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1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione

    • Product Name 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione
    • Alias heptafluorodimethyloctanedione
    • Einecs 221-508-0
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    988129

    Chemical Name 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione
    Molecular Formula C7HF10O2
    Molar Mass 316.07 g/mol
    Cas Number 1516-16-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 120-122 °C at 14 mmHg
    Density 1.631 g/cm³ at 25 °C
    Purity Typically ≥97%
    Solubility Soluble in organic solvents, insoluble in water
    Refractive Index n20/D 1.338
    Flash Point 73 °C (closed cup)
    Stability Stable under recommended storage conditions

    As an accredited 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A sealed amber glass bottle containing 25 grams of 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione, labeled with safety and hazard information.
    Shipping ***1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione*** should be shipped in tightly sealed containers, protected from moisture and incompatible materials. Use appropriate labeling in compliance with applicable chemical transport regulations and ensure the packaging prevents leaks. Handle with gloves and eye protection; ship at ambient temperature unless otherwise specified by the supplier's safety guidelines.
    Storage 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-heptanedione should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong bases and oxidizers. Store it in a cool, dry, and well-ventilated area, away from sources of ignition. Keep the container protected from physical damage and clearly labeled. Handle using appropriate personal protective equipment.
    Application of 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione

    Applications of 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione in Industrial Manufacturing

    1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione finds established applications in a select range of advanced manufacturing segments, where its fluoroalkyl diketone structure plays a crucial role as a complexing agent, building block, or auxiliary in high-value downstream processes. We focus our supply on those industries where technical data, compliance, and usage parameters are robustly documented.

    1. Synthesis of Metal β-Diketonate Complexes for CVD/ALD Thin Film Deposition

    This fluorinated diketone supports precise chelation in the formation of metal-organic precursors, especially for Chemical Vapor Deposition (CVD) and Atomic Layer Deposition (ALD) processes in semiconductor and advanced ceramic manufacturing. The fluorinated nature of the molecule confers high volatility and thermal stability to the resulting metal complexes, which are critical for vapor phase transport and uniform thin film formation on substrates.

    Industry compliance standards

    • SEMI MS standards for wafer material purity (e.g., SEMI MS2, MS4)
    • JEITA IT-1000 for semiconductor production chemicals
    • International Technology Roadmap for Semiconductors (ITRS) guidelines
    • ISO 9001:2015 for quality management in chemical supply

    Typical usage ratio

    • Used in molar excess ranging from 1.05:1 to 1.2:1 relative to transition metal ions (precise ratio optimized for target metal complex formation and volatilization profiles)

    Downstream process integration

    • Introduced during the synthesis of metal diketone chelates, reacted in controlled solvents with metal halides, followed by vacuum distillation or sublimation to yield volatile metal complexes

    Final product types

    • Volatile metal-organic precursors (e.g., hafnium, lanthanum, or strontium β-diketonates for CVD/ALD)
    • Wafer-scale dielectric, conductive, or barrier thin films in integrated circuits

    2. Lithium Ion Battery Electrolyte Additive Manufacturing

    The compound functions as a fluorinated ligand or functional additive in the development of high-voltage-stable lithium battery electrolytes, contributing to enhanced chemical stability, flame retardancy, and improved compatibility with high-nickel cathodes. Its strong electron-withdrawing groups reduce unwanted side reactions, extending cell life and reliability in demanding applications.

    Industry compliance standards

    • IEC 62660-2 for lithium-ion traction battery safety
    • UN 38.3 transport regulations for rechargeable batteries
    • ISO 16949:2016 for automotive and E-mobility battery supply chains
    • IEC 62133 for portable battery safety

    Typical usage ratio

    • Incorporated at 0.5–2.5 wt% of total electrolyte composition; dosage tailored according to required electrochemical window, cell design, and compatibility with co-solvents

    Downstream process integration

    • Dissolved in selected carbonate or fluorinated solvent blends along with lithium hexafluorophosphate and other electrolyte additives, followed by filtration and moisture removal using molecular sieves under inert conditions

    Final product types

    • High-performance electrolyte solutions for electric vehicle (EV) and energy storage batteries
    • Lithium-ion pouch, prismatic, and cylindrical battery cells

    3. Photolithography and Microelectronics Photoresist Applications

    The diketone structure, with its multiple fluorinated substituents, provides unique attributes for photoactive formulations in advanced lithography. Its capacity to fine-tune resist solubility and boost etch resistance enables manufacturing of semiconductor features below 20 nm node sizes, particularly in extreme ultraviolet (EUV) and deep ultraviolet (DUV) lithographic processes.

