3084-47-7

Usage

Uses

Used in Organic Synthesis:
TRI-N-AMYL PHOSPHINE OXIDE is used as a solvent and in organic synthesis for its ability to dissolve a variety of substances and facilitate chemical reactions.
Used in Pharmaceutical Production:
In the pharmaceutical industry, TRI-N-AMYL PHOSPHINE OXIDE is utilized in the production of various pharmaceuticals, contributing to the synthesis of medicinal compounds.
Used in Polymer Production:
TRI-N-AMYL PHOSPHINE OXIDE is also employed in the creation of polymers, where it aids in the formation of complex polymeric structures.
Used as a Catalyst:
TRI-N-AMYL PHOSPHINE OXIDE serves as a catalyst in numerous chemical reactions, enhancing the rate of these processes without being consumed in the reaction itself.
Used as a Reagent:
Furthermore, it is used as a reagent in a variety of chemical processes, playing a crucial role in the analysis and synthesis of organic compounds.

InChI:InChI=1/C15H33OP/c1-4-7-10-13-17(16,14-11-8-5-2)15-12-9-6-3/h4-15H2,1-3H3

Upstream product

• 110-53-2 1-Bromopentane 
• 10496-10-3 tripentylphosphine 
• 79-92-5 camphene 

Relevant academic research and scientific papers

Single-stage synthesis of alkyl-H-phosphinic acids from elemental phosphorus and alkyl bromides

Elemental phosphorus (red or white) reacts with alkyl bromides at 60–62 °C in the phase-transfer catalytic system KOH/H2O/PhMe/Et3BnNCl to afford alkyl-H-phosphinic acids in up to 47% yield.

Effect of electrolysis conditions on the process of anodic oxidation of tertiary phosphines in the presence of camphene

Anodic oxidation of tertiary phosphines (Et3P, Pr3P, Bu3P, i-Bu3P and Am3P) in the presence of camphene and heterogenic base (trisodium phosphate) on platinum anode in acetonitrile solution of sodium

Preparation of epoxides from olefins using bis(triorganosilyl) peroxides in the presence of activators based on metallic acid derivatives

PCT No. PCT/EP97/00982 Sec. 371 Date Sep. 2, 1998 Sec. 102(e) Date Sep. 2, 1998 PCT Filed Feb. 28, 1997 PCT Pub. No. WO97/32867 PCT Pub. Date Sep. 12, 1997Epoxides are prepared from olefins using bis(triorganosilyl) peroxides in the presence of activators based on metalic acid derivatives of the formula where M is a metal of transition groups IV to VII, in particular molybdenum, tungsten or rhenium L is an uncharged ligand selected from the group consisting of amine oxides, phosphine oxides, arsine oxides, phosphoric triamides, formamides and pyridine N-oxides X is an inorganic ligand x is from 1 to 5 y is 0, 1 or 2, Z is 1 or 2 and n is 1 or 2.

SUPERBASE-INDUCED GENERATION OF PHOSPHIDE AND PHOSPHINITE IONS AS APPLIED IN ORGANIC SYNTHESIS

A series of new direct reactions of red phosphorus (or white) with organyl halides, alkenes and acetylenes have been developed.Reactions occur in superbasic systems, such as alkali metal hydroxide-dipolar aprotic complexing solvent (DMSO, HMPA) or under phase-transfer conditions to afford earlier inaccessible triorganylphosphines and -phosphine oxides including unsaturated ones in good yield.