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55517

Supelco

Methanesulfonic acid concentrate

0.1 M CH3SO3H in water (0.1N), eluent concentrate for IC

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Synonym(s):
Methanesulfonic acid solution
Linear Formula:
CH3SO3H
CAS Number:
Molecular Weight:
96.11
Beilstein/REAXYS Number:
1446024
MDL number:
PubChem Substance ID:
NACRES:
NB.21

Quality Level

concentration

0.1 M CH3SO3H in water (0.1N)

technique(s)

ion chromatography: suitable

SMILES string

CS(O)(=O)=O

InChI

1S/CH4O3S/c1-5(2,3)4/h1H3,(H,2,3,4)

InChI key

AFVFQIVMOAPDHO-UHFFFAOYSA-N

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This Item
682791635550972
vibrant-m

55517

Methanesulfonic acid concentrate

vibrant-m

68279

Sulfuric acid concentrate

vibrant-m

16355

Nitric acid concentrate

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

technique(s)

ion chromatography: suitable

technique(s)

ion chromatography: suitable

technique(s)

ion chromatography: suitable

technique(s)

ion chromatography: suitable

General description

This eluent concentrate for ion chromatography is determined by potentiometric titration. Content and expiry date can be found on the certificate.

Linkage

Visit the IC Portal to learn more

Preparation Note

Prepared with methanesulfonic acid and high purity water (18.2 MΩ, 0.2 μm filtered)

Related product

Product No.
Description
Pricing

Storage Class

12 - Non Combustible Liquids

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


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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
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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
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Nanostructuring of semiconductor films offers the potential means for producing photoelectrodes with improved minority charge carrier collection. Crucial to the effective operation of the photoelectrode is also the choice of a suitable electrolyte. The behaviour of the nanostructured WO(3) photoanodes
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Data from two phase 3 studies of eribulin were pooled in analyses initially requested by the European Medicines Agency to assess whether specific patient subgroups, previously treated with an anthracycline and a taxane, benefited from eribulin. Study 305/EMBRACE included women
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The cyclopropenone catalyzed nucleophilic substitution of alcohols by methanesulfonate ion with inversion of configuration is described. This work provides an alternative to the Mitsunobu reaction that avoids the use of azodicarboxylates and generation of hydrazine and phosphine oxide byproducts. This

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