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3-Ethyl-2,4-Pentanedione

    • Product Name 3-Ethyl-2,4-Pentanedione
    • Alias Ethylacetylacetone
    • Einecs 217-925-4
    • 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

    412145

    Name 3-Ethyl-2,4-Pentanedione
    Chemicalformula C7H12O2
    Molecularweight 128.17 g/mol
    Casnumber 539-82-2
    Appearance Colorless to pale yellow liquid
    Boilingpoint 188-190 °C
    Meltingpoint -18 °C
    Density 0.95 g/cm3 at 20 °C
    Refractiveindex 1.441 at 20 °C
    Flashpoint 74 °C (closed cup)
    Solubilityinwater Slightly soluble
    Odor Fruity

    As an accredited 3-Ethyl-2,4-Pentanedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100 mL amber glass bottle labeled "3-Ethyl-2,4-Pentanedione" with hazard symbols, tightly sealed for safe chemical storage.
    Shipping 3-Ethyl-2,4-Pentanedione is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It should be transported in accordance with local, national, and international regulations for flammable liquids, ensuring proper labeling and documentation. Protect from heat, sparks, and open flames during transit, and store in a cool, well-ventilated area upon arrival.
    Storage 3-Ethyl-2,4-pentanedione should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizing agents. Avoid direct sunlight. Ensure proper labeling and keep away from moisture. Store at room temperature and handle with appropriate personal protective equipment to prevent inhalation or skin contact.
    Application of 3-Ethyl-2,4-Pentanedione

    Applications of 3-Ethyl-2,4-Pentanedione in Industrial Manufacturing

    As a global manufacturer of 3-Ethyl-2,4-Pentanedione, we supply this diketone compound for critical roles in specific downstream industries that require high selectivity and purity. The following application scenarios reflect established industrial use where our product enables precise synthesis and controlled chemical transformation. Each sector described leverages the unique chelation, reactivity, and volatility properties necessary for advanced manufacturing.

    1. Organometallic Catalyst Preparation for Polymerization

    Industrial production of advanced polymerization catalysts relies on 3-Ethyl-2,4-Pentanedione as a complexing ligand for transition metal centers such as iron, manganese, chromium, and titanium. Downstream manufacturers use the diketone to synthesize stable, high-activity organometallic complexes for controlled polymer formation in polyethylene, polyester, and specialized copolymer resin lines. The diketone's selectivity in complexation supports consistent catalyst activity while controlling residue profiles in plastics.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management Systems
    • CFR Title 21 FDA for polymer additive trace levels
    • Chinese National Standard GB/T 24186—Industrial catalyst additives

    Typical usage ratio

    • 0.1–0.6 molar equivalents based on metal precursor, with exact ratio determined by targeted catalyst performance and downstream application requirements

    Downstream process integration

    • Introduced during the chelation step in catalyst synthesis; reacted under inert atmosphere with metal salts prior to downstream application in polymer reactors

    Final product types

    • Polyethylene and polypropylene resins
    • High-performance polyester fibers
    • Linear alpha-olefin copolymer pellets

    2. Synthesis of Metal Acetylacetonate Precursors in Electronics

    In the electronics industry, precision vapor-phase deposition and thin film manufacturing require metal acetylacetonate compounds as volatile precursors. The ethyl-substituted diketone forms complexes with metals such as copper, nickel, and zinc, delivering controlled volatility and decomposition profiles in CVD and ALD processes for semiconductors, displays, and energy storage. Consistency in ligand purity ensures high-yield deposition and minimized process contaminants.

    Industry compliance standards

    • SEMATECH Quality Initiative for precursor materials
    • IPC-6012D (Printed Boards Qualification and Performance)
    • IEC 60749-20:2018 for semiconductor reliability
    • IATF 16949:2016 for automotive electronics

    Typical usage ratio

    • 1.0–1.2 molar equivalents per metal atom in precursor synthesis; process engineers optimize according to vaporization rate and film thickness targets

    Downstream process integration

    • Reacted with hydrated metal salts in organic solvent under heating to form acetylacetonate complexes, followed by solvent removal, volatilization, and introduction to vapor-phase reactors

    Final product types

    • Transparent conductive oxide layers for displays
    • Copper and nickel metallization films for microelectronics
    • Zinc oxide coatings for photovoltaic cells

