Methanesulfonic Acid (Highly Pure)

Product Description

Methanesulfonic Acid (Highly Pure)
Catalog number: B2016267
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 mL
Molecular Weight or Concentration: 96.11
Supplied as: Liquid
Applications: a molecular tool for various biochemical applications
Storage: RT
Keywords: Methanesulfonic Acid
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Britschgi J, Kersten W, Waldvogel SR, Schüth F. Electrochemically Initiated Synthesis of Methanesulfonic Acid Angew Chem Int Ed Engl. 2022 Oct 10;61(41):e202209591.
2: Chen J, Lane JR, Bates KH, Kjaergaard HG. Atmospheric Gas-Phase Formation of Methanesulfonic Acid Environ Sci Technol. 2023 Dec 19;57(50):21168-21177.
3: Elm J. Clusteromics II: Methanesulfonic Acid-Base Cluster Formation ACS Omega. 2021 Jun 23;6(26):17035-17044.
4: Wu N, Ning A, Liu L, Zu H, Liang D, Zhang X. Methanesulfonic acid and iodous acid nucleation: a novel mechanism for marine aerosols Phys Chem Chem Phys. 2023 Jun 28;25(25):16745-16752.
5: Huff AK, Love N, Leopold KR. Microwave and Computational Study of Methanesulfonic Acid and Its Complex with Water J Phys Chem A. 2023 Apr 27;127(16):3658-3667.
6: Johnson JS, Jen CN. Role of Methanesulfonic Acid in Sulfuric Acid-Amine and Ammonia New Particle Formation ACS Earth Space Chem. 2023 Mar 7;7(3):653-660.
7: Shen J, Scholz W, He XC, Zhou P, Marie G, Wang M, Marten R, Surdu M, Rörup B, Baalbaki R, Amorim A, Ataei F, Bell DM, Bertozzi B, Brasseur Z, Caudillo L, Chen D, Chu B, Dada L, Duplissy J, Finkenzeller H, Granzin M, Guida R, Heinritzi M, Hofbauer V, Iyer S, Kemppainen D, Kong W, Krechmer JE, Kürten A, Lamkaddam H, Lee CP, Lopez B, Mahfouz NGA, Manninen HE, Massabò D, Mauldin RL, Mentler B, Müller T, Pfeifer J, Philippov M, Piedehierro AA, Roldin P, Schobesberger S, Simon M, Stolzenburg D, Tham YJ, Tomé A, Umo NS, Wang D, Wang Y, Weber SK, Welti A, Wollesen de Jonge R, Wu Y, Zauner-Wieczorek M, Zust F, Baltensperger U, Curtius J, Flagan RC, Hansel A, Möhler O, Petäjä T, Volkamer R, Kulmala M, Lehtipalo K, Rissanen M, Kirkby J, El-Haddad I, Bianchi F, Sipilä M, Donahue NM, Worsnop DR. High Gas-Phase Methanesulfonic Acid Production in the OH-Initiated Oxidation of Dimethyl Sulfide at Low Temperatures Environ Sci Technol. 2022 Oct 4;56(19):13931-13944.
8: Rasmussen FR, Kubečka J, Elm J. Contribution of Methanesulfonic Acid to the Formation of Molecular Clusters in the Marine Atmosphere J Phys Chem A. 2022 Oct 13;126(40):7127-7136.
9: Eberlin AR, Eddleston MD, Frampton CS. Methanesulfonic acid salt forms of carbamazepine and 10,11-dihydrocarbamazepine Acta Crystallogr C. 2013 Nov;69(Pt 11):1260-6.
10: Liu Y, Xie HB, Ma F, Chen J, Elm J. Amine-Enhanced Methanesulfonic Acid-Driven Nucleation: Predictive Model and Cluster Formation Mechanism Environ Sci Technol. 2022 Jun 21;56(12):7751-7760.

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