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4419-47-0

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4419-47-0 Usage

Description

Tetrakis (diethylamino) titanium is useful Ti-source precusor. Tetrakis (diethylamino) titanium is useful in TiN film deposition using the atomic layer deposition method1,2. It is also a useful compound during the process of etching a layer of diamond like carbon.

Reference

Kim, Ju Youn, et al. "Comparison of TiN Films Deposited Using Tetrakisdimethylaminotitanium and Tetrakisdiethylaminotitanium by the Atomic Layer Deposition Method." Japanese Journal of Applied Physics 42.7A (2003):4245-4248. Katamreddy, Rajesh, et al. "Ti source precursors for atomic layer deposition of TiO2, STO and BST." Ecs Transactions 16.4(2008):660-71. Shoemaker, Erika Leigh, et al. "Process for reactive ion etching a layer of diamond like carbon." US, US8409458. 2013.

Chemical Properties

Clear dark red liquid

Uses

Precursors Packaged for Depositions Systems

General Description

Atomic number of base material: 22 Titanium

Purification Methods

Dissolve it in *C6H6, filter if a solid separates, evaporate under reduced pressure and distil it. It is an orange liquid which reacts violently with alcohols. [Bradley et al. J Chem Soc 3857 1960, Beilstein 4 IV 313.]

Check Digit Verification of cas no

The CAS Registry Mumber 4419-47-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4419-47:
(6*4)+(5*4)+(4*1)+(3*9)+(2*4)+(1*7)=90
90 % 10 = 0
So 4419-47-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H11N.Ti/c1-3-5-4-2;/h5H,3-4H2,1-2H3;/q;+4

4419-47-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (40469)  Tetrakis(diethylamino)titanium(IV), 99.99% (metals basis)   

  • 4419-47-0

  • 2g

  • 309.0CNY

  • Detail
  • Alfa Aesar

  • (40469)  Tetrakis(diethylamino)titanium(IV), 99.99% (metals basis)   

  • 4419-47-0

  • 10g

  • 1241.0CNY

  • Detail
  • Alfa Aesar

  • (40469)  Tetrakis(diethylamino)titanium(IV), 99.99% (metals basis)   

  • 4419-47-0

  • 50g

  • 4936.0CNY

  • Detail
  • Aldrich

  • (469866)  Tetrakis(diethylamido)titanium(IV)  99.999% trace metals basis

  • 4419-47-0

  • 469866-5G

  • 1,519.83CNY

  • Detail
  • Aldrich

  • (469866)  Tetrakis(diethylamido)titanium(IV)  99.999% trace metals basis

  • 4419-47-0

  • 469866-25G

  • 6,037.20CNY

  • Detail
  • Aldrich

  • (407399)  Tetrakis(diethylamido)titanium(IV)  technical grade

  • 4419-47-0

  • 407399-5G

  • 1,891.89CNY

  • Detail
  • Aldrich

  • (725536)  Tetrakis(diethylamido)titanium(IV)  packaged for use in deposition systems

  • 4419-47-0

  • 725536-10G

  • 16,684.20CNY

  • Detail

4419-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetrakis(diethylamino)titanium

1.2 Other means of identification

Product number -
Other names diethylazanide,titanium(4+)

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:4419-47-0 SDS

4419-47-0Relevant articles and documents

Synthesis, characterization and catalytic activity of the complex titanium bis(dimethylmalonate)-bis(diethylamido) in the polymerization of propylene

Gueta-Neyroud, Tal,Tumanskii, Boris,Botoshansky, Mark,Eisen, Moris S.

, p. 927 - 939 (2007)

In this account we present the synthesis, characterization and catalytic activity in the polymerization of propylene of a bis(dimethyl malonate) titanium bis(diethylamine) complex (1). The complex exhibits in solution a dynamical isomerization following an internal Bailar twist. The activation of complex 1 was obtained by its reaction with methylalumoxane (MAO). The activated complex in solution shows a different dynamic process involving an equilibrium between a monodentate η1 and bidentate η2 binding of the dimethylmalonate ligand to the metal center. This equilibrium is responsible for the formation of, at least, two active species for the polymerization reaction bearing major symmetry differences. The monodentate coordination (opened form) of the ligand was found to be the major form of the active species of the complex when activated with MAO, most probably due to a strong interaction of the oxygen atoms in the ligand with the strong Lewis acid co-catalyst. The active species in the polymerization were studied by NMR and ESR spectroscopies. The resulting polypropylene showed elastomeric properties with low tacticites.

PROCESSES FOR PRODUCING TRANSITION METAL AMIDO AND IMIDO COMPOUNDS

-

Page/Page column 7-8, (2009/10/21)

Processes are provided for producing transition metal amidos and/or imidos. In methods according to this invention, at least one halogenated transition metal, an amine compound and a solvent are combined, followed by the addition of an alkylated metal or a Grignard reagent to produce the transition metal amide and/or imido.

Dihydrocarbylamino metal compounds

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Page/Page column 8-12, (2008/06/13)

This invention provides a process of preparing dihydrocarbylamido metal compounds. This process comprises bringing together, in a liquid reaction medium, at least one metal halide, MX4, where M is titanium, zirconium, or hafnium, and X is a halogen atom, with at least one dihydrocarbylamine, such that a mixture of (i) halometal amides in which the atom ratio of halogen to metal is greater than about 0.1 and less than about 2, and (ii) dihydrocarbylamine hydrohalide is produced. Then (i) and (ii) are separated from each other, and (i) is brought together with an alkali metal amide, ANR2, where A is an alkali metal, and R is a hydrocarbyl group, in a liquid medium, to produce a product comprised of substantially halogen-free dihydrocarbylamido metal compound. This invention further provides for purifying dihydrocarbylamido metal compounds by contact with a nitrile.

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