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ACETYLACETONATES INFORMATION CENTER
AE Acetylacetonates ™

32.4 (A)/00.022


Hydrogen                                 Helium  
Lithium Beryllium                     Boron Carbon Nitrogen Oxygen Fluorine Neon
Sodium Magnesium                     Aluminum Silicon Phosphorus Sulfur Chlorine Argon
Potassium Calcium Scandium Titanium Vanadium Chromium Manganese Iron Cobalt Nickel Copper Zinc Gallium Germanium Arsenic Selenium Bromine Krypton
Rubidium Strontium Yttrium Zirconium Niobium Molybdenum Technetium Ruthenium Rhodium Palladium Silver Cadmium Indium Tin Antimony Tellurium Iodine Xenon
Cesium Barium Lanthanum Hafnium Tantalum Tungsten Rhenium Osmium Iridium Platinum Gold Mercury Thallium Lead Bismuth Polonium Astatine Radon
Francium Radium Actinium Rutherfordium Dubnium Seaborgium Bohrium Hassium Meitnerium Darmstadtium Roentgenium Copernicium Ununtrium Ununquadium Ununpentium Ununhexium Ununseptium Ununoctium
                                   
    Cerium Praseodymium Neodymium Promethium Samarium Europium Gadolinium Terbium Dysprosium Holmium Erbium Thulium Ytterbium Lutetium    
    Thorium Protactinium Uranium Neptunium Plutonium Americium Curium Berkelium Californium Einsteinium Fermium Mendelevium Nobelium Lawerencium      


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Acetylaceton Formula Diagram (C5H8O2)

Acetylacetonate is an organic compound formally named pentane-2, 4-dione. Acetylacetonate is a building block for the synthesis of heterocyclic compounds and is a precursor to acetylacetonate (acac).

Purities include 99%, 99.9%, 99.99%, 99.999% and 99.9999% which are sometimes referred to as 2N, 3N, 4N, 5N and 6N.

Physical properties may include nanopowder, nano particle, submicron, - 325 mesh, rod, foil, and high surface area carbonate with particle distribution and particle size controlled and certified. We produce larger - 40 mesh, - 100 mesh, -200 mesh range sizes and < 0.5 mm, 2 mm, 5 mm and other mm size shot, granules, lump, flake and pieces, too.

American Elements maintains industrial scale production for all its acetylacetonate products.

American Elements will execute Non-Disclosure or Confidentiality Agreements to protect customer know-how.

Please select from the table an Acetylacetonate Material


Aluminum Acetylacetonate
Barium Acetylacetonate
Beryllium Acetylacetonate
Cadmium Acetylacetonate
Calcium Acetylacetonate
Cerium Acetylacetonate
Chromium Acetylacetonate
Cobalt Acetylacetonate
Copper Acetylacetonate
Dibutyltin bis(acetylacetonate)
Dysprosium Acetylacetonate
Erbium Acetylacetonate
Europium Acetylacetonate
Gadolinium Acetylacetonate
Gallium Acetylacetonate
Diisopropoxytitanium bis
 (acetylacetonate) Solution

Dimethyl Gold Acetylacetonate
Hafnium Acetylacetonate
Holmium Acetylacetonate
Indium Acetylacetonate
Indium(III) Acetylacetonate
Iridium Acetylacetonate
Iron Acetylacetonate
Lanthanum Acetylacetonate
Lead Acetylacetonate
Lithium Acetylacetonate
Lutetium Acetylacetonate
Magnesium Acetylacetonate
Manganese Acetylacetonate
Manganese(III) Acetylacetonate
Neodymium Acetylacetonate
Nickel Acetylacetonate
Palladium Acetylacetonate
Platinum Acetylacetonate
Potassium Acetylacetonate Hemihydrate
Praseodymium Acetylacetonate
Rhenium Acetylacetonate
Rhodium Acetylacetonate
Ruthenium Acetylacetonate
Samarium Acetylacetonate
Scandium Acetylacetonate
Silver Acetylacetonate
Sodium Acetylacetonate
Strontium Acetylacetonate
Terbium Acetylacetonate
Thallium Acetylacetonate
Thorium Acetylacetonate
Thulium Acetylacetonate
Tin Acetylacetonate
Titanium(IV) Oxide Acetylacetonate
Vanadium Acetylacetonate
Vanadyl Acetylacetonate
Ytterbium Acetylacetonate
Yttrium Acetylacetonate
Zinc Acetylacetonate
Zirconium Acetylacetonate

French Acétylacétonate German Acetylacetonat Italian Acetilacetonato Portuguese Acetilacetonato Spanish Acetylacetonate 乙酰丙酮 アセチルアセトネート Swedish Acetylacetonate



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Recent Research & Development for Acetylacetonates

  • Unfairly forgotten member of the iodocarborane family: synthesis and structural characterization of 8-iodo-1,2-dicarba-closo-dodecaborane, its precursors, and derivatives. Safronov AV, Sevryugina YV, Jalisatgi SS, Kennedy RD, Barnes CL, Hawthorne MF. Inorg Chem. 2012 Feb 20;51(4):2629-37. Epub 2012 Feb 1. PMID: 22296243 [PubMed - in process]

  • A thermolysis approach to simultaneously achieve crystal phase- and shape-control of ternary M-Fe-O metal oxide nanoparticles. Huang CC, Chang CN, Yeh CS. Nanoscale. 2011 Oct 5;3(10):4254-60. Epub 2011 Aug 31. PMID: 21879122 [PubMed - indexed for MEDLINE]

  • Chemical fluid deposition of monometallic and bimetallic nanoparticles on ordered mesoporous silica as hydrogenation catalysts. Yen CH, Lin HW, Phan TD, Tan CS. J Nanosci Nanotechnol. 2011 Mar;11(3):2465-9. PMID: 21449408 [PubMed - indexed for MEDLINE]

