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Diphosphoric acid tetrakis(trimethylsilyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18395-45-4

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18395-45-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18395-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,9 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18395-45:
(7*1)+(6*8)+(5*3)+(4*9)+(3*5)+(2*4)+(1*5)=134
134 % 10 = 4
So 18395-45-4 is a valid CAS Registry Number.

18395-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetrakis(trimethylsilyl) pyrophosphate

1.2 Other means of identification

Product number -
Other names tetrakis(trimethylsilyl) diphosphate

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:18395-45-4 SDS

18395-45-4Relevant academic research and scientific papers

Novel synthesis of nucleoside 5′-phosphoramidates through reaction of nucleoside triphosphates with amines mediated by trimethylsilyl chloride

Zhu, Jigang,Han, Bo,Fu, Hua,Jiang, Yuyang,Zhao, Yufen

, p. 6676 - 6679 (2005)

Reaction of nucleoside triphosphates (NTPs) with amines in pyridine mediated by trimethylsilyl chloride produced nucleoside 5′- phosphoramidates in moderate yields without any preprotection of nucleosides and amino acid methyl esters. The reaction pathway is very similar to the mechanism of the RNA capping reaction, DNA or RNA ligation reaction, and catalysis of hydrolases and nucleases involving the formation of covalent enzyme-NMP (nucleoside 5′-monophosphate) intermediates in biological systems, which could provide a valuable clue for the enzymatic reactions.

Lifetime limit of tris(trimethylsilyl) phosphite as electrolyte additive for high voltage lithium ion batteries

Qi, Xin,Tao, Liang,Hahn, Hendrik,Schultz, Carola,Gallus, Dennis Roman,Cao, Xia,Nowak, Sascha,R?ser, Stephan,Li, Jie,Cekic-Laskovic, Isidora,Rad, Babak Rezaei,Winter, Martin

, p. 38342 - 38349 (2016/05/19)

The tris(trimethylsilyl) phosphite (TMSPi) is considered as an ideal electrolyte additive for lithium ion batteries. In this work, its positive effect as well as its failure mechanism in a LiPF6 containing electrolyte was studied by means of selected electrochemical, structural and analytical techniques. The LiNi0.5Co0.2Mn0.3O2/graphite cells with TMSPi as electrolyte additive were cycled between 2.8 and 4.6 V. Thanks to the compact cathode electrolyte interphase formed by the oxidative decomposition of TMSPi in a freshly prepared TMSPi containing electrolyte, both the discharge capacity and the cycling stability of cells were enhanced. However, our results also show that TMSPi actually reacts with LiPF6 at room temperature. TMSPi is consumed by this spontaneous reaction after aging for certain time. In addition, a part of the fluorophosphates, generated from the hydrolysis of LiPF6, is bonded to one or two TMS groups, causing a decrease in the fluorophosphate content in the CEI film. Consequently, the cycling stability of the lithium ion cells with aged TMSPi containing electrolyte deteriorates. The obtained results offer important insights into the practical application of TMSPi, which means that TMSPi can only be used as an effective additive in a freshly prepared LiPF6 containing electrolyte.

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