    Industry compliance standards

    • IPC-6012E for rigid printed circuit board qualification
    • SEMI C92 for photolithography chemical purity
    • ISO 14644 for cleanroom management during resist processing
    • SEMI S2 for environmental, health, and safety in semiconductor fabrication

    Typical usage ratio

    • Added at 0.1–1.0 wt% in photoresist formulations, optimized according to target pattern resolution and substrate compatibility

    Downstream process integration

    • Blended with base resin and photoacid generator system, then filtered at sub-micron levels before spin-coating on silicon wafers or glass panels in photoresist production

    Final product types

    • EUV and ArF photoresists for semiconductor and flat panel display manufacturing
    • Micro-patterned glass, sensors, and MEMS components

    4. Fluorinated Ligand for Organometallic Catalysis in Fine Chemical Synthesis

    In precision catalysis and fine chemical synthesis, this diketone enables the preparation of fluorinated organometallic complexes with high thermal and chemical stability. Such complexes serve in catalysts for stereoselective or fluorine-introduction steps, widely adopted in agrochemical and pharmaceutical intermediate production for improving process kinetics and reducing side reactions.

    Industry compliance standards

    • EU Regulation (EC) No 1907/2006 (REACH) for chemical safety
    • ISO 9001:2015 for GMP fine chemical manufacturing
    • ICH Q7 GMP for active pharmaceutical ingredients
    • Responsible Care® program guidelines for safety and environmental management

    Typical usage ratio

    • Used in 1.0–2.5 equivalents relative to central metal ion in catalyst complex synthesis, determined by specific metal and desired ligand field effects

    Downstream process integration

    • Charged to reaction vessels under inert or controlled atmosphere, introduced during ligand exchange or pre-complexation steps preceding catalytic runs in batch or continuous fine chemical synthesis reactors

    Final product types

    • Fluorinated metal catalysts for pharmaceutical intermediates
    • Agrochemical actives and advanced fluorinated building blocks

    5. Functional Intermediate in Fluoropolymer and Fluoroelastomer Modifier Synthesis

    Manufacturers use the diketone as a building block or co-monomer modifier, designing performance fluoropolymers with enhanced thermal endurance, low surface energy, and tailored dielectric profiles. The diketone supplies functional fluoride content and beta-diketone reactivity for targeted copolymerization, helping tailor specialty material grades for critical electronics, wire coating, or architectural membrane markets.

    Industry compliance standards

    • ASTM D2116 for melt processible fluoropolymers
    • UL 94 flame rating for insulation polymers
    • IEC 60811 for electrical insulation and sheathing materials
    • FDA 21 CFR 177.1550 for certain fluoropolymer applications in food contact

    Typical usage ratio

    • Blended at 0.2–3.0 mol% of total monomer content, depending on desired copolymer architecture, melt properties, and target application

    Downstream process integration

    • Fed to pre-polymerization reactors alongside base monomers under controlled temperature and radical initiation conditions, then worked up via solvent removal and extrusion or granulation

    Final product types

    • Specialty fluoropolymer resins for cable, wire, and microelectronics
    • High-performance fluoroelastomer compounds for seals, gaskets, and protective films
    Free Quote

    Competitive 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

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    Certification & Compliance
    More Introduction

    1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione: Advanced Specialty Intermediate

    Decades in Fluorinated Chemistry: Why 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione Earns Attention

    Manufacturing fluorinated diketones in our facility often means the environment smells faintly sharp, and strict steps shape every batch. Among the family of diketones, 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione, known among colleagues by its short name, DFHD, commands the most focus on our lines. Over the years, chemistry teams—and industrial users—brought up the same set of reasons for choosing this molecule over other synthetics, no matter whether they work in OLED materials, specialty coatings, or catalysis.

    From raw material selection through formulation and QC, we see demand stem not from novelty but from what the structure delivers: high thermal resilience, strong volatility differences compared to perfluoropentanedione or trifluoro analogs, and an ability to act as a robust ligand in metal-organic processes. Unlike run-of-the-mill diketones, this compound’s chemistry comes alive through the unique combination of perfluorinated tails flanking the central methyl and carbonyl units.

    Structural Template: How Its Configuration Unlocks Function

    The backbone of 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione is unmistakable on any NMR chart and in day-to-day handling. Perfluoroalkyl ends bring down hydrogen count, so the molecule is resistant to degradation under the harshest synthetic conditions. Years in scale-up prove that minimal hydrogen content drops side reactions during organometallic complex formation, especially for industrial users working with sensitive metals. We’ve watched those using alternative diketones face stray reactivity and complicating impurities. In comparison, the starker fluorine profile in this compound means fewer process interruptions and simplified purification, both upstream and downstream.

