18115-70-3

Basic information

• Product Name: LITHIUM ACETYLACETONATE
• Synonyms: ACETYLACETONE LITHIUM SALT;(2,4-PENTANEDIONATO)LITHIUM;2,4-PENTANEDIONE, LITHIUM DERIVATIVE;LITHIUM 2,4-PENTANEDIONATE;LITHIUM ACETYLACETONATE;pentane-2,4-dione, monolithium salt;Lithiumacetylacetonate,98+%;2,4-Pentanedione lithium derivative, Acetylacetone lithium derivative, Li(acac)
• CAS NO: 18115-70-3
• Molecular Formula: C₅H₇LiO₂
• Molecular Weight: 106.05
• EINECS: 242-008-9
• Product Categories: Classes of Metal Compounds;Li (Lithium) Compounds;Typical Metal Compounds;metal beta-diketonate complexes
• Mol File: 18115-70-3.mol

Chemical Properties

• Melting Point: 250 °C (dec.)(lit.)
• Appearance: white/Powder
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility: Soluble in water
• Sensitive: Hygroscopic
• Stability: hygroscopic
• BRN: 4575087
• CAS DataBase Reference: LITHIUM ACETYLACETONATE(CAS DataBase Reference)
• NIST Chemistry Reference: LITHIUM ACETYLACETONATE(18115-70-3)
• EPA Substance Registry System: LITHIUM ACETYLACETONATE(18115-70-3)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38-63
• Safety Statements: 26-36/37/39
• WGK Germany: 3
• F: 3
• Hazardous Substances Data: 18115-70-3(Hazardous Substances Data)

Usage

Uses

Used in Energy Storage Industry:
LITHIUM ACETYLACETONATE is used as a precursor for the preparation of LiMn2O4 nanoparticles, which are essential components in the development of high-performance lithium-ion batteries.
Used in Electronics Industry:
LITHIUM ACETYLACETONATE is used as an efficient electron injection layer in organic light-emitting devices (OLEDs). When covered with aluminum, it enhances the performance and efficiency of these devices by facilitating better electron injection.
Used in Nanotechnology:
LITHIUM ACETYLACETONATE is used in the fabrication of electrospun graphene-embedded Li4Ti5O12 nanofibers, which are crucial for the development of advanced lithium-ion batteries with improved energy storage capabilities and longer cycle life.

InChI:InChI=1/C5H8O2.Li/c1-4(6)3-5(2)7;/h3H2,1-2H3;/q;+1

Upstream product

• 110-18-9 N,N,N,N,-tetramethylethylenediamine 
• 917-54-4 methyllithium 
• 14284-89-0 manganese(III) acetylacetonate 
• 16853-85-3 lithium aluminium tetrahydride 
• 3264-82-2 nickel(II) acetylacetonate 

Downstream Products

• 1104640-61-0 6-(1-acetyl-2-oxoprop-1-yl)-5-phenyl-1-ethyl-1,6-dihydropyrazine-2,3-dicarbonitrile 
• 1104640-62-1 6-(1-acetyl-2-oxoprop-1-yl)-5-(4-fluorophenyl)-1-ethyl-1,6-dihydropyrazine-2,3-dicarbonitrile 

Related news

Measurement and correlation of binary diffusion coefficients of LITHIUM ACETYLACETONATE (cas 18115-70-3) in supercritical carbon dioxide and in liquid ethanol07/17/2019

The infinite dilution binary diffusion coefficients D12 of lithium acetylacetonate were measured in supercritical carbon dioxide by the chromatographic impulse response (CIR) method at 308.15–333.15 K and pressures up to 36.00 MPa. The D12 values were also measured in liquid ethanol at 298.15–...detailed

Relevant articles and documents

Permethyl Manganates. Synthesis and Characterization of Divalent 2->, Trivalent 2->, and Tetravalent 2->

The potential use of alkyl manganates in organic alkylation reactions and the need for high-valent organomanganese species to model the oxidation of organic substrates by high-valent manganese porphyrins has prompted us to study a series of permethyl manganates.We report the synthesis and characterizarion of the +> salts of 2->, 2->, and 2->.

Formation of the cobalt hydrogenation catalysts at the action of lithium aluminum hydride and lithium tri(tert-butoxy)aluminohydride and their properties

The interaction of Co(acac)2(3) with LiAlH4 or LiAlH(t-BuO)3 was studied using NMR, UV, IR, ESR spectroscopy, electron microscopy, and volumometry. The basic stages of formation of cobalt catalysts for hydrogenation were suggested. The formation of the nanoparticles that are active in the hydrogenation process is shown to occur at a ratio of reagents 5 ≤ Red/Co ≤ 12. The nanoparticles are stabilized by an excess of LiAlH4 or LiAlH(t-BuO)3, as well as by the products of their catalytic decomposition under the action of cobalt in the reduced state. At the ratio LiAlH4 / Co> 12 to obtain the particles active in catalysis their activation by a proton-donor compound is required.

Formation, nature of activity, and hydrogenation catalysis by nickel bis(acetylacetonate)-lithium tetrahydroaluminate systems

A new approach to synthesis of nickel catalysts under the action of lithium tetrahydroaluminate was proposed which allows preparation of high-performance nanosized catalytic systems with well-reproducible properties. The major stages of formation and the

Hydrogenation catalysts based on palladium bisacetylacetonate and lithium tetrahydroaluminate: Formation mechanism and reasons for modified effect of water

Mechanism of formation, nature of activity, and properties of species active in hydrogenation catalysis in systems based on Pd(acac)2 and LiAlH4 were studied. The effect consisting in activation of catalytic systems was observed and