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1470-83-3

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1470-83-3 Usage

General Description

Lithium p-toluenesulphonate is a chemical compound that is commonly used as a lithium salt in battery electrolytes and lubricants. It is a salt of lithium and p-toluenesulfonic acid, and is known for its high thermal stability and solubility in non-aqueous solvents. It is used in lithium-ion batteries to improve the cycling performance and stability of the battery. In lubricants, it is used as an additive to enhance the anti-wear and friction-reducing properties. Additionally, lithium p-toluenesulphonate is also used as a catalyst in organic synthesis reactions. Overall, it is a versatile chemical compound with various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1470-83-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1470-83:
(6*1)+(5*4)+(4*7)+(3*0)+(2*8)+(1*3)=73
73 % 10 = 3
So 1470-83-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O3S.Li/c1-6-2-4-7(5-3-6)11(8,9)10;/h2-5H,1H3,(H,8,9,10);/q;+1/p-1

1470-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Lithium 4-methylbenzenesulfonate

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:1470-83-3 SDS

1470-83-3Upstream product

1470-83-3Relevant articles and documents

Synthesis of copolyamides based on PA 66 bearing lithium sulfonate groups and having unique thermal properties

Cammage, Geoffroy,Spitz, Roger,Boisson, Christophe,Rossin, Rene,Jeol, Stephane,Touraud, Franck

, p. 5057 - 5062 (2011)

Copolyamides of PA 66/6 lithium 5-sulfoisophthalic acid (LiSIPA) containing up to 40 mol % of LiSIPA were prepared in a 1L-pilot reactor operating at high pressures and high temperatures. Interestingly, the presence of lithium sulfonate moieties highly impacted the glass transition temperature of the polyamide. The Tg increased from 59 °C for PA 66 to 155 °C for a copolymer containing about 40 mol % of LiSIPA. 1,3- Dihexylbenzenedicarboxamide and lithium p-toluenesulfonate were synthesized as model compounds to investigate the interaction of lithium sulfonate moieties and amide functions. Infrared spectroscopy using ATR technology performed on mixture of both compounds showed that the carbonyl group of amide functions interacts with the lithium cation of lithium sulfonate moieties. Similar S-O and C-O adsorption bands were observed in copolyamides PA 66/6LiSIPA and in mixture of model compounds, which strongly suggest the formation in the copolyamides of physical cross-linking points centered on lithium cations coordinated by carbonyl groups of amide functions.

Fluorinated diazabicycloalkane derivatives

-

, (2008/06/13)

Fluorinated diazabicycloalkane derivative of the following Formula I: STR1 wherein n represents 0, 1 or 2; R represents a quaternizing organic group; each R1, R2, R3, R4 and R5 independently represents hydrogen, C1 -C6 alkyl, aryl, C1 -C6 alkyl-substituted aryl or aryl-substituted C1 -C6 alkyl and each X- independently represents a conterion or 2X- represents a single divalent counterion, are electrophilic fluorinating agents.

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