3126-95-2

Usage

Uses

Used in Epoxy Resin Industry:
N-PROPYL GLYCIDYL ETHER is used as a reactive diluent for the formulation of epoxy resins, enhancing their properties and performance.
Used in Polymer Industry:
N-PROPYL GLYCIDYL ETHER is used as a crosslinking agent for polymers, improving their structural integrity and durability.
Used in Solvent Applications:
N-PROPYL GLYCIDYL ETHER is used as a solvent in various industrial applications, providing a versatile and effective solution for dissolving and processing materials.

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 
• 71-23-8 propan-1-ol 
• 106-89-8 epichlorohydrin 
• 106-92-3 Allyl glycidyl ether 
• 27491-84-5 triethyl hydrogen silicate 
• 1471-03-0 allyl propyl ether 

Downstream Products

• 38578-22-2 1-t-Butylperoxy-3-propoxy-2-propanol 
• 105920-40-9 (3-Butoxy-phenyl)-carbamic acid 1-propoxymethyl-2-pyrrolidin-1-yl-ethyl ester 
• 105920-42-1 (3-Pentyloxy-phenyl)-carbamic acid 1-propoxymethyl-2-pyrrolidin-1-yl-ethyl ester 
• 105920-56-7 (3-Butoxy-phenyl)-carbamic acid 2-piperidin-1-yl-1-propoxymethyl-ethyl ester 
• 105919-59-3 (2-Butoxy-phenyl)-carbamic acid 1-propoxymethyl-2-pyrrolidin-1-yl-ethyl ester 
• 105920-44-3 (3-Hexyloxy-phenyl)-carbamic acid 1-propoxymethyl-2-pyrrolidin-1-yl-ethyl ester 
• 105920-58-9 (3-Pentyloxy-phenyl)-carbamic acid 2-piperidin-1-yl-1-propoxymethyl-ethyl ester 
• 143503-53-1 (3-Butoxy-phenyl)-carbamic acid 2-azepan-1-yl-1-propoxymethyl-ethyl ester 
• 105920-34-1 (2-Pentyloxy-phenyl)-carbamic acid 1-propoxymethyl-2-pyrrolidin-1-yl-ethyl ester 
• 105920-48-7 (2-Butoxy-phenyl)-carbamic acid 2-piperidin-1-yl-1-propoxymethyl-ethyl ester 
• 105920-60-3 (3-Hexyloxy-phenyl)-carbamic acid 2-piperidin-1-yl-1-propoxymethyl-ethyl ester 
• 105920-46-5 (3-Heptyloxy-phenyl)-carbamic acid 1-propoxymethyl-2-pyrrolidin-1-yl-ethyl ester 
• 143503-51-9 (3-Pentyloxy-phenyl)-carbamic acid 2-azepan-1-yl-1-propoxymethyl-ethyl ester 
• 105920-36-3 (2-Hexyloxy-phenyl)-carbamic acid 1-propoxymethyl-2-pyrrolidin-1-yl-ethyl ester 

Relevant academic research and scientific papers

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.

Ambient Hydrogenation and Deuteration of Alkenes Using a Nanostructured Ni-Core–Shell Catalyst

A general protocol for the selective hydrogenation and deuteration of a variety of alkenes is presented. Key to success for these reactions is the use of a specific nickel-graphitic shell-based core–shell-structured catalyst, which is conveniently prepared by impregnation and subsequent calcination of nickel nitrate on carbon at 450 °C under argon. Applying this nanostructured catalyst, both terminal and internal alkenes, which are of industrial and commercial importance, were selectively hydrogenated and deuterated at ambient conditions (room temperature, using 1 bar hydrogen or 1 bar deuterium), giving access to the corresponding alkanes and deuterium-labeled alkanes in good to excellent yields. The synthetic utility and practicability of this Ni-based hydrogenation protocol is demonstrated by gram-scale reactions as well as efficient catalyst recycling experiments.

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.

