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TRIS(TRIMETHYLSILOXY)BORON, also known as Tris(trimethylsilyl) borate, is a clear colorless liquid with unique chemical properties. It is a versatile compound that finds applications in various industries due to its distinct characteristics.

4325-85-3

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4325-85-3 Usage

Uses

Used in Organic Synthesis:
TRIS(TRIMETHYLSILOXY)BORON is used as an intermediate in organic synthesis for its ability to facilitate various chemical reactions and improve the efficiency of the synthesis process. Its unique properties make it a valuable component in the creation of complex organic molecules.
Used in Lithium Battery Electrolyte:
TRIS(TRIMETHYLSILOXY)BORON is also used as an additive in the electrolyte of lithium batteries. Its incorporation enhances the performance and stability of the batteries, making them more efficient and reliable for various applications, such as portable electronics and electric vehicles.

Check Digit Verification of cas no

The CAS Registry Mumber 4325-85-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4325-85:
(6*4)+(5*3)+(4*2)+(3*5)+(2*8)+(1*5)=83
83 % 10 = 3
So 4325-85-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H27BO3Si3/c1-14(2,3)11-10(12-15(4,5)6)13-16(7,8)9/h1-9H3

4325-85-3 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (L06277)  Tris(trimethylsilyl) borate, 98%   

  • 4325-85-3

  • 5g

  • 227.0CNY

  • Detail
  • Alfa Aesar

  • (L06277)  Tris(trimethylsilyl) borate, 98%   

  • 4325-85-3

  • 25g

  • 662.0CNY

  • Detail
  • Aldrich

  • (348635)  Tris(trimethylsilyl)borate  99%

  • 4325-85-3

  • 348635-25G

  • 647.01CNY

  • Detail
  • Aldrich

  • (348635)  Tris(trimethylsilyl)borate  99%

  • 4325-85-3

  • 348635-100G

  • 2,871.18CNY

  • Detail

4325-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Tris(trimethylsilyl) borate

1.2 Other means of identification

Product number -
Other names Tris(trimethylsilyl) Borate

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 -
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More Details:4325-85-3 SDS

4325-85-3Relevant academic research and scientific papers

Synthesis of high-purity tris(trimethylsilyl) borate

Voronkov,Basenko,Mirskov,Adamovich

, p. 1721 - 1722 (2006)

A method was developed for synthesis of high-purity tris(trimethylsilyl) borate by reaction of trimethylacetoxysilane with powdered boric acid. Nauka/Interperiodica 2006.

Catalyseurs pour la transformation de polydimethylsilanes en polycarbosilanes

Duboudin, Francoise,Birot, Marc,Babot, Odile,Dunogues, Jacques,Calas, Raymond

, p. 125 - 132 (1988)

The conversion of polydimethylsilanes into the corresponding polycarbosilanes has been studied using liquid monomeric catalysts such as B(OR)3 (R = Me, Pr, SiMe3) or the B-N bonded compounds: Me2BN(SiMe3)2 and B(NEt2)3.Using this route it is possible to obtain polycarbosilanes which are more stable than the Mark III synthesized by the Yajima route and have a smaller polydispersity.These precursors obtained at 380-400 deg C do not require the use of an autoclave.

A three (three hydrocarbyl silicon-based) borate synthesis method

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Paragraph 0048; 0049, (2019/03/28)

The invention discloses a three-(three hydrocarbyl silicon-based) borate synthesis method, to the drying of the reaction bottle adding boric acid and three hydrocarbyl silicon amine, in heating, stirring and reflux condensation conditions steams-born into the lower side of the reaction of the amine, the reaction liquid is precision filtering, rectification, to obtain high-purity of three (three hydrocarbyl silicon-based) borate. This invention adopts the boric acid and three hydrocarbyl silicon amine reaction, on the one hand the reaction by-product can be recycled, efficient use of raw materials, effectively reduce the generation of wastes, the process route is green environmental protection; on the other hand, high conversion rate of boric acid, almost complete conversion, the yield of the reaction is high, three (three hydrocarbyl silicon-based) borate of the yield is 90% or more, reaction solution three (three hydrocarbyl silicon-based) borate content is high, there is little impurity content, the crude reaction solution through the pressure reducing and rectification, the resulting three (three hydrocarbyl silicon-based) borate pure product purity of 99.9% or more, in accordance with the requirements of the lithium ion battery electrolyte additive.

Three (trimethyl silicon-based) borate synthesis method

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Paragraph 0016-0017, (2017/08/31)

The invention discloses a synthesis method of boric acid tris(trimethylsilyl)ester, wherein the synthesis method comprises the steps: mixing boric acid and hexamethyldisilazane, then adding a catalyst sulfonic acid type cation dry hydrogen resin, next heating up to 60-80 DEG C, vacuumizing in a reaction process, adsorbing ammonia gas generated in the reaction, after the reaction is finished, cooling, filtering, and thus obtaining a filtrate boric acid tris(trimethylsilyl)ester crude product and a filter residue; and then carrying out reduced pressure rectification on the filtrate, and collecting a fraction to obtain the high-purity boric acid tris(trimethylsilyl)ester. The synthesis method simplifies the technological process of synthesis and rectification operations, the catalyst can be reused, the product yield reaches more than 85%, and the production cost is reduced.

Preparation of phenylalkyl ethers and phenyl esters from benzenediazonium tetrafluoroborate with alkoxytrimethylsilanes and trimethylsilyl esters

Olah,Wu

, p. 204 - 206 (2007/10/02)

Sonication assisted reaction of benzenediazonium tetrafluoroborate with alkoxytrimethylsilanes and trimethylsilyl esters gives phenylalkyl ethers and phenyl esters, respectively, with trialkyl(aryl) borates as byproducts. The scope of the reaction, experimental conditions and proposed mechanism are discussed.

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