3126-95-2

Basic information

• Product Name: N-PROPYL GLYCIDYL ETHER
• Synonyms: N-PROPYL GLYCIDYL ETHER;(2,3-Epoxypropyl)-propylether;(Propoxymethyl)oxirane;1,2-epoxy-3-propoxy-propan;1,2-Epoxy-3-propoxypropane;2-(Propoxymethyl)oxirane;Ether, 2,3-epoxypropyl propyl;ether,2,3-epoxypropylpropyl
• CAS NO: 3126-95-2
• Molecular Formula: C6H12O2
• Molecular Weight: 116.16
• EINECS: 221-509-6
• Mol File: 3126-95-2.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 151.1°Cat760mmHg
• Flash Point: 39.2°C
• Appearance: /
• Density: 0.958g/cm³
• Vapor Pressure: 4.74mmHg at 25°C
• Refractive Index: 1.427
• CAS DataBase Reference: N-PROPYL GLYCIDYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: N-PROPYL GLYCIDYL ETHER(3126-95-2)
• EPA Substance Registry System: N-PROPYL GLYCIDYL ETHER(3126-95-2)

Safety Data

• Hazardous Substances Data: 3126-95-2(Hazardous Substances Data)

Usage

General Description

N-PROPYL GLYCIDYL ETHER is a chemical compound with the formula C6H12O2 and a molecular weight of 116.16 g/mol. It is a clear, colorless liquid with a mild odor and is commonly used as a reactive diluent in the formulation of epoxy resins. N-PROPYL GLYCIDYL ETHER is also utilized as a crosslinking agent for polymers and as a solvent in various industrial applications. It is known to be an irritant to the skin, eyes, and respiratory system, and appropriate safety measures should be taken when handling this substance. Additionally, it is important to carefully follow regulatory guidelines for the safe handling and disposal of N-PROPYL GLYCIDYL ETHER to prevent harm to human health and the environment.

InChI:InChI=1/C6H12O2/c1-2-3-7-4-6-5-8-6/h6H,2-5H2,1H3

Upstream product

• 6943-58-4 1-chloro-3-propoxy-2-propanol 
• 106-92-3 Allyl glycidyl ether 
• 27491-84-5 triethyl hydrogen silicate 
• 1471-03-0 allyl propyl ether 
• 71-23-8 propan-1-ol 
• 106-89-8 epichlorohydrin 

Downstream Products

• 20040-25-9 2-Propyloxy-1-phenoxy-propanol-(2) 
• 14714-99-9 1-Propargyloxy-3-propoxy-2-carbamoyloxy-propan 
• 143503-49-5 (2-Heptyloxy-phenyl)-carbamic acid 2-azepan-1-yl-1-propoxymethyl-ethyl ester 
• 143503-47-3 (2-Hexyloxy-phenyl)-carbamic acid 2-azepan-1-yl-1-propoxymethyl-ethyl ester 
• 105920-54-5 (2-Heptyloxy-phenyl)-carbamic acid 2-piperidin-1-yl-1-propoxymethyl-ethyl ester 
• 143503-57-5 (3-Heptyloxy-phenyl)-carbamic acid 2-azepan-1-yl-1-propoxymethyl-ethyl ester 
• 143503-45-1 (2-Pentyloxy-phenyl)-carbamic acid 2-azepan-1-yl-1-propoxymethyl-ethyl ester 
• 105920-52-3 (2-Hexyloxy-phenyl)-carbamic acid 2-piperidin-1-yl-1-propoxymethyl-ethyl ester 
• 105919-56-0 (2-Heptyloxy-phenyl)-carbamic acid 1-propoxymethyl-2-pyrrolidin-1-yl-ethyl ester 
• 105920-62-5 (3-Heptyloxy-phenyl)-carbamic acid 2-piperidin-1-yl-1-propoxymethyl-ethyl ester 
• 143503-55-3 (3-Hexyloxy-phenyl)-carbamic acid 2-azepan-1-yl-1-propoxymethyl-ethyl ester 
• 143503-43-9 (2-Butoxy-phenyl)-carbamic acid 2-azepan-1-yl-1-propoxymethyl-ethyl ester 
• 105920-50-1 (2-Pentyloxy-phenyl)-carbamic acid 2-piperidin-1-yl-1-propoxymethyl-ethyl ester 
• 105920-36-3 (2-Hexyloxy-phenyl)-carbamic acid 1-propoxymethyl-2-pyrrolidin-1-yl-ethyl ester 

Relevant articles and documents

Reaction of 1-amino-3-propoxy-2-propanol with aldehydes

The reaction of 1-amino-3-propoxy-2-propanol was examined as a route to the corresponding 1,3-oxazolidines.

PERFUMES IN THE FORM OF AQUEOUS MICROEMULSIONS

An oil-in-water microemulsion including, in weight percentages: between 70% and 94% of water; between 1% and 15% of at least one perfumed hydrophobic substance; between 4% and 20% of at least one preferably volatile solvo-surfactant, which is a monoalkylated glycerol derivative of formula (I); and between 0.1% and 15% of at least one anionic surfactant and at least one alkyl glucoside as a hydrotropic agent. The microemulsion can therefore be used to produce a fine fragrance composition or a cosmetic or personal hygiene composition.

The synthesis and curing kinetics study of a new fluorinated polyurethane with fluorinated side chains attached to soft blocks

Fluorinated polyurethane (FPU) with fluorine in the side chain was obtained using fluorinated polyether glycol (FPO) with fluorinated side chains and 4,4′-diphenyl methane diisocyanate (MDI). The direct visual inspection of microstructures by SEM revealed that the separation degree of soft and hard segments decreased with the introduction of fluorinated groups into polyurethane soft segments, leading to a decrease in the crystallinity of FPU. The glass transition temperatures (Tg) measured by DMA indicated that the optimal working temperature window of FPU separating soft and hard glass transitions became narrow. And the mechanical properties and surface properties of the FPU were also measured. Curing kinetics of FPU was studied using a rotational rheometer, and the activation energy of FPU was obtained. The relationship between the curing temperature and the mobility of fluorinated groups was characterized by XPS. The result showed that F content in the FPU surface decreased with increasing curing temperature.