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18115-70-3

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18115-70-3 Usage

Uses

Lithium acetylacetonate [Li(acac)] is used in the preparation of LiMn2O4 nanoparticles. Li(acac) covered with aluminium was used as an efficient electron injection layer in organic light-emitting devices (OLEDs). Fabrication of electrospun graphene-embedded Li4Ti5O12 nanofibers for lithium ion batteries has been reported.

Check Digit Verification of cas no

The CAS Registry Mumber 18115-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18115-70:
(7*1)+(6*8)+(5*1)+(4*1)+(3*5)+(2*7)+(1*0)=93
93 % 10 = 3
So 18115-70-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O2.Li/c1-4(6)3-5(2)7;/h3H2,1-2H3;/q;+1

18115-70-3 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (30529)  Lithium 2,4-pentanedionate, 99.5%   

  • 18115-70-3

  • 10g

  • 175.0CNY

  • Detail
  • Alfa Aesar

  • (30529)  Lithium 2,4-pentanedionate, 99.5%   

  • 18115-70-3

  • 50g

  • 400.0CNY

  • Detail
  • Alfa Aesar

  • (30529)  Lithium 2,4-pentanedionate, 99.5%   

  • 18115-70-3

  • 250g

  • 905.0CNY

  • Detail
  • Aldrich

  • (413046)  Lithiumacetylacetonate  97%

  • 18115-70-3

  • 413046-25G

  • 428.22CNY

  • Detail

18115-70-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name LITHIUM ACETYLACETONATE

1.2 Other means of identification

Product number -
Other names Li(acac)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18115-70-3 SDS

18115-70-3Downstream Products

18115-70-3Related 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

18115-70-3Relevant articles and documents

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

Morris, Robert J.,Girolami, Gregory S.

, p. 6245 - 6246 (1988)

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

Schmidt, F. K.,Titova, Yu.,Umanets, V. A.,Khutsishvili, S. S.,Belykh, L. B.

, p. 1334 - 1341,8 (2012)

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.

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

Belykh,Titova,Rokhin,Belonogova,Shmidt

, p. 956 - 964 (2008/12/22)

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

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