75-75-2

  • Product Name:Methane sulfonic acid
  • Molecular Formula:CH4O3S
  • Purity:99%
  • Molecular Weight:96.107
Inquiry

Reputable factory supply Methane sulfonic acid 75-75-2 in bulk at low price

  • Molecular Formula:CH4O3S
  • Molecular Weight:96.107
  • Appearance/Colour:colourless or light yellow liquid 
  • Vapor Pressure:1 mm Hg ( 20 °C) 
  • Melting Point:19 °C 
  • Refractive Index:n20/D 1.429(lit.)  
  • Boiling Point:167 °C (10 torr) 
  • PKA:-2.6(at 25℃) 
  • Flash Point:>230 °F 
  • PSA:62.75000 
  • Density:1.511 g/cm3 
  • LogP:0.58480 

Methanesulfonic acid(Cas 75-75-2) Usage

Preparation

Methanesulfonic acid is produced predominantly by oxidizing methylthiol or dimethyl disulfide using nitric acid, hydrogen peroxide, chlorine or by employing electrochemical processes.

Hazard

Toxic by ingestion, skin irritant, corrosiveto tissue.

Safety Profile

Poison by ingestion and intraperitoneal routes. May be corrosive to skin, eyes, and mucous membranes. Explosive reaction with ethyl vinyl ether. Incompatible with hydrogen fluoride. When heated to decomposition it emits toxic fumes of SOx. See also SULFONATES.

Purification Methods

Dry the acid, either by azeotropic removal of water with *benzene or toluene, or by stirring 20g of P2O5 with 500mL of the acid at 100o for 0.5hours. Then distil it under vacuum and fractionally crystallise it by partial freezing. Sulfuric acid, if present, can be removed by prior addition of Ba(OH)2 to a dilute solution, filtering off the BaSO4 and concentrating under reduced pressure; and is sufficiently pure for most applications. [Beilstein 4 IV 10.]

description

Methanesulfonic acid (CH3SO3H, 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.The aqueous MSA solution has been considered a model electrolyte for electrochemical processes.Methanesulfonic acid is an alkanesulfonic acid in which the alkyl group directly linked to the sulfo functionality is methyl. It has a role as an Escherichia coli metabolite. It is an alkanesulfonic acid and a one-carbon compound. It is a conjugate acid of a methanesulfonate.

Chemical properties

Methanesulfonic acid, the simplest alkanesulfonic acid, is a colorless or slightly brown oily liquid, appearing as solid at low temperatures. It has a melting temperature of 20 °C, the boiling point of 167 °C (13.33 kPa), 122 °C (0.133 kPa), ?the relative density of 1.4812 (18 ℃) and refractive index 1.4317 (16 ℃). It is soluble in water, alcohol and ether, insoluble in alkanes, benzene and toluene. It will not subject to decomposition in boiling water and hot alkaline solution. It also has strong corrosion effect against the metal iron, copper and lead.

Definition

ChEBI: An alkanesulfonic acid in which the alkyl group directly linked to the sulfo functionality is methyl.

InChI:InChI=1/2CH4O3S.Fe/c2*1-5(2,3)4;/h2*1H3,(H,2,3,4);/q;;+2/p-2

75-75-2 Relevant articles

A high-yield approach to the sulfonation of methane to methanesulfonic acid initiated by H2O2 and a metal chloride

Mukhopadhyay, Sudip,Bell, Alexis T.

, p. 2990 - 2993 (2003)

Low temperatures and low pressures suffi...

Direct catalytic sulfonation of methane with SO2 to methanesulfonic acid (MSA) in the presence of molecular O2

Mukhopadhyay, Sudip,Bell, Alexis T.

, p. 1590 - 1591 (2003)

Methane is transformed selectively to me...

A novel method for the direct sulfonation of CH4 with SO 3 in the presence of KO2 and a promoter

Mukhopadhyay, Sudip,Bell, Alexis T.

, p. 754 - 757 (2003)

Direct sulfonation of methane with SO3 t...

75-75-2 Process route

p-nitrophenyl methanesulfonate
20455-07-6

p-nitrophenyl methanesulfonate

4-nitro-phenol
100-02-7,78813-13-5,89830-32-0

4-nitro-phenol

methanesulfonic acid
75-75-2,98527-29-8

methanesulfonic acid

Conditions
Conditions Yield
With water; hydroxide; In 1,4-dioxane; at 25 ℃; Rate constant;
 
Florfenicol
73231-34-2

Florfenicol

methanesulfonic acid
75-75-2,98527-29-8

methanesulfonic acid

para-methanesulfonylbenzaldehyde
5398-77-6

para-methanesulfonylbenzaldehyde

C<sub>4</sub>H<sub>4</sub>Cl<sub>2</sub>FNO<sub>2</sub>

C4H4Cl2FNO2

C<sub>12</sub>H<sub>13</sub>Cl<sub>3</sub>FNO<sub>4</sub>S

C12H13Cl3FNO4S

C<sub>11</sub>H<sub>11</sub>Cl<sub>3</sub>FNO<sub>2</sub>

C11H11Cl3FNO2

C<sub>11</sub>H<sub>12</sub>Cl<sub>2</sub>FNO<sub>2</sub>

C11H12Cl2FNO2

(1R,2S)-2-amino-3-fluoro-1-<4-(methylsulphonyl)phenyl>-1-propanol
76639-93-5,105182-37-4,118015-48-8

(1R,2S)-2-amino-3-fluoro-1-<4-(methylsulphonyl)phenyl>-1-propanol

benzaldehyde
100-52-7

benzaldehyde

benzoic acid
65-85-0,8013-63-6

benzoic acid

Conditions
Conditions Yield
With water; hypochloric acid; at 15 ℃; for 0.5h; pH=5.7; Reagent/catalyst; Kinetics;
 

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