both shop floor staff and customer support.

    We treat every failed synthesis or returned batch as a data point, not just a write-off. Operators compare each production cycle’s profiles and learn what feeds, temperatures, or hold times correlate with drift in assay or color. These ongoing reviews give our staff greater confidence when recommending product lots for particularly sensitive research programs. Clients who run large campaigns—multi-step, high-value projects—come back both because of the molecule’s chemical fit and because they trust our continuous vigilance in quality control.

    We encourage client involvement. Some send analytical results back after receiving samples from a new lot, allowing us to cross-verify findings. If discrepancies turn up at the atomic level—shifts in NMR, unusual IR peaks, or erratic crystallinity—our laboratory team flags the shipment, investigates, and updates both sides with findings. Through this two-way information stream, we sharpen specifications over time, sometimes going beyond initial regulatory or pharmacopoeia minimums.

    Supporting Documented Research: Building on Real-World Data

    Across major research facilities worldwide, 1,3-Diphenylacetone features in patents, process development files, and publications. We funnel updates from the literature directly into our product and process reviews, surfacing user-reported performance feedback—whether successes or challenges. Our technical library continuously incorporates these findings, refining both application notes and FAQ resources for clients entering new synthesis space.

    Regular communication with research teams uncovers trends: a rise in use for asymmetric catalysis, surging activity around aromatics functionalization, and even new eco-friendly syntheses that swap out more toxic or less stable reagents. Our staff supports these areas by piloting small-batch runs under client-recommended conditions, sharing data back to speed up their method development loops.

    Application support isn’t limited to published chemistry. We track changes in industrial demand driven by emerging policies—such as restrictions on precursor chemicals or greener processing mandates. Our supply chain adapts quickly to these trends by locking in sustainable sourcing, upgrading manufacturing to waste-minimizing cycles, and adopting transparent reporting. These moves build trust with multinational clients striving to demonstrate responsible practices in their own reporting.

    Day to day, we see the molecule's impact multiply through licensing new product lines, opening joint development with customer labs, and supporting postgraduate research groups looking for a trusted supply of high-purity reagents. The accumulation of small improvements—sometimes overlooked in boardrooms—adds up on the factory floor, where each tweak directly impacts end-users working on the next generation of medicines, materials, or chemical insights.

    Shaping the Future: Our Commitment to Quality and Service

    As a producer of 1,3-Diphenylacetone, we put deep value on long-term relationships. Our partners count on unwavering consistency—every drum, jar, and kilogram matching the past shipment, every technical query met by a team that’s run the full process over many cycles. By emphasizing traceable provenance, direct support, and clear communication, we bridge the usual gaps separating the shop floor from advanced chemistry labs.

    Over time, the company’s spirit shifted from just volume production to crafting a molecule that enables breakthroughs. Whether your work sits in pharmaceutical innovation, material advancements, academic teaching, or speciality manufacture, our approach grows out of respect for practical needs and continuous learning. Open lines with clients, disciplined production, full traceability, and well-shared expertise make the difference between commodity supply and true partnership.

    As research sciences keep pushing the envelope, we’ll stay tuned to both technical demands and the on-the-ground realities of safe, reliable, and innovative chemical supply. Every step—from factory synthesis through QC bench to your doorstep—draws upon years of craft, feedback, and the drive to see chemistry move forward in the real world.