Skip to Content
Merck

550256

Silver methanesulfonate

solid

Synonym(s):

Silver methylsulfonate, Methanesulfonic acid silver salt

Sign In to View Organizational & Contract Pricing.

Select a Size

All Photos(2)

About This Item

Linear Formula:
AgSO3CH3
CAS Number:
2386-52-9
Molecular Weight:
202.97
NACRES:
NA.22
PubChem Substance ID:
24879101
UNSPSC Code:
12161600
EC Number:
219-199-2
MDL number:
MFCD00064795

Product Name

Silver methanesulfonate,

InChI key

MLKQJVFHEUORBO-UHFFFAOYSA-M

InChI

1S/CH4O3S.Ag/c1-5(2,3)4;/h1H3,(H,2,3,4);/q;+1/p-1

SMILES string

[Ag+].CS([O-])(=O)=O

form

solid

reaction suitability

core: silver
reagent type: catalyst

mp

252-256 °C (lit.)

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Gold Catalysts — 21st Century ′Gold Rush′
Catalyst for:
  • Heterocyclization reactions
  • CO2-mediated rearrangement of propargyl alcohols for the synthesis of a,ß-unsaturated ketones and esters

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCZ6307
MKCS7124
MKCR3717
MKCR8945
MKCQ5160

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Tsung-Ming Shih et al.
Chemico-biological interactions, 187(1-3), 207-214 (2010-03-13)
This study compared the ability of nine oximes (HI-6, HLö7, MMB-4, TMB-4, carboxime, ICD585, ICD692, ICD3805, and 2-PAM) to reactivate in vivo cholinesterase (ChE) in blood, brain, and peripheral tissues in guinea pigs intoxicated by one of four organophosphorus nerve
Cassandra J Gaston et al.
Environmental science & technology, 44(5), 1566-1572 (2010-02-04)
Dimethyl sulfide (DMS), produced by oceanic phytoplankton, is oxidized to form methanesulfonic acid (MSA) and sulfate, which influence particle chemistry and hygroscopicity. Unlike sulfate, MSA has no known anthropogenic source making it a useful tracer for ocean-derived biogenic sulfur. Despite
Wenyuan Liu et al.
Journal of pharmaceutical and biomedical analysis, 52(4), 603-608 (2010-02-09)
10-O-(N,N-dimethylaminoethyl)-ginkgolide B methanesulfonate (XQ-1H), a novel active derivative of ginkgolide B, is a platelet-activating factor antagonist which is being under clinical trial. Two unknown related impurities were observed in analysis of XQ-1H bulk drug. A scaling up preparative liquid chromatography
Benedetto Natalini et al.
Talanta, 85(3), 1392-1397 (2011-08-03)
The successful enantioseparation of five 6-desfluoroquinolones with three polysaccharide-based stationary phases (namely, the cellulose-based Chiralpak IB and the two amylose-based Chiralpak AD-H and Lux Amylose-2) is herein described. The investigated species differ for the nature of substituents and/or the position
Neal W Sach et al.
Organic letters, 14(15), 3886-3889 (2012-07-18)
A general synthesis of aryl ethers from primary and secondary alcohols and aryl mesylates is presented. The reaction proceeds via a sulfonyl-transfer mechanism. In this paper, we compare the sulfonyl transfer reaction to Mitsunobu ether formation. The reaction can be
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service