15336-73-9

Usage

Uses

Used in Flame Retardant Industry:
DIETHYL (1-HYDROXYETHYL)PHOSPHONATE, 97 is used as a flame retardant to enhance the fire resistance of materials, thereby improving safety standards in various applications.
Used in Plasticizer Industry:
As a plasticizer, DIETHYL (1-HYDROXYETHYL)PHOSPHONATE, 97 is employed to increase the flexibility and workability of plastics, making them more suitable for a range of manufacturing processes.
Used in Polymer Stabilization:
DIETHYL (1-HYDROXYETHYL)PHOSPHONATE, 97 is used as a stabilizer for polymers to prevent degradation and extend the lifespan of plastic products.
Used in Agricultural Chemical Production:
In the agricultural sector, DIETHYL (1-HYDROXYETHYL)PHOSPHONATE, 97 is utilized in the production of chemicals that aid in crop protection and enhancement of agricultural yields.
Used as an Intermediate in Organic Synthesis:
DIETHYL (1-HYDROXYETHYL)PHOSPHONATE, 97 serves as an intermediate in the synthesis of other organic compounds, contributing to the development of new chemical products and innovations.
Used in Metalworking Fluids Manufacturing:
DIETHYL (1-HYDROXYETHYL)PHOSPHONATE, 97 is used in the manufacturing of metalworking fluids to improve the performance and longevity of these fluids in industrial applications.
Used as a Solvent in Pesticide Production:
In the pesticide industry, DIETHYL (1-HYDROXYETHYL)PHOSPHONATE, 97 is employed as a solvent to facilitate the production and application of effective pest control agents.

InChI:InChI=1S/C6H15O4P/c1-4-9-11(8,6(3)7)10-5-2/h6-7H,4-5H2,1-3H3

Upstream product

• 117365-25-0 diethyl α-tert-butoxyethylphosphonate 
• 75-07-0 acetaldehyde 
• 122-52-1 triethyl phosphite 
• 919-19-7 diethyl acetylphosphonate 

Downstream Products

• 87278-63-5 diethyl α-(2-nitro-5-hydroxyphenoxy)ethyl phosphonate 
• 1023289-17-9 diethyl 1-(4-nitrobenzenesulfonyloxy)ethylphosphonate 
• 86099-56-1 α-(O,O-diethylphosphono)ethyl α'-4-(5'-trifluoromethylpyridin-2-yloxy)phenoxypropionate 
• 54788-35-1 diethyl 1-aminoethylphosphonate 
• 124811-02-5 {1-[1-(3-Trifluoromethyl-phenyl)-eth-(E)-ylideneaminooxy]-ethyl}-phosphonic acid diethyl ester 
• 124811-01-4 {1-[1-(2,4-Dichloro-phenyl)-meth-(E)-ylideneaminooxy]-ethyl}-phosphonic acid diethyl ester 
• 145459-66-1 (1-{N-[5-(2-Chloro-4-trifluoromethyl-phenoxy)-2-nitro-phenyl]aminooxy}-ethyl)-phosphonic acid diethyl ester 
• 78-38-6 ethylphosphonic acid diethyl ester 
• 55264-86-3 diethyl 1-(tosyloxy)ethylphosphonate 
• 55264-89-6 diethyl (1-(phenylthio)ethyl)phosphonate 
• 1188266-63-8 C₁₃H₁₉O₅P 
• 705302-86-9 C₁₃H₁₉O₅P 
• 475207-81-9 (S)-diethyl-1-hydroxyethanephosphonate 

Relevant academic research and scientific papers

Hydrogenation of α-oxophosphonates with molecular hydrogen catalyzed by palladium on carbon carrier as synthesis procedure for α- hydroxyphosphonates

Hydrogenation with molecular hydrogen of substituted benzoylphosphonic acids ethyl esters provides a convenient preparation method for diethyl [hydroxy(aryl)methyl]phosphonates. Both the palladium on activated carbon and the palladium immobilized in a chitosan matrix applied on a carbon carrier sibunit can be employed as catalysts.

The preparation of dialkyl 1-hydroxyalkylphosphonates in the reaction of trialkyl phosphites with oxonium salts derived from aldehydes or ketones

The reaction of trialkyl phosphites with aldehydes or ketones in the presence of hydrogen chloride gives dialkyl 1-hydroxyalkylphosphonates via Arbusov-like reaction of oxonium salts derived from aldehydes or ketones. This reaction is a very convenient instant method for the preparation of dialkyl 1-hydroxyalkylphosphonates with a good yield as an alternative to the well-known Abramov reaction. Georg Thieme Verlag Stuttgart.