Sodium methanesulfonate

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Reagent Code: #234661
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CAS Number 2386-57-4

science Other reagents with same CAS 2386-57-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 118.09 g/mol
Formula CH₃NaO₃S
badge Registry Numbers
MDL Number MFCD00064389
thermostat Physical Properties
Melting Point 17-19 ℃
inventory_2 Storage & Handling
Density 1.481 g/cm3
Storage 2~8℃

description Product Description

Sodium methanesulfonate is utilized as a reagent and intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. It facilitates the introduction of the methanesulfonate group to form mesylate esters, which serve as excellent leaving groups in nucleophilic substitution reactions, providing mild conditions with good selectivity and yield. It is also used in electroplating baths as a conductive salt to enhance deposit uniformity and brightness. Furthermore, it acts as a precursor for sulfonate-based surfactants and catalysts, owing to its favorable reactivity and solubility. Its stability in aqueous and polar organic solvents makes it ideal for large-scale industrial applications.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿310.00
inventory 25g
10-20 days ฿490.00
inventory 100g
10-20 days ฿1,160.00
inventory 2.5kg
10-20 days ฿11,360.00
inventory 500g
10-20 days ฿3,200.00

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Sodium methanesulfonate
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Sodium methanesulfonate is utilized as a reagent and intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. It facilitates the introduction of the methanesulfonate group to form mesylate esters, which serve as excellent leaving groups in nucleophilic substitution reactions, providing mild conditions with good selectivity and yield. It is also used in electroplating baths as a conductive salt to enhance deposit uniformity and brightness. Furthermore, it acts as a prec

Sodium methanesulfonate is utilized as a reagent and intermediate in organic synthesis, especially in pharmaceutical and agrochemical industries. It facilitates the introduction of the methanesulfonate group to form mesylate esters, which serve as excellent leaving groups in nucleophilic substitution reactions, providing mild conditions with good selectivity and yield. It is also used in electroplating baths as a conductive salt to enhance deposit uniformity and brightness. Furthermore, it acts as a precursor for sulfonate-based surfactants and catalysts, owing to its favorable reactivity and solubility. Its stability in aqueous and polar organic solvents makes it ideal for large-scale industrial applications.

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