55517
Acide méthane sulfonique solution
0.1 M CH3SO3H in water (0.1N), eluent concentrate for IC
Synonyme(s) :
Methanesulfonic acid solution
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About This Item
Formule linéaire :
CH3SO3H
Numéro CAS:
Poids moléculaire :
96.11
Numéro Beilstein :
1446024
Numéro MDL:
Code UNSPSC :
12161700
ID de substance PubChem :
Nomenclature NACRES :
NB.21
Produits recommandés
Niveau de qualité
Concentration
0.1 M CH3SO3H in water (0.1N)
Technique(s)
ion chromatography: suitable
Chaîne SMILES
CS(O)(=O)=O
InChI
1S/CH4O3S/c1-5(2,3)4/h1H3,(H,2,3,4)
Clé InChI
AFVFQIVMOAPDHO-UHFFFAOYSA-N
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Catégories apparentées
Description générale
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).
Liaison
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Notes préparatoires
Prepared with methanesulfonic acid and high purity water (18.2 MΩ, 0.2 μm filtered)
Produit(s) apparenté(s)
Réf. du produit
Description
Tarif
Code de la classe de stockage
12 - Non Combustible Liquids
Classe de danger pour l'eau (WGK)
nwg
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
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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A general synthesis of aryl ethers from primary and secondary alcohols and aryl mesylates is presented. The reaction proceeds via a sulfonyl-transfer mechanism. In this paper, we compare the sulfonyl transfer reaction to Mitsunobu ether formation. The reaction can be
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Dimethyl sulfide (DMS), produced by oceanic phytoplankton, is oxidized to form methanesulfonic acid (MSA) and sulfate, which influence particle chemistry and hygroscopicity. Unlike sulfate, MSA has no known anthropogenic source making it a useful tracer for ocean-derived biogenic sulfur. Despite
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