32541-58-5

Basic information

• Product Name: 4-ISOPROPOXY-2-BUTANONE
• Synonyms: 4-ISOPROPOXY-2-BUTANONE;Isopropoxybutanone;4-ISOPROPOXY-2-BUTANONE 95+%;4-Isopropoxybutane-2-one;Methyl 2-isopropoxyethyl ketone
• CAS NO: 32541-58-5
• Molecular Formula: C₇H₁₄O₂
• Molecular Weight: 130.18
• Mol File: 32541-58-5.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 75 °C / 35mmHg
• Flash Point: 46.7°C
• Appearance: /
• Density: 0,89 g/cm3
• Vapor Pressure: 1.71mmHg at 25°C
• Refractive Index: 1.4070 to 1.4100
• CAS DataBase Reference: 4-ISOPROPOXY-2-BUTANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ISOPROPOXY-2-BUTANONE(32541-58-5)
• EPA Substance Registry System: 4-ISOPROPOXY-2-BUTANONE(32541-58-5)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: UN 1993 3/PG III
• HazardClass: 3
• PackingGroup: III
• Hazardous Substances Data: 32541-58-5(Hazardous Substances Data)

Usage

General Description

4-ISOPROPOXY-2-BUTANONE, also known as 4-Isopropoxybutan-2-one, is a chemical compound with the molecular formula C7H14O2. It is a colorless liquid with a fruity odor and is primarily used as a solvent in various industrial applications, including paints, coatings, and adhesives. It is also used as a flavoring agent and fragrance in the food and cosmetic industries. The chemical is known to be flammable and should be handled with care to avoid potential hazards. Additionally, it is important to follow safety guidelines and regulations when using this compound in any manufacturing or production processes.

InChI:InChI=1/C7H14O2/c1-6(2)9-5-4-7(3)8/h6H,4-5H2,1-3H3

Upstream product

• 78-94-4 methyl vinyl ketone 
• 67-63-0 isopropyl alcohol 
• 689-97-4 3-buten-1-yne 
• 139571-54-3 1-[2-(2,4-Dimethyl-[1,3]dioxolan-2-yl)-ethoxy]-propan-2-ol 
• 7664-93-9 sulfuric acid 
• 4630-06-2 6-methylhept-5-en-2-ol 

Downstream Products

• 40091-57-4 4-isopropoxy-2-butanol 
• 78-94-4 methyl vinyl ketone 

Relevant articles and documents

Synthesis of novel β-functionalized α-oximinoketones via hetero-Michael addition of alcohols and mercaptans to enones

A new methodology has been developed for the preparation of β-alkoxy and β-sulfenyl ketones by hetero-Michael addition of the corresponding alcohols and thiols to enones under acidic and basic conditions. The direct conversion of enones into β-alkoxy and

2-AMINO-1,3,4-THIADIAZINE AND 2-AMINO-1,3,4-OXADIAZINE BASED ANTIFUNGAL AGENTS

The invention provides a compound which is a diazine of formula (I) or a tautomer thereof, or a pharmaceutically acceptable salt thereof, for use as an antifungal agent: (I) wherein X, N', C', A and E are as defined herein. The invention also provides a compound of Formula (I) as defined herein.

Acidic ionic liquid [NMP]H2PO4 as dual solvent-catalyst for synthesis of β-alkoxyketones by the oxa-Michael addition reactions

Acidic ionic liquid N-methyl-2-pyrrolidonium dihydrogen phosphate [NMP]H2PO4 was prepared and used as efficient catalyst and reaction medium to synthesize β-alkoxyketones by the oxa-Michael addition reactions for the first time. The