    3. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Several API manufacturers utilize 3-Ethyl-2,4-Pentanedione as an enolizable carbonyl building block in multi-step pharmaceutical synthesis, particularly for heterocyclic condensation reactions and chelation steps in metal-containing drugs. Reliable supply of GMP-compliant diketone contributes to intermediates for dihydropyrimidines, triazoles, and coordination complexes, supporting stringent impurity controls and traceability in regulated drug manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF monographs (where required for intermediates)
    • European Pharmacopoeia 10.0 general chapter 2.2.46 Residual Solvents
    • 21 CFR Part 211 for process controls

    Typical usage ratio

    • 0.15–0.5 molar equivalents as a reactant per synthesis route; chemists adjust to balance yield, reaction time, and by-product minimization

    Downstream process integration

    • Charged to the condensation stage as a key carbonyl source or chelating agent; processed in enclosed reactors with temperature and pH control prior to isolation of intermediates

    Final product types

    • Heterocyclic drug intermediates
    • Metal chelate pharmaceutical excipients
    • Key starting materials for specialty APIs

    4. Functional Dye and Pigment Manufacturing

    Colorant producers select 3-Ethyl-2,4-Pentanedione for synthesis of specific metal-complex dyes, lake pigments, and chelated colorants. The compound acts as a ligand, stabilizing dye-metal complexes and enhancing solubility, lightfastness, and color uniformity required by high-value textile, plastics, and ink manufacturers. Controlled diketone addition supports reproducibility in shade development and end-use color stability.

    Industry compliance standards

    • OEKO-TEX ECO PASSPORT (for textile dyes)
    • EN 71-3:2019 (Toys safety—migration of certain elements, for inks and coatings)
    • FDA 21 CFR 73 (Color additives for polymers and food contact materials)
    • ISO 18451-1 Pigments and extenders definitions

    Typical usage ratio

    • 0.1–0.3 parts diketone per part metal in the complexation stage; ratios fine-tuned per pigment shade and stability requirement

    Downstream process integration

    • Mixed with appropriate metal salt in solvent system under controlled temperature, forming the dye or pigment complex prior to downstream milling and dispersion

    Final product types

    • Reactive metal-complex textile dyes
    • Lake pigments for plastics coloration
    • Inks for packaging and printing applications

    5. Crosslinking Agent in Industrial Coatings and Varnishes

    Manufacturers of specialty coatings and varnishes use 3-Ethyl-2,4-Pentanedione as a crosslinking component for alkyd, acrylic, and polyurethane binder systems, especially where chelated drying catalysts or controlled film formation profiles are needed. The diketone introduces crosslinking points via enolization and coordination with metal driers, effectively influencing drying rate and final film hardness in protective and decorative applications.

    Industry compliance standards

    • ISO 12944-6:2018 (Coating systems for steel structures)
    • ASTM D1640 (Drying, Curing, Film Formation tests)
    • REACH Annex XVII (volatile organic compound restrictions)
    • Directive 2004/42/EC (EU VOC Directive)

    Typical usage ratio

    • 0.05–0.15% on total binder solids; formulations adjust for film thickness, metal drier concentration, and end-use drying profiles

    Downstream process integration

    • Blended during resin synthesis or directly into finished coating formulations; dosed prior to addition of metal driers to maximize crosslink density and uniformity

    Final product types

    • Protective industrial alkyd coatings
    • High-gloss architectural varnishes
    • Specialty metal protective clear coats
    Free Quote

    Competitive 3-Ethyl-2,4-Pentanedione prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3-Ethyl-2,4-Pentanedione: The Workhorse Ligand in Metal Complex Synthesis

    From the reactor floor to the quality control lab, we see 3-Ethyl-2,4-Pentanedione every day as an essential chelating agent that helps coordinate metal ions, especially in research and industrial settings. In our own facility, we draw this compound straight from our reactors after a multistep condensation and distillation process—a procedure that has yielded dependable purity for years. Consistency matters most to our customer base. Most users rely on clear, colorless to pale yellow liquids with a specified boiling range and a strict minimum for assay, keeping contaminants or side products from interfering with downstream applications. We routinely reach over 98% purity, minimizing residue issues for users making high-performance catalysts, stabilizers, or custom metal organics.