    For researchers and plant chemists alike, the molecular symmetry matters. Flanked by decafluorinated segments, 2,4-heptanedione creates metal chelation that’s tighter and more predictable. Large-scale practitioners find yields hold up batch after batch—even as cycle frequency grows. We saw early adopters note improved signal clarity in NMR and FTIR spectra for metal complexes using this ligand, especially compared to the pentafluorinated cousins. Thermal instability and sublimation issues are rare in our day-to-day accounts of bulk handling, which supports broader adoption in fields where other diketones lose performance at scale.

    Performance in Metal Complexation and Deposition Processes

    As a manufacturer, practical stories from our line operators often highlight how this diketone’s fluoroalkyl configuration aids metal-organic chemical vapor deposition (MOCVD) and atomic layer deposition (ALD). Forming stable metal chelates matters for producing thin films and specialty catalysts. The traditional go-to, 2,4-pentanedione (acac), works well for basic aluminum or chromium complexes; but we hear about volatility mismatches, thermal decomposition, and residual contaminants in sensitive equipment. The experience shifts with our DFHD: these issues become background noise rather than daily concerns. Layers of metal oxides turn out smoother, purer, and exhibit fewer mid-process failures or post-treatment variances.

    Clients scaling up in electronics and thin film industries saw lower off-gassing artifacts and tighter thickness control when substituting traditional chelating agents for this highly fluorinated diketone. Transitioning pilot lines to full production, plant managers noted how the predictably high volatility and stability trimmed restart times, limited maintenance, and improved uptime. Our own batch records show that switching to DFHD ligands reduced both the need for downtime cleaning and the exchange rate on wear parts.

    Longevity in pipelines and reactors drew our attention as much as those running synthesis. Where less fluorinated diketones often fume through seals or corrode gaskets, this perfluorinated variant stays compliant longer under pressure, reducing part failure and helping users maintain safe process boundaries.

    Specifications and Purity: Quality Lessons from Direct Manufacturing

    Our teams put every batch through multi-point analysis—GC, NMR, IR, and Karl Fischer—since purity slips are hard to undo after complex formation. We consistently deliver material at >99% purity (water and acid scavenged), because every percent below that mark brings on unexpected side reactivity in downstream chemistry. Trace metal screening features in-house; over-oxidized fractions or non-fluorinated side products undermine metal-ligand stability and can poison catalysts in catalytic cycles.

    From day shifts to graveyard, everyone involved in production hears feedback from world-class labs: the absence of trace acetyl, hydrocarbon, or alcohol byproducts from our process means that metallization or photolithography lines run cleaner. Our R&D staff, working alongside quality, tailors parameters for every batch, minimizing the loss during recrystallization or distillation.

    Early on, we learned that even minor solvent residues can disrupt high-vacuum deposition equipment. Now, attention to drying and packaging procedures sets our process apart; the same batch may undergo multiple low-temperature vacuum cycles before final QA. Much of the positive reputation now enjoyed by this diketone stems from these quality priorities and not just its base chemical structure.

    Usage: From Organometallic Chemistry to High-Value Thin Films

    Seeing how DFHD's characteristics play out on the floor brings tangible evidence. One of the most direct uses involves complexing with transition metals and rare earths—key steps for making volatile, thermally stable precursors needed in the microelectronics sector. In our experience, pilot lines running oxide, fluoride, or mixed metal thin films see smoother nucleation and greater uniformity when shifting away from non-fluorinated analogs to our decafluorinated diketone.

    OLED manufacturers and display engineers regularly report cleaner device performance and longer lifetimes from adopting this structure. Enhanced stability under plasma or electron beam exposure comes from backbone rigidity and resistance to in-situ breakdown under high voltage or reactive atmospheres. Custom catalyst shops overcame parasitic reactions occurring with mixed ligand feeds by tightening to a single, highly fluorinated diketone supplier—feedback suggests yield increases and fewer post-synthesis purification steps. Our own technical support logs show the same for those in specialty agrochemical synthesis, where multi-stage derivatization benefits from lower water uptake and minimal peroxide formation.

    Solvent choices in our operation drive home these advantages. While less fluorinated diketones form parasitic adducts, this molecule’s high fluorine count nearly eliminates those issues in diazotization or Grignard-related organofluorine chemistry. Where other ligands bring volatility mismatches or trace hydrocarbon impurities, we offer a product built for cleaner reactions and fewer safety incidents on the shop floor.

    Difference From Closest Alternative Products

    Chemists and engineers using other diketones in both lab and plant settings see clear lines dividing decafluoro-2,4-heptanedione from pentafluorinated, hexafluorinated, or trifluorinated diketones. We track several main advantages highlighted in their feedback and our trials.

