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1,4-bis(trimethylsiloxy)benzene, also known as tetramethyldisiloxane, is a colorless liquid chemical compound with the molecular formula C14H22O2Si2. It possesses a fruity odor and is recognized for its relatively low toxicity and environmental impact, making it a preferred choice in various industrial applications.

90162-40-6

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90162-40-6 Usage

Uses

Used in Silicone Polymer and Resin Production:
1,4-bis(trimethylsiloxy)benzene is used as a crosslinker for enhancing the structural integrity and performance of silicone polymers and resins. Its ability to form stable crosslinks contributes to the improved mechanical properties and durability of the final products.
Used as a Solvent:
In various chemical processes, 1,4-bis(trimethylsiloxy)benzene serves as a solvent due to its ability to dissolve a wide range of substances. Its compatibility with different materials makes it a versatile component in the formulation of various products.
Used in Chemical Synthesis:
1,4-bis(trimethylsiloxy)benzene is utilized as an intermediate in the synthesis of other chemicals, particularly in the production of specialty chemicals and materials. Its role in chemical synthesis allows for the creation of a diverse array of products with specific properties and applications.
It is important to handle 1,4-bis(trimethylsiloxy)benzene with care, adhering to proper safety guidelines during storage and use to minimize any potential risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 90162-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,6 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90162-40:
(7*9)+(6*0)+(5*1)+(4*6)+(3*2)+(2*4)+(1*0)=106
106 % 10 = 6
So 90162-40-6 is a valid CAS Registry Number.

90162-40-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(trimethylsiloxy)benzene

1.2 Other means of identification

Product number -
Other names Hexa-Si-methoxy-Si,Si'-aethindiyl-bis-silan

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:90162-40-6 SDS

90162-40-6Downstream Products

90162-40-6Relevant academic research and scientific papers

Hierarchically porous monolithic silica with varying porosity using bis(trimethoxysilyl)arenes as precursors

Von Der Lehr, Martin,Ellinghaus, Rüdiger,Smarsly, Bernd M.

, p. 4455 - 4463 (2016/06/09)

The ortho-, meta- and para-isomers of bis(trimethoxysilyl)benzene and bis((trimethoxysilyl)phenyl)dimethoxysilane were synthesized from their corresponding diarylbromides. Mixtures of these bis(trimethoxysilyl)arenes and tetramethoxysilane (TMOS) were used as organosilica precursors for the preparation of macro-mesoporous silica monoliths using different amounts of the porogen poly(ethylene glycol) to investigate the effect on the porosity of the final materials. The prepared samples were characterized by nitrogen and dibromomethane sorption measurements, mercury intrusion porosimetry and scanning electron microscopy. The analysis of dibromomethane isotherms indicated a significantly lower polarity of the mesopore surface compared to that of pure SiO2 monoliths, proving the presence of arene units at the mesopore surfaces.

METHOD OF PRODUCING ORGANOSILICON COMPOUND

-

Page/Page column 5, (2011/04/24)

A simple method of producing an organosilicon compound of a formula R2n(OR4)mSi—R1—Si(OR4)mR2n is disclosed. The method comprises the following two steps, [

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