3814-55-9

Basic information

• Product Name: GLYCIDYL ISOBUTYL ETHER
• Synonyms: GLYCIDYL ISOBUTYL ETHER;ISO-BUTYLGLYCIDYL ETHER;(isobutoxymethyl)oxirane;2-(isobutoxymethyl)oxirane;[(2-Methylpropoxy)methyl]oxirane;2-(2-methylpropoxymethyl)oxirane
• CAS NO: 3814-55-9
• Molecular Formula: C₇H₁₄O₂
• Molecular Weight: 130.18
• EINECS: 223-303-1
• Product Categories: Epoxide Monomers;Monomers;Polymer Science
• Mol File: 3814-55-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 159.5 °C750 mm Hg(lit.)
• Flash Point: 120 °F
• Appearance: /
• Density: 0.909 g/mL at 25 °C(lit.)
• Vapor Pressure: 3.08mmHg at 25°C
• Refractive Index: n20/D 1.416(lit.)
• CAS DataBase Reference: GLYCIDYL ISOBUTYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: GLYCIDYL ISOBUTYL ETHER(3814-55-9)
• EPA Substance Registry System: GLYCIDYL ISOBUTYL ETHER(3814-55-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38-10
• Safety Statements: 26-37/39
• RIDADR: UN 3271 3/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 3814-55-9(Hazardous Substances Data)

Usage

General Description

Glycidyl Isobutyl Ether, also known as 1,2-Epoxy-3-isobutoxypropane, is a chemical compound used in a variety of industrial applications, primarily as a solvent, reactive diluent and plasticizer. It's an organic compound which is colorless and generally has a low viscosity. Its chemical formula is C7H14O2. GLYCIDYL ISOBUTYL ETHER is known for providing excellent long term stability and superior properties like moisture and chemical resistance in various applications such as adhesives, sealants, coatings, and paints. However, due to its epoxy nature, it can cause skin and eye irritation, and prolonged exposure may have negative health effects. Despite these potential risks, it remains a vital component in many industrial processes due to its versatile properties.

InChI:InChI=1/C7H14O2/c1-6(2)3-8-4-7-5-9-7/h6-7H,3-5H2,1-2H3

Upstream product

• 78-83-1 2-methyl-propan-1-ol 
• 106-89-8 epichlorohydrin 
• 13259-29-5 sodium isobutoxide 
• 42314-08-9 1-chloro-3-isobutoxy-propan-2-ol 

Downstream Products

• 61940-72-5 3-isobutyloxy-1,2-propanediol 
• 100066-46-4 Phenyl-carbamic acid 2-isobutoxymethyl-8,8-dimethyl-1,4,6-trioxa-spiro[4.4]non-9-yl ester 
• 856245-85-7 3,4-bis(4-chlorophenyl)-6-(2-hydroxy-3-isobutoxypropyl)imidazo[1,5-b]pyridazin-7(6H)-one 
• 1206669-52-4 C₁₃H₂₁NO₂ 
• 1174746-99-6 1-isobutoxy-3-(phenylamino)propan-2-ol 

Relevant articles and documents

Liquid-Liquid-Extraction of Metal Ions with Lariat Ethers

Lariat ethers of various ring size and substitution are synthesized and characterized by physical data and chemical analysis.The extraction behaviour of the crown compounds towards Na+, K+, Cs+ and Ag+ in a picric acid solution has been investigated.The extraction constants for 1:1 and 1:2 complexes are determined using the equilibrium distribution data.The results show that the flexible side chain in the investigated compounds has in no case a positive effect on the metal picrate extraction.

Synthesis and β-Adrenergic Blocking Activity of New Aliphatic Oxime Ethers

New β-adrenergic blocking agents, most of which do not contain an aromatic nucleus, were synthesized.They were derived either from alkylamino-aliphatic oxime ethers, or alkylamino-aliphatic ethers.Most active among these are O-acetoxime (8; trachea pA2=7.65) and 1-isobutoxy-3-(tert-butylamino)-2-propanol (15, trachea pA2=7.49), both of which displayed bronchoselectivity (β2/β1 ratio ca. 15).The role and importance of the aromatic nucleus in this class of compounds are discussed