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Hexamethyl diorthosilicate, with the chemical formula Si2O(CH3)6, is an organosilicon compound composed of silicon, oxygen, and methyl groups. It is a volatile, oily liquid that is mildly volatile and has poor solubility in water.

4371-91-9

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4371-91-9 Usage

Uses

Used in Silicone Production:
Hexamethyl diorthosilicate is used as a precursor in the one-step production of high-quality silicone, due to its ability to penetrate deep into surfaces.
Used in Adhesives and Sealants:
Hexamethyl diorthosilicate is used as a primer on diverse substrate materials for facilitating bonding and adhesion, enhancing the performance of adhesives and sealants.
Used in Coatings:
Hexamethyl diorthosilicate is used as a component in coatings to improve their adhesion and bonding properties, providing a better finish and durability.
Used in Electronics:
Hexamethyl diorthosilicate is used in the electronics industry as a component in the manufacturing of certain types of silicone-based materials, such as encapsulants and conformal coatings, which protect electronic components from environmental factors.
Used in Construction:
Hexamethyl diorthosilicate is used in the construction industry as a component in the production of silicone-based sealants and adhesives, which are essential for sealing joints and bonding materials in various construction applications.
Safety Considerations:
Hexamethyl diorthosilicate is potentially dangerous if inhaled, swallowed, or if it comes into contact with skin, hence necessitates careful handling and adherence to safety protocols during its use and production.

Check Digit Verification of cas no

The CAS Registry Mumber 4371-91-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,7 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4371-91:
(6*4)+(5*3)+(4*7)+(3*1)+(2*9)+(1*1)=89
89 % 10 = 9
So 4371-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H18O7Si2/c1-7-14(8-2,9-3)13-15(10-4,11-5)12-6/h1-6H3

4371-91-9SDS

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 Hexamethyl diorthosilicate Hexamethyl diorthosilicate

1.2 Other means of identification

Product number -
Other names -

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:4371-91-9 SDS

4371-91-9Downstream Products

4371-91-9Relevant academic research and scientific papers

Formation of two- and three-dimensional hybrid mesostructures from branched siloxane molecules

Sakamoto, Shigeru,Shimojima, Atsushi,Miyasaka, Keiichi,Ruan, Juanfang,Terasaki, Osamu,Kuroda, Kazuyuki

, p. 9634 - 9635 (2009)

(Chemical Equation Presented) We report the design of a new precursor having three branching disiloxane units capable of forming 3D mesostructures with a cubic Pm-3n and its orthorhombic and tetragonal variants Cmmm and P4 2/mnm, in addition to a conventional 2D hexagonal (p6mm) mesostructure, thus creating a novel research area of mesostructural design in silica-organic nanohybrid materials.

Reaction of silicon with alcohols in autoclave

Krylova,Egorov,Nefedov

, p. 260 - 266 (2017/07/11)

A reaction of activated silicon with alcohols in an autoclave at 240—270 °C was studied. It was found that primary alcohols form tetraalkoxysilanes Si(OR)4 with high selectivity (up to 97%), while the secondary PriOH gave a mixture of compounds HSi(OPri)3, Si(OPri)4, HSi(OPri)2OSi(OPri)2H, HSi(OPri)2OSi(OPri)3, and Si(OPri)3OSi(OPri)3 with the predominance of trialkoxysilane (up to 67%). Carrying out the reaction under the indicated conditions has the advantage of experimental simplicity, reagent availability, high conversion of silicon, good isolated yields of products.

High-temperature reaction of SiO2 with methanol: Nucleophilic assistance of some N-unsubstituted benzazoles

Chibiryaev, Andrey M.,Kozhevnikov, Ivan V.,Martyanov, Oleg N.

