993-48-6

Basic information

• Product Name: Propanoic acid, 2-hydroxy-2-Methyl-, MonosodiuM salt
• Synonyms: Propanoic acid, 2-hydroxy-2-Methyl-, MonosodiuM salt
• CAS NO: 993-48-6
• Molecular Formula: C₄H₇O₃*Na
• Molecular Weight: 126.08635
• EINECS: -0
• Mol File: 993-48-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Propanoic acid, 2-hydroxy-2-Methyl-, MonosodiuM salt(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 2-hydroxy-2-Methyl-, MonosodiuM salt(993-48-6)
• EPA Substance Registry System: Propanoic acid, 2-hydroxy-2-Methyl-, MonosodiuM salt(993-48-6)

Safety Data

• Hazardous Substances Data: 993-48-6(Hazardous Substances Data)

Upstream product

• 80-55-7 ethyl 2-hydroxy-2,2-dimethylethanoate 

Downstream Products

• 19444-23-6 benzyl 2-hydroxy-2-methylpropanoate 
• 938-36-3 1-methyl-2-phenylpyrrolidine 
• 19444-21-4 allyl 2-hydroxyisobutyrate 
• 19444-28-1 1,3-Bis-(α-hydroxy-isobutyryloxymethyl)-4,6-dimethyl-benzol 
• 19444-26-9 α-Hydroxy-isobuttersaeure-p-phenyloxy-benzylester 
• 19443-91-5 Bis--aether 
• 19444-24-7 α-Hydroxy-isobuttersaeure-2,4-dimethyl-benzylester 

Relevant articles and documents

The Influence of Hydrophobic Solvation on the Alkaline Hydrolysis of Ethyl Esters of Polar Substituted 2-Methylpropionic Acids in Water

The rate constants of the alkaline hydrolysis of 2-methylpropionic acid ethyl ester, α-hydroxy, α-bromo, α-cyano, and α-nitro-2-methylpropionic acid ethyl ester have been measured in water between 5 deg C and 45 deg C with the help of an appropiate conductance bridge developed in our laboratory.The influence of the polar substituents on the rate constant, a powerful probe for discussing two-particle interactions in solutions, is characterized by an intramolecular structure parameter of the activated complex and a dielectric parameter of its surroundings.The dependence of the reaction rate on the structure parameter is compared to that of substituted acetic acid derivatives.The smaller dielectric parameter of 2-methylpropionic acid esters reveals the increasing hydrophobic solvation in comparison to acetic acid derivatives.