Thermo Scientific Chemicals

Methanesulfonic acid, 98+%, Thermo Scientific Chemicals

Catalog number: A13565.36
500 g, Each
Thermo Scientific Chemicals

Methanesulfonic acid, 98+%, Thermo Scientific Chemicals

Catalog number: A13565.36
500 g, Each
Quantity
Catalog number: A13565.36
also known as A13565-36
Price (USD)
Quantity
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Chemical Identifiers

CAS
75-75-2
IUPAC Name
methanesulfonic acid
Molecular Formula
CH4O3S
InChI Key
AFVFQIVMOAPDHO-UHFFFAOYSA-N
SMILES
CS(O)(=O)=O
Appearance (Color)
Clear colorless to pale yellow or pale brown
Form
Liquid or low melting solid
Assay (Aqueous acid-base Titration)
≥98.0 to ≤102.0% (non-U.S. sourced material)
Assay from Supplier's CofA
≥98.0% (U.S. sourced material)
Comment
Material sourced in the U.S. and in other countries

Description

Methanesulfonic acid is used as a catalyst in organic reactions namely esterification, alkylation and condensation reactions due to its non- volatile nature and solubility in organic solvents. It is also involved in the production of starch esters, wax oxidate esters, benzoic acid esters, phenolic esters, or alkyl esters. It reacts with sodium borohydride in presence of polar solvent tetrahydrofuran to prepare borane-tetrahydrofuran complex. It finds application in batteries, because of its purity and chloride absence. In pharmaceutical industry, it is used for the manufacturing of active pharmaceutical ingredients like telmisartan and eprosartan. It is useful in ion chromatography and is a source of carbon and energy for some gram-negative methylotropic bacteria.It is involved in the deprotection of peptides.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Methanesulfonic acid is used as a catalyst in organic reactions namely esterification, alkylation and condensation reactions due to its non- volatile nature and solubility in organic solvents. It is also involved in the production of starch esters, wax oxidate esters, benzoic acid esters, phenolic esters, or alkyl esters. It reacts with sodium borohydride in presence of polar solvent tetrahydrofuran to prepare borane-tetrahydrofuran complex. It finds application in batteries, because of its purity and chloride absence. In pharmaceutical industry, it is used for the manufacturing of active pharmaceutical ingredients like telmisartan and eprosartan. It is useful in ion chromatography and is a source of carbon and energy for some gram-negative methylotropic bacteria.It is involved in the deprotection of peptides.

Notes
Moisture, light and heat sensitive. Hygroscopic. Keep container tightly closed in a dry and well-ventilated place. Incompatible with amines, strong reducing agents, ethyl vinyl ether, hydrofluoric acid, strong oxidizing agents and bases.
RUO – Research Use Only

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