(2N) 99%  •  (3N) 99.9%  •  (4N) 99.99%  •  (5N) 99.999%  •  (6N) 99.9999%

ACETYLACETONATE INFORMATION CENTER

AE Acetylacetonates™

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Acétylacétonate Acetylacetonat Acetilacetonato Acetilacetonate Acetilacetonato 乙酰丙酮 アセチルアセトネート Acetylacetonat

32.4 (A)/00.012


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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.

AE Acetylacetonates™ products include:


 
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Production Catalog Available in 36 Countries and Languages

Recent Research & Development for Acetylacetonates

  • Elizaveta P. Shestakova, Yuri S. Varshavsky, Victor N. Khrustalev, Galina L. Starova, Sergei N. Smirnov, Rhodium(III) cationic methyl complexes containing dimethylformamide ligand, cis-[Rh(β-diket)(PPh3)2(CH3)(DMF)][BPh4] (β-diket = acetylacetonate or benzoylacetonate), in comparison with their acetonitrile analogs, Journal of Organometallic Chemistry, Available online 7 October 2014
  • Debraj Dhar Purkayastha, Bedabrat Sarma, Chira R. Bhattacharjee, Surfactant controlled low-temperature thermal decomposition route to zinc oxide nanorods from zinc(II) acetylacetonate monohydrate, Journal of Luminescence, Volume 154, October 2014
  • L. Castañeda, A. Maldonado, J. Vega Pérez, M. de la L. Olvera, C. Torres-Torres, Electrical and optical properties of nanostructured indium doped zinc oxide thin films deposited by ultrasonic chemical spray technique, starting from zinc acetylacetonate and indium chloride, Materials Science in Semiconductor Processing, Volume 26, October 2014
  • Mei Ling Chua, Youchang Xiao, Tai-Shung Chung, Using iron (III) acetylacetonate as both a cross-linker and micropore former to develop polyimide membranes with enhanced gas separation performance, Separation and Purification Technology, Volume 133, 8 September 2014
  • Željka Petrović, Mira Ristić, Svetozar Musić, Development of ZnO microstructures produced by rapid hydrolysis of zinc acetylacetonate, Ceramics International, Volume 40, Issue 7, Part B, August 2014
  • Fengzhu Lv, Liling Fu, Emmanuel P. Giannelis, Genggeng Qi, Preparation of γ-Fe2O3/SiO2-capsule composites capable of using as drug delivery and magnetic targeting system from hydrophobic iron acetylacetonate and hydrophilic SiO2-capsule, Solid State Sciences, Volume 34, August 2014
  • Qiuli Yang, Xin Tan, Sujuan Wang, Jianyong Zhang, Liuping Chen, Jie-Peng Zhang, Cheng-Yong Su, Porous organic–inorganic hybrid aerogels based on bridging acetylacetonate, Microporous and Mesoporous Materials, Volume 187, 15 March 2014
  • M. Srinidhi Raghavan, Piyush Jaiswal, Nalini G. Sundaram, S.A. Shivashankar, A composition-dependent “re-entrant” crystallographic phase transition in the substitutional metal acetylacetonate complex (Cr1−xGax)(acac)3, Polyhedron, Volume 70, 9 March 2014
  • Sandra A. De Pascali, Antonella Muscella, Carla Vetrugno, Santo Marsigliante, Francesco Paolo Fanizzi, Synthesis, characterization and cytotoxicity of novel Pt(II) κ2O,O′-acetylacetonate complexes with nitrogen ligands, Inorganica Chimica Acta, Volume 412, 1 March 2014
  • Dmitry S. Suslov, Mikhail V. Bykov, Marina V. Belova, Pavel A. Abramov, Vitaly S. Tkach, Palladium(II)–acetylacetonate complexes containing phosphine and diphosphine ligands and their catalytic activities in telomerization of 1,3-dienes with diethylamine, Journal of Organometallic Chemistry, Volume 752, 15 February 2014