55517
Methanesulfonic acid concentrate
0.1 M CH3SO3H in water (0.1N), eluent concentrate for IC
Synonym(s):
Methanesulfonic acid solution
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About This Item
Linear Formula:
CH3SO3H
CAS Number:
Molecular Weight:
96.11
Beilstein:
1446024
MDL number:
UNSPSC Code:
12161700
PubChem Substance ID:
NACRES:
NB.21
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Quality Level
concentration
0.1 M CH3SO3H in water (0.1N)
technique(s)
ion chromatography: suitable
SMILES string
CS(O)(=O)=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
This eluent concentrate for ion chromatography is determined by potentiometric titration. Content and expiry date can be found on the certificate.
Application
- Design of a new nanocomposite based on Keggin-type [ZnW(12)O(40)](6-) anionic cluster anchored on NiZn(2)O(4) ceramics: Explores the synthesis of advanced materials using Methanesulfonic acid, contributing to developments in energy storage and catalysis technology (Rezvani et al., 2024).
- Nanosuspensions in ophthalmology: Overcoming challenges and enhancing drug delivery for eye diseases: Discusses the role of Methanesulfonic acid in the formulation of nanosuspensions, enhancing therapeutic efficiency in ophthalmologic applications (Fathi-Karkan et al., 2024).
- Building Flame-Retardant Polymer Electrolytes via Microcapsule Technology for Stable Lithium Batteries: Methanesulfonic acid may be utilized in the synthesis of flame-retardant materials for safer lithium battery technologies, addressing critical needs in electronic manufacturing (Zhang et al., 2024).
- Catalysts for C-N coupling in urea electrosynthesis under ambient conditions from carbon dioxide and nitrogenous species: Highlights the application of Methanesulfonic acid in developing catalysts for green chemistry processes, particularly in the efficient synthesis of urea from environmentally benign sources (Yang et al., 2024).
Linkage
Visit the IC Portal to learn more
Preparation Note
Prepared with methanesulfonic acid and high purity water (18.2 MΩ, 0.2 μm filtered)
related product
Product No.
Description
Pricing
Storage Class Code
12 - Non Combustible Liquids
WGK
nwg
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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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
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The solvation effect of 1H-1,2,4-triazole towards imidazolium methanesulfonate was studied by blending imidazolium methanesulfonate and 1H-1,2,4-triazole. Upon addition of 1H-1,2,4-triazole, the melting point of imidazolium methanesulfonate was lowered to less than 100 °C while maintaining the high ionic conductivity for
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