PERFUMES IN THE FORM OF AQUEOUS MICROEMULSIONS

Disclosed is a microemulsion of oil-in-water type including, preferably consisting of, by weight relative to the total weight of microemulsion: ? 70% to 94% of water, ? 1% to 15% of at least one hydrophobic fragrancing substance, ? 4% to 20% of at least one preferably volatile solvo-surfactant, and ? 0.1% to 15%, preferably 1% to 13%, of at least one hydrotropic agent or at least one surfactant selected from anionic surfactants, cationic surfactants, amphoteric surfactants and non-ionic surfactants. The solvo-surfactant is selected from monoalkylated glycerol derivatives of following formula (I): wherein the “alkyl” group is a linear or branched alkyl group including from 1 to 8 carbon atoms, and R and R′ are each independently H or a linear or branched alkyl group including from 1 to 5 carbon atoms, with the proviso that R is different from R′, and mixtures thereof.

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.

OXAZOLOBENZIMIDAZOLE DERIVATIVES

The present invention is directed to oxazolobenzimidazole derivatives which are potentiators of metabotropic glutamate receptors, particularly the mGluR2 receptor, and which are useful in the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which metabotropic glutamate receptors are involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which metabotropic glutamate receptors are involved.

Crystalline MWW-type titanosilicate catalyst for producing oxidized compound, production process for the catalyst, and process for producing oxidized compound by using the catalyst

A crystalline titanosilicate catalyst which is usable as a catalyst in the oxidation reaction of a compound having a carbon-carbon double bond and at least one other functional group, a process for producing the catalyst, and a process for producing an oxidized compound by an oxidation reaction using the catalyst. It has been found that a crystalline titanosilicate having a structural code of MWW effectively functions as a catalyst in an oxidation reaction of a compound having a carbon-carbon double bond and at least one other functional group, or a compound having a carbon-carbon double bond a functional group and having a total carbon number of not smaller than 2 and not larger than 5, wherein the carbon-carbon double bond of the compound is oxidized by using a peroxide as an oxidizing agent, thereby to highly selectively provide an intended oxidized compound.

Crystalline mww-type titanosilicate catalyst for producing oxidized compound, production process for the catalyst, and process for producing oxidized compound by using the catalyst

A crystalline titanosilicate catalyst which is usable as a catalyst in the oxidation reaction of a compound having a carbon-carbon double bond and at least one other functional group, a process for producing the catalyst, and a process for producing an oxidized compound by an oxidation reaction using the catalyst. It has been found that a crystalline titanosilicate having a structural code of MWW effectively functions as a catalyst in an oxidation reaction of a compound having a carbon-carbon double bond and at least one other functional group wherein the carbon-carbon double bond of the compound is oxidized by using a peroxide as an oxidizing agent, thereby to highly selectively provide an intended oxidized compound.

Synthesis, first structures, and catalytic activity of the monomeric rhodium(I)-siloxide phosphine complexes

Four new square-plane rhodium siloxide complexes of the general formula [Rh(cod)(PR3′)(OSiR3)] (where R = Me, i-Pr, O-t-Bu, R′ = Cy, Ph) were synthesized and the structures of three of them were resolved by the X-ray method. [Rh(cod)(PCy3)(OSiMe3)] (1) appeared to be a very efficient catalyst for hydrosilylation of allyl glycidyl ether to yield, selectively, 3-glycidoxypropyltriethoxysilane, a commercially important silane coupling agent. Catalytic measurements and stoichiometric experiments of 1 with triethoxysilane suggest a mechanism where an unsaturated Rh-H species is responsible for the catalysis.

An immobilized homogeneous catalyst for efficient and selective hydrogenation of functionalized aldehydes, alkenes, and alkynes

An immobilized cationic rhodium(I) catalyst bearing the diphosphine 1,1′-bis(diisopropylphosphino)-ferrocene (DiPFc, 1) allows efficient and chemoselective hydrogenation of a range of functionalized aldehydes, as well as alkenes and alkynes, under mild conditions. This heterogenized catalyst system is convenient to prepare, is stable to air and moisture over extended periods, and is readily recycled.