  • Hydrolytic synthesis and structural characterization of lanthanide-acetylacetonato/hydroxo cluster complexes--a systematic study. Wu Y, Morton S, Kong X, Nichol GS, Zheng Z. Dalton Trans. 2011 Feb 7;40(5):1041-6. Epub 2010 Dec 14. PMID: 21152668 [PubMed]

  • Notes on the photo-induced characteristics of transition metal-doped and undoped titanium dioxide thin films. Kment S, Kmentova H, Kluson P, Krysa J, Hubicka Z, Cirkva V, Gregora I, Solcova O, Jastrabik L. J Colloid Interface Sci. 2010 Aug 1;348(1):198-205. Epub 2010 Apr 8. PMID: 20466384 [PubMed]

  • Clewlike ZnV2O4 hollow spheres: nonaqueous sol-gel synthesis, formation mechanism, and lithium storage properties. Xiao L, Zhao Y, Yin J, Zhang L. Chemistry. 2009 Sep 21;15(37):9442-50. PMID: 19672904 [PubMed - indexed for MEDLINE]

  • Nickelacyclic-cobaltocene vs. nickelacyclic-nickelocene. Synthesis, X-ray structures, electron transfer activity, EPR spectroscopy, and theoretical calculations. Buchalski P, Kaminska E, Piwowar K, Suwinska K, Jerzykiewicz L, Rossi F, Laschi F, de Biani FF, Zanello P. Inorg Chem. 2009 Jun 1;48(11):4934-41. PMID: 19405491 [PubMed]

  • Organometallic red-emitting chromophores: a computational and experimental study on cyclometallated Nile Red complexes of palladium(II) and platinum(II) acetylacetonates and hexafluoroacetylacetonates. Pugliese T, Godbert N, Aiello I, La Deda M, Ghedini M, Amati M, Belviso S, Lelj F. Dalton Trans. 2008 Dec 14;(46):6563-72. Epub 2008 Oct 10. PMID: 19030618 [PubMed - indexed for MEDLINE]

  • Well-defined N-heterocyclic carbenes-palladium(II) precatalysts for cross-coupling reactions. Marion N, Nolan SP. Acc Chem Res. 2008 Nov 18;41(11):1440-9. PMID: 18774825 [PubMed]

  • Colloidal chemical synthesis and formation kinetics of uniformly sized nanocrystals of metals, oxides, and chalcogenides. Kwon SG, Hyeon T. Acc Chem Res. 2008 Dec;41(12):1696-709. PMID: 18681462 [PubMed]

  • Generalized nonaqueous sol-gel synthesis of different transition-metal niobate nanocrystals and analysis of the growth mechanism. Zhang L, Garnweitner G, Djerdj I, Antonietti M, Niederberger M. Chem Asian J. 2008 Apr 7;3(4):746-52. PMID: 18335422 [PubMed - indexed for MEDLINE]

  • One-minute synthesis of crystalline binary and ternary metal oxide nanoparticles. Bilecka I, Djerdj I, Niederberger M. Chem Commun (Camb). 2008 Feb 21;(7):886-8. Epub 2007 Dec 19. PMID: 18253537 [PubMed - indexed for MEDLINE]

  • EPR study on ligand-exchange reaction between bis(diethyldiselenocarbamato)copper(II) and some bis(acetylacetonato)copper(II) complexes. Dimitrova A, Taseva C, Yordanov ND. Spectrochim Acta A Mol Biomol Spectrosc. 2008 Oct;70(5):953-7. Epub 2007 Oct 2. PMID: 17988937 [PubMed - indexed for MEDLINE]

  • Metal acetylacetonate domains grown on H-terminated porous silicon at room temperature and their specific I-V behavior. Chao J, Wang HT, Xia B, Liu HB, Xiao ZD, Xiao SJ. J Phys Chem B. 2006 Dec 7;110(48):24565-70. PMID: 17134216 [PubMed]

  • Organic reaction pathways in the nonaqueous synthesis of metal oxide nanoparticles. Niederberger M, Garnweitner G. Chemistry. 2006 Sep 25;12(28):7282-302. PMID: 16927442 [PubMed]

  • Chemisorption and thermodynamic data of the interaction between a chelate free acidic center with basic groups attached to grafted silicas. Arakaki LN, de Sousa AN, Espínola JG, Oliveira SF, Airoldi C. J Colloid Interface Sci. 2002 May 15;249(2):290-4. PMID: 16290599 [PubMed]

  • FT-IR studies of acetylacetonates in supercritical CO2 using a capillary cell at pressures up to 3.1 kbar. Henry MC, Yonker CR. Anal Chem. 2004 Aug 15;76(16):4684-9. PMID: 15307777 [PubMed]

  • The way into the bridge: a new bonding mode of tertiary phosphanes, arsanes, and stibanes. Werner H. Angew Chem Int Ed Engl. 2004 Feb 13;43(8):938-54. PMID: 14966876 [PubMed]

  • Calculated and experimental geometries and infrared spectra of metal tris-acetylacetonates: vibrational spectroscopy as a probe of molecular structure for ionic complexes. Part II. Diaz-Acosta I, Baker J, Hinton JF, Pulay P. Spectrochim Acta A Mol Biomol Spectrosc. 2003 Jan 15;59(2):363-77. PMID: 12685911 [PubMed - indexed for MEDLINE]

  • Detection of inorganic species by chemical reaction laser desorption ionization mass spectrometry. Matsumoto K, Ajiro H, Habaue S, Okamoto Y. Rapid Commun Mass Spectrom. 2003;17(7):678-84. PMID: 12661020 [PubMed]

 




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