Product classification

85857-16-5

Product Name：1H,1H,2H,2H-Perfluorooctyltrimethoxysilane
Molecular Formula：C₁₁H₁₃F₁₃O₃Si
Purity：99%
Molecular Weight：

Inquiry

Product Details;

CasNo： 85857-16-5

Molecular Formula： C₁₁H₁₃F₁₃O₃Si

1H,1H,2H,2H-PERFLUOROOCTYLTRIMETHOXYSILANE 85857-16-5 Best Price

Molecular Formula:C₁₁H₁₃F₁₃O₃Si
Molecular Weight:468.287
Vapor Pressure:0.197mmHg at 25°C
Melting Point:<0 °C
Refractive Index:1.335
Boiling Point:217.3 °C at 760 mmHg
Flash Point:85.2 °C
PSA：27.69000
Density:1.393 g/cm³
LogP:4.99340

High Purity 1H,1H,2H,2H-PERFLUOROOCTYLTRIMETHOXYSILANE 85857-16-5 Usage

Chemical Properties

liquid

Flammability and Explosibility

Nonflammable

InChI:InChI=1/C11H13F13O3Si/c1-25-28(26-2,27-3)5-4-6(12,13)7(14,15)8(16,17)9(18,19)10(20,21)11(22,23)24/h4-5H2,1-3H3

85857-16-5 Relevant articles

Method for synthesizing flurosilicon compound by using continuous flow microreactor

-

Paragraph 0045; 0046, (2019/04/10)

The invention belongs to the technical field of a fluorine-containing material, and particularly relates to a method for synthesizing a flurosilicon compound by using a continuous flow microreactor. The synthesis method is characterized in that the continuous flow microreactor is used as a reaction device; the method comprises the following steps of (1) flowing fluoroolefin, alkoxy silane and catalysts dissolved into organic solvents into a mixed reaction module M with the preset temperature T for mixed reaction respectively through metering pumps P1, P2 and P3 via a material passage A, a material passage B and a material passage C; (2) after the mixed reaction is completed, flowing reaction liquid flows out of an outlet D; performing post treatment by flow-out reaction liquid to obtain the flurosilicon compound. The synthesis method provided by the invention has the advantages of scientificalness, reasonableness, simplicity and easy implementation. The problems of serious heat release, difficult operation control, rigorous equipment requirement, low yield, long reaction time and the like in the existing chlorsilane silicon and hydrogen addition can be solved.

PERFLUORO-ALKYL MODIFIED ORGANIC SILANE

-

Paragraph 0095; 0096, (2017/05/27)

The present invention relates to a method for preparing perfluoroalkyl modified organic silane, and the method for preparing perfluoroalkyl modified organic silane comprises a step for adding a pyrolytic radical initiator and a tin-based organic metal compound to a mixture of a perfluoroalkyl iodide compound and an organic silane having a double bond. The method for preparing perfluoroalkyl modified organic silane suppresses an additive reaction of the pyrolytic radical initiator and smoothens the reduction of iodine, thereby forming perfluoroalkylalkoxy silane at high efficiency and high purity, causes no chlorine gas, which is a toxic gas, thereby making less environmental loading, such as gas purification facilities, and does not use an expensive metal catalyst and hydrogen gas, thereby preparing perfluoroalkyl modified organic silane easily and economically.COPYRIGHT KIPO 2016

Syntheses and Reactions of Metal Organics. XVIII. Syntheses of (1H,1H,2H,2H-Polyfluoroalkyl)trimethoxysilanes and Surface Modification of Glass Plate

Yoshino, Norio,Yamamoto, Yasushi,Hamano, Katsumi,Kawase, Tokuzo

, p. 1754 - 1758 (2007/10/02)

Four silane coupling agents, (1H,1H,2H,2H-polyfluoroalkyl)trimethoxysilanes ((1H,1H,2H,2H-henicosafluorododecyl)trimethoxysilane, C10F21C2H4Si(OCH3)3, (1H,1H,2H,2H-heptadecafluorodecyl)trimethoxysilane, C58F17C2H4Si(OCH3)3, (1H,1H,2H,2H-tridecafluorooctyl)trimethoxysilane, C6F13C2H4Si(OCH3)3, and (1H,1H,2H,2H-nonafluorohexyl)trimethoxysilane, C4F9C2H4Si(OCH3)3), were prepared by the hydrosilylation of trichlorosilane with the corresponding 1H,1H,2H,-polyfluoro-1-alkene in the presence of hydrogen hexachloroplatinate-(IV), followed by reaction with sodium methoxide.The surface modification of glass plate was attempted using these products.From measurements of the contact angles θ (deg) of water and oleic acid against a modified glass plate surface, the coupling agents were found to have high modification ability.The modification produced a glass surface with high oxidation resistance.

85857-16-5 Process route

: 2487-90-3
trimethoxysilane

: 25291-17-2
3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene

: 85857-16-5
(1H,1H,2H,2H-tridecafluorooctyl)trimethoxysilane

Conditions

Conditions	Yield
With chloroplatinic acid; In isopropyl alcohol; at 25 ℃; for 0.133333h;	98.2%

: 2768-02-7
(vinyl)trimethoxylsilane

: 355-43-1
n-perfluorohexyl iodide

: 85857-16-5
(1H,1H,2H,2H-tridecafluorooctyl)trimethoxysilane