    A Well-Characterized Structure

    Chemists recognize 3-Ethyl-2,4-Pentanedione through its structure—an asymmetric diketone featuring an ethyl substitution at the 3-position of the pentane backbone. That small structural tweak lends a markedly different set of behaviors compared to the simpler acetylacetone. The ethyl group not only increases the ligand’s steric bulk but also improves volatility and solubility in certain organic media. In practice, this translates to better isolation and purification of many metal complexes. For makers of metal-organic frameworks, battery electrodes, and photoinitiators, these are not minor details.

    Our production line tunes every batch’s water content and acid number based on batch history, ensuring users can draw on high reproducibility run after run. Subtle batch-to-batch variation can dramatically change the performance of a catalyst or a deposition process. We sample every batch before shipment for moisture, residual solvents, and byproduct content, and log all values for reference. There’s no better insurance than controlling your own feedstocks at the level of raw synthesis.

    What Does 3-Ethyl-2,4-Pentanedione Actually Do?

    3-Ethyl-2,4-Pentanedione’s real edge appears in its chelation tendencies. Ligand field strength and bite angle combine with the added bulk, which nudges certain transition metals toward distinct coordination modes. For example, copper, nickel, zinc, and rare earth metal derivatives made with this diketone show marked improvements in both solubility and volatility versus those made from parent acetylacetone. That makes the ethyl-substituted variant attractive for vapor deposition, solution-phase thin films, and in the synthesis of magnetic and electronic materials.

    Our own clients in the metal oxide and catalysis world provide extensive feedback about processability. Process conditions often demand that the precursor exhibit a low melting point, high volatility, and precisely measured reactivity. 3-Ethyl-2,4-Pentanedione offers this ideal blend, especially when paired with early transition metals or rare earth elements where the extra steric shielding resists hydrolysis—key in ambient-pressure synthesis scenarios.

    Some Key Differences from Similar Diketones

    Not all beta-diketones behave the same way. Plant operators know from experience that a single added methyl or ethyl group can change reaction rates and product yields when switching from acetylacetone to its analogues. 3-Ethyl-2,4-Pentanedione’s ethyl group increases both boiling point and hydrophobicity. This feature reduces water pickup under typical process conditions, which directly benefits those making moisture-sensitive precursors.

    Looking back at process data, the switch to 3-Ethyl-2,4-pentanedione always signals different solubility trends for metal complexes compared to acetylacetone or 1,3-diphenylpropane-1,3-dione. Many customers adopt this molecule after direct side-by-side studies with HPLC or gravimetric analysis, reporting higher yields of metal chelate, less loss during filtration, and a cleaner distillate profile.

    Unlike symmetrical diketones, the asymmetry here further impacts ligand exchange rates. This feature proves quite valuable in kinetic studies or in flow reactors, where predictable behavior saves costly reruns and troubleshooting. It also opens more room for tailoring metal-organic properties for secondary applications like olefin polymerization or thin-film transistor production.

    Demands from Advanced Industrial Users

    Down on the floor, end users invest real money in developing runs that only work if all reactants hit specific specs. Plant operators want the color, acidity, and purity to stay well inside narrow windows to keep their metal-organic complexes consistent for every batch. We have seen even slight color changes warn of unwanted side-reactions—sometimes long before you notice an assay shift. This is why we keep visual inspection in our routine, alongside analytical chromatography and Karl Fischer titration.

    The growing market for high-purity materials by electronics firms—those crafting OLEDs, perovskite solar cells, or new dielectrics—has shifted our quality priorities. Halide and metal contamination limits are set just as carefully as in the pharmaceutical world. Some clients want less than 0.1% total residue after distillation, with sulfated ash and trace chloride at parts-per-million levels. These benchmarks are serious, and meeting them consistently only works out for companies willing to reinvest in purification and finer analytics.

    Workhorse Applications Beyond Synthesis

    In our labs, we see orders for 3-Ethyl-2,4-Pentanedione for more than just synthesis. Some use it in analytical chemistry as a target-specific derivatization agent for identifying trace metals via UV-Vis or luminescence. Lab managers concerned about low-level heavy metal detection trust the product’s batch consistency; if contaminating metal ions appear, false positives and skewed data follow.