, p. 159 - 167 (2013/06/26)

SiO2-containing materials (quartz, Pyrex glass, silica gel, and H-Y zeolite) react slowly with methanol at 350 C under both supercritical and gas-phase conditions. The amount of SiO2 reacted with supercritical methanol depends on the kind of the material and is varied from 0.05 wt% for quartz sand to 4.0 wt% for wide-porous silica gel for 5 h of the reaction. The main products of the reaction are methyl orthosilicates, mainly tetramethyl orthosilicate. N-Unsubstituted 1H-indole, 1H-benzimidazole, and 1H-indazole additives considerably increase the amount of reacted SiO2-containing material. Noteworthy, quartz sand solubility is increased ca 14-fold when indole is used at the same reaction conditions. These benzazoles provide a nucleophilic assistance to the reaction between SiO2 and methanol. During the assistance, the azole ring is methylated by methanol, and the participation of SiO2-surface or tetramethyl orthosilicate molecule facilitates the alkylation reaction of benzazole used.

Practical conversion of chlorosilanes into alkoxysilanes without generating HCl

Wakabayashi, Ryutaro,Sugiura, Yasushi,Shibue, Toshimichi,Kuroda, Kazuyuki

supporting information; experimental part, p. 10708 - 10711 (2011/12/05)

Alcohol-free: A versatile, efficient, and practical synthesis of alkoxysilanes without generation of HCl involves the reaction of chlorosilanes with unsymmetrical ethers in the presence of a Lewis acid (see scheme). The reaction proceeds through selective cleavage of C-O bonds and is superior to conventional processes. Industrially feasible reagents are used and only one by-product results. Copyright

Nonhydrolytic synthesis of branched alkoxysiloxane oligomers Si[OSiH(OR)2]4 (R = Me, Et)

Wakabayashi, Ryutaro,Kawahara, Kazufumi,Kuroda, Kazuyuki

scheme or table, p. 5273 - 5277 (2010/10/21)

Beyond silanol: A branched siloxane oligomer bearing terminal dialkoxysilyl groups was nonhydrolytically synthesized by direct alkoxysilylation of a tetraalkoxysilane with a chlorodialkoxysilane in the presence of the Lewis acid BiCl3 (see scheme). The reaction proceeds without the formation of intermediate silanol groups, and provides a selective route for siloxane-based oligomers. (Chemical equation presented)

Multi-functional cyclic siloxane compound, siloxane-based polymer prepared from the compound and process for preparing dielectric film by using the polymer

-

Page 15, (2010/02/10)

Disclosed herein are a multi-functional cyclic siloxane compound (A), a siloxane-based (co)polymer prepared from the compound (A), or the compound (A) and at least one of Si monomer having organic bridges(B), acyclic alkoxy silane monomer(C), and linear siloxane monomer (D); and a process for preparing a dielectric film using the polymer. The siloxane compound of the present invention is highly reactive, so the polymer prepared from the compound is excellent in mechanical properties, thermal stability and crack resistance, and has low dielectric constant resulting from compatibility with conventional pore-generating materials. Furthermore, low content of carbon and high content of SiO2 make enhance applicability to the process of semiconductor, therefore, this film is of great use as a dielectric film.

Chemistry of Silicon-Nitrogen Compounds, CLXVI: Organylamino Substitutions on Hexachlorodisiloxane

Wannagat, Ulrich,Bogedain, Gabriele,Hajibegli, Hamid,Moretto, Hans-Heinrich

, p. 865 - 874 (2007/10/02)

Reaction of hexachlorodisiloxane with primary and secondary amines leads - in dependence of stoichiometry - to numerous partially and totally organylamino substituted disiloxanes.Partially aminosubstituted chlorodisiloxanes are very sensitive to moisture and can be converted into disiloxanes with different organylamino groups.Exhaustive alkanolysis substitutes amino as well as chloro groups giving hexaalkoxydisiloxanes, but partial alkanolysis may substitute amino in preference to chloro groups.Mass spectra can be interpreted by abstraction of RR'N., RR'N+, RR'NH and (RR'N minus H) units.Most of the compounds are colourless liquids but hexakis(piperidino)-disiloxane melts at 270 deg C.

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