TRIOCTYLSILANE

  • Name:TRIOCTYLSILANE
  • CAS:18765-09-8
  • Purity:99%
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Factory Sells Best Quality TRIOCTYLSILANE 18765-09-8 with ISO standards

  • Molecular Formula:C24H51Si
  • Molecular Weight:368.762
  • Melting Point:< 0 °C 
  • Refractive Index:n20/D 1.454(lit.)  
  • Boiling Point:163-165 °C0.15 mm Hg(lit.)  
  • Flash Point:> 230 °F 
  • PSA:0.00000 
  • Density:0.821 g/mL at 25 °C(lit.) 
  • LogP:9.29500 

TRIOCTYLSILANE(Cas 18765-09-8) Usage

General Description

Trioctylsilane is a chemical compound with the molecular formula C24H52Si. It is a clear, colorless liquid with a faint odor and is insoluble in water. It is commonly used as a silane coupling agent in the production of various materials such as plastics, rubber, and coatings. It is also utilized as a surface modifier in the manufacturing of nanocomposites and as a protective coating for metals and ceramics. Additionally, trioctylsilane is a key ingredient in the production of semiconductor devices and is used as a lubricant and anti-corrosion agent in various industrial applications. It is important to handle trioctylsilane with care as it may cause irritation to the skin, eyes, and respiratory system upon contact or inhalation.

InChI:InChI=1/C24H51Si/c1-4-7-10-13-16-19-22-25(23-20-17-14-11-8-5-2)24-21-18-15-12-9-6-3/h4-24H2,1-3H3

18765-09-8 Relevant articles

Regioselective Hydrosilylation of Olefins Catalyzed by a Molecular Calcium Hydride Cation

Schuhknecht, Danny,Spaniol, Thomas P.,Maron, Laurent,Okuda, Jun

supporting information, p. 310 - 314 (2019/11/26)

Chemo- and regioselectivity are often di...

Olefin hydrosilylation catalyzed by cationic nickel(II) allyl complexes: A non-innocent allyl ligand-assisted mechanism

Mathew,Nakajima,Choe,Urabe,Ando,Sato,Shimada

supporting information, p. 6723 - 6726 (2016/06/01)

The arene-supported cationic nickel ally...

SATURATED AND UNSATURATED SILAHYDROCARBONS VIA IRON AND COBALT PYRIDINE DIIMINE CATALYZED OLEFIN SILYLATION

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Paragraph 0122; 0123; 0124, (2014/11/13)

The present invention relates to process...

18765-09-8 Process route

trihydrogeno(octyl)silane
871-92-1

trihydrogeno(octyl)silane

oct-1-ene
111-66-0,25068-25-1

oct-1-ene

tri-n-octylsilane
18765-09-8

tri-n-octylsilane

Conditions
Conditions Yield
With (IPr2,6-(2,6-iPr2C6H3N=CMe)2C5H3N)Fe(N2)2; at 65 ℃; for 1h;
With C28H66Ca2N8O(2+)*2C32H36B(1-)*2.5C4H8O; In tetrahydrofuran-d8; at 70 ℃; for 24h; regioselective reaction; Catalytic behavior; Inert atmosphere;
trihydrogeno(octyl)silane
871-92-1

trihydrogeno(octyl)silane

oct-1-ene
111-66-0,25068-25-1

oct-1-ene

dioctylsilane
872-24-2

dioctylsilane

tri-n-octylsilane
18765-09-8

tri-n-octylsilane

Conditions
Conditions Yield
With C19H31NiO(1+)*C32H12BF24(1-); In dichloromethane; at 25 ℃; for 24h; Inert atmosphere;
17%
9%

18765-09-8 Upstream products

  • 871-92-1
    871-92-1

    trihydrogeno(octyl)silane

  • 111-66-0
    111-66-0

    oct-1-ene

18765-09-8 Downstream products

  • 56318-67-3
    56318-67-3

    Trioctyl-pentafluorophenyloxy-silane

  • 18768-14-4
    18768-14-4

    Trioctylchlorosilane

  • 367967-63-3
    367967-63-3

    N-[(1,1-dimethylethoxy)carbonyl]-3-formyl-L-tyrosine methyl ester

  • 18765-47-4
    18765-47-4

    PhOSi(n-Oct)3