    As one customer described from a large batch ALD line, “Swapping from hexafluoro-2,4-pentanedione to DFHD cut our precursor waste by almost half and raised quality consistency enough that we gained another day of target operation per week.” From our side, the lower levels of post-deposition cleaning and fume hood maintenance have been obvious.

    Production Observations: Experience Shapes The Process

    Handling perfluorinated diketones over many years, we learned early that standard acetylacetone processes fall short once the hydrogen count drops. Our facility runs modified fluorination conditions, using vented reactors that stay stable under higher backpressure. In our labs, scaling from a flask to kilo-scale reactors brought out key lessons, such as the reactivity of partially fluorinated intermediates and the benefit of ultra-dry glassware to avoid side reactions.

    Every shift coordinator and lab tech finds storage a real-world concern. The product’s volatility means we cycle through cold-chain packaging and limit light exposure in drums, all to avoid byproduct formation. In the field, customers using the same tactics saw longer shelf life and less yellowing, a strong improvement over short-chain analogs with more hydrogens. We frequently field requests for stability studies in unusual solvents or with specific metal complexes—side-by-side trials show a strong advantage in catalyst stability, often attributed to the compound’s unique perfluorinated structure.

    Cleaning is another area where experience brings change. Any spill evaporates rapidly, but leaves almost no residue, which translates into less downtime for lab or production staff and fewer errors linked to cross-contamination. Proper facility airflow and high-grade PPE safeguard operators against skin or inhalation exposure, something we see repeated in technical calls with buyers as well.

    Looking Ahead: Reliability and Application Expansion

    We see fluorinated diketones moving from specialty labs into broader chemical manufacturing. The transition comes from material reliability and performance across evolving markets—whether for OLED dielectrics, next-generation sensors, or custom catalysis platforms. Several long-term partners reported moving away from traditional ligands in favor of decafluoro-2,4-heptanedione for both cost reasons (reduced waste, better yields) and for practical gains in safety and environmental risks.

    The regulatory landscape pushes for greater transparency and lower environmental impact. Our production teams have modified processes to capture and recycle outbound solvents and vapors; direct customers remark on improved safety records and tighter inventory control. Commitment to low residual contamination harmonizes product stability with operational needs. As markets evolve, user demands for optoelectronic applications, battery chemistries, and high-value polymers will likely pull this specialty diketone into further demand, not simply as a ligand, but as an enabler for new synthesis routes.

    Our own technical teams continue to test this diketone’s potential in areas like green chemistry, controlled-release electronics etching, and fluorinated surfactants. It’s not just the unique structure that matters, but the track record—across years and thousands of batches—demonstrating real process improvement. Every week brings new requests for custom blends, modified purities, or co-crystallization studies, each reflecting the shifting needs of advanced material production.

    Supporting Sustainable and Safe Manufacturing

    As the industry looks towards stricter emissions controls, our approach includes vapor phase scrubbing, drum reclamation, and routine operator health monitoring. Years of safe production provide guidance for greener, tighter process runs. We hear from partners and users that process safety isn’t an afterthought but an integral part of ongoing adoption, especially with highly fluorinated compounds like 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione.

    Mitigating risks means oil-free handling for all transfer steps, built-in containment for line breaks, and filtered reclamation on vent exhausts. Operators share in process improvement, driving protocols for drum cleaning and secondary containment that cut waste and improve production room safety metrics. The lessons here influence not only our operations, but those of the downstream users who trust our product on their most sensitive lines. Regulatory trends across global markets—tightening VOC requirements, trace impurity restrictions in electronics, and higher worker safety standards—find our product portfolio adapting and improving batch-to-batch.

    Collaboration and Open Feedback Drive Product Evolution

    Chemists, line engineers, and plant operators keep our process rooted in real-world requirements, always feeding new experience into the production workflow. Through these conversations, we identify adjustments—from quicker solvent stripping protocols to tighter container sealing practices—to bring out the best in each shipment. The push for higher purity hasn’t just pushed analytical limits but also improved long-term stability for those creating advanced catalysis, OLED materials, or cutting-edge thin films.

    Problem-solving goes both ways. Customer feedback about trace impurities led R&D to adjust our workup filtration and solvent selection. Reports of line fouling prompted modifications to in-plant cleaning schedules and drum specification upgrades. Each incident, logged and analyzed, feeds improvements into both production and user practice recommendations.

    For those thinking about switching to 1,1,1,5,5,6,6,7,7,7-Decafluoro-2,4-Heptanedione, hands-on support from seasoned production teams and field technicians can smooth the transition and extract the maximal process benefit. For any operation aiming to improve reproducibility, contamination resistance, and long-haul performance in metal-organic or high-vacuum applications, direct manufacturer experience, alongside rigorous QA, holds the key to extracting the full potential from advanced fluorinated diketones.