Summary
Methanesulfonic acid (MsOH) or methanesulphonic acid (in British English) is an organosulfuric, colorless liquid with the molecular formula CH3SO3H and structure H3C−S(=O)2−OH. It is the simplest of the alkylsulfonic acids (R−S(=O)2−OH). Salts and esters of methanesulfonic acid are known as mesylates (or methanesulfonates, as in ethyl methanesulfonate). It is hygroscopic in its concentrated form. Methanesulfonic acid can dissolve a wide range of metal salts, many of them in significantly higher concentrations than in hydrochloric acid (HCl) or sulfuric acid (H2SO4).[3]
| |
| |
| Names | |
|---|---|
| Preferred IUPAC name
Methanesulfonic acid | |
| Other names
Methylsulfonic acid, MSA; Mesylic acid
| |
| Identifiers | |
| |
3D model (JSmol)
|
|
| 1446024 | |
| ChEBI |
|
| ChemSpider |
|
| ECHA InfoCard | 100.000.817 |
| EC Number |
|
| 1681 | |
PubChem CID
|
|
| UNII |
|
| UN number | 2585 |
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| CH4O3S | |
| Molar mass | 96.10 g·mol−1 |
| Appearance | Clear, colourless liquid |
| Density | 1.48 g/cm3 |
| Melting point | 17 to 19 °C (63 to 66 °F; 290 to 292 K) |
| Boiling point | 167 °C (333 °F; 440 K) at 10 mmHg, 122 °C/1 mmHg |
| miscible | |
| Solubility | Miscible with methanol, diethyl ether. Immiscible with hexane |
| log P | −2.424[1] |
| Acidity (pKa) | −1.9[2] |
| Hazards | |
| GHS labelling: | |
| |
| Danger | |
| H314 | |
| P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, P501 | |
| Safety data sheet (SDS) | Oxford MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 verify (what is   ?)
Infobox references
| |
History and manufacturing edit
The first commercial production of MSA, developed in the 1940s by Standard Oil of Indiana, was based on oxidation of dimethylsulfide by O
2 from air. Although inexpensive, this process suffered from a poor product quality and explosion hazards.
In 1967, the Pennwalt Corporation (USA) developed a different process for dimethylsulfide (as a water-based emulsion) oxidation using chlorine, followed by extraction-purification. In 2022 this chlorine-oxidation process was used only by Arkema (France) for making high-purity MSA. This process is not popular on a large scale, because it co-produces large quantities of hydrochloric acid.
Between years 1970 and 2000 MSA was used only on a relatively small-scale in niche markets (for example, in the microelectronic and electroplating industries since the 1980s), which was mainly due to its rather high price and limited availability. However, this situation changed around 2003, when BASF launched commercial production of MSA in Ludwigshafen based on a modified version of the aforementioned air oxidation process, oxidising dimethyldisulfide with nitric acid which is then restored using atmospheric oxygen. The former is produced in one step from methanol from syngas, hydrogen and sulfur.[4]
An even better (lower-cost and environmentally friendlier) process of making methanesulfonic acid was developed in 2016 by Grillo-Werke AG (Germany). It is based on a direct reaction between methane and oleum at around 50 °C and 100 bar in the presence of a potassium persulfate initiator. [5] This technology was acquired and commercialized by BASF in 2019.[6]
Applications edit
Since ca. 2000 methanesulfonic acid has become a popular replacement for other acids in numerous industrial and laboratory applications, because it:
- is a strong acid,
- has a low vapor pressure (see boiling points in the "Properties" inset),
- is not an oxidant or explosive, like nitric, sulfuric or perchloric acids.
- is a liquid at room temperature,
- is soluble in many organic solvents,
- forms water-soluble salts with all inorganic cations and with most organic cations,
- does not form complexes with metal ions in water,
- its anion, mesylate, is non-toxic and suitable for pharmaceutical preparations.
The closely related p-toluenesulfonic acid (PTSA) is solid.
Methanesulfonic acid can be used in the generation of borane (BH3) by reacting methanesulfonic acid with NaBH4 in an aprotic solvent such as THF or DMSO, the complex of BH3 and the solvent is formed.[7]
Electroplating edit
Solutions of methanesulfonic acid are used for the electroplating of tin and tin-lead solders. It is displacing the use of fluoroboric acid, which releases corrosive and volatile hydrogen fluoride.[8]
Methanesulfonic acid is also a primary ingredient in rust and scale removers.[9] It is used to clean off surface rust from ceramic, tiles and porcelain which are usually susceptible to acid attack.
See also edit
- Trifluoromethanesulfonic acid, the more acidic trifluoro analogue
References edit
- ^ Towler, Christopher S.; Li, Tonglei; Wikström, Håkan; Remick, David M.; Sanchez-Felix, Manuel V.; Taylor, Lynne S. (December 2008). "An Investigation into the Influence of Counterion on the Properties of Some Amorphous Organic Salts". Molecular Pharmaceutics. 5 (6): 946–955. doi:10.1021/mp8000342. PMID 19434850.
- ^ Guthrie, J. Peter (September 1978). "Hydrolysis of esters of oxy acids: pKa values for strong acids; Brønsted relationship for attack of water at methyl; free energies of hydrolysis of esters of oxy acids; and a linear relationship between free energy of hydrolysis and pKa holding over a range of 20 pK units". Canadian Journal of Chemistry. 56 (17): 2342–2354. doi:10.1139/v78-385.
- ^ Gernon, M. D.; Wu, M.; Buszta, T.; Janney, P. (1999). "Environmental benefits of methanesulfonic acid: comparative properties and advantages". Green Chemistry. 1 (3): 127–140. doi:10.1039/a900157c.
- ^ US patent 6531629B1, Matthias Eiermann, Christian Tragut, Klaus Ebel, "Method of producing alkanesulfonic acid", issued 2003-03-11, assigned to BASF SE
- ^ Lobree, Lisa J.; Bell, Alexis T. (2001). "K2S2O8-Initiated Sulfonation of Methane to Methanesulfonic Acid". Ind. Eng. Chem. Res. 40 (3): 736–742. doi:10.1021/ie000725b.
- ^ Binnemans, K.; Jones, P. T. (2022). "Methanesulfonic Acid (MSA) in Hydrometallurgy". Journal of Sustainable Metallurgy. 20. doi:10.1007/s40831-022-00641-6.
- ^ Lobben, Paul C.; Leung, Simon Shun-Wang; Tummala, Srinivas (2004). "Integrated Approach to the Development and Understanding of the Borane Reduction of a Carboxylic Acid". Org. Process Res. Dev. 8 (6): 1072–1075. doi:10.1021/op049910h.
- ^ Balaji, R.; Pushpavanam, Malathy (2003). "Methanesulphonic acid in electroplating related metal finishing industries". Transactions of the Imf. 81 (5): 154–158. doi:10.1080/00202967.2003.11871526. S2CID 91584456.
- ^ "Archived copy" (PDF). Archived from the original (PDF) on 2016-03-04. Retrieved 2015-12-01.
{{cite web}}: CS1 maint: archived copy as title (link)