13716-12-6

  • Product NameTri-tert-butylphosphine
  • Molecular FormulaC12H27P
  • Molecular Weight202.32
  • Purity99%
  • AppearanceColorless to light yellow liquid
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Product Details

Quick Details

  • CasNo: 13716-12-6
  • Molecular Formula: C12H27P
  • Appearance: Colorless to light yellow liquid
  • Purity: 99%

Tri-tert-butylphosphine,TTBP 13716-12-6 In Stock, Immediately Delivery

  • Molecular Formula:C12H27P
  • Molecular Weight:202.32
  • Appearance/Colour:Colorless to light yellow liquid 
  • Vapor Pressure:0.105mmHg at 25°C 
  • Melting Point:30-35 °C(lit.) 
  • Boiling Point:229.4 °C at 760 mmHg 
  • Flash Point:94.6 °C 
  • PSA:13.59000 
  • Density:0.861 g/mL at 25 °C 
  • LogP:4.86380 

Tri-tert-butylphosphine(Cas 13716-12-6) Usage

Reaction

Useful as a ligand in a variety of palladium-catalyzed C-N, C-O and C-C bond-forming reactions under mild conditions.

Chemical Properties

Colorless to light yellow liqui

Uses

Tri-tert-butylphosphine is used primarily in the preparation of mono- and bidentate phosphine ligands in metal complexes for catalytic chiral asymmetric hydrogenations and other asymmetric reactions as well as transition metal coupling reactions. This reagent is also used in the preparation of other phosphines in catalytic polymerization reactions. Tri-tert-butylphosphine is an efficient promoter for the trifluoromethylation reactions of aldehydes, ketones, imides and imines.

InChI:InChI=1/C12H27P/c1-10(2,3)13(11(4,5)6)12(7,8)9/h1-9H3

13716-12-6 Relevant articles

Reactivity of [Pt(PtBu3)2] with Zinc(I/II) Compounds: Bimetallic Adducts, Zn-Zn Bond Cleavage, and Cooperative Reactivity

Hidalgo, Nereida,Romero-Pérez, Carlos,Maya, Celia,Fernández, Israel,Campos, Jesús

, p. 1113 - 1119 (2021)

Metal-only Lewis pairs (MOLPs) based on ...

Raney-Ni reduction of phosphine sulfides

Demchuk, Oleg M.,?wierczyńska, Wioletta,Dziuba, Kamil,Frynas, S?awomir,Flis, Anna,Pietrusiewicz, K. Micha?

, p. 64 - 68 (2017)

A variety of tertiary phosphine sulfides...

Plasma enhanced atomic layer deposition of crystallized gallium phosphide on Si with tri-Ethylgallium and tri-tert-Butylphosphine

SeongUk Yun , Cheng-Hsuan Kuo , Ping-Che Lee , Scott T. Ueda , Victor Wang , Harshil Kashyap , Aaron J. Mcleod , Zichen Zhang , Charles H. Winter , Andrew C. Kummel

Applied Surface Science Volume 619, 15 May 2023, 156727

However, a GaP ALD process has not yet been reported using TEGa and safer tri-tert-butylphosphine (tri-TBP) since the tri-TBP needs a high temperature to be reactive on Si (1 0 0), …

13716-12-6 Process route

tert-butylmagnesium chloride
677-22-5

tert-butylmagnesium chloride

phosphorus trichloride
7719-12-2,52843-90-0

phosphorus trichloride

tri-tert-butyl phosphine
13716-12-6

tri-tert-butyl phosphine

Conditions
Conditions Yield
With lithium bromide; copper(l) iodide; In diethyl ether; hexane; at -20 - 20 ℃; for 4h;
88.3%
tert-butylmagnesium chloride
677-22-5

tert-butylmagnesium chloride

tri-tert-butyl phosphine
13716-12-6

tri-tert-butyl phosphine

Conditions
Conditions Yield
With boron trifluoride-tetrahydrofuran complex; phosphorus trichloride; In tetrahydrofuran; at -10 - 0 ℃; for 3h; Reagent/catalyst; Inert atmosphere;
94.3%
With phosphorus trichloride;
 

13716-12-6 Upstream products

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