13259-29-5

Basic information

• Product Name: sodium 2-methylpropanolate
• Synonyms: sodium 2-methylpropanolate;Sodium 2-methylpropoxide;Sodium isobutoxide
• CAS NO: 13259-29-5
• Molecular Formula: C₄H₉O*Na
• Molecular Weight: 96.10343
• EINECS: 236-254-6
• Mol File: 13259-29-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 105°C at 760 mmHg
• Flash Point: 27.8°C
• Appearance: /
• Vapor Pressure: 16.4mmHg at 25°C
• CAS DataBase Reference: sodium 2-methylpropanolate(CAS DataBase Reference)
• NIST Chemistry Reference: sodium 2-methylpropanolate(13259-29-5)
• EPA Substance Registry System: sodium 2-methylpropanolate(13259-29-5)

Safety Data

• Hazardous Substances Data: 13259-29-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C4H9O.Na/c1-4(2)3-5;/h4H,3H2,1-2H3;/q-1;+1

Upstream product

• 94584-18-6 2-isopropoxy-4,4,5,5,-tetramethyl-1,3,2-dioxaborane 
• 78-83-1 2-methyl-propan-1-ol 

Downstream Products

• 29206-04-0 2,2-dimethyl-3,3-diphenyl-propionic acid 
• 30895-05-7 2,4,6-tris(2-methylpropoxy)-1,3,5-triazine 
• 17071-47-5 1-(2-methylpropoxy)butane 
• 100532-58-9 1-isobutoxy-2-o-tolyloxy-ethane 
• 541-47-9 3-Methylbutenoic acid 
• 64-18-6 formic acid 
• 17860-06-9 α-isobutoxy-isobutyric acid 
• 79-31-2 isobutyric Acid 
• 108-11-2 Methyl isobutyl carbinol 
• 115-11-7 isobutene 
• 53146-47-7 glycerol-1.3-diisobutyl ether 
• 7779-75-1 isobutyl acetoacetate 
• 61940-60-1 glycerol-1-isobutyl ether-3-allyl ether 
• 24133-46-8 isobutoxy-acetic acid 

Relevant articles and documents

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Magnesium-catalysed hydroboration of aldehydes and ketones

The heteroleptic magnesium alkyl complex [CH{C(Me)NAr}2Mg nBu] (Ar = 2,6-iPr2C6H3) is reported as a highly efficient pre-catalyst for the hydroboration of aldehydes and ketones with pinacolborane. The Royal Society of Chemistry 2012.

Solubility of sodium sulfide in alcohols

The solubility of sodium sulfide in methanol, ethanol, 2-propanol, 2-methyl-1-propanol, and benzyl alcohol and the acid-base interaction of these compounds have been determined at (20 and 35) °C. The reactions result in the formation of sodium alkoxide and hydrosulfide. The reported values on the solubility of sodium sulfide in alcohols differ essentially from the data described in the literature.