    Many fine-chemical processors take advantage of its tunable volatility. In metal alkoxide manufacture, this diketone acts as a replacement for more volatile, odorous ligands, delivering gentler evaporation and easier recovery under vacuum. In the field, users have reported fewer odor complaints and reduced solvent losses. The ethyl group not only fine-tunes chelation, but also directly governs how quickly product loads out of a vacuum oven or deposition chamber. In coatings, it functions as a strengthener for crosslinking agents; formulators crafting specialty resins and adhesives share feedback about improved shelf-life and storage stability compared to those built on simpler ketones.

    Universities and research teams have shared published data supporting these effects, especially in newer lithium battery technologies and heterometallic catalyst systems. The last five years have brought a clear climb in requests from these fields, shaping our internal product roadmap and the rhythm of our plant schedule.

    Managing Risk: From Storage to Environmental Impact

    3-Ethyl-2,4-Pentanedione offers cost savings in process safety because its higher boiling point translates to reduced vapor flammability when transferring bulk loads. Occupational health standards still apply; operations crews respect its known central nervous system and mucous irritation effects, keeping closed systems and suction hoods operating at full efficiency. Storage under a nitrogen blanket has sharply reduced off-odors and batch darkening caused by oxygen and light. We rely on stainless steel vessels lined with compatible polymers during scale-up, resisting long-term corrosion or leakage, especially when shipping drums across regions with big temperature swings.

    Environmental compliance matters more every year. Ongoing waste audit reports detail lower organic vapor release numbers since we shifted from bulk storage of simpler, higher-volatility diketones. This change has earned specific mention in external environmental audits. In process wastewater treatment, our effluent profiles match tighter local regulation due to the molecule’s lower water solubility and reduced biological oxygen demand byproducts, as supported by published environmental fate studies.

    Outlook and Opportunities

    The future of 3-Ethyl-2,4-Pentanedione lies in customization. As more electronic and energy storage customers push for coatings, functionalized nanomaterials, and new ligand-catalyst systems, batch-by-batch customization becomes both a technical and commercial imperative. We have run pilot tests that vary starting material source and condensation temperature, resulting in batches with highly differentiated water contents, impurity levels, and isomer distributions. R&D teams constantly reach out for these specific variations—tailoring product not by generic grade, but by subtle shifts in impurity fingerprint and overall reactivity.

    We also see that synthetic chemists sometimes undervalue the knock-on effects of using subpar diketone. When a catalyst batch fails QC or an electrode coating thins out during scale-up, the investigation often traces back to off-spec ligands. Our QC department fields daily calls about trace “background” peaks in gas or liquid chromatography, and most issues resolve at the ligand purchase step. Having direct synthesis experience, our plant teams can advise labs and production floors about subtle quality questions—reactivity byproduct trends, best storage practices, and compatibility with sensitive analytical workflows.

    Technical support now means more than shipping out a batch. We collaborate on spectral assignments, impurity removal procedures, and alternate synthetic routes when clients face regulatory or supply hurdles. Intellectual property in our field sometimes hinges on switching from one diketone ligand to another. Developers in battery, OLED, and catalysis fields keep us posted about their project deadlines and property goals—predictability gets rewarded with repeat business.

    Moving Technology Forward

    This material’s path through the industry is shaped by both technical need and real-world production realities. As manufacturers, we continuously invest in new distillation equipment to tighten residue limits, fresh chromatography to track low-level byproducts, and advanced sensors to flag storage or transport problems before they reach a client site. The increasing complexity of regulatory and reuse demands—especially for products destined for electronics, energy, and pharmaceutical sectors—sets the bar high on every order.

    Looking at global supply chains and logistics, preparedness matters more each year. Plant shutdowns, shipping slowdowns, and raw material shortages appear without warning and test every producer’s ability to deliver on schedule. Rather than relying on spot markets or resellers, pulling material directly from your own line enables greater agility when customers need reliability as costs and lead times fluctuate. We put this into practice by holding safety stocks, pre-certifying raw material sources, and maintaining two or more synthetic routes where possible.

    Building Trust Through Manufacturing Know-How

    At the end of the day, direct experience in synthesis, purification, and logistics determines the true value and dependability of specialty chemicals like 3-Ethyl-2,4-Pentanedione. Real-world production, batch analytics, and user support create a trust that outlasts market fads or commodity price fluctuations. We draw lessons not just from instrument readings but from years in the reactor hall, handling unplanned shutdowns and refining processes through trial, error, and unexpected feedback. This direct engagement lets us stand behind every shipment, support technical troubleshooting, and anticipate the next wave of applications as industries keep evolving.