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HEXAKIS(TRIMETHYLSILOXY)DISILOXANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18602-90-9

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18602-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18602-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,0 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18602-90:
(7*1)+(6*8)+(5*6)+(4*0)+(3*2)+(2*9)+(1*0)=109
109 % 10 = 9
So 18602-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H54O7Si8/c1-26(2,3)19-32(20-27(4,5)6,21-28(7,8)9)25-33(22-29(10,11)12,23-30(13,14)15)24-31(16,17)18/h1-18H3

18602-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(trimethylsilyl) tris(trimethylsilyloxy)silyl silicate

1.2 Other means of identification

Product number -
Other names 1,1,1,7,7,7-Hexamethyl-3,3,5,5-tetrakis-trimethylsilyloxy-tetrasiloxan

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:18602-90-9 SDS

18602-90-9Downstream Products

18602-90-9Relevant academic research and scientific papers

A new selective approach to unsymmetrical siloxanes and germasiloxanes via O-metalation of silanols with 2-methylallylsilanes and 2-methylallylgermanes

Hreczycho, Grzegorz,Pawluc, Piotr,Marciniec, Bogdan

experimental part, p. 2743 - 2746 (2012/01/11)

A scandium(iii) trifluoromethanesulfonate-catalyzed O-metalation of silanols with 2-methylallylsilanes and 2-methylallylgermanes leading to siloxane or germasiloxane bond formation under mild conditions with evolution of isobutylene is described.

Preparation of Alkyl-substituted Partial Trimethylsilyl Silicates from Olivine

Kuroda, Kazuyuki,Koike, Tetsuhiro,Kato, Chuzo

, p. 1957 - 1960 (2007/10/02)

The direct trimethylsilylation reaction of olivine has yielded partial trimethylsilyl derivatives of ortho- and di-silicates whose unsilylated silanol groups have been esterified with the alcohol used as the organic solvent in the trimethylsilylating reagent.Gas chromatographic-mass spectroscopic measurements indicate the presence of the tri-, di-, and mono-alkyl-substituted trimethylsilyl derivatives of monosilicic acid in addition to the fully silylated monomeric derivative .Dimeric derivatives have also been detected which contain both the completely trimethylsilylated derivative and alcohol-esterified derivatives .The ratio of the esterified products varies with the volume of alcohol or water in the silylating reagent as well as the reaction time.

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