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2,2-dimethyl-3,6,9,12-tetraoxa-2-silatridecane is a compound that can be used as a redox shuttle in lithium-ion batteries (LIBs) to prevent overcharging and enhance safety and stability.

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  • 864079-62-9 Structure
  • Basic information

    1. Product Name: 2,2-dimethyl-3,6,9,12-tetraoxa-2-silatridecane
    2. Synonyms: 2,2-dimethyl-3,6,9,12-tetraoxa-2-silatridecane
    3. CAS NO:864079-62-9
    4. Molecular Formula: C10H24O4Si
    5. Molecular Weight: 236.38066
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 864079-62-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: colorless/liquid
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2-dimethyl-3,6,9,12-tetraoxa-2-silatridecane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-dimethyl-3,6,9,12-tetraoxa-2-silatridecane(864079-62-9)
    11. EPA Substance Registry System: 2,2-dimethyl-3,6,9,12-tetraoxa-2-silatridecane(864079-62-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 864079-62-9(Hazardous Substances Data)

864079-62-9 Usage

Uses

Used in Lithium-ion Batteries (LIBs):
2,2-dimethyl-3,6,9,12-tetraoxa-2-silatridecane is used as a redox shuttle for overcharge protection in LIBs. It helps to prevent thermal runaway and catastrophic failure, thereby increasing the safety and stability of the batteries.

Organosilicon Electrolytes for Lithium Ion Batteries

Silicon based electrolytes with polyethylene glycol oligomers improve thermal and electrochemical stability of lithium-ion batteries. Increases battery long-term stability. Are less flammable than conventional organic carbonate-based solvents and maintain the safe operation of batteries. Improves conductivity and kinetics of the lithium salts.

Check Digit Verification of cas no

The CAS Registry Mumber 864079-62-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,0,7 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 864079-62:
(8*8)+(7*6)+(6*4)+(5*0)+(4*7)+(3*9)+(2*6)+(1*2)=199
199 % 10 = 9
So 864079-62-9 is a valid CAS Registry Number.

864079-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(2-methoxyethoxy)ethoxy]ethoxy-trimethylsilane

1.2 Other means of identification

Product number -
Other names 3,6,9,12-Tetraoxa-2-silatridecane,2,2-dimethyl

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:864079-62-9 SDS

864079-62-9Relevant articles and documents

Process for the production of low flammability electrolyte solvents

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Page/Page column 6; 7, (2016/03/13)

The invention provides a method for producing electrolyte solvent, the method comprising reacting a glycol with a disilazane in the presence of a catalyst for a time and at a temperature to silylate the glycol, separating the catalyst from the silylated glycol, removing unreacted silazane; and purifying the silylated glycol.

Highly conductive trimethylsilyl oligo(ethylene oxide) electrolytes for energy storage applications

Zhang, Lingzhi,Zhang, Zhengcheng,Harring, Scott,Straughan, Megan,Butorac, Rachel,Chen, Zonghai,Lyons, Leslie,Amine, Khalil,West, Robert

experimental part, p. 3713 - 3717 (2010/03/01)

Monomethyl ethers of oligoethylene glycols with different chain lengths were converted to trimethylsilyl derivatives by reacting with trimethylchlorosilane in the presence of triethylamine, or by directly refluxing with excess trimethylchlorosilane or hex

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