2870-30-6

Basic information

• Product Name: sodium diethyl phosphate
• Synonyms: sodium diethyl phosphate;Phosphoric acid, diethyl ester, sodium salt;Phosphoric acid diethyl=sodium salt;Phosphoric acid sodium diethyl ester salt;Einecs 220-697-7;Phosphoric acid, diethyl ester, sodium salt (1:1);Diethyl Phosphate SodiuM Salt
• CAS NO: 2870-30-6
• Molecular Formula: C₄H₁₀O₄P*Na
• Molecular Weight: 176.083331
• EINECS: 220-697-7
• Product Categories: Aliphatics;Phosphorylating and Phosphitylating Agents
• Mol File: 2870-30-6.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 200.3oC at 760 mmHg
• Flash Point: 74.9oC
• Appearance: White Solid
• Vapor Pressure: 0.137mmHg at 25°C
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility: Methanol (Slightly), Water (Slightly)
• CAS DataBase Reference: sodium diethyl phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: sodium diethyl phosphate(2870-30-6)
• EPA Substance Registry System: sodium diethyl phosphate(2870-30-6)

Safety Data

• Hazardous Substances Data: 2870-30-6(Hazardous Substances Data)

Usage

Description

Sodium diethyl phosphate is an organic compound with the chemical formula (C2H5O)2PO2Na. It is a colorless liquid that is soluble in water and has a slight odor. Sodium diethyl phosphate is a derivative of phosphoric acid and is commonly used in various industries due to its unique properties.

Uses

Used in Cosmetic Industry:
Sodium diethyl phosphate is used as an ingredient in cosmetic compositions for treating keratin materials. It serves as a conditioning agent, providing smoothness and manageability to keratin fibers such as hair. sodium diethyl phosphate helps to improve the overall appearance and texture of the hair, making it an essential component in hair care products.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, sodium diethyl phosphate can also be used in the pharmaceutical industry as an intermediate for the synthesis of various drugs and pharmaceutical compounds. Its ability to interact with biopolymers and macromolecules makes it a valuable component in the development of new medications.

InChI:InChI=1/C4H11O4P.Na/c1-3-7-9(5,6)8-4-2;/h3-4H2,1-2H3,(H,5,6);/q;+1/p-1

Upstream product

• 108-85-0 1-bromocyclohexane 
• 2303-76-6 sodium diethyl phosphite 
• 64-67-5 diethyl sulfate 
• 1454305-46-4 diethyl 4-(trifluoromethyl)phenyl phosphate 
• 311-45-5 paraoxon 
• 2510-86-3 O,O-diethyl O-phenyl phosphate 
• 7301-86-2 cyclohexyl diethyl phosphate 
• 2737-00-0 n-butyl diethyl phosphate 
• 78-40-0 triethyl phosphate 
• 31268-20-9 bromomethyl phenyl sulfoxide 
• 135-02-4 ortho-anisaldehyde 
• 109-89-7 diethylamine 
• 76211-53-5 4-cyano-2-methylphenyl diethyl phosphate 
• 100-52-7 benzaldehyde 

Downstream Products

• 1080-32-6 O,O-diethyl benzylphosphonate 
• 2682-86-2 diethyl (pyridin-3-ylmethyl)phosphonate 
• 78-40-0 triethyl phosphate 
• 77047-42-8 4-<(diethylphosphono)methyl>pyridine 
• 107-49-3 Tetraethyl pyrophosphate 
• 1474-74-4 unsymm. Dimethyl-diethyl-pyrophosphat 
• 17323-83-0 Dinatriummonoethylphosphat 
• 136103-79-2 C₁₆H₂₄IO₄P 
• 119011-23-3 Phenylhydroxyiodonium diethyl phosphate 

Relevant articles and documents

New Triazole-Containing Branched Bis(dipeptidomimetic) - Switching from Self-Dimerization to Anion-Binding Properties

A triazole-containing branched bis(dipeptidomimetic) 2 using l -lysine as a flexible branching unit was synthesized and characterized. The compound was found to form weak dimers (K dim = 19 M -1) in chloroform as shown by vapor pressure osmometry (VPO) and concentration-dependent 1 H NMR studies. On the other hand, the compound was capable of binding chloride and monobasic diethyl phosphate (DEP) in chloroform. Job plot analysis, MALDI-TOF mass spectrometry, and NMR titration studies revealed a 1:1 binding stoichiometry with good binding affinities (K a ≈ 640-780 M -1). Structural studies using ROESY NMR spectroscopy and molecular modelling on the 2 -DEP complex indicated the adoption of a helix-like conformation by the host with the guest situated near the branching juncture.

Cetyltrimethylammonium hydroperoxide: An efficient reagent for promoting phosphate ester hydrolysis

Cetyltrimethylammonium hydroperoxide solutions are easily prepared by mixing cetyltrimethylammonium hydroxide and hydrogen peroxide and are very efficient in promoting paraoxon (diethyl p-nitrophenyl phosphate) hydrolysis.

Predicting the hydrolytic breakdown rates of organophosphorus chemical warfare agent simulants using association constants derived from hydrogen bonded complex formation events

Organophosphorus (OP) chemical warfare agents (CWAs) represent an ongoing global threat, through either purposeful environmental release or the need to dispose of historic stockpiles. This presents a need for the development of novel decontamination technologies. Due to the toxic nature and legal limitations placed on OP CWAs, the use of appropriate OP simulants that mimic the reactivity but not the toxicity of the agents themselves is vital to decontamination studies. Herein, we show that association constants derived from non-specific hydrogen bonded complexation events may be used as parameters within models to predict simulant reactivity. We also discuss the limitations that should be placed on such data.

Destruction of toxic organophosphorus and organosulfur pollutants by perpropionic acid: The first stable, industrial liquid water-miscible peroxyacid in decontamination

Use of commercial perpropionic acid (PPA), the first stable, industrial and water-miscible peroxyacid, allows the destruction of toxic organophosphorus and organosulfur compounds under micellar conditions. The destruction of paraoxon (O,O-diethyl O-p-nitrophenylphosphate), di-n-butyl sulfide and 2-chloro-2′-phenyldiethyl sulfide has been studied.