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Methanesulfonic acid, lithium salt, also known as lithium methanesulfonate, is a chemical compound with the formula LiCH3SO3. It is a white crystalline solid that is soluble in water and is commonly used as a catalyst, reagent, and electrolyte in various chemical processes. This lithium salt is derived from methanesulfonic acid, a strong acid that is widely used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. The lithium salt form is particularly useful in applications where a non-toxic and non-flammable substance is required, such as in lithium-ion batteries, where it can serve as a component of the electrolyte solution. Its properties, including high thermal stability and good electrochemical performance, make it a valuable compound in the field of energy storage and chemical synthesis.

2550-62-1

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2550-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2550-62-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2550-62:
(6*2)+(5*5)+(4*5)+(3*0)+(2*6)+(1*2)=71
71 % 10 = 1
So 2550-62-1 is a valid CAS Registry Number.

2550-62-1SDS

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 methanesulfonic acid , lithium methanesulfonate

1.2 Other means of identification

Product number -
Other names lithium mesylate

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:2550-62-1 SDS

2550-62-1Downstream Products

2550-62-1Relevant academic research and scientific papers

Mechanism and Anion Activation in Solid-Liquid Phase-transfer Reactions Catalysed by Cyclophosphazenic Polypodands. Comparison with Cyclic Analogue Crown Ethers

Landini, Dario,Maia, Angelamaria,Podda, Gianni,Secci, Daniela,Yan, Yong Ming

, p. 1721 - 1724 (2007/10/02)

A kinetic study of the nucleophilic substitution of the methanesulfonic group by anions (Cl-, Br-, I-, SCN-, C6H5O-, C6H5CH2COO-) catalysed by cyclophosphazenic polypodands has been performed under solid-liquid phase-transfer conditions.The results obtained show that the mechanism of PTC previously found for cyclic ligands (crown ethers, cryptands) also operates in the case of these open-chain ligands: the attack by the anionic nucleophile on the substrate occurs in the organic phase and is rate determining of the overall process.The nucleophilicity scales found (I- > C6H5O- ca.SCN- > C6H5CH2COO-; I- > Br- > Cl-) as well as the anion activation are comparable with those found for cyclic crown ethers.This indicates that the anionic reactive species involved are similar in the complexes of both ligands.

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