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471356

Sigma-Aldrich

Methanesulfonic acid

≥99.0%

Synonym(s):

Mesylic acid, MsOH

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About This Item

Linear Formula:
CH3SO3H
CAS Number:
Molecular Weight:
96.11
Beilstein:
1446024
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

vapor density

3.3 (vs air)

Quality Level

vapor pressure

1 mmHg ( 20 °C)

Assay

≥99.0%

form

liquid

refractive index

n20/D 1.429 (lit.)

bp

167 °C/10 mmHg (lit.)

mp

17-19 °C (lit.)

solubility

water: soluble 1,000 g/L at 20 °C

density

1.481 g/mL at 25 °C (lit.)

SMILES string

O=S(O)(C)=O

InChI

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

InChI key

AFVFQIVMOAPDHO-UHFFFAOYSA-N

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General description

Methanesulfonic acid (MSA) is a strong organic acid. The chemical oxidation of dimetyl sulfide in the atmosphere leads to the formation of MSA in large quantities. MSA undergoes biodegradation by forming CO2 and sulphate. It is considered a green acid as it is less toxic and corrosive in comparison to mineral acids.1 The aqueous MSA solution has been considered a model electrolyte for electrochemical processes.

Application

Methanesulfonic acid may be used:
  • As a catalyst to produce linear alkylbenzenes by the addition reaction between long-chain olefins and benzene.
  • To prepare polyaniline (PANI)/graphene composites with enhanced thermal and electrical properties.
  • As a catalyst for the transformation of glucose/xylose mixtures to levulinic acid and furfural.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

372.2 °F - closed cup

Flash Point(C)

189 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Customers Also Viewed

Facile in-situ preparation of polyaniline/graphene nanocomposites using methanesulfonic acid.
Kim DH and Park SY.
Polymer, 55(12), 2928-2935 (2014)
Use of methanesulfonic acid as catalyst for the production of linear alkylbenzenes.
Luong BX, et al.
J. Catal., 226(2), 301-307 (2004)
Methanesulfonic acid-catalyzed conversion of glucose and xylose mixtures to levulinic acid and furfural.
Rackemann DW, et al.
Industrial Crops and Products, 52, 46-57 (2014)
Microbial metabolism of methanesulfonic acid.
Kelly DP and Murrell JC.
Archives of Microbiology, 172(6), 341-348 (1999)
Environmental benefits of methanesulfonic acid. Comparative properties and advantages.
Gernon MD.
Green Chemistry, 1(3), 127-140 (1999)

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