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2386-56-3

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2386-56-3 Usage

Uses

Potassium Methanesulfonate is used in preparation method of Fatty Acyl glycinate surfactant.

Check Digit Verification of cas no

The CAS Registry Mumber 2386-56-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2386-56:
(6*2)+(5*3)+(4*8)+(3*6)+(2*5)+(1*6)=93
93 % 10 = 3
So 2386-56-3 is a valid CAS Registry Number.
InChI:InChI=1/CH4O3S.K/c1-5(2,3)4;/h1H3,(H,2,3,4);/q;+1/p-1

2386-56-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (39505)  Potassium methanesulfonate, 99%   

  • 2386-56-3

  • 25g

  • 453.0CNY

  • Detail
  • Alfa Aesar

  • (39505)  Potassium methanesulfonate, 99%   

  • 2386-56-3

  • 100g

  • 1380.0CNY

  • Detail
  • Alfa Aesar

  • (39505)  Potassium methanesulfonate, 99%   

  • 2386-56-3

  • 500g

  • 5641.0CNY

  • Detail
  • Aldrich

  • (83000)  Potassiummethanesulfonate  ≥98.0% (dry substance, T)

  • 2386-56-3

  • 83000-5G-F

  • 606.06CNY

  • Detail
  • Aldrich

  • (83000)  Potassiummethanesulfonate  ≥98.0% (dry substance, T)

  • 2386-56-3

  • 83000-25G-F

  • 2,297.88CNY

  • Detail

2386-56-3SDS

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 potassium,methanesulfonate

1.2 Other means of identification

Product number -
Other names Methanesulfonic Acid Potassium Salt

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:2386-56-3 SDS

2386-56-3Relevant articles and documents

Removal of alkyl alkanesulfonate esters from alkanesulfonic acids and other organic media

-

Page/Page column 6, (2008/06/13)

Methods of removing alkyl alkanesulfonate esters from aqueous or anhydrous compositions are provided. The invention provides methods for the conversion of alkyl alkanesulfonate esters of the formula RSO3R′ to the corresponding acids of the formula RSO3H. The alkyl alkanesulfonate esters are present in an organic medium, which may contain significant amounts of water or which may be anhydrous or substantially anhydrous. In some embodiments, the invention provides methods for purifying aqueous or anhydrous alkanesulfonic acids by removing alkyl alkanesulfonate esters.

Linker compounds, linker-compound-ligands and linker-compound-receptors

-

, (2008/06/13)

Novel immunoassay which utilizes an enzyme linked ligand or receptor wherein the enzyme is bacterial luciferase; mercantile kit useful in performing said immunoassay; and compounds utilized in performing said assay.

Polymer-Supported Cryptands. Problems Arising in the Synthesis of Highly Loaded Polymers

Anelli, Pier Lucio,Montanari, Fernando,Quici, Silvio

, p. 4910 - 4914 (2007/10/02)

The attachment of a hydroxymethylcryptand to lightly loaded chloromethylpolystyrene (1 mequiv of Cl/g) cross-linked with divinylbenzene leads to polymer-supported cryptands that are highly efficient catalysts in anion-promoted reactions carried out under phase-transfer conditions.However, the condensation with polystyrenes having a higher content of chloromethyl groups occurs in low yields, apparently affording immobilized cryptands with very low catalytic activity.This behavior results from extensive structural modifications of the bicyclic ligand, most likely promoted by neighboring chloromethyl groups.

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