1809-14-9

Basic information

• Product Name: dioctyl phosphonate
• Synonyms: dioctyl phosphonate;Phosphonic acid, dioctyl ester;Dioctylphosphonat;PHOPHONIC ACID-DIOCTYL ESTER
• CAS NO: 1809-14-9
• Molecular Formula: C₁₆H₃₅O₃P
• Molecular Weight: 217-315-6
• EINECS: 217-315-6
• Mol File: 1809-14-9.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 381.265 °C at 760 mmHg
• Flash Point: 203.539 °C
• Appearance: /
• Density: 0.926[at 20℃]
• Vapor Pressure: 0mmHg at 25°C
• Water Solubility: 47.2mg/L at 20℃
• CAS DataBase Reference: dioctyl phosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: dioctyl phosphonate(1809-14-9)
• EPA Substance Registry System: dioctyl phosphonate(1809-14-9)

Safety Data

• Hazardous Substances Data: 1809-14-9(Hazardous Substances Data)

Usage

Flammability and Explosibility

Notclassified

InChI:InChI=1/C16H35O3P/c1-3-5-7-9-11-13-15-18-20(17)19-16-14-12-10-8-6-4-2/h20H,3-16H2,1-2H3

Upstream product

• 111-87-5 octanol 
• 762-04-9 phosphonic acid diethyl ester 
• 5843-26-5 tetramethylphosphorodiamidous acid 
• 124-07-2 Octanoic acid 
• 1809-19-4 dibutyl hydrogen phosphite 
• 41662-35-5 Phosphorochloridous acid dioctyl ester 

Downstream Products

• 103326-65-4 <α-Anilino-benzyl>-phosphonsaeure-di-n-octylester 
• 62343-55-9 [(2-{[(Bis-octyloxy-phosphoryl)-phenyl-methyl]-amino}-ethylamino)-phenyl-methyl]-phosphonic acid dioctyl ester 
• 145593-32-4 Pyridin-2-ylmethyl-phosphonic acid dioctyl ester 
• 598-02-7 Diethyl phosphate 
• 45163-08-4 phosphoric acid ethyl ester-octyl ester 
• 3115-39-7 phosphoric acid dioctyl ester 
• 32766-70-4 phosphoric acid butyl ester octyl ester 
• 52258-89-6 phosphorochloridic acid dioctyl ester 
• 6156-13-4 dioctyl ethylphosphonate 
• 1806-41-3 octyl hydrogen-(α-anilinobenzyl)-phosphonate 

Relevant articles and documents

New series of green cyclic ammonium-based room temperature ionic liquids with alkylphosphite-containing anion: Synthesis and physicochemical characterization.

A new series of 12 cyclic ammonium-based room temperature ionic liquids (RTILs) containing an alkylphosphite anion have been synthesized by an alkylation reaction between cyclic tertiary amines and dialkylphosphite. This method constitutes an eco-friendly

Lipid-mimicking phosphorus-based glycosidase inactivators as pharmacological chaperones for the treatment of Gaucher's disease

Gaucher's disease, the most prevalent lysosomal storage disorder, is caused by missense mutation of the GBA gene, ultimately resulting in deficient GCase activity, hence the excessive build-up of cellular glucosylceramide. Among different therapeutic strategies, pharmacological chaperoning of mutant GCase represents an attractive approach that relies on small organic molecules acting as protein stabilizers. Herein, we expand upon a new class of transient GCase inactivators based on a reactive 2-deoxy-2-fluoro-β-d-glucoside tethered to an array of lipid-mimicking phosphorus-based aglycones, which not only improve the selectivity and inactivation efficiency, but also the stability of these compounds in aqueous media. This hypothesis was further validated with kinetic and cellular studies confirming restoration of catalytic activity in Gaucher cells after treatment with these pharmacological chaperones.

Method for preparing phosphorus-based extreme pressure anti-wear agent capable of avoiding corrosion or rust formation on metal surface

The present invention relates to a method for preparing a phosphorus-based extreme pressure anti-wear agent, comprising: mixing phosphorus trichloride and benzene in a reaction bottle with nitrogen gas circulating in the bottle to obtain a reaction mixtur