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SAFC

Methanesulfonic acid

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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
NACRES:
NA.21

biological source

synthetic

Quality Level

vapor density

3.3 (vs air)

vapor pressure

1 mmHg ( 20 °C)

Assay

98.0-102.0% (1 M NaOH, T)

form

liquid

impurities

≤5 ppm ethyl methansesulfonate (GC)
≤5 ppm isopropyl methanesulfonate (GC)
≤5 ppm methanesulfonyl chloride (GC)
≤5 ppm methyl methanesulfonate (GC)

evapn. residue

≤0.1%

refractive index

n20/D 1.429 (lit.)

bp

167 °C/10 mmHg (lit.)

mp

17-19 °C (lit.)

density

1.475-1.485 g/mL at 20 °C
1.481 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤50 ppm
sulfate (SO42-): ≤200 ppm

cation traces

Ta: ≤5 ppm

suitability

corresponds for IR spectroscopy

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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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


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Renata Solarska et al.
Nanoscale, 4(5), 1553-1556 (2012-02-01)
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Solvejg Jørgensen et al.
Physical chemistry chemical physics : PCCP, 15(14), 5140-5150 (2013-03-02)
The gas phase reaction between methane sulfonic acid (CH3SO3H; MSA) and the hydroxyl radical (HO), without and with a water molecule, was investigated with DFT-B3LYP and CCSD(T)-F12 methods. For the bare reaction we have found two reaction mechanisms, involving proton
Chris Twelves et al.
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Eric D Nacsa et al.
Organic letters, 15(1), 38-41 (2012-12-15)
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
Gabriel Nowak et al.
Neuropharmacology, 84, 46-51 (2014-05-07)
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